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 10-05-2012, 01:33 PM #12
melanie75 melanie75 is offline
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Join Date: May 2010
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melanie75 melanie75 is offline
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Join Date: May 2010
Posts: 2
10 yr Member
Default Started Naltrexone & Ketamine Troches - CRPS, MS, & TM

Quote:
Originally Posted by Millerprof View Post
Has anyone used this med, or know anything about it? Apparently it has been helpful for many MS patients, and it seems it might be helpful for many people with autoimmune disorders (and there is some thinking out there that RSD is autoimmune).
Hi, I've been a Dr. Schwartzman patient since 2008 when I had my first Transverse Myelitis onset. Since then I've gotten MS and CRPS (stage IV) (diagnosed & treated rigorously by Dr. S... until recently as he seems to be heading toward semi-retirement).

I just began seeing Dr. Datta in Hackensack, New Jersey, an amazing, brilliant anesethesiologist and human being, who is working on what seems to be a trial of Naltrexone and Ketamine Troches (lozenges 3x/day). I'll also be getting my IV ketamine boosters with him from now on, and he'll be adding IV lidocaine, as well as increasing the dosage of Ketamine.

I hadn't heard about the Naltrexone for MS, but I'm a lucky multi-neuro-ite if this CRPS treatment will help both.

I'll keep you posted.

But if you want to get in touch, feel free to email me at ** I don't check my email often anymore - low-vision, etc; but if you make the subject clear hopefully I'll get back to you quickly.

Dr. Datta seems very excited about this new treatment regimen and states that he's seen patients (not stage IV,....) have complete remission or reduction of symptoms, though I'm not sure how long it takes. I think I recall him saying about a year, but my memory is unreliable.

Best to all.

Your neuro sister,
Melanie
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