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Re: New Person with Pudendal Nerve Disorder

Posted: Sun Mar 24, 2013 4:01 am
by helenlegs 11
This all sounds so very positive Kone :) This treatment is something I would chose to try given the opportunity. I know that the ESWT equipment is something that is used in Britain but it has not been employed for pelvic issues at all
Very glad it has helped you.
Helen

Re: New Person with Pudendal Nerve Disorder

Posted: Thu Mar 28, 2013 7:44 pm
by spizer
I too went to see Dr Andrew and feel that I am slowly improving. My improvement has not been as quick as I would have liked but it doesnt help that I'm an accountant and in the middle of tax season right now working long hours. I still require a special seat in order to sit for long periods of time. I do feel the muscles in my lower body are slowly improving. However I've ran into a few stumbling blocks with pain in other areas along the way as my body adjusts. I got orthotics from Dr. Andrew and I think my body may be having a tough time adjusting to them. I too will soon be contemplating a second visit to Dr. Andrew.

Presently I'm still working on developing a team of therapists locally who can help me. I've recently stopped going to physiotherapy and started going to a fitness trainer. The trainer has changed some stretches Dr. Andrew gave me that were causing me to have knee pain. My knees are back to normal after implementing the trainers modifications and new stretches. We are going to start working on strengthening this week.

Kone, I'm glad you've benefited so much from Dr. Andrews treatment. Did you modify your daily activities a lot since seeing him? I have continued working 8 hours a day at a desk and am wondering if I would have seen better results if I had taken time off.

Re: New Person with Pudendal Nerve Disorder

Posted: Fri Mar 29, 2013 2:32 pm
by helenlegs 11
Hi spizer,
A belated Welcome :) to HOPE.
Glad that the ESWT and revised physio with your fitness trainer has been of some benefit. I hope this improves further of course. My nephew is a fitness trainer and keeps giving me helpful tips (although I don't always see it that way ;) ) It will be interesting to see how well you do on your second visit to Cornwall. I have to admit that this is something I am very interested in as if scar tissue can actually be broken down with this procedure I do think I could benefit too. I hope you are able to update us on your experiences there.
Wishing you all the best.
Helen

Re: New Person with Pudendal Nerve Disorder

Posted: Mon Apr 01, 2013 10:56 pm
by konedog4
Spizer,

I can't really answer your question with any degree of accuracy. It seems like the less we sit the better, but that said, I no longer avoid sitting as it does not seem to make matters worse. However, I still sit on a pad just because I want to limit pressure on the perineum. I am happy to hear you got better. I am still not convinced that I can get "cured" by following the Shockwave protocol, however, I cannot deny that I feel better and can do more things. My first visit I made the most progress, perhaps 50% better. The second visit I got another 10-15% better. I still have a ways to go and am doing my stretches and exercises hoping to make more improvements. I will consider a third visit if i have a relapse. This may be the best I can get through shockwave. It's not great, but it is better.

kone

Re: New Person with Pudendal Nerve Disorder

Posted: Wed Apr 24, 2013 11:38 pm
by konedog4
Has anyone on this board, or does anyone know of anyone who was cured of PN by the steroid injections? If the answer is "no", then why do PN doctors keep giving them? (I heard the rate of cure was less than 5%).

My shockwave therapy gains have stayed. I can still for hours at a time, which makes my life much more enjoyable. My only therapy is stretching - I stretch for 1/2 hour daily, mostly my legs, perineum and buttocks. I was walking quite a bit, but developed a bad ankle and now need surgery on it to repair a torn ligament. Plan to swim and walk to rehab the ankle.

kone

Re: New Person with Pudendal Nerve Disorder

Posted: Sat Apr 27, 2013 4:44 am
by Violet M
Kone, this is my 9th year of moderating the PNE forum and I can't remember anyone who has posted that they were cured by nerve blocks. I remember a few people have posted improvement and a few people who have posted long-term worsening of symptoms. My understanding is that nerves blocks are done partly for diagnostic purposes and that the protocol of a series of 3 steroid nerve blocks was developed from the protocol used for carpal tunnel syndrome. I haven't read any literature on the protocol for carpal tunnel so I can't say for sure if that's true. I think the conventional wisdom is that nerve blocks are less invasive with less risks than surgery so it's worth trying them first. It would be interesting to see more studies/peer-reviewed literature on how effective they really are.

Glad to hear your are still experiencing pain relief after ESWT. ;)

Violet

Re: New Person with Pudendal Nerve Disorder

Posted: Sun Apr 28, 2013 5:58 pm
by ritak
Kone,
I have only heard of injections being used for the same as what Arlene posted. I am happy to hear that your shockwave therapy produced some lasting results. Sorry to hear about your ankle though. Watch your rehab. I have a bad foot that lead to incorrect walking thus putting strain on my legs,pelvis and low back. I still cannot get the hang of walking correct but my chiro has a huge bag of tricks so we are continuing to keep trying and headed in the right direction. I hope that your ankle just heals and does not kick up a flair with your PN. Good to hear your updates.
Rita

Update

Posted: Mon May 13, 2013 1:12 am
by konedog4
Severely sprained right ankle needed surgery, so had it done last Wednesday. Casted from knee to toe. Very difficult to get around (on crutches). More PN symptoms as a result of crutching and hopping around. Hope I can make it through this 6-8 week recovery without making PN much worse.

kone

Re: New Person with Pudendal Nerve Disorder

Posted: Sat May 18, 2013 1:14 pm
by Violet M
Sorry about your ankle, Kone. I hope you are taking it easy. ;)

Violet

Re: New Person with Pudendal Nerve Disorder

Posted: Sun May 19, 2013 8:21 am
by konedog4
Thanks Violet,

The ankle needed fixing, so after the improvement in the two sessions of Shockwave Therapy, and now with the ability to sit down again, I decided to have it done. So far, I have not noticed any intensification of symptoms. Once the cast comes off in 2-3 more weeks, I can begin stretching again and start strengthening my withered frame. Laying around all day is not good for one's constitution!

God bless,

kone