Your monthly dose of ms life - offering insights, encouragement, and real support for every step of the Multiple Sclerosis journey.
June 2025 - Nutritional tips for living with Multiple Sclerosis
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The June ms life newsletter focuses on gently resetting through supportive nutrition, simple routines, and self-compassion. It offers practical tips to boost energy, reduce inflammation, and encourage small, consistent habits for a healthier summer.
May 2025 - Travel tips for living with Multiple Sclerosis
Travel - while it’s one of the most exciting ways to create lasting memories, it can also bring some added challenges for those living with multiple sclerosis. With several trips on the horizon, it's a great time to reflect on how to make traveling with MS as smooth and enjoyable as possible. Below are some practical tips designed to help anyone with MS travel more confidently, whether it's a quick weekend getaway or a far-off international adventure.
April 2025 - ms life is now an official partner of the National Multiple Sclerosis Society
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ms life is now an official affiliated partner of the National MS Society! This partnership marks a significant step forward in expanding our reach and impact within the MS community. You can now find ms life listed on the National MS Society’s affiliated partners page for online communities. This makes it easier than ever for individuals affected by multiple sclerosis to discover ms life community’s platform and take advantage of the resources, support, and community we provide.
March 2025 - MS Awareness Month
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Over 2.8 million people worldwide are living with MS, yet so many still don’t fully understand what it is or how it impacts lives. MS is unpredictable, often invisible, and unique to each person. Some days, we feel strong; other days, we battle overwhelming fatigue, pain, or cognitive challenges. By raising awareness, we help break down misconceptions and advocate for better support, treatments, and policies. The more we talk about MS, the more we help others understand it.
February 2025 - Meds, Meds, Meds – Stay informed on the latest FDA-approved treatments for MS!
Let’s talk medications - a necessary evil when you’re diagnosed with MS. While it’s not the most exciting topic, it’s an important one. When you’re first diagnosed with MS, one of the big conversations is about starting a disease-modifying therapy. While we’re not medical experts at ms life, we’re here to break things down in a way that’s easy to understand. We’ll walk you through the different types of medications out there, so you can feel more confident exploring your options. MS treatments generally fall into three categories: oral medications, intravenous (IV) therapies, and injectables.
January 2025 - Congress passes legislature in December and MS athletes take on Paris in the Olympic games.
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In December, Congress passed a spending bill that includes telehealth expansion and increased funding for MS research; a significant milestone for the MS community. Telehealth expansion offers improved access to care, especially for those facing mobility challenges or living in rural areas with limited access to MS specialists. Telehealth expansion offers improved access to care, especially for those facing mobility challenges or living in rural areas with limited access to MS specialists.
December 2024 - Learn more about ms life and the National MS Society's Bike MS event held in NYC.
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Bike MS is an event close to our hearts, and this year’s New York City ride was nothing short of inspiring. It was a powerful reminder of the strength and resilience within the MS community, bringing together people from all walks of life to raise awareness, fund critical research, and support one another. Participants had the option to ride either a 30-mile or 50-mileroute on traffic-free roads, all while raising money for the National MS Society.
Monthly Newsletters
November 2024 - the ms life flyer
Living with Multiple Sclerosis can be overwhelming, but you don’t have to face it alone.
Welcome to ms life — an inclusive and supportive community where individuals affected by MS can discuss experiences, share knowledge and engage in conversations.​