Since most of the people that know me in one way or another haven't made it on to the Dreamwidth boat yet, I thought I should give some background on myself for the inevitable new people I get to meet.

I'm disabled. This is not always readily apparent, either online or in person. Sometimes I'm in a wheelchair, sometimes I can walk for a few hours without significant impairment. I've had a progressively debilitating muscular/neurological problem for years, but only received a diagnosis a few weeks ago. It's called Postural Orthostatic Tachycardia Syndrome (or POTS). It's essentially a failure of the autonomic nervous system (that's the portion in charge of things you don't have to think about to do, such as breathing or blood circulation). Here's a relatively quick list of my symptoms: severe myofascial (muscular) pain, exercise intolerance, extreme fatigue, muscle spasms, spasticity, fasciculations, cold extremities, disorientation, shortness of breath, muscle weakness, severe tremor, visual disturbances (I see flashing lights around the edges of my vision that look like a cloud of fireflies or the sparks flying off of a sparkler), nausea, vomiting, brain fog, short-term memory loss, problems finding words, depression, insomnia and hypersomnia (a lovely combo, I might add), sleep apnea, fear, nervousness, orthostatic hypotension, ataxia/poor coordination, and difficulty concentrating. I think I remembered everything in there. I've been repeatedly misdiagnosed with things ranging from anxiety (it stopped once we started treating the POTS) to malingering. I've had supposedly reputable neurologists tell me to find God and "examine my lifestyle choices" because medicine could never help me, I had one tell me that I was eating tainted chickpeas (except that hasn't happened since the 18th century and that was in Spain)... it's been an interesting journey in to the vagaries of medical science. I also have high functioning Asperger's syndrome, though that's a subject for another entry on another day.

The amazing thing in all of this is that once we discovered the actual problem, we got rid of most of those symptoms. We're still fine-tuning medications, but I went from nearly bedridden to shopping for a gym membership literally overnight. It will still be a while before I can do things such as exercise given that the medications are still being adjusted, but I will be able to, and that's something I never thought I'd even get to consider again. An even happier realization is that I'll be able to work again. I'm a visual artist, and an artist with a severe tremor can't accomplish much. It makes it a bit hard to draw or paint, for one.

I'm happy to answer any questions that anyone has on this. Feel free to ask away!
brigid: close up of my face a week or so post partum (Default)

From: [personal profile] brigid


I get that kind of visual disturbance when I have migraines, right before I go blind. WHEE.

I'm glad your illness is being treated. After decades of being fat and oily I'm now being treated for PCOS and am losing weight like crazy and my skin and scalp are COMPLETELY different. I no longer have to wash my hair twice a day to not look like an oil slick. It makes such a huge difference.
brigid: close up of my face a week or so post partum (Default)

From: [personal profile] brigid


I don't always get pain with my migraines! Which is insane! but very very welcome, actually. LOL

I like your icons, btw.
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