Home » Our People » EndoChampions » James Fidanza

Dr Jane Chalmers (PhD, B.Physio) is a Senior Lecturer in Pain Sciences at the University of South Australia. She is the leader of the pelvic pain theme under the Innovation, Implementation And Clinical Translation in Health (IIMPACT) research concentration at the University of South Australia.

James Fidanza


James is studying to be physiotherapist and works part time as a Patient Service Assistant at a hospital transferring patients, supporting them with any of their needs. James loves to see patients reach their goals and has always wanted to work in the healthcare industry. James loves anything to do with sports and is a bit of an adrenaline junkie. James also enjoys travelling and wishes to continue to volunteer his time in third world countries.  

On his journey and experiences with endometriosis, James has said:  

“Endometriosis (endo) was something I never heard of until I met my girlfriend Brooke, back in 2019. After learning about it, I was in total shock of what my girlfriend went through at such a young age and what she still continues to go through to this day. Brooke was diagnosed in 2016. She had two surgeries resulting in 4 keyhole scars to remove the endo and ovarian cysts, she’s seen multiple doctors and has had many appointments, ultrasounds and blood tests. I’ve seen her in agonising pain on the floor in tears. I’ve seen her skip social events because the pain is that bad and she can’t even move. I’ve seen her carry multiple cysts up until the point that they rupture (at least 8). As her partner it kills me seeing her in excruciating pain and not being able to get rid of it. As being one of her support systems, I try play my part and help with whatever I can to reduce the pain. This can be from heating up her heat pack, to getting a hot bath/shower ready and even attending the ongoing doctor or radiology appointments.  

After introducing her to my mother, I found out that my mother also suffered from endometriosis. I was completely unaware, that someone so close to me suffered from this chronic condition and made me realise that this is a huge silent pandemic. Brooke has been an inspiration to many and me as she has started her own endo account on Instagram where she is breaking down the stigma by raising awareness about endometriosis and her own sharing her own endo story. After learning about endo I’ve learnt that endometriosis is heavily under researched and underfunded, so I wanted to help support all the EndoWarriors out there suffering endometriosis and put my body on the line, just as you amazing people do every single day”.