About Us/Contact

The Pheo Para Project was founded in 2015 as a platform to showcase stories about pheochromocytoma and paraganglioma, made by patients and their families, and to provide information about these rare neuroendocrine tumors. Since that time, we’ve produced two videos for World NET Cancer Day directly, and served as consulting producers for Attiya Khan’s 2017 offering, “Pheochromocytoma: The Last Episode.”

The Pheo Para Project’s mission is to increase awareness of pheochromocytoma and paraganglioma, and to support patients with these rare tumors, as well as their families and caregivers. On our site, you’ll find stories from patients and their families, documenting their paths to diagnosis and their lives as they move forward with the disease. In addition, in early November of each year, we’ll post our annual video contribution to NET Cancer Day.

We are always accepting stories! If you’d like to participate, please contact us: