What is Multiple Sclerosis MS
Multiple sclerosis (MS) is a chronic disease which affects the brain and spinal cord. MS can cause a variety of symptoms, including changes in sensation, visual problems, muscle we...
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Multiple sclerosis (MS) is a chronic disease which affects the brain and spinal cord. MS can cause a variety of symptoms, including changes in sensation, visual problems, muscle we...

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I Need HELP!!
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I am really in a dilema with my DMD and I want to know if anybody has stopped taking Copaxone and after a couple of months, started back up with it. If so, did you have initial issues that went away or when you restarted, you didn't have major site issues, etc...........
I also need to know if I can take Copaxone with LDN.............. I have had a TON of depression issues with Copaxone and am trying to figure out what to do and just wanted to know experiences for the very knowledgable group. Please let me know!! Thanks and Take care.... Posted on 07/05/09, 06:07 pm |
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wish I could help you on this one, have taken Betaserone and Avonex, my Doc tried to get me started on Copaxone, wouldnt shell out the $$, now is trying to get me to start Rebif, once again dragging my feet, I think I am really starting to piss my nuero off, guess I am not a gambler, for that kind of $$ I want some guarantees and since I cant get one, I will just hang with my friend LDN, week 6 and still living, some prozac and some LDN... HA! not feeling to bad for a dude with MS!!!!!
MS Sucks Attitude is Everything
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Thanks so much everyone!! I want to get moving on a DMD but have been going back and forth with a decision as to what is my best option right now. Your responses are really appreciated.
Thnaks again and be well!!
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Have never done rebiff or copaxone over all my 20plus yrs with RRMS. I've stayed in remision for 9yrs now with a wide array of supplements,
B12 shots weekly & LDN. best of luck to you
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I started taking LDN a month ago. I was also taking Copaxone until the monthly shots ended and I needed a refill. Because I started walking better on LDN, I stopped taking Copaxone because I have been on it for 4 years and my MS was progressing slowing anyway. So, I told my neuro that I stopped and he said that it was fine. I am just tired of taking a shot every single night without knowing if it is helping me or not.
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