Pheochromocytoma and Paraganglioma


Have you wondered if NETs might be hereditary? What do you know about pheochromocytoma and paraganglioma (pheo/para)? NET expert Dr. Jaydira Del Rivero gives a full update on these rare and often misdiagnosed conditions. Recorded on February 17, 2022.
To download a copy of Dr. Del Rivero's presentation slides, go to bit.ly/slides_feb2022.
This presentation is also available in Spanish, found here: youtu.be/moN-iwvoTsI
Speaker:
Jaydira Del Rivero, MD, Endocrinologist, Oncologist, National Institute of Health
To learn more about LACNETS, visit www.LACNETS.org.


Aimee Powell, a caregiver and advocate for family members diagnosed with pheochromocytoma and paraganglioma shares what led her to a life of patient advocacy and assisting patients with these rare tumors. Aimee is the founder of The Pheo Para Project – www.pheoparaproject.org.
To learn more about LACNETS, visit www.LACNETS.org.