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The Margaret Hackett Family Program in CNS Congenital Anomalies
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Вміст надано Eric Jorgensen. Весь вміст подкастів, включаючи епізоди, графіку та описи подкастів, завантажується та надається безпосередньо компанією Eric Jorgensen або його партнером по платформі подкастів. Якщо ви вважаєте, що хтось використовує ваш захищений авторським правом твір без вашого дозволу, ви можете виконати процедуру, описану тут https://uk.player.fm/legal.
Judie Holleman, APRM, PCNP-BC, CPNP-AC, CCRN, is a Nurse Practitioner for the Margaret Hackett Family Program. During this interview, we explore what the Margaret Hackett Family Program (MHFP) does and how families can advocate for themselves. I feel it's important to stress this program is available to ANYONE from ANYWHERE in the country.
Through a generous donation from the Margaret Hackett Family Center, the Margaret Hackett Family Program (MHFP) is available to help patients and families with CNS congenital anomalies navigate UChicago Medicine’s resources and establish collaborative communication between patients and their providers. The MHFP aims to provide well-rounded, compassionate patient care, resources in support of the community and education for patients and their families, and steps in advancing the research and recognition of CNS congenital anomalies.
Here's how you can connect with MHFP
Website: https://mhfcp.uchicago.edu/
Phone: 773-795-0622
Email: mhfcp@bsd.uchicago.edu
Link to my interview with Amanda Garzon, COO of the Hydrocephalus Association - https://anchor.fm/abcs-disability-planning/episodes/22-Hydrocephalus-Association-with-Amanda-Garzon-e19cpbd
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