Rebif message boards
Common Questions and Answers about Rebif message boards
rebif
When I went to get my rebif refilled last week was tokd they were out and its on border and they don't kniw when it will come in and could be a couple months. I called every pharmacy in town and got.same.story. Then called rebif and they know.if.no shortage. Is anyone else.having this problem? In meantime I am out so no shots.
Just trying to get my head around starting drugs have known had MS since 06 listed as proable until next relapse although they were sure I had it two weeks ago half head went numb now have to decide which I want to take I am leaning towards rebif any would be great .
I'm new to this app and I just realized there were message boards.. I'm wondering if the boards are designed to go By your weeks or age? Sorry If I sound like an idiot but I was just checking..
t see Lyme as a truly serious illness may try to cause trouble for MDs who *do* take Lyme very seriously, and the result could be problems for the Lyme docs with the state medical boards. (The medical boards tend to hold to the old belief that Lyme is no big deal.)
Over time, the medical profession will work itself out, but for now, please do NOT post names of any MDs here, in order to protect them.
What is usually the cost of these meds? ( I am considering trying Rebif or Avonex) I have heard they run about $1500/month. I have to meet a $3000 deductible which means I may have to pay for my first dose. I don't have an extra $1500 floating around. I am really starting to freak out! But then again part of me figures I have probably had MS for 15-20 years an I am fine so far. I guess waiting another 1-2 months to start taking DMDs can't hurt. Can it?
Oh, and here is a message board for ALS. Maybe it will help you to hear other stories and see if they match yours.
http://www.************.com/boards/forumdisplay.php?
what MS shots copaxone, rebif, betaseron & avonex has the smallest recetage of blood fractions
Are you familiar with the 'private message' function on this website? I can send you a recommendation there, since we keep our doc's names out of the public area of this site, to protect our Lyme docs -- in some jurisdictions, the Lyme docs need to keep very very quiet to avoid the state and local medical boards from trying to shut the docs down.
can I? post a new message to the other Heart Rhythm medical questions board. Do I need to create a whole new profile? Use another email and password? Seems that way but hoping I am wrong and someone can give me a clue here:-)
Thanks!
I have MS and have been taking Rebif foe 7 years. It has worked very well. I just learned that my current drug insurance plan from Humana will not cover Rebif in 2015. What plans cover at least some of the Rebif cost? My copay with Humana was about $300 per month. Would like not to exceed this amount.
Yes, I am on rebif for 11 months and must take advil liquid gels
To stave off headache fever that wakes me up!
So the ins company wont pay for Copaxone or Gilynia until my daughter first tries Rebif (i guess because its cheaper for them.) I have a concern with her being on an interferon due to the possible mental health side effects. She is already on Lexapro for anxiety and mild depression. I dont want anything adding to the issue. We have dr app tomorrow to discuss Rebif but I dont want her on it. Anyone have bad side effects with Rebif??? Any advise for me?? Thank you.
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