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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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#1 | ||
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Hey everybody! I'm so sorry I haven't been on in a long time. After the miscarriage I didn't do much of anything online. I'm way better in that regard. So the CROS might be going into remission in my left arm. However they think it's moving to my legs. ..... I already spent 2 months in a wheelchair over the summer. Then I lost my job and since I haven't had to be on my feet anymore it's a little bit better. I can walk on my own now but the massive swelling is coming back... I'm getting a little bit overwhelming and scared but trying to stay positive. There's a new specialist that has spent her entire education/career studying crps and PN so I might be able to get a much clearer diagnosis! I love you all! Wish me luck!
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#2 | |||
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Hi Bird,
I'm sorry for your lose. Battling CRPS is bad enough without all that else can happen to us. Much luck on the new doctor. I hope she helps you find relief...
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Hope for better days..... Russ okska'sssini ómahkapi'si . Last edited by Russell; 09-25-2014 at 01:54 PM. |
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"Thanks for this!" says: |
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#3 | ||
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Senior Member
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Hi Songbird. I'm so sorry for your loss. I am also sorry that your rsd is causing you so much pain and has spread. I hope that the new specialist you're seeing can help you. Don't give up hope my friend. My thoughts and prayers are with you. Take care.
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RSD ME . |
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"Thanks for this!" says: | CRPSsongbird (09-26-2014) |
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#4 | |||
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Hey Bird!
Great to hear from you, but sorry for your struggles. I have been thinking about you and wondering how you are doing. I hope that new specialist can help you out...wish I could find one around me that knew something about this horrible disease! I have not been on here much myself, but do pop in on occasion. Been having a rough time myself too. Anyway, so good to hear from you. Sending you hugs ![]() ![]() Nanc |
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"Thanks for this!" says: | CRPSsongbird (09-26-2014), Phaedra (09-25-2014) |
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#5 | ||
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Quote:
Hugs right back at you! I hope you're feeling as great as you possibly xan! Sometimes what helps me most is to just focus on the wonderful things that are all around us. Sometimes they're hard to see, when we're blinded by the fog of pain, but love, especially God's Love, can burn that fog away just like the beautiful sun! I'm having one of the most severe flare ups tonight. I can't sleep, I just barely stopped crying from it, but I think the worst is passing. Love to you! Stay strong! |
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"Thanks for this!" says: | Nanc (09-27-2014) |
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#6 | |||
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Wisest Elder Ever
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I would like to suggest that you get tested for B12 deficiency and if you are below 400pg/ml--- get that result in numbers--- to
begin B12 supplementation ASAP. Neuropathy that spreads to legs can be due to combined degeneration of the spinal cord, which is a serious life threatening form of low B12. Since you have one opinion of "neuropathy" this should be looked at before you become permanently disabled. Also get Vit D tested... low D impacts chronic pain in many patients with chronic pain. Sometimes just fixing this, leads to relief. (we have had PN patients here on our board who discovered this result). This long video explains more: http://www.youtube.com/watch?v=BvEizypoyO0 It is very sobering!
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All truths are easy to understand once they are discovered; the point is to discover them.-- Galileo Galilei ************************************ . Weezie looking at petunias 8.25.2017 **************************** These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here.
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"Thanks for this!" says: | CRPSsongbird (09-27-2014), visioniosiv (09-27-2014) |
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