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CMT Awareness Week is almost here and the CMTA (Charcot-Marie-Tooth Association) has set up this special website: www.wearethecmta.com
Please take a moment to browse through the site where you can find facts about CMT, events going on this week, the many faces of CMT (can you spot me in the crowd?), and most importantly, donate. If you can, please donate to CMT research so hopefully we can have some form of treatment or medication in the near future and who knows? Maybe even a cure....
My life with CMT and trying to deal with constant chronic pain with a positive attitude...
Wednesday, September 15, 2010
I am CMT
CMT Awareness Week is almost here and the CMTA (Charcot-Marie-Tooth Association) has set up this special website: www.wearethecmta.com
Please take a moment to browse through the site where you can find facts about CMT, events going on this week, the many faces of CMT (can you spot me in the crowd?), and most importantly, donate. If you can, please donate to CMT research so hopefully we can have some form of treatment or medication in the near future and who knows? Maybe even a cure....
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About Me
- Michele
- CT, United States
- I'm a girl with hopes and dreams who has Charcot-Marie-Tooth (I know! You've never heard of it!). In this blog, I talk about my journey with this invisible disease and 2 reconstructive foot surgeries (and a 3rd minor surgery) I've gone through in the last 18 months. And I try to do it all with a positive attitude and a smile on my face :)
Highlights of My Journey
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3 comments:
Happy (almost) CMT week. Does this call for cake? Like a super moist cake slathered in buttercream frosting? Um...I think it does! :)
Hmmm I'll go for a cupcake cake any day :) Should we skype? LOL
Ok, so I'm reading all of your back-posts....and I see a picture of myself! Aaahhh! I feel so popular! LOL
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