The mission of the Anne Arundel County Food Bank is to alleviate food insecurity in Anne Arundel County by partnering across the community to obtain and distribute nourishing food to neighbors in need.

The Arthritis Foundation is a nonprofit organization that helps people manage arthritis and improve their quality of life. They offer trusted resources, support programs, and fund research to find better treatments.

BGE offers programs and services to help those in need, including energy assistance, help for customers with special needs, and ways for neighbors to help neighbors.

A nonprofit organization of health care professionals dedicated to raising awareness of gout arthritis, with the aim of improving the overall quality of care and minimizing the burden of gout.

The Arthritis Foundation is a nonprofit organization that helps people manage arthritis and improve their quality of life. They offer trusted resources, support programs, and fund research to find better treatments.

The Lupus Foundation of America offers support, education, and resources for people living with lupus. They also fund research and advocate for better treatments and care.

The Spondylitis Association of America (SAA) provides education, support, and resources for people living with ankylosing spondylitis and related diseases. They also fund research, raise awareness, and advocate for better treatments to improve quality of life and work toward a cure.

The University of Maryland School of Dentistry offers comprehensive dental care for patients, including cleaning, exams, specialty treatments, and emergency services. Care is provided by students, residents, and faculty using the latest techniques and technology.

The U.S. Pain Foundation provides support, education, and resources for people living with chronic pain. Founded by people with pain, they work to validate the experiences of those affected and advocate for better care and awareness.

Gladstone is a psychiatry and counseling center providing affordable, in-network mental health care to individuals across the Baltimore and Washington, DC regions. 

The Ehlers-Danlos Society provides education, support, and resources for people living with Ehlers-Danlos syndromes (EDS) and hypermobility spectrum disorders (HSD). They also fund research and advocate for better treatments and care.

The Osteogenesis Imperfecta Clinic at Kennedy Krieger Institute specializes in diagnosing and managing patients with osteogenesis imperfecta (OI) and hypermobility disorders. The clinic provides comprehensive care, including medical management, therapy, and genetic counseling, to improve patient outcomes.

The Relapsing Polychondritis Foundation provides support, education, and resources for those affected by relapsing polychondritis, a rare autoimmune disease. They also fund research and raise awareness to improve understanding, treatment, and care.

The mission of The Myositis Association is to improve the lives of people affected by myositis, fund innovative research, and increase myositis awareness and advocacy. Their programs and services provide information, support, advocacy, and research for the myositis community.

The Vasculitis Foundation is a leading organization dedicated to supporting patients, raising awareness, and funding research for vasculitis, a group of rare autoimmune diseases that cause inflammation of blood vessels. It provides education, advocacy, and resources to improve patient outcomes worldwide.

The Bone Health & Osteoporosis Foundation provides education, support, and resources to help prevent osteoporosis and promote strong bones. They also raise awareness and fund research to improve bone health and reduce fractures.

IgG4ward! is dedicated to serving the unique needs of the IgG4-RD community through: building an online patient community, providing credible disease information and offering resources for patients, caregivers, and healthcare provider.

The Sjögren’s Foundation is the first and only national nonprofit dedicated to conquering Sjögren’s, a complex and life-altering autoimmune disease. They provide education, support, and resources for patients, while also funding research and advocating to raise awareness and improve care.

The Scleroderma Foundation offers education, support groups, and resources for those affected by scleroderma, a chronic autoimmune disease. They also fund research and advocate to improve care and raise awareness.