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UK fertility regulator could propose scrapping donor anonymity law
HFEA to revisit the 1990 Human Fertilisation and Embryology Act

The fertility watchdog says that a rise in genetic testing websites is likely to make it impossible for donors to stay anonymous.
The Human Fertilisation and Embryology Authority (HFEA) is considering whether to recommend scrapping anonymity for future sperm and egg donors as part of a future overhaul of UK fertility laws, according to the Guardian.
Peter Thompson, the chief executive of the HFEA, said an increase in consumer genetic testing websites could threaten donor anonymity and therefore, the law needs to be brought into line with this new reality.
“We feel that the technology of cheap DNA tests throws into question the underlying assumption [of anonymity],” said Thompson for the newspaper. “Given that, the responsible thing to do is to start a conversation about where we as a society want to go on these things. It’s a big change.
“You can see a position in the future where confidentiality just becomes impossible, whatever the attitude of families, the honest truth is that people will just find out,” he added.
Under the current rules introduced in April 2005, people conceived from donated sperm, eggs or embryos are able to find out the identity of the donor once they reached the age of 18. However, donors can choose to keep their anonymity until then.
Scrapping anonymity from birth could mean more contact between donors, donor-conceived people and their parents, but is likely to spark controversy.
The HFEA is planning to look at the 1990 Human Fertilisation and Embryology Act and propose draft legislation by the end of this year.
The Guardian reports that the regulator is expected to demand greater powers to fine fertility clinics found selling ineffective “add-on” treatments and wants to make it easier for same-sex couples and single people to access treatment.
The HFEA chief executive said that the watchdog had not decided on a proposal around anonymity, but that one option under consideration is “a presumption of openness almost from the word go”, with the anonymity of donors being lifted at birth.
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Endometriosis documentary profiles stars including Marilyn Monroe and Amy Schumer

A non-profit has launched an endometriosis documentary featuring Amy Schumer and Marilyn Monroe as it pushes for changes in how the condition is treated and understood.
The Endometriosis Collective has launched to change how endometriosis is researched, treated and understood, starting with a documentary featuring stories from people including Amy Schumer and Marilyn Monroe.
The feature-length documentary, “End of the Cycle”, will premiere in New York on Tuesday, and The Endometriosis Collective is making the film free to stream online.
Schumer, a comedian, writer and actor, has previously spoken of how endometriosis left her “on the floor in pain, vomiting from the pain, the pain that nobody can see.”
Schumer is one of several celebrities featured in the documentary. Other contributors include dancer Julianne Hough, Olympic medallist Brittany Brown and actors Janel Parrish and Folake Olowofoyeku.
The Endometriosis Collective timed the documentary premiere to coincide with the 100th anniversary of Marilyn Monroe’s birth.
Monroe, who died in 1962, starred in films such as “Some Like It Hot” and “Gentlemen Prefer Blondes.”
According to a biography published in 1985, Monroe’s endometriosis was so severe that it destroyed her marriages, her wish for children, her career and ultimately her life.
The Endometriosis Collective said the documentary shares newly uncovered information about Monroe’s experience with endometriosis.
The non-profit said the information connects Monroe’s story to the experiences of women across generations, highlighting how far awareness, research and care still have to go.
A representative of the Marilyn Monroe Estate said: “By sharing this part of her story through ‘End of the Cycle,’ we hope to honour her legacy in a way that brings visibility to endometriosis, encourages more open dialogue and helps inspire the research needed to create change.”
As part of the premiere, The Endometriosis Collective is holding a panel discussion.
Schumer, Brown and Olowofoyeku, the documentary’s co-directors Sammy Jaye and Soraya Simi, and medical experts are due to be part of the premiere.
AbbVie’s Orilissa and Sumitomo Pharma’s Myfembree are among the approved drugs for endometriosis pain.
Hough, one of the participants in the documentary, starred in an Orilissa campaign in 2017.
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