EndoEdition @EndoEdition

🔅 Reliable endometriosis facts, research, and awareness 🔅 Advocating the largest women's health crisis of our time, also affecting trans & non-binary. instagram.com/endoedition West Midlands, England Joined April 2018

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EndoEdition @EndoEdition

2 months ago

We call on the UK Government to introduce statutory paid menstrual leave of up to 3 days per month for people with conditions such as endometriosis and adenomyosis, following the model introduced in Portugal in 2025. Help us get to 100,000 signatures 📝 petition.parliament.uk/petitions/7323…

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EndoEdition @EndoEdition

3 months ago

This is our pain. Powerful speech, thank you @PearseDoherty. Post via @Kathleen_M_King. #endometriosis #adenomyosis

Pearse Doherty @PearseDoherty

3 months ago

This is our pain. Powerful speech, thank you @PearseDoherty. Post via @Kathleen_M_King. #endometriosis #adenomyosis

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EndoEdition @EndoEdition

4 months ago

Working women are too often left to deal with endometriosis alone. But big changes could be coming... Via @Kathleen_M_King theconversation.com/working-women-…

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Kathleen M King @Kathleen_M_King

6 months ago

Endometriosis: 'I'm disgusted with the NHS after our daughter took her own life' news.stv.tv/east-central/f…

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Sara Keenan @SaraKeenan16

7 months ago

I spoke with the amazing @AnitaNnekaJones about her long journey with endometriosis as says she was ‘gaslit by doctors for 14 years’ independent.co.uk/life-style/hea…

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Beth McColl @imbethmccoll

7 months ago

waited 18+ months for a referral, diagnosed with a serious mental illness, had to move in with my parents because I wasn’t able to work enough to pay rent, move meant I was dropped from local services & am back at square one & can work less than ever. what a worm this man is

Saul Staniforth @SaulStaniforth

7 months ago

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hate zine @hatezine

7 months ago

Any journalist or commentator talking about PIP being easy to get should see for themselves how hard it is. Far too many people talking about things they know nothing (and don’t care) about.

Anne Greensmith 💙 @snowleopardess

7 months ago

Any journalist or commentator talking about PIP being easy to get should see for themselves how hard it is. Far too many people talking about things they know nothing (and don’t care) about.

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Sarah Harris @sarahhasendo

8 months ago

So excited to be starting the next stage of my PhD which will involve interviewing those with a lived experience of #endometriosis about their interactions with primary health care physicians. If you are interested please drop a message to email on poster or scan the QR code 🎗️

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EndoEdition @EndoEdition

a year ago

Annalise Weckesser "UK folks - if know a young person (10-18 years) who experiences *period pain* - there is this amazing study being conducted by my friend and colleague @UniofOxford....." @EndoSRN @VQ_Birmingham phc.ox.ac.uk/research/group…

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The BMJ @bmj_latest

a year ago

"Studies of how quickly doctors interrupt patients find that the median time is 11 seconds. Nobody feels listened to in 11 seconds." @Richard56 discusses the healing power of being listened to bmj.com/content/385/bm…

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Victoria Rubadiri @VickyRubadiri

a year ago

A life well lived. Rest Jahmby🕊️

EndoEdition @EndoEdition

a year ago

A life well lived. Rest Jahmby🕊️

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The Endometriosis Coalition @theendoco

a year ago

Our hearts are shattered by the loss of @JahmbyKoikai, an extraordinary endometriosis advocate for all. She was a warrior in every sense of the word. Her passion, strength, & relentless dedication inspired us all and touched the lives of so many in our community and beyond.

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The Nairobi Times @TheNairobiTimez

a year ago

BREAKING NEWS Njambi (Jahmby) Koikai alias Faya Mama has passed away😢💔 Mary Jahmby Koikai passed away following a long fight with endometriosis. Her friends and family have confirmed that she died in hospital on Tuesday morning. Rest In Peace🕊️

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Endometriosis UK @EndometriosisUK

a year ago

Research Opportunity👇👇 This study asks questions on your expectations and experiences of treatments for endometriosis and adenomyosis. Those living with either or both conditions are invited to take part at: forms.office.com/pages/response… #UniversityOfLiverpool #TEPEAstudy

Hapangama Research Group @Hapangama_Lab

2 years ago

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Cysters 🎗 🍉 ✊🏿 @cystersgroup

a year ago

We're tackling healthcare disparities for people of color % the delayed diagnosis of endometriosis Despite widely cited statistics, they don't accurately represent communities of color. Rejected for funding, we're pursuing this research voluntarily, committed to inclusion 👇🏾