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 08-28-2013, 11:55 AM #1
tkayewade tkayewade is offline
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Default Oral Ketamine

My pain doctor referred me to a doctor today who is doing oral ketamine for crps/rsd patients that are not having a lot of success in other areas. Y'all have seen my struggles of late in finding relief. Has anyone tried this? Please give me good and bad experiences. I've been reading research that make it seem like giving it a try is worthwhile, but I am not sure as it doesn't seem like they have been using it long.

Also, it seems like insurance doesn't pay as it is "off label" use for crps.

Any help would be appreciated!
Thanks. I hope everyone is having low pain days!!

TK
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Old 08-28-2013, 12:19 PM #2
alaska49 alaska49 is offline
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What kind of oral ketamine, in pill form, nassal spray, or lozanges?
I take the lozanges amd nassal spray and it has done wonder for me. Before I was doing the ketamine infusions, but still ending up in the hospital every 2-3 weeks in a flare. Now I am going up to 5 months sometimes without a flare up. I have also tried the pill form but that didnt give me any relief. For the pill form my insurance wouldnt pay for it, but they are paying for the nassal spray and lozanges. I havent had any bad side affect only positive outcomes.
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Old 08-28-2013, 02:09 PM #3
Jimking Jimking is offline
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I've always gotten the impression oral ketamine was used primarily as a booster after ketamine infusions?
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Old 08-31-2013, 06:08 PM #4
89danboy 89danboy is offline
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Default Nasal spray

Quote:
Originally Posted by alaska49 View Post
What kind of oral ketamine, in pill form, nassal spray, or lozanges?
I take the lozanges amd nassal spray and it has done wonder for me. Before I was doing the ketamine infusions, but still ending up in the hospital every 2-3 weeks in a flare. Now I am going up to 5 months sometimes without a flare up. I have also tried the pill form but that didnt give me any relief. For the pill form my insurance wouldnt pay for it, but they are paying for the nassal spray and lozanges. I havent had any bad side affect only positive outcomes.
I think u said your nasal spray is 50 mgs per spray , and take 2 sprays x3 aday for 300 mgs,what does your prescription say ,I'm taking the 10% ketamine that isn't helping much,10 mgs per spray 8 sprays aday.thats the main reason it's not helping,but my dr is retarted.i tell her the starting dose is 100 mgs 3 to 4 times aday. The dr in sandiego and your dr in Rhode Island or somewhere in the north east.both drs are really making a difference .the sandiego dr is nancy sajben.if you haven't looked her up yet,check out her web site ,she goes in to detail about her ketamine nasal spray,also she starts out with 100 mgs x4 aday and losanges.and she does this low dose naltrexone,.i just wanted to know if your spray says 50% ketamine on it and what compound pharmacy do u use,cause my pharmacy is a mess trying to compound it.thanks hope your doing well
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Old 08-31-2013, 06:56 PM #5
BrokenHealer BrokenHealer is offline
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Shocked I've seen your posts about Ketamine therapy

Hi,

Would you be kind enough to share what you've discovered about nasal spray and lozenge treatment. CRPS robs me of my humanity, sleep and civility.
If I had a dog in my condition, I would have it put down humanely.

I'm in the Chicago area. Do you know of a physician who uses oral ketamine? Thanks
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