Chance to voice your concerns

This is an area to share and learn about new Medical Advances and Techniques where we can be educated and educate.
TracyB7777
Posts: 196
Joined: Mon Sep 27, 2010 3:42 am
Location: Vail, Arizona

Re: Chance to voice your concerns

Post by TracyB7777 »

Completed!!
Have been dealing with burning pain since Jan 2010.
No sitting since April 2010.
Seen the following dr's: DO, GYN, Dermatologist, Accupuncturist,
URO GYN (his RN is the one who suggested the pain could be PN), Neurologist
Had ECG and MRI both inconclusive, only the SSEP said Pudendal reaction was abnormal and they lost that test result.
Saw Dr. Castellanos April 6, 2011. Next steps, MRI and botox. Having PT while waiting.-Botox denied, appealing to Insurance company now. :(
pianogal
Posts: 437
Joined: Mon Sep 20, 2010 2:11 am
Location: Orange County, CA

Re: Chance to voice your concerns

Post by pianogal »

I DID IT! Thank you for posting.

also...
If you have additional thoughts about advancing pain research, care, and education or would like to share that information related to the committee's work, please use the space provided below to do so. You may also email documents or articles to support your testimony to iompainstudy@nas.edu.
We should send them the HOPE Paperwork. ALL OF US SHOULD. Please download it and email it to them. The more of us do it, the greater the impact. Thank you!
Attachments
Overview of pudendal neuralgia for medical professionals(3).pdf
HOPE PNE document for awareness
(80.59 KiB) Downloaded 188 times
-straddle fall age 4-7 w/bleeding labia, tampons hurt in teens, papsmere started annoying pelvic 'tingling' & pne in 02
-obturator surgery w/ Filler in 05 (useless, created sciatic & plantar fascitis pain)
-TIR surgery w/ Bautrant in 08 and vestibulectomy in 08 in France (vest. removed pain w/intercourse, pain w/sitting increased post surgery)
-chronic fatigue & food allergies/migraines (gluten, milk) from pain meds in 08
-want a life back. I'm 34 w/8+ years of pain
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