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 08-08-2007, 11:04 PM #31
Goodn'Plenty Goodn'Plenty is offline
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Hey DwT and Lin Marie

I think somewhere in this thread I went over the protocol I just went through but I can cover it again.It is not in place of the going to Germany next year ,I just had to do something to get my flare under control!

On another note this is my my personal opinion of the Mayo.I have heard the same from several others- If you have cancer - get your butt to the Mayo .Nerve disorders run the other way - it's not their thing- they are light years behind.
I had a horrible time when I went to the Mayo. If you want more info PM me

Back to ketamine -This current protocol began with a SGB ( which is optional) followed by a 4 hour ketamine infusion a la Scwatzman protocol which is 20 mg /hr for 4 hr total 80 mg. It is what he calls his boosters .
This was followed by an at home oral ketamine regimen of 2 days at 40 mgs and then up to 60 mg a day .I think I was on it orally for a total of 12 days .
The oral dose is based on what you can handle .
I am 5'5 and weigh 105 .I would assume a larger person might be able to handle more .
However I was very highly motivated to feel better and I didn't care if I felt poorly .
This was what I wanted to do for me so maybe this was a good dose.
I was given ativan as a neuro protective agent .There are studies that prove that ketamine works better with a neuroprotective agent not just as an adjunct therapy to stop the hallucinations(at this dose hallucinations are unlikey but you do feel odd or other worldly).

Yes DwT I did feel rather odd the first week. You don't build up a tolerance to ketamine as it has a short half life and leaves the body very quickly (thanks T) but you do grow accustomed to the feeling.
I don't think I would be able to exist on that high a dose but I am going to discuss with my PM doc on Friday adding a lower dose to my med protocol-
maybe 10 mg AM and 20 mg PM . I notice the difference already in 3 days without.


Any highly motivated pain management doctor can get this going in their own area .
All that is needed in the outpatient setting is a RN to oversee the infusion of ketamine which is available in any hospital setting as it is an anaesthesia .
Oral ketamine is made in a compound pharmacy and is very inexpensive ( which is probably why it is taking so long for all of us to get it )


Please talk to your doctors about this .It is not rocket science and it works.
It can be made available to you if you make your doctor make it available.

Germany is next year
I get induced into a coma for 5 days and get massive doses of ketamine - way to much too handle while awake .
The goal is to reboot the computer.
When I wake up my brain will be working the way it used to - no messages of pain where there are no injuries

When I saw Dr, Schwartzman he told me I could do his wide awake coma treatment and I could have a 50% chance at a 50% chance of a reduction of symptoms.
With the full on coma treatment I have more than 50% chance at a CURE.

I like those odds .

The decision is much more complex than a simple matter of math but I have decided that the coma dose is the best option for me.
I believe I went over it all in my thread on " what Dr.S said ;trip to Philly and denial over" or something along those lines a few pages back.

Peace

GnP

Last edited by Goodn'Plenty; 08-09-2007 at 12:08 PM. Reason: who knows:)
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Old 08-11-2007, 01:01 PM #32
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I saw my PM doc and asked for oral ketamine as part of my meds protocol.
You know you have a great doc when he is receptive to any new ideas.

He told me that as of right now there are not enough published studies on the long term use of ketamine for him to feel comfortable treating me that way. As it is very toxic to the liver ,he would prefer that I only use it on an emergency basis for really bad flares( he will be happy to write the script) then as part of my regular med protocol.
As soon as more positive research is published that long term use of the drug is safe, he would write the prescription,but for now it is on an emergency basis .Good doc - cares about my liver.I do too
He did however call the compound pharmacy and have them make a topical ketamine cream for me right away .It is a 2% ketamine gel.It does give some relief to the burning pain - an option I can live with for now.

So that is it from the ketamine front for now.

I hope this information has been helpful to at least one other person out there.
I think it is really important that when any of us get to try new treatment options that we share them with others so that we are all at the forefront of groundbreaking news and treatment in the fight against RSD
That way we have more choices available to us
when looking at whats next for us in our in our approach to this disease .

Good Luck to all

GnP
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Old 08-11-2007, 03:47 PM #33
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Hi GnP,

The biggest fear that they have with Ketamine P/M Docs or Anesthesiologists is that your throat could close with Ketamine. Because you are not monitored.

Their 2nd, maybe some their first is being sued. This is why in the States they are more cautious. Much Love, Roz xxx
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Old 08-13-2007, 04:33 PM #34
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Hey Roz and all

I think it would be worthwhile to read this wikipedia article on ketamine

http://en.wikipedia.org/wiki/Ketamine

Ketamine is the safest and least restrictive of any sort of drugs in this class to the throat, nor is it prone to promote any breathing difficulties
The only reason my PM doc would not give it to me ( I do not speak for other PM docs ) is because of it's toxicity to the liver.

I would hate to end a very informative thread with questionable information.
it goes against all the information I have been told,
read or researched .

Roz hon - if you can find me some fact based evidence to back this up I would be happy to read it .OK

Much love and peace

GnP
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