It’s our mission to alleviate food insecurity in Anne Arundel County by partnering across our community to obtain and distribute nourishing food to our neighbors in need.

Learn more about arthritis, connect with other patients,
and find resources.

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.

Compare prescription drug prices and find coupons at more than 70000 US pharmacies. Save up to 80% instantly!

Lupus Foundation of America educates, empowers, and connects you to resources and support so that you can live your best life with lupus.

SAA strives to be a leader in the quest to cure ankylosing spondylitis and related diseases, and to empower those affected to live their lives to the fullest.

The University of Maryland School of Dentistry Predoctoral Dental Clinic provides high quality dental services at significant savings.

An organization created by people with pain for people with pain, U.S. Pain recognizes and validates the challenges 50 million Americans endure every day.

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 is a global organization dedicated to advancing and accelerating research and education in Ehlers-Danlos syndromes (EDS) and hypermobility spectrum disorders (HSD). They support the development of effective and equitable EDS and HSD therapies and work collaboratively to improve the lives of individuals affected by EDS and HSD.

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.

Relapsing Polychondritis (RP) is a rare and degenerative autoimmune disease that affects cartilage in the body. Not much is known about RP. That’s why we’re funding research to better understand and treat it.
Relapsing polychondritis (RP) causes a systemic inflammatory response that can be fatal without proper care and treatment. RP can affect multiple organs in the body; however, it primarily affects the cartilaginous structures in the ears, nose, airways, and joints. It can also affect the eyes, skin, heart valves, and brain.

The mission of The Myositis Association is to improve the lives of persons affected by myositis, fund innovative research, and increase myositis awareness and advocacy. They 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 (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.

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 proud to be the first and only national non-profit health organization leading the charge to conquer Sjögren’s. While focused on increasing research, education and awareness for this disease, the Foundation works on behalf of all Sjögren’s patients and is dedicated to conquering the complexities of this life-altering and debilitating disease.

The Scleroderma Foundation is a nonprofit organization dedicated to supporting patients, raising awareness, and funding research for scleroderma, a chronic autoimmune disease that affects the skin and internal organs. It provides education, advocacy, and community support to improve the lives of those affected.