Has Anyone Had Endo Symptoms After Having A Hysterectomy?
I had a hysterectomy 7 years ago . My overuse were attached to my Bowles and other organs due to endrometriosis. I had stage four endo. It had traveled up into my abdomen and other parts of my body. My pain is gone and not as bad as it use to be . But I still get some symptoms in my bowls , back stomach and lungs .
Can relate. Started taking Emma & I am more regular now than I can remember.
After my hysterectomy I ended up having 2 more laparoscopies and the last surgery they had to leave live endometriosis in my ureter and pelvic cul de sac due to the depth.
Many years later I know have gastroparesis, IBD, gastritis, and pressure under my rt rib cage. I just got out of the hospital where I had Enteritis and gastritis. They thought I had a 70% blockage but after another scan they said no it’s not but never said what it was.
I know I have a belly full of adhesions that is screwing with my intestine. I’ve had 8 abdominal surgeries from Endo.
I was working part time but I asked my boss to let me go. I’m nauseous most of the time and the pressure in my upper belly is terrible.
Does anyone relate to all the digestive issues from most like adhesions on their colon?
Thanks for letting me vent
Diane
I hope your having a good day
I am sorry to hear that . It’s such a battle . I feel like know one understands how I feel in my family and even my Drs.
I had a hysterectomy in December of 2020 and im currently still struggling with endometriosis! Ive had 4 surgeries to remove endometriosis and it's come back within months of being removed.
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