new to this is my ms but i wish it weren't
Posted: Wed Apr 22, 2015 6:40 am
hi,
I am curious to find people on Gilenya and find out how likely side effects to it are.
personally I am the side effects queen - to almost all pharmaceuticals. my entire ms history is one with a wide trail of discarded meds I could not tolerate.
fortunately I was on Novantrone and Copaxone which detuned my initial lesions then kept me lesion free for about 10 years. then I had to switch and luckily went to Tecfidera without mishap (!) which worked perfectly for another year.
now that I am turning 65 and forced to go on Medicare, they are taking me off Tecfidera and forcing me to experiment with Gilenya.
If I can take it at all - which I very much do not want to do after reading the S.E. list it carries (I have never balked at one before , but that one is over and beyond the pale!) i am curious about the likelihood of side effects it is apt to have.
Back Ground: Dx '04 after being put in a wheelchair almost overnight with a back injury. sent to hospital for op., expected to walk out. neuro surgeon discovered lesion at exact location of surgery site (C-5,6), left H 7 days later w/ definitive MS diagnosis instead - "thoracic demyelination syndrome" (which NOBODY has ever heard of - means almost all lesions at T 8,9, +10)
I am glad I found this forum , and to see how well informed people on it are!! THANK YOU FOR HAVING ME.
I am curious to find people on Gilenya and find out how likely side effects to it are.
personally I am the side effects queen - to almost all pharmaceuticals. my entire ms history is one with a wide trail of discarded meds I could not tolerate.
fortunately I was on Novantrone and Copaxone which detuned my initial lesions then kept me lesion free for about 10 years. then I had to switch and luckily went to Tecfidera without mishap (!) which worked perfectly for another year.
now that I am turning 65 and forced to go on Medicare, they are taking me off Tecfidera and forcing me to experiment with Gilenya.
If I can take it at all - which I very much do not want to do after reading the S.E. list it carries (I have never balked at one before , but that one is over and beyond the pale!) i am curious about the likelihood of side effects it is apt to have.
Back Ground: Dx '04 after being put in a wheelchair almost overnight with a back injury. sent to hospital for op., expected to walk out. neuro surgeon discovered lesion at exact location of surgery site (C-5,6), left H 7 days later w/ definitive MS diagnosis instead - "thoracic demyelination syndrome" (which NOBODY has ever heard of - means almost all lesions at T 8,9, +10)
I am glad I found this forum , and to see how well informed people on it are!! THANK YOU FOR HAVING ME.