Rezultati pretraživanja
  1. “One of the biggest problems with flare ups is the fact that you don’t know how long they will last. This very fact can cause… and frustration…and isolation. flare-ups can last hours, days, weeks or even months.”

  2. Top 12 CRPS & Chronic Pain Articles You Need To Read from inc 🧡5 Common Myths of CRPS Flare Ups 🧡Complete Guide to Dorsal Root Ganglion stimulation for CRPS

  3. 31. sij

    Thought of the day Chronic illness will show you two things very clearly: The amazing compassion of some people you hardly know at all, and the disgusting selfishness of some people you thought you knew very well.

  4. Thought of the day Imagine waking up every day, not sure if you can go to a store, take a shower, eat a meal. Chronic illness requires learning the balances between surrendering and fighting. And no one even knows you are in a battle.

  5. Have you been diagnosed with Complex Regional Pain Syndrome or your partner or family member has been affected by CRPS? Join us at our next CRPS support group in Manchester on Thursday 13 February 2020

  6. prije 1 sat

    Everything went well so far. I‘m awake again. My back burns but it will be fine. My legs pain is worse. Now waiting for the doctor and everything. But look at that view 😍

  7. 2. velj

    Are you affected by Complex Regional Pain Syndrome either as a patient or loved one? Our next support group in Manchester is 13 Feb 2-4pm This is a chance to meet with others, to learn more about the condition & know you’re not alone with this

  8. Why a picture of sneakers? Because it's the first time in about 13 years my pain levels have been controlled enough to wear shoes I like (with leather and laces!) all damn day.

  9. I have learned a new taping method to reduce swelling! And yeah, my leg’s red. thing.

  10. 5. velj

    Thought of the day My pain is real. In this age of technology ignorance is a choice. If you don’t know or understand my pain my Google it, read a book or just ask me. . . .

  11. Odgovor korisniku/ci

    People don't get what we live with. Stay strong sister!!

  12. 30. sij

    Thought of the day The worst thing about chronic illness is the unknown. It’s always a part of your life regardless of how you’re feeling. Even on your best day, it’s just lurking in the shadows, ready to strike at any moment.

  13. Odgovor korisniku/ci

    Hi! We need more of this positivity :D I have and general depression/anxiety. But I stream to make friends and take me out of these 4 walls my life is reduced to 👌 I do lots of charity work because we need to keep trying to make the world a better place ❤

  14. prije 7 sati

    Fellow warriors, has anyone heard of pain affecting multiple areas? had chronic pain in my right neck/arm for 5 years now. But 2 years ago I also started getting nerve issues in my right foot. always wondering if I truly have CRPS or if multiple things are at play.

  15. prije 9 sati
    Odgovor korisnicima

    For me the pin head is the hundreds of little tiny pin prick electrical taser shocks I get on my face/jaw & inside my ears. Talk about pain! This is a million fold type pain.

  16. prije 12 sati

    You know that horrible nerve pain you feel when you eat something too cold and you need a root canal? Imagine that nerve pain, constantly, in your knee. That’s my reality today. Happy freaking Wednesday y’all.

  17. prije 16 sati

    the HAS REMOVED A MEDICATION THAT HAS BEEN HELPING ME SINCE JULY 2019. I WAS GETTING KETAMINE INFUSIONS FOR COMPLEX REGIONAL PAIN SYNDROME . THEY BELIEVE IT DOES NOT HELP. MY HAND SAYS OTHERWISE SIR. I DO NOT HAVE THE MONEY TO PAY FOR TREATMENT

  18. Yes... Flaring for almost a week now.. 😵😩

Čini se da učitavanje traje već neko vrijeme.

Twitter je možda preopterećen ili ima kratkotrajnih poteškoća u radu. Pokušajte ponovno ili potražite dodatne informacije u odjeljku Status Twittera.