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 03-13-2016, 02:54 PM #1
89danboy 89danboy is offline
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Default Woke up in a painful flare

I was having a decent month ,first time in a while.today I woke up and wasn't able to get walk without extreme pain,feet and legs are burning and feels like I have 105 fever.the anxiety really effects me ,any noise or conversation aggravates my mind and it's unbearable .hoping it doesn't last too long,my lady flare I suffered badly for almost 3 months it was very hard to get thru and I feel that way now,I hope every one is feeling well .no of us deserve to feel this way.
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Old 03-13-2016, 08:21 PM #2
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Sorry to hear this...hope is passes quickly. Keep us posted...you are in my thoughts and prayers.
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Old 03-13-2016, 08:41 PM #3
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Quote:
Originally Posted by 89danboy View Post
I was having a decent month ,first time in a while.today I woke up and wasn't able to get walk without extreme pain,feet and legs are burning and feels like I have 105 fever.the anxiety really effects me ,any noise or conversation aggravates my mind and it's unbearable .hoping it doesn't last too long,my lady flare I suffered badly for almost 3 months it was very hard to get thru and I feel that way now,I hope every one is feeling well .no of us deserve to feel this way.
I really hope that this flare passes quickly for you. Many of us know exactly what you mean by others conversations being difficult to bear sometimes. It's just the noise. You are in my prayers as well. Hang in there!

-Spike-

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Old 03-13-2016, 09:16 PM #4
RSD ME RSD ME is offline
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hi dan. i'm so sorry you are having a bad flare. rsd is hard enough to deal with without the flares. i also understand how you feel. i have lived through some horrible flares and also anxiety and pain from noise due to rsd. i think the pain from noise is called alloydnia (sp?). not all people who have rsd understand this pain but we all do here. when i have a flare i get my emergency rsd kit out. i learned how to do this from a dear friend here a while back. they are made up of things that provide comfort during an rsd flare. the kit can vary from person to person. mine usually includes the following: heating pad, lavender epsom salts, chamomille tea, shortbread cookies (lorna doones) i know i'm old lol, soft cotton lightweight short sleeved pajamas, a nice comfy bed and a favorite tv show or music to calm my nerves. my pm dr and physchiatrist (sp again?) also have prescribed breakthru pain meds for the rsd and fibromyalgia pain and antianxiety and antidepressant meds to help with the panic attacks from the pain. and last but not least i keep reminding myself that my flare will eventually pass and i can get through it in the meantime because i have done it in the past. you can do it to. having a support system from my family and NT gives me strength to face each painful day with rsd. you are not alone here and i am sending some soft hugs your way. i hope your flare ends soon my friend and i wish everyone here a painfree as possible night tonight.
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Old 03-18-2016, 10:12 AM #5
Seaglass1972 Seaglass1972 is offline
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Default Flare ups

I am still new to all of this and trying to find ways to help my flare ups.

I hope you are feeling better today.
Keeping you in my prayers.
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