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Nerve biopsy

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Hi ,

Best of luck with your nerve biopsy. I have had absolutely no

problems with anything since my sural nerve biopsy in 1987.

As others have stated, relax, and all should go well.

Blessings,

P.

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My husband had the nerve biopsy when he was three and has had

no problems because of it and my daughter who is now 6 has DNA

testing as the doctor said that it was a lot less painfull. She

was only 1 when the blood tests were done but we were postive

she had it as she showed all the same symptoms as her father,

so it was more just a thing to make it definite.

Thanks.

Kerri

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  • 2 weeks later...

To Kruser:

Yes, you did do the right thing for yourself! While no one likes to undergo

invasive procedures, sometimes those procedures are necessary. You've been

in my thoughts.

Blair

You are not alone with !

Recent Neurocast Statistics show 50% of us have CMT Type 1; 20-40% of us

have CMT Type 2; 10-15% of us have CMT Type X; And 20% of us show NO family

history. For

more information on these and other statistics, visit http://www.neurocast.com

and click on

'previous sessions'. Look for the title " Diagnosing Peripheral Neuropathies " .

is Charcot Marie Tooth Universal Services - for you, your loved

ones, the medical and scientific community, and anyone who wants to learn

how CMT/HMSN affects each of us through experiential sharing.

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  • 2 years later...

,

I, too had a normal sural nerve biopsy, but my muscle biopsy was

abnormal. That lead my neurologists at Mayo Clinic to my diagnosis of

Distal Predominant Motorneuronopathy. (A disease of my lower motor neuron;

in the same family as Lou Gehrig's disease, but not fatal.) Originally it

was thought that I had CMT, because many of the symptoms are almost

identical. Don't give up searching for answers.

K.

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Wow!!! Our 14yr old daughter is having a muscle biopsy in a week. Could you

tell me where your nerve biopsy was done. How long of a recovery. They think

she has cmt and also a artritis conditon called polyomytois. Thanks for the

post. Faye in Fla

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Mine was done on the out side of my foot just above the ankle bone. A 2 1/2

inch incision. Took the doctor a while to find the nerve. He was surprised

that I didn¹t feel him cut it cause even if you numb things he told me when

they make the cut people usually jump. I didn't. I don¹t have feeling on

the top of my foot and parts of the bottom of my feet. Mine is still

healing. It hurts. The skin is really tight so now that the wound is

looking better I'm putting vitamin E on it to help the skin stretch. The

procedure didn't hurt for me but afterwards it hurt really bad. I'm still

walking funny cause I'm feeling less. I¹ve been soaking my foot in epson

salts at night and keeping it elevated cause it still swells up. This is

three weeks after the procedure.

For me I'm kinda disappointed that I¹ve gone through this and it came back

normal.

, Denver CO

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  • 5 months later...

In a message dated 2/26/2005 8:32:41 P.M. Pacific Standard Time,

cbentzin@... writes:

" It is no longer necessary to do nerve biopsies for diagnosing CMT

Well that is good news. I never let anyone biopsy my nerves. I could never

see the reason for it.

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WOW,

That is great news about skin biopsies for diagnosis of CMT. Especially at

this time when it appears a couple of my children (we have 5) may be

showing signs of CMT. It certainly would be easier than an EMG/NCV study also.

P.

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