My Neuro team wants me to start this . So I singed up for the 3 month trial. I am cleared by the maker and will be receiving it soon. I will keep everyone updated with progress.
I got my first injection yesterday! Keeping my fingers crossed that if anything it lessens the pain.
My ins covers it and I'm on my 4th or 5th shot and my dr bumped up my dose to 140mg(2 shots each dose) and it worked at first but then I went off my depo lupron and went on a pill called orlissa and I've been getting migraines daily:(
So how is it so far?
Not covered here in Canada by drug benefits. So it is out of the question for me at $500.00 per dose. It is a huge finacial commitment with no drug benefits.
Glad for so many that they are finding positive results.
Iβm Newly On Medicare (this Month) And Have Found It Impossible To Get Drug Coverage For My Aimovig Injections. Any Advice From Anyone?
Has Anyone Had Worsening Migraines For The First Week After Aimovig Inj. Before Feeling Better?
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