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Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS) |
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August First is my birthday and it was last year on my birthday 2008 that my (ex...) orthopedic surgeon told me I had RSD
...gasp...racing heart...cold sweat.. I went home and stayed in the fetal position for a few hours from shock, panic, and fear... I had done some research on the net trying to figure out what was wrong with my foot and ankle, so I knew the 'kaboom' impact of those words.. I had mentioned in another post that I had asked him in June if he thought I had RSD and he said "no." So, I continued to ice and wear a tight brace to help me walk..then on my birthday, August 1st, yup, I remember the day vividly, he said the words...all wrapped up and with a pretty red bow lol, lol "I think you have RSD..." I had complained for five months after surgery of the inordinate pain..but he kept saying..it'll get, better..and essentially didn't HEAR me..or chose not to... A year has gone by..is this really my new life?? I can walk a few yards and .... no more walking,hiking etc,etc, etc...hey, but I still have my sight, i can hear the ocean and the birds...I am still working... One year later, as with all of us, I have made adjustments in my life, and trying to make friends with my new self.....I know my old self is still around..I guess my old self and new self will have to get along.. You, who have had RSD for years are my heroes, my guides... Those of you just diagnosed, it gets better as you become more knowledgeable and feel more in control as you learn how to become your own healer in many ways..sometimes out of necessity.. I've become quieter, more contemplative, more observant.. The gift of this site makes up a thousand-fold for that day last year.. Thank you friends, Hope4thebest xoxoxoxo |
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