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 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 battled sickle cell disease—this nonprofit was born out of love, grief, hope, and a fierce desire to create lasting change for those affected by this life-altering condition.
We believe that every person living with sickle cell disease (SCD) deserves not only access to proper care and support, but also dignity, respect, and community. ENJAH-SCF is here to provide just that.
Sickle cell disease impacts individuals and families across African, Hispanic, Middle Eastern, and Indian communities. 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 & Jacqueline (“Jackie”) Antoinette Holmes Sickle Cell Foundation (ENJAH-SCF) was created to honor the lives and legacies of two remarkable women who faced sickle cell disease with strength and grace. Today, their journey fuels our mission to bring hope, care, and advocacy to others impacted by this chronic illness.
Sickle cell disease disproportionately affects African, Hispanic, Middle Eastern, and Indian populations. These individuals often encounter pain, stigma, and inadequate access to medical support. ENJAH-SCF exists to address these disparities through community outreach, support services, and meaningful action.
Our mission is to empower, educate, and uplift those affected by sickle cell disease through:
At ENJAH-SCF, we focus on advocacy, education, and support to change the narrative for individuals and families affected by sickle cell disease. Our work is rooted in compassion and powered by the 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 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.
Together, we can build a future where no one faces sickle cell disease alone.
With your help, we turn compassion into action.
Let’s create lasting impact—one donation, one volunteer, one voice at a time.
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:
Sickle cell disease doesn’t wait—neither do we.
Through every program, partnership, and donation, we are rewriting the future.
This is more than a cause—it’s a call to action.
Together, we are building hope where it’s needed most.
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.
“ENJAH-SCF helped me feel seen and supported.” As a college student living with sickle cell disease, I often felt overwhelmed—until I received a scholarship from ENJAH-SCF. It wasn’t just financial help—it was emotional support that reminded me I’m not alone.
“They turned our crisis into comfort.” When our son was hospitalized, ENJAH-SCF stepped in with financial assistance that helped us cover unexpected bills. Their kindness made a painful time a little more bearable.
“Volunteering here changed my perspective.” Helping at an ENJAH-SCF awareness event opened my eyes to the challenges the sickle cell community faces—and the strength they show every day. I’ll always be part of this mission.
“This foundation gives our community hope.” From educational workshops to advocacy efforts, ENJAH-SCF is doing vital work. They're not just raising awareness—they're changing lives.
Frequently Asked Questions (FAQs)
Hello@Email.co
+62 123 456 789
Yes, ENJAH-SCF is a registered nonprofit organization. All donations are tax-deductible to the extent allowed by law.
ENJAH-SCF is a nonprofit organization founded in memory of twin sisters who bravely battled sickle cell disease. We support individuals and families impacted by SCD through education, advocacy, scholarships, emergency assistance, and awareness initiatives.
We provide scholarships to students with SCD, offer emergency financial aid, host awareness events, advocate for policy change, and support community education around sickle cell disease and healthcare access.
Absolutely! We welcome volunteers to help with event planning, digital outreach, mentorship, and fundraising. Visit our Get Involved page to sign up and learn more.