Rare Disease Day 2023: Cast an Even Brighter Light on hATTR
For this rare disease patient, it is reassuring to discover online groups and organizations that connect me with others who live with hATTR.
Jackie Rubick-Gomez
Jackie Rubick-Gomez was recently diagnosed with familial amyloidosis (hATTR) and has the P.Glu74Gly variant. She is eager to share how her life has changed and how she’s managing her rare disease. “I am honored to have been given this amazing opportunity to discuss my experiences with my disease,” Jackie said. “I have 3 young children who may carry the gene.” And that, among other factors, motivates Jackie to hope that her knowledge about the disease and treatment experiences are readily available for others with hATTR.
