After 10 years, I got my endometriosis diagnosis this year in April. I could go into how underfunded the NHS is, how little knowledge and research there is on the female body and endometriosis - we don't know what causes endo, what can cure it or how to cope with it.

I'm taking part in endometriosis UK walk for endo not only to raise money for this amazing charity who help us who suffer from endo feel heard, who advocate for more research, for easier diagnosis but I am doing this to also raise awareness of this invisible condition and to push myself. 8,000 steps a day doesn't seem like a lot however for someone with endometriosis the thought of it is daunting. There's going to be days where I can easily walk over 8,000 steps and there will be days where 8,000 is a struggle. I'm doing this to show myself that endometriosis does not need to rule my life and dictate what I do.

This will be a challenge in itself to face fatigue, pelvic pain and cramps and all things inbetween. I will use a mix of techniques including outside walks, using the treadmill at the gym and following walking exercise videos for those days I really can't leave the house. I will be documenting my fundraiser over on my instagram.

Endometriosis UK's recent report found that it now takes an average of over 8 years to receive a diagnosis in the UK - that is far too long! I'm taking part in Walk for Endo this Summer to help raise awareness and vital funds to support the 1in10 on their journey with endometriosis and take steps towards a time with quicker diagnosis and access to appropriate care.