Can Do Multiple Sclerosis is putting together a two-day program to help newly or recently diagnosed patients and their caregivers learn more about multiple sclerosis (MS), meet others with the disease, and find strategies to adapt to a new lifestyle. Called Take Charge, the free program will…
advocacy
I was once very good at getting out of the way. This skill served me well in dodgeball games when I was younger, and then later during my military career. Given my various injuries, you might be skeptical about that last comment, but I was actually renowned for my ability…
I choose to fundraise for the National Multiple Sclerosis Society through Bike MS, which the society’s website says is “the largest fundraising cycling series in the world.” Approximately 50,000 cyclists and 5,000 teams ride each year, and the community has raised $1.4 billion to support the society’s…
My mom always wished for a son and a daughter. Ten years after I was born, her dream became a reality with the arrival of my baby brother, Michael. Because I was the only child for so long, I had never considered becoming a big sister, nor did I understand…
In previous columns, I’ve shared that I’m a graduate student at the University of Texas at Austin, but what exactly does that entail? Almost every time I tell someone I’m pursuing a doctorate in educational psychology, I’m met with the question, “What do you do?” Let’s unpack the answer.
The focus is on diagnosis for this year’s World MS Day, officially “a day of global solidarity, collective action, and hope” for the multiple sclerosis (MS) community, according to a campaign webpage boasting information in more than 100 languages. While the event officially occurs on May 30,…
Canada has one of the world’s highest rates of multiple sclerosis (MS) in the world, and this month residents are being urged to come together to raise awareness of and funds for people affected by the neurodegenerative disorder. May is Multiple Sclerosis Awareness Month in Canada, and…
With this year’s fundraiser, the Multiple Sclerosis Association of America (MSAA) is marking its 10th annual Improving Lives Benefit — an event that shines a light on uplifting members of the multiple sclerosis (MS) community and outstanding corporate partners. The affair will take place on May 15 at…
Renowned experts in multiple sclerosis (MS) healthcare, research, and advocacy will again gather at the annual meeting of the Consortium of Multiple Sclerosis Centers (CMSC), slated this year for May 29 to June 1. The event, now in its 38th edition, will return to the Music City Center, in Nashville,…
Given how much my life has changed because of multiple sclerosis (MS), anytime an opportunity arises for me to support an MS charity, I jump at the chance — figuratively, of course. I recently learned that the MS Society UK is organizing another of its zip line…
Lynne Denise, right, and her dad, Don Collins, attend last year’s MS walk in Edwardsville, Illinois. (Photos courtesy of Lynne Denise) Day 30 of 31 This is Lynne Denise’s story: Hello, multiple sclerosis (MS) warriors! My name is Lynne Brush, and I was diagnosed with relapsing-remitting…
Kathy Young toasts a beautiful day with a glass of red wine in her backyard. (Photos courtesy of Kathy Young) Day 23 of 31 This is Kathy Young’s story: I was diagnosed with multiple sclerosis (MS) in 2008. It took about a month to get the diagnosis which,…
I have not been kind to my body over the years. I was very active in my old life, although I was a little clumsy even before multiple sclerosis (MS) started affecting my balance. Active and clumsy aren’t a great combination. I accumulated plenty of bumps and bruises along…
Hi! I’m new — not to having multiple sclerosis (MS), but to being a columnist. I’m a daughter, wife, mother of two young adults, dog mom, sister, aunt, friend, college professor, pharmacist, avid reader, nature lover, and an MS warrior. I was diagnosed with MS in 2014, although…
Nora Cherubini poses with Stanley, her service dog, during a beach walk. (Photos courtesy of Nora Cherubini) Day 18 of 31 This is Nora Cherubini’s story: “Thank God it’s not MS … because you would wind up in a wheelchair.” This is what a neurologist told me after…
Tori Henderson receives her monthly infusion at an appointment. (Photos courtesy of Tori Henderson) Day 9 of 31 This is Tori Henderson’s story: Henderson, left, poses with her daughter, Kerriyah, for her birthday at Disney World. Thanksgiving 2017 will forever hold a special place in my memories. I…
Sam Roman, MD, travels to Montana to conduct home visits for patients enrolled in the TREAT-MS clinical trial. (Photos courtesy of Sam Roman) Day 6 of 31 This is Sam Roman’s story: It was during a particularly stressful period of medical school in 2015 when I had my first…
Rocco Mangel, the founding partner of Rocco’s Tacos & Tequila Bar, is joining the Walk MS: West Palm Beach 2024, in Florida, to raise funds for the National Multiple Sclerosis Society (NMSS). Walk MS events, taking place in numerous locations in the U.S., focus on raising disease…
Geographical proximity to neurologists and multiple sclerosis (MS) speciality care centers is lower for people living in rural regions of the U.S. relative to metropolitan areas, according to recent research. Areas with higher proportions of Hispanic individuals, uninsured people, and those with disabilities generally also were more likely to…
Multiple Sclerosis News Today has been chronicling MS advocate and podcaster Mike Parker’s journey leading up to a skydiving jump he made on Oct. 29 to benefit the MS Society U.K. Learn more about Mike at mikesmsjourney.com. You can also donate to his fundraiser. Last…
Multiple Sclerosis News Today is chronicling MS advocate and podcaster Mike Parker’s journey, leading up to a skydiving jump he’ll make Oct. 29 to benefit the MS Society U.K. Learn more about Mike at mikesmsjourney.com. You can also donate to his fundraiser. Third in a…
Multiple Sclerosis News Today is chronicling MS advocate and podcaster Mike Parker’s journey leading up to a skydiving jump he’ll be making Oct. 29 to benefit the MS Society U.K. Learn more about Mike at mikesmsjourney.com. You can also donate to his fundraiser. Second in…
Multiple Sclerosis News Today is chronicling MS advocate and podcaster Mike Parker’s journey leading up to a skydiving jump he’ll be making on Oct. 29 to benefit the MS Society U.K. Learn more about Mike at his website mikesmsjourney.com and click here to donate to his fundraiser.
MS Bike‘s cycling fundraiser events have raised at least $4.3 million over the last four months to support MS Canada and people with multiple sclerosis (MS) in a country with one of the highest rates of the progressive neurodegenerative disorder. The organization predicts up to $4.6 million…
You’d think that people with multiple sclerosis (MS) and other disabilities would have easy access to healthcare services. That’s not always so. A small study in the journal Health Affairs that I wrote about last year said many physicians “expressed explicit bias toward people with disabilities and described…
People with multiple sclerosis (MS) in the United Kingdom are less likely to be on disease-modifying treatments (DMTs) compared with MS patients in other countries in Europe, a new study reports. “We know that getting early treatment with disease-modifying MS therapies can improve long term health and wellbeing.
People with multiple sclerosis (MS) in the U.S. who have access to a Shields Health Solutions care model pay an average $10 out of pocket each month for their MS treatments, according to the company — which noted that this amount is considerably less than the national average…
Ocrevus (ocrelizumab) will be funded in New Zealand for treating certain people with primary progressive multiple sclerosis (PPMS) about six years after being approved there. The decision from the Pharmaceutical Management Agency (Pharmac), which decides what medicines are funded in New Zealand and to what extent, makes Ocrevus…
A day of golfing is in store for those who want to support Johns Hopkins Hospital’s efforts on behalf of research for multiple sclerosis (MS) and to raise awareness about the progressive neurodegenerative disorder. The #spreadingORANGE event will aid the Johns Hopkins Multiple Sclerosis Center along with MS…
I nearly jumped for joy — well, I would’ve if I could’ve — when I saw a new TV commercial for the Expedia travel company the other day. It shows a woman in winter who’s obviously had enough of the cold, ice, and snow. She is desperate to…