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Old 06-17-2013, 11:53 AM #1
kaylee_s kaylee_s is offline
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kaylee_s kaylee_s is offline
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Default hi from a newbie
I'm brand new here. I was diagnosed with CRPS/RSD a few months ago. This scares me a lot. So I'm here to find some advice and support. Thanks!
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Old 06-17-2013, 03:34 PM #2
Lara Lara is offline
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Hi kaylee s,
Welcome to the NeuroTalk Support Groups.
I'm sorry you're dealing with such a painful condition. I'll post the link to our RSD/CRPS forum below where I'm sure you will find a lot of support and information.

Reflex Sympathetic Dystrophy (RSD and CRPS)
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Old 06-18-2013, 01:03 AM #3
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Darlene Darlene is offline
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Wink Nice to meet you!!
kaylee,

It is great to have you come and be with us. You will fine a great number of dear friends to listen when you are in need of ears. Please, just let us know how we can help you out. You will find out we are supportive and relaxing place.

Looks like Lara has given you the CRPS/RSD, and as she said there are a great number of friends there to help you with questions.

Please keep us up to date on your situation. Again welcome, looking forward to seeing you around. My thoughts and prayers are with you.
__________________

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"Life without God is like an unsharpened pencil -- it has no point.
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Old 06-21-2013, 08:33 PM #4
JcRush JcRush is offline
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Hi Keylee,
I was told I have RSD 4 years ago, I have it in my feet, I eat right, cause beleive it or not the food you eat does make a diffrence. in the winter i keep 2 pairs of socks on my feet to keep the senitivity down. If the air can't get to the skin it won' hurt. LOL In the winter I soak my feet in epson salt well the whole body the epson salt helps the whole body feel better plus it makes the skin feel soft. I hope you feel better.
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