Category: Help With Cancer and Other Medical Issues
A Breath of Hope Lung Foundation is dedicated to fighting lung cancer by funding innovative research, educating the public for improved disease awareness, and supporting patients and caregivers on the path to survivorship.
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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.
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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.
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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.
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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.
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Hope for Two…The Pregnant with Cancer Network offers free support for women diagnosed with cancer while pregnant. We connect women who are currently pregnant with cancer with other women who have experienced a similar cancer diagnosis.Our mission here at Hope for Two is to provide women diagnosed with cancer while pregnant with information, support and hope.
Our Guiding Values:
We serve women in all socioeconomic, ethnic and religious backgrounds world-wide.
Volunteers with a history of cancer while pregnant are the mainstays of our support network.
We strive to remove barriers to women obtaining complete and accurate information about their options for dealing with cancer while pregnant.
We respect and support every woman’s personal decisions without judgment.
If you are looking to request support or become a volunteer support women you can visit our website at http://www.hopefortwo.org/
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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.
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Hope in Bloom provides the beauty of nature for breast cancer patients living in Massachusetts. The all-volunteer non-profit plants indoor, outdoor patio and in-ground vegetable or flower gardens at the homes of people in active treatment for the disease. Gardens deliver their own special brand of medicine and recipients enjoy the benefits as they look toward the future.
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Babies affected with Turner Syndrome require a lifetime of specialized care beyond the pediatric setting. Obstacles often impede an early diagnosis for girls to receive critical health screenings and timely, life-altering, interventions. The Foundation’s advocacy efforts identify these gaps and give voice to leaders who can make a difference. The vision to improve the understanding of TS and to render support for women and children living with TS is made possible by advancing communications and inspiring relevant interest in this women’s health issue. Legislative advocacy, education, and research are cornerstone to improved outcomes. For more information about Turner Syndrome, please visit https://turnersyndromefoundation.org/welcome/ or call 1-800-594-4585.
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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.
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