Marion Jones, vice president of workforce development in the solar energy industry and ambassador for The Sumaira Foundation, ...

CAMBRIDGE, Mass., July 21, 2025 (GLOBE NEWSWIRE) -- Vor Bio (Nasdaq: VOR), a clinical-stage biotechnology company transforming the treatment of autoimmune diseases, today announced the appointment of ...

Avery Russek, 17, is fighting an extremely rare autoimmune disease called opsoclonus myoclonus, a condition she was first diagnosed with at 3 years old. FOX 9's Corin Hoggard has the full story.

A Buffalo teenager is getting treatment for her second bout with an extremely rare medical condition that can literally take away control of her body. In 2009, FOX9 covered the treatments that helped ...

The Purdy family shares their insights on navigating their child’s rare neurodegenerative disease and their direct ...

Vitamin D is not only an essential nutrient, but also the precursor of the hormone calcitriol, indispensable for health. It ...

BANGOR -- Autumn Scott, a 17-year-old from Dixmont, is facing a tough battle with a rare autoimmune disease called Degos.

Findings from a cohort of 1.2 million children indicate aluminum-adsorbed vaccines do not raise the risk of autism, asthma, ...

An experimental AstraZeneca (NASDAQ:AZN) drug, anselamimab, failed to extend survival or cut heart-related hospitalizations in patients with a rare plasma cell disorder, disappointing hopes it could ...

A massive Danish study of over 1.2 million children has found no evidence that aluminum in early childhood vaccines increases the risk of neurological, autoimmune, or allergic disorders.

As the future of rare disease research at Cincinnati Children's is threatened, parents of 13-year-old Charlie Evans plead for its reinstatement.

A bill signed into law by Governor Dan McKee on July 3 created a Rare Disease Advisory Council in Rhode Island. State Senator Val Lawson and Warwick mom Erin Vazquez joined Shannon Hegy on 12 ...