Update ... : Instead of asking a... - Charcot-Marie-Too...

Charcot-Marie-Tooth UK

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Update ...

Ashley_x profile image
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Instead of asking a million questions I thought I would create a post. Had follow up appointment with neurologist he says I DO NOT have cmt and only suffer from HNPP. Have no reflexes in my ankles (?) and I've to be aware of what I do that can cause pressure palsies. He was also wanting to refer me for carpel tunnel surgery (which I have declined) and have to be referred to occupational therapy. Does anyone else here go to ot?? As always I hope you are all well xxxx

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Ashley_x
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Amanita profile image
Amanita

After my initial diagnosis with a "polyneuropathy", and before it was pinned down months later to CMT, I was referred to an OT (as well as a physiotherapist and an orthotist). She spent several sessions determining the degree of weakness and lack of sensation in my hands before giving me a pile of exercises to do daily , and wrist/hand splints to wear at night. She also strongly recommended a medical driving-assessment (which resulted in my having to buy an automatic car). After about a year she discharged me, rather to my surprise, but said I could be referred to her again should it prove necessary. This means that when the CMT progresses further and I need more help, I shall have to wait another 3 months to see her again.

lordie profile image
lordie

Pardon me to ask this but is hnpp the same as cmt or different

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