Reflex Sympathetic Dystrophy Support Group

Reflex sympathetic dystrophy syndrome (RSDS), also known as complex regional pain syndrome, is a chronic condition characterized by severe pain following injury to bone and soft tissue. The most common symptom is burning pain. The patient may also experience muscle spasms, local swelling, increased sweating, softening of bones, joint tenderness or stiffness, restricted or...

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336 Posts

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Am I going to be the only active member?

Posted by: Maui1992

Posted: 07/06/2019

0

Hi anyone? No new posts since 2018. What happened anyone?I have a hybrid of RSD and erythromelalgia.
is this RSD?

Posted by: deleted_user

Last Reply: rachlynne 08/01/2018

5

I was just diagnosed with RSD. They say it happened because of all the procedures I have had on my left hip and back. I... READ MORE
CRPS Life

Posted by: MoonKitten

Last Reply: MoonKitten 07/30/2018

2

I was diagnosed with CRPS when I was a freshman in high school. At first I thought I had a sprained ankle but days... READ MORE
Is this group active?

Posted by: Greeneyegirl

Posted: 07/23/2018

0

Does anyone post messages here?
It's so hard to deal with...

Posted by: LaBrock

Last Reply: RachMoore 06/01/2018

7

I was diagnosed with CRPS about 4 and a half months ago. The change it has made in my life has been so hard to deal... READ MORE
Fairly New Still

Posted by: RachMoore

Last Reply: RachMoore 06/01/2018

2

So, I have only been dealing with CRPS for about a year and a half. I was diagnosed in September of 2016 after I fell... READ MORE
3 years

Posted by: Panicxtori

Last Reply: DAnn 04/29/2018

2

I'm 17and have been suffering with full body RND since I was 14. I was diagnosed when I was 15 and was lucky enough to... READ MORE
rsd life sentence

Posted by: mylife315

Posted: 04/29/2018

0

my name is Catherine and I have had rsd for 34 years now. Boy Iam I tired of this!!! Just moved to New Mexico and... READ MORE
Over it.

Posted by: EmilyBee

Last Reply: EmilyBee 03/06/2018

2

Looking over some of these other posts makes me feel dumb. Like I shouldn't complain. I've only been dealing with CRPS... READ MORE
Anyone else being affected by new CDC guidelines?

Posted by: jenthalia

Last Reply: CasMac1 01/30/2018

6

Hi,I've been a member of DailyStrength for years. I used to be thaliajen. I've had RSD for 19 years. I had 3 great... READ MORE
A little lost

Posted by: belle007

Posted: 11/22/2017

0

Hi there ! I was first diagonosed with Crps when I was 14 I’m now 19 and it’s for sure been a journey but I’ve... READ MORE
Just feel lie giving up!!

Posted by: TIREDBDA

Last Reply: djbritt 11/16/2017

1

I've had RSD/CRPS for over 13 years now. It has been a long, hard battle and I just want to end it all. Laying awake... READ MORE
Angry and frustrated

Posted by: Mickeymouse-ct

Posted: 09/06/2017

0

I have been dealing with crps for 3 years now in my foot. I feel that no one understands. My husband thinks I am... READ MORE
RND and POTS treatment

Posted by: kaybriden

Last Reply: djbritt 01/31/2017

6

I have been sick for two years, but I was just diagnosed with POTS and RND this past March. I've tried an increase of... READ MORE
Hoping

Posted by: marion

Last Reply: jenthalia 10/07/2016

2

I have had RSD for 29 years. It started in my left arm and now is throughout my body, including face. This summer I... READ MORE