New PNer

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.
pn_person
Posts: 94
Joined: Fri May 13, 2011 10:11 pm

Re: New PNer

Post by pn_person »

LiveStandingUp wrote:Thanks, Doreen. It's worst at night -- that's when I lose sensation in the genitals. I can't stay asleep or get comfortable right now and I'm sure the anxiety is playing a big part, too. What's also frustrating is how long its taking to get the additional tests like "Sayer(?)" and EMG (not until the 30th). I can't imagine going three more weeks without sleeping. I have reached out to a practice in Bergen, NJ with a PTA named on this site and hope to get a visit there very soon. Thanks for reaching out - your input is so helpful! -Matt
LiveStandingUp,

please send me PM if you like..seems like we have a similar situation with numbness as opposed to pain, which most participants here are dealing with

would like to compare symptoms. tests. treatments, etc..perhaps we can help each other

thanks
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