We’re thrilled that you’re keen to help us out! Endometriosis New Zealand relies on our generous community across New Zealand to continue to provide unique and professional services and programs to improve health outcomes for those living with endometriosis and persistent pelvic pain. We don’t receive any government funding, so it’s people like you who make all this possible.
Jamie was on a mission to commit to run over 10 days a total distance of 100 kilometres to symbolize the 1 in 10 kiwi girls who are impacted by this condition. However, she has been inspired to push herself to a further 20 kilometres and run a total of 120 kilometres to reflect the estimated 120,000 women in New Zealand who live with endometriosis.
“For over a decade, I have battled with the debilitating effects of endometriosis, enduring chronic pain, as well as countless challenges and not knowing why. In 2022, I finally received a diagnosis of severe endometriosis, marking a pivotal moment that allowed me to have answers to what I was experiencing unknowingly for so long and have the reassurance that it wasn’t all just in my head.
My aim is to shed light on this often misunderstood disorder, advocate for early detection, support improved treatments, and ultimately enhance the quality of life for those affected.”
Dayna is competing in the Sunshine Coast Ironman 70.3. This is her second ever triathlon which is 4 times the distance of her first one, and she is doing it to raise money for Endometriosis New Zealand, and spread awareness for this horrible disease.
“Earlier this year I was supposed to do the Taupo 70.3 Ironman however had to put it off due to having my first (and hopefully last) surgery for endometriosis.
I struggled to train due to experiencing excruciating pain at random timings. I used to think that the level of pain I experienced was “normal” so it was a relief when I was eventually told it was not.”
Kirsten ran her first ever half marathon on May 18, 2024, in the La Roche-Posay Marathon in Napier.
“Endometriosis has impacted my life and the lives of so many people close to me. My endo experience started at 13, and after 12 years of pain, doctor’s visits, and frustration, I was finally diagnosed at 25 years old when I had my first surgery.
It’s so important for people, especially our younger generation, to be able to recognise the signs and symptoms of endo, and to have the confidence to advocate for themselves rather than feeling alone in their journey.”
Please let us know the details of your fundraising event by filling out this form and we will be in touch and provide you with promotional resources to help you spread the word about your event.