Pain that worsens with movement

[alice2800]

Hi, I have been experiencing lower right pelvic pain for a few months now but the past few days it’s gotten a lot worse and worsens dramatically with movement, I can hardly walk! What should I do?

[bantam12]

Seeing your GP would seem like a wise move.

[alice2800 in reply to bantam12]

I have tried lots of times but he won’t do anything about it :/

[bantam12 in reply to alice2800]

Have you had scans ? You just have to keep on at him or see a different GP and ask for a referral to a specialist.

[J3ndoll]

It’s your health. Guide you own medical road— only because you are the ONLY person that knows your body.. trust your gut girl, that’s how I found I have PNE. the US federal laws are “F’n” our QOL up. When’s ur last pap?

Have you ever been diagnosed with endometriosis,or interstitial cystitis ? I basically lived in the ER getting every procedure in order to try and diagnose and pain sent me packin... they call PN the suicde disease, “clinical nightmare” only because inadequate pain control due to how poorly understood the CPP syndromes are in the states. It breaks my heart,.. ruins relationships w/ every single kind I’d date .. (they felt helpless and when I’d be in bed for 2days)

Work with your PCP and ask for a referral to a Pelvic specialist .

PN/PNE is quite rare and since it affects your central nervous system along with motor sensory it’s important to research and compare symptoms. I JUST got diagnosed in ‘17 (after 12 years) there are MANY chronic pelvic pain syndromes.. I’d check it out if I were you. PN/PNE.requires 6 specialist believe it or now. Definitely ask for a new referral

Most of all🙏🏼 whatever it is , spread awareness.

I act strong in front of people/family but there will deeeefinity be days where you’re crying alone, feeling alone and that no one understands you.

Follow your intuition/gut feeling

Good luck

I’ll send some good vibes ur way!💁🏻‍♀️✨

[Nicknicks58]

Hi, I have similar problems to you, I have visceral hypoalgesia with activated muscle trigger points, that was the diagnosis 12years ago but since I have been on this site it sounds like p n, nobody understands the amount of pain I'm going through either you have my sympathy hope you can find some meds that help