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

Donna Seebo Interviews Linda Elsegood about LDN (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Linda Elsegood shares her Multiple Sclerosis (MS) and Low Dose Naltrexone (LDN) Story on the Donna Seebo Show with Donna Seebo.

In 1969 at the age of 13, Linda had glandular fever (Epstein-Barr virus). She was seriously ill and away from school for six months. 

Late 1999 Linda’s mother had a serious heart attack and the trauma affected her badly. She was working full time, travelling two and a half hours every day and running the home. This excessive workload and stress began to take its toll on her health, and by May 2000 she had lost her balance, lost feeling in the left side of her face and her head, tongue and nose were numb with pins and needles.

In early December 2003 Linda started Low Dose Naltrexone (LDN), and the results were incredibly positive. By Christmas Linda was functioning again, and her liver tests were back to normal. She felt like herself again.

Linda founded the LDN Research Trust in May 2004. In this interview she says that it is the most exciting thing she has ever done. She is able to give many hours a week to the Trust, helping people to get LDN and trying to get it into clinical trials.

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

Donna - US: Sjogren's, Multiple Sclerosis (MS) (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Today, we're joined by Donna from the United States and Donna takes LDN for multiple sclerosis and Sjogren's syndrome. Thank you for joining us, Donna.

Donna: This is Donna. I'm doing well. Thank you.

Linda Elsegood:  could you tell us when you first noticed there was something wrong with you?

Donna: Well, I was diagnosed with multiple sclerosis amass 2006 this month. So it's spent this sentence.

Linda Elsegood: And what about the Sjogren's? When, when did you develop that?

Donna: Yeah, well, I always had something wrong. I knew with me. And just to give you a little background, it's been. Ten years or more before I was back most with ms. And I was always told her I was working too hard at witness stressful for situations. And I kept telling the doctors, no, that's not it. And so finally the test came back positive. Not, but they couldn't have a tell me 100% certainty. That's what I had, but all everything pointed to in Austin. So that's the name? They did it in 2006.

Linda Elsegood: Okay. How old were you when you first notice that, you know, you've got these symptoms?

Donna: Oh, gosh. I would say when I first started receiving, sometimes it happened then as far back as the 19 late 1980s.

So in 2006 is when I first was diagnosed, but it was intermittent from the 1980s until I was actually diagnosed. But it slowly to grow.

Linda Elsegood: How old were you in the 1980s.

Donna: Okay. Yeah. Okay. Well, now I have no problem with my age. I'm 57 now. So the 1980s, I was what? 30, the early thirties. So with that point, I was diagnosed 47.

Linda Elsegood: Okay. If it makes you feel any better im 60 this year Um, and I've got MS.

Linda Elsegood: so when you were in your thirties, and you had these symptoms, what, what were you experiencing at that time?

Donna: I was just For no reason, numbness in my feet and in my fingers. And I, as it progressed, I kept dropping things, and I would stand up and become dizzy. And we all know that if we stand up too quickly, it can make us dizzy, but. It doesn't matter what, no matter with me as it was quickly or slowly. And at some point, my husband had to literally push me out of bed because I couldn't move.

I would get a headache, my double visions, and my sense of smell changed acutely was either I could not smell. And then another day. Everything nauseated me. Then they smell nice here. I didn't mean my eyes; my appetite drastically change in which I didn't eat a lot at all. And I love food, and that turned me off the just general achiness and my, my headache.

I constantly got migraine headaches. They slid out of my words. I could remember. The day, the last day I worked, and this was ten years ago, and I wish I had a client. I a very effective job. And I was called a client service that then I was visiting a client, and we were talking and all of a sudden my tongue would not move.

And it was so I can remember thinking this is embarrassing. Not thinking where it's something that, which mom with me health-wise, but when I'm on video, that's this point. So I looked at her, thank goodness. She would have seen the front of mine, as well as the client. I looked at her, and I guess I had panic in my eyes and three really concerned.

And so it seemed like it lasted forever, but I'm sure it was less than a minute. And I tried to function my tongue. I tried to get worse to come out of nine. Now I tried to fall on your leg was, and anything I could do, but I could not. So eventually everything loosened up my tongue loosen up, and I turned to her and told us that I need to go.

I'm so sorry. I need to cut this short. And I immediately drove home. And that next day I have a doctor's appointment. I told him what happened. He did an MRI and tried the lesions on my brain. And he recommended to me. He called it. He called in a neurologist. He, it went up, and that'd be one of the top ones here in this part of this, the country.

And he agreed to see me. And that's when the lumbar punchy with Don. And that's not what happened. That's my story. So it was the motion does and thing Elva and think, okay, this is it because I would have worked hard and I've worked since I was ten years old. So, this was extremely devastating to me, very depressing I would cry every day.

I mean, I could not get ahold of my emotions. That was another side effect. And so those are the things that I had to deal with. I went to the Mayo clinic. You've heard of them, Minnesota. I went through this stage with my husband for a week and a half, and they also told me I have fibromyalgia. That was the first time it was diagnosed as fibromyalgia in conjunction with them.

They could never find out anything. Concrete about, well, maybe it's this, maybe it's that. And so, but that's the stood everybody's different with math. So, unfortunately, they could not tell me anything different. So I came back home, my husband and I, and we were just exhausted. We used to give up, we've had to find something we knew there was something out there that could help.

And lo and behold, this plan of my husband friend, who happens to live in Colorado, his wife has lupus. She was sent home, and she was bedridden, and they've heard about, and so she started taking it two weeks later. She was hiking. They gave her a death sentence. Two weeks later, with LDN, she was hiking in the mountains with her husband.

He called my friend, and he said, bonnet need to try this and see what happens. And I didn't Diana, I research so much, and I found it was able to do the research. And then what happened is that. At that point, I said, okay, let me try it. And I thought it was going to be something that was very simple to do, but I couldn't find a doctor who would prescribe it.

No doctor knew about LDN, and I thought, are you kidding? So I ended up having to go to a doctor that was close to Chicago, and that's about five hours away from where I live. So initially he's prescribed it over the phone, and he said, let me see everything that you have. And I did that. And lo and behold, he did prescribe it's for my insurance company, witnessed it.

So, but $30 was a nominal fee for me. So. I said, why not? I can tell you within two days I felt that definitely in my entire body, the way I was thinking, the way my limbs were working, the way I walk because my game was easy. I could fall. If someone blew on me. Okay. And so I was very active on the phone.

That's how I discovered LDN. And I used it. But to me, he is, and after three years, because I was shooting myself for ten years, what did nothing for me every single day. The quality of my life is going down, and with LDN, it was nothing but up with my quality of life, just shot through the roof and I'm thinking, you gotta be kidding me.

How can this miracle pill help me This quickly, and this much didn't drastically change my life, that too near Norman, Steve, that I am used to. So, my husband, I didn't want him to. We told everyone we could, he's heard about it. All the, you heard about this and. Yeah, she had problems with, um, for non they were heightening or if I can't forgive me again, I cannot remember what a prominent disease is.

And they said to her to death in six months. They said she would be dead. And I just so happened to she's a bed and breakfast owner with my husband and my husband. And I didn't go there. Awesome. And we've stayed ahead of that bed in park. And when she told us about what she was going through, and we just exchange voice, and I said, you need to try on the end.

And she wasn't resistant for almost a year, but I kept corresponding with her. You need to try this. You really do need to try this. So eventually she found a doctor, and she started it. She had told me on LDN, and her name is Lori Dawn. And she's on the LDN for him as well. She told me the second night, after 30 years of being in pain, she woke up one morning.

There was no pain in her fingers. And they wish because of the LDN right now. So doctors have no idea how she is living and functioning, and she's wonderful. Well, I can't say enough about it. I, I, I don't know what else to say.

Linda Elsegood: Well, that's an amazing story. If you had to have rated your quality of

 life on a score of one to 10 before you started LDN and ten being the best, what would it have been?

Donna: Oh, it's the lowest point. I mean the, before LDN, I was below a one with the idea IDN, I would say I can go from eight and a half to over 10.

Seriously. Wow. And it depends upon because I'm going through menopause right now. That's not too much information. And so my body goes up and down with that. If anybody out there knows about it, menopause, of course, we, most women do who is this age group, and it's sometimes, you know, just flushed it, but it's been more upward now with, and I thought out too, no complaints whatsoever.

And people look at me, you know, in us as I often did use. And it's. Also, you don't look sick type of statement. Well, as you're feeling miserable on the inside and your food and all of the time, 24 seven, I don't have that anymore inside of me every now and then other twins, but there's nothing to write home about it.

Nothing to complain about. I keep my doctor's appointment to most straighten that I'm addictive, how I'm doing. But other than that, am I new biologist? See the change, but still, to describe LDN, he wouldn't do it. He has one other patient besides myself who is on LDN. Now I, after three years, let's see, I would say about two and a half years ago, I stopped taking LDN, and I see a wonderful.

And I still, I just, I'm still on LDN, but I take no medication at this point in my life. And I was diagnosed, uh, on, uh, the last 20 minutes. So, um, I'm good. My doctors are astonished. You should be on a wheelchair by now. I'm not in a wheelchair. I can walk. I wear me still at hours. Sometimes I trip, but that's okay.

But, but I can't say enough about that's it that's a miracle drug this in college. Uh, my face had been asked to do this, so, I mean, it has increased my faith in my Lord and then increase my face and us, there is something out there, but. Autoimmune diseases for cancers for those type of things. I mean, suddenly I could drive.

Linda Elsegood: before we started talking, you told me about exercising. Would you like to tell everybody what exercises you've been doing?

Donna: Well, I use the leprechaun daily. And each day I do that with emails, and that takes about an hour. I don't push myself too high. I do a little weight lifting, not a whole lot. We wished I had 10 pounds.

I do. A lot of stuff is very important that keeps your tendons doable so that you. Won't hope. And your elbow is a bin. When you want them to bend your knees a bit when you want them to be on. I used to have terrible, terrible pains in my leg, which only casting with FIC. I don't have that anymore. So if the, you know, you keep your stuff, you are yoga.

He left the walk-in. And if you can learn, it's very important. It's important for your state of mind. It's also important to keep your body in as much shape as you can because your body will fight for you. If you fight for it, that's the only way you can beat this thing. And do you, and of course, That's the first and foremost, the number one thing I would, I would tell everyone in the distance, you have to believe in something.

If you don't, you're doomed, because if you don't believe that you can do this, if you're not telling your body, you can do this and keep a positive attitude, you've already defeated, just and used to come to this.

So that does not answer your question.

Linda Elsegood: Thank you very much for sharing your experience with us. We do appreciate it. And I'm so pleased that LDN has worked so well for 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.

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

Don from United States shares his LDN for secondary progressive Multiple Sclerosis (MS) experience.

He started seeing symptoms around 2002 when he would go running he would constantly and have to stop and rest so he knew something was wrong.

He did research after his diagnoses and decied to try LDN. His qaulity of life before LDN was at a 5/10 now it is at a 8/10. He has improved by alot.

To listen to the full interview play the video.

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

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

Dominique from Belgium shares his Multiple Sclerosis (MS) and Low Dose Naltrexone (LDN) story on the LDN Radio Show with Linda Elsegood.

Dominique recognised something was wrong in 2005, when he had a couple falls which led to him breaking both of his wrists. At the age of 48, he had never previously experienced major problems with his balance in the past. While his diagnosis took a while, he was eventually diagnosed with Multiple Sclerosis (MS).

Dominique’s overall health went downhill from this point, as his overall energy levels decreased and fatigue began to settle in. Fortunately, he came across Low Dose Naltrexone (LDN) which has completely revived his health.

“LDN has completely transformed my life. I’ll never stop taking it. I’m back doing the things I was doing before and I feel great.”

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

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

Diane from the US shares his LDN story she takes for multiple sclerosis. 

She was 34 when she first got diagnosed with MS. She has trouble with vision that got progressively worse and had balance issues and fatigue.

She heard about LDN on the internet and decided to give it a try.  She has taken LDN since 2010 and had mild side affects with sleeping.

She found a lot of improvements with fatigue and balance. Her quality of life improved and she was able to do daily task again.

To listen to the full interview play the video.

Any questions or comments you may have, please email us at Contact@ldnresearchtrust.org. I look forward to hearing from you. 

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

Diane from Canada shares her Low Dose Naltrexone (LDN) and Multiple Sclerosis story.

I was very active socially and at work. I was actually a hotel sales manager, and that kept me on the road quite a bit. So I was very active.

One day, in a meeting at work,  I was making some notes, and everything came up as scribble.

I couldn't write my name. I couldn't spell D I A N E period. So I immediately went off to the hospital. I was seeing the Neurologist beforehand because I had one night double vision in my eyes, and they were doing some testing on me.

Anyways, I went to the hospital and they diagnosed me with Multiple Sclerosis. It was devastating. He sent me home and told me to come back and see him if any changes happened.

So, all of a sudden I couldn't lift my right leg and my speech was totally slurred. So my mom rushed me back to the hospital, and then I hadn't eaten anything but I was throwing up, I shook the bed, and I throw up, and I was doing this for a full day until the point where they were saying to my mother that I would never make it for the night.

And  by the morning, everything just settled down. My symptoms were still the same so I was there for a week. When they sent me home, they said I would have to order a wheelchair for me.

So I went home. We're a Christian family so my mother took me to the church. The missionaries prayed over me, and they were there for a few hours while I forget I had this really weird feeling afterwards.

The following week I left from this whole wheelchair-bound and going back to work in the hotel and being active.

And 14 years later I kept falling. I had really pushed myself to the max. And one day I tripped on the concrete and bang my back, my spine against this concrete wall and then thereafter I found I couldn't keep my balance and I got a call on my cell phone. I had a muscle spasm that lasted three weeks so I was bedridden.

Doctors took me off work. So I've been off work since 2001.

Because I am a computer savvy, I went on to the MS Resource Centre, and I was reading up different things and I found about Low Dose Naltrexone (LDN). So I looked further into it and then I noticed they had a pharmacy in Toronto.

And so he wrote me the prescription. That was November 2010.

I have been ok. I had to use a walker outside and inside and got a scooter now. And then I would say January, I was able to go upstairs.

I went upstairs, went to bed. In the morning when I woke up, I opened the door and looked, and there was no walker. The walker was all the way down to the entrance.

And I got up and started to walk. I was so happy. It has given me a little bit of strength in my mind. I have had problems with my bladder. My bladder is totally controlled and I don't take any bladder medications.

Fatigue is still there. I didn't have side effects from LDN except that I couldn't sleep right.

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

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

Linda Elsegood: Today. We're joined by Diana from United Kingdom who takes LDN for primary progressive MS. Thanks for joining me, Diana.

Diana: Okay.

Linda Elsegood: Could you tell us when you first noticed that there was something wrong with you?

Diana: Yes, it was January 2010. I had gone to pick my daughter up from, uh, from the airport. My husband had driven, I was in the passenger seat, and I went to get out, and my left leg wouldn't move properly.

And I thought. It's a crime or something where it started dragging. Um, and it sort of didn't really recover much. Um, so I'll store a doctor who said, I need to see a physio. And I saw the physio who said, this is not for me. It's neurological, which was good that he sort of spotted that. So it was about. February 2010, when I saw a neurologist whose aim said, right, we're going to give you some, an MMR MRI, which they did from my waist down. And I come back, and they said they couldn't see anything. I was still having problems.

So, um, then I went and saw another. A neurologist who's at the same hospital who said, right, we're going to give you another MRI, which they did from the neck down.

And nothing really showed set for the usual wear and tore on the back. And then they said, no, you need another MRI, which was on the brain. And that's when they said, Oh, you've got lesions on your brain. And I've got the letters telling me I had the million station, which I'd not heard of myelination yet.

Thank you. And, um, obviously they said, Oh, well, that's MS. Multiple sclerosis. And I was like. It's really weird. Cause I didn't know about it, but you talk to everybody else. And I do as soon as they say MS. Um, so then they, um, said to Cruz it, we need to give you a, a lumber punch. So this is by now June 2010.

So I had around with punch, and they said, yes, it's definitely MS. And then they asked me about the history previous to, to, you know, um, my diagnosis. And it turned out that I possibly had it for years because back in 1982. I was having problems where I was like, told me I had temporal lobe, epilepsy.

I never had a fit, but I used to, um, Get these really weird sensations where I couldn't speak properly, and my stomach would blow. And I couldn't cope. I had two children by then, and I was under the London hospital, neurology hospital up in Holborn, and they told me I temporal lobe epilepsy and put me on phenytoin.

And then I had to come up with that. Cause I fell pregnant with my daughter in 1984 and went on to take her child, which I stayed on for quite a few years. Cause I still was insisting. That's probably what it was. And then I went back in about a couple of years after my daughter was born and saw another person up there who said, Oh no, you've got stomach migraine.

Come straight off the Tegreto. So I did. And between 86 I had a few episodes of, um, this, this sensation where, uh, I couldn't cope my, uh, Functioning my eyes go funny. My words were slow and everything. And because I just thought of, they've told me what it is.

I'm not going back down that route. I just put up with it, but it was every so many months. It wasn't all the time until 2010. Obviously when this thing with my leg happened, and I was getting the weird sensations where it felt like I was having. Bits of Woodward attaching themselves to me. And I was having running water was all running down my leg and my, my feet as they still are now totally numb.

And he just carried on from there. Really. And so they, first of all, they said, I had relapsing-remitting, MS. They put me on Gabapentin and, um, But every time I went back, that's what they told me the first time it was relapsing-remitting. And then when I went back and thought and urologist, I think it was about three months later, they said, no, you're not relapsing-remitting.

Cause it hadn't gone away. Your primary progressive. And then I decided, they said that I should take this Rebif, you know, where you inject yourself, which I. So, well, if it's going to help, I will try anything. I don't like this. This is awful. Or, cause I couldn't was beginning to not function. I put grandchildren.

And so I did the Rebif. I did it for two weeks. It was terrible. I was so ill on it. Plus the fact I bruised everywhere, but I just had, they said you might get flu-like symptoms. And that's what I constantly had. The whole two weeks, I was really ill. I said I'm not doing that. And then I said, well, you don't.

And then when I went back again, she said, we shouldn't have been put on it because you've got primary progressive MS. And it's not going to help anyway. So she shrugged us older by then. I'd met up with some other MSP people. And one of them said to me, Have you heard of LDN? I said, Nope. What is it? She said I take it.

I found it very beneficial. I, once again, I went to my doctor who said, no, you can't have it because it's not licensed here. So I said, well, I'm going to have it. She gets it. So I pay for it from Dixon's. Is it Dickenson's the chemist in Scotland? Yeah. And, um, From that day. Uh, I can't, uh, I still have my moment, obviously.

I'm still constantly got this, uh, with my legs, numb and date, and I can't walk very far, but it's allowed me to keep working, and I do work three days a week. I teach adults. Um, with, uh, Mental illness and that it, but I can get up and I can do my job three days a week. And, uh, being able to look after my grandchildren, the only thing I will say I did, um, uh, I started, um, I started off at 1.5, and I was on three milligrams.

I was finding that I was having really bad episodes. Um, if I was taking it every day, I don't know if this makes sense to anybody. So I, I cut it down, that what I do now, I take, and also I better, if I take it in the morning, I've been doing little tests on myself, and I found that what has worked for me now, I take one every other day at seven o'clock in the morning, three milligrams.

And that has worked for me. Better than if I was taking it every day. Um, but, and, uh, I, I don't take anything else now because I've also gone. I don't know if this is simply through this, but I've also gone down the homoeopathic home route. So I only take Gabapentin and LDN now. And, um, Touchwood feeling a lot better than I have done for ages.

Um, in myself, my MS. I still struggle. I couldn't say I could. I still do. I use the stick. Um, and I couldn't walk from one into my high street to the other. I haven't, I can only do one shop at a time, but mentally and more focused on. I do feel this is the inner ODM. And I'll tell you why as well because I did come off its two weeks because I wasn't, well, I had a virus and all, so I wasn't functioning very well.

I come off of it, and I felt the fatigue was terrible. And the, so I do feel as soon as I went back on it, the fatigue is a lot better, a lot better.

Linda Elsegood: Well, that's a good result.

Diana: It is a good result. And, um, And the other friend that takes it to sort of at my stage a little bit further on with RMS, actually, she's a bit older than me.

And she said it's a longer, she, she also swears by it. And, uh, she wouldn't, she only takes that and has a painting and a couple of other things she's taken, but I don't know what they are, but for her. Um, you know, I'm glad I found it, and I've recommended it to other people.

Linda Elsegood: I was a very good story.

Diana: Oh yeah. Um, I just wish that all those years ago that maybe somebody had, I don't know because there are no cure forms. There's no answer. They don't know what the cause is. So I don't know. I don't know where it Roy, where, but if there is something that LDL in that can help here, I'm going to stick with it.

And I sit really in the home. You've passed that on. I think that's a lot of mind over matter. I don't care from feeling better. I don't care. I'll try anything.

Linda Elsegood: What would you say to other people with primary progressive ms. Who is thinking of trying

Diana: LDN? Oh yeah, definitely. They've got to try it. I've got to try it.

I mean, my friend gets hers. Her doctor gives her hers. My mom point blank refuses, you know? But then he didn't want to give me LDN cause it was going to cost him 10 pounds a month. So why would he pay for LDN if he doesn't have to? You've got, you know, you've got every right to say, you know, it's not licensed, so we can't give it to you.

Yes, fortunately,

Linda Elsegood: thank you very much for sharing your story with us. I really do appreciate it, Diana.

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.

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

Di from Australia has multiple sclerosis (MS). She started receiving symptoms in 1996, where she had vision problems, stress of her sick mother could have potentially played a part. Di had blurred vision in one eye. She was gradually diagnosed with optic neuritis, which she started taking steroids. For the next 17 years she felt rather well with no symptoms. In the year of 2005, Di had noticed problems with walking. Where she had progressed to secondary progressive multiple sclerosis. Symptoms include tingling and facial numbness, pins and needles, as well as awkwardness in her right side and right leg.

Di was prescribed with Low Dose Naltrexone (LDN) three years ago, she started noticing changes after one month. Recent symptoms included urinary problems. The tingling, the pain, the needles, and numbness all resolved, where she now feels more stabilized.

Overall, Di recommends Low Dose Naltrexone (LDN) and found our website helpful when researching. 

Please play the video to listen to the full story. 

Any questions or comments you may have, please contact us.

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

Derek from England shares their Multiple Sclerosis (MS) and Low Dose Naltrexone (LDN) story on the LDN Radio Show with Linda Elsegood.

Derek first noticed his Multiple Sclerosis (MS) symptoms in 2001 when he had a lot of pain his left leg meaning he had developed a serious limp. He wasn’t diagnosed until a year after, when his neurologist informed him that he probably had been undiagnosed with MS for over 20 years.

Derek’s fatigue began to settle in but luckily he came across Low Dose Naltrexone (LDN) swiftly meaning his symptoms didn’t develop much further. He recommends LDN thoroughly to all those who are intrigued.

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

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

Denny from England shares her experience of LDN for multiple sclerosis.

She was diagnosed in 98 after a car crash where they found scars on her brain. She first heard about LDN through facebook groups and she decided to give it a try, before LDN she would sleep all day.

She felt like her life was getting stripped away. After taking LDN her life has improved, she is now able to stay awake and work on a novel.

 

To listen to the full interview play the video.

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