Guest guest Posted July 27, 2005 Report Share Posted July 27, 2005 > . If you have MS and > only take Naltrexone please let me know. I have questions about how it > works, what are the side effects, what doctor gave you the script for > it, primary or nuro? __________ Welcome to the group. Have you checked out www.low dose naltrexone.org website? That will tell you a lot of info. Goodshape.net has instructions to make homemade low dose naltrexone(LDN). I have one brain lesion and only used the LDN. I had symptoms for 10 years with last two rapidly progressing. Got my first MRI last summer to find the brain lesion. Started Dec. 17, 2004 with the crushed Revia way. I got most all symptoms relieved such as Pain, unbalance, pins sensations, cognitive dysfunction, memory loss, numb all over etc but still had extreme Fatigue. I changed to the liquid homemade LDN and got instant fatigue relief. Started the liquid in June and still doing that way at 4.5mgs. I tried the 4.5mgs of compounded and it didn't have the same affects on me. Some people absorb liquid meds better and I'm one of them. I would suggest you try this way first. After taking the LDN for 5 months, last MRI showed my lesion Inactive and all I have is a little numbness left. I got my first Revia from www.medsmex.com and then told my neuro my great results and he prescribe the Naltrexone 50mgs to me. I also take supplements. The generic has the same ingredients as the name brand Revia. I checke with the lab that makes the generic and got ingredients. So the LDN halted my progression. Goodluck! Rhonda Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 28, 2005 Report Share Posted July 28, 2005 A search of even recent messages will give you some answers to your questions. search isn't the best, though. My wife has been on only LDN for 13 months and is doing so much better than ever before on beta-seron or copaxone that words can't do it justice. I hestitate to use the word " miracle " , but it isn't completely inappropriate. dotsbaby7 wrote: > Hi! Does anyone on this site have MS and if so are you on any of the > current meds for MS Ex- Avonex etc. I am on avonex and it makes me > throw up everytime I inject , thats once a week. If you have MS and > only take Naltrexone please let me know. I have questions about how it > works, what are the side effects, what doctor gave you the script for > it, primary or nuro? Please write to let me know everything you know. > I would love to get off my current med. I really hate it. Thanks Patty > e-mail trinkabarnes@... or I'll try to check this site for your > answers. Thank You agian Patty > > > > > > Quote Link to comment Share on other sites More sharing options...
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