Hi
I am new here
Hi
I am new here
Hello to Lordie ....
Welcome to the HealthUnlocked website, which is mainly used by people who have Charcot Marie Tooth Disease (CMT) : Always call CMT a 'DISEASE, not a condition, or an abnormality :
This great website allows Cmt sufferer's to ask questions, and seek further information, and most importantly 'SHARE' with each other their ongoing experiences:
CMT is an inherited disease, usually 96% of sufferers, the defective gene(s) is passed on from a parent to their offspring : Its symptom vary tremendously from person to person, each individual case stands alone : Some symptons occur in childhood, but mainly present themselves in the teenager years :
Currently their is NO cure for CMT : Your damaged 'long' peripheral (near to the surface) nerves, which carry very weak, and slow electrical signals "to and from" your brain to your affected muscles cause them to waste :
Cmt is a progressivly worsening neurological disease, its not an orthopaedic defect, but does cause many bone "pes-cavus" (high-arches) etc, that may require attention :
You must use POSITIVE MANAGEMENT to your own symptoms in a positive manner : Accept, and adjust your mental outlook, and including your lifestyle accordingly to suit your ongoing, and ever changing circumstances !
Best of luck ....
John (Glasgow)