The Use of Human Milk During Parent-Newborn Separation
This evidence-based Clinical Practice Guideline was developed for the Association of Women’s Health, Obstetric and Neonatal Nurses (AWHONN) as an informational resource for nursing practice.
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This evidence-based Clinical Practice Guideline was developed for the Association of Women’s Health, Obstetric and Neonatal Nurses (AWHONN) as an informational resource for nursing practice.
This fund is designed to help mito patient and families obtaining or seeking care at CHOP. These funds can help supplement travel related costs, uncovered medical expenses, or other financial hardships given the underlying diagnosis. Our families can apply once a year to this fund for support. To find out more information or if your needs qualify you can reach out to our social worker Addie Fishstein fishsteina@chop.edu.
In this episode of the Primary Care Perspectives podcast series, David Levine, MD, pediatrician and board member, Postpartum Support International, discusses perinatal mood and anxiety disorders (PMADs) in dads, partners, and adoptive parents.
Global Genes is committed to providing information, resources and connections to all communities affected by rare disease.
Includes information on the anti-bullying initiative, “Don’t Laugh at Me,” as well as professional development workshops and school assembly programs.
Support research and advocacy, networking among families, provide factual information and resources.
Liam’s Land’s focus is research, a registry, funding genetic testing and clinical trials.
Lipedema Foundation focuses on research for cause & effective treatment of lipedema.
A 501c3 not-for-profit organization dedicated to improving the lives of Proteus patients by funding AKT1 research. We focus on providing family support in the form of education and networking individuals living with Proteus syndrome with other families and medical professionals.
Education, financial assistance, research and awareness.