Co-Founder/CEO of Onevoice shares how his new community building software solution supports the rare disease community.
All in Patient Advocate
Co-Founder/CEO of Onevoice shares how his new community building software solution supports the rare disease community.
Patient advocate talks about her hereditary cancer syndrome and offers her expertise and experience.
Patient advocates Bernadette Scarduzio and Allison Moore share about CMT, their documentary and the Hereditary Neuropathy Foundation.
Former camper and current camp counselor, Ester Wasserman shares the magic of camp, how it was founded, what it offers to seriously ill children campers and her own experience through the years.
February 29th is the rarest day of the year and that means it's Rare Disease Day! Throughout the world NORD (The National Organization of Rare Diseases) has hosted Rare Disease Day events. I attended the Connecticut Rare Disease Day at the State House in Hartford and interviewed a few of the presenters including Jackie and Eloise Stager, founders of JaxLegacy, John Hopper, the director of the Fibrolamellar Cancer Foundation and Maddie Shaw, leader of Maddie's Herd.
Maddie Shaw is an active advocate with the Immune Deficiency Foundation and has a Primary Immune Deficiency Disorder (PI). She is also the Founder & Leader of Maddie’s Herd.
Hereditary cancer experts share about Lynch syndrome, breast cancer, genetic counseling, and genetic testing.
Presentations at the Rare Disease Day 2015 are recapped. Presentors include Dr. Anton Alerte, Juliet and Tara Lynn, Dr. Caroline Dealy and Ethan Talbot.
Attend the Rare Diseases Awareness Event 2015 at UCONN Health Center on February 25th. Sophia Walker explains the celebration of individuals who have rare diseases and the many researchers and physicians who are fighting to find cures for these conditions.
Noel Lloyd from the Alliance for Aging Research explains how they advance science and enhance lives through education campaigns and working with legislation.