HippraConnects
Welcome to HippraConnects where we give a voice to those battling complex illnesses, challenging medical conditions or rare diseases and the healthcare providers who treat them as well as the support system that nurtures and sustains them.
Episodes
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.
Support this podcast at — ...
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...
An informative discussion with Louise Vetter, President and CEO of the Huntington's Disease Society of American. Learn more about this rare disease and how this non-profit organization offers support through community service, advocacy, research and education. https://hdsa.org/
Support this podcast at — https://redcircle.com/supporting-physicians/donations
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...
8. Interview with Melissa Bryce, Executive Director, The Global Foundation for Peroxisomal Disorders
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/.
Support this ...
This is an informative discussion with Rebecca Aune, Director of Education Programs for the National Organization for Rare Disorders (NORD). Ms. Aune shares how NORD supports the rare disease community, those struggling with orphan or rare disorders, their families and healthcare providers.
Support this podcast at — https://redcircle.com/supporting-physicians/donations
Learn how Renee Moten helps individuals minimize knee pain and increase activity levels to maximize quality of life for those bothered by ongoing knee discomfort.
Support this podcast at — https://redcircle.com/supporting-physicians/donations
Join us in learning about the world of pharmacy, its impact on our lives and ways in which this profession has become frontline in healthcare to help us overcome challenges from personal medical needs to community disease prevention.
Support this podcast at — https://redcircle.com/supporting-physicians/donations
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!
For more information on ...
Hippra's vision on the future of healthcare.
For more information on Hippra Check us out on:
https://linktr.ee/hippra
https://www.facebook.com/hippraapp/
https://twitter.com/hippra1
https://www.linkedin.com/company/hippra
Support this podcast at — https://redcircle.com/supporting-physicians/donations
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...
Janice McRae, founder, introduces to the mission of Hippra and what to expect from the HippraConnects podcast!
Thank you and please share with your friends!
For more information on Hippra Check us out on:
https://linktr.ee/hippra
https://www.facebook.com/hippraapp/
https://twitter.com/hippra1
https://www.linkedin.com/company/hippra
Support this podcast at — https://redcircle.com/supporting-physicians/donations
Do you want to learn more about the latest updates in all things medicine and healthcare? Keep up with current medical events and news from an array of medical professionals with HippraConnects bi-weekly. If you’re interested in the healthcare or medicine please checkout the podcast.
For more information on Hippra check us out on:
Popular Podcasts
Does hearing about a true crime case always leave you scouring the internet for the truth behind the story? Dive into your next mystery with Crime Junkie. Every Monday, join your host Ashley Flowers as she unravels all the details of infamous and underreported true crime cases with her best friend Brit Prawat. From cold cases to missing persons and heroes in our community who seek justice, Crime Junkie is your destination for theories and stories you won’t hear anywhere else. Whether you're a seasoned true crime enthusiast or new to the genre, you'll find yourself on the edge of your seat awaiting a new episode every Monday. If you can never get enough true crime... Congratulations, you’ve found your people. Follow to join a community of Crime Junkies! Crime Junkie is presented by audiochuck Media Company.
The latest news in 4 minutes updated every hour, every day.
If you've ever wanted to know about champagne, satanism, the Stonewall Uprising, chaos theory, LSD, El Nino, true crime and Rosa Parks, then look no further. Josh and Chuck have you covered.
Listen to 'The Bobby Bones Show' by downloading the daily full replay.
Latino USA is the longest-running news and culture radio program in the U.S. centering Latino stories, hosted by Pulitzer Prize winning journalist Maria Hinojosa Every week, the Peabody winning team brings you revealing, in-depth stories about what’s in the hearts and minds of Latinos and their impact on the world. Want to support our independent journalism? Join Futuro+ for exclusive episodes, sneak peaks and behind-the-scenes chisme on Latino USA and all our podcasts. www.futuromediagroup.org/joinplus