Medical trauma is more common than we think, and rarely talked about. In this post, Matilda psychologist Sophie Callen explores what medical trauma is, how it might show up in your life, and offers grounding tools, self-advocacy language, and healing strategies for moving forward.

Bladder and bowel dysfunction are frequently under-recognised components of the endometriosis experience, yet they are often among the most distressing.

Matilda Health’s Beyond the Pain event in Broome brought together community and clinicians to discuss endometriosis and pelvic pain. We explored the gaps in care, the importance of pre- and post-surgery support, and how digital programs can improve recovery and connection in regional Australia.

Some days, just getting to an appointment feels like a huge effort. When my pain is bad, even sitting in the car can be exhausting, and by the time I arrive, I’m often too tired to fully take in the information or ask all my questions. And if I can’t make the trip at all, it means waiting longer for answers and delaying the care I need.

Scars, bloating, and self-doubt- Anna shares how endometriosis shaped her body image and how she’s learning to love her body again, exactly as it is.

When it comes to endometriosis, there’s no one-size-fits-all approach and choosing to have surgery is a deeply personal decision. It’s not something I ever took lightly, and it’s not the only path to relief. But for me, at three different points in my journey, surgery felt like the right choice. Looking back, each of those decisions came from a place of wanting to protect my health and quality of life and I do not regret undergoing any of those procedures.

The words we use in endometriosis care can either build trust or cause harm. In this blog, clinician Jo shares how subtle shifts in language can help avoid medical gaslighting, validate lived experience, and foster safer, more compassionate care for people with endometriosis.