advertisement
 
 
Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 09-04-2016, 11:09 AM #13
LouLou1978 LouLou1978 is offline
Member
 
Join Date: Feb 2015
Location: UK
Posts: 153
8 yr Member
LouLou1978 LouLou1978 is offline
Member
 
Join Date: Feb 2015
Location: UK
Posts: 153
8 yr Member
Mad

Quote:
Originally Posted by Healthgirl View Post
There is Ehlers Danlos Syndrome that runs in families and can go undetected or misdiagnosed. This can cause neurological and connective tissue problems and very commonly dysautonomia. I'm pretty sure I have it...or at least I have every single symptom, but autoimmune diseases can look similar. I'm betting they will check me for this when I go to Columbia.

Also there are metabolic disorders that run in families. I'm finding that people go years with out a proper diagnosis until they finally get a geneticist. My one neurologist didn't see the point since I already have a "diagnosis", but I think it's important to find a cause so you know what to treat and not to treat and to stop guessing.
Thank you Health Girl, i am fuming today as i have just read my sister's letter from her Neurologist. It says " As her nerve conduction test is normal, this is consistent with Small Fiber Neuropathy" She would like the biopsy to be absolutely certain. However my diagnosis is Small Fiber Neuropathy.

My sister has not had burning as what we know. She says she has hot feelings on her skin which are not painful, it also goes away for months and does not bother her in the slightest. I still feel really cross that her neuro does not think a biopsy in necessary as there would be nothing they could do if it was genetic. I would have thought it would be very important considering they have agreed an IVIG trial for myself on the NHS. Obviously the IVIG won't work if its genetic, so surely they would need to get a firm diagnosis before i went ahead with expensive treatment and the possibility of having a bad reaction to it!
LouLou1978 is offline   Reply With QuoteReply With Quote
 

Tags
confirmed, genetic, hot, sfn, skin


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
Reccomendations for small fiber neuropathy expert in Boston pg600rr Peripheral Neuropathy 0 08-14-2012 04:20 PM
Neuropathy Expert spoke at our meeting last night MelodyL Peripheral Neuropathy 15 03-18-2012 12:47 PM
Genetic clue to idiopathic neuropathy: mrsD PN Tips, Resources, Supplements & Other Treatments 6 09-27-2011 07:49 PM


All times are GMT -5. The time now is 07:19 AM.

Powered by vBulletin • Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise v2.7.1 (Lite) - vBulletin Mods & Addons Copyright © 2024 DragonByte Technologies Ltd.
 

NeuroTalk Forums

Helping support those with neurological and related conditions.

 

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.