Hi, I can barely type, I can barely use the phone, I can’t drive anymore, can’t take walks. Deteriorating over the past 2 weeks. I am just shuffling around a friend’s house waiting to see the vestib specialist. I have been on the MAV diet for 10 days, on magnesium for a week, tried Topamax for a week but couldn’t handle the side effects. Just waiting for a miracle! (Or the doctor in 3 days, whichever comes first.)
Have been on Betahistine for 2 years for Meziere’s. Is it possible that it’s making it worse? Anyone take betahistine for MAV?
Also, is there a MAV crisis drug? Prednisone work? I have to pick up my daughter for Thanksgiving and move into a new home, etc. etc. My husband lives overseas. I need a solution fast!