Well, I just found out that Copaxone is a no-go for me. All because I'm on Medicare, and there are no funds left for Medicare patients for assistance. That really sucks the big one. I guess if I had NO insurance at all, I would be better off. Oh well, the neuro's office is researching all my options, looks like it will be either Rebif or Tysabri. I'm leery of Rebif because it's still an interferon, and I'm leery of Tysabri because.....well, it's Tysabri. Who knows what I will end up on, I just know I can't take the BetaMonster anymore. Stay tuned for further updates............
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I too am on Medicare, sorry to hear the news on the copazone, They are doing some big cutting on everything including physical therapy too. I hear the Tysabri is really doing well for many people...I don\'t think I would want to go the interferon way.....Please keep me informed. Good Luck and Have a Wonderful Weekend. Smile, Love Ya
I am so bummed. You mean they won\'t pay for any of it? Mother-F\'ers. That is just wrong. Wrong. A co-workers husb is on Rebif and he feels like he has the flu all the time, so I would really think that one over. I don\'t know anything about Tysbri, but I will read up on it. I am praying for a good result for you. I hope things change when we get a new president in office. Love ya,
J