Over 1.8 million nonprofits and charities for donors, volunteers and funders

Childrens Alopecia Project

Rating: 4.91 stars   11 reviews 1,726

Address:

Post Office Box 6036 Wyomissing PA 19610 USA

Mission:

CAP will help any child in need who is living with hair loss due to all forms of Alopecia."We raise awareness of Alopecia and the self-esteem in children so the become stronger teens and productive adults.

Results:

We have helped thousands of children, friends, family and others associated with alopecia with awareness! We continue to grow self-esteem because we can't grow hair but next up is our biggest challenge yet! We are now in need of more funds so we can accomplish a CAP Kid Group that is registered and active in each State. We are also looking have the first comprehensive feasibility study of how children and parents deal with this incurable autoimmune hair loss disease. We need to find another $200,000 to be able to do these things while continuing our mission for the kids!

Target demographics:

He help kids and their family fro birth until 18 years old. We do encourage CAP Kids 18 and above to stay active, volunteer and mentor children that come after they have reached adulthood.

Geographic areas served:

Worldwide Reach!

Programs:

See www.ChildrensAlopeciaProject for a full listing

Write a Review
Donate
Invite Reviews Share This Nonprofit

See How 3Hrs Can Help

More Info

610-468-1011
www.childrensalopeciaproject.org

Reviews for Childrens Alopecia Project

Rating: 5 stars  

1 person found this review helpful

CAP is all about the children with alopecia not the alopecia in a child. They focus on self-esteem and confidence and not treatments and cures. They try to let kids know that everyone is different and that is normal!

 
Flag review
Rating: 5 stars  

1 person found this review helpful

Children's Alopecia project helped my daughter see she was not alone and the only little girl like her. She struggled with bullies and the groups at one of the summer activities helped her to learn to cope. She was given this opportunity free because of the love and hard work put in to making these camps free for the kids with alopecia.

 
Flag review
Rating: 5 stars  

1 person found this review helpful

CAP is a wonderful organization that helps children with any form of Alopecia. It allows these children to meet others that have the same incurable condition, which causes them to lose their hair. The focus is to help the children grow self-esteem and to spread awareness. To see these kids interact with each other is just amazing!

 
Flag review
Rating: 4 stars  

1 person found this review helpful

This is an organisation that is what all organisations should aspire to....its about the kids. Building lifelong friendships, self esteem, and a level of confidence someone with our without Alopecia of any brand would want to achieve. It has done wonders for our son, who i turn, instills confidence around the world, with a condition he is not afraid of or worries about, but loves and owns.

 
Flag review
Rating: 5 stars  

1 person found this review helpful

Childrens Alopecia Project is an amazing, life changing, self esteem boosting, loving organization! I lost all my hair at the age of two and started volunteering with CAP 6 years ago and it's been the best 6 years to be able to meet, learn from, grow with and be apart of the family! I've never felt as accepted and loved in my entire life until I joined CAP! I'm thankful everyday for this organization, the people it's blessed me with as well as all the opportunities! CAP truly is life changing and I can't say enough about all of the great work and events it does!

 
Flag review
Rating: 5 stars  

2 people found this review helpful

Children's Alopecia Project is truly a magical organization. CAP has brought our family together with many other families that are facing the same challenges that we do -- and there is an instantaneous bond. We help each other get through the tough days and celebrate the amazing days. CAP focuses on building each child's self esteem. Through CAP, our family has had so many special experiences. We are all so grateful to this organization! We have become not only clients served, but also want to give back to this community and have become avid volunteers and advocates! We LOVE CAP!!!

 
Flag review
Rating: 5 stars  

2 people found this review helpful

My daughter (who was in Kindergarten) has Alopecia Universalis and lost all the hair on her head and the rest of her body last January. It was very quick and shook her self as teem. It mad her feel different and worried about making friends. We went to camp this year, so she could meet other children like her. My daughter never goes bald in public and at camp she ran out of the car with nothing to cover her bald head. She made friends and asked questions to others about how they cope and manage living with this condition...and yes all from someone about to enter the first grade. My daughter had a great experience and now she knows, she is not the only child like this and she is not alone.

If I had to make changes to this organization, I would...

I would like to see more branches spread in more areas of the country.

How would you describe the help you got from this organization?

Life-changing

How likely are you to recommend this organization to a friend?

Definitely

How do you feel you were treated by this organization?

Very Well

When was your last experience with this nonprofit?

2013

 
Flag review
Rating: 5 stars  

1 person found this review helpful

I am a parent of a bald child with Alopecia. CAP is the only entity devoted to just kids with Alopecia.

How would you describe the help you got from this organization?

Life-changing

How likely are you to recommend this organization to a friend?

Definitely

How do you feel you were treated by this organization?

Very Well

When was your last experience with this nonprofit?

2012

 
Flag review
Rating: 5 stars  

1 person found this review helpful

4 years ago our daughter was diagnosed with Alopecia. At this time we didn't know a single thing about Alopecia. A family friend recommended I contact the Children's Alopecia Project. At first I was hesitant b/c that would make Alopecia affecting my daughter "real." I wasn't ready yet. After about 6 months I finally put my fears aside and our family attended the CAP summer picnic in Wyomissing. Our entire family grew that day because we made friends with other families in our situation. CAP is a part of our life and without it our entire family would be at a loss with this disease. We love CAP and know you will too!

Will you volunteer or donate to this organization beyond what is required of board members?

Definitely

How much of an impact do you think this organization has?

Life-changing

Will you tell others about this organization?

Definitely

When was your last experience with this nonprofit?

2012

 
Flag review
Rating: 5 stars  

1 person found this review helpful

Children's Alopecia Project is amazing! They're focus is on self-esteem for kids with alopecia and they really know how to make a kid feel good about themselves! My son went from not taking his hat off at all to not wearing a hat and saying he loves his alopecia all because of this group!

How would you describe the help you got from this organization?

Life-changing

How likely are you to recommend this organization to a friend?

Definitely

How do you feel you were treated by this organization?

Very Well

When was your last experience with this nonprofit?

2011

 
Flag review