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 10-15-2016, 10:01 AM #24
Shay08 Shay08 is offline
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Join Date: Sep 2016
Location: Northeast PA
Posts: 86
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Shay08 Shay08 is offline
Junior Member
 
Join Date: Sep 2016
Location: Northeast PA
Posts: 86
5 yr Member
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Quote:
Originally Posted by PurpleFoot721 View Post
Yesterday I had a follow up appointment with my PM. I learned a little about his background and experience with Ketamine and patients with CRPS while going through a handful of questions that I had for him. He loves having me as a patient, because I always have a list of questions to ask.

I was wondering where he ended up getting his Ketamine protocol from, and his answer surprised me. The team of doctors that work in the practice he is at, put their protocol together based on what all 4 of them felt comfortable doing. He doesn't like using it much because based on his past experience, it is usually an ineffective protocol for treating CRPS.

I underestimated his knowledge and experience dealing with CRPS patients. It turns out, he did his residency and fellowship at Thomas Jefferson University Hospital working under Dr. Schwartzman when he was there back in the late 80's and into the early 90's. During his time there, they were doing studies on the effects of Ketamine for, RSD/CRPS. During my PM's time there, he saw over 200 RSD/CRPS patients.

With all of the work that he has done with Ketamine and CRPS patients, he does not feel that I would benefit enough from the protocol that his office uses, even though I did manage those 3 days of a fair amount of relief, allowing me to moisturize, and massage my foot during that time. He feels that because of the severity of my case, I would only benefit from an inpatient infusion done in an ICU. Since I did manage to get some relief though, he prescribed a compounded cream for me that has a combination of Ketamine, Gabapentin, Amitriptyline, Lidocaine, and I think there was something else in there as well, but I do not remember. I will find out when it comes to me next week. He is not sure if it will help, but feels that it may help a little. Every little bit helps, so I am willing to try.
Alaina,

Thank you so much for the update. It really explained a lot of questions that I had with the protocol that you received. I really wondered how effective such a low dose over so few days would be for you. I was really happy when you reported some pain relief.

I now understand why your doctor made some of those comments to you about your pain levels during the week you had the infusions. When I saw Dr. Schwartzman in 2011, he felt the 10 day low dose outpatient would work for me. The other protocol was a five day moderate dose inpatient infusion. I have continued with the two day boosters every three months and they do help.

Please keep us updated on the compounded cream and let us know if you decide to go further with the ketamine infusions. It is so great that people on this forum are so willing to share their experiences with different treatments.

Thank you

Shay
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"Thanks for this!" says:
BioBased (10-15-2016), Littlepaw (10-19-2016), PamelaJune (10-15-2016), PurpleFoot721 (10-16-2016)
 

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crps, day, experience, ketamine, outpatient


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