RSD Patient Seeks Community Support
In a telephone interview yesterday May 14, 2013 a Reflex Sympathetic Dystrophy patient stated she has temporarily lost custody of her 16 year old son to Department of Services for Children, Youth and...
View ArticleA New Beginning: My Life with RSD
A New Beginning: My Life with RSD. The above blog belongs to featured Blog Talk Radio Host Trudy Thomas. The Living with HOPE Radio Show is Sponsored by the Power of Pain Foundation. Living with HOPE...
View ArticleReflections Of…
The last week has been a bit overwhelming and my previous post somewhat confrontational. That is not the image I want left etched in the minds of my readers, followers or the communities in which I’m...
View ArticlePower of Pain Gets Ready for September: Pain Awareness Month
Pain Awareness Month is right around the corner. September is always a busy time for most of us. These are just a few of the Power of Pain Foundation’s events and activities during that time. Please...
View ArticleFight for Tomorrow
Always have faith that a better tomorrow will come. We have to or we won’t survive. The life of chronic pain becomes a family disease. In the last few months we have lost over a dozen people in the...
View ArticleStepping Up and Stepping Out with POPF (Power of Pain Foundation)
So many don’t realize what isolation is until they find worth in something or worth finds you. 14 years ago the injury, a right foot mid metatarsal separation changed my life. In my story Emotional...
View Article3 Girls with RSD/CRPS
Megan 15, Tori 15, and Gracie 11. Help These Girls Get the RSD/CRPS Treatment they need! Megan Manuel (15) http://www.gofundme.com/2f7l8g Megan needs a Spinal Cord Stimulator Tori Quinton (15)...
View ArticleThe Communities in which we strive for
I first began to advocate in 1985. I’ve told the story before at least in part. I was 15. I started college later that year. Majoring in Criminal Law, a minor in Drama/Professional Acting. It should...
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