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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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boston rsd doctor needed

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Old 04-13-2010, 02:09 PM #1
glevine glevine is offline
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Default boston rsd doctor needed
Can you recommend a doctor in the Boston area who specializes in RSD?
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Old 04-13-2010, 02:46 PM #2
SandyRI SandyRI is offline
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I use Caritas St Elizabeth's Pain Clinic 617-789-3100.

Good luck. Sandy

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Can you recommend a doctor in the Boston area who specializes in RSD?
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Old 04-14-2010, 06:12 AM #3
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Originally Posted by SandyRI View Post
I use Caritas St Elizabeth's Pain Clinic 617-789-3100.

Good luck. Sandy
There is a doctor I believe her name is Ann Oaklander, MD or something along those lines. If you put it in a google the way I spelled it it should come up with the correct spelling and then go from there. I don't think she' out of Boston exactly but around the Boston or CT area. She is all over the internet so you should be able to find her if you have a problem write back and I will see if I can help...


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Old 04-14-2010, 06:13 AM #4
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Quote:
Originally Posted by SandyRI View Post
I use Caritas St Elizabeth's Pain Clinic 617-789-3100.

Good luck. Sandy
SandyR,

I forgot completely about her for you. I saw her name in an article in NYC just yesterday that's what made me remember. But maybe see if it's for you.
Sorry again.

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Old 04-14-2010, 06:17 AM #5
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Default Correct doctors spelling
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I use Caritas St Elizabeth's Pain Clinic 617-789-3100.

Good luck. Sandy
I looked it up myself it's Anne L. Oaklander, MD a neurologist out of Mass General, Harvard Grad.

Good Luck.

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Old 04-14-2010, 07:46 AM #6
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Hi Gabby,

Mass General and my WC insurance adjuster couldn't work out a fee agreement. I tried to get in there a long time ago. Thanks for thinking of me...

Sandy


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I looked it up myself it's Anne L. Oaklander, MD a neurologist out of Mass General, Harvard Grad.

Good Luck.

Gabbycakes
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Old 04-15-2010, 12:59 AM #7
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I am pm'ing you the name of the neurologist that I see. He was helpful in getting me dx'd and helping with the SSDI application process, but I don't think he is exactly cutting edge on RSD (meaning, he has suggested SGB. etc, but never mentions HBOT, ketamine, SCS, or implantable pain pump)
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