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The mission of the Ehlers-Danlos Syndrome Research Foundation is to improve the care of people with Ehlers-Danlos Syndrome (EDS), Hypermobility Spectrum Disorder (HSD) and related disorders by 1) advancing innovative research on treatment modalities, efficacy, and delivery and 2) educating healthcare providers across disciplines on the diagnosis and management of this patient population.

The overall mission of Blue Hope is to raise funds, resources, social awareness, and provide other support for a variety of self-sustaining social development projects and programs, both domestically and abroad, in order to effectively fight social injustice at a grass roots level. As of its founding, Blue Hope is primarily focusing on working with education, poverty, and children’s issues in Tanzania, East Africa and has done so by constructing and supporting a residential and educational facility and its outreach program. House of Blue Hope pulls kids off the streets and puts them into a safe living and learning environment. With such access to one of the top schools in the country, the current and future residents of the House of Blue Hope will be provided with top-notch educational opportunities in a country in which only about 12% of the population receives a secondary education. Furthermore, the facility has become a large part of the local high school’s community service program, as well as a catalyst to keep alumni involved and connected after graduation.

To serve, educate and fund research for families coping with the effects of SYNGAP mutations.

The Indiana Recovery Alliance operates under the philosophy of harm reduction to educate the community about health risks and to promote the health and dignity of the individuals and communities impacted by drug use. We respectfully collaborate with people to assist in any positive change, as a person defines it for themselves, beginning where the person is at with no biases or condemnations for the person's chosen lifestyle. Our efforts advance policies, practices and programs that address the adverse effects of drug use including overdose, HIV, hepatitis C, addiction and incarceration.

The mission of the Northwest Parkinson's Foundation is to establish optimal quality of life for the Northwest Parkinson's community through awareness, education, advocacy and care. NWPF achieves our mission by supporting specialty care, producing and distributing free educational and support resources, raising awareness of Parkinson's disease and developing self-care tools that help improve the quality of life for patients, families and caregivers.

MISSION:  In response to Christ and the Church, the mission of the Methodist Home for Children and Youth is to be a model agency that restores childhoods, strengthens families and cultivates a people-building organization.VISION:  . . . those we serve receive more grace, understanding, care and support than they are likely to experience elsewhere . . . VALUES: Servant Ministry, Nonviolence, Emotional Intelligence, Social Learning, Democracy, Open Communication, Social Responsibility, Growth and Change

The mission is to be the leading community resource for providing patients and families with compassionate physical, emotional and spiritual end of life care with comfort, dignity and respect.

Mission: BVA serves as ambassadors and mentors for all veterans and their families coping with sight loss.Vision:BVA continually strives to better the lives of all who served in the Armed Forces living with sight loss through: expert advocacy, engaged membership, clear communication, and peer inspired self-reliance. Our BVA family epitomizes respect, honor, dedication and commitment to sustain a thriving, informed, patriotic and connected community.Why: BVA is the only congressionally chartered Veterans Service Organization created for, consisting of and led by visually impaired veterans focused on the issues, advocacy and mentorship vital to all veterans and families coping with sight loss regardless of service connection

To promote the empowerment of Deaf Internationals living or staying in America.

COLN is the first organization of its kind in Nevada. We are devoted to raising Lupus awareness, improving the quality of life, & supporting each other.

AuthoraCare Collective empowers people to be active participants in their care journey, enabling them to live on their own terms through personalized support for mind, body, and spirit.

To engage, educate and empower people to prevent bone loss, osteoporosis, and fractures and to keep strong bones for long and independent lives.