Journalist seeking interviewees for feature series on endometriosis & adenomyosis [London/UK-based]

Hi everyone,
I'm a journalist working on a series of features about endometriosis and adenomyosis, and I'm looking for people who'd be willing to share their experiences. I want these pieces to be led by the voices of those actually living with these conditions, so if any of the following resonate with you, I'd love to hear from you.
I'm working on three stories:
1. The case for statutory menstrual leave — Are you someone whose endometriosis or adenomyosis has affected your ability to work? I'd like to speak with people about their experiences in the workplace, and what statutory menstrual leave would — or wouldn't — mean for them in practice.
2. The diagnosis gap — The average diagnosis time for endometriosis has grown to over 9 years. If you've experienced long waits, dismissal by healthcare professionals, or a particularly difficult road to diagnosis, I'd really like to hear your story.
3. NHS women's health services — Have you struggled to access specialist care, or felt let down by the system despite finally having a diagnosis? I'm exploring what underfunding looks like from a patient's perspective.
You don't need to be based in London — I'm happy to speak by phone or video call. Participation can be anonymous if you'd prefer, and I'll always ask for your consent before using anything you share.
If you're interested or have any questions, feel free to DM me or drop a comment below.
Thank you so much for reading — I know this community's time and energy is precious, and I really appreciate it. 🌸