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End Well is dedicated to the belief that all people should experience the end of life in a way that matches their values and goals. When faced with issues of mortality, we often suffer needlessly for a variety of reasons, from cultural and clinical to matters of access. End Well brings together a multidisciplinary community that unites design, technology, health, policy and activist initiative to transform how the world thinks about caregiving, grief, illness and the end of life experience with the ultimate goal of creating a future where ending well becomes a measure of living well.

We are honored to provide resources and support to the millions of people living with Alzheimer's disease and to their families, friends and caregivers who support them on a daily basis. If you or someone in your family has been diagnosed with Alzheimer's disease or another form of dementia, we are here to help. You can get free, confidential counseling and support today. The End Alz Association is proud to be a leader in the fight to #EndAlz but we couldn't do it without your support. Please join us and make a donation today. Together, we can #EndAlz!

TO IMPROVE THE HEALTH OF THE PEOPLE OF WASHINGTON STATE. IN 2014, WHF MADE THE DIFFICULT DECISION TO END ITS PERSONAL HEALTH ADVOCATE PROGRAM AND OTHER ACTIVITIES AND ESSENTIALLY SUSPENDED OPERATIONS AS THE BOARD EVALUATED ITS OPTIONS. IN 2015, THE BOARD CONTINUED TO ASSESS ITS FUTURE OPPORTUNITIES AND ALSO CONCLUDED THAT IT WAS BEST TO ALLOW ANY POSSIBLE PAST CONTINGENT LIABILITIES TO BE IDENTIFIED AND SATISFIED BEFORE PROCEEDING FURTHER. THE FOUNDATION BOARD HAS NOT IDENTIFIED ANY SUCH LIABILITIES BUT HAS DECIDED TO MAINTAIN ITS CURRENT LIMITED APPROACH FOR ANOTHER YEAR OR TWO. ACTIVITY IS CURRENTLY LIMITED TO COMMUNICATING ITS PAST ACHIEVEMENTS AND LEGACY THROUGH ITS WEBSITE WWW.WHF.ORG

To provide support to parents of children born with rare chromosome disorders, gather together and share information, and to promote research and a positive community understanding of these disorders. CDO envisions a time in the not too distant future when doctors will have a great deal of information available on each and every chromosome disorder. They will be able to tell parents symptoms associated with a particular deletion, duplication or other disorder as well as what not to worry about. It is also our hope that appropriate therapies or other treatments will be recommended specific to particular disorders and that affected individuals will have a much greater chance of a fuller life. This is already beginning to happen and it is CDO's goal to further support this research in any way possible.

Move it Nation, Inc. is a health, well-being, and leadership 501c3 non-profit organization whose mission is to empower youth to move their minds, bodies and souls. Collectively, we motivate, educate and inspire the future generation to live well: physically, mentally and emotionally.OUR FOCUSOur focus is well-being particularly among multicultural, urban youth. Recent research has shown that women and adolescent girls of African descent are disproportionately affected by chronic disorders such as cardiovascular disease, diabetes, and are more physically inactive than their racial or ethnic counterparts.In response to this, we have narrowed our focus with programs and interventions for this population. Our secondary focus is education and enrichment among youth in Southern Africa.

The mission of the Southern Arizona AIDS Foundation (SAAF) is to cultivate a healthy & stigma-free society through transformative action. In 1997, three AIDS service organizations in Tucson (Tucson AIDS Project, PACT for Life, and Shanti Foundation) merged to form SAAF. In 2014, SAAF took over several initiatives from Wingspan, formerly Southern Arizona's LGBTQ community center. In 2015, SAAF celebrated 30 years of providing services and continues to be the only community-based organization in southern Arizona providing case management and ancillary support services for people living with HIV/AIDS and their families; culturally appropriate prevention and education programs to reduce the rate of infection; & LGBTQ community outreach & engagement.

At Dentists on Wheels (DOW) our mission is to reach and treat patients with limited accessible oral healthcare service located in and around Contra Costa County. DOW works to promote health equity in our local community while simultaneously teaching proper oral health care practices.Volunteers, including dentists and assistants, work collectively to help underserved and uninsured individuals become free from dental health issues. DOW is proud to have a team of dedicated individual that help provide low to no cost, high-quality restorative and preventative dental care to uninsured and underserved individuals. At DOW, our ultimate mission is to address and rectify the issue of limited accessible oral healthcare services within our local community.

The Tivoli Fund supports organizations with a focus on improving lives. This fund will split donations evenly between No Dogs Left Behind, One Mission, World Central Kitchen, GLAD, and One Tree Planted. No Dogs Left Behind is a leader in global animal rescue. Through international alliances and local resources, we engage in every step of rescue. From emergency response to dog adoption, No Dogs Left Behind stands by our survivors every step of the way. One Mission programs make living in the hospital less lonely and stressful, bring back joy in a time of fear and uncertainty, and give kids and their loved ones the support they need to get through the emotional and financial challenges of treatment. World Central Kitchen uses the power of food to nourish communities and strengthen economies through times of crisis and beyond. Through strategic litigation, public policy advocacy, and education, GLBTQ Legal Advocates & Defenders (GLAD) works in New England and nationally to create a just society free of discrimination based on gender identity and expression, HIV status, and sexual orientation. ONE TREE PLANTED A NON-PROFIT ORGANIZATION FOCUSED ON GLOBAL REFORESTATION

Lori Hartwell founded Renal Support Network (RSN) in 1993 to empower people who have kidney disease to become knowledgeable about their illness, proactive in their care, hopeful about their future and make friendships that last a lifetime. Lori was diagnosed in 1968 with kidney failure and knows how important hope, peer connection and knowledge is to survive and thrive with an illness. RSN’s hopeful and life-enriching, non-medical programs help people who have kidney disease and their families, whether they are in the early stages of the disease, are on dialysis, or have received a transplant. People we connect with come to see kidney disease in a totally different light – that although it’s difficult, it is manageable. We help them recognize the need to take control of the course and management of their illness through storytelling. Learning from another patient’s experience and point of wisdom to live successfully and navigate care is vital for success. An Illness is too demanding when you do not have hope. RSN strives to make a lasting and positive difference in the lives of people with kidney disease and ensure that healthcare professionals and regulatory agencies legislative leaders that serve us hear what our needs are to have the best care and health possible.

Delta Gamma Foundation fosters lifetime enrichment for members, promotes Service for Sight, and partners with the Fraternity to ensure the future of our sisterhood.

To provide free medical care in the San Francisco Bay Area for those who have the greatest need and the least access.

Oasis Free Clinics is a non-profit, no-cost primary care medical practice and dental clinic, providing patient-centered care to uninsured adults in Midcoast, Maine.