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    • Home
    • About Us
    • Dream Transportation
    • LV SCD WALK
    • Events & Announcements
    • DONATE
    • SCD Support Group
    • Our Purpose
    • Our Programs
    • Patient Assistance
    • The Dream Team (Board)
    • Volunteers
    • Nevada Resources
    • SCD/SCT Fact Sheets
    • Photo Library
    • NV SCD Care Concern Form
    • Dreamsickle Partners
    • UNLV Intern Opportunities
    • *UNLV Internship *
    • Dream Scholarships
    • Thank You Sponsors
    • Press
    • Reviews/ Connect with Us
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DREAMSICKLE KIDS FOUNDATION

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  • Home
  • About Us
  • Dream Transportation
  • LV SCD WALK
  • Events & Announcements
  • DONATE
  • SCD Support Group
  • Our Purpose
  • Our Programs
  • Patient Assistance
  • The Dream Team (Board)
  • Volunteers
  • Nevada Resources
  • SCD/SCT Fact Sheets
  • Photo Library
  • NV SCD Care Concern Form
  • Dreamsickle Partners
  • UNLV Intern Opportunities
  • *UNLV Internship *
  • Dream Scholarships
  • Thank You Sponsors
  • Press
  • Reviews/ Connect with Us
  • Icing Smiles Application

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dream PROGRAMS

Dream Kids

 A program for children with SCD or Rare Diseases from age 0 to 13. The Dream Kids program allows children to learn about their illness and taking care of their health while having fun doing what any child would love to do. 

Dream scholarship

  

The Dream Scholarship is for those affected by SCD and other Rare Disease, their siblings and parents looking to achieve a higher education. The Dream Scholarship is also available to medical students in Nevada as well as Public Health students as an incentive to advocate and practice in the field of hematology, oncology, genetic, and R

  

The Dream Scholarship is for those affected by SCD and other Rare Disease, their siblings and parents looking to achieve a higher education. The Dream Scholarship is also available to medical students in Nevada as well as Public Health students as an incentive to advocate and practice in the field of hematology, oncology, genetic, and Rare Diseases.

* Scholarship amounts may vary from year to year with a minimum of $500*

Dreaming of a Cure

Dreaming of a Cure

This program works to educate those in the community about the importance of blood and bone marrow donation , which can be very essential to the quality of life for people with SCD and other Rare Diseases. Education and awareness of its importance is achieved through workshops and health fairs throughout Nevada.

Programs cont'd

Dream Rare

Dream Transportation

Dream Transportation

  

There are 7,000 Rare Diseases which affect 30 million Americans. Sickle Cell Disease and Childhood Cancer are just two of the thousands of Rare Diseases affecting Americans. We work to ado things like send Rare Kids to camps, Support caregivers, participate in national Rare Disease advocacy events and initiatives, offer scholarships, cr

  

There are 7,000 Rare Diseases which affect 30 million Americans. Sickle Cell Disease and Childhood Cancer are just two of the thousands of Rare Diseases affecting Americans. We work to ado things like send Rare Kids to camps, Support caregivers, participate in national Rare Disease advocacy events and initiatives, offer scholarships, create literature to educate the Nevada's community on Rare Diseases. 

Dream Transportation

Dream Transportation

Dream Transportation

 Our Transportation Assistance Program helps reduce barriers to care by providing reliable, flexible options for individuals and families impacted by sickle cell disease. Through our Patient Assistance Platform, eligible participants can request transportation support for medical appointments, hospital visits, and sickle cell–related even

 Our Transportation Assistance Program helps reduce barriers to care by providing reliable, flexible options for individuals and families impacted by sickle cell disease. Through our Patient Assistance Platform, eligible participants can request transportation support for medical appointments, hospital visits, and sickle cell–related events across the Las Vegas area. Depending on individual needs and funding availability, we offer rideshare services such as Uber and Lyft, limited shared rides when appropriate, bus tokens or public transit support, and gas cards for those with access to a personal vehicle. Our goal is to ensure patients can access the specialized care they need without transportation being a barrier, while maximizing available resources to serve as many families as possible. 

Dream Cares

Dream Transportation

Dream Cares

  

Patients with Sickle Cell and other Rare Diseases often rely on caregivers to support them in managing their health from parents, grandparents, siblings and spouses. Dreamsickle Kids wants to acknowledge and support caregivers as they are the biggest support system for those battling Sickle Cell and other Rare Diseases. Caregivers exper

  

Patients with Sickle Cell and other Rare Diseases often rely on caregivers to support them in managing their health from parents, grandparents, siblings and spouses. Dreamsickle Kids wants to acknowledge and support caregivers as they are the biggest support system for those battling Sickle Cell and other Rare Diseases. Caregivers experience many changes when they assume the role to take care of and support their loved one with a chronic illness from financial changes such as job loss, mental and emotional challenges, familial hardships. We strive to provide a support system for caregivers to better manage stress and to practice selfcare along with supporting financially when needed. We strive to provide gifts to our adult caregivers at events and to ensure gifts are tailored to benefit caregivers from health and wellness certificates to vacations. 

Dream Assistance

complete form for assistance

SSI ASSISTANCE FOR NV RESIDENTS

Are you an SCD patient and need SSI? Get your SSI questions answered and/or assistance with SSI clai

Dreamsickle Kids has partnered with Big Horn Law to offer those with SSI legal assistance with new or existing SSI claims from initial application to appealing denials. Contact Big Horn Law for assistance.

Contact Big Horn Law

Contact for Consultation

Dreamsickle Kids Foundation, Inc is a 501 ( C) 3 nonprofit registered in the state of nevada. tax id 82-4557748. Dreamsickle Kids Foundation, Inc  provides many types of support not listed, please contact us via phone or email for more information on the available assistance we can provide to families impacted by Sickle Cell or Rare Diseases.


Permission to use the Dreamsickle Kids Foundation name or logo in any variation, is subject to the terms and conditions expressly agreed upon in writing with approval from the Dreamsickle Board of Directors. Unauthorized use is prohibited and subject to legal ramifications.
 


Permissibon to use the Dreamsickle Kids Foundation name or logo in any variation, is subject to the terms and conditions expressly agreed upon in writing with approval f+rom the Dreamsickle Board of Directors. Unauthorized use is prohibited and subject to legal ramifications.
.

 

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Registration is now open!

 

Celebrate our sickle cell warriors, families, and community at this powerful, family-friendly event filled with inspiration, resources, and fun!

🗓️ April 25, 2026
🕐 1:00 PM – 4:00 PM
📍 Cambridge Community Center
3900 Cambridge St, Las Vegas, NV 89119

✨ What to Expect:
• Warrior stories & community spotlights
• Superhero-themed fun & activities
• Vendors, resources & giveaways
• Food, music & family connection

⚠️ Limited Availability — Registration Required!
Spots are filling quickly. Don’t miss out on this unforgettable experience!

👉 Register today to secure your spot!



RSVP Warrior Drive