RESOURCES

/

FIND A SPECIALIST

/

CONTACT

Bedford Mother Shares Her Story at Rare Disease Day

On February 23, 2014, aka Rare Disease Day, Lisa Cimino – a member of the NephCure family and mother to FSGS patient Brianna – shared her story and talked about what living with a rare disease is like at the State House in Boston. Read her story here. 

Sign up to get NephCure’s latest updates.

SIGN UP
This field is for validation purposes and should be left unchanged.