GACI Global Is Now Brighter Hope Foundation: A New Name, the Same Mission of Hope

For years, GACI Global has been a trusted source of support, education, and advocacy for families affected by Generalized Arterial Calcification of Infancy (GACI), ARHR2, ENPP1 Deficiency, and ABCC6 Deficiency. Today, the organization is proud to announce a new chapter: GACI Global has officially rebranded as Brighter Hope Foundation.

While the name has changed, the mission remains the same: connecting families, advancing awareness, supporting research, and creating hope for those impacted by ultra-rare genetic diseases.

Why the Organization Rebranded

The transition from GACI Global to Brighter Hope Foundation reflects the evolution of the organization and the growing community it serves. Over the years, the foundation’s reach has expanded beyond GACI awareness alone to include broader education, support, and advocacy for families affected by related rare diseases, including ENPP1 Deficiency and ABCC6 Deficiency.

The new name, “Brighter Hope Foundation,” better represents:

• Hope for newly diagnosed families
• Hope through medical research and treatment advancements
• Hope through community connection and education
• Hope for a brighter future for children and adults living with rare genetic conditions

The rebrand also creates a more inclusive identity that reflects the resilience of patients, caregivers, researchers, and supporters around the world.

Continuing the Mission to Support Families Affected by GACI and Rare Diseases

Brighter Hope Foundation continues to focus on improving the lives of individuals and families affected by:

• Generalized Arterial Calcification of Infancy (GACI)
• ARHR2 (Autosomal Recessive Hypophosphatemic Rickets Type 2)
• ENPP1 Deficiency
• ABCC6 Deficiency

The organization provides educational resources, patient support, webinars, conferences, fundraising initiatives, and community connections for families navigating these complex diagnoses.

Families affected by rare diseases often face challenges including delayed diagnosis, limited treatment options, and difficulty finding knowledgeable medical providers. Brighter Hope Foundation works to bridge those gaps by helping families connect with medical experts, research opportunities, and others who understand their journey.

Supporting Rare Disease Research and Awareness

Research remains a central focus of Brighter Hope Foundation’s work. Because GACI and related disorders are ultra-rare, awareness and funding are essential to improving diagnosis, treatment options, and long-term outcomes.

According to the organization, GACI affects approximately 1 in 64,000 pregnancies, and survival rates for infants remain a serious concern, especially during the first months of life.

Through fundraising campaigns, global awareness initiatives, patient conferences, and partnerships with researchers and medical professionals, Brighter Hope Foundation continues to advocate for advancements that could change the future for affected families.

A Global Community Built on Connection

One of the most important parts of the organization’s mission is helping families feel less alone. A diagnosis of GACI or ARHR2 can be overwhelming, especially because many healthcare providers may never encounter these conditions during their careers.

Brighter Hope Foundation creates opportunities for connection through:

• Patient and family support groups
• Educational webinars and resources
• Family conferences
• Awareness campaigns
• Community fundraising events
• Patient stories and shared experiences

These connections provide emotional support while also helping families better understand treatment options, research developments, and daily life with rare diseases.

What This Means for Supporters and Families

Although the organization now operates as Brighter Hope Foundation, supporters can expect the same dedication, compassion, and advocacy that defined GACI Global for years.

The rebrand represents growth, momentum, and a renewed commitment to:

• Raising awareness of rare genetic diseases
• Supporting families worldwide
• Funding research efforts
• Expanding educational resources
• Building a stronger global community

The foundation’s new identity reflects a future centered on possibility, progress, and hope.

Learn More About Brighter Hope Foundation

To learn more about the organization, upcoming events, educational resources, and ways to support the mission, visit Brighter Hope Foundation.

Whether you are a patient, caregiver, medical professional, donor, or advocate, Brighter Hope Foundation continues to work toward a brighter future for families affected by GACI, ARHR2, ENPP1 Deficiency, ABCC6 Deficiency, and related rare diseases.