Three years ago, we brainstormed during the winter about ways to enable camp to have a broader, more meaningful impact on our campers.\u00a0 We know that camp is fun and that the kids love being here, but we also want campers to appreciate the boundless opportunities and advantages in life that they have.<\/p>\n
In 2012, Woody discovered The Pihcintu Multicultural Chorus, which is comprised of young women refugees from all over the world.\u00a0 Through music, these young women have adapted to new cultures and reclaimed their lives.\u00a0 We invited a group of girls to spend the day at Robin Hood, and the experience proved to be extremely memorable for both Chorus members and campers.\u00a0 The girls enjoyed lunch, spent some quality time with campers in girls\u2019 camp, played gaga, did arts and crafts, swam, and enjoyed a cookout on the beach.\u00a0 After dinner, they performed for us, which was very special.<\/p>\n
Last year, we partnered with Dare2Tri Paratriathlon Club, a group that serves youths, adults and injured service members. Its mission is to provide athletic opportunities for disabled individuals and to inspire the community at large.\u00a0 Six amazing Dare2Tri members spent a few days at camp with us, running, biking and doing the island swim with us.\u00a0 Our guests made deep impressions on our campers, demonstrating how to face challenges with positive attitudes and determination.<\/p>\n
We are excited to share with you our plans for this summer.\u00a0 Today, Paul Frase will be visiting camp to help inspire campers.\u00a0 Paul grew up just 45 minutes away in Concord and played football at Syracuse.\u00a0 He went on to a hugely successful career in the NFL, having played for the New York Jets, Jacksonville Jaguars, Baltimore Ravens and the Super Bowl Green Bay Packers.\u00a0 More importantly, Paul founded the Joshua Frase Foundation in honor of \u2013 and now in memory of \u2013 his son, Joshua, who died four years ago at the age of 15 following a life-long battle with the congenital disease myotubular myopathy (MTM). In addition to raising funds to help find a cure for MTM, the Foundation supports the families whose lives are affected by this terrible disease.\u00a0 Paul will speak with the campers, and then over the course of the day, each group will participate in a walk in memory of these special children.\u00a0 If you would like to learn more about the Joshua Frase Foundation, or if you would like to honor your child by making an online donation in his\/her name in support of the walk on Giving Back Day, please visit www.joshuafrase.org.<\/p>\n
We feel strongly that it is crucial for our children to not only appreciate the advantages that they have but also to develop empathy for others and to understand the importance of giving back.\u00a0 What better place to be inspired than right here amidst the magic in the trees.<\/p>\n","protected":false},"excerpt":{"rendered":"
Three years ago, we brainstormed during the winter about ways to enable camp to have a broader, more meaningful impact on our campers.\u00a0 We know that camp is fun and that the kids love being here, but we also want campers to appreciate the boundless opportunities and advantages in life that they have. In 2012, Woody discovered The Pihcintu Multicultural…<\/p>\n","protected":false},"author":5,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[],"class_list":["post-158","post","type-post","status-publish","format-standard","hentry","category-uncategorized"],"yoast_head":"\n