Living with Choroideremia: Cory MacDonald Shares His Journey | CRF 2025 Interview
Join us for an intimate one-on-one interview with Cory MacDonald, co-founder and Engagement Director of the Choroideremia Research Foundation (CRF). Cory opens up about his diagnosis, growing up with choroideremia (CHM), and the challenges he has faced navigating life with this rare inherited retinal disease. This conversation was filmed at the 2025 CRF International Conference, held June 25–28 at the Radisson Blu, Mall of America, Bloomington, MN. 🔗 Learn more about CRF: https://www.curechm.org 🔗 Support research: https://curechm.salsalabs.org/donate #CureCHM #Choroideremia #RareDisease #SavingSight #RetinaResearch #RetinitisPigmentosa #RareDiseaseAdvocacy #BlindnessResearch #Ophthalmology #MedicalResearch #EyeHealth #GeneTherapy #Optogenetics #ClinicalTrials #RareDiseaseCommunity #VisionResearch #EndingBlindness
Cory’s story: Living with Choroideremia; Choosing to live with courage
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