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1,363 total results

Comments (1,296)

Having CRPS in my feet and toes, are there any specific foods that are recommended for...

https://connect.mayoclinic.org/comment/43812/

Having CRPS in my feet and toes, are

Discussion: CRPS - anyone suffering with complex regional pain syndrome

Support Group: Chronic Pain

Posted: Jun 11, 2019

Hi I'm Renee. That's a really weird story , because it's MY story to the T...

https://connect.mayoclinic.org/comment/254844/

diagnoses then I break my ankle and get crps

Discussion: CRPS Question: Itching

Support Group: Chronic Pain

Posted: Mar 13, 2019

Hi I'm renee. I'm very familiar with crps, unfortunately I did a lot of research on...

https://connect.mayoclinic.org/comment/89156/

I'm very familiar with crps, unfortunately

Discussion: Complex regional pain syndrome or reflex sympathetic dystrophy

Support Group: Chronic Pain

Posted: Feb 15, 2019

Hi all, I have just been diagnosed with early CRPS in my right dominant hand and...

https://connect.mayoclinic.org/comment/795300/

have just been diagnosed with early CRPS

Discussion: Complex regional pain syndrome or reflex sympathetic dystrophy

Support Group: Chronic Pain

Posted: Jan 11, 2023

Welcome @socalfp, I know it must be hard for your wife having had to deal with...

https://connect.mayoclinic.org/comment/788004/

your wife having had to deal with the CRPS

Discussion: CRPS - anyone suffering with complex regional pain syndrome

Support Group: Chronic Pain

Posted: Dec 23, 2022

If you have the financial assets, the Spiro Clinic is the only place having su cess...

https://connect.mayoclinic.org/comment/751338/

place having su cess with a cure from crps

Discussion: CRPS - anyone suffering with complex regional pain syndrome

Support Group: Chronic Pain

Posted: Sep 19, 2022

Greetings. While ketamine infusions didn't work for my CRPS, it did for other patients at the...

https://connect.mayoclinic.org/comment/57682/

ketamine infusions didn't work for my CRPS

Discussion: RSD/CRPS

Support Group: Brain & Nervous System

Posted: Feb 6, 2018

I went to the Mayo Clinic summer of 2005 or 2006, can't remember (records in crawl...

https://connect.mayoclinic.org/comment/757230/

looking for a knee replacement for CRPS ... In the end, firm confirmation CRPS,

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

Support Group: Chronic Pain

Posted: Oct 4, 2022

@jeanniem Welcome to Mayo Clinic Connect, a place to give and get support. You have been...

https://connect.mayoclinic.org/comment/335686/

Have you found relief from CRPS? ... /connect.mayoclinic.org/discussion/crps

Discussion: Illusive Diagnosis, Pain Increasing

Support Group: Bones, Joints & Muscles

Posted: Feb 18, 2021

hi Ms Young, I was a nurse working at Seattle Children's hospital when I got covid...

https://connect.mayoclinic.org/comment/1262290/

pain specialist who diagnosed me with CRPS ... I feel some sense of support that CRPS

Discussion: Dealing with Post COVID and Complex Regional Pain Syndrome

Support Group: Post-COVID Recovery & COVID-19

Posted: Mar 19 10:31pm

No one in the family has had gout, my mum also has CRPS but hers is...

https://connect.mayoclinic.org/comment/1321916/

family has had gout, my mum also has CRPS

Discussion: Pain only on right side of body

Support Group: Chronic Pain

Posted: Jun 6 6:18pm

I'm depends on the source of the pain. Mine is due to a combination of CRPS...

https://connect.mayoclinic.org/comment/1146352/

Mine is due to a combination of CRPS

Discussion: Chronic pain people that fall through the cracks!

Support Group: Chronic Pain

Posted: Sep 23, 2024

Hi, I hope things are a bit better for her. Did you ever go to Mayo...

https://connect.mayoclinic.org/comment/1143580/

My 14 y/o has CRPS right ankle/foot/

Discussion: RSD/CRPS

Support Group: Brain & Nervous System

Posted: Sep 18, 2024

Hi, I have no idea what CRPS is, sorry. But you sound like you have an...

https://connect.mayoclinic.org/comment/788877/

Hi, I have no idea what CRPS is, sorry

Discussion: I’ve got the pain for CRPS under control…need help with the disease pr

Support Group: Autoimmune Diseases

Posted: Dec 26, 2022

DO NOT get a spinal cord stimulator as first treatment. Check spero clinic website as they...

https://connect.mayoclinic.org/comment/1040587/

as they treat a lot of people with crps ... One of the few MD crps experts in the ... I have crps in my colon. ... ve written here about my life with CRPS

Discussion: Best initial treatments for CRPS

Support Group: Chronic Pain

Posted: Mar 26, 2024

I have CRPS so my cytokines ate aleays elevated. Does insurance pay for that. It indicates...

https://connect.mayoclinic.org/comment/914172/

I have CRPS so my cytokines ate aleays

Discussion: Has anyone had cytokine testing?

Support Group: Post-COVID Recovery & COVID-19

Posted: Aug 16, 2023

My Grandaugher has CRPS diagnosed over a year a go. It is in both legs, the...

https://connect.mayoclinic.org/comment/629957/

My Grandaugher has CRPS diagnosed over