Dreamsickle Kids Foundation,Inc

What Dreamsickle Kids Foundation,Inc does

Dreamsickle Kids Foundation, Inc is a 501(c)(3) nonprofit organization founded in 2018 and headquartered in Las Vegas, Nevada. It operates as the first and only Sickle Cell Disease (SCD) organization in Nevada, serving approximately 1,000 SCD patients statewide and, since a 2020 mission expansion, the broader rare disease community of roughly 30 million Americans. Its functional activities center on awareness, education, advocacy, and direct family support rather than technology products.

The foundation delivers a portfolio of programs including Dream Kids (ages 0-13), Dream Scholarship, Dreaming of a Cure (blood/bone marrow donation education), Dream Rare, Dream Transportation (Uber/Lyft rideshare and gas cards for medical appointments), Dream Cares (caregiver support), Dream Assistance (emergency financial aid and SSI navigation via Big Horn Law), and recurring monthly SCD support groups at Nehemiah Ministries. It also sells a children's book, 'Tale of the Cell,' in hardcover ($15) and paperback ($10) formats. Annual events include the Las Vegas Sickle Cell Walk (9th annual in 2026), the Swing for Sickle Cell Golf Tournament, Warrior Drive, Dream Juicing Workshops, and a Holiday Brunch and Gift Spectacular.

The business model is donation- and sponsorship-driven. Revenue streams comprise direct donations (via PayPal), corporate sponsorships from SCD-focused pharmaceutical companies (Vertex, Pfizer, bluebird bio, Agios), grants from national rare disease organizations (Global Genes, NORD), book sales, and proceeds from recurring fundraising events. The foundation is led by founder and Executive Director Georgene' "Gina" Glass, with a volunteer-based team of approximately 7 employees and a board of directors spanning healthcare, real estate, logistics, and community health. Notable milestones include the passage of Nevada's first SCD bill (AB254) in 2019, the 2021 Rare Champion of Hope Award, and Congressional Recognition from Congressman Steven Horsford.

Name

Dreamsickle Kids Foundation,Inc

Legal name

Dreamsickle Kids Foundation, Inc

Website

https://dreamsicklekids.org

Company type

Private

Founded year

2018

Operating status

Operating

Headcount range

1–10 employees

Short description

Dreamsickle Kids Foundation is a Las Vegas-based 501(c)(3) nonprofit and the first Sickle Cell Disease organization in Nevada, serving SCD and rare disease patients and families through education, advocacy, direct support programs, and annual fundraising events.

Ownership category

akta.pro rank

Product category

Patient Advocacy Nonprofit Services

NAICS

Voluntary Health Organizations (813212), Individual and Family Services (6241), Child and Youth Services (62411)

SIC

Services-Social Services (8300), Services-Misc Health & Allied Services, Nec (8090)

akta.pro primary industry

Rare Disease & Special Needs Support Organizations (BPAGACAM)

akta.pro secondary industry

Family Advocacy, Parent Training & Support Services (EDAJAKAK)

Keywords

• Sickle cell disease support
• Rare disease advocacy
• Patient assistance programs
• Community health services
• Nonprofit healthcare outreach

Headquarters

HQ city

Las Vegas

HQ country

United States

HQ region

North America

Offices2 records

Markets served

GTM type

B2C

Offering type

Services

Cost components

Personnel, Operations, Marketing or Sales, Others

Revenue model

1. Donations and Fundraising: Primary revenue stream through direct donations, annual fundraising events including the Las Vegas Sickle Cell Walk and Swing for Sickle Cell Golf Tournament, and general charitable contributions. The organization is a 501(c)(3) nonprofit accepting stock donations.
2. Product Sales: Sale of children's educational book 'Tale of the Cell' in hardcover ($15.00 sale price) and paperback ($10.00 sale price) formats. Book is designed to educate children about Sickle Cell Disease.
3. Sponsorships: Corporate sponsorships from pharmaceutical companies (Vertex, Pfizer, bluebird bio, Agios) and local businesses for events and programs.

Pricing tiers

Go-to-market motion1 record

Distribution channels4 records

Marketing channels7 records

Core offering

Dreamsickle Kids Foundation is a 501(c)(3) nonprofit that delivers direct support, education, advocacy, and community programs to individuals and families in Nevada affected by Sickle Cell Disease and, since 2020, all Rare Diseases. Its core offerings include the Dream Kids program for children ages 0-13, Dream Transportation (rideshare/bus tokens/gas cards for medical appointments), Dream Cares caregiver support, Dream Scholarship, Dream Assistance (emergency financial aid and SSI navigation via Big Horn Law), and Dream Rare rare disease support, supplemented by monthly SCD support groups, the children's book 'Tale of the Cell', and signature annual events such as the Las Vegas Sickle Cell Walk.

Product overview

Dreamsickle Kids Foundation, Inc is a 501(c)(3) nonprofit organization providing a portfolio of programs and services for individuals and families affected by Sickle Cell Disease and Rare Diseases in Nevada. The core programs include: Dream Kids (for children ages 0-13), Dream Scholarship (educational scholarships), Dreaming of a Cure (blood/bone marrow donation education), Dream Rare (rare disease advocacy), Dream Transportation (medical transportation assistance), Dream Cares (caregiver support), and Dream Assistance (emergency financial/SSI assistance). The foundation also operates monthly SCD Support Groups and sells the children's book 'Tale of the Cell'. Major annual events include the Las Vegas Sickle Cell Walk (9th annual in 2026), Swing for Sickle Cell Golf Tournament (2nd annual), Warrior Drive, Dream Juicing Workshops, and Holiday Brunch and Gift Spectacular.

Differentiator

Problem solved

Functional benefit

Products and services

• Dream Kids Program A program for children with Sickle Cell Disease or Rare Diseases from age 0 to 13, helping them learn about their illness and health management through age-appropriate activities.
• Dream Scholarship Scholarship program for individuals impacted by SCD and Rare Disease, including siblings and parents pursuing higher education and Nevada medical and public health students, with a minimum scholarship amount of $500.
• Dreaming of a Cure Education program focused on the importance of blood and bone marrow donation for SCD patients, delivered through workshops and health fairs throughout Nevada.
• Dream Rare Program supporting the 7,000 Rare Diseases affecting 30 million Americans, including camp enrollment for Rare Kids, caregiver support, national advocacy participation, scholarships, and educational literature for Nevada's community.
• Dream Transportation Transportation Assistance Program providing Uber/Lyft rideshare services, limited shared rides, bus tokens, and gas cards for medical appointments, hospital visits, and SCD-related events.
• Dream Cares Caregiver support program acknowledging and supporting caregivers who assist patients with SCD and Rare Diseases, providing stress management, self-care, financial support, and gifts including health and wellness certificates.
• Dream Assistance Patient assistance program providing emergency financial assistance and support services, including help navigating SSI claims through partnership with Big Horn Law.
• SCD Support Groups Monthly support groups for patients and families impacted by Sickle Cell Disease, providing a welcoming space to connect, share experiences, and find strength in unity. Held every Thursday at 6pm at Nehemiah Ministries.
• Tale of the Cell (children's book) Children's book about Sickle Cell Disease written by Executive Director Georgene Glass, sold in hardcover ($15.00 sale price) and paperback ($10.00 sale price) formats to educate children about SCD.
• Warrior Drive Annual event celebrating Sickle Cell Warriors, with the 7th Annual Warrior Drive scheduled for April 25, 2026.
• Dream Juicing Workshops Health and nutrition workshops teaching participants how to make fresh juice and adopt healthy dietary routines, with tips on juices beneficial for SCD management.
• Annual Las Vegas Sickle Cell Walk Nevada's only SCD charity walk event, held annually at Lorenzi Park. The 9th Annual Las Vegas Sickle Cell Walk is scheduled for September 26, 2026 and serves as the foundation's signature annual fundraiser.
• Swing for Sickle Cell Golf Tournament Annual golf tournament fundraiser hosted at Las Vegas National Golf Club, with the 2nd Annual Swing for Sickle Cell Golf Tournament scheduled for September 5, 2026 in a four-person scramble format with sponsorships, raffles, and prizes.
• Holiday Brunch and Gift Spectacular Annual holiday event providing food and gifts to community members in collaboration with JET Foundation, serving over 200 community members.

Quantifiable outcome

• AB254 Nevada Sickle Cell Bill passed in 2019, establishing Nevada's first SCD legislation
• +3 more outcomes

Named customers4 records

Segments4 records

Ideal customer profiles3 records

Technology focussed No

API detail

Has API

No

API docs

API detail

Core technology

AI maturity

App detail

Integration6 records

Partnerships

18 partnerships are on record, tiered core and minor.

• Vertex PharmaceuticalscoreStrategic or Co-development PartnerVertex Pharmaceuticals is a pharmaceutical company that has developed Casgevy, the FDA-approved CRISPR-based therapy for Sickle Cell Disease. As a sponsor of the Annual Las Vegas Sickle Cell Walk, Vertex supports the foundation's advocacy efforts and represents a key pharmaceutical partnership for advancing SCD treatment awareness.
• PfizercoreStrategic or Co-development PartnerPfizer is a major pharmaceutical sponsor of Dreamsickle Kids events, having developed SCD treatments. Pfizer's voluntary withdrawal of Oxbryta in 2024 highlighted the foundation's role in community support and education during challenging times for patients.
• bluebird biocoreStrategic or Co-development PartnerBluebird bio is a biotechnology company specializing in gene therapies for severe genetic diseases, including SCD. Sponsors the Annual Las Vegas Sickle Cell Walk as part of their commitment to the SCD community.
• Agios PharmaceuticalscoreStrategic or Co-development PartnerAgios is a pharmaceutical company focused on cellular metabolism and SCD treatments. Sponsors the Annual Las Vegas Sickle Cell Walk to support Nevada's SCD community.
• NORD (National Organization for Rare Disorders)coreStrategic or Co-development PartnerNORD is a leading independent organization committed to the identification, treatment, and cure of rare diseases. Dreamsickle Kids Foundation is a NORD member, providing access to resources, advocacy networks, and national rare disease initiatives.
• Global GenescoreStrategic or Co-development PartnerGlobal Genes is a non-profit organization connecting the rare disease community. Awarded Dreamsickle Kids a Rare Financial Grant and the 2021 Rare Champion of Hope Award. Part of the Foundation Alliance program.
• Sickle Cell Community ConsortiumcoreStrategic or Co-development PartnerSickle Cell Community Consortium is a national organization supporting the SCD community through advocacy and resources. Dreamsickle Kids collaborates with SCCC for leadership summits and community initiatives.
• Nevada 211minorStrategic or Co-development PartnerNevada 211 is a special telephone number providing information and referrals to health, human, and social service organizations. Helps connect SCD patients with essential resources.
• Sickle Cell Center of NevadacoreStrategic or Co-development PartnerNevada's first comprehensive Sickle Cell clinic serving children and adults with SCD. The foundation works closely with the clinic to support patients transitioning from pediatric to adult care.
• AllStripesminorStrategic or Co-development PartnerAllStripes is a platform that helps rare disease patients access their medical records and contribute to research. Dreamsickle Kids partnered with AllStripes to support Nevada's rare disease community.
• Big Horn LawcoreImplementation/ SI/ Consulting PartnerBig Horn Law provides SSI legal assistance for Nevada SCD patients, helping with new or existing SSI claims from initial application to appealing denials. This partnership addresses the financial burden faced by SCD families.
• Nehemiah MinistriescoreStrategic or Co-development PartnerNehemiah Ministries hosts Dreamsickle Kids' in-person SCD support groups every Thursday at 6pm. The church provides space for community gatherings and collaborates on events throughout the year.
• Be The MatchcoreStrategic or Co-development PartnerBe The Match is the world's largest bone marrow registry. Dreamsickle Kids partnered with Be The Match to increase diverse donor registration and give SCD warriors a greater chance at a cure through bone marrow transplantation.
• Red Cross Southern NevadacoreStrategic or Co-development PartnerThe Red Cross Southern Nevada Chapter collaborates with Dreamsickle Kids on blood drives and awareness events. Blood donations are critical for SCD patients who often require transfusions.
• Full Size Run FoundationminorGTM or Marketing PartnerLocal foundation that supports Dreamsickle Kids events and programs, providing community sponsorship and resources for SCD warriors.
• Immaculate Pieces ClothingminorGTM or Marketing PartnerLocal entrepreneur Truman Hopkins hosted a Swinging for Sickle Cell fundraiser in honor of his late brother, raising $5,000 for Dreamsickle Kids in 2025.
• Health Plan of NevadaminorStrategic or Co-development PartnerHealth Plan of Nevada participates in Sickle Cell Walk events, providing resources and support for attendees at community events.
• Pride Logistics FirmminorGTM or Marketing PartnerLocal business sponsored the 8th Annual Las Vegas Sickle Cell Walk, demonstrating corporate support for the SCD community in Nevada.

Scale indicators6 records

Recent moves7 records

Expansion highlights5 records

Broad incumbents

• Global Genes: Rare disease advocacy nonprofit that has awarded Dreamsickle Kids a Rare Financial Grant and the 2021 Rare Champion of Hope Award. Operates globally with comparable advocacy, awareness, and patient-support programming.
• National Organization for Rare Disorders (NORD): The largest U.S. rare disease advocacy and policy organization. Dreamsickle Kids is a NORD member; NORD represents the broader incumbent in the rare disease space the foundation expanded into in 2020.
• EveryLife Foundation for Rare Diseases: Rare disease policy and advocacy nonprofit focused on accelerating biotech innovation and access to therapies. Comparable as a rare-disease advocacy organization pursuing policy change and patient access.

Direct peers

• Sick Cells: SCD-focused advocacy organization working to elevate the voices of people living with sickle cell disease through storytelling, policy, and community engagement. Comparable in mission to expand SCD awareness and drive legislative change.
• Sickle Cell Disease Association of America (SCDAA): The national umbrella organization for sickle cell disease advocacy, support, and research. SCDAA is the most direct peer to Dreamsickle Kids as both pursue SCD awareness, patient support, and policy advocacy, though SCDAA operates nationally rather than within a single state.
• Sickle Cell Community Consortium: National SCD community organization focused on advocacy, leadership summits, and resource mobilization. Already a stated partner of Dreamsickle Kids, it competes for the same national SCD donor dollars and community engagement.
• Sickle Cell Anemia Research and Education Inc. (S.C.A.R.E.): Bay Area SCD nonprofit providing education, advocacy, and patient support. Closely comparable in mission, service mix, and community-based operational model to Dreamsickle Kids.
• American Sickle Cell Anemia Association (ASCAA): Regional SCD patient support, education, and advocacy organization serving Ohio and surrounding areas. Closely comparable to Dreamsickle Kids in mission, community-based service model, and SCD-specific focus.

Others

• Be The Match (National Marrow Donor Program): Bone marrow donor registry that is a stated partner of Dreamsickle Kids for SCD cure-related donor drives. Comparable as a complementary player in the SCD treatment ecosystem rather than a direct competitor.

Regional players

• Sickle Cell Foundation of Georgia: State-level SCD organization providing patient services, education, and screening in Georgia. Structurally analogous to Dreamsickle Kids as a regional/state SCD advocacy and direct-service provider.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks6 records

Key highlights7 records

Customer concentration

• Instagraminstagram.com/dreamsicklekids
• LinkedInlinkedin.com/company/dreamsickle-kids-foundation-inc

Revenue estimate

Valuation estimate

Number of profiles

Profiles12 records

Funding overview

Funding rounds

Investors

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M&A

Investments

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Frequently asked questions about Dreamsickle Kids Foundation,Inc