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 05-01-2009, 07:50 PM #1
AintSoBad AintSoBad is offline
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LWood,
I go to Dr Knobler, he's in Fort Washington, and is slowing down a bit these days.
He was partners with Schwartzman a couple of decades ago @ Jefferson, in Philly.

I can get you his #, if you'd like.

What type of doctors are you seeing now?

I often preach this "triangle of rsd care".

Your Meds = Your Doctor (Neurologist more than likely).

Your Mind = It's good to see a pain management Psych doc for a while, and re-up occasionally).

Your Health otherwise = EXCERCISE, and follow general good health guidelines. RSD is a Use it or lose it disease, as I'm sure you know.

I've had it since 83.

So, do you have a good neurologist? That's what Knobler is, along with Ph.d. (psych).
Start there, do you have a good hospital, best bet is a University hospital. Get to the "Cheif of Neurology". Or someone there who does know RSD.
Use the phone, and ask questions, like you're an employer testing a new hire! (That's exactly what you're doing).
If that doesn't work, find a pain management facility. Many hospitals have them.

I'm sorry that you don't like Dr Schwartzman. It does seem that he is channeling all his energy into his ketamine thing.

I know Dr Knobler is great, but he's almost two hours from Lancaster, but he IS only a mile from the turnpike! He does specialize pretty much in RSD, and MS.

Let me know, if I can help?

Pete
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Old 05-01-2009, 08:17 PM #2
Teresa112757 Teresa112757 is offline
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It's about 75 miles from Lancaster, but Dr. Jhangir Maleki is wonderful. He's in Bala-Cynwyd. His hours are limited so you probably have to wait a few weeks to see him. His number is 610-949-7142. He's a wonderfully compassionate doctor.
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Old 05-01-2009, 08:20 PM #3
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Quote:
Originally Posted by AintSoBad View Post
LWood,
I go to Dr Knobler, he's in Fort Washington, and is slowing down a bit these days.
He was partners with Schwartzman a couple of decades ago @ Jefferson, in Philly.

I can get you his #, if you'd like.

What type of doctors are you seeing now?

I often preach this "triangle of rsd care".

Your Meds = Your Doctor (Neurologist more than likely).

Your Mind = It's good to see a pain management Psych doc for a while, and re-up occasionally).

Your Health otherwise = EXCERCISE, and follow general good health guidelines. RSD is a Use it or lose it disease, as I'm sure you know.

I've had it since 83.

So, do you have a good neurologist? That's what Knobler is, along with Ph.d. (psych).
Start there, do you have a good hospital, best bet is a University hospital. Get to the "Cheif of Neurology". Or someone there who does know RSD.
Use the phone, and ask questions, like you're an employer testing a new hire! (That's exactly what you're doing).
If that doesn't work, find a pain management facility. Many hospitals have them.

I'm sorry that you don't like Dr Schwartzman. It does seem that he is channeling all his energy into his ketamine thing.

I know Dr Knobler is great, but he's almost two hours from Lancaster, but he IS only a mile from the turnpike! He does specialize pretty much in RSD, and MS.

Let me know, if I can help?

Pete
asb


I have tried for different pain clinics in the surrounding hospitals. My nearest is Lancaster General but there a joke when it comes to trying to deal with RSD. I have went from there to Childrens Hospital which was not help and than on to swartzman. I am currently still with my family doc cause all the neurologists around here are scared and morons and dont know what to do so they wont except me. I had been told there was a good pain management center at Geighsinger Hospital so my files were sent up to the chief neurologist who ran the pain management center he looked my file over and told me i was to complicated for him and his center he recommended Dr. Ronald Harbut, but Harbut has yet to restart a center and give recent new info on how to contact him cause all the previous contact info is out of date and you dont get anywhere near reaching him. Sady to get RSD in Lancaster is to be put in the middle of a place that could help you but refuses to as they dont understand rsd and are afraid of it. Lancaster's idea of a rsd patient is one where they go through therapy, get a nerve block, and or are with a pain therapist and than there fine. Well guess what i therapy failed, nerve blocks make mine worse and i have went to pain therapists that have told me after a year of session there is nothing that can be done untill i get somewhat of a relief from the RSD. problem is no one around here will do anything the neurologists hav heard of rsd but wont even try going out of the book to help the advanced like me so they ignore me and i am left screaming to the air cause no one helps. So give me the number of this doctor you see its worth a shot. Sherry and Schwartzman 2 of the top 3 rsd specialists have given up on me cause i am more advanced than they would like and any hopspital i send to replys with your to complicated to help. Thats why i feel so alone cause all of you guys actually have docs and are getting the procedures or meds and are not having to have everyone against you. I would love the luxury of even to have the lidocaine iv or even a pump. But no mine have to be to afraid to do anything out of the book. As well i am tired of all the kids that go to Dr. Sherry and are cured and especially those who find pain meds that work. I want to be in a hospital knocked out in a partial coma for at least a couple of days to give my brain a rest from the constant attacks. And i am tired of over dosing on oxycontin 80's and it doing zip absolutely nothing. i have cannot get to sleep anymore so i take 6mg of xanax at once to knock me out for alittle problem is my body is getting to use to that so its starting not to work so i have to up it more. I need a doctor to help me not these jackasses that just sit on there hands and even though i have done everything they wanted to try none of them will move on to other things. I am so FED UP with it all AHHHHHHHH!!!!
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Old 05-01-2009, 08:28 PM #4
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i understand what you are going thro i have went thro this for years.. being a kid with advanced rsd and everyone telling me that im too complicated to be treated by them.. so yes i understand i had to travel over 500 miles just to get treated from the time i was 17 till i was 18 then i moved here and it took awhile to find someone here to deal with me.. i went years with out ever having anything for pain. so i understand how hard and frustrating that it is for you..not to even add the problems of the rsd and other things goin on..

i hope that your able to find someone to help you i really do i worrie about you alot .. and i know its ruff at best.. hang in there ..

carrie
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rsd DX 99 had since 98 full body and organ involement,fibro ,pelvic pain ,etc,,,,,,




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Old 05-01-2009, 08:54 PM #5
AintSoBad AintSoBad is offline
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K.I.N.D.
Knobler Institute of Neuologic Disease.
520 Pinetown Road
Fort Washington, PA 19034

215.643.9045

You may use my name, my last name is very long, so we've shortened it to just
"Pete Woj".
they'll know instantly.
Tell them how we met.

He had a small heart attack last year, and is slowing down a bit.
I hope you can see him.
I have other friends who travel a long way to see him, and have seen people fly in from other states and countries to see him.
He's a very kind man. Great people there.

I wish you all the best.

But, I''ll tell you this,
I had the ketamine back in 01, when it was 24 hours/day for ten days.
It didn't hurt, but, it had no long term effect other than giving me the ten day vacation from my wife...

PM me if you like.

your friend,
Pete
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Old 05-02-2009, 08:47 AM #6
daniella daniella is offline
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I am sorry and can relate. I am a hard case and have been to so many doctors in every specialty to usually be refered to someone else because they don't want to deal with me. One called me a nightmare patient with all my conditions. Anyhow I have traveled for most of my pain doctors so I understand how hard it is. Do you have university hospitals or teaching hospitals near you that you could call and see if they have someone in their pain management who deals alot with rsd? I am not sure how close you are to NJ but I know University of Princeton hospital is suppsed to be good in general not sure for rsd but something maybe to look into. Have you looked into a scs? Hang in there and I hope you find someone to work for you and to look outside the box.
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Old 05-04-2009, 10:09 AM #7
SandyRI SandyRI is offline
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Hey Lordwood,

Did you try to get an appt with the doc that Pete recommended?

Please keep us posted. BTW - you mentioned that you had been treated at a Children's Hosp - do you mind if I ask how old you are? And who you have for support? Do you live with your parents, or your siblings, or by yourself?

I am REALLY sorry that you are in the shape that you are in. It sounds like you are in a whole lot a pain and feeling very desperate. It must stink to have stomach issues on top of pain issues, like most of us don't have enough to deal with as it is!!

I don't mean to lecture you - BUT - I can tell you that if I repeatedly took my meds in a manner that was contrary to what my PCP ordered, over a long period of time, he might not want me a patient anymore. He's been my doctor (and my husband's) for the last 20 years, and our relationship is built upon mutual trust and respect. When I need help I know that I can call him, and conversely, when he writes a script for me, he knows that I do my best to take it according to his instructions. Also there is a certain level of legal liability when physicians write a script, and I think we owe it to them to be respectful and responsible. In any case, I adore my doctor, and would never want to lose him. So I try pretty hard to follow his insructions, or keep him in the loop when I have issues with dosages, side effects, etc.

It sounds like you HAVE to get a doctor - a really good one (see Pete's message) - and WORK with him as best you can. And you need someone to help you with that, like your parents or a friend or a counselor.

Good luck, Sandy
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