Jennifer Riddle
(Las Vegas, Nevada)
Owner, NV'D Beauty
Account Manager, Barclaycard
Georgene' " Gina" Glass, CHW, Author, Nonprofit Consultant
(Las Vegas, Nevada)
Georgene’ Glass is the founder and Executive Director of Dreamsickle Kids Foundation, Inc, the first Sickle Cell Disease (SCD) organization in the state of Nevada.
Georgene’ serves as a Vice Chair of the Nevada Rare Disease Advisory Council created in 2019, and is a member of the NV SCD coalition created by 4 resilient SCD leaders in Nevada including the top SCD Hematologist, the Sickle Cell Alliance of Nevada (SCAN) As a mother of a child with SCD, Georgene’ has made increasing SCD awareness and support in the state of Nevada a personal mission. With SCD being one of the 7,000 Rare Diseases, in 2020 Georgene' spearheaded Dreamsickle Kids Foundations' expansion to support those in Nevada impacted by Rare Diseases.
Nika Jones
(Las Vegas, Nevada)
CEO Lupus Empire, CCSD Employee
Destiny Morris
(Indiana)
City of Michigan City, Accounting
Savone Grafton
(Illinois)
Stock Investor
Lyn Rivera
(Las Vegas, Nevada)
Red Cross S. Nevada
Jasmine Grafton
(Illinois)
Treetop Products, Inc.,
Certified Holistic Nutritionist
Cosmetologist
Nykolette Boyd
(Los Angeles, California)
Transaction & Marketing Coordinator, Grand B Realty
Owner/Operator, Donnisha FX
Glahnnia Rates, MSHS, CHW II
Epidemiologist
Founder/CEO Black Community Health & Wellness Association
Community Health Advocate
Naja Bagner, CHW
Naja is an Ohio native and Sickle Cell Warrior. Naja is a phlebotomist and community health worker, in her new role as a CHW , Naja will be able to leverage her experience living well with Sickle Cell to support patients and Families in Nevada as they navigate their healthcare journey and everyday life.
Dr. Dan Laird MD/JD
(Las Vegas, Nevada)
Laird Law PLLC, Medical Malpractice Attorney
Tamika Phyfer, PA-C
(Las Vegas, NV)
Owner , The Beauty Bus; The Phyfer Group
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.
Copyright © 2018 DREAMSICKLE KIDS - All Rights Reserve
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🎉✨ Join us for our 3rd Annual Healthy Holiday Celebration Brunch & Gift Giveaway!
Spots are limited—register now for an unforgettable day of treats, gifts, and holiday fun! 🎁🍬
📲 Click here to register!
We are excited to announce that our popular Dream Juicing Workshops are back, and registration is now open! 🌟 This fun and informative event is designed for Sickle Cell patients and caregivers. Space is limited, so be sure to register early!
At the workshop, you'll enjoy raffles, delicious recipes, and tasty treats while learning about the benefits of juicing for improved health and wellne