Hi all,
Diagnosed with this on Friday. Surgery soon. Then a break and radiotherapy for 6 weeks. If anyone has any advice and tips on this rare one, it would be much appreciated. I'm 56 and seven months post total hip replacement. Suffered with a blocked nose and bleeding for 6 months, then casually went to see the doc and got accelerated though cat scans, MRI's, biopsies, the works.Total random diagnosis. Not in my family and no lifestyle indicators to lead here. Can't help but think about the MRNA covid vaccines, but too late for that now.
