At Dreamsickle Kids Foundation, our heartfelt purpose is to advance health and transform lives. We are a charity committed to serving the community through a range of vital initiatives.
We provide comprehensive community health services that directly address the specific needs of the community. From mobile screenings for diseases and symptoms to offering guidance on nutrition and exercise, we strive to empower individuals affected by Sickle Cell Disease and other Rare Diseases. Our goal is to support them in managing their conditions and reducing the risk of complications.
Ensuring access to healthcare is paramount, which is why we offer patient transport services to and from medical centers, bridging the gap for those who may face challenges in accessing necessary care. We believe that every individual deserves equal opportunity to receive the medical attention they require.
In our dedication to fostering excellence in healthcare, we provide training and education for medical professionals, equipping them with the latest advancements in best practices for diagnosing, treating, and managing illnesses. By sharing knowledge and expertise, we contribute to the overall improvement of patient care.
We understand the financial burden that can accompany Sickle Cell Disease and other Rare Diseases, and we are committed to providing emergency financial assistance to those in need. We strive to alleviate the additional stress that financial challenges can bring, allowing individuals to focus on their health and well-being.
Education is a key pillar of our foundation. We are devoted to raising awareness and understanding of Sickle Cell Disease, Rare Diseases, and their impact. We provide comprehensive education to adults, caregivers, the community, and medical professionals, empowering them with knowledge to support those affected by these conditions.
At Dreamsickle Kids Foundation, we are driven by our passion for improving health outcomes, promoting well-being, and transforming lives. Together with our community, we strive to create a future where every individual impacted by Sickle Cell Disease and Rare Diseases receives the support, care, and resources they need to lead fulfilling lives.
In 2018, a groundbreaking milestone was achieved as Dreamsickle Kids Foundation emerged as the pioneering Sickle Cell Disease organization in the vibrant state of Nevada. With unwavering determination, our foundation made history by establishing the first dedicated platform solely focused on addressing the unique needs of individuals impacted by Sickle Cell Disease.
From humble beginnings, Dreamsickle Kids Foundation embarked on a journey to raise awareness, provide support, and advocate for improved healthcare access. In a landscape where knowledge and resources were scarce, we dared to take the first step towards making a profound impact in the lives of those affected by this often overlooked condition.
Our establishment marked a turning point, igniting a beacon of hope and resilience for the Sickle Cell community in Nevada. Through relentless efforts, we shattered barriers, challenged perceptions, and championed the urgent need for increased support, understanding, and resources.
Since our inception, Dreamsickle Kids Foundation has become a symbol of unity and empowerment, bringing individuals, families, and communities together. We have woven a tapestry of compassion, advocacy, and education, nurturing an environment where no one faces the challenges of Sickle Cell Disease alone.
As we reflect on our remarkable history, we carry the spirit of those who came before us, amplifying their voices and striving to create a better future. Today, Dreamsickle Kids Foundation stands as a testament to the power of passion, resilience, and the unwavering dedication to improving the lives of those impacted by Sickle Cell Disease.
Together, we continue to create a lasting legacy, fueled by the conviction that no one should navigate the journey of Sickle Cell Disease alone. We invite you to join us in our mission, as we make history and pave the way for a brighter tomorrow.
To #MakeSickleCellPopular in Nevada and beyond.
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
Powered by GoDaddy