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Re: New Person with Pudendal Nerve Disorder

Posted: Fri Mar 14, 2014 5:10 pm
by Rosemary
So pleased for you.
(I asked you once about the shockwave therapy and you gave me some information - i didn't follow it up as i am in the UK and can't find anything comparable here.)
Best Wishes
Rosemary x

Re: New Person with Pudendal Nerve Disorder

Posted: Tue Mar 25, 2014 4:41 pm
by kathyd
Hi Kone
Wonderful and encouraging new
so happy for you!
Incredible!
I had a one-week visit with Dr. Andrew in2011
5 Days of treatment when he was still with his previous partner
I was able to sit a bit while there! Which I
Improved each day. We were Encouraged!
Then pain flared right before I came home
Got worse after that and bladder symptoms flared for awhile

Dr Andrew said I would need a few visits to get better
I was on the fence about it as I feel dr Andrew's previous partner went a bit too hard on me with shockwave in order to get it done in five days.
ThenDr. Andrew was banned from posting here due to some unkind remarks he made. Cant remember the details but this plus my bad flare after treatment turned me off
However he was kind to speak to my local chiropractor recently about his ART techniques. My chiro thought it interesting but he couldn't learn enough about on the phone
It's apparent that i would have to restart with Dr. Andrew in order to see progress again with this type of treatment
What also is wonderful is that your bladder is calmed-down as well -that's great! Im in an awful flair of urgency right now probably due to one of the medicine interventions tried. Bladder urge /hesitancy my symptoms began seven years ago.
After many treatments and PT etc sitting pain came on as well and later anal pain.

Quick question: I'm not sure what age you are but do you think that plays into your quicker recovery and success?
I am middle aged as are two women who I know had pretty decent success stories with Dr. Andrew 's treatment also.
Anyway something To think about. Thx for posting your story and congratulations again!
Kathy

Re: New Person with Pudendal Nerve Disorder

Posted: Sat Mar 29, 2014 2:26 am
by konedog4
I am 58 years old. I don't know if being older slows recovery from a disorder like this, but I would not doubt it. Usually, us older folks take longer to heal from any kind of injury.

I keep getting better with each passing week. I am doing things I could not even dream about doing this time last year. I shoveled the driveway of heavy wet snow today, and there is NO WAY I would have tried this last year, or a major pain would immediately be present in my perineum.

I am wondering if the traumatized pudendal nerve needed an additional year to heal? I know that if surgery is done, the docs say that a good 12-18 months is needed to feel better. Perhaps something similar to this happens with shockwave???
Anyway, it has been a year and a month since my last visit to Dr. Andrews, and I now believe I am 90% better. My entire life and attitude has turned around 180 degrees. I no longer have that feeling of despair I once had. I was so depressed a year and a half ago, that I dreaded each and every day, knowing I would be in pain, not be able to sit, not be able to do anything I once enjoyed. Now I firmly believe that with more time and more exercising and stretching, I will recover 100%.

Shockwave started my recovery. Prayer furthered it. Stretching every day helped immensely too.

I thought at one time that I would need surgery and that depressed and scared me because the surgical cure/recovery rate is so dismal. I never thought I'd get better without surgery, so that depressed me even more. Then, I came across a posting by a fellow who had gone through Shockwave with Dr. Andrews. He had gotten 80% better and had his optimism back. He encouraged me to go for it, so I did. I am so very fortunate to have taken his advice.

I don't claim that shockwave can cure or even help everyone. But it does have a good track record, just as good, if not better than surgery. So why risk surgery if shockwave has not been tried?

I wish to encourage everyone here to not give up. I once thought I'd be a partial invalid forever. Now I am 90% better and still improving. Consider every option, and then go for your recovery too.

Best wishes to one and all,

kone

Re: New Person with Pudendal Nerve Disorder

Posted: Sat Mar 29, 2014 4:19 am
by Violet M
Yay!!! :D 8-) :D Wish someone in the US would learn how to do this from Dr. Andrew.

Violet

Re: New Person with Pudendal Nerve Disorder

Posted: Sat Mar 29, 2014 4:58 am
by konedog4
Apparently, the procedure to use a shockwave machine for pudendal area has not been approved in the US. Perhaps we need to get together as a group and petition the FDA to approve this use???

Re: New Person with Pudendal Nerve Disorder

Posted: Sun Mar 30, 2014 12:28 am
by Violet M
Interesting idea. Here's some interesting info on how to get a device approved. Doesn't look terribly easy.

http://www.patientnetwork.fda.gov/learn ... t-approved
http://www.patientnetwork.fda.gov/learn ... fda-review

Re: New Person with Pudendal Nerve Disorder

Posted: Sun Mar 30, 2014 6:08 pm
by konedog4
I am going to work through my two state senators and tell them how important it is to get this therapy approved in US.

Re: New Person with Pudendal Nerve Disorder

Posted: Sun Mar 30, 2014 11:59 pm
by janetm2
Thanks Kone - I am sure this would help others. Keep us posted.
Janet

Re: New Person with Pudendal Nerve Disorder

Posted: Thu Apr 03, 2014 12:51 am
by kathyd
Hi Kone
Just saw your post. Thx for posting this encouraging info. Im so happy for you!
I am 57 so it's great to hear that someone my age (middle-aged!) is healing well and able to do all the normal activities again. Thats wonderful.

I can really relate to how you felt in the past. You described just how I feel, depressed / scared of how Im going to get through the pain of the day.
But as parents , my husband's and my lives are very busy with kids activities; our youngest is only 14, and I must keep my spirits up.
I was encouraged also by the prayer that you believe helped you.
I have family, friends. church members etc. praying for me so I try to keep the faith!

Thx for the info on stretches. I had stopped doing them. awhile ago, but I think they could help with my current bladder flare and with my pain and tightness from being on my feet a lot.
I took a long break from PT, based on the advice of one physical therapist.Another one that knows me well, thinks I should re-start, so I may see someone local.

After hearing your success, I am going to call Dr Andrew..and check on possibly seeing him again. Will see what he has to say regarding my current situation.
It can take several visits as he said. He had told me I needed at least 3 visits,, so its something to consider.
Thx again,for posting this encouraging info, and my best wishes on your continued recovery!

Regards,
Kathy

I believe the prayers and the faith helped as welll76


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Re: New Person with Pudendal Nerve Disorder

Posted: Thu Apr 03, 2014 11:11 pm
by kathyd
Hi All
Sorry I noticed my typos... extra text at the end of my post. Pls disregard... I always miss a few typos..