Hello All, Does anybody have any experiences taking Clemastine as part of your MS treatment? Please share with us.
Hi Gabrieiam I think you’d be better asking on the Everyday Living forum. Many of the people with ppms only take meds for their symptoms and you’ll probably get more feedback there where they get DMDs. We’re usually great with questions about symptoms and coping strategies, pain meds, catheters, etc. I hope you get your answers. Cath
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I will try. Many Thanks
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