Sincerely, Sarai Foundation
Providing Comfort & Support for Grieving Families
The Lord is close to the brokenhearted and saves those who are crushed in spirit." — Psalm 34:18
YOU ARE NOT ALONE.
To appoint unto them that mourn in Zion, to give unto them beauty for ashes, the oil of joy for mourning, the garment of praise for the spirit of heaviness... Isaiah 61:3
Our Mission
At Sincerely Sarai Foundation, we walk alongside families facing the unimaginable loss of a child, offering financial support for funeral and burial expenses. Our mission is to lift the weight of financial stress, honor each child’s memory, and build a caring community that surrounds grieving families with love and hope.
Statement
The loss of a child brings immense emotional pain, and many families find themselves unprepared for the associated financial burdens. According to recent statistics:
The average cost of a child’s funeral ranges from $7,000 to $15,000.
Families often struggle to find the funds needed amidst the shock and grief, leading to additional stress and anxiety during a time of profound sadness.
These statistics underscore the necessity for targeted support services for grieving families, particularly in the form of financial assistance to ease the burden of funeral costs.
How We Help
Financial Assistance – Providing funds for funeral and burial expenses.
Community Awareness – Educating others about the financial burdens grieving parents face.
Partnerships – We work with funeral homes, hospitals, and organizations to ease families' burdens.
Support Network – Offering emotional support, counselling, and grief resources.
CEO | FOUNDER
The Sincerely Sarai Foundation was established in 2025 by Meakeal Streeter, in loving memory of her daughter, Sarai. Sarai was a joyful, thriving child who showed typical development until around her first birthday. It was then that Meakeal noticed signs of regression and a concerning large, firm abdomen. Despite her early concerns, initial medical advice was dismissive.
Refusing to be ignored, Meakeal sought a second opinion. A more attentive pediatrician ordered further testing, which revealed Sarai’s enlarged liver and spleen, along with a low blood count. After 21 days of intensive testing and hospitalization, Sarai was diagnosed with Type 2 Gaucher disease, a rare and aggressive genetic disorder, on September 21, 2016.
Sarai’s courage and resilience inspired Meakeal to create the Sincerely Sarai Foundation. Founded with a mission to raise awareness, support affected families, and advocate for better diagnosis and treatment of rare genetic diseases, the foundation carries Sarai’s spirit forward — one of love, strength, and hope.
Sarai & Friend Family Learning Center
In addition to providing financial assistance to grieving families, Sincerely Sarai Foundation supports parents through Sarai & Friend Family Learning Center. We offer affordable childcare and educational support in a safe, loving, and enriching environment
Why Choose our Learning Center?
Affordable childcare options
A loving, family-centered environment
Enrichment programs tailored for early childhood development
Sarai 's Closet
Providing Dignity Through Everyday EssentialsSarai’s Closet is a giving initiative of the Sincerely Sarai Foundation, dedicated to supporting low-income families by providing free clothing and essential hygiene items. We believe that everyone deserves access to basic necessities that promote comfort, confidence, and dignity—especially during difficult times.
Through donations and community partnerships, Sarai’s Closet offers a wide range of new and gently used items including:
Why Choose Sarai & Friend?
Affordable childcare options
A loving, family-centered environment
Enrichment programs tailored for early childhood development
Understanding Type 2 Gaucher Disease & Screening
Type 2 Gaucher Disease is a rare genetic disorder that affects the body's ability to break down fatty substances called glucosylceramides. This buildup leads to severe neurological damage, organ enlargement, and developmental delays.
Symptoms often appear in infants and can include:
Severe brain damage & seizures
Enlarged liver & spleen
Feeding and swallowing difficulties
Muscle stiffness & developmental regression
How Can You Get Screened?
Genetic testing and enzyme activity tests can help detect Gaucher Disease early. If you have a family history or notice symptoms in a child, consult a genetic counselor or healthcare provider for:
Blood Tests – Measures enzyme activity levels
DNA Analysis – Identifies genetic mutations in the GBA gene
Prenatal Screening – For at-risk pregnancies
Early detection can help with management strategies to improve quality of life. If you or a loved one may be at risk, speak with a healthcare professional today.
Meet Our Founder: Meakeal Streeter
Sincerely Sarai Foundation was created in honor of Sarai, a beautiful two-year-old girl who lost her battle with Type 2 Gaucher Disease—a rare and severe genetic disorder.
Sarai’s journey was filled with strength, love, and faith. Despite a devastating diagnosis, she inspired all who knew her.
“I consider that our present sufferings are not worth comparing with the glory that will be revealed in us.” — Romans 8:18
In her memory, Meakeal founded this organization to help parents navigating unimaginable grief, ensuring that no family feels alone in their loss.
How You Can Help
Donate
Your support directly funds funeral and burial expenses for grieving families.
“And do not forget to do good and to share with others, for with such sacrifices God is pleased.” — Hebrews 13:16
Volunteer
Join us in making a difference—from event planning to administrative support.
“Each of you should use whatever gift you have received to serve others, as faithful stewards of God’s grace in its various forms.” (1 Peter 4:10
Contact Us: Meakeal@saraifoundation.org
Thank you for supporting the Sincerely Sarai Foundation. Together, we turn grief into healing and loss into love.