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Old 01-15-2014, 08:20 PM
joby7165 joby7165 is offline
Junior Member
 
Join Date: Jan 2014
Location: New York
Posts: 42
10 yr Member
joby7165 joby7165 is offline
Junior Member
 
Join Date: Jan 2014
Location: New York
Posts: 42
10 yr Member
Default Hello all,new to site and CRPS as well

Hello everyone my name is Joe,

I was diagnosed with CRPS on New Years Eve ( Happy New Year!! ,LOL!! ) Hey,if you can't laugh as they say. Last January I got a bad concussion at work that left me with chronic migraines,dizziness and memory issues. I've been dealing with a great neurologist since September,previous one,not so great. None of the typical drugs have helped so in November he gave me botox injections,still waiting to see if they'll help.Now for the CRPS issue.

On December 3rd I was just getting over a three day monster migraine. I was dizzy,lost my balance and hit my right hip on the outside corner of my metal bed frame. It took me awhile before I could attempt standing and when I did try I fell again but landed on my right arm,too much pain to move.

Went to the ER,nothing broken,just badly bruised. Several days later my right foot swelled up,then my lower right leg,then around my right eye which looked like an allergic reaction.All the swelling went away 2 weeks later but then both my hands began to tingle. A few days later my right hand began to hurt like a sun burn,then worse like I stuck it in a wood stove.Then the pinkie and ring finger on my left hand. It's always worse at night and I no longer sleep at night but during the day when I can. The pain isn't horrible like I've read from other sufferers.

I have started occupational therapy and even though I am confident in the knowledge of my therapist I don't think she has seen my condition that often.I am sorry to run on this long but I wanted to give you all my info for I know that those of you on this site are sufferers as well and you know how I feel. I've read that the sooner you treat this condition the better chance I have of controlling it but that's no guarantee. I guess my main concern is even with rehab how quickly will this disease progress and what should I expect? I know there are no guarantees but any info would be greatly appreciated,thank you so much and to those that created this site words can't express my gratitude.
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