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Jeanie |
Have either of you had a chance to meet other RSDers in person that have been successfully treated with ketamine? I have.....and that is why I have tried so hard to get it. I know people who feel their lives have been literally saved by the infusions.
We have a support group in my area that meets once a month. The leader of the RI RSD Foundation started receiving ketamine in Boston at Beth Israel on April 16, 2009. (The BI's program has since been closed to new patients.) Her story is very compelling. I won't ever give up trying to get better. I HATE being sick. My injury is a WC injury. I want to go back to work ASAP. I've tried everything else. XOXOX Sandy Quote:
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Hugz, kathy |
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How are you ?? Unfortunately, I do not have access to a local support group, other than my friends here. Not one in my area, I checked and I have not met anyone personally who has under gone the Ketamine treatments..but I am keeping an open mind as maybe one day, as we are all being backed into a corner... possibly there will be more Dr.'s who perform this intervention, less travel.. and it becomes the treatment of choice, not pushed aside like the SCS and blocks... and if only the insurance companys would be on board and not deny us.. as far as medicare, I checked into that and once we become a SS recepient, you have to be on it for 2 years before coverage, unless I am all wet on that.....I, like many would be all over it if we could achieve pain relief.. so far I am now on my third appeal with my HMO and I am losing gas as my next appeal is a teleconference with an insurance committee and I can not formally present documentation that the Ketamine is not considered experimental...so they got me again..Plus, I have a NYS dept. of Ins. rep. working on my case but they can't help due to the same reasoning...plus my congressman, who has a disabled daughter..he is a good listener but the juice of choice is our stumbling block!! Is Jeanie still paddling this boat?? Who turn is next???? Hugz, Kathy :grouphug::grouphug::grouphug::grouphug: |
Don't mean to jump in here out of turn - but ketamine has become an "accepted" treatment for RSD. That's what Getson's office tells me, anyway. I understand that Dr. S. is really strong with insurance companies. Has he or his office done any work on your behalf? Has there been any impact on your case because of the 2 double blind studies that were done last year by him and in The Netherlands?
How cool that you in the pharma industry. That means that you really understand this stuff better than the average joe... Interestingly enough, the women to whom I referred to in my previous posting, who has been getting ketamine infusions for a year now in Boston at the Beth Israel, was approved for the treatments by United Healthcare. She is only liable for her deductible. Because she got her life back I am really happy for her - she is really nice and she and husband deserve it (heck - we ALL do!!!). But I often wonder how it could be that it was so easy for her while I'm being tortured for approval over the same treatments by the same health care company....ugghhhh... Take care Kathy, xoxoxo Sandy |
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I love visiting with ya..Yes, I have been knee deep in the pharmaceutical trenches for 25 yrs...and loved it... got the lingo and medical background..sadly my RSD pulled me away from it.. I did crawl with my RSD there for 3 years but could not do it anymore... Dr. S's office said they can only say it is used "off label" as far as they are concerned and the ins. company can't get past that... as their interuptation is saying then it as experimental then... I have been working with Dr. S's in getting documentation together for my conf. with United health Care based, MVP ins. actually..and Dr. S's told me they have never known any private ins. to approve 5 the day sleep, thats where I lost my gas in my tank... still yet to be refilled!! I am tickled for anyone who can go forward..I hope and pray that others will benefit for life!! And I am equally sorry that you, my dear are being tortured also... hang in there..You are a fighter ..we'll see this thru!!! Hugz, K:grouphug: |
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God Bless all Jeanie |
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Oh my... Jeanie..you have been up front paddling for a very long time..as I sit back enjoying the ride..soon we must switch, as I believe I will be causing you reason to drink and take a turn to relax.. after this post....I gotz yur back!! I so appreciate your prayers, my friend.. Luv, Kathy |
I think everyone of you has made a valid point.. I really wont pay for my appointments.. but wc owes me that. I feel that i am never going to be desperate enough to try the scs. I know the risks are too high, i dont want faster spread. I dont want down for the time for the leads to stay placed, i dont want any of that.. On the other hand i will get desperate enough for pain relief.. But my problem isnt the pain per se,, its the burning that gets to me.. The pain i tolerate, the burning drives me insane..However i havent had anything for pain either, so i have had to tolerate it without any aids.I agree that most drs just are out for the money,, and we need a cure. And i believe someday we will get that cure.. But until that happens we still have to deal with those drs to get the meds we need or the treatments we need to stay mobile. I dont think we can really point fingers at just the 2 drs whose names are on this thread, because i can give you several more that are much worse.. Atleast they are trying to help, whether it is just to push the ketamine or the scs..I realize that it is probably just for the money, but we need help, we cant do this without drs. everyone knows this... ok.. I am done rambling. sorry..
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forget my post.. i didnt go all the way through i guess.. ks i really hope and pray you can get your ins to go through and you get the treatments you deserve..
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