Today is a very exciting day for our collaborative CMT blog: Clicks for CMT. The Hereditary Neuropathy Foundation wrote a great article about it (Kudos to Melissa for getting this interview). To read the article, please click HERE. It's so exciting that our Fab Five blog is getting this exposure!!
We have had over 3,500 views this past month alone!!!! When the 5 of us set out to do this, we definitely did not imagine that it would get so much momentum so quickly!!!!
Keep up the wonderful work girls!!!!
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My life with CMT and trying to deal with constant chronic pain with a positive attitude...
Wednesday, September 19, 2012
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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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2 comments:
Hello, I just found this Blog for Michele and Clicks for CMT..... I love how you have embraced this and are working to spread the word.... I see that the last post is from 2012... I hope all is well and you can continue blogging!
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