LDN Video Interviews and Presentations

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

They are also on our    Vimeo Channel    and    YouTube Channel

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

Linda Elsegood: I'm joined today by Dr Bruce Berman from sunny Florida in the US thanks for joining me, Bruce. 

Dr Bruce Berman: My pleasure. 

Linda Elsegood: Could you tell us how long ago it was when you first heard about LDN? 

Dr Bruce Berman: Yes at least five years, I read an article about it.  I'm an addiction specialist, so I was very intimately familiar with naltrexone, and I know that the side effect profile is very negligible. And when the hypothesis came up concerning low dose, I said, it makes perfect sense to me. The benefits certainly outweigh the risks. So I started using it.  Hashimoto's disease, any autoimmune disease, cancer, depression, fibromyalgia. It's sometimes miraculous. I had a 29-year-old woman with ulcerative colitis who was having 15 bloody bowel movements a day that nothing in medicine could stop. We started LDN and in two days her bowel movements were down to two, and they were normal its great for the joint pain in rheumatoid arthritis.

 I use it as I do integrative cancer therapy. So I use it as part of an overall program in cancer. Cause as you know, it's the endogenous opioids that have the antitumor ability.  Plus, they help balance the TH1  to immune cells. So it's a double whammy against cancer cells,  it's just amazing.

The worst side effect I've seen and really not that bad. It's just bothersome, is vivid dreams and sleep may be affected. You may have an early awakening. We've now tried giving patients the LDN in the morning. And it still works, and it doesn't affect their sleep then.

So I'm, I'm a satisfied customer. A lot of patients are coming to me cause they do research on it and they see it. They go on the cancer tutor website and a lot of other websites and just do alternative therapies and my name comes up. And I'm happy to give the service because it's so innocuous. It's such a benign treatment, and the effects can be dramatic. 

Linda Elsegood: And how long would you say, if pushed on average, it would take a patient to notice that there are benefits of taking LDN? 

Dr Bruce Berman: I'd say anywhere from a couple of days to a couple of weeks, usually within a month. You see some dramatic results. I start low.

I start at one and a half milligrams and work up from there. Usually around three milligrams, you're going to see effects, and if you need to push it to four and a half, patients respond. But usually within a month, sometimes within days, patients respond.

Anything you want to treat for,  it's safe. It's inexpensive. It's easy to obtain. It has almost no side effects. It's like the perfect drug. Most conventional doctors are so pigeonholed that they will say, Oh, I can’t prescribe that. It's not indicated. When, of course, as you know in the States, if you have one indication for a drug, you could use it for anything called off label use, but they don't want to do it because most conventional doctors are, they're hamsters on a wheel. They don't know they're spinning. They think they're going forward. That's why I had to do functional medicine. 

Linda Elsegood: Well, he says he taught this like you who think outside of the box. 

Dr Bruce Berman: Well, I was on the hamster wheel, and all I did was give patients drugs to placate symptoms. And now, I mean, yeah, when you address causes the results are dramatic. Really, really dramatic. And it's, that's why I'm here. To find out what's in my patient's highest and best good. 

Linda Elsegood: So, in your practice, you mentioned Hashimoto's and cancer. Do you do all the autoimmune conditions? Do you know ms? 

Dr Bruce Berman: Yeah. We use LDN on all of them. We also use bee sting therapy in autoimmune, quite dramatic the way they work together. They work together to balance the immune system. But here in the States,  the LDN is so inexpensive. It's under $40 a month.

Linda Elsegood: And I'm always being asked by patients who can't travel. Do you do any online consults?

Dr Bruce Berman: Skype  I do. I do phone counsels as long as they can get local blood work if they need to just have a doctor on hand for any conditions that might need local attention. Why not? I do it a lot. I have a couple of patients from England.  I have one from South Africa. 

Your listeners should go to the website, the LDN summit 2016  was just held in Orlando last month. You can download and watch the videos on all the presentations on LDN. It was tremendous. And there's also a book about LDN now.  I know some of the speakers, Marty Gaydon, is right near me in Miami. In our field what we do in functional medicine, people are few and far between. I'll give you an example. Martin is a hundred miles south of me. And the next closest doctor is 150 miles North of me. Nobody in between. 

Linda Elsegood: Wow. 

Dr Bruce Berman: pretty sad. 

Linda Elsegood: It is. And it's a shame. I didn't know about you before. 

Dr Bruce Berman: Well, that's okay. I’m happy just to be able to see people. I had a woman, I just saw her yesterday for a recheck. She came to me last July, so we're coming up on a one year anniversary, psoriatic arthritis, so bad that the inflammation was affecting her joints. Her skin was horrible. Her dandruff was horrible. She's been on it now for ten months. She's about 90% improved. 

Linda Elsegood: wow. 

Dr Bruce Berman: The lesions are going away. She can make a full fist. There's almost no dandruff. Now we did other things. Besides that, you know that I don't know if your readers know readers or listeners know the most common cause of the autoimmune disorder is dairy products, reaction to the casein protein in milk and gluten. Yes. So all my autoimmune patients have to go off that, or I can't promise they're going to get better, but this one has been really, really strict. I have a patient who just told me she found out there's gluten in her Chapstick so who would think, wow, but gluten is everywhere. So you really have to investigate. If you want to take care of yourself because no one's gonna take care of you. The corporations aren’t going to take care of you. They're just going to give you something that's easy to use and appears to work and tastes good. They have no concern about whether or not it's beneficial. 

Linda Elsegood: And how sad is that. 

Dr Bruce Berman: I'm over the sad part, I'll tell you why I understand it. Because corporations have one job to do, their stock price goes up. Truly they don't have a humanistic component or anything else.  My patients need to be educated on what to do.So it's a lifestyle change for all of this. For cancer, for autoimmune. I mean, we've reversed three cases of MS. Well, they are reversing. They're not normal yet, but they're getting better. That doesn't happen in medicine. I had an ALS patient, Lou Gehrig's disease, actually got off a ventilator off a wheelchair onto a Walker.

Linda Elsegood: So 

Dr Bruce Berman: it's not me. We're just reversing the toxicity of this world. So I'm a, as we say, I'm a satisfied customer. 

Linda Elsegood: Wonderful, and thank you so much for sharing your experience. 

Dr Bruce Berman: Of course, my pleasure. And please have your readers, if your listeners go to their doctor and say, can you prescribe this? And the doctor says no, I can educate them.  It's innocuous. And if they have any questions or concerns, they can go to my website. All my contact information is there. 

Linda Elsegood: Wonderful. Thank you very much. 

Dr Bruce Berman: Wonderful. Have a great day.

Linda Elsegood: Do you have LDN experience to share? If so, please email me at contact@ldnresearchtrut.org I look forward to hearing from you.

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

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

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

Dr Brian Udell: Thank you for having me.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

I forgot what the beginning of that question was.

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

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

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

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

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

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

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

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

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

Dr Brian Udell: I didn't say vaccinations.

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

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

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

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

Go ahead.

Linda Elsegood: No, carry on.

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

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

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

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

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

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

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

Usually, you get people rolling their eyes.

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

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

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

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

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

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

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

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

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The conference will examine life-changing breakthroughs for treating Multiple Sclerosis, Crohn's disease, Colitis. Autism, Irritable Bowel Syndrome, Lupus, Fibromyalgia, Rheumatoid Arthritis, chronic pain, mental health issues, Restless Leg Syndrome, and many other conditions using Low Dose Naltrexone. For tickets, slide stream and sponsorship opportunities. Go to www.ldntwentyseventeen.com

Today's show sponsored by CareFirst speciality pharmacy, leading compounders of LDN and other custom treatment serving patients in other 18 states coast to coast. They're credited to provide you with the highest quality to market by the industry and the expert service you expect. To learn more call 844 822 7379 or visit www.cfspharmacy.com

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Linda Elsegood: What about giving children cows milk?

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

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

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

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

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

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

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

Dr Brian Udell: Dr. Flamingo was a genius.

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

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

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

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

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

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

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

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

Today's show, sponsor CareFirst Speciality Pharmacy by leading compounders of LDN and other custom treatment serving patients in over 18 states, coast to coast. They're wise acredited to provide you with the highest quality to market by the industry and the expert service you expect. To learn more call (844) 822-7379 or visit www.cfspharmacy.com.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Linda Elsegood: Yes.

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

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

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

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

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

Yeah, sharing knowledge.

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

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

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

Dr Brian Udell: She can do your next book.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

And how do they contact you, Brian?

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

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

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

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

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

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

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

Today's show sponsors CareFirst speciality pharmacy by leading compounders of LDN and other custom treatments serving patients in over 18 states coast to coast. They are widely accredited to provide you with the highest quality demanded by the industry and the expert service you expect. To learn more call (844) 822-7379 or visit cfspharmacy.com

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

Cheryl - US: Lyme Disease (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Cheryl from the United States takes LDN for Lyme disease and Co infections.

Her story  goes back into childhood. She had always struggled with some sort of illnesses. Gastrointestinal issues,  stomach virus, rashes on her face, etc

In her teens she developed depression and anxiety and later pain.

When she was 21, her dog got very ill and she noticed she had a four to five inches in diameter round bite that  looked like a Brown recluse bite. She was having palpitations and strange symptoms.  That bite stayed for about two to three months on her body and it had a little centre point.

They diagnosed her with fibromyalgia in 1994 because she felt like she had the flu all the time. And it just never went away. She was vomiting all the time, she had to leave school in 1995 and declared total and permanent disability. Then she slept all day and night, was freezing all the time, and nobody paid any attention. And at that time, Fibromyalgia  meant "It was all in your head." In 1996 a  specialist put her on Ambien and Flexeril.

She went into remission after started seeing his current husband from 1996 to 2000 until her children were born.

She started to get all sorts of symptoms,  restless legs and vomiting.

She had twins and just slept one hour each night and by the time they were eight months old, her body was just in terrible pain, her gallbladder had gotten to the size of the liver. She got a two hour surgery.

The months following, she ended up trying Methadone, Oxycontin and all sorts of pain meds. She was freezing, had chills and sweats, had a lot of allergic reactions and scratched all the time, couldn't walk and visibly see swelling in her feet. So by late 2009, she was unable to leave her house, became housebound and couldn't wear shoes.

She would wear earplugs because she was so sensitive to sound and light. Everything had to be covered on windows. She was not eating most of the time and still was vomiting.

Later on she went to a clinic and they told her she had been exposed to Borrelia. She received treatment with herbs and after 3 months was able to at least get out of the house in a wheelchair.

She came off opiates because she had Sjogren's syndrome.  Eyes and mouth were extremely dry and so she started a huge elimination diet. She started  on very low doses of LDN she learnt about LDN through a naturopath.

She started at 0.1 milligram, and  was going to bed at 4:30 AM. So she started taking it at 4.30Am and her schedule readjusted. Now she takes LDN at around midnight. She tried to up the dose but because she is very sensitive to medications, It took 4 months to see any results.

 "I tell people don't quit just because you don't see results right away, my body's been sick my whole life,  so it's not going to turn around in five seconds.

But by three months or four months after starting LDN, I noticed that I really didn't need a coat.

I went out one day to bike, and I wear a normal shirt without not sweating and do not have chills. I was able to come off medications like Neurotin and Flexeril.  By 9 months I could bend and clean.

Before I couldn't even pull my back leg up to 90-degree position I couldn't walk down my stairs.

I think my quality of life is probably about an eight or nine now and some days it's actually 10. I have completed a course successfully at Oregon state university after not being able to go to school for years.

And I do pottery, I am a personal advocate now in Portland for a group.

And so I would say that my quality of life is quite good because I get to talk to my children and I get to eat food, and I get to walk up and down my stairs, and I get to sleep.

I'm not saying it's perfect. But I consider level three pain or level two pain to be really good."

Brittany - US: Multiple Sclerosis (MS) (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Linda Elsegood: I would like to introduce Brittany from the United States who takes LDN for Vasculitis and Multiple Sclerosis. Thanks for joining me, Brittany.

Brittany: Thank you.

Linda Elsegood: Could you tell us when you first started to notice that there's something wrong with you?

Brittany: I was pregnant in 2006 with my second child and he appeared to me to be an exceptionally large baby.

The doctors had said: "Second children always feel larger. He's not that big. That's something you're just worried about." Because my first child had gotten stuck for several hours, and so I was nervous going into the delivery. My first child had been an eight-pound baby, and so towards the end of the pregnancy, they did aside for dates ultrasound and told us that the second baby, my son was only seven pounds.

And so they didn't feel that there would be an issue with getting him out. When the delivery date actually came and he came out he was actually 10 pounds half, and It was delivered vaginally which apparently is not a safe way to deliver a child that large. So in the delivery, obviously,  there's quite a bit of push and pull going on between the doctor and me.

The baby was severely injured and  I apparently had suffered three dissections, a swelling of my vasculature in the brain, multiple pseudoaneurysms. I was just very sick and was bleeding in my brain.  During the delivery, I had told them I have a headache and they said: "You can't stop pushing because his head is delivered and if you stop now, you're going to have a brain-damaged or dead baby. So you got to keep going." So I keep pushing at the advice of the doctors and ended up being released just fine, went home and that headache just persisted, would not go away. And I call the doctors, they say to take Advil, drink diet Coke, caffeine. "You're probably tired because you have two babies." About two weeks after the delivery the headache had gotten so bad that I was having visual disturbances, vertigo and nausea. We called the doctor and they said he needs to go right to the emergency room.

They ran a CAT scan and came back and said,  "You have a spot on your brain. We can't let you go home. We don't know what it is." So I was admitted to the hospital. They did a four-vessel cerebral angiogram and found significant stenosis feeding all through the vasculature in my brain. I had dissected both carotid arteries at the neck level, going into the base of the skull, and I was transferred and admitted to the ICU at Barrow's Neurological Institute, which was one of the premier neurological hospitals here in the States. They essentially told us:" We're doing everything we can." I was on massive blood thinners and massive doses of steroids. They essentially said, "We're doing absolutely everything we can to save you.

It might not be enough." And at the time I had a two week old and a two-year-old at home. I was a stay at home mom. We just have to sit there and hope for the best. We asked what else we can do? And they said to pray. And after several weeks in hospital as they were working on anticoagulation to make sure that the dissections didn't clot and end up in a stroke. They came to me and said, "At this point, we've done all we can do. So you can either go home and spend whatever remaining time that you may have left with your babies, or you can stay in the hospital where if you do have a stroke, we're more likely to be able to catch it."

And I felt that if death were in the cards, I wanted to be home with my kids. I left the hospital, went home. My husband's father is a physician, so I asked if they would allow us to move in with them. In case I did have a stroke, at least we would have a medical professional on-site that could help.

 I was released to my inlaws house where I subsequently had three strokes and was very sick. At that point, they felt that this was simply a postpartum complication. They weren't sure what they were treating. They just knew that the swelling and disturbance in my brain was significant enough that I needed to be on steroids longterm.

I needed to be on various neurological drugs to, you just be able to cope. There were tons and tons of pain from that injured area in my head, daily chronic headaches. It was really awful and slowly over a period of probably six to eight months, I began to recover, but I was still just a little off.

My husband described it as. You know before you were wicked, wicked smart. Now you're just wicked smart. So I lost a wicked by my husband's estimation. Life is really tough. I had very little energy. My thinking wasn't there. It was difficult to be the caregiver for two children.

I was kind of slowly working toward trying to get to my previous baseline. After about a year of recovering, suddenly I started to just not feel well. There was a node that had developed behind my ear, a solid lump feeling. I was exhausted all the time, sleeping a ton, not from depression, just because I was exhausted. I had some skin lesions that had come up. We were really trying to figure out what, what could this be? I went back to the doctor. My neurologist thought perhaps MS. Another team of neurologist said, no way MS and I was sent to a rheumatologist to ran another full battery of tests and said how we found it. "You're actually testing positive for a very rare autoimmune disorder, a very rare form of vasculitis called polyarteritis nodosa." And I began a two year treat the course of treatment with Methotrexate and steroids. By the end of that two year period, I no longer tested positive for it. They considered me to be in remission, but I still didn't feel well.

So I went through probably two more years of just feeling unwell. Like I had the flu all the time, constant body aches, headaches, exhaustion to the point where my kids would get home from school at the end of the day and I would be sitting there trying to help them with their homework, and I would fall asleep sitting up on the sofa.

Eventually, I was not doing housework, not making dinner. I was a walking zombie. Finally came to a head when I had gone to pick up my kids from school, was driving home, and I fell asleep at a red light with my kids in the car. When that happened, I called the doctor and said, there's something wrong with me. I am not okay. I might be in remission from Vasculitis, but I am not okay. Something is wrong. I was concerned about my kids' safety. I was concerned about being able to be an effective mom.  I went back in for another full battery of tests, and at that point, they found a lesion that was suspicious for Ms, and they had already seen a lot of the myelinated spots in my brain.

Because I had no symptomology of MS, my main team of doctors wasn't ready to call it MS. When I went back in for that, next set of MRIs, they found that  I had a new lesion in my spinal cord, and so they said, we are now ready to make a definitive diagnosis of MS on top of the vasculitis, which is in remission.

So we elected to immediately go on MS therapy on Copaxone, which is a daily injection. They put me on Ritalin, and on antidepressants to try and get the energy levels up. And even with all of those pharmaceutical interventions, I was still sleeping 12 to 14 hours a day, just exhausted.

And after I would sleep an entire night, felt like I hadn't slept at all. So it's a very frustrating period of time. I kind of resigned myself to, I guess this is the new normal and life is not what I thought it was going to be.  I'm never going to be able to do the things that I wanted to do.

I had a career in television news. I was a presenter. Giving all that up was a lot of my identity was very difficult. I was constantly looking for things to help. We had tried diet and exercise and all kinds of different interventions that were sort of more along the natural side of things because that's kind of where I naturally align and nothing was working. My husband was exhausted. We were all exhausted. We went on a vacation to Seattle to visit my brother and his family. We went to get a manicure and in the salon, it was a rainy day in Seattle as it often is.

And we live in Arizona, which is the desert and very sunny all the time. I was sitting in the salon and getting my nails done. There was a woman sitting next to me, and she made a comment about the rain, and I said, "I love it. I bet you know if I live here, I probably don't. But I love it because I'm coming from Arizona where it's eternal sunshine, and it's sort of nice to have some different kind of weather."

We started chatting and I said: "The only thing I really get bothered about with the rain is it makes me so tired." And she said: " Oh, why?" And I said: " Well, I had a mass." And she said: "Really? Have you heard of LDN?" And I thought, who is this crazy woman in the salon who's trying to pitch me on?

I thought multilevel marketing or something ridiculous. She started telling about it, and she said: "My naturopath just prescribed this for me. I've been on at three days, and I feel great. I have Hashimoto's thyroiditis and it has completely turned my life around. It's only been three days, but it's night and day, the difference. "And I thought, here's one more thing that somebody tells you about and it gives you false hope.  I can go and ask the doctor, and it's not going to make a damn bit of difference because nothing works and nothing helps. I was very pessimistic and hopeless.  She said: "Please give me your email address right here, and I will email you information about it." I thought that's odd that this stranger is so in passion about this medication. If I give her my email address, I figured I have nothing to lose.

I came back to Arizona and looked over her email and started doing some research and found the information from the UK and thought, wow, if this really does all it says it does, this could be amazing, and this could be the answer. So I called my naturopath and said: " Would you be willing to talk about this?"

And she said: "Sure. Come on him." And we sat down, and she said:" I have a couple of patients who are on. If you're willing to try it, there's no risk. And you can take it with the capacity, and it's not going to hurt you. So let's go ahead and try it." So she prescribed it starting at 1,5 mg, and she said: " Take it slow because you don't want to rush into it."

I started taking the 1,5 mg, and I was just at the cost of a charity event that I had volunteered for and had taken on entirely too much. I had volunteered prior to the Ms diagnosis and thought that  I would have enough energy for it, and I did not have enough energy, and I was tired to the point of tears every night because there was no way that I was going to be able to get it all done. I was so stressed out and worried about letting my kids, friends and the school down. I took that first dose and I noticed right away the next morning I popped out of bed.

And I was like:" That's probably placebo because I'm so hopeful. It's going to do something."

 She had told me you have to take 1.5 for the first several weeks so that you don't overload. After maybe four days, I felt better than I had felt in years. I had energy. My mood was better. I was less irritable.

I just felt like I could cope like I could do things, I could get up in the morning,  take a shower,  get dressed. My shower didn't completely wear me out for the rest of the day. I could do the dishes again, make dinner again. All of a sudden I was a person.

I was human again, a mom and a wife. I thought: "Could this really possibly be this drug?" I called the doctor, and she said:  "If you feel that good, go ahead and increase to three. Like I'm fine with you taking it at your own pace." And I increased to three, and it only got better.

Suddenly I had my whole entire life back. I was able to go back to work.  I work with my husband and in our family business. So I'm back to work now,  a contributing member of my family and my household and our income.  I'm able to care for the house and work and care for my kids and volunteer.

I run a girl scout troop.  I'm like an Uber mom the way that I always wanted to be. And the one thing that made the difference was 3 mg of this little drug. It's been powerfully life-changing for me because I felt like I had lost myself and who I was.

Then all of a sudden this little pill that I take every night is..

My pain is a far decreased. I was daily narcotics from headaches and body pain daily. So I had my narcotics prescriptions came in, doses of 120 at a time because otherwise, I was unable to move sometimes and I haven't taken narcotics in a year because that's when I started taking the LDN. The moment I started taking LDN within maybe three days, any pain that I had was treatable with Motrin. My chronic headaches, I still get them daily, but they don't stop me in the way that they used to. I don't have to retreat to a dark room and put ice on my head and cry and pray.

I can work through my headaches now, whereas it was impossible before. I have almost zero brain fog. I'm a productive person at work. In fact, I was just hired an as independent consultant for another company. All of these things that I thought that I had to give up because of my brain just didn't work anymore.

It's back, and I can communicate, and I can write again and I can earn money and I can be with my kids and my husband and keep the energy level up. And the pain, like I said, is decreased. My mood is not hopeless anymore. It completely gave me energy and hope and less symptomatic pain.

And everybody, I talked to now who has any kind of autoimmune disorder I'm like: "Please go talk to the doctor about LDN." I turned into that woman in the salon now because it made such a huge difference for my life. I'm so grateful that I ran into a stranger who wanted to share that.

Then we had that kind of random conversation. I don't really believe in coincidence. I was very fortunate to have that woman in my past that day because it made such an enormous impact for not only my life but my kids' lives and my husband's life, our life as a family.

 I will never give up my LDN forever and ever because it just completely changed my life. I'm grateful. When I was asked to do the patient testimonial, I felt, you know what? I want to pay this forward because of it's inexpensive, and I have no side effects from it whatsoever and the benefit, it's all been upside, and it's just made an enormous difference. I feel like I can be the mom that I wanted to be, the wife, the person that I wanted to be, and I don't have to compromise because I have an illness. That is a true gift and a true blessing.

So that's my story.

Linda Elsegood: It's fantastic. I mean, most of the story. Are you still on 3 mg? Did you try going up to 4.5?

Brittany: I am still on 3 mg. We have talked about going up to 4,5 mg. I do have some muscle spasm activity, so we've been holding at the 3 mg. It's pretty good.

 If there were ever to be some exacerbation that was to be difficult, I have room to go up. But I don't really feel the need to. I will also say though, that since I started taking the LDN, I have had three lesions completely disappear off the MRI. What I've been told by my neurologist is that it is unusual that the Copaxone certainly is not doing that.

They don't expect Capaxone to take care of lesions, they expect it to prevent new ones. So they were very enthusiastic about the fact that I've had three lesions disappeared. I'm pretty into the answer about that too, because you only have one brain, so you want to preserve that if you can.

It's not only my subjective experience that I can speak to, but it's also the objective image from the MRI that tells the doctors that I'm in fact getting better. That's pretty awesome.

Linda Elsegood: Wow. Well, thank you very much—you sharing it. I mean, wow, just amazing.

Brittany: It really is, and I just feel so fortunate, and I wish that this were more mainstream.

I really wish medical doctors were using it more and considering it more. If I had been given the option at the beginning to try LDN rather than going on Copaxone, life could have been different so much earlier, how lovely that would have been. Do you know?

But in the meantime, I'm just incredibly grateful for what I've gotten back because it's been a life-changer.

Linda Elsegood: Well, thank you.


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.

Bridget - US: Ankylosing Spondylitis, Fibromyalgia, Insterstitial Cystitis, Depression (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Bridget from the United States shares her experience of LDN for ankylosing spondylitis, fibromyalgia, cystic cystitis and depression. 

Bridget first noticed symptoms when she was  ten years old. It was 1994, and she started having problems with her left hip and she ended up on crutches for 3 years, then it started to speed to other joins and the other hip.

By the time she finished high school, she was half-crippled.

When she was 21, 11 years later she was diagnosed with ankylosing spondylitis, fibromyalgia, depressions and interstitial cystitis, she was on a lot of medication which wasn't helping.

Before LDN, her quality of life was 3 or 4 out of 10. on a good day. And now it is a 6 to 10!

To listen to the full story click the video link.

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

Anne (2) - England: Multiple Sclerosis (MS) (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Linda Elsegood: like to introduce Anne from England who takes LDN for multiple sclerosis. Good morning 

Anne (England): Good morning. 

Linda Elsegood: Could you tell us when you were diagnosed with MS? 

Anne (England): I was officially diagnosed in 1980, but I've had about 15 years before. In 1990, I was diagnosed with MS. 

Linda Elsegood: Oh, right, okay. So what symptoms did you have in those 15 years? 

Anne (England): I kept losing my balance that was one thing. And then I started to drag in my right foot, it just wouldn't work properly. You know, I was falling apart it didn't make sense it had to be MS.

Linda Elsegood: So what were your symptoms like by the time you were diagnosed?

Anne (England): Well, I've had very little change. Um, it was very, very slow. I went into a hospital, and they did a lumbar puncture. And as I said, I came at being far worse than when I'd gone in. Whether that was because I realized it was something very serious. And also, I don't know. But my balance and my walking really went down Hill over the weeks.

Um, and then the consultant told me, yes, you've got MS. Thank you very much. 

Linda Elsegood: So before you started LDN if you had to rate your quality of life at that.time on a score of one to 10, 10 being the highest, what would it have been?

Anne (England): Well, I would say it was about seven deteriorating, quite rapidly down to four. Yoga or swimming, all sorts and it was just going out to the window. Plus I got children of six and nine at the time. So it was a big impact. 

Linda Elsegood: So when did you first get these symptoms?

Anne (England) um, well I, I would be, I would say I would be in my mid to late thirties.

Linda Elsegood: And how did you hear about LDN

Anne (England): LDN? It was an article in my local MS magazine, and it turned out there's a guy lived a couple of hundred yards across the road from me, I didn't know because there's the main road and I didn't know him. He just wrote an article singing the praises of LDN. I rang him and took it from there. 

Linda Elsegood: Were you able to get your own doctor to prescribe it or did you have to get it privately? 

Anne (England): Oh, yes. I, I just went and saw my doctor. I took all the information from the LDN side on not only the basic information on its impact on MS, took it up to my doctor, who was very good.

He read it, and he said, you want to try it? Do you think it'll do some good? Here you are. He gave me a private prescription while I'm on the phone. Yes, he was. It was brilliant. 

Linda Elsegood: Yes. So when you started, how long ago was that? Now. 

Anne (England): Um, I can tell you exactly because it was 2003 and I started it just before we were due to go on holiday and I started taking it in liquid form, um, which I, I couldn't really cope with, with messing around with this arrangement and things, cause my fingers don't work very well on some days.

I started in 2003, I'm liquid form, I, within six months I was, I was on the capsules.

Linda Elsegood: So when you first started, did you send the introductory side effects? 

Anne (England): Absolutely nothing at all. Nothing happens in the first two or three days. And then on about the fourth day, I was walking holding my husband's arm to the car. And he suddenly said, you were walking a lot better. And he noticed immediately. I wasn't dragging on his arms so much. I was still using my stick, but I wasn't dragging on his arm so much. And he actually comes into it, and I thought. Well, it's obviously working because I thought it was just me, you know, I will be thinking, 

Linda Elsegood: Oh, that was very quick, wasn't it?

Anne (England): Yes. It was four days and I don't think I've looked back since, you know. 

Linda Elsegood: Right. What would you say your quality of life is now? 

Anne (England): I go out every day. I maintain all the garden, and I want some vegetables going. That's basically a big garden. But I do much better and squat down and, um, do the gardening of sitting on a chair usually. And, um, a couple of years ago, my daughter, got married from here, and we had the reception for 90 odd people in the garden. And I helped paint all the fences and do everything.

Linda Elsegood: If you rated it on a score of one to 10, 10 being the highest, what would you say?

Anne (England): The my quality of life? Yeah. Oh, I'd say I'm on an eight. And I just get on with life, and I thoroughly enjoyed myself. 

Linda Elsegood: fantastic. And would you say LDN has helped lighten your mood?

Anne (England): Uh, yeah. I've had people say why are you always so cheerful? I can't do anything about MS it won't go away. Won't improve with age, so get on with it. You know, what's the point of being miserable about things? 

Linda Elsegood: And what would you say to other people who are thinking of trying LND?

Anne (England): give it a go. There's nothing to lose. Well, you've got maybe a few pounds to lose, and you've got nothing else to do. I've also tried things. I even went down the STEM cell road. 

But just for the sake of a few pounds, give LDN a try, and I certainly found it fabulous. And I continue to recommend it to anybody, and everybody.

Linda Elsegood: Well, thank you for spreading the word and long may your gardening continue. 

Anne (England): You're very welcome.

Linda Elsegood: Any questions or comments you may have. Please email me. Linda, L I N D a@ldnrt.org I look forward to hearing from you. Thank you. You are joining us today. We really appreciated your company. Until next time, stay safe and keep well.

Alan - England: Multiple Sclerosis; MS (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Linda: I would like to introduce Alan from England. Alan has multiple sclerosis.

Alan: Hello. Could you tell us when you first started getting ms symptoms?

Alan: Probably in my early twenties. The best part of 40 years ago. I used to get terrible headaches and tingling in my hands, and, the medical people put it down to migraines and growing pains and that sort of thing. And then they would disappear for years.

I'd get a bad headache, and I'm tingling in my hand now and again but nothing really bad. Nothing that I couldn't cope with. 

I was a young fit man and then back in the early eighties, they came back again. 

The same sort of symptoms came back, but more so, I went to the doctor.  He put me in for an MRI scan but he sort of diagnosed all that symptoms through the stress of my job because I had a massive job that was million times tiring man targets people working for me, travelling all over the country. 

Massive stress job. 

And so I changed my job and all my symptoms disappeared, so I never went back for the results of my MRI scan. 

Probably in 1988, the symptoms came back again.

And so I went back to the doctor and, he said: "Well, I'll send you for another MRI scan but you never came back for your previous scan results ten years earlier", to which I replied: "Well, the symptoms disappeared, so I wasn't really interested. And then he said: " Well, we had a doctor's dilemma that we couldn't tell you, because you didn't come back.

but we suspected you have Multiple Sclerosis at that time. 

 I was really pleased he didn't tell me because I'd had ten years of symptom-free, changed my job, moved house, did all sorts of things, without any worries that I might be able to have later on in my life. 

But when the symptoms all came back again, then they did an MRI again and told me that they were definitely a hundred per cent certain that it was ms.

And, I was totally devastated. I would say I was in the early fifties, pretty fit, playing great tennis, golf nearly every other day. I'm having a great life and all of a sudden they were telling me that in a couple of years I was going to be in a wheelchair. It was some pretty hard time.

Linda: So what were your symptoms at that time?

Alan: Well, my left leg used to get really heavy. If I was doing active things such as playing tennis, I'm like to play one set, and when I play the second set, and if I want it, that was fine. If I lost it, then I'd have to play the third set and I just couldn't run around because it felt as I just had a ball and chain instructed my leg.

So, I was losing the third set, and that was when I went back to the doctor and,  said: "Look, there's definitely something wrong with me, and I want to know what it is." So he told me about the previous MRI scan. 

And then we went from there to see a consultant and a final diagnosis.

Linda: And then what happens further down the road? 

Alan: Well, I got really depressed, terrible. I even attempted suicide and everything. I was succumbing in a terrible state and then all of a sudden I couldn't play tennis, I couldn't play golf. I couldn't go walking in the hills. I couldn't. I couldn't do anything that I used to do before.

I just got myself in a terrible state. I got really down. And then all of a sudden the guy that I was friendly with said:" Well, would you come to play bowls? And I said:" Bowls skim for old men". And he said: "I put his arm around me and said, Alan, you Bleep, bleep, bleep, cripple. And I looked at him and said, do you know what?

You're right. I can't do the things I want to. I'm a semi cripple. Why don't I go and play bowls? And it was like a new lease of life for me. I started playing bowls more than I used to play tennis and golf and things like that and got pretty good at it. Represented England in the Paralympics and, won a silver medal, Linda.

Linda: Oh, wow. 

Alan: Well, bowls saved my life. So, yeah and over the years I've had to manage my MS, until I heard about LDN and, that was just four, five or six years ago. And, I started taking LDN five or six years ago from Bob Lawrence and Swanzey, and I've been on ever since. And, my symptoms have not progressed hardly at all since in five or six years.

I'm virtually no worse now than I was probably six years ago before I started taking it.

Linda: You said you were secondary progressive. Is that right? 

Alan: I was secondary progressive. I was just gradually going down, down, down, and then It's just stopped. I'll go to the oxygen chambers every week and things like this, but,  that didn't really do, it made me feel better, but it didn't really progression.

LDN seems to have stopped it in its tracks.

Linda: Did you have any side effects when you first started?

Alan: Nothing. Absolutely nothing. Within a week of taking it, all the symptoms that I had, was tiredness especially. If I played bowls, I would play in the afternoon.

I'd come home and go to bed and not do anything else for the rest of the day. But that was fine. I could manage that. That's not a problem. Sometimes I would play twice a day, and I'm five years older, and I'm doing a lot more. So I'm like,I will put it all toward him.

Linda: So what else is LDN done to help you? 

Alan: I used to be sore in my muscle all the time, but you learn to live for that, and you don't sort of taking too much of it.

But no, unless I've done an awful lot of like stay, for instance, I drove most of the way now tonight. My leg will be really sore because I'd been sitting around in a car all day and I've done a lot so I take a sleeping pill and, rub some stuff in the leg and things like by tomorrow I'll be back to normal again. The tiredness is the main thing, the pain is another thing. I used to get up three or four times to go to the loo. It may be once or twice now, maybe.

The only thing that I find that affects me is alcohol. Whether that's because of the LDN or ms, I can't drink anything  I used to drink when I was ten years younger. But can anyone of us?

Linda: I don't know. I'm not there yet.

Alan: I can't drink.  Drinking affects my walking and nothing seems to stop that at all. So, I don't drink much at all unless I'm just going from my back patio to the bed and then I might. 

But most of my symptoms are all improved when I started taking LDN.

Linda: Good. So what would you say to other people who have been given that diagnosis of being labelled with multiple sclerosis and they are thinking about the LDN?

Alan: Well, first of all, I would say to anybody that has been diagnosed. It's not the end of the world.

There are certainly lots of worse things you can get it. I'm not saying it's a nice disease, but on the other hand, there's certainly lots worse ones around. And I think a lot of ms is about how well you treat it and your state of mind, etc. So many people say:

how's LDN going to affect my other medicine?" I have no idea but why don't you try it and see what it's like?  My doctor doesn't say I can take it. So, I'm not going to take it. I said:" Fine".  "You know, probably my doctor said, you don't know what it's doing to you in 10 years time"

and I said, will you guarantee I'll be here in ten years?

I say to anybody who's thinking of taking it, try it and see. If it doesn't do you any good, don't take it. But if it does, keep on taking it. So, I'm a big believer that you should try anything that might help you and if it doesn't work, okay.

So you've paid some money, and it cost you some time and effort, I understand but it may have you some good.

Linda: Okay. Well, thank you very much Alan. Any questions or comments you may have. Please email me. I look forward to hearing from you. Thank you for joining us today. We really appreciate it, your company. Until next time, stay safe and keep well.

Pharmacist Kent MacLeod at the LDN Book Event 2020 (Low dose naltrexone) from LDN Research Trust on Vimeo.

Kent MacLeod, RPh., B.Sc., Owner & CEO of NutriChem Compounding Pharmacy & Clinic

Low-dose Naltrexone (LDN) & The Gut Microbiome

Kent MacLeod, RPh., BSc.Phm., is a pharmacist, as well as the founder and CEO of NutriChem Compounding Pharmacy & Clinic in Ottawa, Ontario. He is an international thought leader and award-winning pharmacist, with over 35 years of clinical experience delivering patient-centered healthcare. He is globally recognized as a hormone health and nutrition expert, has lectured at many health conferences, published research, and developed course materials for many professional clinics based on NutriChem’s success. He is the author of the book, “Biology of the Brain: How your gut microbiome affects your brain,” and his focus is on the relationship of the gut microbiome to mental health and immune function.

Pharmacist Kent MacLeod owns and is CEO of NutriChem and held this event to highlight and share information about LDN (Low Dose Naltrexone). He shares his vast knowledge about LDN as a valuable tool in healing the gut and autoimmune system. He gives a thorough explanation on the importance of maintaining good gut health, which is the key to overall health. He shares many other factors that improve our well being and health. 

Review by Ken Bruce

Nutrichem's LDN Book Events with Linda Elsegood (Low dose naltrexone) from LDN Research Trust on Vimeo.

The LDN Book Volume 2 & The Goals of the LDN Research Trust

Linda is a Multiple Sclerosis patient, founder and volunteer CEO of the LDN Research Trust. She has made it her life’s work to help and support people with autoimmune diseases, cancers, mental health issues etc. Her goal is that LDN will be used as a first-line treatment, where appropriate, globally. In the last 16+ years, she’s achieved a lot.

Linda has organised 7 Conferences, numerous talks, and she has edited both of The LDN Books. Linda is the LDN Radio Show Host, has planned 6 Documentaries and the 15th Anniversary eBook. She also oversees the day-to-day running of the charity along with other volunteers.