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

Susan - US: Celiac Disease, 18 Sept 2019 (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

After Susan’s surgery in 1999, she had certain symptoms from her Celiac disease; including diarrhea, weakness and severe stomach ache and from there found the Low Dose Naltrexone (LDN) charity website for the Low Dose Naltrexone medication. Her doctors agreed for Susan to try it. Having no initial side effects, and even after 18 months she is doing fantastic. Now Susan is 73 years old, she quotes that she is “Going to take it for the rest of her life.” As well as being so thrilled for the Low Dose Naltrexone medication to work for her.

Susan rated her quality of life before the Low Dose Naltrexone (LDN) was a 3 out of 10, and it has now significantly improved since then.

She recommends LDN for all, but advises people to be allergy tested beforehand to double check with what is in the medication.

Please watch the video to hear the full interview. Thank you.

Any questions or comments you may have, please Contact Us.

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

Sue from Wales first experienced symptoms seven years ago when she realised that she couldn’t grip things properly and she started to drop things a lot. She had strange sensations while walking that she was going to fall. Sue went to the doctors and had blood tests and was told she was fine despite the problems that she was experiencing. A year later, in a new job which was stressful, things accelerated, eight months into the job she had to leave.  Back at the doctors, she was given more tests and this time she was referred to a neurologist who diagnosed Primary Progressive Multiple Sclerosis.

Now choking on her food and having to walk slowly and getting nothing concrete from her doctor or neurologist Sue decided to research for herself. She found articles about Low Dose Naltrexone and found a prescriber and finally got herself a prescription for LDN. 

Starting at a low dose and working up steadily Sue soon found she felt a lot better in herself, happier and better able to cope. She had more energy and got a spring back in her step within a month. The numbness improved and she has her life back without the anxiety and fear for her future that she was feeling before. 

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

Stephanie from Australia takes Low Dose Naltrexone (LDN) for Multiple Sclerosis (MS). Stephanie first started noticing symptoms in the year 1997, she had tingling in her legs, funny feelings in her right hand and little finger, as well as massive fatigue.

After CT scans and tests, nothing showed up, so they offered her physiotherapy. After travelling to Australia, she then noticed numbness in her forehead and heavy feet.

After seeing a new GP, they confirmed it was a relapse remitting MS.

Near this time Stephanie also had optic neuritis on the right eye optic neuritis on the left eye and relapses would hit her legs. 

Stephanie found out about Low Dose Naltrexone (LDN) through a meditation and wellbeing group, she then researched online and found the LDN trust website. Stephanie then went to her GP where her doctor agreed to have it prescribed for her. 

Before LDN, Stephanie rated her quality of life a 4 to a 5 out of 10, and now a 9 out of 10 after trying LDN.

Stephanie recommends people to try out the LDN medication, saying how worthwhile it is. Quoting it as harmless, and gives a really great chance at stopping the disease where it is.

This is a summary to listen to the entire interview by click the video link.

Stephen - US: Reactive Arthritis, Fibromyalgia (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Steven from the United States takes Low Dose Naltrexone (LDN) for reactive arthritis and fibromyalgia. He first started noticing problems five years ago at 65 years old, and had tremendous body pain, hands and wrists were very swollen.

After researching into LDN, he showed the information to his Rheumatologist who called it “Internet Crap” stating how there is no magic there.

He finally managed to receive a prescription from his primary doctor after some time.

He advises people to try out LDN, as he feels as though many people may be concerned about it. He rated his quality of life, before LDN a 3 ½ out of 10, and now, an 8.

Please watch the video to view the whole interview, Thankyou 

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

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

Stefan from England was diagnosed with Multiple Sclerosis (MS) in 2004 however had symptoms for around four year prior. He was very active but started to realise that his stamina was reducing, as well as weakness and numbness primarily down the left side of his body. Stefan experienced this on and off alongside, dizziness, where he had a spell of passing out, up until his diagnosis. 

Stefan started taking liquid form Low Dose Naltrexone (LDN), around five weeks ago and has already noticed an improvement in his balance and walking. He is also noticing benefiting differences in the other symptoms too.

This is a summary to listen to the whole Low Dose Naltrexone (LDN) and MS interview please click the video link.

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

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

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

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

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

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

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

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

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

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

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

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

Sophie from the United Kingdom takes Low Dose Naltrexone medication (LDN) for Multiple Sclerosis. In her late twenties, she noticed a weakness in her left side, and hands mostly. Then, her speech went funny. After many tests, MRI scans, CT scans and a lumbar puncture scan, she was diagnosed with Tumefactive Multiple Sclerosis (TFMS).

Sophie found out about LDN through a website on Facebook, where her doctor then prescribed it to her. After the first night, she woke up feeling rather positive and now she feels more herself after taking it. She feels more relaxed, no more spasms, pains and aches.

Before LDN, Sophie rated her quality of life a 4 out of 10, and now a 15/20 out of 10! 

Her feel good factor is amazing and fully recommends Low Dose Naltrexone medication (LDN) to other people.

This is a summary to listen to the entire interview by click the video link.

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

Sissi from France has multiple sclerosis. Where she was diagnosed in 2009, at the age of 63. Symptoms included weakness of touch in her fingers on the left side. Tiredness and also limping. Sissi also experienced eczema like circumstances, where she managed to strip her arms and legs, due to a pins and needles, scratching sensation.

Thankfully, Sissi managed to get a prescription easily from her pharmacy.

After two weeks of being on the Low Dose Naltrexone medication (LDN), she found more energy with herself, no more burning sensations, and did not feel tired anymore.

Sissi recommends LDN, after not experiencing bad symptoms after taking it. Also, her Doctor has recommended LDN to other patients where they have also noticed improvements. 

Please watch the video to view the full interview. Thankyou

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

Simon - Canada: Alopecia (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Linda Elsegood: I'm joined by Simon from Canada. He uses LDN for alopecia. Thank you for joining us, Simon. 

Simon: Thank you for having me.  

Linda Elsegood: So could we find out from you how long ago it was when you first noticed that your hair was falling out, how old you were, and how that impacted your life? 

Simon: Yeah, well, I was just turning 40. As I got near my birthday, actually, there were a lot of things going on in my life. It was a very stressful time. Um, it wasn't just turning 40 that, that was causing me to stress, we were moving house, uh, from one house to another. Uh, I was joining our family with my sister in law and, and my, my niece, um, for all kinds of good reasons. And, uh, but it meant moving to a new house and doing rentals and getting ready for that. And it was a really busy time. And, um, and yeah, I just started noticing, I think I, I didn't, didn't shave for a couple of days and I noticed that I had a bunch of bald spots coming in so I started taking some pictures and, uh, you know, about three weeks later I was coming back from my haircut and my daughter said, daddy's do have, uh, eyes in the back of their head. What are you talking about? And she said, well, you got two bald spots in the back of your head. And I said, okay, take me, take a picture for me. And, I had these two little lies spots to the back of my head. And from there in about six weeks, after eight weeks, I had to shave my head because I had so much hair falling out.

It was really distressing. It was, you know because you feel like you know what's going on? None of the health practitioners has any answers. I went to see my doctor said, Oh, you know, I've seen this before. It's not too bad. Um, this was before I actually shaved my head and, you know, don't worry, it'll come back.

It comes and goes, this kind of thing. And so it just proceeded to fall out, fall out, fall out, and it went throughout my whole body. I mean, I kept my eyebrows, and I lost this for a little while, I lost all my chest hair, all my body hair, and it only stopped at my knees when, uh, when I finally got to see a naturopath and changed my diet.

Yeah. It was devastating, and I was really at a loss at trying to figure out what was going on. 

Linda Elsegood: Literally feel naked, I should think.

Simon: And, you know, you identify so much with what you look like, and you know, it's natural for men to lose hair at some point. I actually have been pretty proud of my family, the dark-haired people in my family I had kept my hair the longest, and then suddenly it was all gone. And you really feel like you lose who you are really.

Like some people say they feel naked or they feel like they lost their identity. And I totally relate to that comment. That's you just, you look at pictures of people with alopecia, and you go, everybody looks the same. We're different versions of Mr Clean, and yeah, it's terrible. 

Linda Elsegood: So, what did the naturopath suggest?

Simon: Well, natural path, did a blood test to see what kind of allergies I had to food and designed a diet that was, I, you know, it's kinda like an AIP autoimmune protocol diet. Uh, kind of like a Paleo diet, but custom for, for what I was allergic to. So we took away all the things that I was allergic to.

And then all of the things that cause major inflammation. So no gluten, no dairy, no alcohol, no nothing with any yeast in it. So all anything that could cause a yeast, all the fermented stuff was out. Legumes were out. Corn was out. Um, you know, it was very restrictive and, and essentially it was easier to describe what I was able to eat, which was good quality, lean protein.

And good, vegetables, um, broccoli, cauliflower, the kales and all the stuff. Actually, that's in the betrayal series now. Uh, that was the stuff that I was, uh, asked to eat and, um, and then a lot of, good quality supplements. Um, and then I guess for that she gave me a rice protein powder that I would make shakes with every morning.

That was basically my breakfast. Um, so the Berry Berry shake was with rice protein and some coconut shredded coconut and some good Omega three oil, um, a little Stevia to make it taste okay. And, uh, that's, yeah, just started eating that. And that's about when the hair loss stopped. At least for my body hair, and it's, it stopped at my knees and I, for the longest time I had no hair except for between my knees and my ankles.

Linda Elsegood: So, how did that diet make you feel? I mean, did that give you more energy? Did you feel better inside? 

Simon: I felt better inside. I felt better, very quickly. I started dropping a lot of weight. I wasn't a super overweight person. I'm about six feet tall, and I was about 215 pounds at the time. And, um, I dropped down to 185 pounds within the year anyway.

If I remember correctly, it was about nine months, six to nine months or something. I dropped down to that weight. And felt amazing, super stamina, brain fog, gone. Um, just felt great. Every time I ate, I felt great and I never felt bloated. Uh, you know, lots of bowel movements and just felt, I just didn't understand actually how good it felt to eat properly.

I'd just been used to feeling bloated and gassy and just lethargic after eating, you know, a good: spaghetti meal or something like that. And I felt really good physically, mentally. It was very challenging, um, always being different than everybody else at the table. You know, even though my family, my wife, my sister in law did a really great job of making sure that when they made food, it was kind of, it could be made, you know, my way or their way for the kids and everything.

But it was still very difficult. I felt isolated a lot, and it was a lot of work because there were times when, of course, they couldn't help me and they were out or something like that. And I'd have to make food, and you have to keep thinking like every meal, okay, what am I going to be home next to make food and, oh, I need to prepare for meals.

You know, cause I'm going to be out overnight somewhere or something. And every work function and any social situation, you know, you couldn't, I couldn't have anything. The Naturopath was very strict with me at first and said, you can't cheat ever. And that was hard and very difficult mentally.

Linda Elsegood: I've done it too. So, I do know you have to check the labels, things that you think that couldn't possibly be gluten in the reason but it becomes easier over time, doesn't it? Because you know the foods you can and can't eat, 

Simon: Yes, I guess I check labels and everything, I think my eyes have been opened even more recently to where gluten is hidden. And, uh, you know if I had known what I know now at the start, I think I would have despaired even more. It's just so hard to get what you really need. 

I started to see some results, some funny Brown patches started appearing on my head, and I got armpit hair back, and body hair started to come back. Actually, more body hair came back then, then head hair during that process. But it was hard you know, eventually, we got to about nine months in or so on a diet, and we were celebrating our 15 year anniversary with my wife, and I went to Hawaii, just the two of us, which was, you know, the first time we'd done anything like that, and it was wonderful.

And while I was there, I just let down my guard and decided to eat. You know, just be kind of good what was there in restaurants and I felt terrible, initially and realized, you know, I was married to this diet, and I couldn't cheat, I gained weight.

I felt terrible. I started seeing some hair loss. I went back on a diet. Um. And then went on about another six months and then we made a family trip to Disneyland. And the same sort of process happened. It was impossible to eat properly there. And, came back from there and gained weight, felt terrible, and then my eyebrows and eyelashes all fell out.

So that was terrible, you know, I just realized is there anything else that I can do to help me out? Because I just feel like I'm doing everything humanly possible to make this work. And it's still not. It's still not giving me, you know, full results. What else out there is there? And that's when I heard about LDN from a good friend who is a very naturally focused person, but said, you know, Hey, I've heard about this LDN and it might help you cause it's helping other people with autoimmune issues.

And then my, when I went to see the naturopath, I basically said, you know, I'm frustrated. I'm tired of trying to fight this battle with just the diet alone. Is there anything else we can do? And she said you know what? I was going to tell you the same thing, you're working so hard, and need some more help.

And so I was going to bring up, uh, see if you were willing to take LDN. And that's when I started. That was about two years into the disease cycle. So I started losing my hair in 2013 June of 2013, and I started taking all the end in about June of 2015 

Linda Elsegood: and what did you notice when you first started? Did you have any introductory side effects? 

Simon: I'd read and learned that you might get vivid dreams. So I was actually kind of excited about that. I thought, well, that might be interesting. I've never been one for taking a lot of drugs or anything. So we started slow. We started with a. I think a 1.5 mg dose and then went for about two weeks, went to three, and then about two weeks went to four and a half. Um, I did get some vivid dreams. Um, and I think, uh, it's just, you know, your, maybe your body's reaction to when those endorphins kick in or something that, uh, things go crazy, but it wasn't too bad.

But the first side effect that I noticed that I didn't expect was about two weeks into the 4.5-milligram dose. I noticed I didn't have any anxiety and you know I'm senior-level management position at work. I am a senior person, in my church community do I do a lot of public speaking.

I do a lot of preparations of Bible studies and things like that. And at the time when I started taking LDN, I was getting ready for a, uh, I was going to be doing some teaching at a Bible school for teenagers. And I was really working hard, trying to get classes prepared. And normally that process, uh, creates a lot of anxiety I really get worried about, not having enough time and not making enough progress.

I ended up talking to my wife and she calms me down and says, you know, just keep moving, keep moving. And all of a sudden, I noticed. I wasn't doing that I was just working. I was worried about all this stress, and I was like, wow, I don't care if I never have my hair ever come back the rest of my life because this is a wonderful feeling.

Just not feeling anxious. And I didn't realize how, how it affected me. So that was the first, uh, the first surprise. Um, then I started noticing my nails, uh, improving. As, you know, many will know that LP should also affect your nails and they get pitted and streaked with white, and they get brittle.

And especially my toenails, you know, they looked almost like you had a fungus on your, on your toenail. And, uh, I started noticing that there was this Ridge. And unfortunately, I never ever took a picture of it, but. There was this defined line where, you know, close to the nail bed and the cuticle, it was totally clear and above the nail bed, you know, towards the end of the nail. Um, you know, across the line it was, it was all streaked and pitted, and everything was like overnight, something changed in that area where the nail was growing, and it was getting clear, and I was like, wow, this is amazing. If this can help my nails and my head, I know nails and hair related, then I'm hopeful that my hair will come back to, so then it was about, probably about three months later.

Yeah, September-ish timeframe that I took my next sort of set of pictures of my head because I was still depressed of what my head looked like, and I noticed that the hair that was coming in now before it had come in and these weird patches, it. My kids and I used to laugh because at one point, you know, like, what shape do you see in daddy's head?

With the hair that's growing back, you know, it's like looking at the clouds and seeing things. So we played games with that, but the hair that started on the LDN. It was coming in kind of all over. It was still thin. And, um, but it was coming in all over my head, and I was like, wow, this is really starting to really work.

At this point, I was still doing my diet, and keeping up with the LDN and just sort of kept progressing, uh, you know, slowly, not overnight for sure, but just slowly, slowly, slowly getting more hair, getting more hair. Um, yeah. So that was really exciting. 

Linda Elsegood: And when it came back, was it the same texture as before or was it fine or was it the same colour or had it changed colour?

Simon: I would say it's not the same texture. You know,I finally got to the point where I'm growing it I'm 18 months in, and it was just September of this year, October of this year that I said, I'm just going to let it grow out and see what it looks like.

So it's grey but I was going grey before I lost my hair, but it's greyer for sure. Um, and it, it's a little coarser, I would say at this point than it was when I lost it. Yeah. And I'm just sort of interested to see, you know, how it continues to grow in and if it reverts back or not.

It was browner, it was a Brown sort of colour, and now I would say it's more black and more grey, um, as it comes in. And definitely coarser. 

Linda Elsegood: What about your eyebrows and eyelashes? Have they grown back? 

Simon: I've, I've got a few eyebrows definitely coming in there and my eyelashes

I've got a few that are starting to grow, and I'm interested to see what sort of comes with that. Um, I've got definitely a little bit more facial hair. I was a person that used to wear a sort of big long sideburns. You know, that's the other thing. I guess I used to shave maybe, you know, before the alopecia, I would shave every day or every other day.

I didn't have a heavy beard, but,  then when I had alopecia, I mean, I might shave once every year. It'd be smooth-skinned and no problem. Then just maybe see one weird hair growing out there that just have randomly successfully grown and now I'm back to shaving maybe every three days.

Cause if I don't, I do have enough hair that it's noticeable. Um, so that's coming in more and more too. I see more on the sideburns and more in my or my beard area. 

Linda Elsegood: And what about the colour of your eyelashes? Eyebrows and you say beard, is that a different colour as well? And 

Simon: texture? Um, so far I would say it's pretty normal.

I mean, normally that hair is more coarse. Right? So I'd say it looks fairly normal actually. 

Linda Elsegood: that's really interesting. And how has that made you feel self-esteem wise? 

Simon: Oh, it's, well, it felt great. I mean, I just, um, those guys in the office now that, you know, those guys are normal male pattern baldness that, you know, of course before I had more hair than them.

And then during psoriasis, I had maybe the same haircut as them, and they said, welcome to the club, and they were happy, and now they're jealous again. Uh, so yeah, it's made me feel good. Um, just, you know, I just look like maybe a normal guy who's, maybe receding hairline type guy, and I think as a youth, I probably would've sworn I'd never looked like this. I would've if I was going to lose my hair and shave it all off. But now that it's growing back, you know, I'm, I'm happier to have it. I feel better. And now on the bad side, I've had so much success that it's mentally sort of tricked me into going off my diet.

And I've been off my diet for about seven months. You know, it's hard to say because I definitely am still having progress with hair growth, but I think I'd have more and be doing better if I was back on my diet and having the LDN there as a support.

Um, so I'm sort of steeling myself to moving back towards having my diet. I mean, the other thing was this is the second major autoimmune disease that I've had. I had rheumatoid juvenile arthritis as a child from age nine to 14, I went into remission when I went through puberty.

You know, as part of this journey that I'm on, learning lots from the community around, LDN and naturopaths and stuff like that. I just realized that I can't eat like a normal, person. I've got to take care of myself a lot more because I've had rheumatoid arthritis.

I've had alopecia. I developed massive hayfever allergies when I was 18. They just came out of nowhere. There are probably other things that have come and gone that I haven't noticed, but, I'm one of those people that are super susceptible and I don't want lupus or MS or any of these other really devastating conditions or rheumatoid arthritis again, that was awful. Alopecia is bad, but it's not like those other ones. I also had low thyroid with this condition. And that's the other thing that's changed a lot is maybe even before the hair started growing back in, about the same time as, as I noticed my anxiety going away and my nails changing as I was getting my thyroid tested, um, I started getting, I started noticing that I started out at about 120 milligrams of desiccated thyroid at the start of my journey, and now I'm down to 30 and all along the way. Uh, I keep sort of going above range and feeling kind of jittery, and they said let's take another dosage off.

That's really awesome. It's my thyroid healing. And so that connected with all of this too. So I'm feeling really encouraged that I don't think they could have done it on a diet alone maybe there's too many toxins and things in food that I just can't control, I know I'm not sleeping enough I have a stressful job. So there are some things that you just can't, get out of your life without making, you know, full change. Like quit your job, move to desert Island somewhere and be stress-free. That wasn't going to work for me, I needed some help.

LDN, I am 100% convinced it'd helped me. Um, and I'm really thankful for the people that sort of brought it to my attention. And now the community I'm connected with. It's helped me understand, you know, what other things I might be able to do to make more progress.

Linda Elsegood: Well, I think it's very interesting. For other people with alopecia that you has is not going to come back overnight. You've got to give it time. If the was somebody in your position who's just been newly diagnosed, or they've just found out their hair is falling out, what would you say to them about trying LDN?

Simon: I would, wouldn't hesitate for a minute. And I'm kind of a promoter of it to almost anybody who I come in contact with. I'm trying to say It's showing that it's helped cancer and other people too. But for anybody with alopecia I know there's not a lot of evidence out there yet.

I mean, when I first started I’d say it's helping people with ms. It's helping people with fibromyalgia, and maybe it'll help me too. But definitely, I believe it will help you. It's, it's going to help your body heal itself, and that's the root cause, right? As you've got either leaky gut or whatever going on in you right? Maybe having a problem and it's going to help accelerate your healing process. And I'm proof that even going back to just regular eating, it's still helping me.

That's how powerful I think it is. Uh, and then there are the benefits for me of not having anxiety. So between those things, I have no hesitation at all it's been really, really helpful.

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.

Shinique - Australia: Hashimoto's Thyroiditis (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Shinique from Australia shares her Hashimoto’s and Low Dose Naltrexone (LDN) story on the LDN Radio Show with Linda Elsegood.

Shinique noticed the possibility that she had Hashimoto’s when swelling in her joints limited the distances she could walk and noticed other things such as a lack of growth in her fingernails and allergic reactions to foods she could previously eat.

Shinique was officially diagnosed in 2010 but many doctors refused to prescribe her any medication as although she appeared fine on many MRI scans, her health was in fact the opposite. She took her treatment into her own hands and found Low Dose Naltrexone (LDN) online.

She said “It’s revolutionised my life. The pain in my legs is gone, I have much more energy so I don’t have to go to bed so early. I can eat most foods again. I’ve got most of my life back.”

This is a summary of Shinique’s interview. Please listen to the rest of Shinique’s Hashimoto’s and Low Dose Naltrexone (LDN) story by clicking on the video above.