Dr Conway

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.
Positivepoppy
Posts: 174
Joined: Mon Feb 24, 2014 2:49 am
Location: uk

Re: Dr Conway

Post by Positivepoppy »

Hi just wanted to say I really empathise with everyone suffering with this awful condition and I know first hand the devastating impact it has on family life and loved ones·
Wanted to say that I hugely appreciate surgery is not for everyone but I had bilateral nerve decompression surgery 10 weeks ago and although I know it's going to be a long and frustrating road to a hopeful recovery I am feeling positive· Yes I am still in pain this is not a quick fix but since surgery I have not had the raw stinging electric type shocks down there that used to have me in tears as wanted to physically rip out my vagina and pelvic area· The pain is now more muted and not so angry and somehow easier to manage· I do not wAnt to give false hope but feel certain surgery was right for me and there is a marked difference in the pain pre/post surgery
My heart goes out to everyone and this site has been instrumental in helping with my sanity and thankfully diagnosis and treatment
Good luck and stay strong
Positivepoppy
Posts: 174
Joined: Mon Feb 24, 2014 2:49 am
Location: uk

Re: Dr Conway

Post by Positivepoppy »

Hi just wanted to say I really empathise with everyone suffering with this awful condition and I know first hand the devastating impact it has on family life and loved ones·
Wanted to say that I hugely appreciate surgery is not for everyone but I had bilateral nerve decompression surgery 10 weeks ago and although I know it's going to be a long and frustrating road to a hopeful recovery I am feeling positive· Yes I am still in pain this is not a quick fix but since surgery I have not had the raw stinging electric type shocks down there that used to have me in tears as wanted to physically rip out my vagina and pelvic area· The pain is now more muted and not so angry and somehow easier to manage· I do not wAnt to give false hope but feel certain surgery was right for me and there is a marked difference in the pain pre/post surgery
My heart goes out to everyone and this site has been instrumental in helping with my sanity and thankfully diagnosis and treatment
Good luck and stay strong
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Karyn
Posts: 1655
Joined: Fri Sep 17, 2010 12:59 pm
Location: Lowell, MA

Re: Dr Conway

Post by Karyn »

Patty wrote:Foot in the door for what? What is he going to offer me that I have not already tried except surgery?
Well, I guess it depends on what you're looking for, Patty. At the very least, he may be able to provide you with more definitive information about your medical condition.
He may offer you surgery at some point in time, but whether to go through with it or not is entirely up to you. Based on your posts, it's my understanding that you don't have a definitive diagnosis for anything. If you suspect you have PN(E), Dr. Conway or any of the other Specialists would be your best bet for confirming or ruling it out.
Kind regards,
Karyn
Ultra Sound in 03/08 showed severely retroverted, detaching uterus with mulitple fibroids and ovarian cysts.
Pressure and pain in lower abdomen and groin area was unspeakable and devastating.
Total lap hysterectomy in 06/08, but damage was already done.
EMG testing in NH in 04/10 - bilateral PN and Ilioinguals
3T MRI at HSS, NY in 09/10
Bilateral TG surgery with Dr. Conway on 03/29/11. Bilat ilioinguinal & iliohypogastric neurectomy 03/12. TCD surgery 04/14.
stephanies
Posts: 686
Joined: Mon Oct 25, 2010 3:07 am

Re: Dr Conway

Post by stephanies »

Patty,

I agree with Karyn. You don't know the underlying cause of your pain until you see a doctor who specializes in PN. I don't know how you can sentence yourself to this life of pain without even a consultation. There are many people who get well through many treatments. Many PN patients are on this forum, many are not, and some of those who are don't come back to report in once they have improved.

My best to you,
Stephanies
PN started 2004 from fall. Surgery with Filler Nov. 2006, Dr. Campbell April 2007. Pain decreased by 85% in 2008 (rectal and sitting pain resolved completely), pain returned in 12/13. Pain reduced significantly beginning around 11/23.
Patty
Posts: 158
Joined: Sun Feb 16, 2014 2:14 pm

Re: Dr Conway

Post by Patty »

Was bedridden from debilatating pain yesterday. If were not for my two dogs I would rather go to sleep and never wake up. I have no quality of life. Cannot even get to a friends house to watch a movie. The more I do the worse this gets. I started with a new PT who is supposed to be the best but my pain just keeps escalating.
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Violet M
Posts: 6770
Joined: Mon Sep 06, 2010 6:04 am
Location: United States
Contact:

Re: Dr Conway

Post by Violet M »

Patty, I'm sorry you are having such a rough time right now. I remember the days when I felt like I was in a prison of pain and when I just wanted to sleep and never wake up. I understand what you are going through and I can't blame you. The one thing I always tell people when they are in this stage of their PN journey is that you still have options so it wouldn't make sense to give up yet until you've tried all of your options. I hope you can find what works for you. If PT isn't helping then it's probably not the right option for you.

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.
Patty
Posts: 158
Joined: Sun Feb 16, 2014 2:14 pm

Re: Dr Conway

Post by Patty »

Thanks for all your responses. I just don't have the will to keep seeing doctors with no answers for me. I have lost all hope to return to the once vibrant person I was over a year ago. I have been trying to turn to church more but cannot even sit for that. I fear I will loose my home since work is becoming more difficult . I have no one to support me financially. I feel I am being punished for what I am not sure.
stephanies
Posts: 686
Joined: Mon Oct 25, 2010 3:07 am

Re: Dr Conway

Post by stephanies »

Patty,

I understand how you feel and that, so far, seeing doctors has not been helpful. However, Dr. Conway is a specialist and he knows about PN. Isn't it worth one more appointment to see if he can help? I have been to the place where you are and it is pure hell. There is hope, even when it feels like there isn't.

My best to you,
Stephanies
PN started 2004 from fall. Surgery with Filler Nov. 2006, Dr. Campbell April 2007. Pain decreased by 85% in 2008 (rectal and sitting pain resolved completely), pain returned in 12/13. Pain reduced significantly beginning around 11/23.
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Violet M
Posts: 6770
Joined: Mon Sep 06, 2010 6:04 am
Location: United States
Contact:

Re: Dr Conway

Post by Violet M »

Patty wrote: I have been trying to turn to church more but cannot even sit for that.
Some people might call it crazy but I used to lie down in church. :oops: :shock: Our church had pews you could lie down on but even with that there was a time that I just couldn't even tolerate going much of anywhere and was pretty much glued to my couch and bed.

With pelvic pain and pudendal neuralgia, my conclusion after reading the PN forums for years, is that you may not always be able to come to a 100% definitive conclusion as to the exact cause/mechanism that is causing the pain. But most people find a treatment that helps significantly and many to the point where they can lead a mostly normal life. You are right though, it can be exhausting and it's easy for me to say "don't give up" now that I've come out on the other side of the tunnel.

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.
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