Neuro & IVIG
I live in TX and I use IVIG 2 days every 30 days. That being said, I have no other medication options. I have a severe allergy to Interferon, I've had macular edema so Gilenya is out, Tecfidera caused my WBCs to drop to 1.9, Copaxone gave me migraine headaches, and Tysabri was great until I became JCV+. The only med I haven't tried is Augbagio (which quite frankly scares me).
My insurance is good, but still requires that I meet a deductible every year so that can be difficult, but my neuro believes IVIG is a great alternative and had actually added it as an addition to the Tecfidera until I had to come off that. Now all I do is IVIG. So perhaps he might meet your needs.
My email address is in my profile.
I live in TX and I use IVIG 2 days every 30 days. That being said, I have no other medication options. I have a severe allergy to Interferon, I've had macular edema so Gilenya is out, Tecfidera caused my WBCs to drop to 1.9, Copaxone gave me migraine headaches, and Tysabri was great until I became JCV+. The only med I haven't tried is Augbagio (which quite frankly scares me).
My insurance is good, but still requires that I meet a deductible every year so that can be difficult, but my neuro believes IVIG is a great alternative and had actually added it as an addition to the Tecfidera until I had to come off that. Now all I do is IVIG. So perhaps he might meet your needs.
My email address is in my profile.
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