Hi Everyone!
I'm new to the forum and to the MS. I am 33 years old and diagnosed with RRMS on February 12th, 2015. My doc swiftly got me on Rebif injections. Then in June, I had a doozy of a relapse (i.e. bouncy, diagonal double-vision that made me toss my cookies whenever I opened my eyes).
My doc then swiftly got me on Tecfidera. I can't be sure if it *actually* makes me feel different, but I swear it's like someone caught the right frequency for the TV with old-school rabbit ears. I feel less "buzzy" and "static-E".
But, every time I actually sit down and *think* about the risks of PML and notion that there are no long-term studies of the safety of Tecfidera, I get super panicked and light-headed.
Any takers on talking this scared little rabbit down from this ledge?
Thanks bunches!
-Heather
I'm new to the forum and to the MS. I am 33 years old and diagnosed with RRMS on February 12th, 2015. My doc swiftly got me on Rebif injections. Then in June, I had a doozy of a relapse (i.e. bouncy, diagonal double-vision that made me toss my cookies whenever I opened my eyes).
My doc then swiftly got me on Tecfidera. I can't be sure if it *actually* makes me feel different, but I swear it's like someone caught the right frequency for the TV with old-school rabbit ears. I feel less "buzzy" and "static-E".
But, every time I actually sit down and *think* about the risks of PML and notion that there are no long-term studies of the safety of Tecfidera, I get super panicked and light-headed.
Any takers on talking this scared little rabbit down from this ledge?
Thanks bunches!
-Heather
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