CRPS Warrior Kathleen Coleman's Story

Kathleen Coleman talks about her journey with chronic pain and a brain injury.
Reposted with permission from Jaybird Media (jaybirdmediagr...)
To learn more about complex regional pain syndrome (CRPS) and reflex sympathetic dystrophy (RSD), visit Reflex Sympathetic Dystrophy Syndrome Association (RSDSA)’s website at rsds.org.
#RSDSA #CRPS #RSD

[@PL-vh4qn]

I’m proud of you and TY for serving! I’m thinking of moving my way down to AZ from the Midwest. My suffering has been too long, since childhood crashing into a tree on a snow sled.....how does AZ improve you? TY, PJ

[@luke144]

I've been struggling with CRPS for about 8 years now and have just come to terms with it. A lot of what you said resonated with me. Thank you for sharing your story with me!

[@jesswhycamarz]

I have been living with CRPS for 1 year this month.....I am luckier than a lot of other warriors because I was diagnosed early, but this illness...it has taken a lot from me. Seeing this video was comforting. I don't know how you made it this so far Kathleen, but I am so happy you have. You're a badass. I hope your pain days are manageable and you continue to search for the light and meet new friends who appreciate and understand how rare you are.

[@dr.premlatadangi3676]

Hi jexxx how are you .know you have no pain.id it true ? Is it possible?

[@Shafe-cv5zb]

Hello, you are an angel, your message is heartfelt and beautiful. I needed to hear this today. I am a 14 yr warrior. I hope and dream that new technologies and advancements can help someday. You have a new friend. Much love, joy and peace.

[@kimberlyhoughton3406]

Kathleen you are a shinning ⭐️ and inspiration to us RSD warriors. I was diagnosed in 2006, nursing accident at work. I have CRPS in my right knee that has gone systemic body wide 24/7 severe pain. My grandchildren are my blessings that help me push threw the pain, try to enjoy life in a new way! Soft hugs and you have a friend here ❤️

[@lorahargrove9710]

I have crps / rsd you have a new friend. You are encouraging. 😁

[@jenniferbowman7845]

I have had crps since 2003. I can relate to the hardships. Thanks for sharing your message. It really helped more than you know.

[@nobody-rr5ln]

You were extremelly beautiful madam! ❤❤. I m very sorry for you.. i didn t find more efficient than putting ice scratchs on my extremities, wrists, forearms, elbows, soles of the feet, back neck and occipital skull. What about all other people here? Thanks for your answer.

[@dpauls3351]

Thank you for sharing your story. I too have CRPS. 16 month. I'm a nurse who is finally accepting my whole life has changed and grieved the loss of my old life. Thank you for the advice to look for the shining bright moments God will provide to help me get thru it, as you know very hard to see it this way. Thank you for helping me.

[@syamsai3038]

Can anyone suggest best doctors in India who are dealing crps

[@nancyries2534]

I've had it since 2000. It's not easy .bright side?.

[@franwintermute2046]

I have had crps for 23 years July 1994 it is a very hard ship in side and out some days you dont no how you are going to fill that day I would. Love to share how I got crps on you u tub on live tv or rush sant luck hospital What thay have done for me so far iam so bless right now but I no I have to xsp who iam today and many more day to come in my life god bless you

[@franwintermute2046]

Chicago ill

[@dr.premlatadangi3676]

What type of treatment you get there.

[@dr.premlatadangi3676]

Hi please reply what kind of facility or treatment they provide.