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    Fear, pain, despair: Breaking silence on endometriosis

    PARIS (AFP) – Lorena Garcia was in her 20s when she was suddenly struck with crippling pain associated with her menstrual cycles.

    It was four years before she was diagnosed with endometriosis, a chronic, incurable disease that affects as many as one in 10 women worldwide.

    Before the diagnosis, she recalled feeling fearful and powerless as she sought help from over a dozen doctors, most of whom would tell her the pain was normal.

    “It was bad,” the Barcelona resident, now in her 30s, told AFP.

    “The doctors who look down on you, who call you crazy or even say that you’re hysterical… I felt very alone.”

    Endometriosis occurs when the cells that normally line the inside of the uterus migrate and grow in other parts of the body, mostly the pelvic organs – including the vagina, cervix and uterus – but also the bowel and bladder.

    Lena Dunham (pic above) and Danielle Collins (pic below)

    Chrissy Teigen (pic above) and President of the World Endometriosis Society Lone Hummelshoj (pic below)

    The cells respond to hormonal changes, and their movement or growth often coincides with menstrual cycles. Endometriosis sometimes causes painful lesions and cysts that can result in infertility.

    The only reliable way to diagnose endometriosis is by laparoscopy, which involves inserting a tiny camera into the patient’s abdomen under general anaesthesia.

    Even with a diagnosis and the best care available, finding the right treatment — usually some combination of painkillers, birth control pills and surgery — is a question of trial and error.

    Despite affecting nearly 200 million women around the world, the disease remains largely unknown to the public.

    A lack of research means there is neither an established treatment protocol nor a cure.

    “For centuries women were told that pain during menstrual periods was normal,” President of the World Endometriosis Society Lone Hummelshoj told AFP.

    “That’s the problem and that’s why we are where we are today. Changing that widespread belief will take time. That’s why women need to speak out.”

    In recent years celebrities including model Chrissy Teigen and actress Lena Dunham have used social media to advance a public conversation on endometriosis by sharing their own diagnoses.

    Teigen posted about her surgery to remove endometrial tissue in February.

    In May American tennis star Danielle Collins revealed to the press she needed surgery to remove an ovarian cyst the size of a tennis ball, saying her endometriosis diagnosis had been “shocking”.

    “As most women in the world who have our menstrual cycles, I think it’s something that sometimes when we’re dealing with these painful moments we learn to accept it,” said Collins, 27, who made the French Open quarter-finals last year.

    Institutional support is slowly being established around the world, often through advocacy by experts.

    Hummelshoj founded the Danish Endometriosis Society in 1997 and five years later Denmark began taking steps to increase public awareness and establish medical guidelines for dealing with the disease.

    Over the last decade, dedicated centres have sprung up in the US and in the UK.

    In 2013, Britain’s National Health Service made it policy that endometriosis patients should be seen at clinics staffed with specialised nurses.

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