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National MS Society Commits to Health Equity in Clinical Trials and Data Collection

March 4, 2022

The National Multiple Sclerosis Society has rallied corporate healthcare partners together in their shared commitment to address underrepresentation in clinical trials through the principles identified in the Consensus Statement on Health Equity in Clinical Trials and Real-World Evidence Data Collection.  
 
People with MS need solutions to live their best lives and find a cure. The lack of diversity in clinical trials and the disparity in healthcare delivery are impediments to finding solutions and cures for everyone. Access to high quality, personalized healthcare is vital to ensuring each person with MS can get the treatments and care that is right for them. Inclusivity in clinical trials is critical to better understand what medication is right for each person and achieving the goal of personalized healthcare for all individuals living with MS. And to do so, the design and collection of clinical trials mush ensure that people with MS can contribute their valuable perspectives so they feel involved, welcomed and respected.
 
The National MS Society has created a forum to engage corporate healthcare partners so they can contribute to direct and focused dialogue to address issues that directly impact the MS community. This group is focused on a common vision with shared resources to ensure every person affected by MS can live their best lives. 
 
This group established four principles to increase inclusivity and address health inequities in the healthcare system and are committed to practicing these as individual organizations and in partnership with others.
 
Learn more about clinical trials and how to participate.

About Multiple Sclerosis

Multiple sclerosis is an unpredictable disease of the central nervous system. Currently there is no cure. Symptoms vary from person to person and may include disabling fatigue, mobility challenges, cognitive changes, and vision issues. An estimated 1 million people live with MS in the United States. Early diagnosis and treatment are critical to minimize disability. Significant progress is being made to achieve a world free of MS.

About the National Multiple Sclerosis Society

The National MS Society, founded in 1946, is the global leader of a growing movement dedicated to creating a world free of MS. The Society funds cutting-edge research for a cure, drives change through advocacy and provides programs and services to help people affected by MS live their best lives. Connect to learn more and get involved: nationalMSsociety.org, Facebook, X, formerly known as Twitter, Instagram, YouTube or 1-800-344-4867.

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© 2024 The National Multiple Sclerosis Society is a tax exempt 501(c)3 nonprofit organization. Its Identification Number (EIN) is 13-5661935.