Senate Resolution No. [insert number] proposes to designate May 2025 as Ehlers-Danlos Syndrome (EDS) Awareness Month. EDS is an inherited condition that affects the body's connective tissues, which provide essential support to various structures, including skin, tendons, ligaments, and organs. The resolution highlights the 13 types of EDS caused by genetic defects in collagen and outlines the symptoms associated with the condition, such as joint hypermobility, pain, and digestive issues. It also notes the prevalence of EDS, estimating that it affects at least 1 in 5,000 people worldwide, and emphasizes the significant impact the syndrome can have on the quality of life for those affected.

The resolution calls for increased awareness and research into EDS, as there is currently no known treatment or cure. It stresses the importance of early and accurate diagnosis to improve medical care and quality of life for individuals with EDS. Additionally, the resolution encourages the establishment of support networks for those living with the condition and aims to inform both the healthcare community and the public about EDS. By designating May 2025 as EDS Awareness Month, the Senate seeks to honor those suffering from the syndrome and promote scientific research and funding to find a cure.