inglese
spagnolo
hello, are janet and I write from Italy, excuse my English.
I need your help for two problems.
the first and 'I'm looking for Dr. Potter, to do the MRI in New York, but after more' often spoken with the hospital Special Surgery, I learned that she does not get more 'and do not see patients after MRI.
"Perhaps," signing the report, but does not explain her.
You understand that affronare a trip from Italy with a lot of pain that I have, without being able to see, not 'acceptable. (I ave pudendal neurophaty. Much, much more' serious after block made by Dr. Vincenti, which has ruined me .. I have a terrible pain ... now!)
THE FIRST QUESTION IS IF YOU KNOW WHERE CAN I FIND THE DOCTOR POTTER NOW (NEWS RECENT LAST MONTH), the HSS do not give news .... I would like the number or mail address of his private studio!
The second thing is a piece of advice I suffer from terrible pain of 8 months (is long to explain ...) caused by block without tac, and I do not know if it would be better to do the neurography Dr. Filler or MRI Potter (if I can find it ....)
I can not do one or the other 'cause the last few months I have already' done 3 magnetic resonance imaging (useless) in Italy.
Thank you very much ... Janet
PS Filler just make the neurography also in london ... does anyone know if it 'the same as those in America?
Help..Where is now dott Potter, she is not more at HSS
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janetrossi
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helenlegs 11
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Re: Help..Where is now dott Potter, she is not more at HSS
Sorry Janet
I do not know of any different details for Dr Potter. Hopefully someone else will help with this.
I would say that given the choice most people would have a Potter Scan over a Filler MRN. Dr Filler often gives everyone a piriformis diagnosis, but his imaging equipment does look impressive.
However if it is much easier to get to London I am pretty sure his MRN technology will be the same in London as it is in the USA.
You can find out more atbout this at www.nervemed.com
You are not guaranteed to get any results from imaging of course. What about travelling to France say to see Professor Robert? They diagnose through clinical hands on examination and do not use any imaging as they don't think it is helpful. There are other European doctors of course. http://www.pudendalhope.info/node/57
I do not know of any different details for Dr Potter. Hopefully someone else will help with this.
I would say that given the choice most people would have a Potter Scan over a Filler MRN. Dr Filler often gives everyone a piriformis diagnosis, but his imaging equipment does look impressive.
However if it is much easier to get to London I am pretty sure his MRN technology will be the same in London as it is in the USA.
You can find out more atbout this at www.nervemed.com
You are not guaranteed to get any results from imaging of course. What about travelling to France say to see Professor Robert? They diagnose through clinical hands on examination and do not use any imaging as they don't think it is helpful. There are other European doctors of course. http://www.pudendalhope.info/node/57
Fall 2008. Misdiagnosed with lumber spine problem. MRN June 2010 indicated pudendal entrapment at Alcocks canal. Diagnosed with complex variant piriformis syndrome with sciatic, pudendal and gluteal entrapment's by Dr Filler 2010.Guided piriformis botox injection 2011 Bristol. 2013, Nerve conduction test positive; new spinal MRI scan negative, so diagnosed for the 4th time with pelvic nerve entrapment, now recognised as Sciatic, pudendal, PFCN and cluneal nerves at piriformis level.
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janetrossi
- Posts: 10
- Joined: Mon Sep 24, 2012 1:13 am
Re: Help..Where is now dott Potter, she is not more at HSS
inglese
italiano
spagnolo
thank you very much ...!
Dr. Robert I have not heard very good reviews from people I know, and I did not think much about the French-Belgian doctors (Beco ', Beautrand, De Bisshop ..).
Unfortunately, I know very, very disappointed with them ....
While I hope well of Filler, even as a doctor, as well as for neurography dottorssa Potter ..... and we all know that and 'the best (if I find it ...!)
I just have to understand, as I said, if it 'better for me neurography or MRI ....
Thanks again, Janet
italiano
spagnolo
thank you very much ...!
Dr. Robert I have not heard very good reviews from people I know, and I did not think much about the French-Belgian doctors (Beco ', Beautrand, De Bisshop ..).
Unfortunately, I know very, very disappointed with them ....
While I hope well of Filler, even as a doctor, as well as for neurography dottorssa Potter ..... and we all know that and 'the best (if I find it ...!)
I just have to understand, as I said, if it 'better for me neurography or MRI ....
Thanks again, Janet
Re: Help..Where is now dott Potter, she is not more at HSS
When I searched for Dr. Potter online she is still listed at the Hospital for Special Surgery.
She is a radiologist and usually radiologists don't see patients. They write the report for your doctor and then your doctor can interpret the report and decide on the treatment. Last I heard, you can purchase a CD of the MRI for $50 for your local doctor to read.
Neither the Potter MRI or the Filler MRN are 100% accurate but they may give valuable information. I can't say which is better. If you already had the MRN in Italy it seems like you would want to try the MRI from Potter now because it might give you different information.
Violet
She is a radiologist and usually radiologists don't see patients. They write the report for your doctor and then your doctor can interpret the report and decide on the treatment. Last I heard, you can purchase a CD of the MRI for $50 for your local doctor to read.
Neither the Potter MRI or the Filler MRN are 100% accurate but they may give valuable information. I can't say which is better. If you already had the MRN in Italy it seems like you would want to try the MRI from Potter now because it might give you different information.
Violet
PNE since 2002. Started from weightlifting. PNE surgery from Dr. Bautrant, Oct 2004. Pain now is usually a 0 and I can sit for hours on certain chairs. No longer take medication for PNE. Can work full time and do "The Firm" exercise program. 99% cured from PGAD. PNE surgery was right for me but it might not be for you. Do your research.