Rare Disease Day: Get to know three kid experts pursuing cures
Rare Disease Day is an international day of recognition to raise awareness for conditions affecting fewer than 1 in 2,000 people and the impact they
Rare Disease Day is an international day of recognition to raise awareness for conditions affecting fewer than 1 in 2,000 people and the impact they
The Cystic Fibrosis program was selected for its dedicated multidisciplinary care team, comprehensive trainee education, exceptional patient and family involvement, and communication tools that overcome
Nikki was diagnosed with cystic fibrosis (CF) at the age of 5 and has been fighting through it since. Nikki is now 48 and credits
Over her nine years at Children’s Minnesota, Tami Vance, LICSW, cystic fibrosis (CF) and primary ciliary dyskinesia (PCD) programs, not only shines as an outstanding
Children’s Minnesota was featured as one of the the “bests” for health care in the state in Msp.St.Paul Magazine.
A day for our generous community to join together to ensure that even the tiniest hearts get the strongest possible start.