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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Old 03-09-2010, 04:38 PM #1
mymomsadvocate mymomsadvocate is offline
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Join Date: Mar 2010
Posts: 2
15 yr Member
mymomsadvocate mymomsadvocate is offline
New Member
 
Join Date: Mar 2010
Posts: 2
15 yr Member
Unhappy In need of a miracle..like every victim of this disease.

Hey everyone,
My name is Danielle. I'm a 21 year old EMT-Intermediate, and also my Mother's advocate. My Mom has been suffering with RSDS for ten years now, and has attempted many painful test and trials such as Prolotherapy, and Nerve Blocks. Her symptoms include and are not limited to the swelling of her right lower limb, discoloration, hypersensitivity, severe pain, inability to ambulate for several days on end due to the pain, and many sleepless nights. We live near the Beaumont, Texas area and if not known, the Medical resources here are very limited. My Mom is only 44 years old, and I wish for nothing more than just to see her pain free for once, no matter the cost. I came into the Medical Field with hopes and dreams of helping people, and with the knowledge that comes with that, you feel more helpless because you know what's out there to help, but it's a matter of finding out how to get them there and get them the treatment that they need. It's terrible to know that someone hurts continuously for days to years at a time with no break. We have been to multiple Doctor's, from Beaumont to Arizona who all say the same dreaded sentence. "There's nothing we can do." If anyone knows of a Doctor, no matter how far, or a treatment that could possibly help, please let us know. And hopefully together, we can help build RSDS awareness, build knowledge and help others not suffer the same way.
Praying for a miracle,
Danielle.
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"Thanks for this!" says:
bobber (03-09-2010), hope4thebest (03-10-2010), Kakimbo (03-09-2010), SandyRI (03-10-2010), SandyS (03-09-2010)
 


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