OPACC was established in 1995 and supports families of children with cancer throughout Ontario through our in-hospital Parent Liaison program, which provides non-medical, peer-to-peer and virtual support and financial assistance; by establishing local parent support groups in communities throughout the Province; and by advocating on issues of importance to childhood cancer families. (Read More...)
A Fresh Chapter is a non-profit organization that facilitates life-changing volunteer and leadership experiences to empower individuals both in the U.S. and abroad impacted by cancer. AFC programs blend volunteerism and meaningful travel to connect cancer patients and caregivers around the globe, and focus on healing the often over-looked emotional scars left by cancer. AFC’s perspective-shifting journeys to places like India, Peru and Kenya help participants reframe adversity and discover a new perspective and purpose in their lives. (Read More...)
JAJF, a national 501(c)(3) nonprofit, treats children facing the loss of their young Mom or Dad to cancer to WOW! Experiences®...a prescribed timeout together as a family away from their late stage cancer to create positive, cherished, lasting memories…while they can. (Read More...)
The National Pancreatic Cancer Foundation exists to deliver unwavering support for patients and families fighting pancreatic cancer. NPCF aims to increase awareness for pancreatic cancer and transform the experience of pancreatic cancer by delivering immediate unwavering support to all who seek it. Our primary programs include education, awareness, and financial assistance. Since it's inception in May of 2009, NPCF has helped over 237 families affected by pancreatic cancer with basic living expenses. (Read More...)
No family is ever prepared to hear the four worst words: Your child has cancer. Friends of Karen, New York-based and serving families in the NY-TriState area since 1978, is a non-profit with a vision that every child with a life-threatening illness, and his or her family, will have all that they need to keep them stable, functioning and able to cope. Providing financial assistance, illness education and supportive counseling, among other services, our staff of experienced social workers, child life specialists and expressive arts therapists guide families from their child’s diagnosis through treatment, at no cost, so they have more time for what's most important: each other. (Read More...)
The Cancer Support Center is here to give strength, guidance and support to anyone living with a cancer diagnosis, as well as to their loved ones. We do this as a community-based, volunteer-driven, donor-supported organization. Our programs, resources and services are always delivered by professional therapists, counselors, nutritionists, and experts; and are provided in a warm, welcoming and nurturing setting at no cost to participants. (Read More...)
Teen Cancer America is a change agent improving the lives of young people with cancer. We create youth-centered ecosystems supporting young people with cancer, their families, and the hospitals and healthcare professionals who care for them. We partner with hospitals throughout the United States to develop specialized facilities and services for teens and young adults with cancer. We build teen friendly environments, enhancing the hospital experience. We develop standards for age-targeted care, improve collaboration between pediatric and adult specialists and enable dedicated research to improve outcomes and survival for our young people. (Read More...)
The mission of Lucy’s Love Bus™ is to improve quality of life for children with cancer and life-threatening illness, to support their families, and to mobilize the next generation of cancer activists. Lucy's Love Bus pays for integrative therapies for children with cancer in New England, and holds programs and workshops in Amesbury, MA open to the families of children with cancer, life-threatening illness, or chronic medical conditions not developmental in nature. (Read More...)
Young Adult Cancer Canada (YACC) supports young adults living with, through, and beyond cancer through digital, local, and national support programs. It is a connection to peers, bridge out of isolation, and source of inspiration. Every cancer, every stage, YACC’s got your back. (Read More...)
The Chordoma Foundation is a nonprofit organization working to improve the lives of those affected by chordoma and lead the search for a cure. Chordoma is a rare type of cancer that forms in the bones of the skull and spine and is diagnosed in just one in one million people per year. The Chordoma Foundation envisions a future in which everyone affected by chordoma is able to overcome the disease and maintain their quality of life through better treatments, better care, and a better patient experience. (Read More...)