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

Shannon Garrett, BS, RN, CNN, LDN Radio Show 2016 (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Shannon Garrett, a Thyroid and Auto-immune Women’s Wellness Nurse has been searching for help and a diagnosis on Low Dose Naltrexone (LDN) for many years.

Shannon finally received a diagnosis of Hashimoto’s where she was diagnosed with Celiac Disease and Pernicious Anaemia.

Shannon first found out about LDN through a prison nurse and how it successfully helped her Father who had Multiple Sclerosis (MS). From then on, Shannon started researching, searching social media for information where she came across some helpful support groups.

Shannon broadcasted what she found to her doctor, where they both agreed that the LDN medication was worth trying. She worked nine months on getting her body ready for the medication which could potentially result in nutrient deficiency. This is when she saw a brighter version of herself. 

Shannon began working closely with patients who was wanting the Low Dose Naltrexone (LDN) medication and seeing what would be right for them. Her aim was to empower patients and doctors that LDN does not always work for some, which leads to a protocol and closely monitoring the patient. 

Shannon found a 90-95% success rate for her patients, an improvement in their quality of life even. Despite some patients still having sleep issues and insomnia within the first 2 -3 weeks, there was no other outstanding side effects. A small handful of patients say their anxiety increased at the beginning of the LDN treatment medication, which therefore they would refer the patients to a cream rather than an oral capsule.

You can find Shannon through: shannongarrettwellness.com or holisticthyroid.net

Summary of Shannon’s success story interview, please listen to the video for the full story.

Any questions or comments you may have, please Contact Us.  I look forward to hearing from you

Keywords : Low Dose Naltrexone, LDN, Celiac Disease, Pernicious Anaemia, Multiple Sclerosis, MS, medication, nutrient deficiency, anxiety, insomnia, Shannon Garrett

Dr Sarah Zielsdorf, LDN Radio Show 2016 (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

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

Dr Sarah Zielsdorf is a relatively new prescriber of Low Dose Naltrexone (LDN), yet her knowledge of autoimmune diseases etc. is certainly convincing throughout this interview. 

Having Hashimoto's and Hypothyroidism gives her the perspective of the patient. Her “extra" education in Functional, Integrative, and Holistic medicines makes her very qualified to treat a host of illnesses. She prescribes LDN, but does thorough tests to arrive at the best combination of treatments including diet, exercise, detox, and proper medications.

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

Robert - US: Fibromyalgia, Anxiety, Major Depression (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Robert from the United States shares his Fibromyalgia, Anxiety, Major Depression and Low Dose Naltrexone (LDN) story on the LDN Radio Show with Linda Elsegood.

Robert became very ill in 2015 when he started to get pins and needles all over his body, leading to him becoming very lethargic. He had muscle spasms and an overwhelming sense of fatigue. 

Robert’s doctors prescribed him multiple types of thyroid medications which had little to no impact on his health until he discovered Low Dose Naltrexone (LDN) in early 2016.

“Within a week of starting LDN, I got up one morning and I was able to stand up right with no pain, which was something I hadn’t been able to do for months. I didn’t believe it was real. I had energy again.

To anyone who’s listening and is on the fence about trying LDN, then you’ve got to. Obviously do your research, but the results are worth the work.”

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

Ray - England: Hailey-Hailey Disease (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Linda Elsegood: I'd like to introduce Ray from England who takes LDN for Hailey Hailey's disease. Thank you for joining me, Ray.

Ray: Thank you very much for asking.

Linda Elsegood: could you tell us about your Hailey Hailey's disease when you first started to notice symptoms?

Ray: I first started to notice symptoms on my body about seven years ago.

Linda Elsegood: what kind of symptoms?

Ray: I was getting a breakdown at the skin at that time, which was mainly centred around the neck on the left and the right sides. It was blisters. It was becoming infected, and it was rubbing on shirts obviously when I was working as a teacher.

Linda Elsegood: And what did your doctor say? What medications did they give you to help?

Ray: I was prescribed some cream and then some antibiotics. Basically, what was happening was the outbreaks were lasting for about five to six weeks. And then they were going into slight remission, but the breakdown was starting to come back again.

Over a period of time, the outbreaks were getting worse because it was becoming sorer and it was breaking down with more regularity. In 2009, 2010 I got massive eruptions in my groin area and also on my chest under my arms and my neck was really bad.

Linda Elsegood: Was stress a factor that made it worse?

Ray: Stress is a factor. LDN in the UK is off license, and although I had remarkable effects with it and remarkable benefits, I was going to see my consultant this week. I was anxious that she was going to turn around and wash your hands of me as other people have.

So I was mindful of that. A couple of days beforehand I started getting spots of it coming up on my stomach. But I don't think that stress, he's everything. I think is a contributing factor but it's not the sole actual reason for it.

Linda Elsegood: Well, if I can take you back to before you started LDN, how did you go about obtaining a prescription in the first place? How did you hear about LDN?

Ray: I heard about LDN from the self-help group that I'm involved with which is, Hailey Hailey's Disease New Approaches. This was started off by a lady called Lori and Thomas. And there are 70 people involved in that now. We're trying to help each other through this.

One or a few there had LDN prescribed, and I saw that they had it. So started researching it because once I found out what Hailey Hailey disease was, the congenital effect of the calcium pump and that he was hereditary, I started looking into it. I did a vast amount of research and came across the work of Dr. Bernard Bihari. That's how I found out about LDN.

Linda Elsegood: And how long ago was that?

Ray: That was about January this year when I started, I was formally diagnosed with it in October last year.

Linda Elsegood: So when she heard about LDN, and you could see that other people were taking it, what did you do about getting a prescription?

Ray: I had spoken to my GP to see if there was any chance that he would prescribe LDN for me, and he said he couldn't because all the directives that have come from the local commissioning group on prescribing off licensed drugs. I then spoke to my consultant about LDN, and she said that she couldn't do it either. So I wrote to the commissioning group in the UK asking them if it was possible. I had been referred by my consultant for laser treatment on this which I wasn't really keen on because that was just going to affect the skin surface.

It is a cosmetic reconstruction. It wouldn't affect the cause but they refused as well because he didn't fit that criterion. So I wrote to the chief officer of Dudley in the commissioning group and I wrote to him five times. I tried to phone him three times. He wouldn't speak to me, so I knew I was getting absolutely nowhere. My consultant had used LDN in the past and she was quite happy with the research that I'd done and was willing to give it a try. She wrote the request for LDN for me through the hospital board but was rejected by the commissioning group. So I knew that this is going to happen and I knew that wasn't going to get anywhere. I got 5 letters ignored. I went to my GP, and I said:" Look, if I get this myself, would you supervise me?"

And he responded to me that if I got it, I was taking it he would have nothing to do with it, so I felt right Okay. So I stopped all antibiotics in February, all opioid painkillers. So on the 28th of February, I had filled my supply of LDN, and I gradually started to build up from 1,5 mg up to 4,5 mg over a period of time.

I've now been on it for just over a month. I've been on it for five weeks.

Linda Elsegood: You are very kind to offer us a before and after situation which people can see at the end of the interview and it is absolutely amazing.

Ray: I mean, I would go so far as to say that has changed my life. One little thing that people will suffer from it because of the pain and the pain is constant. It's 24 hours a day. You can't sleep, and there are some people that I know who have this on her back.  They can't sleep on their back. Unfortunately, I don't, but he doesn't matter because in the groin chest and armpits, if you move around in bed, which we all do, then the pain of that wakes you up.

So for the period of time, I was getting on average about two and a half hours sleep at night which was not exactly doing me any good either.  I haven't worked since last June because I can't stand in one place very long. I can't sit for very long.

I certainly can't drive because I can't get into driving position. Now what the LDN has done, it's transformed. It's taking the pain. It's healing dramatically. The groin area is slightly improved, not as the neck. But then again,  I'm not expecting it to work as fully in other areas but my underarms, my chest is clear. I'm able to basically live a more normalized life. I'm bathing four times a day. I'm still not ready for going back in front of the classroom for the kids. I think it's important to say that the support that I've had from the group from LDN research trust and from a consultant is giving me hope, optimism and determination to get this thing kicked into touch.

Linda Elsegood: What about your sleeping pattern now?

Ray: Sleeping is more or less normalized. I might wake up once in the middle of the night one for 15, 20 minutes and then I get comfy again and go back to sleep.

Linda Elsegood: And that in itself has an impact on everything, doesn't it? just being able to get your rest and have asleep?

Ray: You wake up in the morning and you know you still got it, it's still sore in areas, but you're actually seeing the thing getting better. It motivates you that something is happening. I may be on it for the rest of my life. I may get a taxi in the future but at least I will know then that I have something that works, something that is helping me, and something that's restoring my quality of life.

Linda Elsegood: Well, that's excellent.

I think you might find it's a drug for life, but because it's not toxic and it's not going to do you any harm, there's no reason why you shouldn't take it.

Well, that is amazing. How about if we in six months time do a follow up to see how you're progressing?

Ray: That's great. I mean, anything I can do to provide information that will help anybody else that's what we'll do. One of the things that I've done at the moment is, I have been recording everything on a daily basis religiously. I've been taking blood pressure measurements because I do suffer from, blood pressure, which is managed but nevertheless, I have got slightly high blood pressure, and there's been no change in blood pressure. It is stable on both sides. I've been noticing the dosage the symptoms, the areas, sleep patterns, mood, appetite and documenting everything that I'd been doing every day.

And honestly, I can say that I have had absolutely no side effects of this. The literature states that you are the best advice to take this st 1,5 mg and go up, after about a two week period by one milligram, so 1,5 mg, 2,5 mg, and then 3 mg. I did it a bit quicker than that and in about three weeks. I suffered no adverse effects from it whatsoever. And it may well be that because I've taken 4,5 mg quite quickly  I will go down to 3 mg and then see you, and will keep on measuring to see what happens after that.

But there are no side effects that I have come across at all. And that in itself is marvellous. I've also taken steps to engage my MP with this method about it being a full license and he has written to the commissioning group. And if he doesn't get any response, then I'm prepared to take it to the secretary of state for health.

Because I feel that the evidence that I have and the images that I have been living proof that this particular medication is invaluable for anybody who has Hailey Hailey disease.

Linda Elsegood: Well, I'll look forward to speaking to you again in six months time. Right?

Ray: Okay. Thank you very much, indeed.


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.

Paul Battle PA-C, LDN Radio Show 22 Feb 2017 (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Linda Elsegood: today. Our guest is physician assistant Paul Battle from Colorado. Paul is an experienced LDN prescriber and also has personal experience of LDN.

Paul Battle PA-C: Thank you. I really appreciate it.

Linda Elsegood: Well, I know you've been prescribing LDN for many years. How long has it been now?

Paul Battle PA-C:  Since 2008 I believe.

Linda Elsegood: Okay. I thought it was longer than that. At that time, how many different conditions do you think you've prescribed LDN for?

Paul Battle PA-C: Approximately 20 or so. Ones that I can recall right now, all varying different conditions, an autoimmune disease. It does help with cancers that have had treatment already. I can't say it's a cure for cancer, but it's a, like a supplemental treatment, especially for people who've already had cancer therapy, stage four cancers.

And then certainly the autoimmune diseases, which can include Lupus, Crohn's disease, all sort of Colitis, Complex Regional Pain Syndrome. What I generally do is look at the disease mechanism, what the aetiology of it. If it has some antibody-associated mechanism, autoimmune disease, then I consider LDN and the treatment.

Many of these people really don't have any other option. They tried multiple drugs. A lot of the drugs will have side effects and they just are looking for another answer. LDN can help with a lot of people that don't have any other options. 

Linda Elsegood: And from the patients that you've prescribed LDN for, what has been their success rate?

Paul Battle PA-C: I would say the majority of the patients get some positive response. I would say probably close to 85% of people will get some positive response. Some are very dramatic responses. For example, I had a 13-year-old girl with Crohn's disease who after just 3 months, she had already been on the biologics and was losing weight and having difficulty she had no more symptoms. All her inflammatory markers were completely normal and she's still doing well. That was probably about a year and a half ago, just a couple months ago and she's just doing remarkably well. Same with some of the complex regional pain syndrome. This is a terrible disease that plagues people, that causes severe pain due to some dysfunction or dysregulation of the immune system related to the nervous system. It's called the neural glial cells. And some people, I've had 80% relief from complex regional pain syndrome. I first started that in 2010 when this young woman who was attending college couldn't finish college. We had put a spinal cord stimulator in her neck to try and control the pain, but she still wasn't doing well.

That was my first proposal ever for CRPS and Dr Chopra wrote an article, then published an article a couple of years later after I started this young lady on it, and it worked for her. She finished college, got a career, and after a year and a half, she went off LDN without a problem and since then, I've been treating multiple people with that disease with varying success. So it really varies though, like I never can guarantee to somebody that I'm going to cure them or they're going to get 90% relief. We're just trying to improve the quality of their life.

Linda Elsegood: And how long would you say it takes on average for somebody to notice that LDN is doing something for them?

Paul Battle PA-C: Well, I've seen people respond in some positive fashion within 2 to 3 weeks. For example, my son, (that's how I got interested in all this) within 2 weeks with his Crohn's disease started having a positive response, getting a better colour, less pain, fewer symptoms. But I've also had people where it's taken six months.

I had a woman who was a university professor with Complex Regional Pain Syndrome who just persisted. I said," just keep on, keep on. " And she was in a wheelchair. Her symptoms were so bad. She was disabled in a wheelchair.  Then six months later, I got all these Facebook invitations to look at this video, and here she was returning to work, which was a glorious thing.

And now she just texted me last week saying she did a five kms. That's going from a person in a wheelchair totally disabled to now running five kms. That's been about a year and a half now, but she stuck it out. And I asked people to be patient. Sometimes they do not think it's doing anything. For example, in her case, she said: " I don't know if this is working.

I'm just gonna see how it goes without it." So one Friday night, she ran out of it, and that was the last time she ever skipped a dose that she said it was the worst, she described her spinal cord on fire. And I've had a number of other people saying, "well, I'm not sure if it's working."

They stop it, and then they discover it was really a mistake to stop it. So I tell people in where from a couple, three weeks to six months. 

Linda Elsegood: And from all the patients that you have prescribed LDN for, have any had negative side effects?

Paul Battle PA-C: I think some people describe a kind of tiredness or a little fatigue they may have and sometimes it depends on when they take it. For example, most people take it at night, but I have a lot of patients with these syndromes that really creates sleep deprivation anyway. I don't want to have them risk their restorative sleep. So I have them take it in the daytime and I think those people probably have a little bit more fatigued and tiredness than the people take it at night.

I met some people that just like any other medications have a little stomach distress from it, but that's pretty unusual. And you know, I'm not even sure if it's the LDN, but, the sleep deprivation, I really haven't had troubles with that too much, because I titrate them up, fairly solidly over three weeks, sometimes four week time period.

Linda Elsegood: And would you say there's any condition better than any other that you found LDN works best for?

Paul Battle PA-C: I would say the inflammatory conditions of the joints work really well. Dr Berkson,  done great the presentations on Rheumatoid Arthritis, iPad, people who were on the biologics,  that is,  the biologic agents that are what's called tissue necrosis factor inhibitors, who were doing okay on those and, they couldn't afford anymore so they want an LDN and they actually got better results. One patient of mine now was mountain climbing. He wasn't able to move his shoulders for 3 years, went on LDN, and now he's welling up that he's climbing with his kids. So I think that the joint arthritis issues, the inflammatory bowel disease, especially Crohn's. I don't find all sort of colitis as responsive as the Crohn's patients. So I'm careful to say how successful it is with Ulcerative Colitis patients, but it's certainly always a good idea to try it. The gastroenterologists recognize the Ulcerative Colitis and Crohn's that may have some different mechanisms of action.

The cancer patients, I've had several stages for cancer patients. They're living any of them with the same diagnosis. That's been good. And how much of that is the LDN? How much is it good health and a good attitude? I don't know, but I just know the other people that were treated without LDN in their particular type of cancers are no longer with us.

So I think it is a help because of the two mechanisms that LDN works. It inhibits cancer cell reproduction, and it also, according to the new research done last year by Angus, Down in Great Britain where it actually helps change the gene action with apoptosis of the cancer cells. So I think it has a dual benefit therewith, with cancer.

Linda Elsegood: We have a few questions here and we will start with the question from Randy who has Graves' and Hashimoto's. And the question is," I've heard that LDN can lower thyroid hormone and sent a person hyperthyroid, but in the information, it says it can quickly make a person hyperthyroid.

Can it really have such opposite effect."

Paul Battle PA-C: Usually it's hyper because what happens is the Hashimoto's usually has a tendency, depending on what phase of the disease you're in. Graves', usually you're hyper and that could possibly cause the problem but what it is is the Naltrexone interacts with the antibodies so if a person is Hypothyroid from Hashimoto's thyroiditis, I always tell them to reduce their thyroid supplements by half or 25% because there's been a number of people who are hyperthyroid, they're on their thyroid medication, they take the LDN and the next day they're agitated, they are like high, they're hyperthyroid because what happens is it has a tendency to neutralize the antibody action, whether it actually reduces the antibodies or how the antibodies respond to the cellular receptors with antibodies to thyroid.

We don't know, but I always warn people to cut their dose down before they take their Naltrexone. In the case of Graves' disease, I haven't heard of it causing I hypothyroidism. I guess that would be possible if it's, a lot of the inflammation is causing a hyperthyroid state, which you can't get in Grave's disease and you reduce that inflammation, you could possibly reduce the thyroid activity there.

But I haven't had that personal experience with Graves' disease. Mostly I treat the Hashimoto's thyroiditis, and that's the most common cause of hypothyroidism.

Linda Elsegood: Thank you for answering that question for Randy. We have a quite long question here, so bear with me. It's from Shantelle.

She says, "So thank you for being on the show and greetings." And she's a 54-year-old woman diagnosed with disposed systemic CIRCLE DOMA 15 years ago. The only medication she's presently taking is IVIG and Plaquenil a 0.25. She lives in the UK and is currently in the process of finding an LDN doctor.

She says she's noticed that you have experience in bioidentical hormones, and she would be very interested in your views on estrogen and testosterone. Four months ago, she changed from oral HRT to testosterone gel to having biodentical pellet implants of estrogen 50 mgs and testosterone at 100 mg.

And since she's had the pellets, she's never felt so awful in her life in terms of depression, mood and run down. And she seems to catch every bug going around compared with the four months that she was on oral.

Paul Battle PA-C: I didn't quite catch the initial diagnosis but if she's being treated with IVIG that puts it in the same class of diseases that can be treated with LDN because it's going after the same problem. That is an autoimmune disease immune dysregulation. I have a young girl who was also going to be treated with IIVIG  for an antibody associated Peripheral Neuropathy.

She had problems with antibodies to her nerve receptors so she basically did not have a lot of function in her muscles, her GI tract and they were going to give her IVIG, but it wasn't insurance approved here in the United States, at least with their insurance so I offered a LDN, and that has proven to be very good for her.

She's back in school, halftime. She was in bed or missed all of last year. So the answer to her question is: I think LDN would be a very reasonable possibility for her to approach her other disease. Do you want me to answer the question about the hormone?

Linda Elsegood: Hang on. The main question when you get to the bottom there, because the testosterone and the estrogen implant is making her feel very depressed, very down, very moody.

She feels awful. She felt quite good on the oral HRT. So she's saying to you, she wants to go on the LDN, which should she take? Should she stick with the oral or the pellets?

Paul Battle PA-C: Well, I usually use the oral just because it's easier to titrate the dose. Once she got inserted pellets with estrogen, it might've been too high of a dose, and once you put the pallet in the subcutaneous tissue, it's very difficult to adjust the dose.

So she may be running very high. I usually like to estrogen to run around 60 to 100. That's what the literature shows to be protective against osteoporosis and coronary artery disease. But if you have too much, you can certainly have psychiatric side effects just like women get what they are on the birth control pill, they can have depression.

And as far as the testosterone pellets, the same thing, once you insert those, you're kind of stuck with those for 3 or 4 months. So some people love pellets because they don't have to deal with the daily pill and adjusting things but in my experience, it's just easier to adjust. If she has trouble with estrogen, you can just reduce the pill dosage.

I work with compounding pharmacy so I can make it whatever dose I want.1 milligram, 2 milligrams. The oral therapy for estrogen has been shown to be more cardioprotective than for example, a pellet form or a cream form. So for that reason, the dosing can be easier adjusted when it's in a pill or a cream form.

Linda Elsegood: Well, that's good. I think that was the route she was hoping to go down because she felt so ill and so down. So I think you've just confirmed it for her, so thank you for that. Here's a good one. Have you prescribed LDN for migraine headaches?

Paul Battle PA-C: I have. I have several patients with migraines that I prescribed LDN mostly because the current theory on migraine headaches is not our old theory of spasm of the arteries because they've done arteriograms and found that the artery diameter doesn't really change a lot when people have migraines.

So it's really more thought to be an inflammatory process of the nerves and therefore the LDN would be appropriate to try and adjust to an inflammatory condition like that. So I do have several patients with migraines on LDN. I do other things too but it seems like that's helped them.

They were treated in traditional medications for years, probably 5 or 10 years and I seem to be getting better results with the LDN. They stay with me, so obviously I'm doing something right for them.

Linda Elsegood: And I'm talking about headaches and migraines. Have you ever known LDN to cause a migraine headache?

Paul Battle PA-C: I haven't noticed it cause a migraine, but  I have had several patients say it does cause a headache more of the dull headache, not so much the pounding vascular headache type of symptoms.

Linda Elsegood:  And we have another question. It says," Have you seen LDN improve acne breakouts?

Paul Battle PA-C:  I have not seen that. I just haven't noticed that. I use other things for acne so I haven't observed that.

Linda Elsegood: Okay. Thank you. And what it's your opinion of using Ketamine infusions in conjunction with LDN?

Paul Battle PA-C: I think they can be done. I have patients, I just had one last week.  The ketamine works in a different way. it's a dissociative anaesthetic and it works by blocking the NMDA (N-methyl-d-aspartate) receptors. That's the receptor that transmits the pain to the brain and so what it does is it blocks that and so that really doesn't have any interaction with the LDN because the LDN works on opioid receptors, endorphin receptors. I think they can be used synergistically.

Linda Elsegood: And what conditions would you use the combination to for?

Paul Battle PA-C: That would be Complex Regional Pain Syndrome. When I used to operate on people putting in spinal cord stimulators, I would put it routinely. First I would give  IV magnesium prior to surgery and that has been shown in several studies that it can reduce pain 50%. That magnesium also naturally blocks the NMDA receptor, which the ketamine does so that works with ketamine. And then I would give an infusion during surgery and then after I would give an infusion for overnight to blocked the NMDA receptors so that the surgery would not precipitate an exacerbation of the Complex Regional Pain Syndrome or what's known as RSD, or Reflex Sympathetic Dystrophy.

That's only a diagnosis that I've ever used it for and I don't know of any other diagnosis that you would use Ketamine for. Ketamine is a tricky drug. Adults can have a miserable experience whether they can have nightmares and side effects from them can be hypertension, tachycardia, hallucinations, things like that.

So with adults, you do have to be careful with it. There are low dose ketamine infusions, and there are high dose ketamine infusions. Dr Kirkpatrick at the RSD Research Centre in Tampa, Florida, does a high dose. I've been there, and I watched him do his technique there. So that's the only diagnosed I can think of.

Linda Elsegood: Well, thank you very much. We'll just go to a quick break, and we'll be back in just a moment.

To listen to individual radio shows and interviews go to www.mixcloud.com/lldnrt.

This show is sponsored by Paul Battle PA-C. He is a well-respected physician's assistant. He takes a physiological approach for your optimal health using traditional and nontraditional treatments for autoimmune diseases and bone health, using hormone replacement therapy and low dose naltrexone. He has patients throughout Colorado and other states.

Visit www.pabattle.com or call 720 773 9041.

We have a question here, Paul, which you can sympathize with. Amy has a 17 year old daughter got Crohn's disease diagnosed four months ago. She says," Are the children taking LDN with success? What can I expect to see as an improvement besides better sleep, which assist with pain and improve quality of life?

And by that, she means more energy and able to go through a normal school day. Will LDN take her pain away?

Paul Battle PA-C: You're right. That is dear to my heart because that's how I got started with my son. And for her to know, my son was diagnosed with severe Crohn's as he hits at age 10. I think it started at age 9.

He had to have a good part of his small bowel resected that time, 3 years later, he had another severe exacerbation going into hypovolemic shock and so that is a time where I started researching by myself. And that's when I read Jill Smith's article in 2007 about LDN and Crohn's and she's an excellent and respect gastroenterologist who did excellent studies on LDN and Crohn's showing a remission. So if she wants to know if it works within 8 weeks, 69% of the people in her first study, showed that they went into remission, 89% of them showed that they had a significant reduction in the Crohn's index scores.

And what are those? The index scores are more symptomatic scores on a number of stools per day. Cramping, bloody diarrhoea, fevers things like that. Those, that 89% of them had significant reduction scores, so she can't expect a very good possibility that she would have less pain because the inflammation is causing the spasm, which is causing the pain.

So reduces the inflammation. Those symptoms will improve. They also will reduce the diarrhoea if she is having diarrhoea. You can get Crohn's in any section of your GI tract from the oesophagus to the anus. My son now, he's been on LDN for 8 years. He is a weight lifter, a bodybuilder.

He's doing really well. He has a strict diet so the one thing I would tell people that you don't depend on LDN alone. It's multi-system, multiple approaches to solving the Crohn's problem and if you do these other techniques such as dietary control and supplements, probiotics, things like that, you can expect to get good control of it.

As I said, I had a 14-year old that really pretty much doesn't have symptoms anymore. Inflammatory markers are gone, so you can expect chemical markers for inflammation to be reduced when she's on the LDN and yes, they had children on certainly had my own son on it. Dr McCandless treated many thousands of people with autism with LDN, and so it's proven to be very safe with children.

Linda Elsegood: Thank you. That was an ideal question for you, wasn't it?  Robin has asked the question. She's got Multiple Sclerosis. She's had been taking LDN since 2005 and in that time, she's had no new lesions and no active ones. She's had MRIs. She says that she's no better, but she's no worse.

MS has been stable in all that time. She uses a cane away for balance away from home and uses a scooter in large stores. Now what she would like to know is, does she need to continue taking LDN for the rest of her life, or is there a period of where she can stop?

Paul Battle PA-C: That's a good question. I wouldn't because she's been stable now for almost 12 years, I would be very hesitant to stop it. There are not many people with MS that are stable for 12 years. He could have 5 or 6 years where you have this up and down cycle but that's a long time to be stable.

She has no new lesions and the cost and the risk of LDN is so low. I don't know why she would want to consider stopping it. The other thing is the benefits of LDN with your immune system in general. It upregulates many of the things that help protect you from infections. It upregulates the natural killer cells and with the new research and cancer and the old research in cancer with doctors Aegon? it may help. I can't say for sure, but there are no studies on preventing it cancer. But certainly, we've seen the action clinically and how it benefits people with cancers. I would really recommend that she stay on it for the rest of her life.

Like I said before, there are people thought: " There's no benefit here. I stop it." And they paid the price. And MS is not something you want to have an exacerbation, it can be quite devastating for some people.

Linda Elsegood: Exactly. Yes. I certainly wouldn't want to come off the LDN.

We have an interesting question from Kat and, she says that she takes baking soda in water for reflux before she goes to bed, but she also takes her LDN before bed. And will the baking soda stop the LDN from being absorbed?

Paul Battle PA-C: It might. I wouldn't really recommend that because of the baking soda itself, could inhibit the absorption of LDN.

It'd be best if you could take the LDN maybe an hour after that. By then, the baking soda should be out of her stomach and into her small intestine. So that's why we don't recommend compounding pharmacies to put calcium and other minerals in with the pills because it can disturb the absorption.

If she really needs the baking soda then she might consider doing LDN in a topical form with the oil or cream or something like that. If she has that much trouble with reflux she might have eosinophilic esophagitis, which LDN can be helpful for, since it's also an immune-based problem and that seems to be a more common diagnosis. So in the end, I wouldn't recommend her to take it at the same time.

Linda Elsegood: Just on a personal note, I used to have to take an anti-acid every night for acid reflux, which was really bad. It used to burn the back of my throat and absolutely awful. But have changed my diet and not eating gluten or dairy, the acid reflux has gone on.

I no longer have to take that medication, so I'm quite pleased.

Paul Battle PA-C: Excellent. That's the way to do it. Glutamine also was another nice thing to do. It's just an amino acid and that helps with reflux also. That's what most of the intestinal cells are dependent on for energy and also helps with restoring the intestinal cells so that's another thing she could try, but you're right, Linda, that's the best thing to do is just get away from those triggers.  Gluten and dairy are the two most common triggers for many of the diseases we're talking about. We are not used to those kinds of proteins.

Linda Elsegood: And we have a question here from Heidi and she says she's got resistant depression. "I've been on every type of antidepressant and been in counselling on and off for years, and nothing works. I currently attend CBT I am suffering from crippling anxiety, depression, and insomnia. I've read that LDN can help.

I'm very desperate for help. I wish to try what would work"

Paul Battle PA-C: That's a good question. Some of the psychiatrists on our meetings are saying it can help. I mean, it certainly, increases the endorphins or at least the endorphin function. So that in itself can help depression. I don't know if it'll help the anxiety. The cognitive behaviour therapies he's doing is helpful but newer research is showing that many people have depression. It is an inflammatory condition. For example, people who have had a heart attack, the highest risk for reinforce, and that is, another heart attack occurring is depression and it's not an accident because of inflammation from depression. Inflammation in the presence of coronary artery disease can cause the plaque to be released from the wall of the artery causing a coronary thrombosis. So I think it would be worthwhile. There are studies, and I think Sweden and Japan, are showing that people who didn't do well on the medications, did well responding with high doses of fish oil. It is also an anti-inflammatory, and I'm talking large dosages.

For example, 5 to 10 grams per day of fish oil. Because DHA, which is in the official, makes a good part of the brain weight, about 20% of the brain weight so in the studies that Purdue University with children on anyway, so that most of the kids with this kind of psychiatric diseases, 85% had low DHA.

So fish oil is another anti-inflammatory, another option for people with depression. And the other thing that's important, since I do a lot of hormone work is to make sure that the thyroid is optimized. I don't mean in the range or normal. I mean optimized at a good level, healthy level, not just in the range, like 95% of the population and that has been shown in psychiatric journals to be just as good as antidepressants for depression therapy.

Linda Elsegood: I know many people who are using LDN for depression and anxiety, and I found that it really does help. Certainly got nothing to lose by trying it.

Paul Battle PA-C: Right.  It's a great economic thing with really minimal if any side effects.

Linda Elsegood: Exactly. We have a question here from Robert who's got CFS/ME, and he said, "I was originally taking LDN at 4.5 mgs daily.

Now I'm taking it every other day based on an article which I have read recently, which is recommended, taking it every day or every other day.

Paul Battle PA-C: We have all, traditionally been prescribing it every day because the blockade is four hours and the immunological benefits that had been described byDr Dagan and Dr Bihari himself show that the immunological benefits last for about 20 hours. For that reason, I usually do a daily dose. Now for this person, if it's benefiting him every other day, his receptors may be more sensitive, and he does not need the 4.5 mg. What he might try is take half of the tablet and take two 2.25 milligrams a day versus every other day. But then, the pharmacokinetics, that is how the drug works and how long it lasts, it would be generally recommended to be on a daily basis. Now,  you got to understand how LDN works. It is an opiate receptor blocker, and if somebody has more sensitive receptors, they may need a lower dose or not as frequent to make their immune system actually, most beneficial.

That's true. We find with cancer. We don't like to go too high on the dose. Anything above 4.5 I don't think is a good idea because then you're blocking the benefits of the opiate growth factor that Dr Zagon has described in the past. So he just may find a level that's good for him, and that's perfectly fine, but the pharmacokinetics usually indicated it should be a daily dose.

Linda Elsegood: Thank you. We'll just have one more quick break, and we'll be back in just a moment. The LDN research trust has an LDN Vimeo channel. I have interviewed over 550 LDN prescribers, researchers, pharmacists, and patients from around the world for many conditions. You can find the link from the LDN Research Trust website. If you'd like to be interviewed, sharing your experience, these email, linda@ldnrt.org

 I look forward to hearing from you.

This show is sponsored by Paul Battle PA-C. He is a well-respected physician's assistant who takes a physiological approach for your optimal health using traditional and nontraditional treatments for autoimmune diseases and bone health using hormone replacement therapy and Low Dose Naltrexone. He has patients throughout Colorado and other states.

Visit www.pabattle.com or call 720 773-9041

Welcome back. I wonder if you could tell the people listening, Paul, the benefits of attending the LDN conferences, either in person or the live stream.

Paul Battle PA-C: Well, I've my personality. I think I've been to now 4 or 5 of them and the benefits certainly I get as a practitioner, but he can also apply as a patient or interested individual, is that you hear people from all over the world and the different applications that they're using it for. When I look at myself, I'm only one practitioner in my own experience, and I certainly haven't treated everything so it gives me a great advantage to listening to other speakers from anywhere around and what they're using it for, some of which I really never thought of.  The psychiatrists are talking about how it might help depression and may help sexual function, for example.

I certainly never thought of that so I think the biggest advantage is you're seeing some of the top people around the world who've been using this for a while and all the different indications so that if you have a disease that has not been a common one that we told about LDN, like Multiple Sclerosis and Crohn's, but it's one of these more rare diseases, you then can say: " This might be an option for me." And then try to find the LDN prescriber to try it. It's such a low-risk treatment. It certainly would be worthwhile for a lot of different diseases. I think you've counted over 200 autoimmune diseases now that I think we had the experience. It is a lot of diseases to cover and it's great to hear from other people around their experiences.

Linda Elsegood: And this year we're getting case studies and some prerecorded presentations because there was so much information there that we wanted to present to everybody. It would have taken like two weeks just to sit there and watch. So you're limited to what you can do in three days, but there is going to be a lot of extra material there.

But the Q&A sessions I find amazing because not only do people in the room get to submit questions, but the people who are listening online as well, and there are some amazing questions that come up, and it's really interesting to see all these people that have been prescribing LDN for so long.

Some of the questions are very complex and answering them can be tricky. We had feedback last year from one doctor who said she thought the Q&A sessions were amazing, and she had all her questions answered. She had some questions answered that she would have asked herself if she thought of them and the whole thing was unbelievable. She said, because some of the questions that were asked, I think there are only a few where nobody on the panel knew the answer, and they just shook their heads and said, no, I don't know that one. So for her, that meant every time somebody answered a question, they didn't answer it to give an answer.

They answered it because it was a fact. So for her, that made the whole thing believable. So, that was good. But I always find that the conferences, the atmosphere is electric. You've got all these people that are so for LDN. It's just amazing, isn't it? The actual feeling in the room.

Paul Battle PA-C: Well, it is. It's a great comradery because it's still not a well-known treatment and if it doesn't have salespeople doesn't have commercials on TV.

So it's really been pretty much up to people like you, Linda, who's been one of the leaders in promoting LDN around the world and that's been my mission since it says my thumb's life is to speak at international conferences sponsored by you and sponsored by other organizations. I'm going to be speaking at the Age Medical Management conference in Florida in April about LDN and that's a whole different group of practitioners that will be hearing about LDN from myself. It's a nice, progressive movement that's helping thousands of people around the world in a very economical way. I just wish there was a way we can spread it a little bit more, but commercials are expensive, so it depends on all of us to be together.

That's where I feel a real brotherhood and sisterhood about LDN movement. We don't have a lot of help other than us volunteers or in your organization.

Linda Elsegood: And this is where the good thing is in sharing case studies and people getting together to discuss different ways of treating different conditions with LDN.

It's a good way of everybody learning. We do have another question has just come in and it's for Rheumatoid Arthritis. The question is, "How long should I take LDN to treat my Rheumatoid Arthritis?"

Paul Battle PA-C: Well, I'm not sure if he's asking how long should he take it before he notices a difference, or how long should he take it to treat it. I would stick with it at least three or four months before he would expect any dramatic results. Just give it that much time. If he does have a good result in the end, if you can get 70 or 80% improvement then he used to just stay on it the rest of his life. Rheumatoid Arthritis is not one that goes away. I would want to make sure though that it is Rheumatoid Arthritis. I had a patient in my clinic who was told by the rheumatologist she had Rheumatoid Arthritis, and so for 3 years, she's been thinking she had rheumatoid arthritis and I checked her for Lyme disease, through Armin labs, the German lab that we have come to our conferences, and she was positive for Lyme Arthritis. So the question is always make sure you have the right diagnosis also. But if he gets a good relief, Dr Bert Berkson in New Mexico has a great presentation on his patients with Rheumatoid Arthritis showing the serological markers improving dramatically on LDN. Many of the people were able to get rid of most of their rheumatoid medications of which a lot of them have side effects.

Linda Elsegood: Yes. We've had the lady Mary, who's been listening to the show, and she's talking about Complex Regional Pain Syndrome, and her daughter is 15 years old. She says: "Is it safe to take LDN at the same time as Gabapentin". Her daughter is currently on 2,700 milligrams a day, and she'd love to get her daughter off the Gabapentin but it's the only thing that takes the edge off the pain.

"Is it necessary to go gluten-free to find relief?" She said: "I know she should, and I'm gluten-free myself." But her daughter is not ready to accept. That's what she needs to do. "Are there any studies out there on the longterm effects of using LDN in adolescents?" She often searches for weeks and finding studies difficult.

What is the most normal dose for CRPS? She's 5,11 foot and weighs 140 pounds. Thank you for your help.

Paul Battle PA-C: Well, that's interesting she brings that up because I had that exact patient in my office about an hour ago. She's the CRPS patient on Gabapentin, and she's been trying to get off Gabapentine.

I believe the Gabapentin may have been helping her a little bit because Gabapentin can work with the LDN as it helps attenuate the nerve transmission. It's a class of drugs, like anti-seizure drugs, so she can certainly use them together. And is there any studies? There aren't any longterm studies on kids.

We just know that like Dr McCandless had kids on the LDN for years and there's never been any problem longterm. My son's been on it for 8 years without a problem. We have the OB-GYN doctors in Ireland who use the larger dose Naltrexone, 50 mg for infertility during pregnancy, and they have not had any problems.

So I really can't think of any other safer drug and  I've been a PA for 35 years and a lot of different medicines that I prescribed over the years. I can't think of a safer drug then Naltrexone at  3 mg, 4.5. For her at that size, I think the 4.5 milligrams would be the appropriate dose, but I would titrate it up, and regardless of the gluten-free, I think when you have any kind of immune dysregulation gluten-free is a good idea. The gluten proteins are not ones that we have been designed to digest. Dr Tom O'Bryan, who comes to our conferences, is one of the experts on gluten, said to me last year that, even a person without gluten intolerance or the Celiac disease still has inflammatory changes in their intestinal track when they do biopsies 30 minutes later.

So my recommendations would be yes to have her do gluten-free. I know my son with his Crohn's took a while, but when he finally realized, this is his body, this is this future, now he's gluten-free, dairy-free, all that. So I would highly recommend that she go on a gluten-free diet.

Linda Elsegood: Appreciate what she's saying though.

Having a 15-year-old daughter who wants to socialize and go out and be part of the crowd, and then you can't go out for a pizza because you can't eat it. It's difficult, isn't it?

Paul Battle PA-C: You have to do a gluten-free crash. A lot of pizza parts and an Italian place have gluten-free pasta, gluten-free crust. I was just had that last night, as a matter of fact so it's workable now. It's much easier now for gluten-free meals and diet, and she can always bring your own food. That's what my son's done for years, is just pack your own food and have salads and things like that.

Linda Elsegood: Well, it's not very easy in England to find anywhere that is gluten-free.

You'll find that when you come over. When I went to travel and, we were hungry, and I just wanted to grab something. I went to the supermarket, and I said to the lady because I couldn't find it," Do you have a gluten-free section?" So she said: "Yes, but it's not very popular."

We're going to stop it and we've only got what's left on the shelf. And there were like six things, and it was like, then you're going to get rid of all the small section. You do have. I thought that was quite amazing.

Paul Battle PA-C: They need more education there because the Northern Europeans, as I understand it, have a little higher incidence than other population.

That is 1% of the population so I'm surprised at that. That's unfortunate.

Linda Elsegood:  We took our grandson to the cinema last week, and we were looking at menus outside to see what was gluten-free. Many places don't have menus, and we were looking at TJ TG Fridays, and we went inside and they actually have a gluten-free menu. And it was like," Wow, a whole menu of gluten-free!" You can choose it. This is it! Take it or leave it! There was actually a choice. That was very good. I had a gluten-free burger and a gluten-free bun, and it was very tasty.

I was going to say to you, Paul and anybody else out there who's listening, if there are any conferences coming up where you're a speaker, or you're attending a conference, and LDN is going to be one of the topics, let us know. We actually have on our website now an events calendar for talks and lectures so that people can read and have that as a resource available.

So you would have to give me the details, Paul, and we'll put that on there in the event calendar.

Paul Battle PA-C: We can spread the word. I love doing it. If we can help a couple of hundred people. And mostly what I really like doing is teaching the practitioners because I figured each practitioner has 1,000, 2000  patients in his practice. You've helped that many thousands of people at least be exposed to the LDN, by teaching the practitioners that, I think has a big impact on l.

Linda Elsegood: And word of mouth. Taken hold, hasn't it? People are telling friends and social media. I must admit I didn't want to join Facebook. I don't know how many years ago now. Reluctantly thinking that suggest another thing I don't have time for, but I think we have about 18300 members now.

I'm on there and I'll take this opportunity to thank all the wonderful admin people that we have who answered all the questions and help and steer people and give them advice on how to find an LDN prescribing doctor. Without them, Facebook wouldn't continue, but the number of people that pass through, who come, who go, who take the information, go to their doctors and get LDN prescribed It's a wonderful tool.

Paul Battle PA-C: It would just have to educate more people, more practitioners.  Some people may not be open to things that they're not trained in, and certainly the lack of a lot of clinical trials that do make the practitioners a little hesitant to prescribe it, but if you educate yourself, I've read a lot of it, all doctors papers and convinced that it's definitely a good thing for my patients.

I do certainly not hesitate to do that, but you do have to get educated, and that's what we're doing.

Linda Elsegood: Well, I'd like to thank you very much, Paul, for being with us today. We've just about run out of time and you've been amazing. So thank you. And I look forward to meeting you in September, but I might meet you when you come over later in the year.

Paul Battle PA-C: Yes in summer. That'd be great! Okay, Linda, I appreciate it and a really great time. I love helping out.

Linda Elsegood: Thank you very much.

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.

Margaret - US: Cushing's, Hashimoto's, PCOS, Arthritis, Depression (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Linda Elsegood: I'd like to introduce Margaret from the United States who takes LDN. Thank you for joining me, Margaret.

Margaret: Hi,

Linda Elsegood: thank you. Could you tell us when you first started to get sick, how old were you?

Margaret: Well, after the birth of my first child when I was 20, um, I started to have a lot of hormonal problems and symptoms.

And after several years and several doctors, um, my first diagnosis was with the polycystic ovarian syndrome. And, um, I suffered through, uh, many years of trying to find someone to treat me in a way that didn't have a lot of side effects. And I eventually went on Metformin, and that was very helpful. And I kind of had a period of good health for several years, and then when I was about 35 I started to have a lot of new symptoms that were similar but different and more intense.

And after probably four years of that, I finally was diagnosed with having Cushing's disease and having an ACTH secreting pituitary tumour. And I had pituitary surgery, two years ago, in May of 2013. And they found the tumour, they got it out, and I went into remission. And the recovery from that is quite brutal.

You have to slowly wean off of steroids. You have to take them as replacement because your pituitary doesn't work right for a while. And the withdrawal from steroids has been like into heroin withdrawal. So it's very intense. It's very painful. You have a lot of joint pain, muscle pain, um, a lot of psychological symptoms, depression, um, anxiety because not having enough cortisol is almost as anxious.

It is provoking as not as having too much. And so it's, you know, a good year of weaning. And then what happens is because you had high cortisol for so long, a lot of autoimmune things pop up that were being suppressed by the cortisol. And that's kind of where I'm at at this point, where now I have really high Hashimoto's titers and.

You know, I'd have to replace a lot of hormones and I'm still in the recovery process from Cushing's. But, you know, in the meantime, ten other autoimmune things get you.

Linda Elsegood: So, before you, um, started on LDN, could you describe what a typical day for you felt like?

Margaret: Well, I started on LDN when I was about sixteen months postop from pituitary surgery. So I would say that I had very little quality of life. I was still in the place where I was in a lot of pain. I didn't work full time. I was only working part-time and only from home at that point. I could barely do the grocery store by myself and come back home. I still have people taking my kids to school for me and all. It was basically helping me just to survive.

So I would say probably on a scale of one to 10, it was about a three.

Linda Elsegood: Oh, wow. That's not good. Not a good life.

Margaret: I mean, it was better than when I had Cushing's where my life was a zero. Yeah. Before they took the tumour out, I was home-bound and could not work. Didn't think straight. Had severe panic disorder. And anxiety all the time. And how did slept in probably two years by the time I had surgery. Yeah. So it's a really intense disease.

Linda Elsegood: It certainly sounds like it. So how did you hear about LDN?

Margaret: My endocrinologist, who, he is a Cushing specialist. That's what he specializes in. He actually recommends it to a lot of his postop patients because most of us have these underlying autoimmune problems and he gives it out quite frequently, especially if you kind of linger in your recovery.

I mean, some people just snap right back. That wasn't me. Maybe cause I was older, not sure, but he recommended it. And my primary care doctor prescribed it for me. I ended up making my own with a 50 millilitre, uh, 50 millilitres and 50-milligram pills because my insurance doesn't cover compounding.

And that was the most economical way for me to do it. And so my primary care doctors, he's in on it too, and he actually prescribed it for me. And, um, you know, does all the followup for it for me.

Linda Elsegood: When you started, did you notice any side effects at all?

Margaret: Well, I started at 0.5.mg, cause I was doing liquid, it was really easy to change my dose based on whatever I was noticing.

So the very first thing that I noticed was that I started dreaming, like a lot, and they weren't bad dreams. They were actually amazing, wonderful dreams. But when you have Cushing's and you don't sleep for a long time, you don't dream anymore cause you never get to REM sleep. And I'd had several sleep studies. You know when I was sick but didn't know what was wrong with me.

And I never got up. I never had any REM at all. So I will say that the very first thing that happened was it gave me background sleep and I started dreaming on a regular basis. And each increase in dose I would have several days of. Just fantastical dreams, which is a good thing for me. So it's a side effect, but a good one to me.

IThey were never bad dreams or nightmares or anything like that.  I did notice that on each dose increase that I would have a little bit of bowel motility, very short-lived. And when you have hormone issues. That's not unusual. You know, there's a lot of stuff going on in my body, so I don't know if I can particularly attribute it to LDN, but I think so. and it just was, you know, getting used to it. So at this point, I'm, my endo wants me to work up to four, but I'm very slowly working my way up. Right now, I'm on four, and that has been a process of about a year of getting up that high. And I stayed at three for a long time. But my Hashi titers were still very high, and so he wanted me to go up a little higher and see if we could get it to work.

Linda Elsegood: So, what is a typical day like for you now?

Margaret: Well, I attribute some of it to LDN. Some of it is just simply time. And my pituitary is recovering, but I now work full time. I am completely in control of my own life. I still have some chronic pain. It's much better. I do think that the LDN helped with the pain a lot.

It is now where I can take two Motrin a day and be pretty okay. I also use acupuncture extensively, which is, you know, it's not about LDN, but that is a huge part of my recovery as well. And I would say, you know, my life is an eight, and I work full time, probably 60 hours a week. I take my own kids to school.

I have a child in college now. And I take him to school and I grocery shop, clothing shop. I do everything now. And so it's a huge improvement from before I had surgery for my pituitary tumour. And I think LDN is probably half that. I, I won't be stopping it anytime soon.

Linda Elsegood: What would you say to other people who are thinking of trying LDN?

Margaret: You know, I think it's such, it's such a longstanding drug that's been around for so long and they know what the side effects are and it's really easy. So low risk, why not try it? And I think that's how I presented it to my primary care. I said, you know, cause he had other people on it.

And so he had heard of it. He was aware of the drug, and it's such a low dose. He just had no problem letting me try it, even if he didn't really believe in it necessarily. So I would approach it in that way. But I mean, the risks are very low and if it doesn't help, then just quit if it does and amazing.

Yeah. That's what I would say. Try it,

Linda Elsegood: You have such an amazing story and so inspirational for other people. Thank you very much. You're sharing it with us.

Margaret: Oh, you're welcome.

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.

Lexi - US: Parkinson's (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Lexi started having chronic insomnia, one of the non-motor symptoms of Parkinson’s disease; and severe anxiety, bladder spasms, loss of sense of smell, and constipation. Soon she noticed tremors in her right toe, and noticed a right foot drop, which caused her to trip and fall several times, including while walking upstairs. Next she noted her right arm didn’t swing when she walked, and that walking felt like pushing against a river current.  She started having pain, stiffness, weakness in her legs, debilitating fatigue, and her voice and her handwriting became small and scratchy.

Her neurologist’s diagnosis of Parkinson’s was confirmed at Mayo Clinic. Her quality of life was about 3 on a 10-point scale, and she had to quit her job because of her disability. With a no-hope diagnosis she started researching and learned about low dose naltrexone (LDN) in 2009 and convinced her neurologist to prescribe it. She started on 3 mg for 1 year, and quickly noticed improvement, a feeling of wellbeing, and less anxiety. Currently she’s on 4.5 mg, all her symptoms improved, and she has weaned off all Parkinson’s meds. She rates her quality of life at 9 on a 10-point scale.  She still has a few bladder spasms, but otherwise is doing well, including regaining her sense of smell.

Keywords:  insomnia, anxiety, bladder spasms, anosmia, loss of sense of smell, constipation, tremors, foot drop, pain, stiffness, weakness, fatigue, voice changes, Parkinson’s, LDN, low dose naltrexone

Summary of Lexi’s interview, please listen to the video for the full story.

Any questions or comments you may have, please Contact Us.  I look forward to hearing from you

Judy - US: Sympathetic Autonomic Nervous System Disorder, PTSD (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Linda Elsegood: I'd like to introduce Judy from the U.S. She was diagnosed with sympathetic autonomic nervous system disorder due to chronic PTSD and trauma. Thanks for joining us today, Judy. 

Judy: [00:01:13] Thank you. 

Linda Elsegood: [00:01:15] So could you tell us how old were you when you noticed you are experiencing problems with your health? 

Judy: [00:01:26] I didn't experience, I didn't know.

 I think my, now looking back, I think my mental health was, um, was a factor, um, because I, I grew up in a sick family. Basically.

So, um, you know, I mean, well, I'm not physically, I really wasn't a sick child, right. But, um, I was like in the middle of a lot of trauma in the family, a lot. And, um, I guess it affected me since I was younger. My. I, um, felt my, um, uh, like my mother, like really involved me in her life. She was, uh, she was, you know, she told me she was going to commit suicide and she would be bulimic and she, it was just like a mess.

It was until she passed. And, um. I think I think as a child I was very distraught. Uh, I, uh, I just, it just affected me. I see pictures of myself where I had like dark circles under my eyes from when I was little. So, um. You know, it's like, to the extent of it, it just, like, I'm so far past it, but it was, uh, I was in constant turmoil and, uh, and neglected, neglected.

So, um, I, I really think that it had an effect on me. 

Linda Elsegood: [00:03:33] And what about your teenage years 

Judy: [00:03:37] and my teenage years, I was just, um. You know, I, I think I tied myself to people that I shouldn't have tied myself to. I was over empathetic. Um, just did what people wanted me to do, wanted people to like me and felt ugly when I was told the opposite.

It just, um, it was like I looked back at it now and that's just the way I was, but I had no self-esteem. Um. I just, uh, I was a mess. Yeah. I was just, uh, uh, I just, I was like, I was sick and then everybody came and talked to, but it, but I didn't have anybody to talk to. And I did. I wouldn't, I was, I was in bed.

I was ashamed, really. Okay. And I kind of, I buried everything. 

Linda Elsegood: [00:04:31] And how old were you when you got married? 

Judy: [00:04:35] I was 25. 

Linda Elsegood: [00:04:39] And how was your health? 

Judy: [00:04:43] Um, my health was fine. Actually, I haven't had a fever since I was 22. Um, the neurologist actually added in that he thinks that I had an immune disorder also.

Um, and I didn't understand because I said I was checked for autoimmune and it was negative, but he said, he told me no, if there's an immune disorder, which is, he says you can't check for that. And I, I think, I know, I think I understand now a little bit more. But, um, yeah, so, um, yeah, it was a, it was a mental issue.

Then. Like I said, I would be, since I was 22, I haven't had a fever, but, um, my, uh, I see that like certain things, especially with this disease, it, um, it. Really, um, it regulates your temperature. So my temperature always was like 96, uh, regulates your blood pressure. I would, when I got my period when I was a teenager every month, it was extremely painful.

And during those painful periods, I would, uh, my, my, uh, blood pressure would dive down. My heart would race, I would sweat and I would almost pass out. And, uh, this is just the way my life was. I would just, my, my blood pressure always took a dive and, uh, but it felt like my heart was racing out of control.

 I see that even as a youth, I, I felt full fast, couldn't consume liquids, but I didn't know any better. I think that was, that was me. I was. Over concerned about my weight. I just, because I was heavy at one point and then, uh, lost weight and people treated me different and I was just, I've always been consumed about like, I had no self-esteem, no self-awareness you see that now?

And, um, and then just life was. On. I just was, I was, as I got older, I got, I was over empathetic. I was just like, I would take care of everybody and I couldn't untie myself to them. They would, I just, I'm thinking back, I can't believe the way I was, um, until now, until, um, until this pill. I wrote something on the website just saying like, it's not even half of what I thought it was, I was just, I downplayed everything. Molestation, grade, everything.  

Linda Elsegood: [00:07:45] So before you started LDN,  what would you say your health was like? 

Judy: [00:07:53] Okay, so I got to a point. Where I downplayed everything and I absorbed the pain and I would go to the gym and just accept that I would almost pass out afterwards.

And, but then I got pain. I got pain in my neck, like really bad. I couldn't ignore it. Um, and I heard cracking in my skull and even my husband heard it from the outside. Um. And nerve pain, like shot down my arm to my finger, to my trigger finger. And my hips were always inflamed, but I just absorbed it and I went to the gym.

So I, I went to, um, uh, physical therapy and I did about 15 sessions of that. And then my other side, I had an MRI on my neck and it said bone spurs and my other side, um. I had my bicep tendon inflamed. So they gave me an ultrasound, saw was inflamed and gave me a cortisone shot and, um, that didn't help.

The only thing that helped me was, um, I was prescribed Gabapentin at night. Um, and so all I took was Gabapentin and I took Xanax for 36 years to sleep because I never got tired. I had, um, I would rev up at night. Um, and that's, this is after kids if I didn't sleep. Uh, poor days. I was, I was, uh, I would, my body would get tight and I would have heart racing.

My hair was falling out. Um, uh, like in clumps, and they just said panic attacks and alopecia anxiety and gave me Paxil and, and it still was falling out today with breaking off. But now it's not. Now it's growing in. I just thought it was just like regular breakage now, but now I see the new growth and, and um, my husband doesn't see as much hair in the, in the, um, drain.

Um, I thought all this was normal. I had, you know, I just, I thought certain things were cosmetic, um, like I could on the site. My, my feet, my, I mean, people can't believe it, but my feet were blue all the time. My toes started getting numb. My right foot started turning out. Um, my eyes were always dilated. I just, uh, I think pain-wise I hit a wall.

Um, but I at least I got some relief from the Gabapentin at first before the LDN.  so. 

Linda Elsegood: [00:10:54] So when you started LDN, how long did it take before you noticed improvements in those symptoms?

Judy: [00:11:00] Well, in, I just couldn't believe it, and in like three weeks that my feet, what I thought was normal, started turning a regular color and I was, I didn't think that was possible.

I just thought these were my legs when I took that picture. That I put on this site. I, um, I, I took that picture, just sent it to my husband because my toes were down, but I thought it was the shoes and he's, and, but he even like didn't panic cause those were my feet, you know, all the time. Um, so three weeks it cleared like physical things started clearing up.

I had done it corral Asus, um, like I couldn't go to the bathroom. I always use certain things to go to the bathroom. I woke up, I started going to the bathroom. I started drinking fluids easier. Um, I didn't know that. Like that was not my normal. I started my, I wasn't full as fast and have been like that all my life, like just extended full.

Everything physically started changing. Even my depth perception, my eyes. It was like, but most of all. I got really nervous because I didn't know what was going on. I had like, I buried a lot. I had strong reactions. I see. Um. Uh, people wouldn't know this because I was joke around, but I cared about how people felt.

Everything got to me. I just like it really, I couldn't control my reactions, but I didn't voice them. I didn't communicate. And, um, uh, every, all of a sudden I'm just being like, nothing bothers me. It's very, it's very strange. I just like went from one extreme to the other, but without trying, like, without working on myself, not knowing that there was something wrong.

So, um, physically I started changing mentally. It was like just so siding. It was very, um, very straight. And my husband actually said, I think you have PTSD. And I got angry and upset because, um. That's what military people have, not, not me. No, I was embarrassed. So you know, so it just went like that and the answer, I still have the physical changes, but I just, it took me a while to get adjusted to this because it was, I was driven by extreme anxiety.

Like my father had Alzheimer's. I was afraid I was going in that direction. But I think it was the opposite. I was like, I would be so clear-minded when I didn't even know I was foggy before. And  I went into, um, I went into the city, New York with, um, with my husband to see a play with my daughter and her boyfriend.

And I was in the theatre with them and I was, I was still taking low dose naltrexone, but I was in a theatre and the theatre was extremely cold. And like everybody was cold, you know, they just, , but when I came out, I had this reaction where my insides felt weak and they were, I've never felt this way before.

I've trembled before and I used to tremble all the time, but my insides felt like they were going to come out. And now I see it. While I was getting used to this, and because of this condition, my temperature goes 93 like in the house and in the theatre, it must've been like. Dropped, um, because I've, I've actually had hypothermia before, but this was severe.

This was, um, this, I felt like I must've been going into shock. Um, but that's all I can explain too. And every day it took, so it took a while for me to get adjusted to it, um, because I just felt very strange for months. And also not myself. And I was communicating. There were things that just lifted that I didn't even know were there.

And, um, I, it, it scared me. Even sleep. Sleep was so unnatural to me and now I was tired. I was never tired before. I was all hyped up. So physically, I just, even my friend said, I drive better. I was like on and off with a gaseous, my depth perception was. Well, if I was always on guard, I see that now. Um, mentally.

Um, it was, it was hard to get used to because I was just such, I became such a different person, um, than I was. And now I can look back and I feel, I don't feel like my past, I feel like, I know I was my past, I woke up and. I had, I was also somebody who was a compulsive shopper. I woke up and  I looked around, I couldn't believe what I had.

Like I just started getting rid of things. I didn't have that feeling of, of uh, needing stuff. It's just like I, and to me it was, that's a normal person, but I didn't know I was abnormal.  I really. It's, it sounds, I always blame things on, no, just asthmatic or whatever. But as I was getting better, if somebody upset me, I can feel the tops of my, my feet tingle.

Um, my stomach was regurgitating and I actually came home from being upset, shaking, and I, I actually. We went to bed. If I cord blood from, from my rectum, it was an, I thought, well, maybe those are haemorrhoids. But now it was just my whole nervous system affecting my nerves. My feet were tingling back up.

They were called. It was just, my reactions were still getting. Um, I was getting used to it. It was quite a ride. 

Linda Elsegood: [00:17:34] What is your health like now 

Judy: [00:17:35]  It is like never before. Uh, I, first of all, I've, we, uh, my husband's a firefighter and, uh, he's also, um, on the medicine because when I was getting used to, he's also had like, he's his, he, he was like, I can't explain it.

He was like, I see that he didn't take social cues, and that was part of my. Like marriage things. So I like you went to the doctor, he put on medicine. He's totally different now. I am so totally different. I'm easy going. I drink fluids and eat differently. I have self-esteem. I've got nervous. I see that.

I must've lived my life as being nervous. I would never have been able to do this with you. I was just nervous. I see that I was depressed. I feel I guess I, I feel what normal people feel I used to put, getting, you know, this condition, it makes your swallowing like choking. Um, like all your natural reflexes are, they don't, they don't work.

The things that people don't think about. And I looked back and I. I see that I would like, I would choke on food as it younger child. Like it was just because this nervous system, everything that works that you don't think of your eyesight, your swallowing, your temperature, your heart racing, your stomach, your, um, I had chronic kidney disease because I couldn't.

Take in fluids like a normal person. It took me a whole day to drink a little bottle of water, and now I see, I can, I see it now that that's not normal, but I didn't know it before, so, um, yeah, even I was, uh, given medical marijuana and I was just like when I was in pain, I. I would try to smoke it and it would, medical marijuana always made me crazy, but it made my pain heightened and I was, I felt like an Alzheimer's patient and this is like, I didn't, I got a like a severe reaction for medical marijuana.

And now since I've been on low dose naltrexone, it is totally different than my whole life. It just calms me. Go to sleep. Um, before it used to make my whole body shake. It changed something in my body, uh, changed my whole life. And, uh, I just, I find it amazing because I didn't even know anything was wrong with me.

I just, I'm more comfortable with myself. I didn't have a strong sense of self. I never had it before. I don't. I liked my own company. I see myself differently. I don't see myself ugly anymore. I just, my, my body's totally different. I don't, I have very, um, I, I like people more. If I speak my mind, and, and it sounds strange, but I never did.

I always buried it. I was always, I would always listen to people. I was afraid they wouldn't like me. Yeah. Everything has changed. 

Linda Elsegood: [00:21:01] We've come to the end. But what a remarkable story it was amazing.

Judy: [00:21:25] That is amazing. It is amazing. Really. I'm just so grateful that if I didn't walk into that doctor if I didn't find you guys, I don't even know what would become of me so. Um, 

Linda Elsegood: [00:21:42] thank you so much for sharing your experience with us. 

Judy: Thank you, Linda. I appreciate it. 

Linda Elsegood: [00:21:53] This show is sponsored by our members who made donations.

We'd like to give them a very big thank you. We have to cover the monthly costs of the radio station software and with phone lines and phone calls to be able to continue with the show. And thank you for listening.

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

Transcripts are only 90% accurate you can watch the video 

Elizabeth - US: CFS/ME, Lyme (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Elizabeth uses low dose naltrexone (LDN) for chronic Lyme disease, chronic fatigue syndrome (CFS), food sensitivities, and poisoning by Cipro.

When Elizabeth was very young she had anxiety and nausea, feeling on the verge of vomiting, and doctors found no diagnosis. At 12 she was taking Accutane, which interfered with her immune system and her symptoms increased through her teen years. 

She carried diagnoses of chronic fatigue syndrome, hypothyroidism, insomnia, food sensitivities, depression, anxiety, OCD, gastroparesis – all kinds of autoimmune disorders and symptoms - and was disabled. She got some improvement with a holistic treatment called NAET, but in her late 20s took ciprofloxacin (Cipro) and became bed-bound for over ten years. Unfortunately, later she took Cipro again and all her symptoms got exponentially worse.

She was diagnosed with POTS, or dysautonomia, and could not tolerate medications to heal.  She couldn’t tolerate food, heat, the sun, and couldn’t sleep. When she started LDN it made her feel like she had a bad flu, migraines, and a racing heart. Her doctor adjusted her thyroid medication to help with her heart rate and insomnia, but later was able to increase it back up. She learned that taking LDN in the morning, and a lowered dose, reduced those symptoms. Now her symptoms are 85% improved.

In addition, after 10 months, LDN has improved her endometriosis pain and cognitive functioning. She has been able to come off multiple other pharmaceutical medications, including those for her high blood pressure, antidepressants, and medication for CFS. By her research, she hopes to continue improving for up to 2 years.

Keywords:  Lyme disease, chronic fatigue syndrome, CFS, POTS, dysautonomia, hypothyroidism, insomnia, depression, anxiety, OCD, gastroparesis, food sensitivity, poisoning by Cipro, ciprofloxacin, endometriosis, high blood pressure, NAET, LDN, low dose naltrexone

Summary of Elizabeth's interview, please listen to the video for the full story.

Any questions or comments you may have, please Contact Us.  I look forward to hearing from you. Thank you for joining us today.

Dr Sally Boyd Daughtrey, LDN Radio Show 2016 (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Linda Elsegood: This evening. I'm joined by Dr. Sally Boyd Daughtrey, who's a licensed naturopathic doctor from Hawaii. Thank you for joining us. 

Dr Sally Boyd Daughtrey: Aloha. Thank you for having me. This is a great opportunity to share my experience with naltrexone. 

Linda Elsegood: Could you tell me when you first heard about LDN? 

Dr Sally Boyd Daughtrey: Well, this is a very interesting question, because it just sort of - I don't know if you know the word grok, but it just sort of grokked towards me from the universe and just different layers. There's not a particular time that I went, Oh wow, naltrexone is amazing. It just sort of became clear to me. But the first time I prescribed it for a patient, it's something I will never forget. It was astonishing. I'm sitting in my office, and I hear this banging on the wall of my waiting room, just this thump, thump, thump; and my receptionist was at lunch. So I was alone; what is that? So I am flying out to the waiting room, and there's this lovely waifish ill woman laying on the floor of my waiting room, and she was trying to drag herself through the waiting room to get to the reception desk by banging, by grabbing a wall, literally dragging herself through the waiting room; and it was amazing. So I reached out and I picked her up, and I put her in a chair, and I took her in the back and started doing her interview. She was an MS patient who had been through everything and couldn't walk because of the MS, and had no money, low-income, literally stumbled into my office off the street. There was very little I could do for her because I do private medicine, I don't take insurance. But I remembered naltrexone. Someone had told me about this thing called naltrexone. This is about 2007, 2008. I managed to find a compounding pharmacist that knew what the heck it was and prescribed it for her. And within two weeks she walked into my office. Two weeks, and all I had done for her was naltrexone and some vitamin D, because that's all she could afford. I saw her for two years when she could come in and see me. She had no relapses. One more thing we did, I gave her a grounding mat. I don't know if you know what those are. It's just a very simple device that helps connect you to everything, helps you connect to the earth and reduce EMF exposure, basically.

So those were the only things that we really did. And in those two years, she had no relapses at all. And I know people say, Oh, well, MS has spontaneous relapses, but really come on, the chance of that happening was so low. And the only reason I lost track of her is that she got well enough to get married and moved to a different state. So that was the pretty astonishing start and my exposure to naltrexone.

Linda Elsegood: So where did you go from there? 

Dr Sally Boyd Daughtrey: As you can imagine, I was pretty impressed, so I started using it specifically for autoimmune conditions at first. But as you know, autoimmune conditions are epidemic everywhere, and the more you look for autoimmune conditions in a wide variety of symptoms, the more you find them. So I started going with a lot of my Hashimoto's patients next. And it's sort of becoming my go-to if someone has thyroid symptoms; there are hundreds of thyroid symptoms. I have a thyroid questionnaire that's 2-3 pages long, with symptoms and overlapping with other conditions, symptoms, and whatnot. If someone shows a lot of thyroid symptoms I run antibody tests on them, and if they're high at all, then it's pretty much an automatic thing now that I put them on naltrexone. And what I love about running antibodies is because, especially with thyroid patients, you can get a baseline antibody level, and you can put them on the naltrexone, and you can watch that number drop like a rock. I had one person come in with 1200 antibodies, and three months later, they're something like 30 to 60. That's not uncommon, to have those antibodies go down that fast. And ANA and anti-TPO and TBG are well-accepted tests.

And it's a good thing to actually have something they can take to their MDs, who tend to be more in the medical establishment. So there's good about that and bad about that. One of the bad things about being in that system is if you're entrenched in that system, it's harder, there are more social stigma and financial stigma for them to break free of that dogma. So it's really refreshing for me to be able to say, here are the baseline autoantibodies when my patient walked in the door, and here are their antibodies ten times lower three months later, what do you think of that? And the more forward-looking of these that my patients also see, because most of my patients see an MD as well because their insurance covers it now - I use that as an educational tool for, for them to help increase exposure to this treatment. 

Linda Elsegood: So, do you have any other stories? 

Dr Sally Boyd Daughtrey: I can tell you my own story. I've had Hashimoto's thyroiditis for 25 years. I got it in medical school and I remember the reason for getting it, in my mind, was cadaver lab, being exposed to huge, massive amounts of formaldehyde in a high-stress environment, and then autoantibodies started going up from there.

And it was presented to me, even as a naturopath where we treat a lot of things outside the box that isn't supposed to be treatable; even in that context, it was presented as well, we can manage this, but you're always going to have gluten sensitivity and weight problems and fatigue, and we'll check your autoantibodies every now and then, but there's no need to really redo them again because now we know you have this disease and it's not treatable.

So basically the plan that was presented to me - I'm in my early twenties - was here, they'll give me this thyroid medication, and when it stops working, we'll give you more. And then when it stops working, we'll give you more. And then when you reach the max, we'll just keep you on that. And good luck with that. And you think, okay, I'm swimming against the stream by becoming a naturopath, so the things that aren't treatable are supposed to be treatable with our medicine. And you're telling me that this is not treatable, or it's something super elusive like - maybe it's your mercury exposure or something like that. And then 20 years later, take one little pill at bedtime and have that condition dramatically improve, it was amazing. And to be able to actually track that on lab work, and say it's not just me, it's not a placebo effect. I can't really see how a placebo effect would reduce an autoantibody level on a lab consistently. Yes it could take a little bit, but that's obviously not all that's going on here. 

So myself starting to take it resulted in my being able to go from a part-time practice to manage my condition, to a full-time treatment centre. So now I have staff, and I have ancillary services, I have an associative MD, and I have all these things that I'm able to manage now because that condition is successfully - I wouldn't say cured because to me cured means you don't need to take anything to not have your symptoms. So I would say that naltrexone has created the ability for me with a wide range of conditions to successfully manage them, and moderate or eliminate the symptoms. 

I would say maybe 20-30% of my patients that come into this clinic get naltrexone treatment. Part of that's a reflection of the fact that I treat recalcitrant patients in the first place, meaning I treat patients that have pretty much been through regular medical care and have not been fully resolved with that or satisfied with that. So that population is somewhat self-selected to be a more difficult treatment population in the first place, and that's part of what naturopaths tend to do in this country. When you have a success rate that is high with a population that already has failed conventional treatment, you know you're doing really well. It's a very gratifying profession in that way.

I would say it's an appropriate fit for about a third of my patients. Of those patients, about 60 to 80% stay on the therapy and self-refer themselves to stay on it. Meaning I'm not sitting there wondering how to track compliance. They're calling in to get their prescription refilled. They're choosing to stay on it because they perceive that they feel better when they're on it, and that's pretty quick too. 

I'm reading the LDN Research Trust website, which is super useful by the way, this is a great website, and there are all kinds of things on there that I didn't know, that's useful. I've been expecting people to have a significant symptom change within two weeks, and then I'm reading on here that a lot of the chronic pain patients can take three months to have a significant benefit. So I am able to condition people to wait that long to see a benefit. And still I'm seeing 60 to 80% of people staying on it and reporting improvement.

Part of that might be me encouraging them to notice an improvement is having a positive mental effect for sure. Everyone that comes here is paying cash to see me and is paying cash for the therapies because insurance doesn't cover what I can do. So if you're going to keep paying for something, you definitely perceive a benefit from it. 

Linda Elsegood:  On the flip side, has anybody told you that they experienced any negative side effects? 

Dr Sally Boyd Daughtrey: Well, the sleep change, sleep disturbance, insomnia effect is definitely a factor. And for that, I would say maybe 20-30% of people will report that. There are some people of course that come here, see me once to try something and then I don't see them again. I don't know what happened to them. They don't follow up. It's not the right kind of care for them. So I can't say what those people are doing if they have the insomnia effect or not. But people that come in and are consistent and do the therapy, it seems to me like there's a certain subset of patients that have that symptom. I haven't quite pinned down who they are, except that they tend to be more sensitive and more anxiety-prone, more reactive. I do see a lot of chemically sensitive people, canary in the coal mine kind of people, and  their dose-response rate is very individual. So I have people on 0.5 milligrams and I have people on 12 milligrams. That's a huge range, and I've come to that with people through very specific trial and error. 

A lot of my patients are very intelligent too, they're very motivated and follow instructions well, and can do some self experimenting. Which is a wonderful thing about being a naturopath too, that that population kind of seeks you out. So I'll start them on say one milligram for a week and then have them try 1.5 and then try 2, and change the dose, and keep a log and ask, how did I sleep last night? Did I have vivid dreams? Were they pleasant or unpleasant? Were they disturbing? A lot of autoimmune people have disturbed sleep, so they're not used to dreaming at all, or they're not used to remembering their dreams. So they find that startling at first. But then if you take the time to inquire and ask if it was a bad experience, they say no, actually it was a good dream. Well, maybe that's okay. That's not a bad thing. So part of it's how you see it, but definitely, people will have restless or disturbed sleep the first few nights, but I haven't usually found it to last more than three nights. 

What I do now just for simplicity sake is to start them on, let's say three milligrams, but the first night I'll have them open that capsule and pour nearly all of it out. And then the next night I'll have them pour all but a quarter out, and then stay on that for about three nights. And once they're sleeping through the night, then I'll slowly start adding back a quarter of the capsule at a time until they're taking the whole three milligrams without any problems. And that works 99% of the time.

Linda Elsegood: I would say that there are many doctors that actually swapped to morning dosing for people who find sleep is an issue. And it seems to work just as well in the morning. 

Dr Sally Boyd Daughtrey: And they're not noticing any downwards depressions spike at any time after taking it? 

Linda Elsegood: No. And there are some people who have been taking it in the morning, swapped to the evening and feel that actually taking it in the mornings they have less fatigue. I take it for MS, and I've swapped from night to morning and it didn't make any difference. And there are some doctors that prescribe LDN for chronic fatigue syndrome, double dosing, so the dose that they take in the morning they take in the evening as well because the body doesn't see it as double. So if you were taking 4.5, the body doesn't see it as nine, it sees it as 4.5 twice, because at the time you take the second dose, the first dose has been gone. I tried that as well. That didn't give me any more energy either, but I at least gave it a go.

Dr Sally Boyd Daughtrey: That's a really great idea. And I actually just had someone who just on his own decision, started taking it in the afternoon because he was afraid. We have lava here, this volcano that tends to threaten to cover the town every now and then. So he has severe anxiety and he lays awake at night and worries about the lava covering his farm, which I can't say is an unrealistic worry. So he started taking it in the afternoon and reported an immediate improvement in mood within 20 minutes. And thinking about the path of how it's supposed to work in the body, I don't understand how exactly that's happening, but I can't discount this experience. It's a consistent experience and who am I to say to stop doing that, you're doing it wrong; because for him, it's right. So I just put him on doing it in the afternoon and then trying a very small dose in the evening to see if it helps. 

And the wonderful thing about this stuff is that at these doses, it seems so safe that allowing people to experiment with it and find what works best for them, and then tracking their results and making sure that their lab work is in order and they’re progressing in all aspects. I do regular physicals and I can see people's physical parameters improving.

I don't do just naltrexone. In this kind of setting, I'm doing naltrexone and nutrition changes and counselling and lifestyle modification, and I'm doing all of these things together, and it doesn't really serve my patients to just do one thing so we can test it. Now that's a very difficult sell, right? So that's the whole problem with holistic medicine, with testing holistic medicine in general, that it's the sum of its parts and it's a synergistic sum of the parts. So if you try to reduce that down to what's just naltrexone effect versus what's this lovely whole food B-vitamin that I've switched to them too, and taking them off their synthetic kind that was causing anxiety, for example. 

That's challenging for the standard medical paradigm to accept as a real therapy. I don't really know what to do with that, except to compare people that get that holistic treatment with it with people who choose not to have naltrexone because some of my patients are against all pharmaceuticals. I have a subset of the population who are seventh day Adventists or Amish or someone like that. And they will not do a conventional pharmaceutical of any kind. Even this one, even this very benign one. So the only way in my mind, can ever really extract what naltrexone is doing individually is to compare the progress of those people in general, with those other people who do all of that plus naltrexone. I've been doing that admittedly in my own head, keeping a tally in my head, since 2007 or 2008, so that's 30 years, and a lot of people. My overall very strong impression is that the people that do everything plus naltrexone do significantly better than the people that choose not to do it for whatever reason they're choosing not to do it.

Linda Elsegood: And if we have people listening to you in Hawaii and they'd like to come and see you, how did they contact you? 

Dr Sally Boyd Daughtrey: Our practice is called Vitality Integrative Medicine, and we are a comprehensive integrative clinic in Pahoa, Hawaii. Our phone number is 808-965-2233. Our website is http://www.vitalitymedicine.org/

Linda Elsegood: Is there anything else you'd like to add before we finish? 

Dr Sally Boyd Daughtrey: I guess one thing that I'm thinking of doing now is expanding who qualifies for this therapy. What are other doctors finding results with this that are beyond cancer, autoimmune, pain syndrome? That's something that I'm really interested in because it seems like... 

Oh, PANDAS, I had an amazing PANDAS. It's a cross - one of the things that we're seeing more and more now is cross-reactivity is in the human body to past infection. So someone who's had an infection in their childhood, say strep, or staph, or Lyme; then their body will mistake the antibody for that bacteria to a piece of their own body, their own tissue, and then they will have chronic problems with that particular organ. I'm having some really interesting results with people like that. They don't even always know that they have an autoimmune condition. They feel like they have a heart condition or a skin condition; or in this case, a mental, emotional psychosis condition. And naltrexone seems to be helping - kind of in layman's terms, it's helping the immune system be happier and calm down, and recognize what’s a friend and what's foe more accurately. The implications of that are huge.

Linda Elsegood: At the conference in February, we had two psychologists talking about post-traumatic stress. But it seems to work for cravings and all sorts of problems that people have. So the more we are using it, the more conditions are coming along that doctors are treating with it. We now have a list of I think 204. Normally, if there's an altered immune component, LDN could well work; and then there are all the different pain conditions, there are these mental health issues that it's helping with as well. So it's very interesting. We're learning all the time. 

Dr Sally Boyd Daughtrey: One that I also am treating for - I don't have a large population of people partially because they're self-reporting is poor, there are some shame-based issues with the self-reporting, but the euphoric drugs of abuse like ecstasy and Molly and MDNA. Those kinds of drugs. I think people that use those and use them and use them and use them, end up depleting not only dopamine but endorphin and enkephalin as well. They tend to present with this sort of chronic low-grade apathy, dysthymia, hopelessness, lassitude. The only thing that seems to make them happy is when they're actually on that drug. So, although it's not technically “an addiction or an addictive drug” by classification, their life ends up being cycled around the use of that drug. When I can get them to take naltrexone and stop taking that drug of choice, it seems to make them feel normal. And it makes me feel hope for these people because they're self-medicating in a way. If their endorphins are chronically low and they don't know that, but they know that they get to actually have an experience of having normal or high endorphin levels for a few hours, you can see how their life would then end up revolving around wanting that feeling of actually feeling normal. Here we are saying for the first time in your life, you can feel good, not high, but good every day. And that can be your baseline reality from now on. That's incredibly powerful. That's a life-changing experience. 

I've had a couple of patients who have been able to tell me this is the cycle they’re stuck in, and I've been able to say, well, if you can commit to weaning off that drug, not doing it every three nights or every week and/or living for it, and instead, do this because I would think that they would contradict. So I don't want them doing naltrexone and that drug at the same time; I don't know what that would do. So then we actually make a contract: you do naltrexone. If you want to keep doing your illegal drug of choice, don't do naltrexone that day, please. And they find that they need that drug, whatever their drug is, less and less. So that's very successful; that's very satisfying.

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

 

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.