#crps

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It’s too late….
IT’S TOO LATE……. This is something I hear a lot with all the doctors because CRPS NEEDS TO BE DEALT WITHIN THE FIRST 3-5 MONTH.. That is why a lot of this is so frustrating. I’m going on 2 years and 6 month and I waited over 2 years to see a pain specialist and now I’r seen 3 so far.. one was c
Kathy Surmon 🇨🇦

Kathy Surmon 🇨🇦

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Spent the day in the ER
Spent the majority of the day in the ER. Thank you chronic diseases that are slowly killing me. I haven’t eaten in three days and they say they can’t help but rehydrate me. Life with chronic pain and invisible illnesses. 😕😣 #fblifestyle #crps #gastroparesis
Jennie’s Journey

Jennie’s Journey

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Read the caption
You get used to hospital waiting rooms. You really do. You get used to the smell of antiseptic clinging to your clothes. The sound of machines beeping in the background while you sit there, waiting for your name to be called… again. You get used to feeling sick every single day—waking up and alread
Raven

Raven

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Chronic pain
Today… I’m spent. Not just tired — empty. I haven’t really slept in days. Last night, I cried myself to sleep again because the pain in my leg felt like it was going to explode. That deep, burning, pulsing pain that never stops — that’s CRPS. Chronic Regional Pain Syndrome doesn’t care about
Raven

Raven

8 likes

First post on here!
First post here! Not really sure what I should post on here so if you use this app often please lmk! Heres a lil introduction anyway.. Hey! I’m Jess, I post disability content online mainly about my wheelchair, CRPS and JIA. I have had JIA (Juvenile Arthritis) since I was 1 year old, and got di
Jess 🌻🧡

Jess 🌻🧡

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