Dr. Jamie Benham, along with two of our PCOS Patient Advisory Council members, Erin Joslin and Jade Broughton, participated in an interview with journalist Hanan Hammad for News Decoder about how and why people sometimes turn to online sources for medical information — especially when traditional healthcare pathways feel slow or dismissive. The conversation highlighted that many individuals with PCOS first found language for their symptoms and community support through online forums before ever receiving a formal diagnosis, underscoring both the value of peer-to-peer spaces and the risks of misinformation.
Lab News - October 28, 2025
Related News
May 12, 2026
PCOS has a new name! Formerly known as Polycystic Ovary Syndrome (PCOS), the new name Polyendocrine...
MAY 12-13, 2026
Members of our team travelled to Edmonton to attend the 2026 NW SPOR Collaborative Forum. Halle...
May 9, 2026
On May 9th, we gathered with our PMOS Patient Advisory Council (PPAC) to celebrate one year...