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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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Magnate
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I'm in bad shape and have avoided the ER over the years, but due to insurance issues, this is my best option currently to try and stop new spread.
Thanks in advance. |
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#2 | ||
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Elder
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The ER, may be able to get you some temporary help. they also have the inside, on how to get to the best doctors as soon as possible. Can get you in to see a specialist faster. I had no insurance either, and this was the way to go for me. I wish you all the best. ginnie
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#3 | ||
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Magnate
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Ginnie, I am insured, that's not the issue at all. I've been hoping I could avoid having to go to the ER, but I'm experiencing spread due to a hold up of med approval (meds that have kept me stable for years.) I have a good RSD doc, but I can't travel the distance to him in my current state... I'll call him and ask what the ER can offer as well, but I was hoping for advise from others. Spread is in my jaw, starting across my teeth, and it appears my tongue. It hurts to eat and talk. My doc said he'd request a sympathetic block for my jaw at my last appointment, but things are escalating to a point I'm scared.
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#4 | |||
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Member
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The ER in my town took unnecessary x rays, assured me "this is just what happens when your body heals" called it good. Then, instead of billing my insurance, billed my past info and turned me into collections because I live at a new address and never received a bill. I will only go to ER if I was on the verge of death. lol just my experience.
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Synthetic right hamate hook. Rsd type 2 |
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#5 | ||
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Elder
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so very very sorry you are experincing that kind of pain. Hope you can get in touch with your doc. and get some sound advise. Try not to panick, but I do know how bad pain can effect someone. Let me know what you do, and if you can get that injection. My heart goes out to you. ginnie
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#6 | |||
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Member
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I went to the ER for basically the same thing. I specifically asked for a doc at the ER that knew something about RSD. I had to wait quite a while for him, but it was worth it. He told me that it was the Vegus nerves that the RSD was effecting. Meds given Gabapentin, Valium, Percocet, and if it the pain gets out of hand then IV Dilaudid. The trick as I know you know, is to stay ahead of the pain, otherwise it takes more big gun drugs to turn it back around. As far as a permanent solution… I do not know of one. But I do understand. It effects my teeth, gums, jaw, eyes, neck… absolutely no fun. So sorry hon. Hope you get relief soon!
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#7 | ||
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Magnate
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Quote:
Your info is greatly appreciated! It's by far the worst area I've ever had to deal with spread. |
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"Thanks for this!" says: | Vrae (09-20-2012) |
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#8 | |||
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Member
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Quote:
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#9 | |||
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Elder
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I haven't been to the er since being diagnosed with rsd.
I don't want them to think I am seeking drugs as I am already on all kinds of medications....I figure there's not much more they can do for me. I usually just suffer though whatever is going on, take my meds, go to bed, and wait to see what tomorrow brings. Sigh.... Abbie
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My avatar pic is my beautiful niece Ashley! . Rest in Peace 3/8/90 ~~ 4/2/12
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"Thanks for this!" says: | pooh_ac (09-23-2012) |
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#10 | |||
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Junior Member
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Be cautious of the sympauthetic nerv block. weigh your options carefully.i understand your options are limited but I say this because I had a sympathetic nerve block and I regret it wendy day.not to say you will because as we all know everyone responds differently I would just be cautious.i wish you the best.
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