kika
CH.com Veteran
 
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I Love CH.com!
Posts: 122
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hi i have visited this site many times over the past 7 years ( as long as i've lived with CH's), but never posted on your message board before.
i am 36 years old, a mother of 3 and an RN. i live in ontario, canada and got married 2 weeks ago. i began having CH's 7 years ago, and used to get them every fall, for about 6-10 weeks. the cycle then changed a few years back, and now i get them in the late spring/ early summer, and depending on the drugs that i use to treat/ prevent them, they last anywhere from 4-8 weeks.
my pattern has typically been that i get a CH within 1 hour of waking up, which fluctuates since i work shift work ( 12 hour days and nights). i go from pain free to 10/10 pain, in/around my right eye within 10 minutes. Honest to God, when i discovered Zomig, i wanted to write a letter to astra Zeneca and thank them from the bottom of my heart. this drug changed my life. the problem was, i ended up needing to take it twice a day, because the CH's began happening 12 hours apart every day. I was also on an SSRI antidepressant and being on both, developed serotonin syndrome, which landed me in the ER.
I went to see a pain/ headache specialist, who put me on high dose prednisone, DHE shots and isoptin (verapamil), which worked well to abort the cycle, but the side effects of the prednisone were terrible, and i hated injecting myself in the thigh with the DHE, especially since i could never get proper needles for it and had to use subcutaneous needles. hurt like hell.
soooooooooooooooooooo, this winter, in preparation for my wedding in the spring, i started taking isoptin, 260 mg to try and prevent them from starting, BUT, got my first CH on June 8th. they have no pattern at all this time, they come at random times and the zomig does not work as well as it normally does. I have rolled the dice by taking the zomig out of desperation a few times, but am taking my SSRI only every other day to lessen the odds of getting serotonin syndrome again.
my MD started me on topamax on wednesday, and i have weaned myself up to 100 mg so far. feel pretty confused, dizzy, tired and clumsy, but the CH this am was no where near as bad as the others thus far, so here's hoping it's gonna work. if not, i'll be back here looking for advice about occipital nerve blocks.
anyhow, sorry this was so long. glad to have a plce to share and hope i can be of help and support to others here as well.
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