Michigan 2025-2026 Regular Session Status: Passed Senate 1 R cosponsors

SR 48 — A resolution to designate May 2025 as Ehlers-Danlos Syndrome (EDS) Awareness Month.

Last action — ADOPTED

  1. ✓
    Introduced
  2. ✓
    In Committee
  3. 3
    Passed Senate
  4. 4
    Passed House
  5. 5
    To Executive
  6. 6
    Enacted

This bill has passed the Senate. Introduced May 14, 2025. It now moves to the second chamber.

Next likely step: consideration and a floor vote in the House.

Prognosis

Stalled 28% · moderate confidence

Where this bill stands today.

Odds of enactment

High

How often bills like it became law.

  • Passed Senate

    Current position in the legislative process.

  • 1 sponsor

    1 primary, 0 co-sponsors signed on.

  • Single-party support

    Sponsorship is currently within one party (1 R).

Prognosis reads this bill's own signals — stage, sponsorship breadth, committee status, recorded votes and cross-state momentum. Odds come from a model trained on which bills have become law.

Summary

A resolution to designate May 2025 as Ehlers-Danlos Syndrome (EDS) Awareness Month.

Bill Text

What changed in the latest version

39 added · 54 removed

Plain-language change summary

In the updated version of Senate Resolution No. 48, several lines detailing the symptoms and conditions associated with Ehlers-Danlos Syndrome (EDS) were removed. This streamlining may help clarify the resolution's focus on designating May 2025 as EDS Awareness Month, emphasizing the importance of raising awareness about the syndrome without getting into extensive medical details. By simplifying the language, the resolution aims to reach a broader audience and reinforce the significance of understanding EDS and its impact on individuals' lives.

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SR-48, As Adopted by Senate, May 14, 2025 SENATE RESOLUTION NO.
MICHIGAN SENATE Senate Resolution No.
48 Senators Johnson, Chang, Santana and Theis offered the following resolution:
48 Offered by Senators Johnson, Chang, Santana and Theis A RESOLUTION TO DESIGNATE MAY 2025 AS EHLERS-DANLOS SYNDROME (EDS) AWARENESS MONTH WHEREAS, Ehlers-Danlos Syndrome, or EDS, is an inherited condition that affects the connective tissues of the body;
A resolution to designate May 2025 as Ehlers-Danlos Syndrome (EDS) Awareness Month.
and WHEREAS, Connective tissues provide support in skin, tendons, ligaments, blood vessels, internal organs, and bones;
Whereas, Ehlers-Danlos Syndrome, or EDS, is an inherited condition that affects the connective tissues of the body;
and WHEREAS, There are 13 types of EDS caused by genetic defects in collagen, one of the major structural components of the body;
and Whereas, Connective tissues provide support in skin, tendons, ligaments, blood vessels, internal organs, and bones;
and WHEREAS, Symptoms of EDS may include joint hypermobility, loose, unstable joints that dislocate easily, joint pain, skin that bruises easily, digestive problems, dizziness and increased heart rate when standing up, and problems with internal organs, among others;
and Whereas, There are 13 types of EDS caused by genetic defects in collagen, one of the major structural components of the body;
and WHEREAS, Eighty percent of people with EDS also have postural orthostatic tachycardia syndrome (POTS);
and Whereas, Symptoms of EDS may include joint hypermobility, loose, unstable joints that dislocate easily, joint pain, skin that bruises easily, digestive problems, dizziness and increased heart rate when standing up, and problems with internal organs, among EDS Awareness_SR48_AA_1 5cs2dz 1 others;
and WHEREAS, POTS occurs when an individual’s heart rate increases very quickly after getting up from sitting or lying down causing symptoms such as dizziness or light-headedness, fainting or almost fainting, noticeable heartbeats (heart palpitations), chest pain, shortness of breath, and shaking or sweating;
and Whereas, Eighty percent of people with EDS also have postural orthostatic tachycardia syndrome (POTS);
and WHEREAS, Those suffering from POTS may also have additional medical problems including digestion problems such as feeling or being sick, diarrhea, constipation, bloating and stomach pain, headaches and problems with sight such as blurred vision or tunnel vision, hands and feet looking purple, weakness and extreme tiredness and fatigue, and problems with thinking, memory, and concentration;
and Whereas, POTS occurs when an individual’s heart rate increases very quickly after getting up from sitting or lying down causing symptoms such as dizziness or light-headedness, fainting or almost fainting, noticeable heartbeats (heart palpitations), chest pain, shortness of breath, and shaking or sweating;
and WHEREAS, It is estimated that the prevalence of all types of EDS combined affect at least 1 in 5,000 people worldwide with recent research indicating that EDS is likely under diagnosed;
and Whereas, Those suffering from POTS may also have additional medical problems including digestion problems such as feeling or being sick, diarrhea, constipation, bloating and stomach pain, headaches and problems with sight such as blurred vision or tunnel vision, hands and feet looking purple, weakness and extreme tiredness and fatigue, and problems with thinking, memory, and concentration;
and WHEREAS, EDS may significantly decrease both quantity and quality of life for those affected;
and Whereas, It is estimated that the prevalence of all types of EDS combined affect at least 1 in 5,000 people worldwide with recent research indicating that EDS is likely under diagnosed;
and WHEREAS, Currently, there is no treatment for EDS and no known cure.
and Whereas, EDS may significantly decrease both quantity and quality of life for those affected;
and Whereas, Currently, there is no treatment for EDS and no known cure.
and Whereas, Early and accurate diagnosis can help create lifesaving medical plans and improve overall quality of life;
and WHEREAS, Early and accurate diagnosis can help create lifesaving medical plans and improve overall quality of life;
and Whereas, A network of EDS support groups can help connect those managing life with the disease as well as better inform the health care community and the public;
and WHEREAS, A network of EDS support groups can help connect those managing life with the disease as well as better inform the health care community and the public;
now, therefore, be it Resolved by the Senate, That the members of this legislative EDS Awareness_SR48_AA_1 5cs2dz body designate May 2025 as Ehlers-Danlos Syndrome (EDS) Awareness Month.
now, therefore, be it RESOLVED BY THE SENATE, That the members of this legislative body designate May 2025 as Ehlers-Danlos Syndrome (EDS) Awareness Month.
EDS Awareness_SR48_AA_1 5cs2dz
Adopted by the Senate, May 14, 2025.
Secretary of the Senate
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Action History

  1. ADOPTED

Sponsors

Sponsorship breakdown

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1 sponsors · 0 co-sponsors · 146 not signed on

Sponsors (1)

Co-sponsors (0)

None.

Not signed on (146)

146 members have not signed on to this bill.

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"Not signed on" means a member has not sponsored or co-sponsored this bill — it does not imply opposition. Members flagged Voted No have a recorded No vote on this bill.

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Subjects

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Frequently asked questions

What does SR 48 do?
A resolution to designate May 2025 as Ehlers-Danlos Syndrome (EDS) Awareness Month.
Who sponsors SR 48?
SR 48 is sponsored by Ruth Johnson (Republican).
What is the current status of SR 48?
This bill has passed the Senate. Introduced May 14, 2025. It now moves to the second chamber.
Where can I track SR 48?
Track SR 48 free on One Click Politics — get push/email alerts when it moves.

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