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)


advertisement
Reply
 
Thread Tools Display Modes
Old 10-20-2011, 08:48 AM #21
gramE's Avatar
gramE gramE is offline
Member
 
Join Date: Nov 2010
Location: NorthCentral Indiana
Posts: 262
10 yr Member
gramE gramE is offline
Member
gramE's Avatar
 
Join Date: Nov 2010
Location: NorthCentral Indiana
Posts: 262
10 yr Member
Default

We got a wheel chair just for shopping and school events because many times you have to park so far away. And I use a cane when I'm walking, not because I really need it, but it acts as a signal to those "huff and puffers" that think I'm moving at a snail's pace that I do have difficulties. People seem to go around without making comments when I use the cane. Just don't hang it over a chair in a restaurant and forget it. I also have a mobility scooter that I've used at Cross Country meets, tennis matches. I can go, and not be as restricted as sitting in the car is.
__________________

.
gramE is offline   Reply With QuoteReply With Quote

advertisement
Old 10-20-2011, 08:50 AM #22
LIT LOVE LIT LOVE is offline
Magnate
 
Join Date: Mar 2010
Posts: 2,304
10 yr Member
LIT LOVE LIT LOVE is offline
Magnate
 
Join Date: Mar 2010
Posts: 2,304
10 yr Member
Default

It took me 12 hours to make a 3 hour drive a few years into having RSD, but before I had accepted the limitations it brought. It was for my bf's wedding shower. I'd drive 1/2 an hour. Stop. Take meds. Wait to be not too medicated. Rinse & Repeat.

My bf didn't believe that I had really taken that long or required such extreme methods.

So when our nearest and dearest struggle with our illnesses, what can we really expect from strangers?

People will surprise you with their compassion, and others will surprise you with their nastiness. Many will seemingly take your illness personally--which I don't understand at all. It's as if they think you've done something to bring it upon yourself. They don't want to believe it could happen to
themselves I suppose. Everybody will have a cure after doing a 2 minute Internet search. And yeah, maybe trying some of those things are worthwhile, but there can be an expectation that it's easy to go into remission. If you fail to get better in their expected time frame...

My vent for the month...
LIT LOVE is offline   Reply With QuoteReply With Quote
Old 10-20-2011, 09:15 AM #23
3fingers 3fingers is offline
Junior Member
 
Join Date: Oct 2011
Location: Rockland County, NY
Posts: 16
10 yr Member
3fingers 3fingers is offline
Junior Member
 
Join Date: Oct 2011
Location: Rockland County, NY
Posts: 16
10 yr Member
Post Support here is great

Quote:
Originally Posted by Jennifer Q View Post
Thank you Ginnie!

Its amazing how I can be here and feel so much hope and support from people whom I've never met. I am so blessed to have been able to stumble upon this forum! Even though we don't know eachother like I said before, there is a common denominator that binds us together. And if I could I would hug you through this computer to let you know I'm. Grateful for you! I'm new to all this and having to come to terms with it is quite difficult for me. But I thank you so much for your encouragement and hope

Jenn
I feel so llucky that I found this site. Noone seems to understand just how difficult it is for me to deal with RSD and the discomfort I am going through especiallly now when the weather keeps changing. Rain is the worst so far. Wish there was a way we could talk as I feel close here with all of you. I am Grateful for the wonderful people and everyone needs support and to be encouraged. This forum by far is wonderful and without it too relate to all of you, I would feel alone. Thanks.
3fingers is offline   Reply With QuoteReply With Quote
Old 10-20-2011, 10:11 AM #24
Russell's Avatar
Russell Russell is offline
Member
 
Join Date: Feb 2011
Location: Blue Ridge Mnts of NC, USA
Posts: 680
10 yr Member
Russell Russell is offline
Member
Russell's Avatar
 
Join Date: Feb 2011
Location: Blue Ridge Mnts of NC, USA
Posts: 680
10 yr Member
Default

I love this site as well. This is a family of people sharing and caring as if we reach out with open arms being understood by those who also fell victim to this monster. A place to chat, ask questions or just vent. People here don't seem to mind listening to the rambles of me (lol)...
__________________
Hope for better days.....
Russ
okska'sssini ómahkapi'si
.
Russell 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
Totally just had a breakdown... AynaDee Multiple Sclerosis 16 09-15-2010 11:53 AM
Communication Breakdown: What Happens to Nerve Cells in PD Stitcher Parkinson's Disease 0 02-10-2010 09:19 AM
HELP - Surgeon Breakdown olecyn Thoracic Outlet Syndrome 4 03-27-2007 06:07 PM


All times are GMT -5. The time now is 06:44 PM.

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.