Hi I was diagnosed with M.S. at age 12 and now I'm 20. So for almost 8 yrs I have been suffering from M.S. and the pain from the Rebif shots, it is the only medication I have taken but now doctor is say's that it's not working so I'll be taking Tysabri very soon. Wish Me Luck!!
I have been taking Tysabri since last May '10 and its so much better than shots. Rebif was what I took until a doctor at the Cleveland Clinic believed Tysabri would be the best DMD for me. I was diagnosed with MS 5 years ago and will try anything because it is so early on. My boyfriend has MS as well & Tysabri was not around for him when he was diagnosed. Stick with it and see if it helps you. Good luck and God Speed.
You told healthy people have a slim chance of PML? That statement holds no grounds! Having MS takes you off the list of being a healthy person, Tysabri nearly killed meI I was one of the lucky!!! My severe reaction was caught during an infusion next to the hospital! Why are you just settling for the MOST life THREATING drug out there for MS?
Am taking LDN and doing fine and filling why better, and most of all not worried about PML! Good Luck
I'm 24 and was diagnosed with MS at 18. I see a brilliant neurologist here in tx. He recommends copaxone for me. Although it's a daily shot, it's painless compared to avonex and rebif. The only problem with everything for me now is that I no longer have insurance and can't afford my injections and I'm currently beginning to have yet another relapse. These are pretty pricey meds!
Anywho, when I first brought up tysabri to my neurologist, he told me about PML, Progressive multifocal leukoencep
My son had MS and I am waiting to find out if I do. I am so sorry that you have this disease. I am hoping you do well with whatever you take on and that you have family and friends to help you endure.
Sorry to hear that your meds are not working for you. All I have heard about Tysabri is great. Check out laurenvparrott channel. She has alot of great info on tysabri that she talks about.
Hi I was diagnosed with M.S. at age 12 and now I'm 20. So for almost 8 yrs I have been suffering from M.S. and the pain from the Rebif shots, it is the only medication I have taken but now doctor is say's that it's not working so I'll be taking Tysabri very soon. Wish Me Luck!!
5lovejs 4 weeks ago
Comment removed
5lovejs 4 weeks ago
I have been taking Tysabri since last May '10 and its so much better than shots. Rebif was what I took until a doctor at the Cleveland Clinic believed Tysabri would be the best DMD for me. I was diagnosed with MS 5 years ago and will try anything because it is so early on. My boyfriend has MS as well & Tysabri was not around for him when he was diagnosed. Stick with it and see if it helps you. Good luck and God Speed.
AndreaD
Andrea0414D 1 year ago
Hey everyone, I am taking the Tysabri because my Doctor said it's the best course of action in my case.
jrmcg1 1 year ago
You told healthy people have a slim chance of PML? That statement holds no grounds! Having MS takes you off the list of being a healthy person, Tysabri nearly killed meI I was one of the lucky!!! My severe reaction was caught during an infusion next to the hospital! Why are you just settling for the MOST life THREATING drug out there for MS?
Am taking LDN and doing fine and filling why better, and most of all not worried about PML! Good Luck
ThePennygirl 1 year ago
Please consider being screened for CCSVI. Before you do the Tysabri! You will be amazed.
jbaileyl 1 year ago
I'm 24 and was diagnosed with MS at 18. I see a brilliant neurologist here in tx. He recommends copaxone for me. Although it's a daily shot, it's painless compared to avonex and rebif. The only problem with everything for me now is that I no longer have insurance and can't afford my injections and I'm currently beginning to have yet another relapse. These are pretty pricey meds!
Anywho, when I first brought up tysabri to my neurologist, he told me about PML, Progressive multifocal leukoencep
spazticfugliness 1 year ago
My son had MS and I am waiting to find out if I do. I am so sorry that you have this disease. I am hoping you do well with whatever you take on and that you have family and friends to help you endure.
tubegirl41 1 year ago
Sorry to hear that your meds are not working for you. All I have heard about Tysabri is great. Check out laurenvparrott channel. She has alot of great info on tysabri that she talks about.
Pelagaia 1 year ago
Good luck with the tysabri John xx
whyworryabout2moro 1 year ago