Long story short. I’m 26. Officially diagnosed via laparoscopy a year ago. Had the Mirena fitted. I had 3 injections of prostap last year and 3 this year (personally for me it was amazing) I went to see pain management who gave me a 3 stage plan of drugs co-codamol 8/500, zapain 30/500, gabapentin 300 mefenamic acid, buscopan, Buprenorphine.. I’ve taken buprenorphine for a total of 4 days in the past 6 weeks... it’s not helping right now. I’m in constant pain. My bowels are okay not constipated but I have blood and mucus which is common during my flare ups but I’ve had this flare up continuously for 8 weeks now. 3 our of 7 days roughly I’m grtting these very strong severe contraction like pains around my pubic area which last about a minute and come and go every 10-15 minutes or so but that minute feels like forever it takes my breath away and it floors me every time..
Does anyone else get those contracting pains like you want to push and you get all sweaty but there’s nothing to actually push? It honestly feels like I dilate during it...
I’m doing pelvic floor therapy with my physio but each week it’s always an internal and internals are soooooo painful for me.. I have adenomyosis as well 😢
My question is what do you all do to help? Any suggestions? I’ve changed my diet a year ago, I try and keep active when I’m not curled up in a ball.. I try and keep moving even with the severe pain but it’s got that bad the pain goes down my groin legs and back. I have sharp pain in both my left and right and it feels like a dragging pulling pain which is dull but always there (I have reoccurring cysts)
I’m sick of being In daily pain. I’ve tried so many different anti inflammatory too as well as daily tumeric..
Please if anyone can suggest something to help I would be so grateful. It’s a fighting battle against my Drs but thankful I done their heads in that much they sent me back to see gynae.. those in the U.K. might of heard of a mr David rowlands I’m under him again never met him but he operated last year.. we know it’s grown because a cystoscopy confirmed its inside my bladder but my question is... is 12 months too soon for them to go bavkcin and remove all the newly grown endo? Or will they just leave me to carry on suffering! I’ve lost my job over these after collapsing and taking a lot of time out of the office even though I worked from home I wasn’t reliable enough even though I had 7 absences in 12 months to them it’s a lot..
Please any advice on what I can do would be great because I can’t cope.
Ps.. I also use biofreeze cryotherapy gel to rub onto my stomach to try and help 😭😭😭😭😭😭😭😭