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myendometriosis.bsky.social
Advocating for endometriosis awareness 🎗️| Stories and global updates regarding endo & other gynaecological conditions | 1 in 10 | U.K. |
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Can you help us with our research? We'd like to understand more about the uncertainty that people can experience whilst going through fertility treatment (e.g. IVF, IUI) or fertility problems (e.g. PCOS, Endometriosis). More info below! ⬇️ nclpsych.eu.qualtrics.com/jfe/form/SV_...

We are being failed. Those with #Gynaecological conditions deserve better. #NHS #InvisibleIllness #Endo #PCOS #Disability

Over the space of 8 years I’ve had 6 transvaginal ultrasounds, 5 showed nothing. But one showed deeply infiltrative #endometriosis. ALL it took was an endometriosis consultant who is trained in transvaginal ultrasound to diagnose me within 5 minutes. #Medsky #Medicine #Gynaecology #Health

“I feel like I’m being stabbed by a thousand tiny men” A great article from a linguistic perspective delving into the challenges #women face describing #endometriosis pain, the role of metaphors, and how tools like metaphor menus could bridge communication gaps between patients & doctors.

Fellow #Endometriosis sufferers, were you #diagnosed through invasive techniques (e.g., laparoscopy) or non-invasive methods (like transvaginal ultrasound or #MRI)?

General gynaes are treating endometriosis patients, we need more #specialists in the #NHS. Sophie’s story: “Doctors attributed her symptoms to phantom pain, and even appendicitis, which led to her having her appendix being unnecessarily removed.” She was later diagnosed with #endo & #PCOS

PSA to those who suffer from #ChronicIllness 👇

#UnwellWomen by #ElinorCleghorn is my night time read! A great #book which delves into the key topics of how medical research has historically prioritised the male body. With women’s health being profoundly under researched. #Disability #Medicine #Medsky

A #BBC article includes the lived experience of #endometriosis through Vicky’s story: "When I say ‘I’m fine’, I’m in pain," she says. "And when I say ‘I’m in pain’, I’m really in a lot of pain." The popular press must continue to give a voice to those #struggling with endometriosis 🎗️

Reminder: endometriosis is not just a ‘bad period’ 🎗️

I have endometriosis, an #InvisibleIllness, today I feel: Isolated, misunderstood, existing with an unpredictable body. My plans often get cancelled, and the need to explain the condition and its effects become exhausting, I feel like a burden. Does anyone else resonate with this?

Enlightening article by @bmj.com. Really bringing to light how #endometriosis care should not just rely on #surgical management, but should adopt a comprehensive, #multidisciplinary approach that integrates #medical treatments with #psychological support and effective #pain management strategies.

This is one way to put it into perspective... "If all 760,000 #women waiting for #NHS #gynaecological appointments were to stand in a line, the queue would go from London to Exeter". We are being failed.

Kudos to #FlorencePugh for opening up about her journey with #Endometriosis and #PCOS. Building awareness in the media is definitely one step towards battling the ignorance surrounding women’s health. www.dailymail.co.uk/tvshowbiz/ar...

Something that i think more people need to hear, is that #endometriosis is a #disability ‼️

Me today 🥲🌻 #endometriosis #endo #WomensHealth #ChronicPain