LDN Video Interviews and Presentations

Radio Show interviews, and Presentations from the LDN 2013, 2014, 2016, 2017, 2018 and 2019 Conferences

They are also on our    Vimeo Channel    and    YouTube Channel

Dr Deanna Windham, LDN Radio Show (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Dr Deanna Windham shares her Low Dose Naltrexone (LDN) experience on the LDN Radio Show with Linda Elsegood.

Dr Deanna Windham currently works in the Whisker Wellness Institute in California, the United States. She and her institute first heard of Low Dose Naltrexone (LDN) around 12 years ago while establishing their adjunctive cancer treatment program.

However, the process by which she could obtain LDN was difficult. Nevertheless, Dr Bihari phoned Dr Windham to explain the many benefits LDN can have for cancer patients.

At her institute, Dr Windham has established a tried-and-tested prescription program of LDN to ensure that each individual patient starts on the correct dosage of LDN for them personally in order to reap the best possible benefits.

This is a summary of Dr Deanna Windham’s interview. Please listen to the rest of Dr Windham’s story by clicking on the video above.

Dr David Borenstein, LDN Radio Show 28 Dec 2016 (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Linda Elsegood: Today we are joined by Dr. David Bornstein.  Thank you for joining us, David. 

Dr David Borenstein: Thank you for having me. 

Linda Elsegood: For those people who haven't heard of you yet, could you tell us how you got involved in LDN? 

Dr David Borenstein: Absolutely. I'm an integrative physician. My office is in Manhattan, right here in New York; and about ten years ago, I had a patient come to me who was interested in being put on this medication known as LDN, low dose naltrexone.

Now the first thing I said was, like many people who do not know about LDN is, “Oh, we use naltrexone for drug addiction. What's this LDN?” And he said to me that he would give me literature, and I said, you know what, let me take a look at it; and on your next visit, we can talk about prescribing it.

I did some research. I made a few phone calls. And I said, okay, let me give this a try. And the patient just wanted it for general health. They didn't want it for any particular disease. So I prescribed it, and he was happy. No side effects; work beautifully. And then I had patients come in with various different abnormalities or diseases: Crohn's, MS. So I decided to try it for these patients; and lo and behold, two, three, four, five patients, they're doing okay. The patients with MS weren’t progressing, the Crohn's patients are getting better. I put a few patients who had cancer on it, and I started using it, gaining experience with it. And now it's a very big part of my practice. All thanks to that patient who came in ten years ago. 

Linda Elsegood: I can see on your website a list of conditions.  There’s thyroid, autoimmune, menopause, andropause, hormone imbalance, adrenal fatigue, chronic fatigue syndrome, fibromyalgia, chronic pain, polycystic ovary syndrome, insomnia, sleep disorders, metabolic syndrome, obesity, Crohn's disease, irritable bowel, yeast overgrowth, candida, and allergies. That is quite some list. How do you go about assessing patients to see whether they are suitable for LDN? 

Dr David Borenstein: Well, first of all, any patient who comes to see us gets a complete history and physical examination, and then we evaluate their condition.

We go over the lab work. At that point, I can discuss with them if LDN would be something they would want to consider. Now, remember, when they're coming to see me, they have many different symptoms: fatigue, weight gain, hair loss, dry skin, constipation, depression, mood swings, irritable bowel. They can have a laundry list of different symptoms. So what we first need to do is just evaluate, and treat these different symptoms. And then, especially on the first visit, it's a very long visit and we have to go over many things. I generally don't bring LDN up at the first or second visit. I usually wait until a couple of visits down the road, especially to monitor their response.

I mean, I don't want to use it initially for a first-line unless there are other things we can treat.  At that point, a couple of visits later, we see how the clinical condition of the patient is improving or not improving, and then we can throw in LDN. And now remember, most of these people coming to me have no idea what low dose naltrexone is. A few do; I’d say less than 10% of my patients know exactly what I'm talking about. The other 90% have a natural inclination. And what did they tell me? I will Google it. It's the first thing:  I will Google it. I say beautiful, Google it. I give them a couple of websites, give them your website. I give him some keywords to use, and 90% of the time they come back and say, “I want this.” 

Okay, what conditions do we popularly treat with low dose naltrexone Crohn’s, any inflammatory bowel disease, irritable bowel disease, multiple sclerosis; Parkinson's is very popular; fibromyalgia, and chronic fatigue - it's a biggie now, and we have a lot of that, as well as certain types of malignancies that a lot of patients come in for, for LDN. As you can see, we can treat a wide variety of diseases. But we generally have either autoimmune disorders, or malignancies, or certain neurological disorders. Those are the most common reasons for me to put patients on LDN.  

Linda Elsegood: We have a caller here, called Christina, who would like to discuss LDN with you. Would you like to ask your question, Christina, yes? 

Patient: Hi. Thank you. Can you guys hear me? 

Linda Elsegood: We can; or I can, yes. 

Patient: Yes. So, doctor, I have a few things. I have postpartum thyroiditis, I have hypothyroidism, I have pericarditis. And I have Sjogren's syndrome. I started LDN, and I was on it for about a month, and I got very sick. I got flu-like symptoms, a burning feeling in my stomach, and all of my symptoms came back. I also have vertigo, so they think it's autoimmune, inner ear disease. So my chest pain came back, and my vertigo came back, and I went off of it because it got intolerable. I've read a lot that starting off on a very low dose and working slowly can be beneficial. My doctor doesn't want to do that because he feels that it isn't a therapeutic dose unless it's at least 1.5 mg. So I've read a lot of posts in forums, about LDN, where people have had to try three or four times before they can successfully be on LDN; and that they could have a Herxheimer reaction. And, I did the very sensitive test for Lyme, and I am negative for Lyme. So I'm wondering, is a Herxheimer reaction something that does often occur with LDN? And have you found that people have had to go on it several times before they can successfully be on it? And is a low dose, very low dose, like 0.5 mg beneficial?

Dr David Borenstein: Well, it's a very good question. The first thing I would tell you to do is before you even consider the LDN, is you seem to be having some reaction. I think you need to clear up some of the other issues that you're having. For example, you mentioned to me the Hashimoto's. I think that when I hear Hashimoto's, I hear autoimmune. The first thing I would strongly recommend, way before taking LDN, is cleaning up your gut: I can't stress the importance of gut health. You have to clean up your gut. And what do I mean by that? I mean, adding things like probiotics, digestive enzymes, gut change to improve your gut function; looking to see if you have any parasites, bacteria, any sort of viruses.

Gut health is extremely important in treating autoimmune disease. I'd also recommend some treatments possibly for candida, yeast overgrowth. Looking to see if you have leaky gut, and if you have an autoimmune disease, by definition you probably do have leaky gut, and treating the leaky gut with a gluten-free diet, cleaning it up with adding things like L-glutamine and zinc and aloe, and all these sorts of things. So I think the first approach is, before you even consider going on LDN, is cleaning up the gut. Now, that's a lot harder to do than what I just said. I mean, it takes a lot of work; and you would probably need to find some sort of practitioner to help you with this. But again, cleaning up the gut is key to success with LDN. That's number one. Now, starting LDN, even at a very low dose after that's done, I think the issue is not so much the therapeutic effect. You need to build up your LDN tolerance. So even if 0.5 mg may not be very therapeutic, I don't think that matters. I think you just need to build up the dose so you can get up to a therapeutic dose, and I agree you're probably not going to get very much benefit below 1.5 mg. Maybe not, but I think you just have to have the ability to grow tolerance. So the quick answer is clean up your gut, to start slow, work your way up, and you'll get there.

Patient: All right. Thank you, Doctor. Do you notice that you see a Herxheimer reaction, or flu-like symptoms in patients that maybe start to build up too quickly? 

Dr David Borenstein: It's very rare. You know, when I start patients off at 1.5 mg, and then I go up to 3 mg; and after that, it depends on their condition. For example, with MS I don't try to go up above 3.0 mg unless I have to, because there are issues with spasticity; and remember, we always talk about doses. We have to remember these are doses, but it's going to be different for every person. A person who is 250 pounds is going to need more than someone who's 150 pounds. So you give them the same dose, okay; when you go per kilogram, it's a very different dose. So we have to also remember that. In all the LDN pages, and on the Facebook pages and the Yahoo groups, they will talk in doses. And the problem is it's not the most accurate way of dosing, because you need to consider the weight of the patient as well. So 1.5 mg for me is going to be very different from 1.5 mg for you or another person. That's also another important point to remember when prescribing LDN. Also, some of the practitioners like to go up to 4.5 mg.  I like to keep it a little bit below that. We're finding that you're getting the opioid blockade at around 4.0 mg, and after that, it's not as effective. So recently, in the past year, year and a half, I've been keeping my maximum dose to about 4.0 mg; and I don't really go above that unless the patient has been on LDN 4.5 mg for many years. I don't want to touch it. I leave it alone. 

Patient: Okay, and thank you. I appreciate it. Could I just ask one more quick thing? I do a lot of great things for gut health, the L-glutamine and probiotics; and I stay away from gluten and dairy completely. Could you explain a little bit about how one would go about testing for parasites, bacteria and viruses? 

Dr David Borenstein: There is a test called the CDSA 2.0, from a company in North Carolina; I'm trying to remember the name of the company. I use it all the time, I can see the box. But these are special stool kits you can get, and actually, insurances will help pay for a part of the test. You collect a stool sample for three days. The test looks for parasites. It looks for your digestive enzymes. It looks to see how well you're absorbing food. It looks for bacteria and other viruses. It's a very good test. It's called a CDSA 2.0.

Patient:  Great. Thank you so much, doctor. 

Dr David Borenstein: My pleasure. Thank you. 

Patient: Bye-bye. 

Linda Elsegood: Well before we go to the break, I have another question here that's come in. It's from Susan, and she says, “When do I need to stop taking LDN prior to a minor medical procedure which requires anaesthesia?”

Dr David Borenstein: Excellent question. We know that LDN and its metabolites have a half-life of approximately 59 hours. So 60 hours; you know, technically it's two and a half days. I would at a minimum do probably a week before, and that would be a minimum I would do. Yeah, I'd say two and a half days; or at least about a week before you'd play it safe. And that would be  a good thing to do, especially if you're receiving any sort of narcotics before or after the procedure. So I just say a good solid week would be a good number. You know, you can do a little more. Wouldn't hurt, but I think to keep it safe at least a week. 

Linda Elsegood: And how long would you say to wait after you'd had narcotics before you restarted LDN 

Dr David Borenstein: Let's see, two and a half days. So I would say at least five days afterwards would be a good number. From the last point of taking a narcotic. 

Linda Elsegood: Okay. Thank you. We'll just have a quick break. If anybody would like to call in with their questions or email them, and we'll be back in a moment. 

The LDN research trust is very proud of the LDN book, which was launched at the LDN 2016 conference in Orlando, and it's been a great success, not only for the medical profession but for patients wanting to learn more about low dose naltrexone. Full details can be found on the homepage of the LDN Research Trust. Discounts are available on bulk orders of the book, which is ten or more. The details: Contact us, telling me how many copies you wish and where you live. I will then be able to get Chelsea Green Publishing to contact you.

Belmar Pharmacy is a nationally respected compounding pharmacy. They compound low dose naltrexone, LDN; bio-identical hormones, and custom amino acids, mineral blends. They're based in Colorado and ship nationwide. Their goal is better patient outcomes through quality compounding, combining effective communication between practitioner, pharmacist, and patient.  Call +1 800-525-9473 or visit Belmarpharmacy.com.

Okay. Welcome back. I have a question here for you, David, from a  lady in Turkey or a gentleman. They have a five-year-old son who was diagnosed with nephrotic syndrome at age three. He takes 4 mg of steroid every other day. They would like him to try LDN, but the doctor said no. And through a year, they've looked for a doctor who would prescribe LDN, without success. They say their son's on steroids, and it's very troublesome. He becomes very sick easily at home, and next year he starts school. So they would like to find a permanent solution. The question was, can LDN be prescribed for a child who takes 4 mg of steroids; and do the steroids affect the LDN.

Dr David Borenstein: Well, the second question first. Yes, it can, and that's why I like to keep the steroid dose as low as possible.  In adults, I like to keep Prednisone below 10 mg per day as a rule, and that's just an arbitrary number. I just find that it works best below 10 mg a day. Many of my patients have a lot of autoimmune immune disease and are on much higher doses. So what I do is I start them on LDN, and I have them slowly taper their Prednisone while the LDN is kicking in, in the hopes that, as the LDN dose increases and the steroid dose decreases, the LDN will start working. So far, it's worked pretty well.

Now with kids, you have to be very, very careful, especially for nephrotic syndrome. And you would need a physician to really keep on top of this. But you could, in theory, try the LDN, 80 micrograms per kilos. You do depend on the weight. He's probably gonna need a lot less than most adults would. And with a child, they tend to like to use the transdermal  - just easier to use. And you can certainly give it a try, but again, you're going to have to be under very close care of a physician when you're doing this, to make sure that everything is being watched. This is very different from a patient who's just taking it for fibromyalgia or for Crohn’s. You can have some flexibility. But with a child, you have to really keep on top of them. I definitely think it's worthwhile to try it and see if it has an effect; but remember, you have to keep on top of this, and finding a physician who's going to do that is not going to be easy. People have had a lot of trouble finding physicians prescribing LDN, just to get it for whatever disease they have. But for a child, needing constant watching, that's going to be a little bit tricky.

Linda Elsegood: Especially in Turkey where I think it's very, very difficult to get LDN prescribed anyway. 

We also had a question from Taja, and she says that she was diagnosed with rheumatoid arthritis in December 2015 and she started LDN in March. Her questions, she's got three. The first one is, do anti-inflammatory drugs have an effect on the efficacy of LDN?

Dr David Borenstein: They generally don't. The main issue when you're taking low dose naltrexone is going to be high dose steroids. Not so much the nonsteroidal anti-inflammatories, generally not. But here's the problem. When you're taking a lot of NSAIDs or nonsteroidal anti-inflammatories, it's not good for you.

It's not good for your liver, it’s certainly not good for your kidneys, and certainly not good for your stomach. So LDN would certainly be of benefit to try to help reduce your need for these anti-inflammatory medications, but they're not going to interfere with LDN. 

Linda Elsegood: And the second question is, have you seen any difference in how LDN works on patients following an anti-inflammatory diet?

Dr David Borenstein: Yes, no question, diet is key to helping patients with rheumatoid arthritis and other autoimmune diseases. Now, what do I mean by that? I mean, I always talk about LDN being a tool, not a cure of disease. It's a tool that one can use to help treat disease. Now, if you can approach disease in multiple different ways, then, of course, there's going to be a much better response. So diet is key, especially in rheumatoid arthritis. With diet, we want to make sure that the patient, especially with rheumatoid arthritis, keeps away from nightshades - tomatoes, potatoes; working on fixing the leaky gut we are treating, having a gluten-free diet. These are very key components for fixing the gut. Probiotics, digestive enzymes, stomach acid. And again, looking for parasites and bacteria in the gut. Treating the gut is extremely important in rheumatoid arthritis and other autoimmune diseases. That in combination with low dose naltrexone is a very powerful tool for treating rheumatoid arthritis and other autoimmune disorders.

Linda Elsegood: Okay. And her third question was, I take 4.5 mg of LDN. Should I change the dose if I feel my symptoms increasing? And if so, in what direction? 

Dr David Borenstein: Well, I don't know the patient's weight or their age, so I really couldn't give a super-accurate answer. That being said, you're not going up.

I mean, that's it. 4.5 mg is the max. As a matter of fact, I would probably recommend the patient lower the dose down to 4.0 mg. I wouldn't be surprised if the response improves, because if you lower the dose to 4.0 mg there may be a more effective opioid blockade. So I would probably give a trial of lowering the dose to around 4.0 mg, not 4.5 mg and see if that works a little bit better, especially if the patient is low weight. 

Linda Elsegood: Thank you. And we have a question from Jen, and she says she has MS, and she has taken LDN for three months with some improvement to her bladder.

She said she started at 1.5 mg, then increased to 3.0 mg.  Should she increase the dose or wait longer, because she's only had some improvement to the bladder? Nothing else. 

Dr David Borenstein: Okay. Well, here's the thing with MS. You have to be concerned about spasticity. Many times we have patients with MS, they have spasticity, but if spasticity is not getting worse, then you can experiment with going up at very small doses - 3.25 mg try that for a little while. Then go up to 3.5 mg, and you can go up a little bit till the spasticity increases. And that's probably the max you want to take.

So yes, that would probably be a way to go. Now, remember, although we've had patients who felt better, the goal in low dose naltrexone for MS is more to prevent exacerbations and to keep disease stable, rather than actually feel a little bit better. So if you had numerous exacerbations in the past, LDN in many cases would prevent exacerbations. If it prevents exacerbations, then LDN has done its job. Okay. So it's more for preventing the disease from coming back and halting in its tracks rather than feeling better. So three months is a little bit short. We'd have to see over a longer period of time. I don't know how many exacerbations this patient has. So the answer will be if the patient has fewer exacerbations than she did, we know the LDN is probably doing its job.

Linda Elsegood: Okay. Thank you. We have another question from Paula, and she asks if LDN is a problem with candida? She took <a medication> to help and it allowed her to get up to 4.5 mg. She stopped the <medication> several months later and some of her old autoimmune symptoms have returned. She says, “Am I getting symptoms of candida, and what would you suggest I do?” 

Dr David Borenstein: Well, the first thing I want to do is, and sometimes patients with severe candida can have problems with LDN. I think the thing you have to do is just clean out your gut and especially with candida. The same treatments that we have getting gluten and dairy-free diets, keeping away from fruits that can contribute to candida, and we all know what they are.

Anything that tastes good or isn’t good for you, it's probably good for candida. And some doctors give a course of Diflucan for a period of a month or two, that may be beneficial. It's not a cure, but it can give what I call an artillery barrage to at least lower the symptoms and then change your ability to do with the candida, with dietary changes and other supplements, cilantro, oregano, garlic, all very good for treating candida.

And just one more, which. I have a little bit of a mental block, but it also works - berberine, berberine-containing substances are very good for treating candida. Treat the candida for a month or two, even three, and then try and restarting the LDN and you'll probably get a better response.  

Linda Elsegood: and we have a question here from Alec. She says, “Could LDN help with prostate cancer and other prostate issues?” 

Dr David Borenstein: We've had patients with prostate cancer who've taken LDN. However, again, when you're treating cancer, you have to use a very combined approach. I've had patients who basically have prostate cancer, but they're not treating it because it's either low-grade cancer or its small cancer, and they don't want treatment yet, but it's certainly worth a try. And as long as your PSA doesn't go up and there are no changes in a digital examination, it's certainly something to consider. That being said, if the patient has received hormone treatments, those who are in a later stage or towards the end stage of receiving hormone treatment, we’re finding the LDN really doesn't work too well with that subset of patients. But as a rule, it's certainly worth a try, as long as you follow the rules, keep away from opioids and do the proper dosing. I think the question is, do you tell your oncologist about it? People ask me this all the time, and you know, I would, and just explain to your oncologist, or your urologist that you're on it and just give them a five-minute debriefing. Bring them some literature. But a lot of the time, urologists and oncologists are not crazy about it. But there'll be someone understanding at least in 2016, 2017. Ten to fifteen years ago, forget about it. Everyone’s mind was closed. I think we're living more open-minded today. So, again, short answer, you should always use LDN with the knowledge that your attending physician, your oncologist, your primary care doctor, whoever's treating you should probably know about LDN and that you're taking it, and just make sure that you don't only use LDN if it's something serious, a more serious disease. Because again, there are other treatment options available for more serious disease.  

Linda Elsegood: And we have a question from Leanora. She says, “What are your thoughts on LDN and a person's genetics, SNPS, and methylation pathways. Are you familiar with MTHFR, COMT, or SNP called CYP-2-D-6?” 

Dr David Borenstein: Well, here's the thing with the MTHFR and the other genetic mutations, there's no problem using LDN with that. You do have to treat the issues of those particular mutations. For example, I'm going to use MTHFR, because that's certainly by far the most common that we see. How do you treat the MTHFR? Even this is controversial, and I think this is going to change, so this is not in stone. When we have MTHFR gene mutations, you have to first evaluate to make sure homocysteine levels are normal. This other test you can use, I'm not allowed to use it in New York state, but there are better ways of checking homocysteine levels than just measuring homocysteine, but that's the tools we have, we have to use it. And making sure that you have the B-6, B-12 and methyl folate - make sure that in all your vitamins there is methyl folate - and use trimethylglycine and cleaning up the gut to detoxify.

So that's the best you can do. That being said, if you do all that and use the LDN, there shouldn't be any issues.

Linda Elsegood:. Okay. And she said, “Would know a person's genetic hiccups help determine the dose of LDN.”

Dr David Borenstein: Not really. We've been dosing LDN well before MTHFR became popular, well before. And I know Dr. Bahari when he was doing it, I, I speak with his wife from time to time also, who is in New York; and again, in the eighties and the nineties, we didn't really use MTHFR, and nothing changed. I mean, the dose is going to be basically based on the disease you have, your weight, and your tolerance. MTHFR and other genetic mutations are really not gonna make a big difference in the way we dose you. 

Linda Elsegood: Okay. And she has another question, and she says” Have you seen success with LDN and endometriosis?”

Dr David Borenstein: I generally don't use LDN for endometriosis. Remember, endometriosis by definition, in most cases, is an excess of estrogen: estrogen dominance, as opposed to anything LDN would treat. So when I have endometriosis, I have to look for estrogen dominance and balancing the hormones. So I really wouldn't be using LDN for that.

There are many other things you can do to improve your hormone balance, like measuring the hormones, either through salivary testing; you can do urinary testing; in some countries, all you have is blood testing. And you have to do it on certain days of the month, balancing the hormones. And in most cases, the problem is either too much estrogen to too low progesterone or both. So balancing the estrogen, treating insulin resistance, and that's a biggie. And once you do that, that tends to be some sort of improvement in the endometriosis. So I would do that before throwing LDN at the problem. 

Linda Elsegood: Okay. And she has one more question, and it says, “LDN might not always help or improve a person's condition, but are you aware of any conditions that are known to exacerbate, or worsen, a condition or disease?

Dr David Borenstein: I have not seen that. I've only seen certain side effects from taking LDN - the vivid dreams, the difficulty sleeping, the increasing candida, and Herxheimer reaction. But I've never seen a condition get worse from the LDN. Now, of course, diseases do progress naturally, and if you don't treat them, they tend to get worse, not get better. So many times, this is the natural course of the disease. But as a rule, no, I've never—seen any detrimental effects from LDN. 

Linda Elsegood: Okay, lovely. Well, we'll just have a quick break, and we'll be back in a moment.

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Belmar pharmacy is a nationally respected compounding pharmacy. They compound low dose naltrexone, LDN; bio-identical hormones, and custom amino acids and mineral blends. They're based in Colorado and ship nationwide. That goal is better patient outcomes through quality compounding, combining effective communication between practitioner, pharmacist, and patients. Call +1 800-525-9473 or visit Belmarpharmacy.com.

Welcome back. We have some questions here from Dr Leonard Weinstock, and he says, “Have you measured pre and post LDN antithyroid antibody levels?” 

Dr David Borenstein: Well, the answer is yes, we have, because anytime I have a patient who has Hashimoto's and hypothyroidism, I always measure their antibodies. So, and as a rule, they come down, and they can come down sometimes quite quickly. And you have to be very careful with these patients because if you have them on thyroid medication and their antibodies come down, and the amount of medicine they take may be the same, but their antibodies come down. That can actually cause them to become hyperthyroid. Think of it as driving a car and all of a sudden you're driving with the accelerator halfway down and the brakes halfway down, right?

So all of a sudden you're lowering the antibody, so the brakes, you're reducing the brake and what happens - the car zooms forward. That's exactly what happens. So you have to watch it, and watch it closely. Now here are some of the problems we have in monitoring the antibodies. Many of my patients’ antibodies are through the roof and the lab that I use, which is a very common lab that most integrative doctors in the New York area use, if it's above a certain level - if the anti-TPO is above a thousand and an antithyroid globulin is above 3000, it just says greater than a thousand, greater than 3000. So if the antibodies dropped from 5,000 down to 3,500, I have no way of knowing that. All I'm seeing is that it's above 3000 or when it gets below 3000, and I can see if it's dropping or not. But as a rule, LDN is a very effective tool for treating Hashimoto's, and the antibodies can drop, and it can drop quickly, so you have to watch these antibodies very closely to make sure the patient does not become hyperthyroid. Now, if the patient's not taking any thyroid medication, then it's a very different story than if it drops, it drops, and then you have to still watch them make sure that they're not becoming hyperthyroid, but it's less of a concern because they're not taking any thyroid medication.

Linda Elsegood: Just out of interest, how often do you check the levels if they're on thyroid medication? 

Dr David Borenstein: It depends. If they're on LDN and I'm starting it, I probably would do it every four to six weeks, and I tend to be very, very conservative in the way I give the LDN. I like to start off at 1.5 mg, and then after a month go up to 3 mg and then go to 4.0 mg. However, sometimes I'll do it a little bit slower than that. Especially when I know the antibodies can drop quickly and they're on a high dose of thyroid medication. So you do it very, very slowly. Sometimes I'll just put them at 1.5 mg and have them come back in two months to see how the levels are. And then, all right, they've dropped, we're going to put you on 3.0 mg. But you know what? We're going to change your medications a little bit. Drop your medications a touch, come back in two months. But when we do it that way, you require a lot of constant monitoring. That's the best way to do it. And the safest now, thank goodness, no problems, but you know, there's a theoretical risk of hyperthyroidism, which you have to watch out for.

Linda Elsegood: Okay? And he also says, “What are your thoughts on using low dose oral methylnaltrexone for systemic inflammatory conditions without CNS pain?”

Dr David Borenstein: You know, generally I don't use it. Most of the time I use straight LDN, and I treat those other conditions other ways. As I said, I don't use the LDN only for treating pathology. I use various different ways to reduce inflammation, and there are many different ways we can reduce inflammation in outpatients. Obviously diet is very big. We know that certain foods are more inflammatory than others. High fructose corn syrup is huge. Red meats, certain nuts are huge. Dairy is huge. All inflammatory foods, so you want to change that. Use of anti-inflammatory supplements like fish oil, curcumin, Boswellia, bromelain; there are many different supplements you can take to reduce inflammation. One of the least evaluated, but very, very commonly associated with inflammation, believe it or not, is insulin. Insulin - you have to be very careful with insulin. We know that people who have hyperinsulinemia are very inflamed, and a lot of doctors aren't aware. Physicians treat blood sugar. They look at glucose. They never look at insulin. And while there is a relationship between the two, it's certainly not direct. You can have perfectly normal blood sugar and very high insulin, and that insulin can be very inflammatory. So I like to treat inflammation, look at the root cause of the inflammation, and then I add the LDN to help for any other issue that we're treating.

Again, not the primary treatment for what I do. But it's just a tool that aids in helping me treat disease. 

Linda Elsegood: And he had one more question, “Did Dr Bihari compare measurements of enkephalins with PM versus AM dosing of LDN?” 

Dr David Borenstein: I believe he may have, and it's usually about a third. As I remember, about a third less in the afternoon than in the evening. So, for example, let's say 2:00 AM in the morning is when you have the peak. It's probably three times as much at two in the morning than it is at two in the afternoon, at least three times, maybe a little bit more than that. That's why we don't recommend taking LDN in the morning. I have this question asked all the time because you don't have anywhere near the amount of endorphin peak at 2:00 PM in the afternoon than you do at 2:00 AM in the morning.

Linda Elsegood: Okay. We have another question here. Can you explain how LDN effects and regulates Th1 and Th2 rather than boosting either one?

Dr David Borenstein: Here's the thing. I've seen the charts on them, and it's probably better to explain visually. I think theTH-1 and TH-2, you know, the humoral immunity versus cellular immunity, I think a lot of this is overblown. But basically, the answer is it does affect the relationship between the two. But there's a huge chart that has all this stuff, and I probably have to do a more of a visual presentation than I can explain over the radio. It would be a very visual thing, but there are charts out there that will explain how LDN may affect the Th1 versus Th2 immunity.

Linda Elsegood: Okay. Thank you. And how does LDN affect allergy testings? 

Dr David Borenstein: Well, in theory, it really shouldn't. I have patients on LDN get allergy testing and they certainly still come up positive, so we've never seen it. I mean, it could very well be, I've never done a study, but just from anecdotal evidence, I don't see how it affects the IgE modulated immune response.  

Linda Elsegood: Another question: we're always being asked, while we're talking about testing, people say if I have to have a drug test for my work, would LDN show up? 

Dr David Borenstein: No. Remember, it's not an opioid, it's an opioid blocker. So there's going to be no problem with you going in and taking LDN and having issues at work. 

Linda Elsegood: And does LDN right serotonin levels in the brain? 

Dr David Borenstein: As far as I know, the relationship is not proven. There may be some relation to that because remember, it's working more on the opioids and met 5-enkephalin. The met 5-enkephalin somehow may have some effect on serotonin, but I haven't certainly seen that in my patients. But that would be something that research can definitely look into.  

Linda Elsegood: And we have a question from Kirsty, and she says, a week ago she started on 1.5 mg of LDN for lichen sclerosis, and she’s curious about at what point should she expect to see some relief of symptoms, and when should she increase the dose? 

Dr David Borenstein: Well I think it's still very early, but I would certainly recommend the next couple of weeks trying to go up to 3.0 mg and see how that works, and then moving up a little bit higher. And if you're not getting any results for a few months after that, it's probably less of a chance that it will work. As a rule, I think after three or four months if we’re not seeing results, either you have to clean your diet out and change what you eat, or it's probably not gonna work for what you're trying to use LDN for.

Linda Elsegood: What is the protocol that you suggest to your patients? I know you have said LDN is just one of the tools that you use and it doesn't always work for everybody, but if we were a new patient coming into you, how would you describe LDN to them if they weren't going to go off and Google it. 

Dr David Borenstein: Well, here's the thing. Usually, if I'm going to prescribe LDN, we'd have a specific reason for doing that. So maybe give me a scenario, which type of patient - one with MS, a patient with Crohn's. You tell me, and I can give you better answers. 

Linda Elsegood: Let’s say Crohn’s.

Dr David Borenstein: Perfect. Perfect. Well, most of the time, people with Crohn's maybe on Humira or other medications that would impair the immune system.

So I would explain to them it's very simple. I tell them that there's this medication that mostly integrative doctors use. It has very good success in treating Crohn's disease. It is inexpensive. A dollar a day on average. It has minimal side effects, and it works in most cases really, really well. So they say, doctor - the most common question I have for this - is, “How come my gastroenterologist didn't tell me about it?” This is the most common question I have. Why are you doing this and they're not doing it. So then I have to explain it again: most integrative doctors use this; this is compounded, not pushed by their pharmaceutical representatives. That, and explain the mechanism of action, that we know that opioids have a very important part of regulating the immune system. Then explain to them what opioid blockade is and the increase in met 5-enkephalin and how that can modulate the immune response. Now we also have to educate the patient that this is not a narcotic, because they think naltrexone, and they think drug addiction, so we have to educate them about that. 

Now, especially with Crohn's, not only do I use LDN, but I also use some of the other techniques I mentioned: treating the gut, the inflammation. But here's some good news about LDN and Crohn's. A lot of my patients don't keep to their diet. A lot of my patients don't do what I tell them. All they do is just take LDN, and that's it. And you know what? They do really well despite not having to change their diet; despite not having to do anything I tell them to do; and they respond really, really well. So that's kind of a good thing. At the same time, patients who don't respond well, we may want to have them change their diet and follow my instructions for cleaning up the gut and taking the proper supplements and diet, and then they tend to respond as well. One thing about Crohn's that works so well in our patients. A lot of the patients don't even - that's it - I want my LDN and goodbye. And it works as they come periodically to see me get their refills, and they're the happiest people in the world. 

Linda Elsegood: I have a question here that always comes up. Now, some doctors, pharmacists, think Tramadol is an opiate. Others will say it's a synthetic opioid and can be taken with LDN. Where do you stand on that? 

Dr David Borenstein: It can be taken with LDN. Don't believe anything they say. If you're in pain and you need a painkiller while taking LDN, Tramadol is what you're going to take. It works. How do I know? I've tried it on myself. You know, it's not a problem. 

Linda Elsegood: Okay. Any particular dose. 

Dr David Borenstein: You know, it’s individualized. But the point is, the question is more in general, will Tramadol have a problem working with LDN, and the answer is no. The dose is as you need it. Every pain situation is different. Certain pains, you don't really need Tramadol, you just need Tylenol or Motrin. But other pain, heavy narcotics. In that case, that's where the Tramadol comes in. That being said, in many of our patients who need high dose narcotics, you may want to just get off of LDN for a little while and hope for the best. And then when your need for narcotics goes away, restart the LDN

Linda Elsegood: So would you say with Tramadol there has to be a gap when you take LDN or can they be...

Dr David Borenstein: No, no gap at all. Just use it as needed. But sometimes Tramadol will not be enough for the pain. You may need opioids, and that's when you're going to have to go off the LDN.

Linda Elsegood: Oh, that's good. Thank you. We have people ask us about weight. We know that LDN is used in some weight loss clinics; and some people say when they start LDN, they gain weight. Do you have any experience of weight with LDN? 

Dr David Borenstein: Usually not. Usually, people don't gain weight. It's usually very well tolerated. I wouldn't use it, again, as a primary weight loss medication, although some patients have claimed that they have lost weight on it. Maybe they sleep better after a while on it, and that improves the metabolic rate. But weight loss is an entirely huge separate issue. We can have ten seminars on weight loss because it's such a complicated factor of hormones, adrenals, thyroid, lecithin, insulin. It's a huge, huge topic; and growth hormone; there are so many things that are involved in discussing weight loss, and that's just hormonally, and obviously, we have diet issues and exercise issues that we can discuss as well. But I think, for the most part, it may be a pleasant, side effect. And if you lose weight, that’s great.  

Linda Elsegood: And does LDN help with sensitivities to fragrance or chemicals.

Dr David Borenstein: Here's the thing. It's certainly worth a shot, but chemical sensitivity, and I've seen a lot of chemical sensitivity in my life; it's a very, very, very difficult thing to treat. First of all, many physicians, if not most physicians in the United States, I don't know how it is in the UK or the EU, but most physicians here don't even think that it even exists. It just doesn't exist. Okay. And I think when we're treating chemical sensitivity, we have to work on detoxification of the body. Working on building the methylating pathways, detoxing with things like charcoal or other things. Also, when I hear fragrance sensitivity, when someone has a problem with perfume, the first thing I think of is candida. Candida is the first thing I think of. Look for yeast. Many times it's a very close clinical association. Now, if you want to try LDN that's great, but I don't think that's gonna cure the issue. I think we have to look at the root cause of the problem and address it. And the LDN may be a tool in fixing, addressing that issue, but I don't think it's a cure-all, but certainly worth a shot. Again, we have a medication that's cheap, little in the way of side effects. It may have good therapeutic potential. Why not use it?  

Linda Elsegood: And another question that's always coming up, and I know you were saying about missing doses for a period of time before and after an anaesthetic. Some people say that skipping a dose is good on a regular basis. Some doctors will say once a week, some will say once a month. What is your view on that? 

Dr David Borenstein: Well for the first few years, I don't think it's necessary to skip a dose, but we're finding probably after a number of different years, and patients who've been taking LDN for many years, it certainly wouldn't hurt to skip a dose maybe once a week. First of all, it saves you a few dollars if that's a concern. But if you can skip the dose once a week. Okay, now I wouldn't do this in the initial couple of years. It's just more people that have been on it for a long period of time. Skip a dose once a week and see how you feel, and see if your clinical symptoms change. We do this, believe it or not, in Parkinson's disease, we take as a drug holiday, and it works really well when the medicine for Parkinson's disease doesn't work very well. We take a drug holiday, and it's kind of like what you're doing here. It wouldn't hurt. I don't think there's an exact protocol. I think this is very anecdotal, and every patient is different, and everyone is different. But you know, 5-6 years of LDN - try stopping it one day a week and see what happens. What's the worst-case scenario? You have to go back on it every day. That's the worst thing that's going to happen.  

Linda Elsegood: And you were saying about Parkinson's - we've got many members that are taking LDN for Parkinson's. What has been your experience with that?

Dr David Borenstein: Pretty well. Now I've been doing a lot of work with Parkinson's, and right now in my practice I've been doing a lot of work with Stem cells, and I find that Stem cells are very beneficial. And what I find is that I get the Stem cells to improve the symptoms of Parkinson's and then the LDN to keep it stable. So I've been using LDN and those patients recently with some good results too. We just keep the disease stable. So they may get a big boost in the way they function with the Stem cells, and we use the LDN to keep them that way. So I think it's a very powerful tool for treating Parkinson's and MS, and some other neurological diseases.  

Linda Elsegood: We have a question for Mary, and she says, “Have you found LDN to be beneficial for Alzheimer's?” 

Dr David Borenstein: I have not used LDN for Alzheimer's. The problem is you have a patient who may not have the best memory, and you have to be very careful with the medication. If there's a provider there with the Alzheimer's patients, you can certainly give it a try. I think there are many other things you can do for Alzheimer's patients: treating their vitamin deficiencies, B12, folic acid, lots of fish oil, making sure their thyroid is okay. And look for other deficiencies: low levels of vitamin D, look for MTHFR mutations, high levels of homocysteine. These are things that - aluminium toxicity is the thing that I would look for in treating patients with Alzheimer's. Again, if you have a physician who can work with you, this is very low risk. And very inexpensive. It's certainly worth a try. That being said, look for the other things that you need to address with patients with Alzheimer's and address those, and you'd be surprised just by giving some B12 shots, a little thyroid, and little fish oil - you may actually see some improvement.

Linda Elsegood: That's good. Well, we have time for one more quick question.

Debbie has bipolar, and she wants to know if LDN would help her. 

Dr David Borenstein: I have not treated bipolar in my practice, and I have not had any patients who would be treated with, let's say, Crohn's or MS or cancer, and also have bipolar and have any change in their symptoms. So I honestly couldn't give you an answer to that.

Linda Elsegood: Well, that's us just about over David, and thank you very, very much for taking all these questions and for your time. It's been amazing. So thank you very much. And next week we're going to be joined by Dr Mark Shukhman, who's a psychiatrist, so maybe he'll be able to answer our question on bipolar. But thank you once again, David.

Dr David Borenstein: Oh, my pleasure. Thank you.

Linda Elsegood: Belmar Pharmacy is a nationally respected compounding pharmacy. They compound low dose naltrexone, LDN; bio-identical hormones, and custom amino acids, amino blends. They're based in Colorado and ship nationwide. Their goal is better patient outcomes through quality compounding, combining effective communication between practitioner, pharmacist, and patient. Call +1 800-525-9473 or visit Belmarpharmacy.com.

Any questions or comments you may have, please Contact Us. I look forward to hearing from you. Thank you for joining us today. We really appreciated your company. Until next time, stay safe and keep well.

Dr Brian Udell on Low Dose Naltrexone, LDN Radio Show 17 May 2017 (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Today our guest would be Dr. Brian Udell who is the medical director of the Child Development Center of America in Florida.

Linda Elsegood: Thank you for joining us today Dr. Brian Udell!

Dr Brian Udell: Thank you for having me.

We're really looking forward to hearing your experience with LDN for Autism. First of all, when did you first hear about LDN?

Dr Brian Udell: I heard about LDN through the, at the time it was called the Defeat Autism Now Protocol. It was called the Dan movement, which started many years ago, in the late 1960s, and that was the first time that the doctors tried to do anything medical to address the Autism that they were seeing.

First of all, it was a very rare disease. Right now in the United States, one in 68 children have it and 2% of boys. So it's five times as prevalent in boys than girls. So 2% of the boys in the United States that have AASD diagnosis. At the time, I first started I think it was one in 110 and the Autism Research Institute became the next version of Defeat Autism Now. And in that time, treatments such as this were beginning to be offered to patients. Previous to the 1970s It was considered to be a psychological, psychiatric disease and it was due to mothers and their refrigerator moms theory was the idea that it was psychological due to lack of love on the caretakers part. And that was actually first proposed by Leo Connor in 1940, and then it was popularized by a self-taught psychologist named Bruno Bettelheim in the fifties and sixties and so that really impeded any kind of understanding for years of what was going on in these children.

And so LDN in 2006 Dr. McCandless, who was a paediatrician wrote her paper in 2006 and a number of us. I  first tried it in 2009 when a patient was in high dose and actually had some effect. But I didn't really recognize how great it could do for patients until about three years later as Low Dose Naltrexone when I rediscovered with the rest of the Autism Research Institute community the use of Low Dose Naltrexone in Autism.

Linda Elsegood: And why do you think that the cases of Autism have increased so greatly?

Dr Brian Udell: There can't be anything like a genetic epidemic. Would be impossible that the two terms are mutually exclusive.

So then it has to be environmental. And in any environmental issue, it's going to act on susceptible individuals. So it is genetic in the sense that susceptive and everyone when the play happened, everyone didn't die the plague, somebody was more susceptible. Very few were not susceptible but the ones that were not were the survivors. So right now we have a toxic environment and susceptible individuals. Obviously, boys are five times more susceptible than girls, so they get five times as many premature babies. There are more and more susceptible babies that are born with congenital anomalies.

Babies born with a genetic, anomalies are more susceptible, but it's that susceptibility whatever the environment is and that's the key is what it is in the environment that's causing havoc. As a paediatrician and a doctor who's a baby doctor for 40 years,

the main things that I see different in the medical environment are a baby's having a lot of reflux. Babies don't breastfeed. If there's anything that parents should attune to now is doctors understand breastfeeding and when a baby doesn't breastfeed, sometimes it's not because they have an allergy or because the mother's milk isn't coming as soon as the baby's not sucking hard enough.

And then the next thing is they have reflux. That's a very common thing that I didn't see in the previous century. And then the next thing It's one or two years of life they have ear infections, which again, I didn't see. I saw plenty of ear infections in my life, but it didn't happen in the first couple of years of life.

And so for the year infections, we give antibiotics, and for everything, we give antibiotics now. And if there's one different thing in the environment that would be the biggest thing is the use of antibiotics. And the second biggest thing is using antacids to stop baby reflux, which is just a total misunderstanding.

And I believe that that starts in the susceptible individual. Many of my cases start with that problem and then it steamrolls into bigger problems that appear in the central nervous system. But as a little baby, if your stomach is hurting all the time and you're refluxing all the time and you have a bad bacteria or organisms in your gut, then the only thing you're going to do is cry. So all it's going to present as in little babies is a really fussy baby who doesn't pay attention. That doesn't get broken until some doctor figures out that that child has been seen by an immunologist and an allergist and a skin doctor, in an ear, nose, and throat doctor.

And the paediatrician can't figure out why the kid's not talking all of a sudden. The effect that I see as being the biggest cause if there's such a thing as a cause.

Linda Elsegood: How old are children when they can be diagnosed with Autism?

Dr Brian Udell: That's a great question. I was a neonatologist, the premature baby doctor and so I saw this in the seventies and eighties a lot of drug and alcohol addicted babies. And I was also the director of the followup clinic until they were three years old for the city. And then in the late eighties and nineties, I mostly saw HIV positive babies.

And I also saw them until they were three years old for the followup clinics. Those years, my first case of Autism was 1975. I knew what autism looked like. Autism is not being misdiagnosed as previously being called mental retardation. Mental retardation is different from a different medical condition. As a matter of fact, most of the children that we see, if they really have a diagnosis of Autism, they're at least normal in many times, above normal intelligence. What happened is that I was interested in trying to help the kids that look like they had medical problems.

I forgot what the beginning of that question was.

Linda Elsegood: Well, if a parent is concerned that their baby has got that.

Dr Brian Udell: So then I started the clinic just for Autism. That's how I got into that. I was doing clinics for babies who weren't developing correctly.

And so I started a clinic in 2008 just for Autism. We would see children between the ages of two to five. The city wasn't seeing them if they were much older than three in my case but the diagnosis in 2008 was really made in five-year-olds. It was rarely made in two and three-year-olds.

I got to see more and more children, and I've seen over 2000 children now with kind of developmental delays. You start to see the second sibling of that child and then it becomes just, or the older sibling, frankly, and it just becomes just as important to me to see how early I can catch it in that second sibling.

Of course, the first question that comes up is the kid going to get childhood inoculations because that's the worry that the parent has. That's why I start seeing them so young. I've seen a good number of those kids. I believe that by the age of six months, there's a certain set that I can see.

Now, there are children who don't get it until the age of 15 to 18 months of developing perfectly, normally.  And then at 18 months, things start going bad. That's what we're told. I can usually tell by the time a child is six to nine months whether I should worry and I do start to intervene.

Yesterday I saw a child, the younger sibling, and she was just under two years old. She wasn't talking, she was walking, she was making good eye contact, everything looks nice, and I wasn't happy with that development and everything else was fine in that child. So sometimes it's a little later, but I would like to think that since I was a neonatologist, I was a premature baby doctor, I'd like to think that I can usually tell by the time they're nine months old. Their tone is already very low. They're not making eye contact. They're not having a responsive eye contact. They usually have another medical problem that's been going on, either diarrhoea or constipation or some feeding problem, and they're not crawling correctly between six and nine months.

A whole book was written a couple of years ago about the earliest diagnosis and the author spent two or three chapters talking about the crawl being abnormal. So if a doctor wants to be stewed about it and really look hard, they might see it that young.

Linda Elsegood: And the military, the question. You mentioned vaccinations there. I'm really pleased that I don't have to make vaccinations.

Dr Brian Udell: I didn't say vaccinations.

Linda Elsegood: Sorry. I said vaccinations. Okay. Inoculations.

Dr Brian Udell: I said childhood inoculate. It is a hard subject.

Linda Elsegood: Yes, it is but children and parents have that decision to make. And as I was saying, my children grew up, so I don't have that dilemma anymore. But if you have a baby you have to make a decision.

Dr Brian Udell: Soon in the US it won't be the parents' decision either. In California, practically it's not at all. I don't know what it's like in other countries. Maybe in your country, it would even because of socialized medicine, maybe they could even make it more forceful, but you can't go to school if you're not vaccinated in California. Now I don't know that it's about panels for decision anymore, which is another all topic on it. But what can I say?

Go ahead.

Linda Elsegood: No, carry on.

Dr Brian Udell: There's no right answer. We were fighting in the United States alone is a $4 billion a year industry. People get murdered for less money than that.  Dr Andrew Wakefield, I think the man is a gentleman and a scholar, and he's vilified.

You can't write an article about anything that has to do with Autism nowadays and not mentioned the devil, dr Wakefield, is wonderful gentlemen and just trying to help everybody. And just that alone keeps physicians like me from talking much about it. I have 10% of my patients that have a picture of the child before the vaccination and a picture of the child after the vaccination and it's a different child. And that means 90% of my patients, and I've seen, like I say, over 2000, 90% of them don't think it's the vaccination. So it's not in everybody. But as I said in the beginning, it's the susceptible child with the environmental stimulus. And for some people that could be an environmental stimulus.

Unless you believe that all vaccinations are good for all children all the time, and that would be an impossible statement. So it would beg the issue, it would beg the question, which vaccinations for which children went and no study got, and there's not even something close to that.

The best thing I can do when they put for booster shots is I can check tastes called titers.

I can check the moon immune titers to see if the children are already immune to measles, mumps, rubella for example, the MMR shot. And I've checked about three dozen so far in the last year, and every single one of those children has numbers that are flagged by the lab as extremely hot, okay.

That means that that person could kiss a person with the disease and not get it. And my question to the public health departments is, how do you give someone who's allergic to peanuts. Peanuts you don't because they're allergic to peanuts because they have a reaction to it. We are just in no man's land with this. Snd I don't know if there are listeners who think that I'm anti vacs, which I'm not. I'm 66 years old, and I had to stay indoors in the summertime because of the polio scare. That's what happened in the 1950s In the summer. It was big. And so I recognized the value of vaccination.

I also recognize the weakness of the science and just when our colleagues just keep saying the science is clear, the science that is far from clear. When they're really faced with that science, usually they'll say, well, I see what you're talking about. That's about the best you'll get.

Usually, you get people rolling their eyes.

Linda Elsegood: And when you see a small child that you think may be susceptible to having Autism, what steps can you take to try and prevent the Autism from developing?

Dr Brian Udell: Right. The first thing is finding out if they have a medical problem at the time.

So a child who has diarrhoea or constipation or frequent rashes where frequent illnesses, that kid is an immunologic, sort of a no man's land. He needs to have an immune system evaluated and gotten on a steady keel. The diet is important. When you see that, that's a child that you start to worry about, and if you can move it in the right direction.

I see these younger children, younger siblings already diagnosed autistic patients. And as soon as they show any of these signs, we address their diarrhoea, we address them constantly and their nutrition.

And if I have a question I usually get a blood count on the kids. I'll get a couple of labs when that young child, and you know, this is something in other countries, in the South American countries when I get patients from there, they do a lot more laboratory testing than the US. I don't know if the UK does it at all, but we don't know if these children are anaemic.

We don't know. And here in the United States, a huge amount of vitamin D deficiency you correct that. The women are walking around, and they say, well, my doctor told me how to vitamin D. Well, if you have a low vitamin D, your kid has a low vitamin D. It did transfer any to the kid, and they don't go outside as often.

And then you have low vitamin D levels. So that's optimizing nutrition, optimizing their health. And it makes me feel a lot better. And if I have a question, as I say, some laboratory work will make me say: "Why don't you wait a few months? Why don't you ask the doctor to just give seven at a time instead of 14 at a time?"

Linda Elsegood: Okay. Well, we'll just have a quick break, and we'll be back in just a moment.

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Welcome back! The question that parents are always asking is "What dosage do you give a child? How do you work out what the optimum dose is?"

Dr Brian Udell: One of the interesting things about Naltrexone is it's almost the same dose for everybody. So it's hard to believe that I get results in a 15-year-old or a 20-year-old and I almost get the same result in a three-year-old with 3mg after 9:00 PM.

Sometime I'd like to give it as late as I can in the night so the cream is great for me. First of all, children don't have a choice. And second of all, they're already asleep after 9:00 PM. and that's the dose. If I'm really worried about one of those young children under 18 months, and their immune system looks like it's kind of a mess, I want to see what kind of improvement we could see with naltrexone  I may only start them with 1,5 mg or 2 mg every night. But the highest I go right now in a bigger person is 4,5 mg as a single dose or 3 mg at night, 3mgs in the morning, which I was surprised to get results from that.

Through the years now going up higher doesn't get us any better results. And frankly, I don't exactly understand what the mechanism is, why the second dose is helping them. I suspect it's helping more in a different sort of physiologic mechanism than the rise of endorphins because the parents will say: "If I don't give that morning dose, they don't seem the same."

That would be something that I'd love to see studied and I'm sure that what you're doing and the people that you're involved with would be great if there were some studies because as I'm saying,  that 3 mg dose do take care of people who don't have autism. They have other immunologic conditions and get a lot of relief with that 3 mg dose.  Higher than 4,5 mg at one time has never been helpful. And more than 3 and 3 have not been helpful either.

Linda Elsegood: And how long does it normally take before you notice that LDN is working?

Dr Brian Udell: The quickest I'll see is in the first week but depends on what I'm looking for. The original article by dr McCandless was "The use of Low Dose Naltrexone for immune modulation and mood regulation." So we are using it for two different reasons so if I'm using it right for mood regulation, we'll usually see that in the first week to say three or four weeks, and that's why a parent will continue it. Or a parent may stop it after three or four weeks, and this is rare. Most of our parents continue it, but they may stop it because what we were looking for was the mood regulation.

Now, if we're doing it for immune modulation, then I asked the parents: "How many times a year does the kid gets sick?" Usually, they get an infection or cold every other month and so I'll say: " Okay, so let's do it for three months." And then we'll look back, and we'll see whether or not, in this last three months the kid never got sick, which is what I see practically all the time. So usually the parents that see their modulation improvement that is, he stopped getting sick,  keep giving it for years because they just don't want the kids to get sick. And, and the ones that are given it for mood regulation, we'll do it until some other mood problem comes along. What'll happen is that's usually for about a year, that they'll see it's working, and then they may say that's not working and there are other psychological issues that are coming in, but that's usually how I do that.

The people that have autism have a lot of different symptoms.

The three core features of autism are speech delay, repetitive behaviours and social isolation. If that speech delay takes the form of speech apraxia that is,  they really don't say anything at all and they are two, three, four years old then we have only a very few protocols that have been proven to instigate speech. And those protocols are very sort of stimuli as we call. When an autistic person flaps, jumps or does repetitive things, we call that stimming self-stimulatory behaviour and I believe that a lot of that behaviour is communication. So if I can make them talk more, they could stymie less. So in order to get those protocols on board, I use Naltrexone even if the parents don't notice that there's a particular problem with mood regulation or immune modulation.

I'm using it in preparation of giving supplements that will sort of wake up the brain a lot and so I use the LDN so that they won't be so hyperactive.

Linda Elsegood: And how long does that take to notice that?

Dr Brian Udell: I don't know. I don't let it get noticed so well. I usually just do a protocol where I tell the parents the child is not speaking and are very hyperactive.

The two protocols have to do with methylation.  MTHFR is a big thing that many of your audience members who know about LDN probably know about the MTHFR gene. So we excite that gene. We get that gene work harder with either methyl B12 or methyl folate, glucosamine, antioxidant products. And those products tend to make patients even more hyperactive, less attention may be even more aggressive. So I'll start the child on Naltrexone for three weeks, and then the fourth week of the Naltrexone I start whatever protocol I picked to get speech started. And I don't know. Again, I'm a clinician.

I don't do studies. I found Naltrexone to be successful doing it that way and that I'm more successful getting children to speak because, for a child who's not speaking, who's three and a half, four years old, regardless of their behaviour,  the important thing over that next year is going to find some way to get them to start to talk because if they don't really talk under the age of seven there's going to be significant ongoing problems and there aren't protocols that necessarily help that.

Linda Elsegood: Okay. Are there any foods or drinks that children shouldn't be given if they are having development problems?

Dr Brian Udell: Do you live in a small village? I don't know how many McDonald's are within five minutes of you but  the worst thing I hear in my practice is when a parent says: " I can't pass that McDonald's without going in."

Okay. That drives me crazy because as far as I know, the parent is the one driving, not the kid and of course, a dad can pass them.  So just start a healthy diet and stop eating processed foods whether or not gluten-free, casein-free. It depends on what country you're in.

All the gluten in the United States has been exposed to a fair amount of glyphosate and pesticides. And I think the reason that so many people feel so much better when they're gluten-free, maybe is not to be the gluten, but it may be the pesticides and likewise in the children who seem to improve when they're taken off the gluten.

That's one part of it. And then the other part of it is the casein. And the feeling is that the casein can be allergenic or it can lower the immune response. And I test for that.

So when parents ask, what's the best diet,  my answer is,  in this century, there is the capability to tell parents exactly what diet your child should be on to not have an immune response. So the best diet starts with a healthy diet with not a lot of steroids and not a lot of antibiotics.

Over here, that's called a natural diet. If a parent wants to test for food immunity, I think it's a valuable test. The test that is usually done around the world is an immunoglobulin E test. They're testing for a scratch test or something that would cause you to get a rash or the hives or allergies, like a stuffy snuff nose. What I'm testing for is IgG antibodies, which are antibodies that your body has to get rid of it. So it's not that big antibody response to the milk, let's say, is the thing causing the problem.

The antibody response is using up energy, and these kids come in with very low tone, very low activity and the tone that seems to be the lowest is in the midline and, speech is affected. So it starts with a good diet, a healthy good diet. I can't stress enough that if I have a breastfed child that is autistic, that didn't mean that the breast milk didn't work. When I see a breastfed child who's autistic, I can tell the parents, you prevented a lot of the other signs and symptoms of autism by breastfeeding your child. So I see children who breastfeed as long as three years, believe it or not, and they may have autism, but it's not as significant as their siblings who only breastfed for a month. And the mother was more determined maybe the second time to do that.  And frankly, it starts in utero. It's not just the food that the mothers eat. They have to take the correct vitamins and not too many vitamins. They can have a vitamin D deficiency, and  there may be doctors that are listening or patients that hear this, but my object to any kind of drugs given during pregnancy end up in the fetus. Parents and saying:" Well, the mom has enough anxiety and it's better to give her Prozac than to have the anxiety." And I point to the 3 million years prior to Prozac that moms had babies, and there were plenty of hard times through those 3 million years, and we didn't have Autism.

So I object to any kind of medication. Tylenol during pregnancy can be a big factor leading to it. It uses glutathione, and the baby has to supply glutathione to the mother. When I started doing babies in the 1970s, people were actually telling me that cocaine wasn't going to cost harm the baby. There's no way that a drug doesn't get into the fetus, and, if it works on our brain, how can it not work on a forming fetal brain? So it really even starts with that. And then it actually starts two generations past. There are people who look at the flora of grandparents.

They're looking at smoking and the grandparents as being related to the second generation problems. So it's sort of a lifestyle that you want to live that might get us away from this epidemic.

Linda Elsegood: What about giving children cows milk?

Dr Brian Udell: At the end of his career and his life, Dr.

Frank Oskie, who was one of the premier paediatricians of the 20th century, wrote a book that I think probably got a kick out of being a paediatrician. And the book that he wrote was, "Don't drink your milk."

He felt that was causing a lot of allergies and asthma that he hadn't seen in previous centuries because he had seen the growth of infant formula in his lifetime from the 1940s. It wasn't really until the forties and fifties that women really got started using the formula all the time which is all cows milk-based.

Cows, milk protein carries a lot of potential problems of the allergic responses. And I see thousands of them every year I tested. I test thousands of allergic responses, and I would say casein, which is proteins in milk and then the sugar is lactose, and then there's water.

So I see much more casein intolerance than lactose intolerance. Lactose is the sugar and I don't think that we're intolerant, especially babies to the lactose. The best substitute, if you can't use human milk, goats milk.

Goat's milk may be number two on my best list. It's not camels, and it's not cow. Obviously, camel and cow have a lot of the same protein to our bodies.

Linda Elsegood: As children become toddlers, parents sometimes to keep their children quiet, give them what we call sweets, or you'd call candy giving children sugar. How is that affect children?

Dr Brian Udell: Dr. Flamingo was a genius.

There were studies, prospectively randomized, double-blind controlled studies it would be hard to do but it is high fructose corn syrup and that is poison.

Anything that has a number in front of it is not food.

I worry more about the high fructose corn syrup has a fair amount of lead in it. And it's not a natural food. So refined sugar has been around. I try to look at things that weren't around before.  I'm old, and I took care of kids for 25 years in the previous century, and I've taken care of kids for 17 years now in this century, and there are certain things that just don't make sense to me.

High fructose corn syrup wasn't around in the old days, and we didn't have autism. And I was there when ADHD started happening until the seventies or eighties. By then, they were putting in artificial colours, artificial flavours, steroids in the animals, antibiotics in the animals.

Dr Feingold Diet which is a low sugar is a very healthy diet. I think should be followed by everyone. If you were to do a study about sugar, I would be more interested in doing a Skittle study, Skittles are these things M&Ms that were colouring one  and are a lot worse for children. But a lot of times I'll have a mother who says he gets crazy every time he gets sugar. It's like, so why would you give them sugar? To me, you don't have to get a study for that.

Do you think I should give them sugar? No, I think you shouldn't. If it hurts when you do that, don't do that.

Linda Elsegood: I just have one more quick break, and we'll be back in just a moment.

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Wellcome back! And today we have Dr. Brian Udell with us and it has been amazing all the information that you've given us. So we've talked about what autism is and the use of LDN, and you also use LDN, as you were saying, for other conditions. How effective have you found LDN to be in autoimmune conditions?

Dr Brian Udell: The autoimmune conditions that I deal with other than some that cause what people call Autism,  are Juvenile Rheumatoid Arthritis, Systemic Lupus, general allergies all the time, they have asthma, some kind of reactive airway disease problem and I find it to be great at a first-line. When I give it for a lot of immune conditions, either the drug that they're on can be lowered or at least they don't go up on the drug that they're on. I mean, Juvenile Rheumatoid Arthritis is a

pretty severe condition and my child, who has and takes Methotrexate which is a really strong drug, he finds that it, without the Naltrexone, his days are very much harder to deal with. So, I think it's an adjunct.

I think that it's not the be-all and end-all for an autoimmune condition but it certainly can be a beginning, or it can be an adjunct for kids. Some autism, we now measure these antibodies in their brain, and we're now able to measure without doing a spinal tap, antibodies binding and blocking antibodies in their brain that could be causing  5 to 10% of autism. And so even if the autoimmune condition that I'm helping is asthma, and I have a child who has autism and asthma, a lot of children who have autism have other autoimmune conditions.  And so just by giving them the Naltrexone for whatever I'm getting either immune modulation or mood regulation, the parent will say that they don't get their attacks as often as they used to, or that if they forget to give it, they run out, they wish they had it. Again, I'm not specific in it because it's a clinical practice, but if sort of amazes me the worry, the concern that some people have about Low Dose Naltrexone. I think It's been a godsend for my practice.

I don't have to give it for a lot of reasons. I don't have to give anywhere nearly the amount of drugs that everybody else has to give, I don't have to give repeated courses of antibiotics because they don't get sick as much. So the LDN helps that. I don't have to give a stimulant medication because the child's focus is better or I don't have to give antianxiety medication because the kids settled down.

All these things have turned out to be great, and I practically give it to all my children, ADHD and ASD and autism because to me is so safe. The two biggest side effects that I see are about 1 in 20 of the children that get it will have a little hyper from the stuff and last for two or three days sometimes. I usually ask the parents to start it on a weekend night, on a Friday night or Saturday nights so many hyperactivity gets away by the time Monday comes around. And about 1 in 20 that the hyperactivity sort of continues weeks into it, and the parent doesn't want to do it anymore,

I'll try lowering the dose from 3 to 2 or 3 to 1,5 mgs. The number of people who don't continue it, only about 10 to 20%. Everybody else just continues to get it. And that's sort of an underlying thing that I'm always giving. And then I don't have the question of." I wish I was giving that too." because what traditional medicine does is, we drop a big bomb from the top Adderall or Ritalin or Abilify Risperidone.

We drop these big bombs from the top, and we see what's happen until the smoke clears to the patient. What I'm trying to do is add vitamins and supplements to take away foods that might be causing the problem. To me, the safety of the Naltrexone is, that is the only thing that it will stop it if they get too hyper. The only other problem I ever have in it is maybe 1% of kids will get a little rash. We ask them to rub it on their wrists and somewhere thin where it'd be absorbed. So 1% of kids might get a rash and usually the rash is due to the vehicle that they're mixing it in.

And I ask the pharmacist to change whatever the vehicle is. I don't have a problem so far in this. Thousands that I've given to children. One child who turned out that was allergic to Naltrexone because we put it in pill form and he got high and the highest went away when I stopped the Naltrexone. So I just see it as a wonderful treatment because it has such a high safety index and it works in so many cases that it's almost a crime that it's not tried more. I'm an allopathic doctor, I'm board-certified and everything.

and I can only figure that they don't try because nobody's making money off it. It's a very inexpensive thing and maybe that's the reason.

Linda Elsegood: And you were saying that when diagnosing a child, they usually have stomach upset, diarrhoea. Do you find that the LDN helps with that?

Dr Brian Udell: I don't know. I wouldn't address one without the other anyway. None of my patients who are on LDN aren't on something for their gut anyway because especially in the US their guts are totally poisoned, and they have to be on some kind of probiotic, they have to be on some kind of an antioxidant and in their gut. I really don't know if the LDN by itself helps. The only way I would ever know is if a patient ran out of the probiotics. I recently had one patient ran out of the probiotic, but continued the LDN and the kid's gut was okay when she came and saw me. So maybe it held things together, but I don't give it a chance. I like it so much.

Linda Elsegood: I was only just wondering because it's used in pediatric Crohn's and so on. So I just thought maybe it would help.

Dr Brian Udell: And that's interesting because they don't choose probiotics in Crohn's.

You'll find a lot of kids in Crohn's who aren't on a probiotic or who haven't had their gut flora checked, and they're not on maybe the correct antibiotic that they should be in their gut. They have C diff growing in their gut, and they're calling it Crohn's, you know? And so I'm glad that it could work by itself. It shouldn't be by itself in a Crohn's patient.

Linda Elsegood: Yes.

Dr Brian Udell: That's just my little opinion.

Linda Elsegood: Well, we got you as a speaker at our conference in September, so I know there are many doctors who would like to discuss LDN in children with you.

Dr Brian Udell: I'm looking forward to it. I really am. You guys have been great to me.

Linda Elsegood: But it's sharing that knowledge, isn't it? That is just so amazing.

Dr Brian Udell: I didn't know it was given to adults and you told me you weren't sure that it was giving little kids for autism.

Yeah, sharing knowledge.

Linda Elsegood: Exactly. And bringing all the people together. And the Q&A sessions I think are so much fun at the conference with all the experts pull all the knowledge together.

Dr Brian Udell: And I think the people who attend really get a sense of, they get empowered with a lot of knowledge.

Linda Elsegood: Yes. And there was one doctor who had notepads there last year and she filled two notepads with information, whether she's actually read it all or not.

Dr Brian Udell: She can do your next book.

Linda Elsegood: Yes.  And you've got an hour prerecorded, which we still have to do when you have time. If you can get your PowerPoint together then tell me and we'll record the audio. The title is "Low Dose Naltrexone and the Autism spectrum disorder". Last year you had 30 minutes live, which was nowhere near long enough, so you've even got less this time.

So that means it will be turned into a video and it's available for everybody for a year to watch as many times as they like, and they'll be able to download your PowerPoint. As you know doctors love the PowerPoints to go through and check.

It's a quick way of  doing it and the information you give help and guidance to doctors is amazing. So thank you very much for everything that you do and all those children that you treat. It's amazing. And last year we had the little boy who played the piano, Jacob. What an amazing little boy. He sat down and everybody just sort of stood there. I don't know whether they were expecting him to play chopsticks or something, but it was truly amazing.

Dr Brian Udell: He keeps moving along in his career.

Linda Elsegood: Can you just tell us very briefly of what LDN did for Jacob?

Dr Brian Udell: Sure. It take place when he was about four years old when I met him, and he just had a new little sister. His biggest problem was, I don't know if he didn't like her crying or he was jealous of her.

He wasn't talking. He was developing slowly. But the parents started to get scared that he was going to hurt her. He was very aggressive, abusive self-injurious on others. So when he came to see me, it was because the regular medical community used to give strong drugs to stop the negative behaviour.  We don't do anything to find out why they have negative behaviour. He wasn't really autistic at the time. I saw him but all he ever did was scream and hit.

The mother wanted me to use B12 because everybody reads that B12 helps speech and I do use a lot of  B12 shot in my practice, but he was so aggressive that I felt that I gave him B12 at that time he may increase the risk that he could hurt somebody. So we started him on the Naltrexone. Then his mother was not necessarily on board on that and within days he told his mother he loved her and his life turned around.

And then within a couple more days,this is obviously just one case, she heard the piano playing, and she thought it was her husband. But she thought he's not that good. And it was her son playing the piano, and it turned out that he's a prodigy. He just was listening all those years and looking, and then that's how he got it. I thought it was an amazing story.

Linda Elsegood: Absolutely amazing. And I interviewed her and she said that all he was doing was,  slapping her around the face all the time. She kept telling him, "I love you, Jacob."  Even though it was difficult sometimes, and then as you say, one day he just turned around, and I hugged her and kissed her and said, and I love you, mommy.

And she called for her husband to get the video camera and said:" I'm going to save it in case he never ever says it again we will have it to look back on." But it was amazing to hear him playing. It was as though somebody in their forties that had been playing classical music.

Dr Brian Udell: And I can tell you that is not uncommon in my practice. I have more talented kids in my practice now than in any practice I've ever had.

I've had several different kinds of children, and they were very good artists, musicians, speakers. One was a public speaker. He can't speak when he's by himself.  He stutters, and he doesn't do things but then when he starts doing public speaking, it's perfect. It's amazing how the brain works.

Linda Elsegood: And I think the takeaway message here is if your child has been diagnosed with autism or ADHD or anything like that, or it's a development problem, then it's not the end of the world. There are things and treatments and doctors like yourself that they can consult with.

And how do they contact you, Brian?

Dr Brian Udell: My organization is a child development centre of America, and my blog that I write every week is TheAutismDoctor.com.

And it's free, and you don't have to register. My purpose is to get the word out there, just like you said in a lot of my blogs, I just want the parent to take it to the paediatrician and say, what do you think about this?

And the organization around the world that we all belong to is called The Medical Academy of Pediatric Special Needs which is where we train. So we go twice a year, and we spend three days, eight to 10 hours a day, three days in a row learning about the basic science and Autism from each other. So that's a good place if you're not seeing me.

Linda Elsegood: Well, thank you very much. Our time is up, and it was an honour and a privilege to have you here with us today. The LDN research trust Facebook group has almost 18,000 members around the world.

It is a great place to start your research, connect with others, www.facebook.com/groups/LDNRT

It is a closed group, and only members can see your post. Nothing is shown on your page or feeds. Posts can't be shared. We do also have the page where you can share links. It's www.facebook.com/ldnrt

Check out our books constants pages by searching on Facebook. The LDN Research Trust also has a Twitter account, and you can find us on twitter.com/ldntrust.

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Linda Elsegood: 
Any questions or comments you may have, please Contact Us.  I look forward to hearing from you. Thank you for joining us today. We really appreciated your company. Until next time, stay safe and keep well.

Dr Alena Guggenheim on Low Dose Naltrexone, LDN Radio Show 11 Oct 2017 (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Naturopathic physician with 10 years experience in direct patient care. Dedicated to improving patient outcomes through evidenced based integrative medicine with an expertise in rheumatologic and gastrointestinal diseases. Working to improve patient care through clinical practice, publication, teaching, mentorship, seminars, and research. Research interests include the intersection of autoimmune inflammatory disease, HLA haplotype and the microbiome.

Dr. Alena Guggenheim does extensive testing and observation like a detective, to solve the case and heal her patient. She stumbled onto Low Dose Naltrexone while still in medical school over 10 years ago, and sees it as one her most valuable tools. But like all great doctors, she also concentrated on diet, nutrition, exercise, and checking labs for problems. She specializes in rheumatologic and other autoimmune diseases.

Review Ken Bruce
Summary from Diane's interview. Listen to the video for the full story.
 

Diane - US: Rheumatoid Arthritis (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Linda Elsegood: I'd like to introduce Diane to the United States to takes LDN for rheumatoid arthritis. Thank you for joining me, Diane.

Diane: You're welcome. Linda beauty. A pleasure to speak with you again.

Linda Elsegood: Could you tell us when you started to notice the pain

Diane: from rheumatoid arthritis? Um, I began having daily pain with my feet, the week of labor day of 2012.

That would have been early September. I had been canning tomatoes, and I thought my feet just got sore from being on them. And I figured with some rest after a couple of weeks, the pain would go away, but it didn't. And after about six, four to six weeks, I said, this is not normal. I need to have this look at.

So I went to my doctor and talked to him, and he agreed that it's probably arthritis and he prescribed Tylenol, which was not acceptable to me. He told me it was safe to take Tylenol for the rest of my life, which it is not. And I had told him that earlier in the year, just a couple of months prior to my pain, my brother was diagnosed with rheumatoid arthritis and I was concerned that I might have the same thing.

He dismissed my concerns. I chose to seek a second opinion. Um, I went to an orthopaedic doctor who did, when I went there and told me they didn't do feet only above the ankle. So I had pain in my knee. So I had him look at that, and he diagnosed me with osteoarthritis in my knees and told me I should go see a podiatrist.

So we have one that comes into the town where I live to the hospital as an outreach clinic, I made an appointment, and I went to see him, could not confirm rheumatoid arthritis, but did do an examination and some x-rays of my feet. He did say that rheumatoid arthritis can frequently show symptoms first in the feet.

Where I had the pain, and he referred me to a rheumatologist, and you basically have to be referred to a rheumatologist in order to get an appointment. You can't just call up and make an appointment yourself. A doctor will have to refer you. So I chose to go to the doctor where my brother had once and was diagnosed, which was in Sioux Falls.

It's about 90 miles from my home. And they did blood tests and some additional x-rays there. And the day, the Monday after Thanksgiving in November, I got a phone call from the doctor confirming that I had rheumatoid arthritis. He wanted me to take methotrexate Plaquenil folic acid. And potentially prednisone as treatment.

I refused. I asked him if it would harm me to wait to start treatment for a short period of time, so I could explore alternative treatment protocols. He agreed that a short timeframe to look into alternative treatments would be okay. We felt I was fairly early in my disease and that a short delay would not unduly harm me.

So I started to do research on my own, and I prayed, and I went to the library and requested some books. One of the books I found at the library. Um, I believe it was through an interlibrary loan was honest medicine written by Julius Shopee. Hope I pronounce her last name correctly, and I read that book after a very long heartfelt prayer.

And believed once I had read through the book that I may have found the treatment I wanted to try, and that was low dose naltrexone. I didn't stop just with her book. I further researched it online. Um, I Googled it. I found some Yahoo health groups. About rheumatoid arthritis and others about taking low dose naltrexone.

All of my research confirmed for me that this was a treatment that I wanted to try as an alternative to the harmful or biologic drugs normally used to treat rheumatoid arthritis. So I went back to my primary physician who I'd been with for many, many years. And I went back first to the rheumatologist in Sioux falls and ask about getting a prescription for low dose naltrexone.

The rheumatologist refused to prescribe it. He said that it's not an approved treatment based upon the American college of rheumatology. Treatment protocols for rheumatoid arthritis. He did say I could go and try to get it from my primary physician. And if, um, I would get the prescriptions and the physician would, you know, he would monitor my treatment from that point forward.

I then went back to my primary physician and. Asked about getting the prescription for low dose naltrexone. And my primary physician refused to prescribe it. He seemed to be more concerned with lawyers and any potential liability for giving me an off label prescription for a drug that's been approved by the FDA.

I did not like that response from my physician because he seemed more concerned with malpractice and liability that in treating me the patient, I then fired my doctor and have not gone back to him since. So I looked for a physician that would prescribe the low dose naltrexone for me.

 Through online support groups on Facebook, including your group, Linda and another group.

There is a woman who keeps a list of doctors that will prescribe. I was also doing acupuncture treatment in 2012, and the acupuncturist had recommended a doctor for me. And it was the same doctor that was on the list kept by one of our angels in the group. So I made an appointment, and I went to see the doctor in January of 2013.

He prescribed the low dose naltrexone for me. I started February 1st of 2013. With a three milligram dose for two weeks. And then I bumped up to 4.5 milligrams, and I've been taking that ever since.

Linda Elsegood: And what was your experience when you first started?

Diane: Well, when I first started taking it, um, I'm not a sensitive, a person that's sensitive to meds.

Some people are, but I seem to tolerate most medications fairly well. I had positive thoughts going into it. This was my treatment of choice. Prior to starting the low dose naltrexone, my rheumatoid arthritis was getting worse. Um, the fatigue and brain fog from the disease was not well, was not good. Um, I get up in the morning, and I'd feel I say about 80 years old.

Um, I was like 50, 51 at that time and I could barely walk. To the bathroom from my bedroom, which is just across a very short hall, um, six feet or less. And it was very difficult getting out of bed in the morning and getting to the bathroom when I started taking low dose naltrexone at nighttime before bed.

I could feel little tingles in my legs, almost like when your legs are waking up from being asleep. Um, If anybody, you know how it goes. If you sat on your leg too long or something, your leg will go to sleep cause of blood flows, net going. And when you get up in the blood flow is restored. You get a sharp tingling sensation in your leg.

As your blood flow is getting back and your nerve endings are waking up and so on. It wasn't that severe, that tingling I felt, but I could tell that something was happening. Um, by the time I jumped up to the 4.5-milligram dosage in two weeks, I felt a lot more like myself. Um, being a 50, 51-year-old woman, instead of 80 years old, I had more energy.

Um, the pain in my feet was less, it wasn't totally gone, but it was a lot more comfortable to walk.

Linda Elsegood: If you had to rate your quality of life before you started LDN on a score of one to 10 and 10 being the highest, what would it have been?

Diane: Well, I was still able to walk,  um, the rheumatoid arthritis was mainly in my feet, so I would probably say maybe a five at that 0.5 or six. The fatigue was pretty bad.

So a five or six seems fair. Um, I know that there are people out there in a lot more pain than I am, and some are using canes or walkers, or even in wheelchairs. And I would have to say there's just a lot worse than mine.

Linda Elsegood: What would you say your quality of life is now on that same scale?

Diane: let's go back to when I first started with the LDN and, and how it improved.

I would say it went from a five or six to maybe two or three because I did feel more like myself. 

Diane: Dan is good. Then I would say it went from. I kind of did that backwards. Then I would have said that my quality of life was probably like a four or five then.

Um, and then it improved to like a seven or eight. Um, I still had the daily pain from the rheumatoid, but it was better. And the brain fog and fatigue improved. So instead of feeling 80, I was more feeling my own age of 50. There's a big difference there. Um, to be fair, um, I have to say that LDN was not enough for me.

Um, it, it served me very well for months. But in the summer of 2013, I had a lot of stress at work. They were basically trying to terminate me. Um, there's a long process that they had to go through to do so. And I had requested reasonable accommodation at work to try and help deal with some problems caused by my rheumatoid arthritis.

Which were denied to me and the stress and the disease was very active and aggressive. It got worse for me in the summer of 2013. Um, I had to choose another treatment to go along with the LDN. It is again, considered an alternative treatment, but I have been taking antibiotics since the fall of 2013, and together the two are working very well for me.

Linda Elsegood: I mean, any condition where you've got an autoimmune disease, stress and trauma

are really big

triggers. So hopefully. Once your life calms down, things hopefully will improve tremendously as well.

Diane: I agree with you. Linda stress plays a very, very big role with my disease, and I'm sure with many others, such as what you have ms.

Um, in our online support groups on Facebook, you hear that all the time stress can trigger flares. Um, whether. For rheumatoid can trigger flares. There are different things that can trigger it for different people. It's been amazing. It's been quite a journey of learning and awareness since I been diagnosed in 2012, um, there's a whole world out there, not just my little corner of, of the earth.

Where people are suffering from these diseases, many doctors, not all of them, but many doctors are trained in medical school. How to treat symptoms of diseases. Some doctors look for causes. Some doctors try to treat the cause instead of the symptoms. It can be frustrating when a patient has a doctor that only wants to treat symptoms and not look at causes.

Um, I was fortunate in that I got to a doctor he's an osteopath where they try to treat the cause of a disease instead of the symptoms. And that's one reason I'm doing the antibiotic therapy in conjunction with the LDN. Um, for anyone listening to this interview with you today, I encouraged them to educate themselves.

Do your own research. If you don't feel comfortable with a treatment that is suggested to you, you have the right to refuse it and search for your own solution. Like I did. Um, look at side effects of medication that are prescribed for you. Decide. If you are willing to take that medication based upon what it can do for you and your condition and the side effects that could affect you at some point.

And if you're not comfortable with that medication, don't take it, find something else because there are alternatives out there. From the online community, Yahoo groups, Facebook groups, particularly, there are so many people that are successfully using what is termed alternative medication, low dose naltrexone, successfully to treat their conditions.

Um, I know you're doing interviews with many people with many different diseases, but I've seen people online testifying from firsthand experience of the success they're having with low dose naltrexone for multiple sclerosis, thyroid issues, fibromyalgia, rheumatoid arthritis. It's. Very individualized.

Your dosage may be different. Even 4.5 is considered an optimum dose for some things, but with ms and smother diseases, thyroid issues, the dosage can be very particular to you as an individual. And. One of the groups. I have an online support group for people taking or interested in taking LDN for rheumatoid arthritis disease.

And there's one woman that takes five milligrams per day. Some women do better at three; it's very much up to how an individual body works with medication. And I think for rheumatoid arthritis, diet can also play a very big part. It's not to be ignored. I have not done autoimmune protocol diets or gluten-free although, should I choose to do that?

At some point, I do believe it will enhance the treatment that I'm already taking.

Linda Elsegood: What can I say? What an amazing interview. Thank you so much, Diane, for sharing

Diane:  Yes. Are there any other questions that you would like addressed Linda?

Linda Elsegood: I'm going to ask is if you can write an article for our newsletter.

Diane: Yes. Um, I'll try my best. I, I'm not much into writing these days, but, um, I'll give it my best shot for you because it's worth it.

This medication low dose naltrexone is like a miracle for some people. It doesn't have harmful side effects. It may not work for everyone, but no medication does. Um, I applied you and your charity and the work you've done over the years to make this, um, more well known out in the world. And I attended for people listening.

I attended the LDN conference near Chicago in 2013. Because I was taking the medication and I wanted to, to go and hear from experts. It was well worth the time and money to attend. So if anyone wants to get more information, I encourage them to order the CD of the conferences that are available. Um, pays a small fee to listen to them online, do the streaming site.

Um, it's just, people call it a miracle drug. It's not really a miracle, but for some that are sick, it can seem like a miracle. Um, I find it an answer to a prayer that I found it when I did. And I'm so happy that it was available to me and I could find a doctor to prescribe it. Um, it has many health benefits, side effect benefits that people have experienced.

No more allergies symptoms after they started taking LDN for, uh, an autoimmune disease. Um, no more flu maybe or no more sinus infections, many, many different things are beneficial from taking this medication what's even better is longterm usage. There are no harmful side effects at this low dosage. And. So I just strongly encourage people that have an autoimmune illness of any kind to look at it as either an alternative treatment or something to take in conjunction with your other treatments.

Um, more information is becoming known through research. Um, hopefully, it will become more widespread with the doctors. It is up to us, the patient. To make our doctors aware of the medication and the uses for it and get them on board to prescribe it for their patients. So I encourage people to do that. Um, Julia halts, um, Teleseminars via phone for people that want to go to their doctor and talk about taking the low dose naltrexone and she'll have helpful articles and papers that you can print out and take to your doctor to help educate them.

Linda Elsegood: Thank you very much for sharing your experience with us.

 

Any questions or comments you may have, please email us at Contact@ldnresearchtrust.org. I look forward to hearing from you. Thank you for joining us today. We really appreciated your company. Until next time, stay safe and keep well.

Barbara (2) - US: Fibromyalgia, Sjogren's Syndrome Arthritis, Hypothyroidism (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Barbara from the United States shares her Sjögren's Syndrome and LDN story on the LDN Radio Show with Linda Elsegood.

Barbara suddenly noticed something was wrong with her health when she began to experience sudden pain without an apparent cause. The pain eventually intensified until the point where it hurt to lift her foot onto the sidewalk to avoid the curb.

After the pain naturally died down, it returned a few years later which is when Barbara was then diagnosed with Sjögren's Syndrome. Upon hearing about Low Dose Naltrexone (LDN) through her cousin, she decided she must try it.

Barbara is now able to enjoy time with her family without any serious pain and do the simple things like climbing the stairs without any stiffness in her legs.

This is a summary of Barbara’s interview. Please listen to the rest of Barbara’s story by clicking on the video above.

Barbara - US: Polymyalgia Rheumatica (PMR) (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Barbara from the United States shares her Polymyalgia Rheumatica and LDN story on the LDN Radio Show with Linda Elsegood.

Barbara began to notice symptoms of arthritis around late 2013 shortly after participating in the jury of a murder trial. The stress from the trial certainly took its toll, leaving her with a stiff neck, hips, shoulders and muscle pains.

Having refused conventional treatment, Barbara was determined to find another solution which is how she came across Low Dose Naltrexone (LDN). Within a week of starting on LDN, her pain had begun to decrease and she was able to walk the dog again and complete other simple activities without the usual pain.

This is a summary of Barbara’s interview. Please listen to the rest of Barbara’s story by clicking on the video above.

Teresa shares her Fibromyalgia, CFS, Thyroid disfunction, Spondyloarthritis, IBS and LDN Story (low dose naltrexone, LDN) from LDN Research Trust on Vimeo.

Teresa is from Portugal and suffers many autoimmune conditions. The worst is Fibromyalgia which doctors don’t recognize easily and don’t have a treatment for. But she did her research and tried LDN. She suffered many years but has an improved quality of life thanks to the Low Dose Naltrexone.

Bev uses LDN for Graves, Psoriasis and Psoriatic Arthritis - 12th August (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Bev from Israel shares her Graves Disease and Psoriasis and Low Dose Naltrexone (LDN) story on the LDN Radio Show with Linda Elsegood.

Bev has lived across the world in South Africa and Australia, but it wasn’t until she returned to Israel that she began to experience her symptoms of Grave’s disease. This coincided with her pregnancy, leading to an enormous amount of stress on Bev’s body.

Combined with the usual symptoms of pregnancy, Bev then began to suffer from blurred vision and lost a lot of weight rapidly. Concerned about the health of her unborn child, Bev was determined to find a solution.

Thankfully bev was able to give birth to a healthy baby girl, but her symptoms still progressed afterwards. She reached a point where she described herself as a “walking skeleton”, but fortunately had come across Low Dose Naltrexone (LDN) after researching it thoroughly.

Once starting on LDN, Bev has never looked back. She no longer has severe headaches in the evening and is now back to “nearly 100%”. She recommends LDN to anyone who’s even remotely interested.

This is a summary of Bev’s interview. Please listen to the rest of Bev’s story by clicking on the video above.

Michelle Resendez FNP-C - 15th Jan 2020 (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Michelle  Resendez is a certified family nurse practitioner. She combines her love for alternative and natural medicine alongside traditional medicine.


She has successfully treated patients with a diverse range of health conditions that have not responded well to conventional medical treatments.

She said" I first learned about LDN about 10 to 12 years ago, first learned about it from a naturopathic medical. The first patients I treated had thyroid conditions, Hashimoto's, Graves thyroiditis. And so I was really using it to try to the modulator assist the thyroid in functioning better. And from that point, it really expanded and opened the horizons, treating other things.

So we found that people with thyroid conditions, if they're taking thyroid medication, usually have to reduce the amount of thyroid medication.

When I start someone on Low Dose Naltrexone (LDN), easily around 0.5 to one milligram at night, and I will either reduce their thyroid medication in half, or I will just reduce, if they're on a T three medication, I'll reduce that down.

 A lot of times, their autoantibodies will start going down, and that will help the thyroid function better.

Sometimes you'll get some adverse side effects like tremors or palpitations, or just feel a little bit more excitable than her used to feel.

I have a lot of patients start noticing the effect almost immediately within a couple of days. Depends on what condition I'm treating.

A osteoarthritis type pain or structural type pain people usually notice the effects within a week of taking that.

Once they move out to one or two milligrams, they start feeling some relief.

Antibodies are a little bit more resistant, and it might take, two to three months to see antibodies go down with LDN. And that's because of the treatment approach for that is really multifactorial.

And the LDN is just an adjunct to that. And usually, we do lifestyle modifications and diet and, and other interventions to help those antibodies come down as well.

Anyone starting Low Dose Naltrexone (LDN) can experience negative side effects. The most common would be that when they get a rebound effect it at night with those endorphins kicking up, they can get some anxiety. They can get some insomnia.

Patients that we treat for viral conditions or reactivation syndromes like Chronic Fatigue Syndrome, they can actually get more severe adverse side effects such as sweating, fevers, flu like symptoms, feeling sore throat, things like that.

All of that is expected and typical. I don't like to stop treatment if they're experiencing those side effects because that's telling you that it's working. We're getting the endorphin release that we're looking for, and we're getting the immune system enhancements that we're looking for.

Those side effects are what I would consider good responses.

I haven't had anyone had any side effects that  I would consider to be adverse like hives—rashes, vomiting, anything so severe that I'd have to stop them on it.

I treat GI conditions as well. I've had probably the most success with gut issues. It's one of my top responders. Some of my earlier patients were Crohn's patients.

LDN seems to work pretty well for the exhaustion, the fatigue and the pain.

The conditions that I treat teenagers for could be anything from Attention Deficit Disorder, Depression, pain conditions, allergies, sleep issues.

Some of my kids are on the autism spectrum, so I do treat that as well.

I do have quite a few teens and young children on LDN. And I'll actually have them on liquid if they're too young to swallow a pill or won't tolerate a gummy or a sublingual lozenge.

I do have a traditional medical doctor referring to me, Neurology, Cardiology, Rheumatology. Dermatology because there's a lot of dermatologic conditions that can be treated very successfully with both topical LDN called Xeno top and then oral LDN.

The skin conditions I am treating it for it would be the Legos, Psoriasis, Rosacea, Eczema. Those are probably the top of all the skin conditions that respond really well to it. It takes normally 3 months to see results.

There's trials to find if there are some food triggers associated with that.

A lot of it is when they're having fires and because it's triggered by something and I want to find out what that trigger is.

And then the LDN just helps the body heal itself. So it's keeps them in a remission state.

When I first see a patient I typically wll do labs tests first that looks at allergies, hormones, thyroid, inflammatory markers, genetics, things like that. I try to find triggers if I can identify any and remove those before then starting on LDN. I like to see how they respond first to that.

I like to do things in stages so we can really see how impactful each thing is at each stage. So I'll take away the food triggers first if I can identify them and then add LDN onto that at some point.

Right now we've just moved into our new office. So my business partner and I have been here for three months. I'm at a two-month waiting list right now. Once we hire some more back-office staff, I'll be able to stack more appointments and that will trim down for maybe a month or two and then we'll probably get booked up again. I do keep appointments open early morning and sometimes I'll see patients after my last appointment for the day. If there's something urgent or somebody's not responding favourably to meditation or something.

I leave those time slots available for that so I can get people in if I really need.

I would say on average, patients see me every three months. That would be somebody who is stable, doing well on their regimen and not needing any further testing or imaging or interventions done.

So some patients I will see on a monthly basis if they have a lot more chronic illnesses and conditions because I like to do those steps, plan out, maybe CBO treatment, diet.

Also with hormones, thyroid continue to add things to optimize how they're doing and their quality of life.

I have some come in annually. They're probably not my patients on LDN. They're probably more. They're doing our mono treatments, pellets, injections. Yhey're doing other treatments other than just LDN.

Summary from Dr Michelle  Resendez YouTube interview. LDN Radio Show Listen to the video for the full interview.