// BBC HEALTH NEWS — SALUTE
Doctors said I was too young to have endometriosis at 13 - I had to take morphine to cope
Grace struggled with severe period pain before she was diagnosed with endometriosis
Every month, at about the time of her period, Grace has to be taken to hospital.
She is often in so much pain her parents have to carry her to the car. She can wait hours to be seen in A&E, only to be sent home in tears with more strong painkillers.
For a long time, Grace - who's now 14 and is from Yorkshire - felt doctors were dismissive of her pain. "I feel like I was seen as a girl who didn't want to go to school and was being dramatic," she says.
She was given multiple possible reasons for her symptoms: irritable bowel syndrome, a cyst, anxiety and "just a bad period". But, she says, "I knew it was more than that."
Doctors told her time and again that it could not be endometriosis - an incurable condition causing lesions and scarring on internal organs and around the body, external - because she was too young. Grace says her requests for further investigation were ignored.
Grace's periods began when she was 11, and by 13, she was having excruciating pains around the time of menstruation. She describes it as if "heated barbed wire" were wrapped around her abdomen: "It's like my organs are being pulled apart."
She is often bedbound and, whenever she has exhausted the painkillers she has at home, she has to go in to hospital, where she is regularly given morphine. She has also been given co-codamol and tramadol.
Dependency on strong drugs like opioids worries her. "It's scary," she says, "because I don't want to have to rely on them for the rest of my life."
Grace has been hospitalised and regularly given opiods like morphine for her pain