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An Immune Disease? Low Dose Naltrexone (LDN) Fibromyalgia Study Suggests FM Has Inflammatory Side
"Low dose naltrexone (LDN) is becoming more and more widely used in fibromyalgia (FM) and chronic fatigue syndrome (ME/CFS). You can chart that use right back to Jarred Younger’s two small FM trials in 2009 and 2013. Now Younger’s back with a third trial that aims to do two things: a) further validate
"Low dose naltrexone (LDN) is becoming more and more widely used in fibromyalgia (FM) and chronic fatigue syndrome (ME/CFS). You can chart that use right back to Jarred Younger’s two small FM trials in 2009 and 2013. Now Younger’s back with a third trial that aims to do two things: a) further validate
Mdaisy
in
Fibromyalgia Action UK
7 years ago
Shortness of breath and LDN
I am looking for a reliable place in the UK where I can purchase Low Dose Naltrexone. Does anyone have any suggestions? Thank you!
I am looking for a reliable place in the UK where I can purchase Low Dose Naltrexone. Does anyone have any suggestions? Thank you!
Anap38
in
Fibromyalgia Action UK
7 years ago
Ra sufferer
When I get home from rehab I am going to look for a Dr that prescribes low dose naltrexone but what responses have people here who are on or tried humirs
When I get home from rehab I am going to look for a Dr that prescribes low dose naltrexone but what responses have people here who are on or tried humirs
Rocky07
in
NRAS
7 years ago
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Ra sufferer
Has anyone tried low dose naltrexone I have done a lot of research utube and read the ldn book and honest medicine by Julia schopik worth reading and researching I approached my senior rheumatologist she showed no interest which I expected through my research they seem more interested in giving you
Has anyone tried low dose naltrexone I have done a lot of research utube and read the ldn book and honest medicine by Julia schopik worth reading and researching I approached my senior rheumatologist she showed no interest which I expected through my research they seem more interested in giving you
Rocky07
in
NRAS
7 years ago
Low dose Naltrexone (Ldn)
Was diagnosed with RA in Feb, so far no medication regime helpful. Has anyone experience of taking Low Dose Naltrexone which is proving very successful for MS and having some success with other autoimmune diseases?
Was diagnosed with RA in Feb, so far no medication regime helpful. Has anyone experience of taking Low Dose Naltrexone which is proving very successful for MS and having some success with other autoimmune diseases?
Peterborough67
in
NRAS
7 years ago
Shannon Garrett, autoimmune specialist- Low Dose Naltrexone
https://vimeo.com/223058917
https://vimeo.com/223058917
liveurlife
Volunteer
in
LDN Research Trust
7 years ago
Why can't I stop drinking?
Hello, this is my first post. I have been drinking excessively for over 35 years. Wine. Up to a bottle a night. Blood tests are usually normal or slightly elevated but I know they don't tell the whole story. I've been referred to community addiction at my request but they only tell me what I already
Hello, this is my first post. I have been drinking excessively for over 35 years. Wine. Up to a bottle a night. Blood tests are usually normal or slightly elevated but I know they don't tell the whole story. I've been referred to community addiction at my request but they only tell me what I already
Hidden
in
British Liver Trust
7 years ago
LDN
Hi all anyone heard of LDN or low dose Naltrexone? There seem to be good results for ms sufferers and other autoimmune disorders although there is no mention of PMR specifically. It is an opiate antagonistic was was originally put on the market to help addicts but there is growing interest in it to
Hi all anyone heard of LDN or low dose Naltrexone? There seem to be good results for ms sufferers and other autoimmune disorders although there is no mention of PMR specifically. It is an opiate antagonistic was was originally put on the market to help addicts but there is growing interest in it to
blackstone1
in
PMRGCAuk
7 years ago
Ra sufferer
Hi all thank you all for your advice which is very much appreciated you all know my situation I have a difficult decision to make but the final decision is mine for me I need to think of my dignity (having to wait for nurses take me to the toilet in my present situation I can't go on my own at home I
Hi all thank you all for your advice which is very much appreciated you all know my situation I have a difficult decision to make but the final decision is mine for me I need to think of my dignity (having to wait for nurses take me to the toilet in my present situation I can't go on my own at home I
Rocky07
in
NRAS
7 years ago
Has anyone tried LDN Low Dose Naltrexone?
Hoping that someone with autoimmune condition will share their experience with LDN. I have myasthenia gravis, Hashimotos and chronic urticaria. I have changed my eating habits (on autoimmune paleo diet) which helped a lot and switched from levothyroxine to ndt. However, I still suffer from fatigue,
Hoping that someone with autoimmune condition will share their experience with LDN. I have myasthenia gravis, Hashimotos and chronic urticaria. I have changed my eating habits (on autoimmune paleo diet) which helped a lot and switched from levothyroxine to ndt. However, I still suffer from fatigue,
Monima
in
Thyroid UK
7 years ago
Gabapentine
Has anyone tried this to get rid of the horrific itch. I have tried questran,rifampin and naltrexone. My liver specialist has now prescribed this as the itch is destroying me x
Has anyone tried this to get rid of the horrific itch. I have tried questran,rifampin and naltrexone. My liver specialist has now prescribed this as the itch is destroying me x
Melwoods
in
PBC Foundation
7 years ago
LDN
Hi again everyone! I just want you to know that the Low Dose Naltrexone (LDN) is still working well for me. I continue to gradually get better and better, thank God.
Hi again everyone! I just want you to know that the Low Dose Naltrexone (LDN) is still working well for me. I continue to gradually get better and better, thank God.
positiveness
in
My MSAA Community
7 years ago
Feedback please!
I'm doin pretty good at the moment but I recently got off of Lexparo due to weight gain issues. Im now on Bupropion, which works well for depression but not so much for anxiety. Would like to know of some ways to cope with the anxiety!!! Im taking magnesium supplements and excersizing regularly.
I'm doin pretty good at the moment but I recently got off of Lexparo due to weight gain issues. Im now on Bupropion, which works well for depression but not so much for anxiety. Would like to know of some ways to cope with the anxiety!!! Im taking magnesium supplements and excersizing regularly.
Sweetsoul36
in
Anxiety Support
7 years ago
Trying Fluoxetine(Prozac) for Raynauds
I was recently diagnosed with limited systemic sclerosis with secondary Raynauds. Honestly, the Raynauds and hand swelling has been the worst ongoing symptoms that I've had. Getting muscle and joint pain, fatigue under control with Celebrex, Plaquenil, and low dose naltrexone. I also take a lot of vitamins
I was recently diagnosed with limited systemic sclerosis with secondary Raynauds. Honestly, the Raynauds and hand swelling has been the worst ongoing symptoms that I've had. Getting muscle and joint pain, fatigue under control with Celebrex, Plaquenil, and low dose naltrexone. I also take a lot of vitamins
Boisecgm13
in
Scleroderma & Raynaud's UK (SRUK)
7 years ago
Naltrexone
Hi. Just had to weeks holiday in Spain lanzarote went in and asked if I could buy naltrexone the offered me 28 tablets of revia genteric naltrexone for 20.45 euros buy as many packets up to a limit of ten without any problem bought 10 packets picked them up next day both farmicas offered them to me hope
Hi. Just had to weeks holiday in Spain lanzarote went in and asked if I could buy naltrexone the offered me 28 tablets of revia genteric naltrexone for 20.45 euros buy as many packets up to a limit of ten without any problem bought 10 packets picked them up next day both farmicas offered them to me hope
Huskyblade
in
Thyroid UK
7 years ago
rra sufferer
pt 4 final pt Well I have told most of my ra story sometimes I regret not listening to doctors re medicatios but expereince with prednisoloe and methotrexate along with anxciety got the better of me and I feel that surgery is the only choice get me back on track, it wont be easy but I will be
pt 4 final pt Well I have told most of my ra story sometimes I regret not listening to doctors re medicatios but expereince with prednisoloe and methotrexate along with anxciety got the better of me and I feel that surgery is the only choice get me back on track, it wont be easy but I will be
Rocky07
in
NRAS
7 years ago
Low dose naltrexone
Hi all - has anyone tried Low Dose Naltrexone - and what were the results?
Hi all - has anyone tried Low Dose Naltrexone - and what were the results?
Slosh
in
PMRGCAuk
7 years ago
~Progress update on low dose Naltexone~
I wrote several months ago on a fairly controversial topic regarding starting the use of Low Dose Naltrexone (orally 0.5mg) which in a short time made me feel nauseous even on such a low dose. Pharmaceutical Compounding made me a paraben free cream & I apply to areas of inflammation or where it hurts
I wrote several months ago on a fairly controversial topic regarding starting the use of Low Dose Naltrexone (orally 0.5mg) which in a short time made me feel nauseous even on such a low dose. Pharmaceutical Compounding made me a paraben free cream & I apply to areas of inflammation or where it hurts
Megams
in
PMRGCAuk
7 years ago
Low dose Naltrexone
Has anyone had experience with LDN? You can Google LDN or go to http://www.lowdosenaltrexone.org/index.htm#What_diseases_has_it_been_useful_for
Has anyone had experience with LDN? You can Google LDN or go to http://www.lowdosenaltrexone.org/index.htm#What_diseases_has_it_been_useful_for
Don_oregon_duck
in
Cure Parkinson's
7 years ago
Itching
I have been "itching" since 2014. I have slowly worked my way through GP recommendations and since January I am in the care of a specialist here in the UK. I started colestyramine last summer, naltrexone was added later but I could not tolerate it. I was given Rifampicin at 150mg twice a day. The
I have been "itching" since 2014. I have slowly worked my way through GP recommendations and since January I am in the care of a specialist here in the UK. I started colestyramine last summer, naltrexone was added later but I could not tolerate it. I was given Rifampicin at 150mg twice a day. The
butterflyEi
in
PBC Foundation
7 years ago
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