Yesterday I had the monthly infusion of Solu-Medrol. Already you can feel a difference as far as strength goes and coordination. Unfortunately, this feeling does not last the full month. In the past it has lasted for a few weeks then I go downhill. It is amazing what the heavy-duty, steroids can do. Is my understanding that they reduce swelling of the nerves in that way your body works better. It would certainly be nice if there was a drug available to all. On this site I have addressed some of the drugs that are available, as we all know they work a little, they are not a cure. Personally, I have taken them at this point. The only thing I take is the Solu-Medrol infusion. I would love to try Tysabri. It seems strange to me that the drugs that are approved for Relapse Remitting MS are available to you, no matter what type you have been diagnosed with yet. The one drug that has been approved by the FDA for relapsing forms is not available to you. Even though this category is broader than the others. Confusing?
Here is today's picture from another country:
Thursday, August 6, 2009
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About Me
- Steve
- North Grafton, Massachusetts, United States
- Well-educated, disabled at this point with Multiple Sclerosis. I am very glad that I was able to do the things that I have been able to do over the years. had to change the picture, this one's more realistic.
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