HippraConnects

Join Laura Byer, Program Manager of the Alzheimer's Association of the National Capital Area for an informative discussion aimed at those supporting individuals with Alzheimer's. Learn about the resources offered by the Alzheimer's Association of the National Capital Area and valuable tips for engaging with someone with this progressive disease that not only impacts the individual, but the family and friends who care fo...

Dr. Tammy Smith serves as the Regional Epidemiologist with the Communicable Disease Branch at the Department of Public Health in Raleigh, NC. Dr. Smith is also the CEO and President of Inspired Now Networks, Inc., a nonprofit organization focused on health awareness, education, and research.

Dr. Smith has a Doctorate of Public Health and an extensive background in research and public health. She has worked at Duke University Medical...

In this episode, we chat with two individuals committed to the study and practice of Orthopedic Medicine, Dr. Oluwadamilola Kolade an Ortho resident at Howard University and Ms. Moriah Martindale, a medical student at the University of Buffalo. Their focus is on sharing important information about orthopedics and addressing healthcare disparities/barriers to treatment in underserved communities.

Rev. Deneen Robinson discusses Reproductive Health (RH) Impact and the Collaborative for Equity & Justice, a fiscally sponsored program of The Praxis Project, a 501(c)(3) public charity. RH Impact is one of the nation’s leading experts and an advocate for change in the Black maternal health and infant mortality crises. RH Impact works to create transnational solutions that optimize Black maternal, infant, sexual, and reproduct...

In this podcast, we welcome Miranda Klassen, Executive Director of the Amniotic Fluid Embolism Foundation (AFE), for an enlightening and valuable discussion of a condition that may severely impact the health of pregnant women. Amniotic Fluid Embolisms occur when a mother has an allergic-like immune response to amniotic fluid or fetal material that enters her bloodstream during labor or after. This birth complication can be life-thr...

We are so pleased to have with us, Lonnie Somers, Co-Founder of The Fetal Health Foundation. The Fetal Health (or Hope) Foundation’s mission is to support families receiving a fetal syndrome diagnosis. fetalhealthfoundation.org. The foundation provides life-saving research, increases the awareness of fetal syndrome and shares leading medical information on this disorder. Learn more about the fascinating story of Lonnie and his wife...

We are quite pleased to present Laura Castillo, Executive Director of the 5 P Minus Society. The 5 P Minus Syndrome is a disorder of chromosome deletion that impacts a small number of children in this country (50-60). Also known as Cri du Chat Syndrome, it is typically accompanied by physical and developmental delays often requiring life-time support for those impacted. The 5 P Minus Society provides crucial education, inform...

Join this enlightening conversation with Dr. McCamey, the Founder and President of Doctors of Nursing Practice of Color (DNPs of Color) and her journey to enhance the medical profession by supporting and encouraging those working in advanced nursing or seeking degrees in advanced nursing. DNPs of Color is a non-profit organization and their mission is to serve DNPs of Color through networking, mentorship and advocacy to increase di...

Ana Rath, Director of Orphanet shares how this valuable resource gathers information on rare diseases to improve the diagnosis, care and treatment of patients who are diagnosed with these challenging medical conditions. The goal of Orphanet, with a global outreach, is to provide high-quality information on rare diseases and ensure equal access to knowledge for all stakeholders. For more information contact Orphanet: https://www.orp...

We welcome Melissa Bryce, Executive Director, The Global Foundation for Peroxisomal Disorders. Join us to hear about these rare genetic disorders and how they impact the lives of many children and families. The Foundation's mission is to improve the lives of individuals with Peroxisomal Disorders by funding research, championing scientific collaboration and empowering families and professionals through educational support servi...

Join us for this fascinating interview with Diana Gray, the President and CEO of an amazing organization, the Hydrocephalus Association whose mission is to find a cure for hydrocephalus and support those living with this rare disease. Ms. Gray provides and informative overview of hydrocephalus and how it impacts patients and families. We urge you to support their efforts: https://www.hydroassoc.org/about-us/.

In this episode of HippraConnects, Eesha Imam interviews her cousin Mehreen about her journey of living and growing up with Microphthalmia. Mehreen talks about some small challenges living with the condition, overcoming mental barriers, not letting Microphthalmia hold her back, doing what makes you happy, finding a support group and much more!

Thank you to Mehreen for coming on the show and take care!

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Janice McRae, Founder and CEO of Hippra, interviews Heather Ferguson, Founder and Executive Director at Lymphedema Advocacy Group.

Get in Contact with the Lymphedema Advocacy Group!

Website: https://lymphedematreatmentact.org/

Instagram: https://www.instagram.com/lymphedematreatmentact/

Twitter: https://twitter.com/LymphedemaAct

LinkedIn: https://www.linkedin.com/company/lymphedema-advocacy-group

Facebook: https://www.facebook.com/ly...