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My Stupid Body

So in the past three days, I have had TWO migraines. Friday morning I awoke with twinges, took some Excedrin and the damned thing continued to persist. So, because I had somewhere Friday I *had* to go, I took one of the "melt in your mouth" migraine tablets my doctor gave me. And.... it worked! The migraine faded within the hour and, unlike the last time I took migraine medicine, I didn't even get nauseated! And I was able to focus and concentrate the rest of the day, go to my meeting and then out to dinner afterward.

Yesterday I had headache twinges but the Exedrin I took kicked it pretty well. I still felt kind of tired and blah but at least my head didn't hurt.

This morning, however, I awoke with the migraine already well on its way to critical mass. I started my treatment of it with a cup of coffee, thinking maybe it'd been brought on by caffeine deprivation. But no, that didn't do anything other than wake me up a bit. (Nice side effect, however.) I moved on to the Excedrin which did nothing and, about 75 minutes ago, I took a dose of the "orally disintigrating" Maxalt. And, thankfully, it has finally kicked in and the pain is gone!

Of course, I still feel kind of crappy - my arms are rather sore and feel very heavy, but that is tolerable. The pain part of these migraines? Intolerable.

So, to recap: Maxalt good. Pain bad. And I'm off to take a nap now before I pick back up on my studying. Let's hope I can go more than a day between these aggravating things this time!

Comments

Hope you are feeling better!!


"I could have me a million more friends, and all I'd have to lose is my point of view."

~John Prine

My Multiple Sclerosis Diagnosis

On June 23, 2006, I was diagnosed with Multiple Sclerosis. Among other topics, this blog is devoted to my ongoing experience with the disease.

Pharmaceuticals

Shortly after my MS diagnosis, I began taking Avonex. Although I managed to mitigate the "flu-like" side effects, for the most part, the drug unfortunately seemed to exacerbate my clinical depression.

So, on July 19, 2007 I switched to Copaxone.The Copaxone worked quite well for a couple months - except for some minor issues with injection-site reactions - and I felt much better.

Unfortunately, the Copaxone also exacerbated my depression. So I met with my psychiatrist to find a mix of anti-depressants that would counteract the debilitating depression I experienced. After spending most of December 2007 in a complete funk and - some days - being totally unable to leave the house, I finally stopped taking the Copaxone on my own. I immediately began to feel better and with some help from my primary care doc - who discovered I also had a mild case of hypothyroidism - I started to feel like myself again.

On May 16, 2008, I had my first infusion of Tysabri. With the exception of some anxiety issues, I've had no trouble with it so far. Still, it's early and the jury is still out... stay tuned for ongoing updates!

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