I’m considering stopping my injections of Rebif. I know I probably “shouldn’t” but fuck, if i have to do them myself, I’d just rather find an alternative. I’m thinking that a monthly treatment, Tysabri or Low Dose Novatrone.
So, I’m trying to read up on both of those as a primary treatment. I know they are sometimes used as a secondary line of treatment optimization, but I don’t know about primary treatment and either medication. Hell, I may not even be an acceptable candidate for either medication.
I just know I can’t do the shots myself. Thus, one would think that makes me a potential candidate, at the least.
Have I mentioned that I hate having MS?
I hate the shots even more—so much so that I’m considering doing chemotherapy as an alternative.
Fucking wordpress. I can’t get my post formatted the way I want.
Oh, my 6 year diagnosis anniversry is Friday.
It’s also the first time I’ve been recalled for a second blood-draw because my liver function is “off”.
I was anxiously expecting that the first couple of years, and it never happened. Now, when I’ve stopped thinking about it altogether, my results are a minor cause for concern.
I guess I can always hope that my LFT is so off that I’m forced to stop the interfuron injections.
My LFT was normal. I still haven’t resumed giving myself the injections. Sporadically, a friend does them. At this point, it’s been two weeks since my last one. I think about it occasionally. I’m much more concerned with the other chronic illness, and I’m going to start weaning off those meds today. See Hair Loss post.