LDN Video Interviews and Presentations

Becca - England: Crohn's Disease (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

I would like to introduce Becca from England who takes LDN for Crohn's disease.

Thank you for joining me, Becca.

Becca: Hello Linda.

Linda Elsegood:  Could you tell us a bit about your experience? What led to your diagnosis?

Becca: Five years ago I was bedbound with chronic diarrhoea, couldn't keep any food down. It went on for about six weeks before I was finally admitted into a  MI and I was in the hospital for over a month, and they diagnosed Crohn's disease.

Linda Elsegood: Were you bleeding at that time?

Becca: Yes, absolutely. I was losing a lot of blood and mucus. Not a normal bowel movement at all.

Linda Elsegood: So did you become anaemic?

Becca: Yes, I did. I lost five stone in weight. Couldn't keep any food down at all.

So by the time I was admitted to my organs started to fail and my family were told to prepare for the worst.

Linda Elsegood: Oh goodness. How old were you even then?

Becca:  I'm in my late thirties, and I had two young children at home.

Linda Elsegood: Oh, that must've been devastating. Absolutely devastating.  What happens then?

Becca: After some intravenous steroids and lots of different treatments I was sent home after six weeks with lots of different medications. I was on 20 different medications a day. But nothing really seemed to have to work, and nothing was really settling it down.  I think to be in a continual flare-up of the Crohn's for over six months.

So during that time, I couldn't leave the house. I was completely incontinent. I was terrified to even go into the garden in case I have an accident. I wouldn't really leave anywhere unless I had a toilet right next to me. It was a very scary time.

Linda Elsegood: Were you able to sleep?

Becca: My normal day's bowel movements were about 20 a day so I'd be up to five, six times in the night to sit in on the toilet sometimes for up to an hour. I can joke about it now. My husband would say to me: "I'm just going to move you into the toilet." to stop disturbing his sleep. It was a pretty difficult time.

Linda Elsegood: I can imagine. And how did your children cope with that?

Becca: I couldn't take them to school anymore, so they were finding it really hard. And they will be in total don't stress mummy hell because she is got this bowel disease. They found it really hard. I wasn't really a hands-on mama in that period.

I had to really take a back seat.

Linda Elsegood: How old were they?

My youngest daughter was eight at the time, and my oldest daughter had just started secondary school. So it was a bit of a crucial time for her. And I just wasn't there for her at that time. I couldn't be.

Linda Elsegood: What led you to find LDN? How did you hear about LDN?

Becca: I heard about LDN from a friend who has Ms. She read a little bit on the website about other illnesses that LDN could help. She'd had a lot of success with LDN. I didn't really take her word for it. I just thought: " It's another miracle cure, and nothing's going to really help me."

It wasn't till about six months later that I actually did my own research into it. Did take me a while to come around to the idea of something would again help me. I just didn't think it would.

Linda Elsegood: Did your own GP prescribed it for you or did you have to get it privately?

Becca:  My own GP was quite happy for me to take it but didn't know anything about it.

So they didn't want to prescribe it. I wrote various letters and sent things that sent through the LDN research to my own consultant at the Royal Boucher hospital and he said, he was happy to do more research, but it would take him up to a year. So I knew I didn't have that long to wait because my life was pretty much impossible. So I did a private prescription via clinical on private.

Linda Elsegood: What were your experiences? Did you notice any initials side effects?

Becca: Yes, when I first started taking it symptoms were a little bit worse for a couple of weeks, and then they became a lot better. As I increased the dose, every time I would have a couple of days of discomfort, but then again, the benefits would kick in then after a few days. So now up to 4.5 mg. I take it every day and there are no side effects at all now when I increase.

Linda Elsegood: How are you feeling now? I mean, how often are you happy to go to the toilet?

Linda Elsegood: About twice a day, which is pretty much a miracle.

I have no inflammation. I have no blood. I lead a normal life. I don't have to wear nappies or incontinence pads. I've been abroad since I've been taken LDN, which was something I could never even consider before and I've actually had another child. I've got a two-year-old son and a perfectly normal pregnancy all the way through. And I really do think that's all down to LDN. Because I wouldn't have been able to even live a normal life or even think about having a relationship with my husband. And now I'm a normal mum, and I go swimming with my son and, do the school runs and just work as well. So it's been a real transformation.

Linda Elsegood: When did you start the LDN? Was it before you got pregnant with your youngest child?

Becca: Yes. I've been taking the LDN for a little while now. So when symptoms settled, and I felt WEDI, then we considered having a baby. I've had no problems taking LDN through pregnancy and just had no problems since cyber.

My consultant is pretty impressed. Colonoscopy showed that I have no inflammation at all and he was astounded. So he's now decided that he's going to prescribe LDN to others with similar symptoms. I think it's fabulous because he's quite a well-known guy in the crimes world in this area.

 I'm really, really impressed that I managed to sway him.

Linda Elsegood: And what does your GP think?

Becca: GP is just absolutely delighted with it. As I said, when I first came out of the hospital, I was taking 22 tablets a day and now down to four, which is fabulous. So  I've slowly tailed off all my medication apart from the four essentials and just take these four and my LDN every day. And that's it.

Linda Elsegood: And your husband's got his wife back and your children.

Becca: Yes, I've got my life back as well which is so important.

Linda Elsegood: What a success story! That is absolutely amazing! So what would you say to other people with Crohn's who are contemplating trying LDN but are a bit scared?

Becca: I would say, don't hesitate. You're already suffering. You've already got all the problems. Your symptoms might flare a little bit initially for the first two days. When I was at my worst I was in a wheelchair for about six weeks. I had a blue badge because obviously I was too weak to walk anywhere. And the steroids that I have on affected my bones which meant I had so much weakness, I could hardly even wash myself. And my husband had to bath me on a daily basis. So I was pretty much totally disabled for a short time and really opened your eyes to how much you take for granted when you're like that.

Linda Elsegood: And how close were you to having surgery?

Linda Elsegood: I was told that I needed a colostomy bag urgently and if I refuse, I was at risk of my bowel bursting and actual death. But when I spoke to the colostomy nurse, and I had my markings for surgery, something in me just said, "No, actually this isn't for me."

I just need to see if I can manage this on my own. There must be some other way. So I pulled out an hour before surgery and said, "No, I'm changing my mind." And that was the best decision I ever made.

 

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.

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

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

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

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

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

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

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

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

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

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

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

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

Linda Elsegood: I'd like to introduce Barbara from Germany, and Barbara has multiple sclerosis. Welcome, Barbara.

Barbara:  Hi, Ninja. 

Linda Elsegood: When were you diagnosed, Barbara?

Barbara: I was diagnosed in 2007. Okay. 

Linda Elsegood: And how old were you at the time? 

Barbara: I was 45 just when I was diagnosed, um, which came exactly two days after I tuned. 45.

Linda Elsegood: What were your symptoms at that time? 

Barbara: At the time, I had very few symptoms I was living in Australia at the time, and I'd been out on a Bushwalk with a group, um, and we'd after we'd been walking, or I'd been walking for, I don't know, three-quarters of an hour, so my legs sort of started to give I couldn't carry on walking. It was very, very strange and I just had to stop the walk. Luckily, we didn’t walk in the Bush. We were just walking along the beach, and there was a road run in parallel to where they were walking. So, um, somebody came with me, and we just walked very slowly, sort of onto the road and waited there, sitting on a bench, and then eventually somebody else from the group came to the car. Um, so it was very lucky, you know, the circumstances. Um, because I could have been out with that group in the Bush, and it would have been very, very difficult to get me back.

After I'd been sitting with the person for a while I started to feel fine again, and then I had a lift back into town and then took the bus back to where I was living, I only remember getting off the bus feeling perfectly fine and walking home without any problems.

But obviously this kind of incident kind of shook me up a bit. And I went to see my doctor, my GP and told her about it and she said, well, I really don't know what this could be, but I'm going to take it seriously and I'm going to refer you to a neurologist. And that's what she did.

I went to see the neurologist and described what had happened to me, and she said I'm going to send you for an MRI, which she did, and I have the MRI. When she had the films back, she said this is what I thought, you prove she came, but I wanted to make sure before I said anything to you. You've got multiple sclerosis, and at the time she said it was relapsing-remitting. And now last year. Summer. Um, I had a major episode and I, after I'd been in hospital and had the steroids, um, I went into a clinic for them as sort of rehabilitation places, um, brought about five weeks and the doctors there said he was, um, secondary progressive and I mean, I now have symptoms all the time.

You know, I mean, until, when was it, 2009 I had very few symptoms. Then, you know, I had problems and, um, I couldn't run. I mean that I noticed that even before you have this sort of incident on the walk that I couldn't run, I tried to run and I couldn't do it.

Linda Elsegood: The doctor said that you were secondary progressive, what were the symptoms then?

Oh, this was last year, you mean? Well, I sort of, now when I go out, I have to really use a stick most of the time because my balance has been affected really quite badly and I can't walk I mean, it depends, you know, it’s different from day to day, some days are better than others, and I'm sure everybody who has MS experiences that, um, some days I find it really difficult to walk more than 10 minutes at a time.

Um, and I also feel very stiff after I've been sitting down for a while you know, so you have been sitting at a desk for quite a while working and then I have to get up, to go to the toilet. Um, I do find the kind of, really difficult it takes me a little while to get going, but then I'm okay.

That is just the sort of initial other symptoms like fatigue and bowel and bladder and sleep. Obviously, I'm tired at the end of the day, but because I do things all day and I mean, you know, I don't think I'm, I'm usually tired.

So that's, that's not an issue. Um, my balance really isn't very good.

Linda Elsegood: What about cognitive problems? 

Barbara: I don't have cognitive problems. I, that, I mean, in this clinic they did do ten cognitive tests, and I was fine. I mean, it was well within the range of, uh, you know, um, healthy person and, um, those, that there's no problem there. Um, and I had to come in early enough. I had an appointment with my new biologist on Monday, and he did this, um, kind of things. Okay. Whereas, you know, for example, he has a tune in for, can you put different places, you know, on the arm and on the, on the ankle and stuff.

And I remember when you did it last time, I hardly had any agree with anything in my uncle. Um, and to, and on Monday I could kind of feel a little bit, and he sort of. Said afterwards, well, they sued me in the pool in an improvement there that you use, sort of seem to be able to feel the little vibration bit better.

I go and have a monthly  B12 injection there. And he said, well, he's determined B, I mean, not sure. You said that there is an improvement. They use the test by hand, you know, when you have to tune your race and stuff like that. And he said, well, your hands are really very good.

I mean, I, in the summer when I have this major episode, my left hand was sort of paralysed and I my index finger was sort of permanently bent it was sort of like crooked. It was horrible, and I couldn't eat with that hand, and that is all gone now. Luckily that is all gone back to normal.

So my hands are fine. So that is a great relief, obviously. 

Linda Elsegood: So when did you discover LDN? 

Barbara: LDN? I was diagnosed in 2007 when the neurologist diagnose me, want you to put me on to some drugs right away, you know? And I sort of said, you know, I don't, I want to explore some other things.

And then I've found the Best diets. And I spoke to Andrew a few times as well, and then I researched that, and then I found the resource centre. I mean, the website, you know, I'm talking about, and I went on the website, and I think I read about LDN there. I mentioned it to my GP at the time, and she was originally from Yugoslavia.

And she said I've used in Yugoslavia to treat, um, alcoholics. Um, and I didn't really realize it could be, you know, used as a treatment for MS. And she was quite supportive. And she said, you know, if you want to get it a try, I'll support you in that. Um, and when I mentioned it to my urologist.

I changed neurologists because the woman I originally see retired for health reasons, and I went to see another neurologist, and I asked him what he thought of LDN or whether, you know, of it, he said no, he didn't think there was anything to be gained by that. I didn't pursue it in the end, because at the time I had so few symptoms, you know, and  I kept to the diet. I didn't really need to do anything else. 

I started LDN at the end of November of last year. 

Linda Elsegood: Right. And did that do anything immediately for you? 

Barbara: Yes. Well, it was more or less immediately.

That's still going on. Now. I sleep really, really well. That's mean fantastic. I mean, I didn't really have any problem I was, you know, sort of suffering from insomnia and new things like that. But I have noticed that I go to sleep really quickly. I sometimes used to have problems going to sleep, you know But I go to sleep really quickly now and. Sometimes I don't even have to get up for the toilet in the night at all. Um, some now I, um, I do have to get up once to go to the toilet. Then like last night I did, but I then go back to sleep more or less straight away, you know, so fine. Um, I’m kind of had very happy.

Sometimes the backs of the back of my leg, it was sort of like, muscles, you know, like when you've been hiking a lot. Yeah. Would the next day your legs to the field a bit strange and you want to sort of have these pains, and it was like that. The pain was like that, and that has more or less gone.

Since I've started taking LDN, I do sometimes have them still these pain you know, my muscles, but I'm not anywhere near as often as I used to have them. So those are, I would say, the most obvious improvement. I also. Find that when I do things like cleaning, which I find sort of physically quite strenuous, I do a lot of walking.

I do recover more quickly. I do have to still sit down, you know, take a rest, kind of have a bath. I do think that it's quicker and better. Like last week I did some cleaning, and then I did sort of sit down for a while we did something else, but then I went for sort of 20-minute walk that park and then walked back for 20 minutes.

And it was, I mean, I wouldn't say it was difficult, but you know, I instead of wasn't, I did feel my legs, but I, I was able to do it, you know. 

Linda Elsegood: So your doctor prescribed the LDN for you, is that right? 

Barbara: No, no, no, no, no. I know. I told my doctor LDN. Um, I mean, here in, Germany, it's not really well known.

Um, I said to him, I told him about it, and I gave him all information I downloaded all the stuff from me and MS. For him and gave it to him, and he'd read through it. And then next time I went to see him, he said, well, would you like to do that? And I said, well, yes. And he said, okay, well let's, you know, the only thing is I'm not quite sure how you'd be able to get it.

And I'd try to get it. There's an international pharmacy here, and they said they weren't able to get it they have never heard of it either. I mean, they should know what I'm talking about. Anyway, I called Dickson pharmacy in Glasgow, and they were very helpful. Very nice. Um. And Paula said you have to get a UK prescription for him to send you that.

You get via email, and that's what I did, and it was really easy. I was surprised at the end. Once I got onto it, you know how quick, how easy it was. I filled in the form on the web, and I sent them a letter. And just within a couple of days, they sent the prescription to him, Glasgow, and then the book in a few days.

Linda Elsegood: Did you have any initial side effects when you started? 

Barbara: No. No. The only thing is as happened of time. I did have vivid dreams back then. I mean, they were not nightmares or anything like that, but that happened to a couple of times in the beginning.

But I mean, I wouldn't really call that a side effect, you know what I mean? Yeah. It may have happened even if I hadn't been taken LDN, you know, you have no, no, no. 

Linda Elsegood: So how would you say your life has been since you started LDN? 

Barbara: Um. I think it has improved in, as I said, no, I sleep better, and that makes such a difference, I think to anybody.

Barbara - England: Chronic Fatigue Syndrome (CFS/ME) (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Barbara, from England was diagnosed with Chronic Fatigue Syndrome (CFS) after experiencing symptoms eleven years ago. She started undergoing exhaustion, confusion, memory loss and constant discomfort in her legs. And after a cold/flu, Barbara never really fully recovered. After seeing a GP, it was put down to menopause. 

Barbara stumbled upon LDN a few months ago whilst searching the internet for medication for CFS. After printing off all the details regarding LDN, she went to see if her GP would prescribe it. She was told no, due to government guidelines. So after getting in contact with Linda, she was given LDN. 

Upon initially taking the medication, Barbara experienced strange dreams as the only side effect. These dreams only lasted two weeks. Barbara has noticed improvements in her energy reserves and other symptoms.

When asked what she would say to those contemplating trying LDN, Barbara urges people to go for it and reiterated the fact that “it does not seem to be anything but benefits.”

This is a summary of the entire interview, click the link to watch the video.

Barb - US: RSD (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Barb from the United States shares her RSD and Low Dose Naltrexone (LDN) story on the LDN Radio Show with Linda Elsegood.

Barb suffers from Reflex Sympathetic Dystrophy (RSD) which impacts upon the nervous system. This was exacerbated following foot surgery she had in 2003, leaving both of her feet in severe pain and discomfort.

She was initially put onto a Ketamine treatment which had mixed results, but upon finding Low Dose Naltrexone (LDN) her recovery skyrocketed. She is now back to working 30 hours a week on her feet. Having recovered miraculously herself, Barb now tried to help others diagnosed with RSD by promoting alternative treatments such as LDN.

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

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

Austin from England shares his Multiple Sclerosis (MS) and Low Dose Naltrexone (LDN) Story on the LDN Radio Show with Linda Elsegood.

Austin first started to notice symptoms of Multiple Sclerosis (MS) around ten years ago, suffering from intense brain fog which limited his ability to read and write. His vision was also impaired, as well as his constant fatigue and bladder issues.

After Austin obtained his Low Dose Naltrexone (LDN) prescription, his life drastically improved.

“The very first thing I noticed was that I had more energy, which was major. I no longer have frequent muscle spasms. My overall quality of life is definitely higher than before.”

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

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

Linda Elsegood: I'd like to introduce Audrey from England who has multiple sclerosis. Welcome. Audrey, could you tell us how old you were when you were diagnosed with MS. 

Audrey: I was 12 years old when I was, no, we're not. Not when I was diagnosed at 28, but I was 12 when I first started getting symptoms of MS.

Linda Elsegood: Right. Okay. And what was your life like if you were having symptoms from the age of 12, you know, what were you experiencing? 

Audrey: Um, well, when I was 12, I had, um, diplopia, um, and, uh. Then throughout my teens, I remember I had like burning down my legs. Then I, when I was 20, I went for my first lumbar puncture and MRI scans and, um, yeah, I, I, that was such a long time ago.

I can't remember. I remember, um, I was having numbness in my hands, which is quite bad. I couldn't use my hand, my right hand. Um, and I was an artist. I couldn't draw. And then throughout my twenties, where was, um, basically I was, I would pull myself and retest, although my neurologist says I was benign.

And, uh, um, but yeah, I, I just have eye problems and like my side lesson diplopia and numbness down my legs and all my body and problems with my hands and stuff. Um, and immediately before I started the LDN, I had five relapses in a row. Um, and I ended up losing my job as a result of it. And, uh, I was only sent for diagnosis because I ended up in tears in front of my doctor.

And, and I had. Tried once before to get diagnosed, but, uh, no. 

Linda Elsegood: You said that you had five relapses, um, yeah. What period of time that was over? 

Audrey: Um, I don't know. Usually a relapse per month. 

Linda Elsegood: Really? 

Audrey: Yeah. 

Linda Elsegood: And did you find that with each relapse you were going further downhill? 

Audrey: Yeah, I actually, I would have thought, I remember thinking at the time that I was moving into a secondary progressive, and that was scary.

I noticed I was driving like a drunk sort of swerving and stalling and cars picking at me and I received a speeding ticket. And, um, yeah. 

Linda Elsegood: How did you learn about LDN? 

Audrey: Um. Yeah, I was living in America at the time, and I just found it over the internet and some LDN forum that, I'm not sure what it's called, but I only, www.lowdosenaltrexone.org probably. Yes. That was a very helpful one. And, uh, yeah, I thought it was quite informative, and I decided before I moved back to the UK, I knew I was going to try and get hold of it. And by the time I moved back to the UK, things were starting to move on, and I found you. 

Linda Elsegood: Good. And did you find getting a prescription easy? Would your GP prescribe it for you? 

Audrey: Um, when I went to a private GP on Holly Street first to get it prescribed. Then then, because it made such a massive improvement in my health, I then went to my GP, and she said, wow, you look fantastic. Of course, I'll prescribe it for you. So that was, and I'd been turned down by another male GPS, um, when I'd ask for it to be prescribed before. And they said no outright no. And my neurologist said no. 

Linda Elsegood: So how long have you been taking LDN now? 

Audrey: I’ve been taking it four years now. 

Linda Elsegood: Then how would you say, how have you worked? Do you say it's helped with your MS? 

Audrey: Um, it helped me with symptoms. Um, I sleep a lot better. Um, my energy is a lot better. My blood is better. I haven't had any eye problems and, uh, yeah. 

Linda Elsegood: What about relapses? 

Audrey: Um, I wouldn't, I don't know if I'd call them full-blown. Relapse is more sort of exacerbation kind of. I've had some symptoms, uh, nothing major, even, you know, if I eat the wrong thing and me, it’s been difficult. And then really candidly, I try to be careful most of the time, but now and then I will have something I shouldn't have.

Linda Elsegood: Um, and so for the results, you know, did you have any side effects, initial side effects when you started LDN? 

Audrey: Um, I had quite, um, yeah, I started to have a dream that I would call them nightmares actually, but they were controllable cause you just avoid taking the LDN. Um, I quite enjoy it. I do, I do take the LDN before I get there, maybe half an hour before I go to bed, but sometimes I forget to take it at bedtime, and it might not have the vivid dreams and before the sleep that I don't mind having nightmares.

I quite enjoy it because it doesn't happen that often. 

Linda Elsegood: Hmm. So what do you continue taking? LDN? 

Audrey: Um, definitely I can see myself taking it, you know. 

Linda Elsegood: Have you ever taken a break? 

Audrey: Uh, um, yes, our house at Christmas time and we had the snow problems and probably the Royal mail. I didn't take it for five days. I think that's the longest I haven't taken it for, but sometimes I'm out, but the chemist can get it to me quickly. I might miss a day or two, but it's not a problem or so. 

Linda Elsegood: What, what did you find with missing it for five days? Did you notice anything? 

Audrey: I didn't notice anything. No, I didn't. No, I didn't see anything. 

Linda Elsegood: What would you like to say to other people that are considering trying LDN? 

Audrey: Um, I'll say, go for it. You've got nothing to do at all. Just give it a go. Cause I know, um, the, the good results I had were within the first week, and it made me feel fantastic. I remember. I remember dancing to the radio. I could, I felt that good, you know, and I had an appointment with my, um, an F nurse, and I remember walking to the hospital, which I couldn't have done before. I walked from the base about a mile to the hospital, and that was, that was the start of my progress. 

Linda Elsegood: Brilliant. Fantastic. And I understand, you have a dog you take for walks as well. 

Audrey: I, I, um, yes. I've had. I got Lucy. I think it was before I started. Yeah. I've had her for four years now, so I got her before I started the LDN. So she, I called her my gift from God because she's just been so good for me. So I walked her a lot. Yes. That's a definite. There'd have been times where either I maybe not had that much energy, I have to admit. But a majority of the times she gets many walks a day.

Um, if you have a dog, you don't have the chance to sit. You have to go out for a walk. Which, yeah. It's a good reason for making you do it, isn't it? So, yeah. That's very good. 

Linda Elsegood: Well, thank you very much for sharing your thoughts with us. 

Audrey: Thank you, Linda. Thank you. Bye. Bye. Bye.

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

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

Linda Elsegood: Today, I'd like to introduce Astrid from Norway who uses LDN for MS. Thank you for joining us today, Astrid. 

Astrid: You're welcome. My pleasure. 

Linda Elsegood: Can you tell us how long ago was it when you first noticed your MS symptoms? 

Astrid: That's a good question. I was diagnosed in 1996 at 29 years old, and I was diagnosed during a period where our boss was getting sick too and the diagnosis was three weeks.

I have all kinds of strange methods for this because normally people are kind of sick for a long time and don't figure out what's wrong with them. But my MS was like a big surprise for me when I got this, I was kind of shocked. But I had a friend who I had grown up with, who had played with us.

Both these ladies were real role models. I can say they were very happy, had a good life, even though they were using a wheelchair and you can really see they were sick, but they have a very good life and are very happy. I was like, not so scared, but of course, very surprised when I got the diagnosis.

But when I look back, from a research perspective, I can find episodes and also some issues that had been bothering me. During the year before I got MS but I didn't recognize it as something. The doctor would. I got to the Agnos and at the moment I was kind of … didn't manage to put the buttons on my blouse and had the talk that I needed to use the wheelchair for a while, but kind of recovered, kind of. I felt like it was nothing to worry about, so kept ongoing, as I did before, and didn't want to recognise that I was sick really. This went on, for almost two years.

Then I had to have surgery for my back and a couple of weeks after that surgery, I got another attack which kind of put my feet away. Then the doctor explained the reason for this attack was the... what do you call it? I was completely awake during the procedure and they explained that it was you that triggered this attack, they explained. 

I still didn't get any offer for any medicine for MS. Only for pain. I use all this bad stuff for this medicine for epileptic normally and I was kind of more and more affected by the fatigue, the new neural pain, because of MS more and more. 

Then the doctor couldn't really help me. I wasn't qualified to get the medicine to slow down the MS because I was still considered different. Or whatever you can call it in a different category at the time, considered to give medicine to slow down their progress.

Today, I know the Norwegian doctors are starting to give this right away, but in 96 and 98 when I had these two big episodes, it was not common yet. Then I had my daughter in 2002 and I had a really good pregnancy and I was feeling very sick. MS unusually got better during pregnancy.

Of course, I was concerned that the birth could trigger another attack. I was right because this is what I did during the birth. I did use only the needles for pain relief and I didn't get any help to do it all or things like that.

They were careful with what they gave me when my daughters started to grow, I had more fatigue and more pain. Whatever the doctor was giving me didn’t help with the pain or fatigue. There wasn’t really any medicine which was working. I was trying it and it's something called for a while, but… What do you call it? A tree gets it. It was like more fatigue. Then I met this lady, I don't know if you know about this program that we had in Norway in 2013, it was the program in general. The lady with MS who was telling her story in that program, I met her in a training camp for MS and she told me about LDN, and then I figured out that this is something I want to try because she was like all over the place, the allergy and I find out I would give it a try. I ask the doctors, they said this is not proven, so we can't give it to you.

But they told me how to get it. They said if I go to a primary doctor and the primary doctor was given the risk perception... But prescription, it's okay, and we can't really say that you shouldn't take it, because of policy and blah, blah, blah, they have decided that all of the Norwegian neuro doctors will not write this prescription.

In May 2012 I started using LDN, and I have been reading a lot on Facebook because it started to pop up groups in Norway and in Denmark. Sharing stories and also a special group only MS and LDN and I read and concluded that if I start, I need to start with the low dose, very low dose and increase very slowly.

And I did. So I started in May and at the end of July, I was able to go on holiday with my family for 10 days. We started at a wedding which normally was so exhausting that I would be on the couch for the rest of the week after just one night. We went on to a park for my daughter who was 10.

I was for the first time able to spend the whole day walking around in the park together with her. Then we went on for a long ride with the car and we were away for 10 days and when I came back I was exhausted.  It was like, wow, something has changed.

Some radicalized change. I still was taking some pain medicine but I started reducing it. By February 2013, my doctors stopped prescribing the drugs with the opioids for me.

I went back to work, not full time, but I have been 100% since then. Like you call it auto work since 2001. I have been more or less, sometimes also in more than a hundred percent in hours working in pay and stuff today, no pain at all. I very often had this problem with my bladder, so I had to... what is the name of it in English? I didn't really manage to consolidate. So I had a lot of accidents, of course, but I also got a lot of infections. 

Linda Elsegood: In your bladder? 

Astrid: Yeah, yeah. In my bladder. Yeah. It was constantly infected and two times it almost cost me my life more or less because I got this sepsis, what they call it in Norway, the blood then got infected. So two times I went to the hospital and was really, really critical. After I started on LDN I have never any cold or any flu or things like that. My allergy has gotten better. I also use the catheter to help to empty the bladder because it didn't empty completely itself. That's the reason. 

Linda Elsegood: So you're self catheterizing?

Astrid: Yes, I did for several years. Of course, that was a nope. Done that. I haven't done that since I started on that. All-day I can feel like I need to go to the bathroom for an hour and I don't have the accidents anymore either. So definitely affected my bladder in a very good way. Who is really saying that you can't?

You are, so you can't see it. I feel like I'm more or less without any diagnosis really at the time. It's the combination with the LDN and I also take something called… natural medicine based on D mannose. Take it to flush out your bladder. I think it's like a drink. I drank it and the oils from seeds with black cumin seed in it. It's like the respiratory seed and it's shadow make rapeseed.

Then this is also very good for them. For infections, prevent the faction infections and so this should combination with the LDN. So it's been like life-changing. 

Linda Elsegood: If you were to say, what's your quality of life was like before you started on LDN and 10 being the best, what would it have been?

Astrid: I would say between three and four, maybe. 

Linda Elsegood: What would you say it is today? 

Astrid: Wow. Wow. Yeah. Amazing. Oh, I can do whatever I like to do. I can say yes to what I like to do and I don't need to say no. I'm measuring. If anything was supposed to happen, I needed to value, is this going to cost me too much or is it gonna give me any value? Everything was like that. Of course, since I have a little daughter, everything was focused to give her the best possible life. So when she went to kindergarten and school, I was residing on the sofa, doing nothing so that I can play with her. When she came back from her with school so that she could have friends over and so on.

So everything was kind of focusing on giving her the best what I really wanted. I'm the kind of person who is used to, I went to school and I went to college and high school and university, I was working. Besides, I have also been always using use to have a very high capacity of what I thought something used to work a lot and to enjoy working and always kind of this.

Suddenly I had to be this no person in many aspects. Even though I wanted, I knew that this is gonna cost me, so it wouldn't be worth it. Everything is back to where it was, I'm the person I am. I can say yes to what I like to do. It works.

Linda Elsegood: Oh, that's fantastic. You don't get the pain anymore? 

Astrid: I said, that's gone. No. That was really the big difference. The biggest, I think because the pain gave me a sleep disorder because I was having very bad sleep, even though I was always tired and being on the couch, I didn't really like... if I was lying on the couch and I felt like going to the bathroom because I needed to, it was like, I wait a minute, did two, I wait the five minutes. It was exhausting just to go to the toilet. So everything was so hard. It was like constantly like something was going on. I felt like my whole body is like when you take your muscles on you, you squeeze them as hard as you can and you feel like how the body's anxious and in a strain, it felt like this all the time, even though I was lying in bed.

The body was relaxed, but it didn't feel like it. This pain is all gone. When I lay down now it feels like I'm relaxed and I don't have any pain or neuro pains. They’re gone. Also, it's more like pain in the ears, eyes, and mouth.

It's like lightning balls coming and give you pain for just a few seconds to a minute. I had a lot of these neuro pains and they are also all gone. It's very good. It's so many things that disappeared. I don't remember all the pain though, because it's since 2013 I felt like my life, we started again.

I'm talking a lot about it and gave everybody's psyche, you have to try. So they are always asking me all, you're selling this or what? I say you have to go to the doctor and ask for it. So when I started, I had to order a box with a special delivery to my pharmacy in my city. So in the beginning that was like a special order. Out of curiosity, asking if I go to a new pharmacy and if the people know about them, ask them if they have a lot of customers and a lot of them say that it's been common and there are more and more people using it for more and more sickness. They recognize that this is something that is working. It’s good for so many people for so many reasons and different reasons to use it. They recognize it in the pharmacy too.

Linda Elsegood: We've come to the end of the show and we're so pleased to have heard your story today, Astrid. Thank you so much for sharing it with us. 

Astrid: My pleasure and I hope everybody is able to try it, LDN, because I think it's worth a try. Anyway, thank you very much. 

Linda Elsegood: My pleasure. 

This show is sponsored by our members who made donations. We'd like to give them a very big thank you. We have to cover the monthly costs of the radio station software, bandwidth, phone lines, and phone calls to be able to continue with the radio show and thank you for listening.

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

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

Linda Elsegood: Malcolm is going to read his story. Welcome, Malcolm!

Malcolm: Thank you Linda.

Art's MS LDN story. 1988 to 2012. I was diagnosed with Multiple Sclerosis, April 1988. I was very ill for two years after the initial attack. I couldn't walk straight and be actually partially blind for a few weeks.

I never thought I would recover and become independent again. I was very depressed and briefly considered suicide. I was hospitalized for over one month. And out of work for over four months. It took me many, many months to get back into the swing of things. I gradually pulled out of the attack with the help of much Ivy Solu-Medrol and oral Prednisone, which is all the doctors had to offer back then.

I made a full recovery and was symptom-free until around 1994. It was like I was never had MS. I was under the care of a neurologist, which in hindsight was a mistake. In 1994 is when I started seeing him again on a regular basis. I was originally diagnosed with a Relapsing-Remitting type of Ms.

But after a few years, the neurologist upgraded it to the next level called Secondary Progressive Multiple Sclerosis. In 1996 there was a very rough winter here in New York. It was a major blizzard followed by heavy snowfall after heavy snowfall. I work as a maintenance supervisor for a Real Estate company, and part of my job is to see that the snow is removed from their properties.

It was a very stressful winter for me, both mentally and physically. My Ms returned with a vengeance, and my Neurologist put me on Avonex, which I took for over three years self-injected. I eventually developed neutralizing antibodies against interfering on medicines, so my Neurologist put me on Copaxone, which I took for over three years.

You also had me on eight treatments of the Novantrone. I had many, many Ivy Solu-Medrol, Prednisone taper offs in between all of this. Nothing was holding the MS. He then wanted to put me on Betaseron, and I asked him why as I thought I was immune towards the Interferon.

He said:" Well, we have to try something." He also thought about putting me on Tysabri right before it started harming people and was pulled from the market. It was then I realized he was only experimenting on me and really didn't have any definite answers. I am 6,7 foot and weigh 240 pounds, but my eyes filled with tears in his office.

Fortunately, his nurse saw me and suggested I look into LDN even though the neurologist was against it. She also suggested pro-Karen, which I took for a few months. They've been on LDN since March 2005 and shudder to think where I'd be without it, among other things, it has helped my blurry vision and balance. Improved my bladder control and lessened to my fatigue and give me a general sense of wellbeing.

It has slowed the progression of my disease. My only regret is that I didn't start LDN sooner than I did. I am certain I wouldn't be dealing with the physical problems I now have. Besides taking 4.5 milligrams of LDN from Skip's pharmacy every night around 10:00 PM, I also take a variety of supplements which include a multivitamin, vitamin D3, Calcium citrate, a B complex vitamin, a B12 vitamin. He also takes 4-Aminopyridine, also known as Amphora, which helps with, walking and nerve transmission for Ms patients. And he also takes fish oil and magnesium L-Threonate and um. Glucosamine and that concludes his statement.

I try to avoid eating foods containing gluten, casein, sugar, corn, soy, legumes, red meat, eggs. The foods I tried to eat are fresh fish, fresh wild fish, organic chicken and turkey, brown rice, fresh raw, organic fruits and vegetables. I believe highly in the benefits of coconut oil, tart cherry juice, and stevia.

I walk as much as possible. Moderate stretching, deep breathing, lift light weights. I use toothpaste free of florid and two soap. I try to get to bed by 10:00 PM.

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.