Reply
 
Thread Tools Display Modes
Old 08-30-2012, 05:18 PM #1
hula77 hula77 is offline
New Member
 
Join Date: Aug 2012
Location: St. Louis, MO
Posts: 5
10 yr Member
hula77 hula77 is offline
New Member
 
Join Date: Aug 2012
Location: St. Louis, MO
Posts: 5
10 yr Member
Default

Anyone else have any thoughts?
hula77 is offline   Reply With QuoteReply With Quote
Old 08-31-2012, 08:56 AM #2
Susanne C. Susanne C. is offline
Member
 
Join Date: Jul 2011
Location: Mid-Atlantic coast
Posts: 721
10 yr Member
Susanne C. Susanne C. is offline
Member
 
Join Date: Jul 2011
Location: Mid-Atlantic coast
Posts: 721
10 yr Member
Default

Quote:
Originally Posted by hula77 View Post
Anyone else have any thoughts?
It is very hard for most of us to improve on Mrs. D's advice. She is a wealth of accurate, not anecdotal, information. It is also hard and not particularly helpful in the short run, but may be very important to come to terms with in the long run: many patients with PN never get a firm diagnosis, there is often no treatment, and palliative care is about it for pain and disability.

That doesn't mean that you are in this camp. Many things you mentioned could point to possible causes that are treatable. It takes a bit of detective work to tease out the information that applies to you.

I hurt my back badly when we adopted an infant who didn't sleep though the night for five years. He was tiny, but carrying him, swaying, rocking, and walking the floor with him resulted in two ruptured discs and surgery. While that kind of back problem and surgery can cause PN, mine is hereditary, so you can also have two things going on at once, or more than two.

Your suffering sounds intense. Good pain management is a must, and there are combinations which are better than others. I hope that you get an actual diagnosis soon and are able to recover. I still have three kids at home. I cannot imagine having this, raising children, and working.
Susanne C. is offline   Reply With QuoteReply With Quote
Reply


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
The "Official" Merry Christmas NeuroTalk Thread Chemar Community & Forum Feedback 0 12-24-2009 01:06 PM
saving the "when did you get your initial rsd/crps dx" thread JOAN_M Reflex Sympathetic Dystrophy (RSD and CRPS) 2 09-10-2007 08:59 AM


All times are GMT -5. The time now is 08:46 PM.


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.

 

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.