Looking for support with CRPS

Hi! Yeah I do. Mine is in my hands and feet (mostly hands). I see you are a zebra as well🦓💜🥄

Hey, yeah I do, mine is full body.

I do have CRPS full body and EDS.

I have it in my right foot but if the pain is bad it goes up my leg

Wide spread CRPS🙋🏼‍♀️ So, who thought this would be a club we’d all join one day 💁🏼‍♀️

I also full body crps now and have internal organs involved. Never thought I would be joining a club/family like this

Look at Spero clinic in Arkansas. I had CRPS for years and this place actually worked. I occasionally get a flare but I am able to get through it quickly. I am living a much more fulfilled life with much less pain. It was expensive and I was there for 3 months but worth every penny to get my life back.

I have it bad in my legs

Hi! I have type 2 in (mainly) my left leg and my right foot. I had cauda equina and CRPS was a result of that spinal cord injury.

Robby, I had virtual consultation with Spero clinic, whats involved in going for full treatment?