Personal stories
Lily's Story
"I've never felt relief and validation to the extent I did on the day of my surgery because I finally had answers to my pain and knew I wasn't imagining it all these years."
This is Lily’s Story.
Anahita's Story
"I’ve missed so much time at school, university, work, social events because of my symptoms. It’s frustrating being that person that’s always unwell."
This is Anahita's story.
Ria's Story
"Talking about endometriosis is so important and I tell all my friends to feel free to ask questions as I know how hard the journey can be."
This is Ria's story.
Jessica's Story
"Over my whole journey it has felt like there has been a lack of willingness to help me, that the pain is in my head, I just needed to wait."
This is Jessica's story.
Josie's Story
"With Pride Month upon us, I wanted to share my story and how my sexuality has impacted my endometriosis journey."
This is Josie's story.
Mollie's Story
"I'm so exhausted and I genuinely feel bad for having to cancel on friends. It's easy for them to think I just can't be bothered, but actually I'm in agony."
This is Mollie's Story.
Daniela's Story
"Your struggles are valid, and you're not alone. Keep advocating for yourself, use a symptom diary and seek second opinions if needed. You deserve understanding and relief."
This is Daniela's Story
Nicole's Story
"I’ve been fighting for so long and never had the right answers as I was told I was ‘too young’ to have anything serious."
Saffiyah's Story
Content warning: brief mention of suicidal thoughts and feelings. Reader discretion is advised.
Rebecca's Story
Rebecca tells the story of her journey to diagnosis, mixed experiences with medical professionals and the impact of endometriosis on day to day life.
Michelle's Story
This Endometriosis Action Month, Michelle shares her experience of getting diagnosed and the impact of endometriosis on her life.
Tannagh's Story
“All I can say is keep the right people in your corner. My friends, family and colleagues are who get me through.”
Daniel's Story
“Be kind to yourself and remember that this is a long term very unpredictable condition that both of you will be coming to terms with.”
Maeve's Story
“I am so proud of myself for never giving up because knowledge is power and getting a diagnosis has helped me to take back some of the control this condition has had over me.”
This is Maeve’s story.
