Plug-in to Care: Nonprofit Partners
Nonprofit partners and patient advocacy groups play a vital role in Caregiver Action Network’s efforts during National Family Caregiver’s Month and throughout the year.
These organizations amplify our message, extend our reach, and help us provide critical resources and support to the millions of caregivers nationwide. Their collaboration allows us to connect with diverse communities, advocate for caregiver needs, and offer valuable tools and services that would be impossible to deliver alone.
Whether through joint campaigns, shared expertise, or direct outreach, these partners help caregivers receive the recognition, guidance, and encouragement they need to continue their essential work.
Their dedication strengthens the caregiving community and enhances our ability to make a lasting impact.
2025 National Family Caregivers Month Nonprofit Partners
2025 National Family Caregivers Month Nonprofit Partners
Disease-Specific and Health-Related Agencies
For caregivers supporting loved ones with specific medical conditions, access to disease-specific information and resources is essential. Many organizations offer tailored guidance, support, and community connections for particular health issues such as Alzheimer’s, cancer, diabetes, heart disease, and more. By leveraging these disease-specific organizations, caregivers can feel more empowered and informed when navigating the complexities of their loved one’s health needs.
The mission of the Angelman Syndrome Foundation is to advance the awareness and treatment of Angelman syndrome through education and information, research, and support for individuals with Angelman syndrome, their families and other concerned parties. We exist to give all of them a reason to smile, with the ultimate goal of finding a cure.
The IgA Nephropathy Foundation’s mission is to be a patient-centric organization focused on finding a cure for IgA Nephropathy. Using the power of the patient community, we are focused on funding research, using patient advocacy to empower our patients, and building a network of support.
Which everyday cancer problem will we fix today? Livestrong mission is centered around this one question. We make immediate impact on the lives of people affected by cancer and seek out solutions to support quality of life today—and for every step of the journey.
The Cancer Support Community uplifts and strengthens people impacted by cancer by providing support, fostering compassionate communities, and breaking down barriers to care.
The Kidney Cancer Association’s mission is to be a global community dedicated to serving and empowering patients and caregivers, and leading change through advocacy, research, and education
We fight to cure colorectal cancer and serve as relentless champions of hope for all affected by this disease through informed patient support, impactful policy change, and breakthrough research endeavors.
Mental Health America advances the mental health and well-being of all people living in the U.S. through public education, research, advocacy and policy, and direct service.
Triage Cancer® is a national, nonprofit organization that provides free education on the legal and practical issues that may impact individuals diagnosed with cancer and their caregivers, through events, materials, and resources.
Lung Cancer Initiative specializes in connecting patients, survivors, and loved ones with the medical and research community.
Association of Migraine Disorders Logo
The Association of Migraine Disorders® strives to expand the understanding of migraine by supporting research, education, and awareness.
To improve the lives of people with MS. Mission statement: The mission of the Multiple Sclerosis Foundation is to provide programs and support services to those persons affected by MS that help them maintain their health, safety, self-sufficiency, and personal well-being; and to heighten public awareness of multiple sclerosis in order to elicit financial support for the Foundation’s programs and services and promote understanding for those diagnosed with the illness.
Our mission is to improve the lives of everyone affected by Huntington’s disease and their families.
The Bone Health & Osteoporosis Foundation (BHOF) is the leading health organization dedicated to preventing osteoporosis and broken bones, promoting strong bones for life and reducing human suffering through programs of public and clinician awareness, education, advocacy and research. Established in 1984, BHOF is the nation’s largest health organization solely dedicated to osteoporosis and bone health.
Our mission is to unite stakeholders to advance patient-centered COPD policy at the state and federal level.
Cures Collective seeks to unify the neurodegenerative disease field, accelerate finding treatments and cures, and increase and improve access to care through intentional collaboration, and sustained public awareness and mobilization.
The mission of Alamo Head Injury Association (AHIA) is to improve the quality of life and well-being for survivors of brain injury (traumatic or non-traumatic), their caregivers, and their family members.
The Association of Cancer Care Centers (ACCC) is a powerful community of more than 46,000 multidisciplinary professionals from 1,700 organizations nationwide.
Founded in 1974, ACCC brings together healthcare professionals across all disciplines in oncology to promote quality cancer care. It is estimated that 65 percent of the nation’s cancer patients are treated by a member of ACCC.
Blue Faery’s mission is to prevent, treat and cure primary liver cancer, specifically Hepatocellular Carcinoma, through research, education, and advocacy. Our work will improve the quality of life for HCC patients, support their caregivers and give them hope, information, and a voice.
The mission of the Brain Injury Association of New York State is to support, educate and advocate for people and families impacted by brain injury and to minimize brain injury through prevention.
CANCER101’s mission is to simply healthcare – one person at a time – through personalized education, navigation and support.
The COPD Foundation was founded 20 years ago to transform the lives of people with COPD. Over time, our work has expanded to include bronchiectasis and NTM lung disease. What began as a grassroots effort is now a global force in research, education, and advocacy. Celebrate two decades of progress with our 20th Anniversary magazine and article in the Journal of the COPD Foundation.
Our mission is to create a world immune to cancer by driving scientific discovery, accelerating collaboration, and turning breakthroughs into life-saving treatments.
For over 70 years, CRI has driven breakthroughs in cancer immunotherapy by funding groundbreaking research, supporting life-saving clinical trials, and expanding access to the latest treatments. Today, CRI continues to accelerate progress by uniting scientists, funders, and patients around the shared goal of advancing data-driven discovery worldwide.
A local and independent nonprofit, Cancer Services opened in 1959 to serve the tangible needs of people living with cancer in Greater Baton Rouge. For over 65 years, the agency’s scope has evolved to empower cancer patients and their families by helping to meet the financial, physical and emotional needs that arise during the cancer journey. All services are free of charge, and we serve a 10-parish area that includes Ascension, East Baton Rouge, East Feliciana, Iberville, Livingston, Pointe Coupee, St. Helena, St. James, West Baton Rouge and West Feliciana Parishes. Cancer Services operates independently with key support from Mary Bird Perkins Cancer Center in the areas of operational efficiencies in accounting, marketing and vendor services therefore ensuring philanthropic support is fully-directed to mission programs.
Founded in 1944, CancerCare is the leading national organization providing free, professional support services and information to help people manage the emotional, practical and financial challenges of cancer.
Cervivor is a global community of patient advocates who inspire and empower those affected by cervical cancer by educating and motivating them to use their voices for creating awareness to end stigma, influence decision and change, and end cervical cancer.
Our mission is to champion policies and programs that improve the lives of children with cancer and survivors.
The Cholangiocarcinoma Foundation’s (CCF) mission is to find a cure and improve the quality of life for those affected by cholangiocarcinoma (bile duct cancer).
The Community Oncology Alliance (COA) is a non-profit dedicated solely to advocating for independent community oncology patients and practices. Our mission is to ensure that patients can receive the highest quality, most affordable, and accessible cancer care close to home.
Debbie’s Dream Foundation: Curing Stomach Cancer is a 501(c)(3) non-profit organization dedicated to raising awareness about stomach cancer, advancing funding for research, and providing education and support internationally to patients, families, and caregivers. DDF seeks as its ultimate goal to make the cure for stomach cancer a reality.
Enhancing patient outcomes by expanding FDA-approved treatment modalities and fueling research in the pharma/bio/life sciences, device & diagnostic industries and by closing the existing GAP from initial diagnosis to IMMEDIATE AND EXPANDED ACCESS to specialists, researchers, advanced & innovative treatments, clinical trials and critical care with the ultimate goal of improving patient outcomes through updating and improving guidelines and clinical practices related to Standard of Care for brain cancer patients.
EverythingALS is a patient-focused non-profit, part of Peter Cohen Foundation, a 501(3)c organization, bringing technological innovations and data science to support efforts — from care to cure — for people with ALS, by offering a open-data platform for direct engagement with patients, caregivers, researchers and drug companies.
FORCE, Facing Our Risk of Cancer Empowered is a national, nonprofit organization dedicated to fighting hereditary breast and ovarian cancer. With over 50 outreach groups throughout the U.S., their programs provide support, education, advocacy and research on behalf of the individuals and families affected by hereditary cancer.
To improve the lives of individuals and families impacted by liver disease through promoting innovation, encouraging collaboration, and scaling optimal approaches to help eradicate liver diseases.
Head and Neck Cancer Alliance’s mission is to provide hope and support to individuals impacted by head and neck cancer, to raise awareness about prevention and early detection, and to advocate for improved patient outcomes.
To connect people with trusted breast cancer information and a community of support.
LCFA’s mission is the improvement in survivorship of lung cancer patients through the funding of transformative science.
Raising public awareness, serving as a resource for patients or anyone seeking answers, hope, and access to updated treatment info.
The Lupus and Allied Diseases Association, Inc. (LADA) is an all-volunteer national patient advocacy organization dedicated to enhancing quality of life by enlightening and empowering individuals impacted by lupus and allied diseases and other conditions of unmet need to become proactive in their medical care. As a passion-driven charity led by people with lupus and their loved ones, we work to ensure that the patient stakeholder is included as an equal participant in the healthcare, regulatory and public policy arenas and across the research continuum. It is our goal to improve access to care and quality of life by fostering collaboration among stakeholders, promoting unity in the community, and wielding the patient voice as a catalyst to advance innovative advocacy, education, awareness and biomedical research initiatives.
Fueled by our coast-to-coast grassroots community,METAvivor is proud to be the country’s only nonprofit that exclusively funds metastatic breast cancer research through a peer-and-patient-advocate review process. METAvivor strives to sustain hope and make every dollar count as we work with researchers to extend and improve quality of life for MBC patients, to render this disease a truly survivable condition.
NORD was founded after the passage of the Orphan Drug Act of 1983 (ODA) to formalize the coalition of patient advocacy groups that were instrumental in passing that landmark law. Since then, NORD has been a national steward and a steadfast partner helping those who battle and care for rare disease feel seen, heard, supported, and connected. We’re a full-service, mission-driven, and independent nonprofit reimagining a future where every person with a rare disease and their families live their best lives.
The National Psoriasis Foundation (NPF) is a forward-looking, patient-centric nonprofit organization relentlessly driving efforts to cure psoriatic disease and improve the lives of those affected.
Ovarian Cancer Research Alliance is the global leader in research funding and a trailblazer in the race to find a cure for ovarian and gynecologic cancers. Unafraid to challenge accepted wisdom, OCRA has taken powerful stances on everything from new recommendations for prevention to creating innovative, highly effective programs to promote education, advocacy, and awareness.
The Parkinson and Movement Disorder (PMD) Alliance provides essential resources to those living with a movement disorder diagnosis and to the loved ones and professionals supporting them. With on-demand education and local events, PMD Alliance’s programs meet people where they are with the promise: there’s a place for you here.
Project Purple is a non-profit organization empowering the fight against pancreatic cancer. Our unwavering commitment is fueled by the pursuit of raising awareness, driving crucial research, and providing aid for patients who are battling this disease.
SHARE Cancer Support is a national, peer-led 501(c)(3) nonprofit organization that supports and educates anyone who has been diagnosed with breast or gynecologic cancer and provides critical information to the general public about signs, symptoms, diagnosis, and treatment options.
Sharsheret, a Jewish not-for-profit organization, provides personalized support, lifesaving education, financial assistance and genetic counseling to empower those faced with or at increased genetic risk of breast cancer and ovarian cancer.
While our expertise is in young women and Jewish families as related to breast cancer and ovarian cancer, Sharsheret programs serve all women and men.
Sick Cells’ mission is to elevate the voices of the sickle cell disease (SCD) community and their stories of resilience. In highlighting the grave disparities this community faces, we hope to influence decision-makers and propel change.
SPOHNC, a not-for-profit 501 (c) (3) organization, has become a vital component of the healing process for head and neck cancer patients. It has had an enormous positive impact on meeting the psychosocial needs of patients as well as preserving, restoring, and promoting physical and emotional health. A support organization, such as SPOHNC, can also be the foundation for patient and family education and awareness.
The Arc Michigan is a leading advocacy organization dedicated to protecting and promoting the rights of people with intellectual and developmental disabilities (IDD) across the state. As part of a nationwide movement, we work to ensure that individuals and families in Michigan have access to the information, resources, and advocacy they need to support full inclusion and participation in their communities—at school, at work, and in life.
The Arc of Illinois is committed to empowering persons with disabilities to achieve full participation in community life through informed choices.
To inspire hope and improve the quality of life of cardiovascular disease patients and their families through ongoing peer-to-peer support, education, and advocacy.
The Michael J. Fox Foundation is dedicated to finding a cure for Parkinson’s disease through an aggressively funded research agenda and to ensuring the development of improved therapies for those living with Parkinson’s today.
To provide hope and connection to those impacted by breast cancer, fund bold breakthroughs in MBC research, and raise awareness of the disease.
Changing lives by creating a community of support for young adults, and their loved ones, impacted by cancer.
The Urology Care Foundation supports, through philanthropic efforts, the improvement of urological care globally by funding research, clinical education, patient education, and humanitarian programs.
YSC supports the young breast cancer community and ignites global collaboration to improve quality of life worldwide.
Caring for Elders
As our loved ones age, the challenges of providing elder care can increase. Various organizations offer invaluable support and guidance in navigating elder care, from helping with mobility issues to managing cognitive decline. These resources help families manage the complexities of elder care with expert advice and up-to-date information.
The mission of Aging & Disability Resource Center of Barron and Rusk Counties is to empower and support seniors, people with disabilities, and their families to ask for help, find a way to live with dignity and security, and achieve maximum independence and quality of life.
The NHCDD is dedicated to the pursuit of dignity and justice, authentic community inclusion, cultural competency, and self-determination for all people with developmental disabilties.
Organization for Latino Health Advocacy (OLHA) is a national advocacy organization committed to improving Latino health outcomes through research, education, and policy. OLHA applies a community-based participatory research model that elevates Latino voices and drives policy reform through evidence-based strategies.
The National Association of Social Workers (NASW) is a membership organization that works to enhance the professional growth and development of our members, to create and maintain professional standards for social workers, and to advance sound social policies
The mission of BCSSI is to promote independence and provide enriching opportunities for older adults in Boone County.
Aging Forward is a national alliance of 55 dedicated affiliate organizations serving more than 165,000 older adults each year. Together with our committed volunteers and sponsoring partners, Aging Forward has reached more than 2.5 million older adults—and we’re just getting started!
Longer life means that today’s older adults have opportunities unknown to previous generations. Longer life also brings new challenges for both older adults and caregivers. No one understands the new face of aging better than the professionals at Lifespan.
Lifespan helps older adults and caregivers take on the challenges and opportunities of longer life. As a regional nonprofit, Lifespan is a trusted source of unbiased information, guidance and more than 30 services and advocacy for older adults and caregivers. We also provide training and education for allied professionals and the community. Annually we assist thousands of older adults and caregivers. All of our services are provided in Monroe County and several extend to the Pennsylvania border and over to Seneca and Genesee counties.
A man and woman.
Three 90 year-old women.
Lifespan holds informational workshops every month on topics ranging from Medicare to fall prevention. Visit our workshop page to learn more.
Lifespan is a member of the American Society on Aging, the National Council on Aging, the Greater Rochester Partnership for the Elderly, Leading Age NY, the State Society on Aging, the NYS Senior Citizen Action Council, and LiveOn NY.
Three women.
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Foster Excellence, Innovation and Collaboration to Advance Aging Research, Education, Practice and Policy.
USAging represents and supports the national network of Area Agencies on Aging and advocates for the Title VI Native American Aging Programs that help older adults and people with disabilities live with optimal health, well-being, independence and dignity in their homes and communities.
The South Alabama Regional Planning is the designated Area Agency on Aging (AAA) for South Alabama. For more than thirty-five years the AAA has assessed the needs of older persons in the three-county region in South Alabama; distributed funds for the provision of services to older adults; helped agencies and local governments plan services for older persons; and provided information about available resources to older adults and their caregivers. Staff of the Area Agency on Aging are available to assist seniors, persons with disabilities, and their families in coordinating resources and services that support an active healthy lifestyle and maintain independence as long as possible.
AgeSmart Community Resources enhances the lives of older adults, persons with disabilities, and veterans through advocacy, action, and answers on aging.
The Agency on Aging of South Central Connecticut (AOASCC) is an independent non-profit organization serving older adults, individuals with disabilities, and caregivers.
The mission is to champion and serve older adults and individuals with disabilities so that they remain independent and engaged within their communities.
The vision is a society that values older adults and people with disabilities.
The Alliance for Aging Research is the leading nonprofit organization dedicated to changing the narrative to achieve healthy aging and equitable access to care. The Alliance strives for a culture that embraces healthy aging as a greater good and values science and investments to advance dignity, independence, and equity.
The mission is to champion and serve older adults and individuals with disabilities so that they remain independent and engaged within their communities.
The vision is a society that values older adults and people with disabilities.
Founded in 1942, the American Geriatrics Society (AGS) is a nationwide, not-for-profit society of geriatrics healthcare professionals dedicated to improving the health, independence, and quality of life of older people. Our 6,000+ members include geriatricians, geriatrics nurse practitioners, social workers, family practitioners, physician associates, pharmacists, and internists who are pioneers in serious illness care for older individuals, with a focus on championing interprofessional teams, eliciting personal care goals, and treating older people as whole persons.
The mission of the Colorado Gerontological Society is to provide information, education and training, research, and public policy for professionals who work in the field of aging, as well as to provide services for older adults and families.
The Greater Wisconsin Agency on Aging Resources, Inc., is a nonprofit agency committed to supporting the successful delivery of aging programs and services in 70 counties and 11 tribes in Wisconsin. We provide aging lead agencies in our service area with training, technical assistance, and advocacy to ensure the availability and quality of programs and services to meet the changing needs of older people in Wisconsin.
NOAGE, a 501(c)3 nonprofit organization, was created from a steering committee of concerned residents and older adult service providers to address the challenges facing LGBTQ+ older adults in the New Orleans area.
Founded in 1977, NANASP is proud to be a leading organization advocating for community-based senior nutrition programs and staff. Our member programs represent a wide range of essential services providers who support the nutrition, health and life quality of seniors.
The Pennyrile Aging and Disability Resource Center (ADRC) is a fully operational, “no wrong door” approach to accessing aging and disability services in the nine county Pennyrile Region.
The key objectives are to provide comprehensive information and services to citizens and their families in order for them to make informed choices on their care, provide citizens with a single portal of access to area program and services, and to identify gaps in services.
The ADRC provides awareness, information, assistance and access.
The Wisconsin Aging Advocacy Network (WAAN) is a collaboration of organizations and individuals working with and for Wisconsin’s older adults to shape public policy and improve the quality of life for older people. WAAN advocates for all older adults by educating the community and policy makers on particular issues impacting older adults; mobilizing people on priority issues; and advocating for change.
Caregiver Support Organizations, Information & Advocacy
Family caregivers play an essential role in the care of loved ones, often without access to sufficient resources or support. Fortunately, numerous national organizations exist to provide advocacy, education, and hands-on support for caregivers. These groups work to raise awareness about the unique challenges caregivers face while offering a range of resources, from legislative advocacy to educational materials.
Sandwiched KC is a 501c3 nonprofit helping family caregivers in the Kansas City metro area by providing FREE information and referral, support groups, education, and self-care activities. Our mission is to create opportunities for family caregivers to find local support and shared wisdom.
The mission of Courage to Caregivers is to empower and equip carers to navigate their journey. We envision a world where healthy carers lead to healthier families and communities. We’re in the caregiver burnout prevention business! * We use carer and caregiver interchangeably. Carers are who we are; caregiving is what we do–in all forms, for others and ourselves.
Triage Health provides free education on legal and practical issues to help you navigate health care, through resources, materials, and events. This is especially important when navigating a chronic or serious medical condition.
We catalyze system change to build health, wellness, and financial security for all family caregivers through research, policy, and narrative change.
The mission of the ARCH National Respite Network and Resource Center is to assist and promote the development of quality respite and crisis care programs in the United States; to help families locate respite and crisis care services in their communities; and to serve as a strong voice for respite in all forums.
We champion youth who provide care for chronically ill, injured, or elderly family members, as well as those with physical or mental health conditions. We support their role as caregivers and guide their success in school and life.
Patient Advocate Foundation (PAF) is a national 501 (c)(3) non-profit organization which provides case management services and financial aid to Americans with chronic, life threatening and debilitating illnesses.
We support caregivers by investing in their mental, physical and financial wellness. Each year, we host multi-day retreats featuring professional wellness workshops and outdoor activities for family caregivers.
Advance women’s health through science, policy, and education while promoting research on sex differences to optimize women’s health.
AfPA is a national network of healthcare providers who prioritize patient-centered care by advocating for policies that support clinical decision making, limit abusive utilization management techniques, and acknowledge each person’s individual health care needs.
The Movement Disorders Policy Coalition brings together advocacy groups, health care providers, patients and other stakeholders to inform policy impacting patient-centered care for people living with movement disorders.
The mission of the National Health Council is to provide a united voice for the 160 million people living with chronic diseases and disabilities and their family caregivers.
Established in 1982, the ASCP Foundation is a 501(c)(3) charitable organization. The mission of the ASCP Foundation is to carry out the charitable – including scientific, literary, and educational – purposes of ASCP. ASCP is a nonprofit association of pharmacists and pharmacies that manage medications of older people and the medically complex. ASCP is an international organization with members located in all 50 states, Puerto Rico, and 12 countries. The society’s mission is to promote healthy aging by empowering pharmacists with education, resources, and innovative opportunities.
American Red Cross Military and Veteran Caregiver Network’s aim is to prevent and relieve suffering with every action. The Red Cross shelters, feeds and provides comfort to people affected by disasters; supplies about 40% of the nation’s blood; teaches skills that save lives; distributes international humanitarian aid; and supports veterans, military members and their families.
The Red Cross is not a government agency. The Red Cross is a registered 501(c)(3) nonprofit organization that depends on volunteers and the generosity of the American public to deliver its mission.
Thie mission is to empower seniors and their families to make informed decisions about senior living. This is done by providing them with the necessary information and support to find the perfect care options that ensure they can age with dignity, comfort, and joy.
Our mission is to improve the lives of patients and communities by empowering and educating them to be advocates for their health.
Jewish Family Service of Greater New Orleans (JFS) is a social service agency dedicated to preserving, strengthening and enhancing the well-being and self-sufficiency of individuals and families at every stage of life.
Jewish Family Service is a constituent agency of the Jewish Federation of Greater New Orleans and a community impact partner of United Way of Southeast Louisiana.
Jewish Family Services of Washtenaw County (JFS) is a mission-driven non-profit, 501(c)(3), organization that provides a wide range of social services offered to all residents of Washtenaw County. All services are rendered on a non-sectarian basis.
The Independent Living Outreach Movement (MAVI) is the pioneering, non-profit organization that promotes the Independent Living Philosophy and develops skills in people with disabilities to take control of their decision-making about their lives. The independence, equality, productivity, empowerment, integration and inclusion of the human being in all aspects of society is promoted.
The New Mexico Caregivers Coalition (NMCC) was created to enhance and promote family and professional direct care workers, supporting their professional development and advancing issues of importance to the field of long-term and direct care.
NACDD’s mission is to work with State Councils on Developmental Disabilities (SCDD) to empower people with developmental disabilities, their families, and allies to build welcoming and supportive communities through policy and practice ensuring that people with DD can live a self-directed life in the community.
The mission of the National Patient Advocate Foundation is to make the healthcare system work for all of us. As the advocate affiliate of Patient Advocate Foundation, they work at the national level to engage real people and drive system-change in healthcare.
In 2006, Congress authorized the Lifespan Respite Care Program to support community-based respite for family caregivers across the country. The lead federal agency, the Administration for Community Living (ACL), began awarding respite grants in 2009, and in 2010, the ACL awarded the New York State Office for the Aging (NYSOFA) a grant to partner with Lifespan of Greater Rochester and improve access to respite in New York State. The New York State Caregiving and Respite Coalition (NYSCRC) grew out of this partnership. Founded in 2010, the Coalition started small, with just one staff person and a handful of initiatives.
Patient Empowerment Network (PEN) is a 501(c)(3) non-profit organization. PEN’s mission is to offer trusted information to empower anyone impacted by cancer, through health equity, health literacy and shared decision-making.
Our programs provide people impacted by cancer with tools to feel activated and connected with resources that help overcome barriers in accessing care and bridging gaps among underrepresented communities.
PEN is committed to inclusivity in all levels of our organization, governing staff, the Board, volunteers, business partners and all external stakeholders, to deliver on our mission on behalf of cancer patients and their care partners.
Empowering every patient in America to advocate for reforms placing them, alongside their doctors, in control of their healthcare choices.
Improving Health & Safety Through Innovation and Awareness. (PRNewsfoto/Physician-Patient Alliance…)
The Physician-Patient Alliance for Health & Safety (PPAHS) is a national advocacy force for addressing patient health and safety priorities shared by patients, physicians, regulators, and industry. PPAHS identifies, promotes, educates, and certifies clinicians in best practices that promote patient safety and improves the quality of patient care.
To offer you the guidebook, tools and educational information needed to reduce the stress, depression, isolation and economic hardship of caregiving.
The mission of Soldiers’ Angels is to provide aid, comfort, and resources to the military, veterans, and their families.
To enrich lives and strengthen communities through services and engagement for individuals at all ages, beginning with those most in need.
The Empowered Caregiver Show uplifts caregivers through education, advocacy, and support, while also lifting up their invaluable role in society.
The Gateway Family YMCA is a powerful association of men, women, and children of all ages and from all walks of life joined together by a shared passion: to strengthen community.
Jewish Federations work every day to support and strengthen Jewish communal life around the world. We are there anytime, anywhere Jews are in need. We serve Jews of all ages, backgrounds, nations, and stations in life. We help young families with children, Holocaust survivors, victims of terror, survivors of natural disasters and other emergencies, and all those in distress.
Tena Scallan created The Ultimate Caregiving Expert to be the resource she wishes she had when she was caring for her loved ones. Whether you’re juggling a demanding career, raising children, or coordinating long-term care plans, The Ultimate Caregiver is here to help you breathe easier, stay organized, and feel massively supported. The mission is to empower family caregivers like you with the tools, knowledge, and compassion you need to thrive in your caregiving journey.
he staff and volunteers at Volunteers of America in Northern Colorado care about the people we serve. Our desire is to create communities where everyone thrives, especially those who need our help most, including our oldest neighbors and those who have served our country. We are here to provide a hand up, encouragement, and understanding to those in need.
The Wisconsin Family and Caregiver Support Alliance (WFACSA) is a grassroots coalition of family caregivers, professionals, advocates, and educators working together to strengthen support for Wisconsin families.
We believe that family caregivers are the backbone of our care system, providing critical support to older adults and people of all ages with disabilities.
The mission of the Elizabeth Dole Foundation is to empower military and veteran caregivers, their families, and their communities through programs, partnerships, and advocacy that drive innovation and sustainable solutions.
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Caregiver Action Network (CAN) is proud to lead National Family Caregivers Month each year, supporting more than 63 million caregivers nationwide. With trusted resources, advocacy, and education, CAN is here to help you feel less alone in your journey.
