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 07-29-2014, 03:21 PM #1
bchristman bchristman is offline
Newly Joined
 
Join Date: Jul 2014
Location: Aberdeen, SD
Posts: 2
8 yr Member
bchristman bchristman is offline
Newly Joined
 
Join Date: Jul 2014
Location: Aberdeen, SD
Posts: 2
8 yr Member
Default Rsd/crps

HI, I'm Brandy, I'm 28 and I have had RSD since I was 14. I am a single Mom (father not in pic at all), my son is 10 and in the last couple years he has had to grow up real quick. My disease went into remission some years ago, it came back full force in 2012. It started in my right leg and now has moved up my hips and into my left leg now. I have to use assistance when walking now. My son is not ashamed to carry my camo pink purse for me Anyways, I was supposed to start Ketamine treatments last month, than last week, than next week, now I got a call today postponing it once again until September. I have had to wing off my pain meds for this treatment, does anyone know what I can do to relieve some pain?? Any suggestions would help, I have tried everything I can think of and still no relief.

Thanks, and I look forward to getting to know people who suffer with the same thing. I know it's not a good thing but it did make me feel better when I saw this and realized I am not the only one who suffers from RSD.
bchristman is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
eevo61 (07-30-2014)

advertisement
Old 07-29-2014, 04:19 PM #2
Adalaide's Avatar
Adalaide Adalaide is offline
Junior Member
 
Join Date: Feb 2014
Location: Utah
Posts: 91
10 yr Member
Adalaide Adalaide is offline
Junior Member
Adalaide's Avatar
 
Join Date: Feb 2014
Location: Utah
Posts: 91
10 yr Member
Default

I'm sorry you're getting stuck in this position. It seems that for all we have insurance to help us, sometimes all it does is leave us wondering why we have it.

I do a few things for pain relief that aren't drugs. I use microwavable heating pads, I can't stand the electric ones because they're uncomfortable to use. I also use essential oils. For me ylang-ylang and frankincense are helpful, I'm not sure what others will like and find helps. The third thing I use (this is not G rated, sorry) is orgasm. It sometimes takes an iron will to block the pain out of my mind enough, but the pain relief is great. And free!

I hope they see you soon so you can get relief.
__________________
"...it needs to be about 20% cooler."

Celiac DX Dec 2012; over 30 years symptoms to DX
CRPS DX March 2014; 5 years, 1 month from first symptom to DX
Adalaide is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
eevo61 (07-30-2014), visioniosiv (07-29-2014)
Old 07-29-2014, 04:26 PM #3
visioniosiv's Avatar
visioniosiv visioniosiv is offline
Member
 
Join Date: Nov 2013
Posts: 257
10 yr Member
visioniosiv visioniosiv is offline
Member
visioniosiv's Avatar
 
Join Date: Nov 2013
Posts: 257
10 yr Member
Default

Quote:
Originally Posted by bchristman View Post
HI, I'm Brandy, I'm 28 and I have had RSD since I was 14. I am a single Mom (father not in pic at all), my son is 10 and in the last couple years he has had to grow up real quick. My disease went into remission some years ago, it came back full force in 2012. It started in my right leg and now has moved up my hips and into my left leg now. I have to use assistance when walking now. My son is not ashamed to carry my camo pink purse for me Anyways, I was supposed to start Ketamine treatments last month, than last week, than next week, now I got a call today postponing it once again until September. I have had to wing off my pain meds for this treatment, does anyone know what I can do to relieve some pain?? Any suggestions would help, I have tried everything I can think of and still no relief.

Thanks, and I look forward to getting to know people who suffer with the same thing. I know it's not a good thing but it did make me feel better when I saw this and realized I am not the only one who suffers from RSD.
Hi Brandy - I'm sorry you're in so much pain. Cool kid you got there

I don't know how to help much on the meds side, since individuals have such different tolerances and reactions. Many here have had success with lots of different modalities and will be able to chime in. A warm bath with epsom salt and soothing music was always good for me though.

For me, the biggest pain relief came from visualization methods and meditation. Here's how I started: http://neurotalk.psychcentral.com/thread202210.html

Doesn't seem like much but it helped me
visioniosiv is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
eevo61 (07-30-2014)
Old 07-29-2014, 04:31 PM #4
visioniosiv's Avatar
visioniosiv visioniosiv is offline
Member
 
Join Date: Nov 2013
Posts: 257
10 yr Member
visioniosiv visioniosiv is offline
Member
visioniosiv's Avatar
 
Join Date: Nov 2013
Posts: 257
10 yr Member
Default

Quote:
Originally Posted by Adalaide View Post
The third thing I use (this is not G rated, sorry) is orgasm. It sometimes takes an iron will to block the pain out of my mind enough, but the pain relief is great. And free!

I hope they see you soon so you can get relief.
Hahaha Adalaide that's genius and you're frickin' dead on

There is a massive parasympathetic rebound after orgasm that provides long term, natural pain relief.

Pretty much all parasympathetic activities are great for managing and reducing RSD symptoms!! And Addy's recommendation is the most fun
visioniosiv is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
eevo61 (07-30-2014)
Old 07-29-2014, 05:47 PM #5
Kitt Kitt is offline
Grand Magnate
 
Join Date: Aug 2006
Posts: 4,428
15 yr Member
Kitt Kitt is offline
Grand Magnate
 
Join Date: Aug 2006
Posts: 4,428
15 yr Member
Default

Welcome bchristman.
__________________
Kitt

--------------------------------------------------------------------------------------------------------

"It is what it is."
Kitt is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
eevo61 (07-30-2014)
Old 07-29-2014, 10:19 PM #6
Lottie Lottie is offline
Member
 
Join Date: Nov 2013
Location: United States
Posts: 363
10 yr Member
Lottie Lottie is offline
Member
 
Join Date: Nov 2013
Location: United States
Posts: 363
10 yr Member
Default

Welcome Brandy! Glad you found us! This is a great bunch of CRPSy friends here who offer hugs and share info.
Wow. CRPS at age 14, I am so sorry this happened to you so young. Were you injured? Or have surgery that caused it? Mine is in the right leg after multiple spine surgeries. For comfort I use warm baths with epsom salt, heating pad, soft socks, meditation musice, lavendar oil aromatherapy, aquatic therapy in a warm water pool,elevate my leg, and get cyber hugs from my NT friends!! Wishing you wellness - Lottie
__________________
1999 Chronic spine pain related to Degenerative Disc
Disease,
Sept 2001. C6 / C7 discectomy & fusion.
Jan. 2005 L5/S1 discectomy and Artificial Disc Replacement.
July 2011 removal of broken
.
Artificial Disc Replacement.
Woke up in recovery room with RSD Monster.:
.

Aug 2011 Stabilization of spine at L3/L4/L5.
October 2014 Rheumatoid Arthritis.
Lottie is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
eevo61 (07-30-2014)
Old 07-30-2014, 07:36 PM #7
eevo61's Avatar
eevo61 eevo61 is offline
Member
 
Join Date: Aug 2013
Location: California
Posts: 389
10 yr Member
eevo61 eevo61 is offline
Member
eevo61's Avatar
 
Join Date: Aug 2013
Location: California
Posts: 389
10 yr Member
Default

Quote:
Originally Posted by bchristman View Post
HI, I'm Brandy, I'm 28 and I have had RSD since I was 14. I am a single Mom (father not in pic at all), my son is 10 and in the last couple years he has had to grow up real quick. My disease went into remission some years ago, it came back full force in 2012. It started in my right leg and now has moved up my hips and into my left leg now. I have to use assistance when walking now. My son is not ashamed to carry my camo pink purse for me Anyways, I was supposed to start Ketamine treatments last month, than last week, than next week, now I got a call today postponing it once again until September. I have had to wing off my pain meds for this treatment, does anyone know what I can do to relieve some pain?? Any suggestions would help, I have tried everything I can think of and still no relief.

Thanks, and I look forward to getting to know people who suffer with the same thing. I know it's not a good thing but it did make me feel better when I saw this and realized I am not the only one who suffers from RSD.
Sorry you rsd came back so strong , hope soon you find a way to regain control back.
I'm so happy your son is such amazing young men,sure you are so proud mama.
My relief when flare ups are ,heating pads In the most affected areas,rest when possible,take my meds, cry if I have to ,gelato to refresh my belly , light and soft music Tibetan singing bowls to meditate and relax a little, but most important , always try to no fight a bad day,let it pass the only really good advise from my old pm dr.when you fight a bad day the pain gets back at you stronger then ever, sucks for sure.
I hope soon you found some much needed relief and also pamper yourself with something you like and distracted your mind from the pain,is almost impossible but do your best,
Happy you are here and we can in some way give you some source of support and comfort,wish you better days and sending you gentle hugs with love Jesika .
__________________

.
eevo61 is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Lottie (07-30-2014)
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
crps David44 New Member Introductions 6 01-30-2013 02:23 AM
Have I got CRPS ??? pacman New Member Introductions 1 04-18-2012 08:01 PM
Crps/rsd Angelique New Member Introductions 1 06-24-2011 01:45 AM
Crps Greedy Reflex Sympathetic Dystrophy (RSD and CRPS) 6 07-19-2009 06:32 AM
Crps???? sbvcrn Reflex Sympathetic Dystrophy (RSD and CRPS) 1 12-17-2008 05:43 PM


All times are GMT -5. The time now is 11:28 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.