Albert Freedman, PhD, is a psychologist, educator, and rare disease advocate with more than three decades of experience working with individuals and families affected by rare diseases and disabilities.

Dr. Freedman is inspired by his personal journey as the father of Jack, who lived with spinal muscular atrophy (SMA) for 26 years as well as his professional training to provide counseling and consultation. He works with families, advocacy organizations, pharmaceutical companies, and healthcare organizations to create meaningful support systems and impactful change within the rare disease and disability communities.