The Endometriosis Foundation is a patient-led charity dedicated to supporting people affected by endometriosis. We offer educational resources, community support, and awareness initiatives to help individuals understand and manage this long-term health condition.
Our work is built on compassion, collaboration, and lived experience. We partner with medical professionals and those living with endometriosis to ensure our resources are both evidence-based and empathetic.
- Support Groups: Connect with others who understand your journey.
- Speak to a Nurse: Get reliable, up-to-date information and guidance.
- Educational Resources: Access clear, trustworthy information for patients, families, and carers.
- Awareness Campaigns: We work to make endometriosis more visible and better understood.
Founded by Carla Cressy, whose personal experience highlights the challenges of diagnosis and care, The Endometriosis Foundation is committed to driving change and improving lives. Our information is reviewed by specialists and follows current NICE guidelines.
We welcome everyone affected by endometriosis, as well as their loved ones and supporters. Whether you are seeking information, community, or ways to get involved, we are here for you.
Our services are free to access. We rely on donations and fundraising to continue our work. If you find our resources helpful, please consider supporting us.