My functional MD started me on 4.5 mg at bedtime a month ago to prevent breast cancer reoccurrence. I also have sleep apnea but it hasn’t affected my sleep in any way. One fantastic side benefit is it immediately took away all my chronic back and knee pain for which I praise God!
My doctor suggested I start LDN more than 15 years ago when I was diagnosed with RA sjorgens syndrome, painful facet syndrome. I’ve had PRP and prolotherapy for the facet pain which helps for short periods of time. I’ve used LDN on & off for 15 years (2mg) is enough for me. Reason for me going off for periods of time due to nervousness and sleep issues. Which still can occur from time to time. 3 months ago I prayed about going to a rheumatologist and going on an injectable…..(didn’t really want to do that but I needed something to turn my pain around ) I asked my doctor to start prescribing again and started .5, then 1mg now 2 mg. I have been basically facet & fibromyalgia free for 2 & 1/2 months. I’m Thankful and I hope more doctors start prescribing. I agree with Dr Campbell it grieves me that more healthcare providers are not prescribing. Bottomline is many doctors do not have time to research the literature.
Thank you Dr. Campbell & Dr Cohen for covering LDN and being courageous to stand up and speak up against the main stream censorship. Please change the title to include LDN as I've been searching for a while and this just popped up. Ive been suffering from chronic joint pain, fatigue and inflammation since I had covid 3 years ago. This has turned into a spondylitis AxSpa and I finally found a doctor who is willing to try something more than the typical prescription causing so many side effects. I hope LDN helps me. Btw Ive changed my diet to ketovare 6 months now and that has halved my recovery time when I get a flare but not the magic bullet.
I take LDN for severe, painful, inherited restless leg syndrome. It took only 2 weeks to start working and I have never looked back. I have been spreading the word about this drug to anyone who will listen and everyone I have recommended it to with RLS has had the same result as me. It has literally saved my life as I was in a very dark place thinking I would be in this pain forever. Never be able to sit down from about 5.00.p.m or sleep at night.
Low-dose Naltrexone solved my rapid heart rate issue I've been battling for YEARS. And I sleep like a ROCK. The deepest most restorative sleep. On week 3 of the stuff and I feel like layers of trauma are slowly being lifted day by day.
Nice conversation! Great to see a balanced discussion on this pharmaceutical. It is definitely past time for some large clinical trials to begin. - Jarred Younger
Thanks for the informative talk. I suffer from CFS and I am about to start LDN. I live in Australia, and near me on the Gold Coast there is Griffith University which is a world leader in research for ME/CFS, and they are currently undertaking studies using LDN. I look forward to seeing the results of these studies!
@katyb2793 lt had a strong effect on me. It would definitely give me more energy, but I would get very vivid dreams and also bad tinnitus from it, so I had to stop. But I would definitely recommend trying it, as alot of people don't get side effects.
@@TheIceyeddy oh I'm sorry it didn't work out... I don't have much luck with side effects either. I just tried melatonin and had to stop as I immediately got headaches again that I'd been getting since covid.. Do you have any other options available to you? Cfs is really difficult to deal with.. i hope you can find something that works for you :)
@@TheIceyeddy I'm sorry to bother you again, but I just spoke to my gp about it and he can't prescribe it due to rules etc May I ask how you got it prescribed? Did you have a specialist?
Hello to you both, I have been taking LDN for five years. I pay for it from a pharmacy in Glasgow. I have had Fibromyalgia for 15 years. This is the only drug that has helped me with pain reduction. And gives me some semblance of a normal life. I’ve told doctors about it but they always say that they don’t know about it. I say that you could help other fibro sufferers if you prescribed it but as it’s unlicensed and so cheap I guess they’d never make any money out of it. I researched LDN for two years before I decided to give it a try. ( Dr. Jared Younger) I also have come off it twice just to check that it does work and my pain comes flooding back and I’m like a cripple. So I am back on the LDN again. I titrated with liquid to start then gradually upped to 3mg where I am today. I did try 4.5 but the nightmares were too frequent. So went back to 3mg and am ok. I wish more people would know about LDN, I am always telling anyone who will listen about it.
Your comment is very encouraging. Thank you so much. I am excited and happy to hear about your positive experience with ldn, and at the same time upset I could not get it in my part of the world. I think I know what you may be referring to when you mentioned Glasgow.
I’m just about to contact the Glasgow Pharmacy. My GP would not consider it and gave me Gabapentin. I’ve had Fibro/ME/CFS for 40 years. Hoping for good things.
Thank you John Campbell for your honesty. I have ME/CFS/Fibro - I don’t get a positive effect from exercise. I’m looking forward to trying this through a private doctor.
Well done for getting the message out there! And I’m so happy for you that you’ve found a solution for your condition. I’m about to go on it for Hashimoto’s, depression, CPTSD and chronic migraines and am feeling very hopeful about it 🙏🏼☺️
My rheumatologist prescribed me Ldn 4.5 for chronic inflammation for connective tissue disease. It helps with pain and brain fog and no side effects at all.
Someone in my family takes LDN for severe endometriosis every night before bedtime and states it makes her life much easier. It is now being recommended for fibromyalgia.
Thank you both for making this video. It is so important to hear professionals about their experiences with prescribing LDN. I have been on ldn for about 7 years, for ME/CFS, POTS and other things, and I am a huge advocate for ldn. I tell everyone who might benefit about it and try to help them to get a prescription. But it is so difficult, because most doctors will shrug, saying that this is just another ‘alternative thing’ that someone has heard about. I Hope that video’s like this will help convince doctors to give it a try. What other conditions have you prescribed ldn for? It was very interesting to hear about your patient with copd, as it is very difficult to find information about experience with ldn and certain conditions. Please let me know if I can do anything to help awareness further.
I just had a pharmacist recommend this to me for long covid, so hopefully the word is getting out there. I came here to educate myself, and it's given me hope. I hope you're doing well in your health :)
@@katyb2793 thank you! It can be very helpfull with long covid, I hope it works for you. Has the pharmacist given you good information on dosing and titrating? This can sometimes be a bit tricky for people with ME/CFS but also long covid.
@@Boringbetty I also have cfs and just had adverse reactions to melatonin so I am a bit unsure how it would go, but definitely want to try. The pharmacist said up to 4.5mg. But I just spoke to my doctor today and he said he's not allowed to prescribe it as it's not an approved use or dose of the drug.. He suggested seeing if my specialist is allowed to, so will try that. I wish the government cared more about long covid but they're just sticking their heads in the sand like ostriches. Thank you so much for taking the time to offer advice, it's much appreciated :)
I saw the title and got so excited. Dr. John is doing LDN! I take it for fibromyalgia/ dysautonomia neuropathic pain. It works quite well for nerve pain but nothing else unfortunately. I still use cannabis for fibromyalgia, migraine, and myofascial pain. The first line is NOT become stressed or deconditioned whenever you can help it! Paiin flare prevention > pain treatment.
LDN works, start low and go slow. I'm using it for not only a major covid vax reaction, but also chronic pain and Inflammation that got worse after vax. My severe pain was completely gone in 5 hours after first dose. It truly is a miracle drug. I did have a Herx like response the second day and thought I was going to die, lol, but really my immune system is bad and I was in bad shape. The hard part is getting a doctor to prescribe it. Especially in the US.
I talked to three doctors (endo, allergist, and GP) and NONE had heard of LDN and wouldn't prescribe it. I had to go to an online RX, and this is ridiculous. I despise doctors, 99% of them are idiots.
In the USA, usually you need to see a specialist, like a rheumatologist, because it is off label, so most PCPs won’t prescribe. Compounding pharmacies that make it can usually refer you to a local doctor who prescribes. I have used it for several years for ME/CFS.
@@sueregan2782 I saw almost every type of doctor because I was so sick. An none of them would prescribe it. It took me awhile working on an open minded neurologist who was concerned about my brain inflammation and a neuro optometrist who helped explain to him what was going on.
@@angeminc it also has significantly helped my stomach problems which I had before covid jab, but it got so bad after I couldn't eat solid foods for months. They called it covid stomach, but the meds the GI doctor gave me didn't help and had horrible side effects. LDN actually helps the stomach and intestines produce mucosal lining. The reason why I was unable to eat was because the jab caused acute pancreatitis,which caused my body to stop producing Digestive enzymes. So between the LDN and the digestive enzymes I had to purchase and take with each meal I was finally able to eat solid food. When I say my body had a severe reaction I mean it was bad. The entire GI took 1.5 years to resolve and I also lost the ability walk for two days, still have heart issues,etc.. the list goes on. It was disheartening to be turned away by the medical community over and over again because they packed the critical faculty to be proactive and progressive about my case. The second I mentioned it also started after the Jab I was seen as a crazy person and treated like it. Over a two year period I finally got a better group of doctors but it was so much work for me to walk them through my illness what was going on and how to cure it. The alternative medicine doctor jumped on it right away and was the greatest help, but as a DOM she can't prescribe LDN or anything. She was the one who told me to get on it. And she also recommended quercitin, histax by integrative therapeutics, amino acids and other treatments. Peptide infusions help but are too expensive. The acupuncture and cupping helped. You got to think detox.
Never been first before! Good morning both! :) :) How is the glucose monitor you are testing doing Dr C? And, can we have more soup recipes please? :) Love this channel.
@@jamiehowington3 It took about three weeks to notice the difference for me. I used to wake up moaning and groaning, and now I feel a decade or so younger. I am 57. Aches and pains minimized. I take 4.5 mg at bedtime nightly and 2 mg in the day time 3 days a week (I've recently added that because it seems to enhance mental clarity and mood and lower anxiety.) I also have beautiful crazy dreams, psychedelic adventure dreams (while waking up well rested and happy).
I follow Dr Campbel since Covid, but I did not see this episode. This is a great explanation, thank you so much 😊. I came to hear about Naltrexone a couple months ago from other channels, actually from talks addressing Ehlers Danlos syndrome. I finally got a doc to prescribe this to me, and I started beginning of August. I am at 2.3 mg every evening, but at this dose I get sleep problems. Last night I did not sleep again. When I go back to 2 mg, I sleep fine. I tried to up the dose from 2 mg several times, but almost everytime I cannot sleep. So now I will start to take it in the mornings instead. I hope this helps, because almost everything I eat seems to trigger harm to my body, but having such restricted diet also harms my body. And there is no way a Gastroenterologist will help me; I tried so many doctors since 2018, and the Gastroenterologist for about 2 years. They dont take me seriously. I do hope naltrexone will be used to help long covid (post covid and post vax), I am bringing this up with every doctor I talk to, maybe someone will have interest.
I first heard about this drug as an emergency treatment, provided by paramedics, to counteract opioid overdose. Many years ago. It's interesting hearing you two discuss this.
I'm suffering from long covid brain fog/ inflammation, insomnia, Anxiety from last 2 years. It's soo scary and debilitating😢. Should I take this ???
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Victoria can you elaborate how bad your insomnia was? I am literally having to take Unisom or some sleep aid every night and often still dont sleep. I am desperate 😢
Thanks for the video very informative. Unfortunately my situation is quite frustrating medicaly i have long covid an outside the box condition but i also have a doctor that refuses outside the box treatment. Knowing a possible helpful solution is sitting in a pil bottle in the pharmacy a block away from my house has caused me a great deal of medical mistrust.
Am same as u.. was pre med, long cov, long Lyme, mold , gut dysbiosis, wasted 2years w 11drs done now.. using long vivid Drs , naturopathic, mostly USA.. 🙏💓
I just started with 0.125 mg. I am extremely sensitive to all meds. I am praying this helps with my LC and ear pressure and anxiety. Thank you for your help!
@@theancientsancients1769 yes it has helped with some issues. I still have pain but the pain is less. Still having trouble sleeping. Anxiety is less but still there. I am still slowly increasing dosage.
@@briechilli4496 I am doing ok. Did not help my ears but I am better able to tolerate the pain and off balance and pressure. I am thinking I may make a tiny increase here soon.
I have had M.E and Fibromyalgia for 23yrs in severe pain with reactive depression due to this. This gives me some hope. I did ask my pain clinic but they do not issue it. I have heard so many good reviews of this from people who have been able to get this on script. Is it a postcode lottery? Can primary care prescribe it? If not, why not?
If you're in the UK the only compounding pharmacy for LND is in Glasgow (it comes up on google). A private prescription is surprisingly low cost. If it works your GP might agree to a take over the prescription via a shared care agreement. If you're lucky the practice might already be prescribing it off-lable. It's worth asking your GP.
I have had compartment syndrom in my right leg and the after effects of the surgery was very painful flares in my foot and toes with the sensation of it boiling, also I have torn the tendons across my shoulders from golf and this stopped me from lifting my arms above my head, I have been on 4.5mg dose of Naltrexone for about 4 months and all of the pain has ceased and I can now lift my arms above my head without any ANY pain. I also have suffered from OCD and this has caused me to settle down and feel at peace. I cound not reccommend LDN highly enough
I am located in Australia, I originally started with capsules @ $1 each but now dissolve 50mg tablet in 500ml of water and take 45ml of the solution each evening at 9pm. I had read up on the efficacy of the solution and over what period. I have been a couple of months on the solution and my condition continues to improve and fixing issues I hadn't realised I had until they went away.
My daughter, bedbound by me/cfs for 12 months has tried 1 x 0.1 mg once in the evening and could not sleep for several days. It is terrible because we were so hopeful that this would help her improve. What do you do with your patients in such a case?
I'm very sorry to hear that such a small dose had such an effect on your daughter. I'm not yet bed bound, but heading that way ( housebound and getting progressively worse for ages) and I am thinking of trying LDN. Did you dare to try it again in the morning? If so, how did it go? Did your daughter have any sleep problems before taking LDN?
@@tatianagolitsyn675 She did not sleep from one single Tablet for three days, so taking it in the morning would change nothing. However, there are people that say it helped. Most get rather sleepy - that is why you usually take it in the evening.The Doctor suspects that it is a MCAS (She has Mast cell issues) reaction for my daughter. Looking back it was a chance I would take again. It helps many people. If you try it and feel more energy consider not spending it, but leaving it for your body to heal was a recommendation offered to us by a few people.
Thank you, be interesting to know whether it might be possible to help with asthma reduction as well as or instead of drugs like seratide so rather than prohibiting the hypersensitive reaction & its affect from the response of the lungs, it encourages a healthier response. Obviously there may be a few with a variety of allergic reactions to a variety of allergens pathogens & medications both scientific & natural who may be more at risk of a mal event in relation to it so would need to be consulting an immunologist & allergy specialist firs, but if its encouraging a more vitalising & supportive response from the body, rather than deadening it certainly sounds a better wholistic state to have mind body & soul work with each other rather than ignoring or inhibiting each other. Good talk, thanks for offering it.
Wonderful I used it for my skin condition and saw a result after a week..I have an inflammatory skin condition like Psoriasis and it seemed to regulate my immune response to hot water and it reduced my itching caused by the anxiety of having such a disfiguring disease...
Don’t think it’s a game changer. Because it hardly approved my health. did prevent the crashes of post exertional malaise only a little bit. Although I do know of people who have had great success with the same drug. The key is to start low at around 0.5mg and slowly increase up to what you can tolerate over several weeks, but don’t go above 4.5mg per dose
Dr Cohen, I'm from India. I've been diagnosed with Chronic HSP/Fibrotic NSIP. My current treatment is basically Nebulising with a Formoterol fumarate Budesonide inhalation suspension. You mentioned that you had excellent results with LDN on a patient with COPD. Have you also treated HSP/NSIP successfully with LDN? Would you recommend my trying it out?
This medicine sounds awsome. I had Covid in 2021 and I never recovered. My functional doc just put me on this Winston to get it. I have lots of gut issues can’t eat any solid foods without having immediate pain and I have fibromyalgia and chronic migraines. Also this medicine has barley any side effects. I can’t wait to start it.
This is a old video but there are lots of opioid addicts struggling for months because their receptors are shot to shit and finding it difficult to get a dopamine abundance state and often relapse because of that. This would be a great possibility for them.
Also works for thyroid disease I'm taking it now for my hoshimotos instead of meds that didn't help me this is my 2nd week it starts at 1.5 to 3 then 4.5 in a 3 week span.❤
I have very bad wide spread neuropathy literally all over my body from head to toes. It affects my hearing my eyesight I've lost 70lbs I could barely walk at this point. Since after my second shot of the moderna COVID vaccine it's been a down hill. Can this medication help me? Anyone has information?
My neurologist put me on B2 400mg daily, magnesium 400mg twice daily, and CoQ10 10g daily for migraine prevention, it’s helped. I’m also on LDN for neuropathy, my migraines have decreased significantly. I still get them, I know my triggers, laughing, coughing, bending over. I don’t watch comedies anymore!
I'm wondering if LDN might be of use for epiretinal membrane (caused by glial cells migrating to and forming a membrane on the retina) that can cause deterioration in fine detail of eyesight when it progresses to involve the macula. It is a condition that is said to be triggered by inflammation after the vitreous membrane separation that every aging human has.
Dear Dr., I do appreciate your sharing with us about naltrexone. I am also interested in this to see if it helps with severe asthma. When I asked the immunologist/allergist, she said it can depress respiratory rate (I am summarizing). I want to ask you, does naltrexone do that at low dose?
I've never seen respiratory depression listed as an effect of naltrexone at any dose. Opioid agonists like morphine or oxycodone certainly have that effect. There's no obvious reason why an pure antagonist like naltrexone would.
Conventional docs don’t know sh@t. They only do what their hospitals or overlords on boards plus Big Pharma tell them or they are in big trouble. I rarely darken their doors now. My functional doc recommended LDN for my thyroid and immune system. I’m 76 and basically doctor myself. I take 3 mg. The only conventional doc who has helped me these days was the surgeon who fixed my femur when I fell.
I got long Covid from the vaccine. Brain fog and sleep problems stayed with me after the fatigue left. I was prescribed 1mg for sleep; after a week I went up to 2mg. The side effects were skin issues: red welts in my face and neck: herpes on my nose and incredibly chapped lips. I went off for 3 days and the welts started to disappear but the other symptoms did not. I’m starting the LDN again at .25mg. I do not want to stop taking it all together because I’m concerned that the brain fog will return. Any suggestions? I would be very grateful.
@@larryc1616 after stopping for 3 days I started up again at .25mg. Brain fog and sleep were still issues. I just tried upping the dodo to .5mg and the red welts on my neck came back. I’m now off for a few days and will go back to .25mg. I’m hoping to get LDN in a smaller dosage so I can go up more slowly. Interestingly, one of my minor autoimmune issues went away so I’m still hopeful!
@lesleepetersen87 I have CFS/ME and I started at .6mg but that gave me insomnia, body pains from hell and up/down fatigue. I will be restarting at .3mg and slowly work my way up, hopefully without side effects. I'm not giving up as there are no other meds for this horrible disease. Good luck to you!
I've been suffering all of these symptoms for 2 years now and it will be interesting suggesting this medication to my Doctor in New Zealand. We have a massive issue here since CV with the health system dictating to all medical professions NOT to give anyone anything not prescribed by the WHO or other major authorities that shouldn't be, I've had certain drugs for arthritis and gerd red flagged in real time on their computer screens with a warning of police interventions legally if they prescribe certain drugs, which incidentally happen to be alternatives to the CV JAB!
It’s part of the control and elimination of population plan worldwide especially in western countries. Authoritarians are in control now. Especially in Australia and New Zealand. Surely you know that by now.
Hi Dr. Can you discuss Long Covid & what has happened to cause our Heart Rates to be so high on getting up, this causes the feeling of not being able to breath. What can be done?
many potential causes which is why a proper diagnosis must be made. not everything is covid-related and other diagnosis must be considered by a doctor. covid does seem to cause POTS (postural orthostatic tachycardic syndrome) and this is treatable and will usually resolve significantly, if not completely, in time and with some basic medications.
Have you heard of Dextro-Naltrexone? I guess you can take opioids with it, and it targets the autoimmune response even better than low dose naltrexone... I have a theory that taking LDN every 12 hours at 4.5mg might be even more effective...
I have the same question. I did a little googling and found an articel at www.ncbi.nlm.nih.gov/pmc/articles/PMC3962576/ that actually mentions this idea! Here is part of the text:
"The hypothesis that naltrexone and naloxone operate via glial cells to exert their beneficial actions is supported by work with dextro-naltrexone. Dextro-naltrexone is a stereoisomer of naltrexone which is active at microglia receptors but has no activity on opioid receptors [26]. Dextro-naltrexone possesses analgesic and neuroprotective properties [27]. Therefore, the analgesic, anti-inflammatory, and neuroprotective effects of naltrexone do not appear to be dependent on opioid receptors."
I haven't read through the references yet, but it does seem to validate the approach. You should be able to take this at MUCH higher doses than the right-handed version without any ill effects on the opiod receptors. My neurologist increased my prescription to 6mg/day but I think it's likely that the benefits is threshold-dependent with most of the benefits at doses higher than the standard 4.5mg/day for real benefit. Dextro-naltrexone could solve this problem. I can't undertand why there is so little research on this.
After a moment I don't really care what he says. In 4 months of downright reading publications and research, I'm far, far beyond his understanding of long COVID ( - the infinite and beyond - ) so I'm not even losing any time to listen to his approximations. Read the litterature, doc. Do your job. Follow the top world researchers on the matter (dr Akiko Iwasaki, from Yale ; dr David Putrino from Mount Sinai (NY) ; dr Michael Peluso from UCLA ; dr Amy Proal fouder of the consortium for long COVID and ME). Read the litterature on ME, fibromialgia, lake Taohoe and Iraq war syndrome ; on post-acute Ebola and Zika syndromes). My cognitive capacities are debilitated and I'm bedridden. All the while I read probably 1000 times more than you ever will on the subject. So take it seriously. We're not having british tea with biscuits here. People's lives are being ruined.
Hey bud, I’ve had long Covid or post viral syndrome for close to a year now. I’ve poured through the literature too and I’ve been really angry - with my GP, the health system and regulators etc. But these docs are not the enemy, they are trying to help. I met John Campbell last month at a conference on Covid and he is an incredible, principled man who has provided lots of valuable information to people suffering from the virus and the vaccines. I started LDN a few days back and it’s been helping a lot. Keep your head up mate you’ll get through it.
CBD is also hard on the liver. LDN does act as a stimulant for some people at higher doses. I had to stay at 1.5mg because I felt wired and irritable at 2mg LDN.
Not hard on the liver at low doses like are being discussed here (4.5 mg or less). Low dose Naltrexone is *completely* different animal from standard dose Naltrexone. Two different things.
Completely inaccurate trash. LDN is not hard on the liver seeing as Naltrexone even at 100mg is very rarely associated with liver damage and LDN dosage is between 0.2-4.5mg.
I am on LDN, for my primary Progressive multiple sclerosis. For 7 yrs now. I have progressed in the disease, but I felt more energy when I started it! Please, include me in your study, I volunteer! My neurologist doesn't support me in my use of LDN. My primary, naturopath MD, subscribes it to me.😮
I got covid in March 2020 and had a bad case for 2 1/2 months. Occasionally, during this time I took one of my wife's vicodin and it made a tremendous difference in how bad I felt and also helped to stifle my terrible cough. Just an amateur observation.
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My functional MD started me on 4.5 mg at bedtime a month ago to prevent breast cancer reoccurrence. I also have sleep apnea but it hasn’t affected my sleep in any way. One fantastic side benefit is it immediately took away all my chronic back and knee pain for which I praise God!
@Campbell_teaching SC USA
My doctor suggested I start LDN more than 15 years ago when I was diagnosed with RA sjorgens syndrome, painful facet syndrome. I’ve had PRP and prolotherapy for the facet pain which helps for short periods of time. I’ve used LDN on & off for 15 years (2mg) is enough for me. Reason for me going off for periods of time due to nervousness and sleep issues. Which still can occur from time to time.
3 months ago I prayed about going to a rheumatologist and going on an injectable…..(didn’t really want to do that but I needed something to turn my pain around ) I asked my doctor to start prescribing again and started .5, then 1mg now 2 mg. I have been basically facet & fibromyalgia free for 2 & 1/2 months. I’m Thankful and I hope more doctors start prescribing. I agree with Dr Campbell it grieves me that more healthcare providers are not prescribing. Bottomline is many doctors do not have time to research the literature.
Thank you Dr. Campbell & Dr Cohen for covering LDN and being courageous to stand up and speak up against the main stream censorship. Please change the title to include LDN as I've been searching for a while and this just popped up. Ive been suffering from chronic joint pain, fatigue and inflammation since I had covid 3 years ago. This has turned into a spondylitis AxSpa and I finally found a doctor who is willing to try something more than the typical prescription causing so many side effects. I hope LDN helps me. Btw Ive changed my diet to ketovare 6 months now and that has halved my recovery time when I get a flare but not the magic bullet.
I take LDN for severe, painful, inherited restless leg syndrome. It took only 2 weeks to start working and I have never looked back. I have been spreading the word about this drug to anyone who will listen and everyone I have recommended it to with RLS has had the same result as me. It has literally saved my life as I was in a very dark place thinking I would be in this pain forever. Never be able to sit down from about 5.00.p.m or sleep at night.
Low-dose Naltrexone solved my rapid heart rate issue I've been battling for YEARS. And I sleep like a ROCK. The deepest most restorative sleep. On week 3 of the stuff and I feel like layers of trauma are slowly being lifted day by day.
What dose are you on ?
@@ethannewman195 Curious what was your starting dose.
What is the mg level you started & settled at?
Could you please respond what dose you are taking? This is important Information for other Patients😉
@@irisxkx i ran out and quit using it. if forget the dosage, but I experimented a lot
Nice conversation! Great to see a balanced discussion on this pharmaceutical. It is definitely past time for some large clinical trials to begin. - Jarred Younger
Thanks for the informative talk. I suffer from CFS and I am about to start LDN. I live in Australia, and near me on the Gold Coast there is Griffith University which is a world leader in research for ME/CFS, and they are currently undertaking studies using LDN. I look forward to seeing the results of these studies!
Do you have an update on the LDN study ?
I didn't know this! How did you go? Did you find it helpful?
@katyb2793 lt had a strong effect on me. It would definitely give me more energy, but I would get very vivid dreams and also bad tinnitus from it, so I had to stop. But I would definitely recommend trying it, as alot of people don't get side effects.
@@TheIceyeddy oh I'm sorry it didn't work out...
I don't have much luck with side effects either. I just tried melatonin and had to stop as I immediately got headaches again that I'd been getting since covid..
Do you have any other options available to you? Cfs is really difficult to deal with.. i hope you can find something that works for you :)
@@TheIceyeddy I'm sorry to bother you again, but I just spoke to my gp about it and he can't prescribe it due to rules etc
May I ask how you got it prescribed? Did you have a specialist?
Hello to you both, I have been taking LDN for five years. I pay for it from a pharmacy in Glasgow. I have had Fibromyalgia for 15 years. This is the only drug that has helped me with pain reduction. And gives me some semblance of a normal life. I’ve told doctors about it but they always say that they don’t know about it. I say that you could help other fibro sufferers if you prescribed it but as it’s unlicensed and so cheap I guess they’d never make any money out of it. I researched LDN for two years before I decided to give it a try. ( Dr. Jared Younger) I also have come off it twice just to check that it does work and my pain comes flooding back and I’m like a cripple. So I am back on the LDN again. I titrated with liquid to start then gradually upped to 3mg where I am today. I did try 4.5 but the nightmares were too frequent. So went back to 3mg and am ok. I wish more people would know about LDN, I am always telling anyone who will listen about it.
Your comment is very encouraging. Thank you so much. I am excited and happy to hear about your positive experience with ldn, and at the same time upset I could not get it in my part of the world. I think I know what you may be referring to when you mentioned Glasgow.
I’m just about to contact the Glasgow Pharmacy. My GP would not consider it and gave me Gabapentin. I’ve had Fibro/ME/CFS for 40 years. Hoping for good things.
My GP refused when I requested it after I researched LDN for my ME/CFS/Fibro. He gave me Gabapentin- that didn’t suit me. I’m going private.
Thank you John Campbell for your honesty. I have ME/CFS/Fibro - I don’t get a positive effect from exercise. I’m looking forward to trying this through a private doctor.
Well done for getting the message out there! And I’m so happy for you that you’ve found a solution for your condition. I’m about to go on it for Hashimoto’s, depression, CPTSD and chronic migraines and am feeling very hopeful about it 🙏🏼☺️
My rheumatologist prescribed me Ldn 4.5 for chronic inflammation for connective tissue disease. It helps with pain and brain fog and no side effects at all.
Absolutely love the improvements I have experienced! 🎉Improved cognitively. Impressive decrease of pain!😊
So excited that you’re getting this info out there Dr Campbell!!
Someone in my family takes LDN for severe endometriosis every night before bedtime and states it makes her life much easier. It is now being recommended for fibromyalgia.
This is so exciting that the benefits of LDN are getting out. Dr. Campbell will spread this vital information worldwide.
Thank you both for making this video. It is so important to hear professionals about their experiences with prescribing LDN. I have been on ldn for about 7 years, for ME/CFS, POTS and other things, and I am a huge advocate for ldn. I tell everyone who might benefit about it and try to help them to get a prescription. But it is so difficult, because most doctors will shrug, saying that this is just another ‘alternative thing’ that someone has heard about. I Hope that video’s like this will help convince doctors to give it a try. What other conditions have you prescribed ldn for? It was very interesting to hear about your patient with copd, as it is very difficult to find information about experience with ldn and certain conditions. Please let me know if I can do anything to help awareness further.
I just had a pharmacist recommend this to me for long covid, so hopefully the word is getting out there. I came here to educate myself, and it's given me hope. I hope you're doing well in your health :)
@@katyb2793 thank you! It can be very helpfull with long covid, I hope it works for you. Has the pharmacist given you good information on dosing and titrating? This can sometimes be a bit tricky for people with ME/CFS but also long covid.
@@Boringbetty I also have cfs and just had adverse reactions to melatonin so I am a bit unsure how it would go, but definitely want to try.
The pharmacist said up to 4.5mg. But I just spoke to my doctor today and he said he's not allowed to prescribe it as it's not an approved use or dose of the drug..
He suggested seeing if my specialist is allowed to, so will try that.
I wish the government cared more about long covid but they're just sticking their heads in the sand like ostriches.
Thank you so much for taking the time to offer advice, it's much appreciated :)
Excellent and informative video Doctors. Thanks to both of you!
Glad you enjoyed it!
I saw the title and got so excited. Dr. John is doing LDN! I take it for fibromyalgia/ dysautonomia neuropathic pain. It works quite well for nerve pain but nothing else unfortunately. I still use cannabis for fibromyalgia, migraine, and myofascial pain. The first line is NOT become stressed or deconditioned whenever you can help it! Paiin flare prevention > pain treatment.
LDN works, start low and go slow. I'm using it for not only a major covid vax reaction, but also chronic pain and Inflammation that got worse after vax. My severe pain was completely gone in 5 hours after first dose. It truly is a miracle drug. I did have a Herx like response the second day and thought I was going to die, lol, but really my immune system is bad and I was in bad shape. The hard part is getting a doctor to prescribe it. Especially in the US.
I talked to three doctors (endo, allergist, and GP) and NONE had heard of LDN and wouldn't prescribe it. I had to go to an online RX, and this is ridiculous. I despise doctors, 99% of them are idiots.
In the USA, usually you need to see a specialist, like a rheumatologist, because it is off label, so most PCPs won’t prescribe. Compounding pharmacies that make it can usually refer you to a local doctor who prescribes. I have used it for several years for ME/CFS.
@@sueregan2782 I saw almost every type of doctor because I was so sick. An none of them would prescribe it. It took me awhile working on an open minded neurologist who was concerned about my brain inflammation and a neuro optometrist who helped explain to him what was going on.
I have been struggling since the Covid Vax. What dose of LDN did you take? Please update on how you are.
@@angeminc it also has significantly helped my stomach problems which I had before covid jab, but it got so bad after I couldn't eat solid foods for months. They called it covid stomach, but the meds the GI doctor gave me didn't help and had horrible side effects. LDN actually helps the stomach and intestines produce mucosal lining. The reason why I was unable to eat was because the jab caused acute pancreatitis,which caused my body to stop producing Digestive enzymes. So between the LDN and the digestive enzymes I had to purchase and take with each meal I was finally able to eat solid food. When I say my body had a severe reaction I mean it was bad. The entire GI took 1.5 years to resolve and I also lost the ability walk for two days, still have heart issues,etc.. the list goes on.
It was disheartening to be turned away by the medical community over and over again because they packed the critical faculty to be proactive and progressive about my case. The second I mentioned it also started after the Jab I was seen as a crazy person and treated like it. Over a two year period I finally got a better group of doctors but it was so much work for me to walk them through my illness what was going on and how to cure it. The alternative medicine doctor jumped on it right away and was the greatest help, but as a DOM she can't prescribe LDN or anything. She was the one who told me to get on it. And she also recommended quercitin, histax by integrative therapeutics, amino acids and other treatments. Peptide infusions help but are too expensive. The acupuncture and cupping helped. You got to think detox.
Never been first before! Good morning both! :) :)
How is the glucose monitor you are testing doing Dr C?
And, can we have more soup recipes please? :)
Love this channel.
Thank you for educating us. We as individuals can ask our doctors to look into this drug as a potential treatment.
I am taking it right now. 4.5mg for 6 days so far. I am being told by the pain community that it will take 6 months to work.
@@jamiehowington3I heard you sill feel a difference between 2weeks-3months.
@@jamiehowington3 It took about three weeks to notice the difference for me. I used to wake up moaning and groaning, and now I feel a decade or so younger. I am 57. Aches and pains minimized. I take 4.5 mg at bedtime nightly and 2 mg in the day time 3 days a week (I've recently added that because it seems to enhance mental clarity and mood and lower anxiety.) I also have beautiful crazy dreams, psychedelic adventure dreams (while waking up well rested and happy).
I follow Dr Campbel since Covid, but I did not see this episode. This is a great explanation, thank you so much 😊. I came to hear about Naltrexone a couple months ago from other channels, actually from talks addressing Ehlers Danlos syndrome. I finally got a doc to prescribe this to me, and I started beginning of August. I am at 2.3 mg every evening, but at this dose I get sleep problems. Last night I did not sleep again. When I go back to 2 mg, I sleep fine. I tried to up the dose from 2 mg several times, but almost everytime I cannot sleep. So now I will start to take it in the mornings instead. I hope this helps, because almost everything I eat seems to trigger harm to my body, but having such restricted diet also harms my body. And there is no way a Gastroenterologist will help me; I tried so many doctors since 2018, and the Gastroenterologist for about 2 years. They dont take me seriously. I do hope naltrexone will be used to help long covid (post covid and post vax), I am bringing this up with every doctor I talk to, maybe someone will have interest.
Thank you doctors! Great presentation!
Ive ben u-sving this for years now. I had the epstein bar virus and it worked instantli.
I first heard about this drug as an emergency treatment, provided by paramedics, to counteract opioid overdose. Many years ago.
It's interesting hearing you two discuss this.
you are thinking of naloxone which is given intravenously. naltrexone at these low doses works differently.
LDN has been a godsend for my Long Covid brain fog/inflammation and insomnia
Me too
@Campbell_teaching that’s very kind of you! Paris, France.
I'm suffering from long covid brain fog/ inflammation, insomnia, Anxiety from last 2 years. It's soo scary and debilitating😢. Should I take this ???
Victoria can you elaborate how bad your insomnia was? I am literally having to take Unisom or some sleep aid every night and often still dont sleep. I am desperate 😢
How much you take
Thank you DrJohn 🙏🏼🕊️
Way to be, to go❤️
God bless!
I take it for my autoimmune condition.
Thanks for the video very informative. Unfortunately my situation is quite frustrating medicaly i have long covid an outside the box condition but i also have a doctor that refuses outside the box treatment. Knowing a possible helpful solution is sitting in a pil bottle in the pharmacy a block away from my house has caused me a great deal of medical mistrust.
Am same as u.. was pre med, long cov, long Lyme, mold , gut dysbiosis, wasted 2years w 11drs done now.. using long vivid Drs , naturopathic, mostly USA.. 🙏💓
A few doctors prescribe LDN on Internet. I got mine that way through AgelessRx (also called LDNDirect I think). There's another one called LDNDoctor.
Thank u both. I learned a lot.
I just started with 0.125 mg. I am extremely sensitive to all meds. I am praying this helps with my LC and ear pressure and anxiety. Thank you for your help!
How is it going so far?
I hope it works out for you! Any update?
@@theancientsancients1769 yes it has helped with some issues. I still have pain but the pain is less. Still having trouble sleeping. Anxiety is less but still there. I am still slowly increasing dosage.
@@chestnutmair1how are you going now on the LDN ?
@@briechilli4496 I am doing ok. Did not help my ears but I am better able to tolerate the pain and off balance and pressure. I am thinking I may make a tiny increase here soon.
I have had M.E and Fibromyalgia for 23yrs in severe pain with reactive depression due to this. This gives me some hope. I did ask my pain clinic but they do not issue it. I have heard so many good reviews of this from people who have been able to get this on script. Is it a postcode lottery? Can primary care prescribe it? If not, why not?
Have you tried an Integrative Practitioner or functional doctor? They are more familiar with it and could prescribe it to you
I have Hashimoto’s and am about to start treatment with it. It seems to help all autoimmune conditions
If you're in the UK the only compounding pharmacy for LND is in Glasgow (it comes up on google). A private prescription is surprisingly low cost. If it works your GP might agree to a take over the prescription via a shared care agreement. If you're lucky the practice might already be prescribing it off-lable. It's worth asking your GP.
@@nataliebutler can you take it if on an opiate pain relief medication?
@@katinahockney9387 I'd ask the LDN research trust or a prescriber about that.
I have had compartment syndrom in my right leg and the after effects of the surgery was very painful flares in my foot and toes with the sensation of it boiling, also I have torn the tendons across my shoulders from golf and this stopped me from lifting my arms above my head,
I have been on 4.5mg dose of Naltrexone for about 4 months and all of the pain has ceased and I can now lift my arms above my head without any ANY pain.
I also have suffered from OCD and this has caused me to settle down and feel at peace.
I cound not reccommend LDN highly enough
I am located in Australia, I originally started with capsules @ $1 each but now dissolve 50mg tablet in 500ml of water and take 45ml of the solution each evening at 9pm. I had read up on the efficacy of the solution and over what period. I have been a couple of months on the solution and my condition continues to improve and fixing issues I hadn't realised I had until they went away.
By all means
My daughter, bedbound by me/cfs for 12 months has tried 1 x 0.1 mg once in the evening and could not sleep for several days. It is terrible because we were so hopeful that this would help her improve. What do you do with your patients in such a case?
Has your daughter been checked through IgeneX labs for Lyme and coinfections?
Have her try taking it in the morning or another time of day rather than evening.
@@gpet711 As sleeplessness lasted for days it will not help taking it in the morning.
I'm very sorry to hear that such a small dose had such an effect on your daughter. I'm not yet bed bound, but heading that way ( housebound and getting progressively worse for ages) and I am thinking of trying LDN. Did you dare to try it again in the morning? If so, how did it go? Did your daughter have any sleep problems before taking LDN?
@@tatianagolitsyn675 She did not sleep from one single Tablet for three days, so taking it in the morning would change nothing. However, there are people that say it helped. Most get rather sleepy - that is why you usually take it in the evening.The Doctor suspects that it is a MCAS (She has Mast cell issues) reaction for my daughter. Looking back it was a chance I would take again. It helps many people. If you try it and feel more energy consider not spending it, but leaving it for your body to heal was a recommendation offered to us by a few people.
Thank you, be interesting to know whether it might be possible to help with asthma reduction as well as or instead of drugs like seratide so rather than prohibiting the hypersensitive reaction & its affect from the response of the lungs, it encourages a healthier response. Obviously there may be a few with a variety of allergic reactions to a variety of allergens pathogens & medications both scientific & natural who may be more at risk of a mal event in relation to it so would need to be consulting an immunologist & allergy specialist firs, but if its encouraging a more vitalising & supportive response from the body, rather than deadening it certainly sounds a better wholistic state to have mind body & soul work with each other rather than ignoring or inhibiting each other. Good talk, thanks for offering it.
definitely worth discussing with your doctor/immunologist
Prayers coming.. so much can be done these days.. never give keep searching. Hugs 🙏🙏🙏🙏🙏🙏🙏🙏🙏
Wonderful I used it for my skin condition and saw a result after a week..I have an inflammatory skin condition
like Psoriasis and it seemed to regulate my immune response to hot water and it reduced my itching caused by the anxiety of having such a disfiguring disease...
What mg level did you start with and settle at?
LDN slows the cell cycle so natural apoptosis can occur for those fast replicating cancer cells.
Doesn't work on skin cancer
@@juliabarron2122
Cansema for skin cancers 100 % .
@@juliabarron2122
Cansema 100%👍
My functional doc just out me in this. I am waiting for get it shipped to my house. I hope this works.
I take LDN for Crohn’s. I love the vivid dreams 😊
Don’t think it’s a game changer. Because it hardly approved my health. did prevent the crashes of post exertional malaise only a little bit. Although I do know of people who have had great success with the same drug. The key is to start low at around 0.5mg and slowly increase up to what you can tolerate over several weeks, but don’t go above 4.5mg per dose
Dr Cohen, I'm from India.
I've been diagnosed with Chronic HSP/Fibrotic NSIP.
My current treatment is basically Nebulising with a Formoterol fumarate Budesonide inhalation suspension.
You mentioned that you had excellent results with LDN on a patient with COPD.
Have you also treated HSP/NSIP successfully with LDN?
Would you recommend my trying it out?
This medicine sounds awsome. I had Covid in 2021 and I never recovered. My functional doc just put me on this Winston to get it. I have lots of gut issues can’t eat any solid foods without having immediate pain and I have fibromyalgia and chronic migraines. Also this medicine has barley any side effects. I can’t wait to start it.
Have you started it? How did it work?
@@andreas956 yes I would love to know too. I hope you're doing much better now ❤
I started LDN 3mg. I was recently diagnosed with MS also, have Hashimotos
My Mother has been on LDN for over 21 yrs for MS. 4.5mg a day. Wishing you all the best on your journey.
I also have hashimoto’s and have been prescribed it by my integrative practitioner. Functional doctors will also prescribe it
So does it work for tou
Hope you and your loved ones are fairing well in face of the violence and war now in Israel. Our thoughts are with you and Israel!
@Campbell_teaching the state of North Carolina in the United States
This is a old video but there are lots of opioid addicts struggling for months because their receptors are shot to shit and finding it difficult to get a dopamine abundance state and often relapse because of that. This would be a great possibility for them.
It’s a mu antagonist . It blocks the opiate from attaching to that receptor.
Also works for thyroid disease I'm taking it now for my hoshimotos instead of meds that didn't help me this is my 2nd week it starts at 1.5 to 3 then 4.5 in a 3 week span.❤
Have you seen any reduction in your antibody levels?
I took it years ago, I felt too good, ended up getting the worst migraine, and I remember in the end I just felt silly in the head!❤❤❤😂😂😂
What mg level did you start at and settle at?
I have very bad wide spread neuropathy literally all over my body from head to toes. It affects my hearing my eyesight I've lost 70lbs I could barely walk at this point.
Since after my second shot of the moderna COVID vaccine it's been a down hill. Can this medication help me? Anyone has information?
LDN sounds like Lily the Pink’s medicinal compound that’s efficacious in every case.
What time of the day would you recommend taking it? I take it at bedtime for lyme.
??? Has Naltrexone been tried for chronic migraine?
My neurologist put me on B2 400mg daily, magnesium 400mg twice daily, and CoQ10 10g daily for migraine prevention, it’s helped. I’m also on LDN for neuropathy, my migraines have decreased significantly. I still get them, I know my triggers, laughing, coughing, bending over. I don’t watch comedies anymore!
This a very important question. Is the 4.5 dose the same for Long Covid, and Depression the SAME dose?
I'm wondering if LDN might be of use for epiretinal membrane (caused by glial cells migrating to and forming a membrane on the retina) that can cause deterioration in fine detail of eyesight when it progresses to involve the macula. It is a condition that is said to be triggered by inflammation after the vitreous membrane separation that every aging human has.
רק עכשיו הבנתי שאתה בארץ
I take 325 tylenol with 5 ml of opiates I do not know what I would do without It going on 2 years of inflamation from covid
Dear Dr., I do appreciate your sharing with us about naltrexone. I am also interested in this to see if it helps with severe asthma. When I asked the immunologist/allergist, she said it can depress respiratory rate (I am summarizing). I want to ask you, does naltrexone do that at low dose?
I've never seen respiratory depression listed as an effect of naltrexone at any dose. Opioid agonists like morphine or oxycodone certainly have that effect. There's no obvious reason why an pure antagonist like naltrexone would.
Conventional docs don’t know sh@t. They only do what their hospitals or overlords on boards plus Big Pharma tell them or they are in big trouble. I rarely darken their doors now. My functional doc recommended LDN for my thyroid and immune system. I’m 76 and basically doctor myself. I take 3 mg. The only conventional doc who has helped me these days was the surgeon who fixed my femur when I fell.
I thought it blocked endorphins . Isn’t it in the same the same class as narcan ?
Works in the short term for pain ...
I got long Covid from the vaccine. Brain fog and sleep problems stayed with me after the fatigue left. I was prescribed 1mg for sleep; after a week I went up to 2mg. The side effects were skin issues: red welts in my face and neck: herpes on my nose and incredibly chapped lips. I went off for 3 days and the welts started to disappear but the other symptoms did not. I’m starting the LDN again at .25mg. I do not want to stop taking it all together because I’m concerned that the brain fog will return. Any suggestions? I would be very grateful.
Update?
@@larryc1616 after stopping for 3 days I started up again at .25mg. Brain fog and sleep were still issues. I just tried upping the dodo to .5mg and the red welts on my neck came back. I’m now off for a few days and will go back to .25mg. I’m hoping to get LDN in a smaller dosage so I can go up more slowly. Interestingly, one of my minor autoimmune issues went away so I’m still hopeful!
@lesleepetersen87 I have CFS/ME and I started at .6mg but that gave me insomnia, body pains from hell and up/down fatigue. I will be restarting at .3mg and slowly work my way up, hopefully without side effects. I'm not giving up as there are no other meds for this horrible disease. Good luck to you!
@@larryc1616 thank you! And to you too! I’ve heard it can take up to 6 months sometimes before it works so I’m hanging in there!
I've been suffering all of these symptoms for 2 years now and it will be interesting suggesting this medication to my Doctor in New Zealand. We have a massive issue here since CV with the health system dictating to all medical professions NOT to give anyone anything not prescribed by the WHO or other major authorities that shouldn't be, I've had certain drugs for arthritis and gerd red flagged in real time on their computer screens with a warning of police interventions legally if they prescribe certain drugs, which incidentally happen to be alternatives to the CV JAB!
How did it go with your Dr?
(also, 'arthritis and gerd'? what is 'gerd'? Can you say which drugs were red-flagged?)
It’s part of the control and elimination of population plan worldwide especially in western countries. Authoritarians are in control now. Especially in Australia and New Zealand. Surely you know that by now.
It's working for me
Is better to take at night or in the morning?
At night as endorphins released between 2-4am. Take at 9 or 10pm.
If dreams to vivid or you get insomnia, then take every am.
Would LDN be good for Post Vaccine Syndromr
Yes, my integrative dr just prescribed it for my vax injury and has seen excellent results. Good luck!
For Post Viral Syndrome like CFS/ME/Chronic Lyme/ Long covid.
No such thing as post vaccine syndrome
Hi Dr.
Can you discuss Long Covid & what has happened to cause our Heart Rates to be so high on getting up, this causes the feeling of not being able to breath. What can be done?
many potential causes which is why a proper diagnosis must be made. not everything is covid-related and other diagnosis must be considered by a doctor. covid does seem to cause POTS (postural orthostatic tachycardic syndrome) and this is treatable and will usually resolve significantly, if not completely, in time and with some basic medications.
LDN research trust in the US shares great information too
This drug has serious withdrawal issues
I went off for awhile and didn’t experience any at 3 mg. But everyone is different.
❤
Have you heard of Dextro-Naltrexone? I guess you can take opioids with it, and it targets the autoimmune response even better than low dose naltrexone... I have a theory that taking LDN every 12 hours at 4.5mg might be even more effective...
I have the same question. I did a little googling and found an articel at www.ncbi.nlm.nih.gov/pmc/articles/PMC3962576/ that actually mentions this idea! Here is part of the text:
"The hypothesis that naltrexone and naloxone operate via glial cells to exert their beneficial actions is supported by work with dextro-naltrexone. Dextro-naltrexone is a stereoisomer of naltrexone which is active at microglia receptors but has no activity on opioid receptors [26]. Dextro-naltrexone possesses analgesic and neuroprotective properties [27]. Therefore, the analgesic, anti-inflammatory, and neuroprotective effects of naltrexone do not appear to be dependent on opioid receptors."
I haven't read through the references yet, but it does seem to validate the approach. You should be able to take this at MUCH higher doses than the right-handed version without any ill effects on the opiod receptors. My neurologist increased my prescription to 6mg/day but I think it's likely that the benefits is threshold-dependent with most of the benefits at doses higher than the standard 4.5mg/day for real benefit. Dextro-naltrexone could solve this problem. I can't undertand why there is so little research on this.
what is dextro naltrexone?
Got to eliminate sugar sweets all bad for mental health. I suffer w mental health issues exercise is the best.
After a moment I don't really care what he says. In 4 months of downright reading publications and research, I'm far, far beyond his understanding of long COVID ( - the infinite and beyond - ) so I'm not even losing any time to listen to his approximations. Read the litterature, doc. Do your job. Follow the top world researchers on the matter (dr Akiko Iwasaki, from Yale ; dr David Putrino from Mount Sinai (NY) ; dr Michael Peluso from UCLA ; dr Amy Proal fouder of the consortium for long COVID and ME). Read the litterature on ME, fibromialgia, lake Taohoe and Iraq war syndrome ; on post-acute Ebola and Zika syndromes). My cognitive capacities are debilitated and I'm bedridden. All the while I read probably 1000 times more than you ever will on the subject. So take it seriously. We're not having british tea with biscuits here. People's lives are being ruined.
Instead of complaining, share your knowledge
Hey bud, I’ve had long Covid or post viral syndrome for close to a year now. I’ve poured through the literature too and I’ve been really angry - with my GP, the health system and regulators etc.
But these docs are not the enemy, they are trying to help. I met John Campbell last month at a conference on Covid and he is an incredible, principled man who has provided lots of valuable information to people suffering from the virus and the vaccines.
I started LDN a few days back and it’s been helping a lot. Keep your head up mate you’ll get through it.
Are you covid vaxxed. Bingo. It’s long mRNA vax. Wake up.
hard on the liver to take every day, plus it makes you feel like your on an amphetamine. CBD is more effective
CBD is also hard on the liver. LDN does act as a stimulant for some people at higher doses. I had to stay at 1.5mg because I felt wired and irritable at 2mg LDN.
dont consume the cbd just hold it under your tongue though.@@sueregan2782
Not hard on the liver at low doses like are being discussed here (4.5 mg or less). Low dose Naltrexone is *completely* different animal from standard dose Naltrexone. Two different things.
Completely inaccurate trash. LDN is not hard on the liver seeing as Naltrexone even at 100mg is very rarely associated with liver damage and LDN dosage is between 0.2-4.5mg.
What mg level did you start at and settle at?
I am on LDN, for my primary Progressive multiple sclerosis. For 7 yrs now. I have progressed in the disease, but I felt more energy when I started it! Please, include me in your study, I volunteer! My neurologist doesn't support me in my use of LDN. My primary, naturopath MD, subscribes it to me.😮
I got covid in March 2020 and had a bad case for 2 1/2 months. Occasionally, during this time I took one of my wife's vicodin and it made a tremendous difference in how bad I felt and also helped to stifle my terrible cough. Just an amateur observation.
@Campbell_teaching Pennsylvania, USA
Are you covid vaxxed? Sure it’s not that?