MHFP TEstimonials
Meet Margaret!
At 18 months, Margaret was diagnosed with a rare condition called craniometaphyseal dysplasia, which causes thickening of the bones in the skull. It wasn’t until Margaret entered junior high that Margaret was diagnosed with hydrocephalus..
Despite the challenges she faced, Margaret is grateful. The neurosurgery program at UChicago Medicine is one of the few in the country dedicated to providing comprehensive care for both children and adults with CNS congenital anomalies. After all she’s been through, Margaret wanted to share her knowledge and experiences to help others by creating the Margaret Hackett Family Program!
Meet Mary!
Mary is the parent of Emmanuel, who was diagnosed with Cerebral Palsy after being born with a grade four brain bleed. This experience has given Mary hope! Mary’s so, Emmanuel is a miracle and testifies that all things are possible through Jesus and prayer! Watching him grow and become stronger every day gives her strength.
Meet Anne!
Anne shares her journey as the Parent of an adult with Hydrocephalus, and how the Margaret Hackett Family Program has made a positive impact on her and her daughter, Mia’s, life.
Meet Mia!
Mia is an adult that is 22 years old living with Hydrocephalus! Mia has been learning to navigate her own medical journey and has even used resources through the Margaret Hackett Family Program to fund her education.
MHFP Summer Party at the Brookfield Zoo
Karen is the mother of a 14 year old son, who has found various resources and connection through the MHFP.
Submit Your Story Now!
If the Margaret Hackett Family Program has impacted your life, share your story and recieve a $10 Starbucks gift card. Share your photo, a few sentences about your story or submit a video. We would love to hear from you!