Shakespeare once said "To sleep perchance to dream." Unfortunately, those of us with CRPS/RSD don’t see sleep that often and we rarely dream. The question of sleep is one we often bring up.. How did you sleep, did you sleep at all, how long did you sleep.. But no one ever seems to ask us… Continue reading To Sleep, Is To Dream
Category: legacy
Looking Towards The Future
I’ve lived in Groton, Connecticut for the past 23 years. I moved here when I was 4 safe to say I was pretty much raised here. I thought I knew and saw everything that my small town had to offer. I knew the streets, the buildings, the people, the changing of the crazy seasons that… Continue reading Looking Towards The Future
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!
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.
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!
My Journey With CRPS/RSD 