newcomer

Welcome to HOPE. We have tried to provide a place for newcomers to make their introductions. We will try our best to make you welcome and guide you through our website and Forum and assist you as best as we can through any questions you have regarding Pudendal Neuralgia.
molly
Posts: 121
Joined: Wed Aug 29, 2012 7:58 pm

newcomer

Post by molly »

Hi My name is Molly,

I have had pn now for four years which started after a gynae disaster. To date this is what I have had

I have had nerve blocks and neuro modulation in London.
Eighteen months physio with a very good pn aware physio.
Two lots of botox with the lovely Dr Greenslade.

On top of this I,ve tried acupuncture, magnetic therapy, chropracture treatment,and several other alternative treatments, with little or no success.

Earlier this year I finally decided to have surgery, as a last resort.

Having read about Dr Tibet,s new operation I felt it looked very promising.

I visited in February, where I met the team, and Dr Tibet, who is a very nice man. On this visit it was a through examination, from a range of specialists I returned in May for right sided decompression surgery. The hospital and staff were all very nice and Dr Tibet was very attentive.
It was a long operation(six hours), and the nerve was badly entrapped. I did have a haemorrhage, which I wonder has effected my recovery.

Unfortunately, I have made no progress at all in the last four months which I had hoped to do. Most of Dr Tibet,s patients respond very quickly, so I am really disappointed although I still hope I may improve in a longer time frame. Dr Tibet continues to monitor my progress via e-mail as he does all his pn patients.







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helenlegs 11
Posts: 1779
Joined: Fri Sep 17, 2010 9:39 am
Location: North East England

Re: newcomer

Post by helenlegs 11 »

Hi Molly,
Thanks for your honest post, I hope that you will continue to improve and that the complications with the op are the only things holding you back from a speedier recovery.
There are many people on here who have had to pass the operations anniversary to see any great benefits, although that is not with Dr Tibet. I have heard some good reports from his patients but everyone is different and you do sound like you had a big and difficult op.
Would love to be able to keep up with how you are progressing :)
Take care,
Helen
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.
AliPasha1
Posts: 739
Joined: Fri Sep 17, 2010 2:35 pm
Location: New Orleans,Louisiana

Re: newcomer

Post by AliPasha1 »

Hi Molly,

I met Dr. Tibet in May and he seemed like a nice guy.What is Dr. Tibet's reasoning to why you haven't seen any improvement in your symptoms.I would really appreciate if you could elaborate on what your symptoms were in the first place.Do you have aching pain when you sit at your ischial tuberosity(sitting bone) amlong with urinary frequency/urgency etc

I look forward to hearing from you.

Kind Regards,
Ali
Diagnosed for PNE by Dr. Jerome Weiss in June 2007.Started PT with Amy Stein in NYC.
PT for almost 3 years now without any results.
Pudendal Nerve blocks in August,2007 by Dr. Quesda left me with sitting pain.
Unilateral TIR approach with Dr. Bautrant on 18 Febuary,2010 with no major improvements and sitting is much worse.
MRI By Dr. Potter reveals nerve entrapment in the ST,AC and DN.
Dorsal Nerve Decompression surgery on April 8,2011
Redo surgery by Dr. Hibner on July 18,2011
molly
Posts: 121
Joined: Wed Aug 29, 2012 7:58 pm

Re: newcomer

Post by molly »

Hi Ali,


My history is pretty much as are many people,s. The pain started after a painful gynae examination. I started to have trouble sitting and vaginal discomfort. The consultant then procceded to laparoscopy, which showed nothing, he then procceded to hysterectomy.

By this time the pain had become very severe and I also suffered from urinary frequency, rectal pain kicked in and the rest is pretty much standard.

MRI was clear, thankfully got diagnosis quite quickly, thanks to a friend scouring the internet for hours.

Dr Tibet,s last feeling was I had another reason for my pain, but as you can see I,ve had a significant number of investigations, including which I forgot to mention, one caudel block and one sacral nerve root block, so if there is another reason, I really don,t know how to go forward .

Hope this is helpful,

Molly
AliPasha1
Posts: 739
Joined: Fri Sep 17, 2010 2:35 pm
Location: New Orleans,Louisiana

Re: newcomer

Post by AliPasha1 »

Hi Molly,

Any complications from the surgery like restrictions/pain to bending, walking ,lifting etc.

Thanks,
Ali
Diagnosed for PNE by Dr. Jerome Weiss in June 2007.Started PT with Amy Stein in NYC.
PT for almost 3 years now without any results.
Pudendal Nerve blocks in August,2007 by Dr. Quesda left me with sitting pain.
Unilateral TIR approach with Dr. Bautrant on 18 Febuary,2010 with no major improvements and sitting is much worse.
MRI By Dr. Potter reveals nerve entrapment in the ST,AC and DN.
Dorsal Nerve Decompression surgery on April 8,2011
Redo surgery by Dr. Hibner on July 18,2011
molly
Posts: 121
Joined: Wed Aug 29, 2012 7:58 pm

Re: newcomer

Post by molly »

Hi Ali,


Actually funny you should say that, because I did have a significant haemorrhage which resulted in a blood vessel having a clip put on it.
Dr Tibet did wonder if this could be irritating the nerve, but decided probably not and advised me to go home.

I have asked him if he would reconsider this, but he has not replied to me.

Other than that I cannot think of any other problems, a lot of post-op pain, again which was unusual.

The surgery was also very long (six hours), and I wonder if the nerve suffered being stretched
for so long on decompression, but again I do not know how long his surgeries are as he has not answered this question.


Regards Molly
User avatar
Violet M
Posts: 6651
Joined: Mon Sep 06, 2010 6:04 am
Location: United States
Contact:

Re: newcomer

Post by Violet M »

Hi Molly,

Sorry to hear your surgery has not proven successful yet. Most people I know of who have had PNE surgery do not get well by the 4th month and in fact the 4th month can be the worst because the nerve can be waking up. I think it is way too soon to tell if your surgery was successful because nerves take a long time to heal. I was on narcotic pain medications until 9 months post-op and couldn't really count on a good day until 18 months after surgery. I know it sounds like a long time but don't give up hope that you may yet have improvement.

Take care,

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.
molly
Posts: 121
Joined: Wed Aug 29, 2012 7:58 pm

Re: newcomer

Post by molly »

Hi Violet,

Thank you for your kind message.

It is only the fact that Dr Tibet,s patients respond so quickly that makes me despondant. I ,m quite happy to wait if I knew there was light at the end of the tunnel.

Molly
User avatar
GregT
Posts: 135
Joined: Mon Sep 20, 2010 6:51 am

Re: newcomer

Post by GregT »

Unfortunately, I have made no progress at all in the last four months which I had hoped to do. Most of Dr Tibet,s patients respond very quickly, so I am really disappointed although I still hope I may improve in a longer time frame. Dr Tibet continues to monitor my progress via e-mail as he does all his pn patients.

Molly,

Can I ask you what makes you believe that most of Dr. Tibet's patients "respond very quickly"? I don't really know anything about Dr. Tibet, but I do know that some doctors tend to overstate their accomplishments and success rates. My statement to you here has nothing to do with whether or not your recovery will come. Just want to let you know that some doctors really do exaggerate their success rates as well as how long the recovery can take. I wish they wouldn't, but many do it. I suppose it's done to get patients to have surgery with them.

Did he tell you this ("respond very quickly"), or is this something that you'd heard elsewhere?

Greg
Had surgery in Nantes, France in 2001 with Professor Robert. I advocate physical therapy with PTs who specialize in the pelvic floor. I also advocate injections to help diagnose PN and I am in favor of having PN surgery to release the nerve when the diagnoses points to an entrapped nerve.
User avatar
GregT
Posts: 135
Joined: Mon Sep 20, 2010 6:51 am

Re: newcomer

Post by GregT »

Can I ask where Dr. Tibet does surgery? Also, Molly stated earlier that she liked his new surgery (or something to that effect). Can someone briefly tell me what is different about his surgery?

Finally, are there other people on here who've had surgery with Dr. Tibet who have had good successes? I know I could spend time searching this, but if someone could briefly answer these few questions it would save me a decent amount of searching time.

Thank you.

Greg
Had surgery in Nantes, France in 2001 with Professor Robert. I advocate physical therapy with PTs who specialize in the pelvic floor. I also advocate injections to help diagnose PN and I am in favor of having PN surgery to release the nerve when the diagnoses points to an entrapped nerve.
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