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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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#11 | ||
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Junior Member
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#12 | |||
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Co-Administrator
Community Support Team
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Hmm, sounds like he isn't interested in going out of his way at all.
![]() Seems like most up to date Drs would at least know how to find a good referral for a patient. I wonder if you medical insurance provider/carrier has a nurse line or "find a doc" on their website? Or possible your local hospital has a referral service that will be of help?
__________________
Search the NeuroTalk forums - . |
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#13 | ||
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Magnate
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SSDB? I'm familiar with SSI and SSDI...
I just want to clarify before commenting further. ![]() |
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#14 | ||
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Junior Member
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I believe it's like SSDI whereby I worked and paid SS taxes long enough to apply. I believe they refer to it as I had enough credits of working years to apply. It's not SSI.
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#15 | ||
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Magnate
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SS will send out CDRs, but yearly would be very surprising. The short form asks if you've discussed certain things with your doc, but does not require a signature from your doc. Social Security does not require special certification from doctors, all that is required is q valid medical license. Your doc's opinion, both upon initial application and during a Continuing Disability Review, is only one factor in regards to your receiving benefits. Even if you're sent to a "Social Security" doc, they can only give their opinion of the severity of your disability, they don't have the power to grant or deny your SSDI benefits. Your doc may no longer be comfortable supporting your disability claim. Or he might just be misunderstanding what's required of him. Please verify his signature is even required. If you can post the SS form number if you have more questions, that would help. ![]() Last edited by LIT LOVE; 12-16-2011 at 02:03 PM. |
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"Thanks for this!" says: | twocabinet (12-16-2011) |
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#16 | ||
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Junior Member
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#17 | ||
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Junior Member
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Does anyone know if Accupunture and RSD mix. I am thinking of getting it done and wanted to get input from others who may have tried it. Thanks.
I hope I am posting this question in the correct place. |
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#18 | ||
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Magnate
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You could start a new thread, since not everyone looks at every thread.
I've had it done and had some relief. I've also had a very scare experience of mirroring in my "good" hand caused by an IV needle in the same spot two weeks in a row. Accupressure might be safer. You just never really know with RSD... You're also unlikely to find someone with RSD experience. If you try it and have a flare--especially in a new region--treat the problem area quickly and aggressively like you wood with any new problem area. For example, I dropped something on my foot yesterday. A few hours later and my foot was ice cold and RSD pain was creeping up... I through on a Lidoderm patch and took extra breakthrough meds. The pain is reduced to a level that seems appropriate to the injury now, but the temperature regulation is still off... It took me about a week to get my hand back to normal after my IV scare. |
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