Working Together to Support Patient Communities

Patients often need support that goes beyond financial assistance. At HealthWell, we value our relationships with leading patient advocacy groups and national health care organizations. Together, we focus on total patient care, not just a condition. We work with these groups to reach the patients who need us the most and share resources to support patient communities. We refer patients to one another, and, together, we raise awareness for various diseases, especially during national health observance months.

If you work for a non-profit and would like to learn more about partnering with HealthWell, please email us.

Become an Alliance Partner

Spotlight On Alliance Partners

We’re pleased to recognize our alliance partners for their generous support of our mission.

Oxalosis and Hyperoxaluria Foundation (OHF) is a national nonprofit organization that brings together people living with hyperoxaluria, families, care partners,... .

Oxalosis and Hyperoxaluria Foundation (OHF) is a national nonprofit organization that brings together people living with hyperoxaluria, families, care partners, scientists, doctors, advocates, donors and volunteers to join forces to improve lives and advance towards a cure. Since 1989, OHF has partnered with the scientific community to fund game-changing research that provides better outcomes, include the patient voice every step of the way, and convene the best minds from around the world to find new approaches that enhance care and move us closer to a cure.

Community Liver Alliance (CLA) is a national nonprofit foundation promoting liver health through education and support services throughout the nation.... .

Community Liver Alliance (CLA) is a national nonprofit foundation promoting liver health through education and support services throughout the nation. Headquartered in Pittsburgh and with offices in Milwaukee, CLA has grown to have a national presence while still holding true to a mission to invest in local communities and give voice to patients and providers. CLA is dedicated to supporting the community through liver disease awareness, prevention, education, advocacy and research. Supported by a network of patients, caregivers, health care professionals and community leaders, CLA develops and runs educational workshops, coordinates support groups, facilities linkage to medical care and provides education to health care professionals, patients and caregivers. 

Formed in September 2005, the Gout Education Society is a nonprofit organization of health care professionals dedicated to educating the... .

Formed in September 2005, the Gout Education Society is a nonprofit organization of health care professionals dedicated to educating the public and health care community about gout – an extremely painful form of inflammatory arthritis – and the related health care consequences of hyperuricemia. With the aim of improving the quality of care and minimizing the burden of gout, the Gout Education Society offers complimentary resources for both the public and medical professionals. 

The REACH Institute is dedicated to ensuring that the most effective, scientifically proven mental health care reaches all children and... .

The REACH Institute is dedicated to ensuring that the most effective, scientifically proven mental health care reaches all children and families. Led by national leaders in child psychiatry, psychology, and pediatrics, REACH arms individuals and institutions with the best, evidence-based therapies to improve the mental health of children and adolescents. REACH trains pediatricians, family practitioners, child psychiatrists, psychologists, social workers, nurse practitioners, school personnel and parents and their advocates in the most effective therapies, from psychotherapy to pharmacology. 

The Aging Life Care Association (ALCA) is a non-profit association representing more than 2,000 Aging Life Care Professionals® – sometimes... .

The Aging Life Care Association (ALCA) is a non-profit association representing more than 2,000 Aging Life Care Professionals® – sometimes referred to as geriatric care managers. ALCA members act as a guide and advocate for families who are caring for older relatives or disabled adults, ensuring that they live well as they face the challenges of aging. The Aging Life Care Professional is educated and experienced in any of several fields related to Aging Life Care™ / care management, including, but not limited to nursing, gerontology, social work, therapy, or psychology, with a specialized focus on issues related to aging and elder care. To find an Aging Life Care Professional in your area, visit The Aging Life Care Association. 

Founded in 1993, the Alagille Syndrome Alliance (ALGSA) is a non-profit patient advocacy organization dedicated to mobilizing resources, facilitating connections, promoting... .

Founded in 1993, the Alagille Syndrome Alliance (ALGSA) is a non-profit patient advocacy organization dedicated to mobilizing resources, facilitating connections, promoting unity, and advocating for a cure to inspire, empower, and enrich the lives of people affected by Alagille Syndrome. Representing the global community, the ALGSA seeks to connect individuals with ALGS to resources and education while furthering scientific understanding and treatment options for this complex condition. To learn more, visit the Alagille Syndrome Alliance. 

Network of Alliance Partners

As we continue to expand our programs across a variety of disease areas, it’s important to identify alliance partners who share our vision to ensure that no patient goes without health care because they cannot afford it. Thank you to our valued alliance partners for working with us to make a lasting difference in patients’ lives.

Become an Alliance Partner

Support from Our Alliance Partners

In the words of our alliance partners…

Headshot of Susan Gurley.

“We applaud the HealthWell Foundation for recognizing the paramount need for frontline health care workers who are going to heroic measures to save the lives of those impacted by COVID-19 by providing a vital financial resource that will enable them to obtain critical behavioral health services.”

Susan Gurley, Executive Director – Anxiety and Depression Association of America

Headshot of Kim Hollander.

“Hyperoxaluria is a group of rare diseases that require life-long medical treatments. For many living with the disease, treatment options may be unattainable due to cost, which can ultimately lead to an irreversible, potentially life-threatening, situation for the patient. We are honored to partner with the HealthWell Foundation to spread the word about the new fund and to be able to share this critical financial resource with our community.”

Kim Hollander, Executive Director – Oxalosis and Hyperoxaluria Foundation

Headshot of Louise Vetter.

“Facing a neurodegenerative disease like Huntington’s is overwhelming, but the additional diagnosis of psychosis magnifies the complexity of treatment. Financial support programs, such as this new fund from HealthWell, are vital tools for families facing the burden and cost of care.”

Louise Vetter, President & CEO of the Huntington’s Disease Society of America.

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