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HMSN, CMT or ??

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I have a question for the group. My neurologist has diagnosed my

" condition " as hereditary demylenating peripheral (poly)neuropathy. From

everything I've learned about my condition, it seems that it goes under the

heading of CMT or HMSN, both terms seem to be interchangeable to me. Since

I applied to Social Security for Disability, I'm wondering how I should

refer to my condition? In the paperwork I put in, I wrote what my

neurologist diagnosed, then put aka, HMSN or CMT.

What does everyone think? Are HMSN and CMT interchangeable terms to

describe what we experience?

PS, I've been following everyone's comments on SSD with great interest!

Since I applied on June 1, 2000 I've heard nothing, except to get a

supplemental 6 page form to fill out in mid June from the agency that SS

uses here in land to evaluate disability claims, that wanted me to

document my daily activities.

I also get this mailing list in digest format, so anyone responding to

me, it may take me a bit longer to reply. Thanks!

Jim

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<< What does everyone think? Are HMSN and CMT interchangeable terms to

describe what we experience? >>

You need to check. I believe I heard that they know Charot Marie Tooth and

have it listed. However, they are interchangeable terms medically.

http://www.neuro.wustl.edu/neuromuscular/time/hmsn.html

http://www.mdausa.org/disease/cmt.html

http://medweb.bham.ac.uk/http/depts/clin_neuro/teaching/tutorials/hmsn/hmsn.ht

ml

http://www.muscular-dystrophy.org.uk/information/Key%20facts/hmsn.html

Kat

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Hello ,

the demyelenating describes what kind of cmt you have. CMT 1 is demyelenating,

while

cmt 2 is axonal. This is a descripting what kind of the nerve (the myelin-sheet

or the

inside of the nerve is affected. Peripheral means that it starts in the arm and

feet.

A few years ago they thougt it would stop at the elbows or knees but now they

know this is not true.

What your neurologist meant is that you have cmt or hmsn :-))

Bye,

Jim Topper schrieb:

> I have a question for the group. My neurologist has diagnosed my

> " condition " as hereditary demylenating peripheral (poly)neuropathy. From

> everything I've learned about my condition, it seems that it goes under the

> heading of CMT or HMSN, both terms seem to be interchangeable to me. Since

> I applied to Social Security for Disability, I'm wondering how I should

> refer to my condition? In the paperwork I put in, I wrote what my

> neurologist diagnosed, then put aka, HMSN or CMT.

>

> What does everyone think? Are HMSN and CMT interchangeable terms to

> describe what we experience?

>

> PS, I've been following everyone's comments on SSD with great interest!

> Since I applied on June 1, 2000 I've heard nothing, except to get a

> supplemental 6 page form to fill out in mid June from the agency that SS

> uses here in land to evaluate disability claims, that wanted me to

> document my daily activities.

>

> I also get this mailing list in digest format, so anyone responding to

> me, it may take me a bit longer to reply. Thanks!

>

> Jim

>

> ------------------------------------------------------------------------

> Best friends, most artistic, class clown Find 'em here:

> http://click.egroups.com/1/7078/13/_/616793/_/964113768/

> ------------------------------------------------------------------------

>

>

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