I was diagnosed with endometriosis in 2022 following a surgery to remove an ovarian cyst. I had, like many people, been going to my GP for years due to my periods and the symptoms that came along with them. Each time I was turned away with various doctors and nurses telling me that 'it was normal' and 'periods are painful'. It took 12 years to get my diagnosis and it only happened by chance.

I would love to say that this is rare and that generally people don't wait nearly as long but sadly the average diagnosis time for endometriosis is 8-10 years.

There is an array of symptoms that come along with endometriosis including:

- Pelvic pain

- Lower back pain

- Painful periods that interfere with everyday life

- Heavy menstrual bleeding

- Pain during or after sex

- Painful bowel movements

- Pain when urinating

- Difficulty getting pregnant

- Fatigue

It's pretty self explanatory how much these symptoms can interfere with a persons life even more so when the medical professionals we rely on so much are telling you there is nothing wrong.

There is no cure for endometriosis, only management of symptoms. It's incredibly unresearched and unfunded which means those impacted have little to no support.

That's where Endometriosis UK come in, they're the UK’s leading charity for all those affected by endometriosis, determined to ensure that everyone gets prompt diagnosis and the best treatment and support.

They work to break down barriers to access - whether information, treatment or support - wherever endometriosis impacts on lives. They are a powerful voice for those with endometriosis, driving up care standards across the UK.

They lead collaboratively across the community, acting to inform, empower and advocate for all those affected by the disease. The endometriosis community is at the heart of all they do, and they strive to support and represent all experiences.

They fight to make change happen for everyone with endometriosis, to end chronic menstrual related pain being brushed off as normal and raise awareness of endometriosis with the wider public.

They provide vital support services, reliable information and a community for those affected by endometriosis.

And like most charities they receive minimal funding for the work they do.

This is why I've chosen to hold a Tea for Endo, to give back to the charity that has helped me on my journey.