Children’s Alopecia Project Celebrates 20 Years of Empowering Children with Alopecia Hair Loss
Children’s Alopecia Project Celebrates 20 Years of Empowering Children with Alopecia Hair Loss

We have changed the emphasis from growing hair to growing confidence and self-esteem, providing support and raising awareness for 20 years.

I never thought for one minute that the little support group we started 20 years ago would grow into an organization helping kids and their families around the world and witness magic every day.”

— CAP Founder, Jeff Woytovich

WYOMISSING, PENNSYLVANIA, UNITED STATES, June 27, 2024 / — The Children’s Alopecia Project (CAP) is proud to announce its 20-year anniversary of providing support, education, and empowerment to children living with Alopecia hair loss. Founded in 2004, CAP has been a guiding light for thousands of children, helping them embrace their uniqueness and build self-confidence.

Alopecia, an autoimmune condition causing hair loss, often affects children at an early age, making it a challenging experience for them to navigate. However, the Children’s Alopecia Project has been a beacon of hope, fostering a sense of community and acceptance for children and their families.

To mark this significant milestone, CAP is thrilled to celebrate the 15-year anniversary of its beloved camp, Alopeciapalooza. From August 16 to August 19, 2024, Alopeciapalooza will bring together children from across the country for a memorable and empowering experience. The camp offers a supportive environment where children can connect with others who understand their journey and participate in activities designed to boost their self-esteem.

During the four-day event, campers will engage in breakouts, interactive sessions, and team-building exercises aimed at promoting self-acceptance, confidence, and personal growth. From art therapy and confidence-building workshops to outdoor adventures and talent displays, Alopeciapalooza promises an unforgettable experience for every participant.

Since its inception, CAP has worked tirelessly to raise awareness about Alopecia and eliminate the stigma associated with hair loss. Through educational programs, support groups, and community outreach initiatives, CAP has empowered children to embrace their differences and live their lives to the fullest.

In addition to the camp, CAP offers year-round programs and resources to support children and their families on their Alopecia journey. From local support groups to online forums and educational materials, CAP ensures that no child or family feels alone in their experience.

As CAP celebrates 20 years of making a difference in the lives of children with Alopecia hair loss, the organization looks forward to continuing its mission of empowering, educating, and inspiring children to embrace their unique beauty and live without limits.

Media Contact:

Name: Jeff Woytovich

Title: Founder

Address: 906 Penn Ave. Wyomissing, PA 19610

Email: [email protected]

Phone: 610-741-5552


About Children’s Alopecia Project:

The Children’s Alopecia Project (CAP) is a non-profit organization dedicated to providing support, education, and empowerment to children living with Alopecia hair loss. Through its various programs, including Alopeciapalooza, CAP aims to create a positive sense of community, foster self-confidence, and raise awareness about Alopecia.

For more information about the Children’s Alopecia Project and Alopeciapalooza, please visit or contact [email protected].

Jeff Woytovich
Children’s Alopecia Project
email us here
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20 Years of CAP and 15 Years of Alopeciapalooza

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