"I was diagnosed with neuroendocrine tumors in 2022. I had never heard of this disease before, and I lived in a state without a single NET specialist. I was scared and unsure of what to do next. I am so thankful that I quickly reached out to the Neuroendocrine Cancer Foundation (NCF). One of the first NCF emails I received said, ' You are not alone. We are here to help.'  In the midst of uncertainty and fear, they offered hope . From the very beginning, NCF connected me with someone who...