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1,172 total results

Comments (1,123)

I fell and have had butt pain for 5 months. I've had 4 lumbar surgeries so...

https://connect.mayoclinic.org/comment/1099250/

I have CRPS.

Discussion: Gluteus Maximus tear

Support Group: Bones, Joints & Muscles

Posted: Jul 4 1:22pm

I have had bladder changes since covid. I don't have an infection. I'm a nurse, had...

https://connect.mayoclinic.org/comment/778180/

I have CRPS which spread from COVID.

Discussion: Post Covid/Long Covid: Anyone else experienced bladder issues?

Support Group: Post-COVID Recovery & COVID-19

Posted: Nov 28, 2022

I am a 43 yrs old female. Diagnosed 9 years ago when they called it Reflex...

https://connect.mayoclinic.org/comment/157614/

Mayo clinic in Jacksonville, FL has a CRPS

Discussion: Living with Neuropathy - Welcome to the group

Support Group: Neuropathy

Posted: Aug 8, 2019

Lacy, Lioness & all, Not sure I’m replying in the right spot but I have a...

https://connect.mayoclinic.org/comment/119903/

here in the Midwest and it sent my CRPS

Discussion: Fibromyalgia pain: Let's connect

Support Group: Fibromyalgia

Posted: Mar 8, 2021

I was born with scoliosis (adopted). I fell about 15 yrs ago & fractured my left...

https://connect.mayoclinic.org/comment/149466/

in 1996 % developed RSD/now called CRPS

Discussion: Scoliosis - Introduce yourself and meet others

Support Group: Spine Health

Posted: Feb 5, 2018

Hope I'm writing in the right space! I just looked at my first You Tube of...

https://connect.mayoclinic.org/comment/1134687/

I've heard of CRPS, all the letters

Discussion: Gabapentin and Cymbalta side effects

Support Group: Chronic Pain

Posted: Sep 1 7:05pm

I have POTS from Long COVID which attacked my autonomic nervous system causing several life long...

https://connect.mayoclinic.org/comment/984372/

#39;t wear compression socks due to CRPS ... pressure impacts my neuropathy and CRPS

Discussion: Some possible answers: Diagnosed with POTS

Support Group: Post-COVID Recovery & COVID-19

Posted: Dec 21, 2023

fibromyalgia is totally different then CRPS or the original name Reflex Sympathetic Dystrophy. It dates back...

https://connect.mayoclinic.org/comment/1090649/

fibromyalgia is totally different then CRPS ... If anyone has CRPS with spasms especially ... so many doctors have no idea what CRPS

Discussion: CRPS - anyone suffering with complex regional pain syndrome

Support Group: Chronic Pain

Posted: Jun 20 6:34pm

Nearly 21 years with CRPS. Original injury: oilfield accident slipped and fell dislocating my R knee...

https://connect.mayoclinic.org/comment/741782/

Nearly 21 years with CRPS.

Discussion: Complex regional pain syndrome (CRPS) and feeling blank

Support Group: Chronic Pain

Posted: Aug 25, 2022

I look into acupuncture in our area we do not have no one and same with...

https://connect.mayoclinic.org/comment/89092/

Doctor's think it might be CRPS but

Discussion: Complex regional pain syndrome or reflex sympathetic dystrophy

Support Group: Chronic Pain

Posted: Apr 10, 2017

My name is Kathy Vienna( I believe my on line tag is #kvienna) I haven't been...

https://connect.mayoclinic.org/comment/156220/

if there is any new information on CRPS

Discussion: Living with Neuropathy - Welcome to the group

Support Group: Neuropathy

Posted: Sep 19, 2017

@rsnowflake @barbbie I live in New York. I was pretty healthy before my ankle fracture. But...

https://connect.mayoclinic.org/comment/254847/

I’ve been reading that people with CRPS

Discussion: CRPS Question: Itching

Support Group: Chronic Pain

Posted: Mar 14, 2019

I was diagnosed with CRPS after total knee replacement. The pain was so bad I am...

https://connect.mayoclinic.org/comment/903085/

I was diagnosed with CRPS after total

Discussion: CRPS/pain syndrome. is it time for a mobility device. Embarrassed.

Support Group: Chronic Pain

Posted: Jul 27, 2023

I have POTS from having long COVID. I can't imagine having it prior to having long...

https://connect.mayoclinic.org/comment/978969/

about falling and have neuropathy and CRPS

Discussion: POTS, Pre- or Post-COVID: Where did you find treatment and what helps?

Support Group: Post-COVID Recovery & COVID-19

Posted: Dec 12, 2023

Hi, I agree with you. The more you move the better. The more you have mental...

https://connect.mayoclinic.org/comment/728058/

Positivity with CRPS/RSD is awesome

Discussion: CRPS - anyone suffering with complex regional pain syndrome

Support Group: Chronic Pain

Posted: Jul 18, 2022

I have had CRPS for 22 years. I had surgery for Tarsal Tunnel Neuritis on my...

https://connect.mayoclinic.org/comment/797816/

I have had CRPS for 22 years.

Discussion: Complex regional pain syndrome or reflex sympathetic dystrophy

Support Group: Chronic Pain

Posted: Jan 17, 2023

I don't think there is a cure for long COVID. My LC clinic told me that...

https://connect.mayoclinic.org/comment/991308/

non-curable issues - POTS, Neuropathy, CRPS

Discussion: Anyone think that it’s no longer long Covid? just permanent damage?

Support Group: Post-COVID Recovery & COVID-19

Posted: Jan 4 10:04am

Thanks for your comments on spacing ingestion of prednisone throughout the day. I've been spacing it...

https://connect.mayoclinic.org/comment/824417/

levels are extraordinary for PMR (CRPs

Discussion: PMR, prednisone and Poor Sleep or Insomnia

Support Group: Polymyalgia Rheumatica (PMR)

Posted: Mar 11, 2023

Born premature, massive stroke at 6 months old gave me right sided mild cerebral palsy with...

https://connect.mayoclinic.org/comment/812184/

related to the CP), diagnosed with CRPS

Discussion: A Neurological Cocktail , Anyone Else?

Support Group: Brain & Nervous System

Posted: Feb 15, 2023

Very sorry this happened to you. Yes the medical field and judicial system in this country...

https://connect.mayoclinic.org/comment/886106/

the question bc I would end up with crps

Discussion: Anyone been diagnosed with arachnoiditis after spine surgery?

Support Group: Spine Health

Posted: Jun 27, 2023