Guest guest Posted January 23, 2006 Report Share Posted January 23, 2006 Yes, it would be a good idea to have your son " looked at " considering all that you posted. If your son has CMT, he will have the same type that you do. CMT symptoms and progression can be completely different in each family and in each generation. Physical therapy can help in stretching of toes, feet, and legs - in addition to this, the doctor may suggest other ideas that may help - Vitamins, a nutritional plan, perhaps AFOs (Ankle Foot Orthotics or DAFOs - the DAFOs are for kids.) If you can find a pediatric neurologist, this would be ideal. Or take your son to a MD clinic - they provide services for CMT also. I'm not sure what you mean by DSD - do you mean Dejerine Sottas Disease or Duchene Muscular Dystrophy? DSS was once considered to be CMT Type 3, but is now thought to be a variant of CMT 1. DMD is entirely different from CMT, and even the better reason to have your son checked if this is an issue. No questions here are ever silly or stupid. We are ALL learning, that's why we're here ~ Gretchen Quote Link to comment Share on other sites More sharing options...
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