We are dedicated to supporting and advocating for children and families affected by GPT2 Deficiency around the world. Our goal is to raise awareness for this rare disease, while also supporting scientific and medical research focused on finding a cure.
We are just beginning our journey with an objective of creating a network of individuals, clinicians and researchers. Our hope is to connect individuals and families through our support group because we believe that power is in numbers, while also connecting clinicians and specialists who are treating individuals with GPT2 Deficiency to improve patient care and outcomes. We intend on providing resources to anyone seeking out more information on this disease, including ongoing research studies.
We’re looking forward to hearing from you!
Email us at firstname.lastname@example.org