Caleb Duplan, a resilient soul born with Sickle Cell Disease, faced numerous painful crises throughout his life. Despite the challenges, he remained undeterred, embracing his passions and pursuing a life filled with purpose. Wrestling and regular exercise became not just a means to stay healthy but a testament to his unwavering determination.

In addition to his physical pursuits, Caleb was a musician, weaving melodies that reflected his inner strength and optimism. As his journey unfolded, he found solace and purpose within the walls of a church, further enriching his life and connecting with a supportive community.

 

About Us

Awareness of
Sickle Cell Anemia

CDC Foundation is created to support children and families who are suffering from sickle cell disease. 

Program Initiatives

Decoding Sickle Cell Disease: Navigating Challenges with Hope

Sickle Cell Disease (SCD): Unraveling Red Blood Cell Impact

SCD involves inherited disorders altering red blood cells. Instead of their usual round shape, these cells transform into rigid, sticky “sickle” shapes, hindering oxygen transport. The abnormality causes cell death, leading to a shortage and blockages in blood vessels. This results in complications like pain, infections, acute chest syndrome, and strokes. Recognizing SCD challenges is crucial for effective diagnosis, management, and support.

Sickle Cell Disease Genesis: Revealing the Genetic Blueprint

Sickle Cell Disease (SCD): Investigating Genetic Inheritance from Both Parents

Detecting Sickle Cell Disease: Navigating the Path to Diagnosis

Detecting Sickle Cell Disease: Unveiling through Routine Newborn Screening

Advancements in Sickle Cell Disease: Investigating Treatment Breakthroughs

Pioneering Sickle Cell Disease Treatment: FDA-Approved Cure through Bone Marrow or Stem Cell Transplantation

Services We Provide

Education and Emotional Support

Virtual and At-Home Support Program: Providing Education, Emotional Support, and Resources for Individuals and Families Impacted by Sickle Cell Disease.

Education and Emotional Support

Education and emotional support are offered to individuals and families virtually or at home. Individuals and families are able to discuss how sickle cell disease has impacted their lives. Families are provided with coping mechanisms and support to enhance their way of living with the disease.

Routine Outpatient Visit

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Pain Management

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Outreach Services

Community Collaboration for Awareness: Annual Blood Drives and Fundraising Events in Partnership with Other Agencies.

Healthcare and Medical Assistance

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Case Management

Comprehensive Support: Addressing Medical, Social Needs, and Community Referrals, Collaborating with Providers to Provide Necessary Resources.

Caleb was born with Sickle Cell Disease and experienced many painful crises. He had multiple visits to the emergency room because of pains and fevers. Caleb knew of his sickness, but that never stopped him from doing what he wanted. He will do wrestling and complete exercises that were difficult. Caleb was strong willed and wanted to accomplish so much in a short time. Caleb was a beautiful person inside and out. He would light the room with his smile. He was a genuine and caring person and was loved by family and friends. This Foundation was created to honor him and celebrate all of his accomplishments and most importantly to help families and children suffering with the disease.

(Celebration and Memory of Caleb Duplan)

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Meet Our Team

Volunteers Around
The Globe

Monet Jean

Philippe-President and CEO

Myriam Duplan

Executive Vice President

Rony Duplan

Vice Chair

Partners

Our Partners