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Title: Back from MHNI Post by UnsolvedEquation on Sep 6th, 2003, 6:20pm Well...I made it back from my second trip to MHNI and Chelsea hospital. They gave me a 5 day treatment of DHE IV ( @ .5 mg ) and then I had a "Facet Nerve Block". (My neck still hurts) They said this block is temporary ( like the Occipital blocks i've had ). I have to call them on Monday to let them know how I am doing an set up my next appoinment. I'm still going to have the RF ( Radio Frequency ) procedure very soon. Some of you have asked about RF and it's side effects...well...I asked ALOT of questions while I was there...if you'd like more information...send me an e-mail and I'll fill you in on the details. One important detail > Dr. Saper ( The founder of MHNI ) says that RF will stop my clusters for 6 - 48 months .... COOL :) ;D ;D Thanks for the vibes and I"M SURE GLAD TO BE HOME !! PS. I was the only one there with CH !! |
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Title: Re: Back from MHNI Post by Prense on Sep 6th, 2003, 9:50pm on 09/06/03 at 18:20:03, UnsolvedEquation wrote:
!!! ;D |
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Title: Re: Back from MHNI Post by UnsolvedEquation on Sep 6th, 2003, 11:59pm I see what your sayin' ... but I guess nothin's ever really guarenteed ... except that your gonna die someday ! :o Besides...what else am I gonna do...sit here and have multiple MASSIVE headaches everyday for the rest of my life without doing what I can to stop it? No thanks ! If I don't continue to try and stop them...I probably would die...and I'd rather go out with a fight !! >:( 12 years epesodic and another 3 years chronic. ~Unsolved~ ;D |
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Title: Re: Back from MHNI Post by UnsolvedEquation on Sep 7th, 2003, 9:50am The block only lasted about 36 hours ... back to bein' an Imitrex junkie :'( |
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Title: Re: Back from MHNI Post by Prense on Sep 7th, 2003, 10:15am ... :( |
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Title: Re: Back from MHNI Post by taraann on Sep 7th, 2003, 1:55pm Oh that sucks UE im so sorry to hear that. :( |
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