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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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LIDOCAINE PATCHES.....just had a flare up and went to PM doc...he put 2 on me. One under my arm and the other over my bicep(believed injury site). Sigh..........finally a little relief!
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"Thanks for this!" says: | birchlake (12-05-2012) |
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Wisest Elder Ever
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Thank goodness... I am glad you finally got them.
__________________
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 (12-05-2012) |
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#3 | ||
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Junior Member
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Glad you are able to wear them, I have them but I often can't wear them because it just hurts to even have the patch on me because of the hypersensitivity. Was at first this a problem for you?
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"Thanks for this!" says: | CRPSsongbird (12-10-2012) |
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#4 | ||
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Quote:
![]() Last edited by CRPSsongbird; 12-05-2012 at 07:26 PM. |
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#5 | |||
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Wisest Elder Ever
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Sometimes, and I mean sometimes....
The lidoderms will cause a remission. This is only if the nerve is just "overfiring" for some strange reason. You need to use them for about 2 weeks or more daily, to see if this happens. If it doesn't work it doesn't. But if it does, you are very lucky. It happened to me with MP... so it is a possibility for you.
__________________
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 (12-10-2012) |
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#6 | ||
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In Remembrance
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I believe that lidocaine, (and other meds) are available as gels that are 'formulated'. Much, much stronger than something like menthol ice. And, I've NEVER had an issue with contact pain with a formulated med.... You might want to check that out. You may or may not have a formulating pharmacy near you, but your dr will know where there's one that ships.
pete |
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"Thanks for this!" says: | CRPSsongbird (12-10-2012) |
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#7 | ||
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Elder
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My doctor gladly gave me lidocain patches today. I had been told on NT. that medicare and medicaid would cover them. However I was denied. Who has what medicare part D carrier. I have humanna and am sick of writing begging letters. I need some help to find new insurance. I called AARD, and united way with no better results. Can you give me directions? Why would insurance company allow morphine but not this non-opiate patch.? Earlier I was denied medication to breathe for asthma. This is making me very very sad. ginnie
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#8 | ||
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With the new regulations Obama put on insurance comps I though they couldn't do that anymore. Well I'm sorry to hear that! I'm trying to gt the
"claims"through hospital that caused this to approve a regular prescription for me. It's almost worse than the insurance........like trying to squeeze blood from a turnip. ![]() Not sure what you can do other than maybe write a letter again ![]() |
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#9 | |||
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Senior Member
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Quote:
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"Thanks for this!" says: | CRPSsongbird (12-10-2012), mrsD (12-06-2012) |
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#10 | ||
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Member
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I feel like screaming.... pain back meaner than ever Lidocaine finally fully wore off.... PM is out of town until Monday. PCP can't see me for 2 weeks.....Ans Specialist is gone till monday as well....looks like its back to the ER........I am crying from the pain.....or trying not to....
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