Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS)

 
 
Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 12-08-2008, 02:19 PM #10
DianaA's Avatar
DianaA DianaA is offline
Member
 
Join Date: Jun 2007
Posts: 329
15 yr Member
DianaA DianaA is offline
Member
DianaA's Avatar
 
Join Date: Jun 2007
Posts: 329
15 yr Member
Default Hi Lori Lee!

I am so sorry that you must endure this pain. I have said this many times, though I know it is NO consolation "But, you are in good company!" You will find much support here and people who really care. I hate to be a habitual advocate of HBOT, but there are a few of us who find amazing results in this form of treatment. I truly believe that if HBOT was administered on site of injury, as it is for professional athletes, many of us would not be where we are today. I know of a manufacturer of HBO Chambers. They make portable HBO Chambers, that go to athletes when they are injured. I think you can still have a good quality life and not give up your career. For me it requires, planning, exceptions, concessions and HBOT on a regular basis.
I also have some writings of a man that passed this year on RSD and HBOT if you would like I will send them to you. (Heres to you Vic, may you rest in peace!)
Please NEVER give up hope! My doctors said " you are resisting the fact that you have RSD". Each year when I ask "what is new, what is everyone doing for treatment?" I get...no one is doing more than you! So I have to advocate on my own behalf and I do exactly what it takes for me to get by and still be more than reasonably satisfied with my results! I live my life each day to my standards and I am thankful for the progress I have made. If you have read my posts, you know I have a home chamber. I know that not everyone can do this. When I first went to Canada, I sold my car, a white convertible Jaguar. Never yet too be replaced. I had forty dives in a HBO chamber and my results were amazing. I have had many dives since and although it is not a cure for me, my life has moved from the bed to the depths of the ocean. Anything is possible. You will move through this phase and on to the newer phases, as nothing, for sure, stays the same. Look forward with hope. Lots of love and prayers Diana

Last edited by DianaA; 12-08-2008 at 02:33 PM. Reason: Tried to put in picture of Chamber ..unsuccessful
DianaA is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
llrn7470 (12-08-2008)
 


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
Denial ??? msrozhou Multiple Sclerosis 3 05-13-2008 08:10 AM
Just a little more denial Blessings2You Multiple Sclerosis 20 05-11-2008 12:51 PM
In complete denial kittygato Reflex Sympathetic Dystrophy (RSD and CRPS) 16 02-11-2008 10:50 AM
LTD is in denial SBGUY Peripheral Neuropathy 13 11-29-2007 05:18 PM
denial of rsd siccy Reflex Sympathetic Dystrophy (RSD and CRPS) 11 02-08-2007 08:03 PM


All times are GMT -5. The time now is 05:26 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.