About Me

I am Georgene Glass, a passionate consultant, dedicated mother, and a Subject Matter Expert in Sickle Cell Disease (SCD). With my diverse background and expertise, I have made it my mission to advocate for SCD patients, raise awareness for rare diseases, and promote health equity and diversity.

As the founder of Nevada's premier SCD organization, I have revolutionized advocacy and driven advancements in healthcare outcomes for those affected by SCD. My extensive education, including a Bachelor of Science in Criminal Justice and a healthcare leadership certification from Duke University, has equipped me with the knowledge and skills to provide direct support to SCD patients and their families on their healthcare journey.

I am also a certified community health worker, allowing me to offer crucial services and support free of charge to SCD and Rare Disease patients. As a notary public and loan signing agent, I am able to certify important documents, further assisting patients in navigating the complexities of their healthcare needs.

In addition to my advocacy work, I am the author of "The Tale of the Cell," a powerful children's book that sheds light on the SCD journey and empowers others to understand and support those affected. Through my authentic storytelling and personal experiences as a caregiver, I strive to inspire and encourage others on similar paths.

Using the power of social media, I share real-life experiences, fashion, food, and fun, all with the aim of providing hope and inspiration. I am dedicated to using these platforms to raise awareness for sickle cell and rare diseases, promote health equity, and share valuable information on how individuals can start small businesses with less than a thousand dollars and begin and sustain nonprofits in 60 days or less, while also advocating for fair compensation for patients and advocates.

My commitment extends beyond individual advocacy efforts. I also work tirelessly to provide valuable information to pharmaceutical companies, industry organizations, and other healthcare stakeholders, advocating for increased support for minority-led organizations and promoting collaboration for better patient outcomes.

I would be delighted to assist you or your business/organization in tackling these complex issues or elevating your operations to increase impact and sustainability. Together, we can make a significant difference in the lives of individuals and families affected by SCD and other rare diseases.

Join me on this journey as we work together to make a lasting impact and improve the lives of individuals and families affected by SCD and other rare diseases. Let's create positive change and build a brighter future.