Help Us Reach Our Goal of $10,000
Our vision is to create spaces where caregivers feel seen, supported, restored, and valued.

We believe families caring for individuals with disabilities deserve moments of peace, opportunities for healing, and experiences centered around compassion and restoration.

Through community partnerships and support, The Jailynn Amani Foundation, Inc. hopes to provide life-changing respite retreat experiences that remind caregivers they are not alone.

Every dollar brings us closer to life-changing experiences and resources for families impacted — but we can’t do it without you.

Our 2026 Goal:

$10,000

We have a long way to go, and we need your help. Whether you give $20 or $2,000, your donation moves us closer to hope, healing, and breakthroughs for families like so many.

Will you join us?

Together, we can close the gap and make a difference.

DONATE FOR IMPACT!

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Jailynn Amani is an inspiration to many, having persevered through life's obstacles while living with Rett Syndrome. Her family's foundation, The Jailynn Amani Foundation Inc, provides support, awareness, and research to the community and other families with disabilities . We are excited to continue raising funds and awareness while honoring Jailynn's strength and resilience.

About

MORE ABOUT
RETT SYNDROME

Rett Syndrome is a rare genetic disorder that affects brain development in girls. It is caused by a mutation in the MECP2 gene, which is responsible for producing a protein that regulates the expression of other genes. Symptoms of Rett Syndrome usually appear between 6 and 18 months of age and include loss of speech and hand skills, repetitive hand movements, breathing problems, and seizures. There is currently no cure for Rett Syndrome, but treatment can help manage symptoms and improve quality of life.