Senate Resolution No. [number], introduced by Senators Johnson, Chang, Santana, and Theis, aims to designate May 2025 as Ehlers-Danlos Syndrome (EDS) Awareness Month. EDS is an inherited condition that affects the body's connective tissues, which play a crucial role in supporting various structures such as skin, ligaments, and organs. The resolution highlights the 13 types of EDS caused by genetic defects in collagen, along with the symptoms associated with the syndrome, including joint hypermobility, pain, and digestive issues. It also notes the prevalence of EDS, estimating that at least 1 in 5,000 people worldwide are affected, and emphasizes the importance of early diagnosis and awareness in improving the quality of life for those living with the condition.

The resolution calls for increased scientific research and funding to find a cure for EDS, as there is currently no treatment available. It recognizes the significant impact EDS can have on individuals' lives and the necessity of support networks to connect those affected and inform the healthcare community. By designating May 2025 as EDS Awareness Month, the Senate aims to honor those suffering from the syndrome and promote greater understanding and support for the condition.