Living With CMT by Nick - Having CMT
This is a video of a boy named Nick who lives in New York. He was diagnosed with CMT when he was 13 and he is now 18. He has gone through 9 surgeries! This kid has a big heart just like Carter! Just thought I would post it so you all can see what it might be like for him over the next year. Love to all!
Michelle
I started this blog shortly after my two sons were diagnosed with Charcot Marie Tooth Disease, no it has nothing to do with your teeth! Carter and I blog to tell about our journey with CMT, the ups and downs, trials and tribulations and to raise awareness. I hope this blog helps others who are affected by CMT and those who caregivers. Finding A Cure One Step At A Time!
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