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Old 03-02-2010, 09:57 PM
loretta loretta is offline
Senior Member
 
Join Date: Feb 2007
Posts: 1,090
15 yr Member
loretta loretta is offline
Senior Member
 
Join Date: Feb 2007
Posts: 1,090
15 yr Member
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Quote:
Originally Posted by Chrome1972 View Post
Greetings all, I've nothing to hide so I'm not going to beat around the bush. My name is Keith, I'm 38, Live in Denver, CO., I'm married for 15 years, have 2 children and I have CRPS/RSD. When I was 15 I was hit by a van crossing the street on a dirt bike. I broke my left leg intially in 7 places. 2 breaks were compound fractures and one of those was caused by the foot peg going through my calf. The othe compound fracture left an 11" scar on my inner side of my left leg centered around the knee. I spent 3 months in the hospital and 3 months in a rehab center learning to walk again. In 2005 I re-broke the same leg, giving myself a Tibia Plateau Fracture. The surgeons graphed cadaver bone to the site and screwed three screws into my leg. 4 months later I had an arthroscopy done on my knee (spelling?) an Achilles tendon lengthening and a release and fusion done on my left foot. I sat around for 2 years and found a really decent job, in my field of work and right before they were going to hire me I was pulling a lousy pallet jack and tore something in my left knee and haven't worked since. I managed to make that job last 2.5 months, if that.
I was diagnosed with RSD/CRPS, Type I on Aug. 7, 2009. I am quite upset that with all the symptoms and all my complaints of unyielding, mind-numbing pain, as well as a color changing leg, no doctors would tell me what was wrong. Instead they chose to treat me like I was some pill popping junkie. Yeah it's all in my head, right? That's what some of them remarked. In any case I'm happy to have found what seems to be a supportive site. I look forward to chatting and debating things with all of you, take care......
Wow, you have been thru so much. I hope you have a good RSD Dr. that will help you keep mobile and care for the challenges that come up. I, like yourself, went undiagnosed for 4 years. Mine started with surgery and now is spread full body, generalized, along with internal orgn involvement.
Many of us have been helped with psychiatric help. When I was diagnosed full body, I need some help to cope with the pain and growing difficulties.
RSD is known by the government as an acceptable disorder for disability. I've had it for 15 years, but now with meds, and spread, I've decided to apply for disability.I've just lost my health insurance-will be 62 in May-and have my Drs. support.
Welcome again, and please feel free to join right in. One of your new friends, loretta
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