Deep And Burning Pain When Aroused | MyEndometriosisTeam

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Deep And Burning Pain When Aroused
A MyEndometriosisTeam Member asked a question 💭

First of all, I have to say I have not been diagnosed with endometriosis! I don’t want to offend anyone but this is the only place where I found people who had the same pain as mine, so I hope I’ll find here some answers or at least someone who feels the same as me!! Every time I get sexually aroused, I feel like my cervix and vagina are burning or getting stabbed and my labias instantly go numb! Does this happen to any of you? Thank you, and please, do excuse me if I offended you in any way!!

posted March 11, 2020
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A MyEndometriosisTeam Member

option 1:When you're horny, blood flows to your vagina, and that can result in pelvic congestion. What does that mean? If you're horny and you don't orgasm, it can stay there for almost an hour.

option 2: It could be because your clitoris is trapped and can’t expand when it’s being filled with blood, which is called clitoral phimosis.

check this:

https://helloflo.com/yes-women-can-experience-p...

https://www.bustle.com/p/why-does-my-vagina-hur...(Phone number can only be seen by the question and answer creators)

posted April 15, 2020
A MyEndometriosisTeam Member

YES! I've had this for years! If I'm not having sex I get horny dreams and wake up with an orgasm forming and if I don't get a cold shower quickly my whole pelvis explodes with intense cramps that can last for half an hour. I now take an anti-inflammatory when I'm unavoidably triggered, but it's not really a sustainable approach! No one has diagnosed me as I won't have the endoscopy! I already have pelvic scar tissue from an old scar where my appendix was removed in an emergency. This is the closest I've been to understanding this condition, but no doctor has ever really understood so I simply don't ask for treatment as it seems that surgery is the only go to. Having a sexual relationship just to deal with this seems like a lot to ask, of myself and a man. If he has not encountered this it can be a scary thing. Oh well. I shall have to stick to removing wheat and grains from my diet. All inflammatory! Paleo diet works but can be hard to stick to! If in doubt leave the triggers out! Too much heat, inflammatory foods and being lazy and not getting enough exercise can all exacerbate this condition! Thanks for letting me know I am not alone! 😊😎
#horny #cramps #inflammation #dreams #prostaglandins #pelvicpain #orgasm #sex 💞🤘

posted April 7, 2021
A MyEndometriosisTeam Member

You're welcome. I'll just leave the links here; might help your research?

Nancy's Nook on Facebook is a good resource. Lots of articles and a list of excision surgeons. Feel free to read my story and recommendations tab. There's more details on the surgeons I consulted or used.

I've also got a resource list here of stuff that helped me; other users have also found it helpful. I've got tons of other articles, so if you want anything specific, let me know. Some users told me the links don't open; please let me know if that happens to you. Happy to help however I can.

https://www.myendometriosisteam.com/users/5d1ab...

Other articles
Overview of Endo: https://pacificendometriosis.com/what-is-endo/

Excision Surgery Overview: https://pacificendometriosis.com/excision-of-en...

Endo Treatment Options: https://www.vitalhealth.com/endometriosis-speci...

Interviewing a Surgeon: https://www.endofound.org/preparing-to-see-a-do...

Excision vs. Ablation Surgery. WARNING graphic surgical photos. https://www.endometriosisaustralia.org/post/201...

posted March 12, 2020
A MyEndometriosisTeam Member

Welcome and no offense at all. There are many users who suspect they have it, so you’re not alone. It can involve many hoops to get diagnosed, so I’m glad you’re here for support.

I have a lot of Pelvic Floor Dysfunction but I also have Pelvic Congestion Syndrome. That means that the Endo has damaged the lymph channels and nerves. I have pain with sex and sometimes with arousal. I’ve never had my labia go numb. But what you’re saying makes me suspect Pelvic Congestion Syndrome.

Have you looked into consulting an excision surgeon at all? They tend to be the most well versed docs in Endo. Nancy’s Nook on Facebook is a good resource. Lots of articles and a list of excision surgeons. I’ve got a bunch of General Endo info and I do on excision. If you want those, let me know.

posted March 11, 2020
A MyEndometriosisTeam Member

Hi! How do you know you don’t have endo? Did you have a laparoscopy?

I don’t mind you being here, many suggestions should help you, too.

Have you tried pelvic floor PT?

posted March 11, 2020

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