HippraConnects

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 diversity in doctoral studies, clinical practice and leadership: https://www.dnpsofcolor.org/.

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/

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.orpha.net/consor/cgi-bin/index.php.

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 services.

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/.

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.

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.

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.

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 Check us out on:

https://linktr.ee/hippra

https://www.facebook.com/hippraapp/

https://twitter.com/hippra1

https://www.linkedin.com/company/hippra

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