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Many attendees of our group meetings, local camps, and International Annual Camp – Alopeciapalooza have never met someone who looks like them. With your gift, you make it possible for a CAP kids to attend a camp. You also have the option of giving to fund the CAP2U Speaking Tour that brings awareness and community that meets a CAP Kid right where they need it most, their community or school.
Friday, 25 October 2024 7:00 PM – Sunday, 27 October 2024 11:30 AM EDT
2000 Frost Valley Rd, Claryville, NY, 12725, United States
To help any child in need who is living with hair loss due to all forms of Alopecia. We change the emphasis from growing hair to growing confidence. building self-esteem, providing support, and raising awareness.
– Jeff Woytovich, Founder
We desperately need your help! The mission of CAP is to help all children with alopecia, and we will continue do everything in our power to keep CAP Kids free at all camps and events. Charitable giving is at an all-time low, and CAP, like many non-profits, is facing significant financial challenges that could compromise our ability to continue providing free programs and camps for children with alopecia. Alopeciapalooza and all of CAP’s programs are changing lives, and it won’t be the case without the continued support of donors like you!
When you join us at any CAP Camp, you and your child will not leave the same as you arrived. You will meet parents who understand what you’ve gone through and some that can help navigate what’s to come. Your child will meet children of all ages that look just like them.
You both will meet Speakers, Mentors, and Volunteers who have not let Alopecia keep them from accomplishing their dreams.
Keep your eyes open, you might just see your favorite celebrity showing up.
You are more, even if your hair is less.
Know that you are perfect the way you are. You are an original, not a copy.
It is normal to be different because everyone is different, and that makes you normal.
If one person has alopecia in your family, you all have alopecia.
Find a place for you to get connected and get the support you or your CAP kid needs.
Read the stories of those impacted by the Children’s Alopecia Project. Click on Leave a Review to tell us your story!
A: We are the only 501(c) 3 non-profit devoted specifically to helping children living with the hair-loss disease, alopecia areata. We do so by raising awareness about alopecia, providing support for children and their families, and building self-esteem in children living with alopecia.
A: Funds are used for the following:
A: CAP endeavors to keep all expenses to an absolute minimum. As such, we welcome gifts of office supplies, current model computers and other technical equipment, software, premium items such as event t-shirts and other giveaway items, as well as in-kind services. These include but are not limited to publicity, printing, technical support, legal services, and all other professional services. We also welcome sponsors who are willing to make donations to underwrite any expenses or growth opportunities that can help CAP grow and thrive.
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To have Jeff Woytovich speak at your child’s school during a CAP2U Speaking Tour or to make a house visit with a Bag of Books for your CAP Kid to donate to their school library, click a link below.
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