Guest post by Tanya Patel, founder of online maternity and breastfeeding brand Lily and Ribbon
‘My doctor diagnosed me with everything from epilepsy to migraines before realising I actually had endometriosis’
Call out: Research on experiences of endometriosis care (trans-inclusive)
Researcher Jodie Hughes would like to hear from anyone with endometriosis
Continue reading “Call out: Research on experiences of endometriosis care (trans-inclusive)”
Endometriosis: ‘I felt betrayed by my body and the professionals who had failed to recognise my pain’
Adenomyosis: ‘It shouldn’t be up to us to tell our doctors which conditions to look for’
PMDD: ‘By considering my viewpoint, and listening to me talk, my doctor validated my feelings’
Guest post by Laura Teare-Jones, for PMDD Awareness Month
‘Healthcare providers need to understand the impact of untreated endometriosis’
Q&A with Dr Natalya Danilyants from the US
Continue reading “‘Healthcare providers need to understand the impact of untreated endometriosis’”
Endo Art: ‘Women do not even get the privilege of owning their pain’
Guest post by women’s health artivist Alicja Pawluczuk
Continue reading “Endo Art: ‘Women do not even get the privilege of owning their pain’”
Endometriosis: ‘It pains me to say, but I knew I’d be taken more seriously now I could say sex was painful too’
Guest post by Dominique from Switzerland
‘13 hours of surgery, months of recovery. For what? My surgeon had left an ovary inside me’
Guest post by Emma Williams-Tully
‘Why did I have to climb the endometriosis treatment ladder, just to get the procedure we knew would help?’
Guest post by Anusha Gandhi from Canada
Fertility status unknown: ‘I cried almost as if I was already mourning the loss of a child’
‘I chose not to have children so I wouldn’t be in pain anymore. But in fact, I ended up in even more pain.’
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