Guest guest Posted February 3, 2011 Report Share Posted February 3, 2011 I find it quite interesting that the MS clinic I go to nor Tysabri folk have said nothing about a blood test. Seems like that could save a person a whole lot of worry-my family! I have had 2 infusions, and really no change in symptoms yet. Tey said at least 3 months so hopefully soon. The only neg. for me so far is I pretty much have a constant headache-maybe not constant but def. a daily headache. I am on thee Tysabri because due to side effects I cannot take Rebif, nor Copaxone-plus was not going into remission like they expected. TY for info. Sherri Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 3, 2011 Report Share Posted February 3, 2011 I never quite knew the reason, perhaps checking liver enzymes--but I always had bloodwork done prior to each infusion. Should have asked why. I'm just a dumb sheep sometimes, and blindly follow. I need to be more proactive and involved in my own medical care. Live and learn.I hope the TY works as good for you as it did for me. Back on Copaxone, and so far, holding my own.Best wishes,KateTo: MSersLife Sent: Thu, February 3, 2011 10:38:16 AMSubject: Tysabri and Ty for Info. I find it quite interesting that the MS clinic I go to nor Tysabri folk have said nothing about a blood test. Seems like that could save a person a whole lot of worry-my family! I have had 2 infusions, and really no change in symptoms yet. Tey said at least 3 months so hopefully soon. The only neg. for me so far is I pretty much have a constant headache-maybe not constant but def. a daily headache. I am on thee Tysabri because due to side effects I cannot take Rebif, nor Copaxone-plus was not going into remission like they expected. TY for info. Sherri Quote Link to comment Share on other sites More sharing options...
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