My Nonprofit Reviews

I was diagnosed with a PNET 12/2017. I have never heard of Neuroendocrine Cancer prior to this. I get online and start to Google, I came across NCAN's website and requested a patient pack be sent to me. It was so informative and I quickly learned a lot of information. I then spoke to Maryann a few times with questions. In March of this year I got to meet Maryann & Bob along with the rest of the NCAN leaders and I have to say it was the best feeling I have had in a long time. Everyone is so wonderful and the support they have for patients and caregivers is above and beyond. I am so happy that I found another family and great support system.