Anyone else with peritoneal mesothelioma here?
I hear my diagnosis is literally one in a million. Weird to be 43 and have been totally fit & healthy and never really have a doctor then bam, world up side down, loss of everything I value in life and know so few souls experiencing this. I am connected to MARF, just wondering if there are any fellow patients at Mayo who can relate.
Interested in more discussions like this? Go to the Colorectal Cancer Support Group.
Thank you so much for welcoming me! Im NED (no evidence of disease) as of right now thankfully. I would suggest to find a doctor who has expertise in meso research right away. I am a patient at Mayo, but I also go to M.D. Anderson in Houston. I do scans every 3 months between the Mayo and M.D. Anderson. I also am in palliative care. It can feel pretty lonely going through all of this, and was hoping to reach others who are going through this and can understand the constant fear. Please feel free to ask me any questions you might have!