Anyone Using Aubagio?
I want to stop shooting myself and switch to an oral. I have read up on them and Aubagio seems to be the most helpful.
Yes...for about 9 months. At first there was some digestive issues - upset stomach. Now everything ok in that department. I am also having some hair "thinning" (as the support team for Aubagio calls it.) I can't think of the name right now....but Google "Aubagio" and there's a helpful Aubagio support system. Also, I took Copaxone for 10 years, and am so glad to be rid of the shots. Despite the minor side effects, I am very happy with Aubagio. No relapses, and MS symptoms improved.
i've been on it for 6 months. hair thinning in first 2 months. no other symptoms and that has stopped. MRI next week to see if less lesions...i'll let you know.
My MRI came back with "no significant change" so I'll take that as a sign of hope, and a sign that Aubagio is helping.
Use it, love it.
I Have Taken Copaxone, Aubagio, Avonex And Tecfidera. All Gave Me Bad Side Effects. Anyone Using Rituximab?
Anyone Using Aubagio? Have Stopped Ocrevus And Looking Other Option With Spms?
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