sj904fighter
CH.com Newbie
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I Love CH.com!
Posts: 23
Santa Cruz Mountains in CA
Gender:
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Hi all, I'm encouraged to see there's a place here where people truly understand the agony of Cluster H/A.
Here's the abridged version of my story:
I first started having Headaches about 25 years ago. I was 21, and had a headache like nothing I had ever experienced before. It went away fairly quickly, so I thought nothing of it. The next day I had another one, and decided to see my Dr. at the time. After a BRIEF assessment (brief is an understatement here) he said that it was probably from some scar tissue between my clavicle and scapula. He told me to do some stretches, and take some Advil. Needles to say, that didn't work. After a few weeks the Head Aches went away, and I thought all was good. About 2 years later, they started again. Different Dr this time. He was a MUCH better Dr, and did a more thorough assessment, but still thought it was muscle based. He prescribed Flexeril. Flexeril did nothing for the pain, but it DID knock me out at night at least. Many years of this cycle (trying everything I could think of, none of which really worked), until just last week, I was finally diagnosed with CH. I immediately did some research, and the description was DEAD ON with what I have been experiencing. My current Dr prescribed me Imitrex auto injectors. That night I had to use one, and was overjoyed to FINALLY have something that worked. 15 minutes after the injection, the pain was gone!!! The next night, same thing. I called the pharmacy to get a refill, and found that my insurance will only cover 2 doses per month!!!!! My delight quickly turned to despair knowing that the beast would return tonight, and every night for the next month or so, and I was just going to have to tough it out again. My DR is doing everything she can to get approval for more doses (she's very good), but that will take some time.
My wife (who is an RN) suggested trying my CPAP machine, which has been unused for quite some time now. I jumped on the computer to research if anyone had had any success with CPAP, and that's when I found this wonderful site here. I used my CPAP last night, and NO HEADACHE!!!! We'll see if this continues to work, but for now.......big thumbs up.
Thank you all for being here. The few posts I've read seem to be very supportive, and helpful. Those of us that suffer from this need that.
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