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Tue, Jan 29 3:03pm · Chronic severe nocturnal hypnic headaches in Sleep Health

Hi I will be taking my 4 th dose in about 2 weeks and so far it’s going well, migraines have been better, less frequent and less severe. I do have slight headaches … but , tolerable… I do take topamax for prevention and fioracet and promethazine they also have helped me with them as well. I’m pretty excited thus far , life with aimovig is better than before this medicine only downfall is my insurance doesn’t cover it and after my free year not sure what will happen:( I’m staying focused and positive! And enjoying my life day to day for now and prayers for low and hopefully less migraine life …. #gothope

Oct 23, 2018 · Cavernoma in Stroke & Cerebrovascular Diseases

nothing was really mentioned at this time, In the mean time i have been having more migraines with nausea and vomiting , and been taking zofraine. with little relief. my days of having longer migraines seem to be getting more frequent. I am in the waiting trial for the new migraine medicine Aimovig.?? has anyone heard of this or tried it?? I guess people say it is good . so im hopeful for some relief if my insurance company will help with the exspense of it. in the mean time, it seems like i go day by day. I have been continuing to see my neurologist on a monthly basis and getting injections in my head for migraines. they seem to help great for like the first week than slowly sibe side after that. work is hard when i have a migraine, life in general just takes a toll on a person. any feed back ?

Sep 21, 2018 · Cavernoma in Stroke & Cerebrovascular Diseases

Hi,
I had an MRI last october with lesions on my brain, and was diagnosed with "MS", and have had many MRI since then , and recently my headaches have been getting more persistent and also, now i seem to be getting "dizzy " spells, and more nausea. which is a new onset for me. at the time i had the MRI last oct , they had seen a "spot" on my spinal column, which was concerning, but was assuming it was MS , related. and now i had another MRI, with the new onset of symptoms. at this time few weeks ago, they have now diagnosed the spot on my C2, of my spinal column, a cavernoma, not anything MS related, at this time they took me off all my MS medications and i am not to take anything, to wait till the next MRI to see if there is anything changes. to make sure the lesions in my brain are "MS', or tumors, of the cavernoma relation. i am just concerned. if i should be worried?? having these blood vessel type tumors?? he wants to do a biopsy of the one on my C2 spinal column but states it is to risky at this point till we for sure do the next MRI to see what or if there are any changes at that time. has any one else heard of this or anything else related to this. in october i had a second opinion , at the MAYO. and they were pretty consistent with the hospital i am currently going to the doctor with. i just am concerned with my light dizzy spells, etc.
thanks for listening… any information will be greatly helpful 🙂 thx