Educate. Connect. Empower. THRIVE.
Meet the Board
Maya Bloomberg, MSN, FNP-BC
Founder & President
Hematology Nurse Practitioner for 10+ years specializing in sickle cell disease and bleeding disorders. Passionate about mental health, empowering patients to take an active role in their health, and utilizing a holistic approach to treat patients mind, body and soul! Known by many as "TheHemeNP"
Devanne Barr
Board Member
Sickle Cell Warrior, Mother, & Advocate
Robb Williamson
Board Member
Hematology Customer Service Executive at CVS Health with experience in patient experience, program development and planning.
Drew Bloomberg
Board Member
VP of sales for MTB responsible for billions in sales of precious metals during his career. Advising on nonprofit operational strategies.
David Bennett, CPA, CFE, CITP, CFF
Board Member & Treasurer
Partner with a multinational CPA firm, David is a Board member on several non-profit organizations, including the NFL Alumni Association. His connection to Sickle Cell Disease is through a family member and he is passionate about supporting the medical and patient communities to improve the lives of Warriors and their families.
Meet the Patient Advisory Board
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Megan Livisay, LCSW
Megan Livisay is a Licensed Clinical Social Worker and Sickle Cell Warrior (SS). Megan has practiced in the field of social work for over 10 years. She has committed her career to raising awareness, providing resources, and creating safe spaces for those often overlooked by traditional health systems. Megan brings both personal insight and professional expertise to her work, combining compassion with advocacy to drive meaningful change in the Sickle Cell Community.
Vicky Quintana, MSW
Vicky Quintana is a sickle cell warrior (SS), born and raised in Miami, FL. Vicky has a background in social work and has a deep interest in aging, mental health, and grief support. They joined the Patient Advisory Board to connect with other warriors and help build a more compassionate, informed community. Through sharing their own lived experience, they hope to uplift warriors navigating similar journeys and maybe even find their own "warrior tribe" along the way.
Doris Carina Polanco
Doris Carina Polanco has sickle cell genotype SC and has been a dedicated advocate for the sickle cell community for over 20 years. She is committed to uniting the community in the pursuit of innovative, accessible care. Through social media, Doris partners with nonprofits and pharmaceutical companies to empower fellow warriors with knowledge, promote alternative treatments, and help others make informed decisions about their health and healing options.