ENDO ON POD, NOW THINKING POSSIBLE PUDEND... - Endometriosis UK

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ENDO ON POD, NOW THINKING POSSIBLE PUDENDAL NEURALGIA. PLEASE HELP!

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Hello!

If anyone has PN, would you be so kind to share your symptoms with me please, I feel like I am going crazy!

It was a battle to get diagnosed with endo in the first place and during that time I lost my faith in the system and the thought of going through all that to get another diagnosis is scary. Also, I am an anxious person and now tend to get a lot of health anxiety because of the trouble I had. So because of this I have convinced myself I have herpes-2 (although I have no sores), because of the tickling/prickling burning sensations that I get. Ive had these symptoms since just before my lap (2years ago), also had to have bowel detached from pelvic wall so maybe they hit the nerve or endo spread and growing on nerve?

These are my symptoms:

-All located on the right side of my vagina

-Feels like there is something inside my vagina constantly

-Sometimes burning during urination (tested neg for Chlamidya and Gon) (always worse in night)

-Can't wear tight clothing, this seems to make it worse

-Gets progressively worse throughout the day (also started uni and I've done a lot more sitting so I don't know if this has triggered something)

-tickly/burning pain/sensations that can come from inside vagina out to the skin and kind of down to my bum

Thank you in advance!

x

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