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Old 06-30-2013, 12:11 AM
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Dr. Smith Dr. Smith is offline
Senior Member (**Dr Smith is named after a character from Lost in Space, not a medical doctor)
 
Join Date: Oct 2010
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10 yr Member
Dr. Smith Dr. Smith is offline
Senior Member (**Dr Smith is named after a character from Lost in Space, not a medical doctor)
Dr. Smith's Avatar
 
Join Date: Oct 2010
Location: Lost in Space
Posts: 3,515
10 yr Member
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Hi Lizzy,

I've seen you other posts & PM. It's a journey/ordeal for all of us with hard to diagnose/treat chronic migraines. What works for me has taken years to accumulate, and while things are much better than they once were, I'm not migraine free. I had one last week that, if my DW had been home with the car, would have sent me to the ER. But this isn't about me right now...

As I recently posted in another forum:
Quote:
Have you been to a headache specialist? Not a neurologist who treats headaches -- most claim to do that. I mean a doctor (may or may not be a neuro) whose practice is limited solely to headaches/migraines. That's what it took for me; after years of being bounced from neuro to neuro, I found a migraine specialist who was able to dx me the first visit with 3 questions. Treatment took a bit longer, but he was eventually able to reduce my headaches in frequency (>15/month to <10/month) and intensity.
Are you keeping a headache/pain/migraine diary/journal/log?

migraine journal

If not, you can read up on them starting with the above link, and then continue with some of the suggested related searches at the bottom of the first page of links. This is one of the best tools to help your doctor help you, which is, IMO, the key.

Botox was suggested to me at one point (before our insurance would cover it), but after researching it, I opted out even if it were covered. Between the side effects (some of which you've experienced) that may not go away for weeks or months (some for the duration of the injections) and the limited lifespan of a few cycles (the body builds up a tolerance to the botox) it just didn't seem worth it to me for a "band-aid fix". (YMMV)

I tried several prophylactics and abortives. None of the prophylactic meds worked (though our ins. co. played doctor/God and mandated one or they wouldn't cover the abortive. That prophylactic may have caused/contributed to my peripheral neuropathy), but after trying several abortives, Maxalt/rizatriptan works the best for me (again, YMMV). There are natural/herbal remedies that work for some. They did not for me, but IMO they are worth trying (but check for medication interactions beforehand).

Some anti-seizure meds (e.g. topamirate) are being used off-label for migraine prophylaxis. If you haven't been down that road, it might be worth investigating and discussing with your doctor (killing 2 birds...?)

One of my stress-related factors involves certain muscles & nerves at the base of the skull as per this diagram:

I use (with the help of my DW, who actually does the massage/therapy) myofascial triggerpoint therapy on this point as/before the migraine comes on. I have another region along my front hairline that helps to massage once the migraine manifests. You may have similar or different trigger points, acupressure points, etc.

acupressure for migraine

Sometimes, there are groups/systems of these points, which must be treated (attacked) in sequence and in the right order, or the headache can not be averted/relieved. Again, a journey/learning process to find your points and how to treat them. A certified myofascial trigger point therapist helped me, and taught us how to do it and more on our own.

The rest has been finding/figuring out my other triggers -- foods, smells, allergies, computer migraine headaches and other triggers.

That's about all I've got for now. It's late, and past my pumpkin hour...

Doc
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Dr. Zachary Smith
Oh, the pain... THE PAIN...

Dr. Smith is NOT a medical doctor. He was a character from LOST IN SPACE.
All opinions expressed are my own. For medical advice/opinion, consult your doctor.
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