26/01/2026
This is me in September 2015. I’d been diagnosed with endometriosis and adenomyosis, approximately four weeks prior, after experiencing symptoms of both conditions for at least 8 years.
Whilst I had a diagnosis (or two even), I had no idea where to start. I’d had surgery to have my endometriosis lesions cut out, but I was still in pain. I thought all I needed was surgery and I’d be fixed. I didn’t know that it was only one part of a larger picture, puzzle or strategy.
I didn’t know anyone else with endo. I had only just learned that adeno was even a thing. I had no idea where to find information that was reliable, and spent HOURS on google searching for ways to manage my pain and other symptoms I experienced. I saw professionals who were asking ME what endometriosis was, when I was hoping they could help.😬
If I knew what I know now, then, I would have had a MUCH smoother recovery, and would have felt MORE confident managing my illnesses.
That’s why I’ve spent years working to create change for the chronic illness community and particularly my LTP community who are living with Endo, Adeno or PCOS. I’ve done countless hours of education, study and professional development around endometriosis, adenomyosis and pcos, as well as having lived experience myself.
I don’t want anyone else feeling the way I felt.
I don’t want anyone else feeling alone.
I don’t want anyone else feeling overwhelmed, confused and unsure where to turn.
I don’t want anyone else spending hours on google trying to find info that they can trust, but don’t know if they can.
I don’t want anyone else not living their best life because of their chronic illness.
If you are living with Endo, Adeno, PCOS or pelvic pain and don’t know what’s wrong, then I’m here for you! LTP is here for you! There are SO many resources and so much content I’ve created, as well as our LTP community to help you as well, so you never feel alone and always feel supported! 🫶🏼
