A resolution to designate May 2025 as Ehlers-Danlos Syndrome (EDS) Awareness Month.
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Progress
Where this bill stands in the legislative process.
- Introduced
- Passed Senate
- Passed House
- To Governor
- Became Law
Overview
This resolution designates May 2025 as Ehlers-Danlos Syndrome (EDS) Awareness Month in Michigan. It recognizes EDS as a genetic condition affecting connective tissues, leading to a variety of symptoms and often co-occurring conditions like POTS. The resolution aims to raise awareness about EDS, encourage research into potential treatments and a cure, and support individuals and support groups affected by the syndrome.
Key provisions
- Designates May 2025 as EDS Awareness Month.
- Recognizes EDS as an inherited condition affecting connective tissues.
- Highlights common symptoms of EDS, including joint hypermobility and POTS.
- Acknowledges the significant impact of EDS on quality of life.
- Encourages scientific research and funding for EDS treatment and a cure.
Who is affected
- Individuals with Ehlers-Danlos Syndrome (EDS)
- Family members and caregivers of individuals with EDS
- Healthcare professionals
Notable changes
- None – this is a resolution designating a month for awareness.
Bill text
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Document of record
- Version
- Senate Enrolled Resolution
- Published
- Not published in the source record
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