Honoring a Legacy. Empowering a Future. Fighting Sickle Cell Disease.
At The Elizabeth Nicole & Jacqueline Antoinette Holmes Sickle Cell Foundation (ENJAH-SCF), our mission is both deeply personal and profoundly impactful.
Founded in loving memory of twin sisters Elizabeth (“Lizzy”) Nicole and Jacqueline (“Jackie”) Antoinette Holmes—two courageous young women who bravely faced the challenges of sickle cell disease with extraordinary grace and strength—our foundation was born from love, grief, hope, and an unwavering determination to create lasting change.
We believe that every individual living with sickle cell disease (SCD) deserves not only access to quality medical care, but also compassion, dignity, and respect.. ENJAH-SCF strives to uplift, empower families, and bring hope where it’s needed most.
Sickle cell disease (SCD) is a class of rare genetic blood disorders that mainly impacts Black Americans but is also diagnosed in individuals of Hispanic, Mediterranean, Middle Eastern, and Indian ancestry. At ENJAH-SCF, we provide resources, advocacy, and support tailored to those disproportionately affected by this chronic and often misunderstood condition.
We work to eliminate the disparities that limit access to quality care for sickle cell patients.
Our campaigns reduce stigma and spread knowledge in high-impact communities.
We offer emotional, financial, and educational support for those impacted by SCD.
The Elizabeth (“Lizzy”) Nicole and Jacqueline (“Jackie”) Antoinette Holmes Sickle Cell Foundation (ENJAH-SCF) was created to honor the lives and legacies of twin sisters who faced sickle cell disease with remarkable strength and grace.
Born from love and a determination to make a difference, ENJAH-SCF works to bring hope, awareness, and support to families affected by sickle cell disease. Through education, advocacy, and community programs, we strive to improve quality of life and advance health equity for all who live with this condition.
Sickle cell disease disproportionately affects African, Hispanic, Middle Eastern, and Indian populations— communities that too often face pain, stigma, and limited access to quality care. The Elizabeth Nicole & Jacqueline Antoinette Holmes Sickle Cell Foundation (ENJAH-SCF) exists to confront these disparities through education, advocacy, and compassionate support. Our mission is to bring hope, dignity, and equity to every life touched by sickle cell disease.
At the Elizabeth (“Lizzy”) Nicole & Jacqueline (“Jackie”) Antoinette Holmes Sickle Cell Foundation (ENJAH-SCF), our mission is to empower, educate, and uplift individuals and families affected by sickle cell disease.
Through compassionate outreach, advocacy, and community programs, we strive to:
At ENJAH-SCF, we focus on advocacy, education, and support to change the narrative for individuals and families living with sickle cell disease. Our work is rooted in compassion— and powered by the enduring legacy of those we serve.
Through advocacy, education, and direct support, ENJAH-SCF is committed to closing the gaps in treatment and awareness for underrepresented communities impacted by sickle cell disease.
At ENJAH-SCF, we combine compassion with action. From scholarships and emergency support to public awareness and advocacy, our programs are designed to meet the real needs of individuals and families affected by sickle cell disease.
We empower students researching and living with sickle cell disease by providing scholarships that support their academic and career goals, helping them overcome barriers to higher education.
We offer urgent financial support to families facing the economic burden of sickle cell complications—covering expenses like medical bills, transportation, and household needs.
Our outreach campaigns educate communities about SCD, reduce stigma, and promote early diagnosis. We host workshops, share resources, and spread awareness through events and digital platforms.
ENJAH-SCF works alongside healthcare providers, researchers, and policymakers to advocate for improved care, increase funding, and advance life-saving treatment options.
This foundation was created not only to fight for the future, but to honor the past. Lizzy and Jackie’s journey with SCD was filled with both hardship and resilience. By sharing their legacy, we’re turning pain into purpose—empowering others to live boldly and fully.
When you get involved with ENJAH-SCF, you become part of a powerful movement to improve the lives of individuals and families impacted by sickle cell disease. Your time, donation, or advocacy can spark real change.
Ways to Support:
Sickle cell disease remains underfunded and underserved. By supporting ENJAH-SCF, you help break barriers in care, education, and advocacy. Every contribution helps us reach more lives with dignity and hope.
Whether it’s one hour or one event, your time can make a lasting impact.
Start a campaign, organize a local event, or share your story to help raise awareness.
Despite being one of the most common genetic blood disorders, sickle cell disease remains drastically underfunded and often misunderstood. At ENJAH-SCF, we work to bring visibility, support, and systemic change to communities most affected by this condition.
Our Goals:
You don’t need a large organization to make a difference—just a big heart and the willingness to act. Whether it’s a birthday fundraiser, charity run, or school event, your effort directly supports programs that change lives for those living with sickle cell disease.
From bake sales to virtual events, every fundraiser brings more awareness and support to underserved communities. We'll equip you with the tools and guidance to make your campaign a success.
Fundraising isn’t just about raising money—it’s about raising voices. When you host a campaign, you educate others, share real stories, and fuel hope for patients and families affected by sickle cell disease.
Volunteering with ENJAH-SCF means becoming part of a passionate team dedicated to driving awareness, building stronger communities, and offering real support to families facing the daily challenges of sickle cell disease. No matter your background or skill set, your time can make a lasting impact.
Help us organize and run community events, fundraisers, and educational programs.
Support young people living with SCD and advocate for better care in your community.
Sign up for our newsletter to get updates about sickle cell education, upcoming events, scholarship opportunities, and ways to make an impact.
Elizabeth (“Lizzy”) and Jacqueline (“Jackie”) Holmes were twin sisters whose lives, though far too short, left a permanent mark on the world. Their journey with sickle cell disease shaped the mission of ENJAH-SCF—to bring hope, healing, and dignity to others walking a similar path.
Their Impact Lives On:
Their memory lives through every donation, scholarship, and community event hosted by ENJAH-SCF.
We turn their story into support—serving others with the same love they gave to the world.
Celebrate Lizzy and Jackie’s legacy by leaving a tribute, sharing a story, or giving in their honor.











