Home Menu

Site Navigation



NeuroTalk Support Groups > > >

Has anyone been to Johns Hopkins for Neuropathy?

 
 
Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 10-02-2012, 04:18 PM #1
Nervous1's Avatar
Nervous1 Nervous1 is offline
Member
  
Join Date: Jul 2012
Posts: 117
10 yr Member
Nervous1 Nervous1 is offline
Member
Nervous1's Avatar
 
Join Date: Jul 2012
Posts: 117
10 yr Member
Confused Has anyone been to Johns Hopkins for Neuropathy?
Has anyone been to Johns Hopkins that has some form of undiagnosed neuropathy and come out on the other end with a diagnosis?
My neurologist is telling me that he needs an extra set of eyes on me since all of my tests come back negative. And I still pass the reflex and "feeling" tests on my feet. NCT and EMG were OK months ago. Only mild carpal tunnel.
So before I consider traveling to another state, I would like to know if anyone has any experience with Johns Hopkins.

Thanks in advance!
Nervous1
Nervous1 is offline   Reply With QuoteReply With Quote
 

« Previous Thread | Next Thread »

Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts
BB code is On
Smilies are On
[IMG] code is On
HTML code is Off

Similar Threads
Thread Thread Starter Forum Replies Last Post
Good Article on Mitochondria and neuropathy - Johns Hopkins Nervous1 Peripheral Neuropathy 9 10-03-2012 07:25 AM
Back from Johns Hopkins tysondouglass Myasthenia Gravis 7 05-17-2011 06:44 AM
Mayo / Johns Hopkins neuropathy (possible sjogren's) smitty1 Peripheral Neuropathy 6 04-16-2009 02:08 AM
my follow-up at Johns Hopkins RedPenguins Multiple Sclerosis 5 02-15-2009 02:26 AM
HiCy/Revimmune at Johns Hopkins RedPenguins Multiple Sclerosis 30 06-28-2008 11:03 AM


All times are GMT -5. The time now is 02:05 AM.


Powered by vBulletin • Copyright ©2000 - 2025, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise (Lite) - vBulletin Mods & Addons Copyright © 2025 DragonByte Technologies Ltd.
 

NeuroTalk Forums

Helping support those with neurological and related conditions.

 

All posts copyright their original authors.

The material on this site is for informational purposes only,
and is not a substitute for medical advice, diagnosis or treatment
provided by a qualified health care provider.

Always consult your doctor before trying anything you read here.

Home