CHILDRENS ALOPECIA PROJECT
Invite reviews
Invite friends and colleagues to share their experiences with this nonprofit
November 30, 2012
I am a parent of a bald child with Alopecia. CAP is the only entity devoted to just kids with Alopecia.
More feedback...
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
May 1, 2012
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!
More feedback...
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
May 1, 2012
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!
More feedback...
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
July 1, 2009
I am the founder, so I am bias. Please visit www.childrensalopeciaproject.org and see if you think we try to help build self-esteem, provide support and raise awareness. Thank you and take care. Founder, Jeff Woytovich Children's Alopecia Project, Inc.
Photos
The Great!
I've personally experienced the results of this organization in...
Seeing what we do for children living with the incurable autoimmune hairloss disease, Alopecia.
Ways to make it better...
If I had to make changes to this organization, I would...
I do. Help me with your comments.
More feedback...
What I've enjoyed the most about my experience with this nonprofit is...
Knowing that we are helping children from around the world with there self-esteem.
The kinds of staff and volunteers that I met were...
the best out there.
If this organization had 10 million bucks, it could...
Have more events bringing more children from around the world together.
Ways to make it better...
We had more financial support from companies that held self-esteem in high regard.
In my opinion, the biggest challenges facing this organization are...
getting more volunteers to help spread the word.
One thing I'd also say is that...
I am always optimistic and waiting for that phone call that knocks me off my feet. I am still waiting and my number is still, 610-741-5552.
When was your last experience with this nonprofit?
2009
Previous |
Next
Filter by reviewer role:
Support This Nonprofit
Help this nonprofit get more reviews
5 tips for getting reviews