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Support With CRPS

Lately I've been getting several emails from fellow CRPS warriors on how to deal with this diagnosis. I've found a great website that can help you guys out..It's called IPain and they have incredible service and support internationally! I hope this website gives you guys the help, info, and support that we're all looking for!

Blog · Complex Regional Pain Syndrome · CRPS · Invisible Illness · legacy · Life · Personal · Platform · Reflex Sympathetic Dystrophy · RSD · Sponsor · Work

Not Being Able To Work Because Of Invisible Illness.

“No one realizes that a job does more for you than just pay your bills. It is part of what gives you self-esteem. When you can’t work anymore, it is very hard to see yourself as worth something to people. You feel isolated because everyone is so busy with their lives they don’t have time… Continue reading Not Being Able To Work Because Of Invisible Illness.

Blog · Complex Regional Pain Syndrome · CRPS · Invisible Illness · legacy · Life · Personal · Platform · Reflex Sympathetic Dystrophy · RSD · Truth To Power

CRPS FACTS!

I have been living with CRPS for about 4 years now. CRPS is the most painful disease known to mankind. More painful than unprepared child birth, stage 4 cancer, and even amputation according to the McGill Pain Index. The pain never stops and when it flares up I can be in bed for days or… Continue reading CRPS FACTS!

Blog · Complex Regional Pain Syndrome · CRPS · Reflex Sympathetic Dystrophy · RSD

My October 21, 2016 Letter For You. 

Thank You all for your kind words during this rough time in my life once again. I know many of you had no idea that I was going to be having surgery yet again and on the same Right Foot that I was diagnosed with CRPS last year in February.  It was very hard to… Continue reading My October 21, 2016 Letter For You. 

Blog · Complex Regional Pain Syndrome · CRPS · Reflex Sympathetic Dystrophy · RSD

Beauty In The Fragile Fighter 

There is beauty in the courage of the fragile fighter. Those that persevere, despite all they’ve been through.      Yesterday and today I've been getting emails from two women who have been diagnosed with CRPS and don't know what to do. One lives in Canada and the other in Minnesota. It's crazy that I'm… Continue reading Beauty In The Fragile Fighter