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Josh (left), diagnosed in 2019 | |
This MS Awareness Month, we’ve been shining a light on the unseen effects of MS — the fatigue, the cognitive changes, the emotional toll that families navigate every day.
What's even more powerful than awareness is action. Give today and you can make twice the impact. For the next 24 hours, every gift will be matched dollar for dollar up to $25,000 courtesy of the Kalota Family, doubling your support for those affected by MS.
Your matched gift helps fuel life changing research, strengthens programs that connect people to resources and supports MS Activists calling for expanded access to high-quality care. | |
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What I Wish People Knew About MS |
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Check out the firsthand stories of people affected by MS and hear what they wish people knew about living with the disease. | | | | |
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Dr. Bruce Bebo, the National MS Society's chief research and medical affairs officer explains what MS prevention looks like and how experts plan to achieve this remarkable goal. | | | | |
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Kresence (left), diagnosed in 2016. | | |
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Women are disproportionately affected by MS – diagnosed 2 to 3 times more often than men – and experience unique challenges. The National Multiple Sclerosis Society is investing $2.3 million in a new research projects that will focus on women’s health and MS. | | | | |
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5 Recipes For People with MS |
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Explore easy recipes that are designed to make life in the kitchen a little smoother and more manageable for people living with MS. | | |
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MS Activists Heading to Capitol Hill |
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The Society’s Public Policy Conference kicks off next week with MS Activists advocating for more affordable healthcare and federal funding for MS research. Learn more about the policies and help make a difference. | | | | |
© National Multiple Sclerosis Society | 733 Third Avenue, New York, NY 10017 United States
Contact us at nationalMSSociety.org or 1-800-344-4867. This message was sent to [email protected]. To ensure that you continue to receive our emails, please add us to your address book. | | |
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