No fireworks here, just a neuroism on one of my not-meant-to-be neuro-ite blogs.
If you're curious enough to click on the blog title (it links to the blog post as noted), you'll also see where my interest has remained. Actually, it's a blog I started during my the last class I completed of my MFA before Transverse Myelitis Lightening shot that degree out of the (current) ball park.
It might be your last chance to see my previous blog wizardry (choke on water, need speech therapy kind of wink wink), because I'm thinking of shutting down that blog for good.
In case you forgot what this post was about by now (that would be me), here's the link:
http://melanie-miller.blogspot.com/2011/07/quote-of-day-jdmpapgaf.html
Living Obliquely
Approximately 1400 people are diagnosed with Transverse Myelitis (TM) annually.
Similar to Multiple Sclerosis, it attacks your myelin, leading to painful and debilitating side effects.
About 33,000 Americans are currently disabled as a result of this rare neurological disorder.
Not one person with TM will ever know their prognosis.
I happen to be one of them.
I am a neurological soup. Since my TM diagnosis, I have developed encephalitis, MS, RSD/CRPS, Osteoporosis (I am 34, no 35, eek), and Chronic Anemia. Yeah...life sucks, but I still rock.
Similar to Multiple Sclerosis, it attacks your myelin, leading to painful and debilitating side effects.
About 33,000 Americans are currently disabled as a result of this rare neurological disorder.
Not one person with TM will ever know their prognosis.
I happen to be one of them.
I am a neurological soup. Since my TM diagnosis, I have developed encephalitis, MS, RSD/CRPS, Osteoporosis (I am 34, no 35, eek), and Chronic Anemia. Yeah...life sucks, but I still rock.
7.04.2011
2 comments:
Thanks for sharing your comments on my blog. Please stop back soon or subscribe by clicking http://feeds.feedburner.com/NeuroDetour.
If you're a Philly-region person with TM, please consider joining the Transverse Myelitis Philadelphia network (http://www.facebook.com/inbox/?ref=mb#/group.php?gid=44446668472), a new social networking group that I started for people with TM so that we can meet and chat casually. It's only on Facebook for now, so, if you haven't already, join. It's easy.
Best,
Melanie
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In Pictures
Please Note: Some photos may contain partial nudity or depictions of medical procedures. Though I am in many of these photos, my reason for sharing these personal photos is to promote awareness, understanding, and advocacy for people with TM and other rare diseases.
To play the slide show, click the big play button in the center of the screen, then the small one in the bottom left corner. Click here for more advanced viewing instructions, and select "Help."
Please keep the old blog open. It is just as intelligent and vibrant as this one is!
ReplyDeleteNice post..Informative and useful.Thanks for sharing..
ReplyDelete