The diary of a working woman living in Metro Phoenix, and pursuing a healthy life while dealing with Multiple Sclerosis, autoimmune thyroid diseases, and food allergies
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DRAFT TODAY, POST TOMORROW: Some posts may be in draft status until I (aka procrastinator extraordinaire) get around to posting them.
Friday, March 27, 2009
Doctor visit and medical update
I saw Dr Gitt, my neurologist today. He suggested I go into the trial for alemtuzumab. It is an IV drug that has been used for a type of leukemia and is being tested for MS. The results have been promising. Mary sent me this: http://www.medicalnewstoday.com/articles/126550.php It is administered by IV for five days (a few hours each day). Then it is administered for three days a year later. Two thirds of the trial gets alemtuzumab and one third gets Rebif, which is similar to the Betaseron I take now except it is 3x/week instead of every other day. (MS trials do not use placebo groups; they use one of the current treatments for the control group.) The side effects are ITP-idiopathich thrombocytopenic purpura, which is fatal if not treated, but easily treated, and thryroid problems, which are not desirable but also treatable. It's a big decision but the pros as I see it are: careful monitoring (more than standard care), treatment paid for, 2:1 possibility of not giving myself injections for the next two years, and improved MS. The cons are possible thyroid problems, continuing injections if I end up in the control group, and developing ITP.
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