Tophurious
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Life's a bitch then you die.
Posts: 22
Denver, CO
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Well, as I said, they have gotten worse over the years. I wasn't officially diagnosed with them until recently, however I do remember weeks of headaches starting when I was 15 but doctors attributed it to sinuses, allergies, caffeine addiction, etc. So of course, nothing really helped.
In May of 08, I had about 3 weeks of excruciating headaches, to which the only thing that helped even in the slightest was marijuana through a vaporizor. This didn't make the pain go away, but it kind of pushed the pain to the back of my mind so I was at least able to function. I quit smoking, I quit drinking caffeine, I started jogging, trying to figure out why I was getting these headaches. Finally, I went to the doctor and she said "Well it sounds like cluster headaches, but I can't say for certain unless you come in with a headache" so she gave me a prescription for zomig and sent me on my way.
The zomig worked as long as I took the pill RIGHT as it started, but if I missed, it was pretty much useless (not to mention way to expensive). A week or so later they just stopped.
The next attack started on the 20th of December, my new girlfriend and I were up in the mountains for the weekend and when we went to breakfast the morning we were coming back I couldn't function. I was able to drive down the mountain and back to my house. My mother pretty much has a standing prescription for vicodin, so I started taking those at the first sign of a headache (again, like the weed, it doesn't remove the pain just allows me to function). After 2 and a half weeks of these headaches (1-2 a day) I scheduled an appointment with my doctor around the time of day my headaches happen most. I got a call back from her saying she would rather I just go to a neurologist. I convinced her to prescribe me my own vicodin as my mother needs hers and can't be running out.
I saw a neurologist last week, who officially said "Yeah, clusters" gave me some maxalt, frova and verapamil. As it has been over a month since the start of the attack (meaning I should *crosses-fingers* be almost done) I decided save the frova until my next attack as my neurologist said it would only help shorten the clusters if they helped at all. I took the maxalt the next day when it was so bad I couldn't move and man, those things are awesome. Within about 10 minutes, I felt my pain level drop from a 9.5 to a 4. I filled those right away, unfortunately my insurance only covers 4 tablets at $22 a piece). The verapamil is a calcium channel blocker and I can't remember exactly what my neurologist said it would help, but the internet says a side-effect is "headaches", so i'm not sure what to expect from it.
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