Our Partners
The National Pancreas Foundation provides hope for those suffering from pancreatitis and pancreatic cancer through funding cutting edge research, advocating for new and better therapies, and providing support and education for patients, caregivers, and healthcare professionals. The National Pancreas Foundation is a supporter of and key partner in Mission: Cure’s first project, Mission: Cure Pancreatitis.
Rebecca’s Wish provides help and hope for children suffering from pancreatitis through supportive patient care, charitable services and medical research.
The Chan Zuckerberg Initiative was founded in 2015 to help solve some of society’s toughest challenges — from eradicating disease and improving education, to addressing the needs of our local communities. Its mission is to build a more inclusive, just, and healthy future for everyone.
The National Organization for Rare Disorders (NORD) is the leading independent patient advocacy organization representing all individuals and families affected by rare diseases in the United States. NORD improves lives, empowers patients and caregivers, and provides the right information and resources at the right time.
The Collaborative Alliance for Pancreatic Education and Research’s (CAPER) mission is: (a) to facilitate the collaboration of researchers of pancreatic diseases and to support scientifically rigorous multi-center studies in pancreatic diseases; (b) to educate and train healthcare providers in pancreatic diseases; (c) and to increase public health awareness regarding pancreatic diseases.
The purpose of Global Genes is to connect, empower and inspire the rare disease community.
As a member of this strategic advisory council, Mission: Cure will be working on urgent policy issues by collaborating with both industry and patient organizations to create and advance science-based policy for the rare disease community.
Black Women’s Health Imperative launched the Rare Disease Diversity Coalition to address the extraordinary challenges faced by rare disease patients of color. The Coalition brings together rare disease experts, health and diversity advocates, and industry leaders to identify and advocate for evidence-based solutions to alleviate the disproportionate burden of rare diseases on communities of color.
Connecting Pieces is a nonprofit organization dedicated to serving as a beacon of support and resources for individuals and families impacted by Gastrointestinal Disorders (GI) and associated challenges. Their mission extends beyond providing education and support; they actively address health disparities by accepting donations of ostomy supplies and distributing them to those in need, ensuring accessibility for those facing barriers. Additionally, they are committed to hosting retreats tailored for families affected by GI conditions, offering a sanctuary for support and access to vital resources. Connecting Pieces prioritizes mental health and holistic well-being, striving to empower every individual to navigate their journey with resilience and hope.
The Autoimmune Registry Inc. (ARI) is a hub for research, statistics, and patient data on all autoimmune diseases. Its goal is to streamline data on autoimmune diseases so that researchers can better understand the complexity of this class of diseases and discover new treatments. ARI also connects patients to eligible clinical trials to facilitate the research and approval of new treatments for autoimmune diseases.
IndoUSrare is a patient-centric nonprofit that advances cross-border collaboration to shorten the diagnostic odyssey, enable inclusive clinical research, and expand access to therapies for rare diseases. By convening patient organizations, clinicians, researchers, regulators, and industry partners across the US, India, and beyond, IndoUSrare builds pragmatic bridges that turn scientific promise into equitable, real-world impact.
Program Supporters
