Bringing this to the community because I think it speaks to something a lot of people here have experienced.
A local news report from Memphis covered a minimally invasive BPH treatment now being offered at a vascular centre there — likely prostate artery embolisation (PAE), an interventional radiology procedure that treats an enlarged prostate without traditional surgery.
The reason I find this worth sharing: most men with BPH aren't told about this option. They're told about alpha blockers, 5-alpha reductase inhibitors, and eventually a TURP or similar surgical procedure. What tends to fall out of the conversation is the growing landscape of minimally invasive options — often available at centres that aren't even urology practices.
The access gap is real. But so is the information gap.
For those in this community who've navigated BPH treatment decisions: what options were you told about? And — importantly — what weren't you told about until you went looking yourself? I'm curious whether people found the care pathway informative, or whether they had to push to get the full picture.