Quote:
Originally Posted by Kitt
I have been a member of this site for nine years and before that I was on the old forum. If I am reading your post correctly, that I don't quite fit the category, I assure you that I do have CMT. Family history goes back a long, long way. You can have symptoms when you are young, old, or in-between. Or you may not have any noticeable symptoms but you still can have CMT. And, yes, symptoms vary greatly even within the same family. I certainly can see that.
You can have flat feet, normal feet or high arches. You can have hammertoes but not all do. I do not. Hammertoes, drop foot, etc. can be caused by a lot of things. Many in the general public have one or the other. Also, I have normal looking feet. Not everyone has drop foot either. Or it may not be that bad if they do have it. Hands and arms can be impacted as well. Mine at this point are not but time will tell. The rest of the family going way back does have both hand, arm, leg and foot issues/weakness.
CMT progresses no matter what you do. CMT does not come on just like that and all of a sudden there you are. But CMT does progress. I have known about CMT since I was five years old. I have kept up with all the research that is being done - and there is lots - for many years now. And much was before the Internet. This information is all from reputable resources.
As far as EMG/NCV testing they can tell the type via the testing. When the myelin is damaged (CMT type 1), the nerve impulses are conducted more slowly than normal. If the axon itself is damaged (CMT type 2), the speed of nerve conduction is almost normal, but the strength of the signal is reduced. CMT is a multi-gene disorder and so there are many different defective genes which cause the disorder.
CMT affects the peripheral nervous system (PNS) and therefore it results in both motor symptoms (weakness and muscle wasting) and sensory symptoms (numbness). CMT is progressive no matter what you do. A neurologist who is an expert in CMT would be the doctor to see. I cannot say that you have CMT. Only a good neurologist can help you there. You certainly do have something going on. Hope you get to the bottom of it.
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Thanks for all this information!!
I did not by any means mean to come across as insinuating you didn't have CMT. I am sorry. I know you do! I was just stating that I am absolutely un-educated in CMT and most other neurological disorders because this is all very new to me. I just wanted to get the point across that reading things purely online or googling symptoms can be misleading for someone like myself that has not been researching or dealing with this for several years. I have by far gained the most experience and education from this forum, from people like yourself. And I am so grateful there is a forum like this available for people suffering from neuro symptoms and not knowing what the heck to do about it. I know that no one on here can dx anyone, but the support def. helps me and I know so many others like me!! Thanks for educating me in CMT and supporting me in finding some answers