Multiple Sclerosis (MS) Support Group
This community is a place where members can discuss current events and weigh in on what's going on in the world.
This community is a place where members can discuss current events and weigh in on what's going on in the world.
There are several threads about this drug if you want to look them up, they might help you. But we don't have anyone who has taken it in the new form as it has just come out. There are people who have taken it in previous forms, and they seem to have mixed reviews. If you do not get many responses, we sometimes have talked a subject out and take a rest! LOL, please go back an look...the most recent ones are called Amprya, or have it in the title.
very nice of you to be looking for this for your friend. Allso, if cost is s problem, they are offering an assixtance program. Good Luck to your friend. If the yare not on this board, and could be, you might suggest it. We are full of information, again, LOL.
http://www.dailystrength.org/c/Multiple_Sclerosis_MS/forum/9087146-ampyra-fampridine
http://www.dailystrength.org/c/Multiple_Sclerosis_MS/forum/8937569-fda-approves-ampyra
http://www.dailystrength.org/c/Multiple_Sclerosis_MS/forum/9064737-projected-cost-ampyrafampridine/page-2
http://www.dailystrength.org/c/Multiple_Sclerosis_MS/forum/8928366-ampyra
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You might find this interesting too.
http://www.dailystrength.org/c/Multiple_Sclerosis_MS/forum/8824033-reducing-nerve-fatigue
Best wishes,
EP
Isn't it nice that they have at least one thing that we can put in the plus column? My doctor is leaning towards having me try this. She had experience with it as an intern, as she says, "some years ago," but the concern about the side effects was a real problem. She said that as far as a good reaction from patients, yes, absolutely, but the risk was high. She is very hopeful about this new form.
I am glad to hear that you are doing so well with it.