hi golden, i too have vertigo and problems with my ears, namely progressive hearing loss. i was just diagnosed with meniere's disease in addition to migraine. i had been to 5 ent's before i got the...
hi snowy, so sorry to hear you are having such a rough time. I have hemiplegic migraines to and because i get them often i have been put on topamax as a preventative. preventatives take a couple of...
I haven't ever heard of that but maybe he means vestibular migraines or migraine associated vertigo? There is a lot written on that! I get very motion sick with my migraines and I have had vertigo on...
i have been to neurologists that have thought i it was all a psych problem!! please find a headache center that has neurologists who are ALSO headache specialists. it would be worth the money to get...
you are totally right. . . .it is the topamax. i'm on it and cannot drink anything with bubbles. everything tastes wrong, kind of like metal. it totally sucks. sorry but the topamax is totally...
hi!! i am so happy to tell you i am in san diego too and have a great referral to the neurology center. they are worth the drive! they have neurologists there who are also migraine specialists and...
i am on topamax and doing well but i have heard that a LOT of hm people are on verapamil. calcium channel blockers seem to be the way to go often but i have not tried them as yet. i think you are...
dizzykez, you really need to find a neurologist who is also a headache specialist if at all possible. i am on preventative meds that are helping so so much. it is very hard to hear that you are going...
i shake when i try and go off the meds and before i started them, on and off for a few months. it lasts anywhere from 20 min to two hours but the last time, when trying to go off the med, was six...
thanks for the info! a bit of clarification: i have good neuorologist who is also a headache specialist who i just started seeing who put me on 75mg of topamax this month. the middle of the night...
Hi everyone! I am so happy to have found this site and to not be alone, I really have no words. I am just being diagnosed and right now we are just with "migraine with aura." Here is the my story. ....