Honor their memory with a charitable gift.

RSRT was launched in 2008 to drive research toward a cure for Rett Syndrome and related MECP2 disorders. Our mission is urgent: 15,000 girls and women in the United States and 350,000 globally live with the agonizing symptoms of Rett Syndrome.

The Testicular Cancer Awareness Foundation is committed to raising awareness and educating the public about the most common cancer in men ages 15–44, while providing lifesaving support to patients, survivors, and caregivers with compassion and care. Our Mission? Awareness . . Support . . Survivorship We are a nonprofit compassionately dedicated to the fight against testicular cancer through awareness and outreach, promoting the importance of monthly self-exams for early detection, support and guidance to patients and families, providing a resource for the medical community, providing financial assistance to those in need and continuing to save lives. We stress the importance of early detection through the practice of monthly testicular self-exams (TSE), just as women are taught to detect early signs of breast cancer through monthly breast self-exams. We are fighting to make TSE part of health education classes taught at the middle school, high school, and college levels. We seek to reduce the great stigma and taboo associated with talking about testicular health; most teenagers and young men are embarrassed to openly talk about their bodies and the changes taking place. We do this simply by talking about testicular cancer, its impacts and how to recognize the signs through regular testicular self-exams. We assist patients in seeking the most effective treatments for testicular cancer that yield the best outcomes. Testicular cancer is not as common as many of the other cancers and as a result some medical facilities are inexperienced in the treatment of this disease and may be unaware of the most effective protocols. It is crucial when diagnosed with testicular cancer that the patient has access to the most reliable and expert care that yields the best treatment plans and outcomes resulting in lifesaving measures. We seek to reduce the financial burden of a testicular cancer diagnoses by empowering the patient with resource information for financial assistance through the use of online fundraising tools. We also provide limited funding to those in immediate financial need, including helping with gas, groceries and more. We provide an online private support group to help connect those who have been affected by this disease. The role of emotional and psychological support in the management of testicular cancer is extremely important and vital to an individual's overall well-being. We have over 4,000 active members in our private support group, fostering a strong and supportive community through meaningful conversations. Our programs: Financial Assistance Program - Provides direct financial aid as well as other resources for financial assistance. Academic Education Program - Provides academic and health professionals, such as teachers, coaches, doctors and nurses with the knowledge and tools to educate students and patients about the importance of early detection of testicular cancer. Centers of Excellence - Features a comprehensive list of centers recognized for their expertise in the treatment of testicular cancer. Outreach & Awareness Program - Organizes events, fundraisers, and conferences while distributing educational materials nationwide to spread awareness. Utilizes social media as a key tool for outreach. Testicular Cancer Conferences - Brings together an international community of TC patients, survivors, and their loved ones to address the physical and emotional challenges of diagnosis and treatment at a young age. Covers life during and after cancer, lifestyle changes for healing, and features a panel of medical experts providing essential information and long-term survivorship resources. Research Studies - Collaborates with researchers to advance the understanding of testicular cancer survivorship. Today we are making a positive impact in the fight against this disease and saving lives. Visit us at www.testescancer.org to learn more!

The mission of Joslin Diabetes Center is to prevent, treat and cure diabetes. Our vision is a world free of diabetes and its complications.

Brain Support Network (BSN) is a non-profit, charitable organization dedicated to three missions: 1) Providing information and support for anyone living with an atypical parkinsonism disorder (Progressive supranuclear palsy, Dementia with Lewy bodies, Multiple System Atrophy or Corticobasal degeneration) anywhere in the world; 2) Providing a support for care partners of those living with an atypical parkinsonism disorder in the San Francisco Bay Area; 3) Enabling families living anywhere in the US to donate the brain of anyone with any neurological condition (or healthy controls) to confirm the diagnosis and to further neurological research into causes, treatment options and cures.

The Children's Tumor Foundation is a not-for-profit organization dedicated to finding effective treatments for the millions of people worldwide living with neurofibromatosis (NF), a term for three distinct disorders: NF1, NF2, and schwannomatosis.  NF causes tumors to grow on nerves throughout the body and can lead to blindness, bone abnormalities, cancer, deafness, disfigurement, learning disabilities, and excruciating and disabling pain.   NF affects one in every 3,000 people, more than cystic fibrosis, Duchenne muscular dystrophy, and Huntington’s disease combined.  The Children’s Tumor Foundation funds critical research into neurofibromatosis.  In addition to benefiting those who live with NF, this research is shedding new light on several forms of cancer, brain tumors, bone abnormalities, and learning disabilities, ultimately benefiting the broader community.

The Fisher Center for Alzheimer’s Research Foundation is an organization that provides millions of dollars for novel Alzheimer’s research all over the world to investigate the latest, most promising research available. Our mission is to understand the causes of Alzheimer’s disease, improve the care of people living with it, and find a cure. A majority of our funding goes to the Fisher Center Lab at The Rockefeller University that was under the direction of the late Nobel laureate Dr. Paul Greengard, which is now under the leadership of Dr. Nathaniel Heintz. The Center has provided researchers around the globe with a conceptual framework for understanding the disease process and continues to be at the forefront of one day finding a cure for Alzheimer’s disease. We also fund research at NYU Langone, where a handful of clinical trials are taking place. The Foundation’s national comprehensive Alzheimer’s Information Program, the heart of which is the Foundation’s website, www.ALZinfo.org continues to spearhead efforts to increase awareness of and education about Alzheimer’s disease to the general public. The website provides in-depth information on the most current research studies, treatments, and disease management approaches. We also publish a magazine (Preserving Your Memory®) that provides readers with information about Alzheimer’s and how to take the necessary steps to prepare adequately if they or a loved one fall victim to the disease. Another facet of our Information Program is the e-newsletter, which contains updates and helpful tips. Our vision is working towards a future where Alzheimer’s is nothing but a memory.

The mission of the American Brain Tumor Association is to advance the understanding and treatment of brain tumors with the goals of improving, extending and, ultimately, saving the lives of those impacted by a brain tumor diagnosis. We do this through interactions and engagements with brain tumor patients and their families, collaborations with allied groups and organizations, and the funding of brain tumor research.

The Child Cancer Fund was founded in 1994 by a group of Jacksonville, FL parents whose children were being treated for cancer; they understood the stress, anxiety and heartache of a childhood cancer diagnosis. We provide practical, emotional, financial, and educational support to children and their families every step of the way to navigate the challenges of childhood cancer.

To break the cycle of domestic violence by providing comprehensive support, services, and education within and beyond the walls of our shelter

The Pediatric Brain Tumor Foundation works to eliminate the challenges of childhood brain tumors. Our vision is a cure for childhood brain tumors.

The mission of the Hydrocephalus Association is to promote a cure for hydrocephalus and improve the lives of those affected by the condition. This will be accomplished by collaborating with patients, caregivers, researchers, medical professionals and industry, raising awareness and funding innovative, high-impact research to prevent, treat, and ultimately, cure hydrocephalus.

SOME (So Others Might Eat) is an interfaith, community-based organization that exists to help the poor and homeless of our nation's capital. We meet the immediate daily needs of the people we serve with food, clothing and health care. We help break the cycle of homelessness by offering services, such as affordable housing, job training, addiction treatment, and counseling, to the poor the elderly and individuals with mental illness.