Gabbi Lewis is a passionate patient advocate living with the rare genetic condition Classical Homocystinuria. Her personal journey navigating this complex disorder has fueled her mission to raise awareness, support fellow patients, and drive meaningful change within the healthcare and life sciences communities. As an advocate, Gabbi works to amplify the voices of individuals and families affected by rare diseases. She partners with non-profits, biotech companies, and healthcare providers to ensure that the patient perspective is represented in everything from clinical trial design to disease education and policy discussions. With a strong belief in the power of storytelling, Gabbi shares her experiences to highlight both the challenges and triumphs of living with a rare condition.