advocacy

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,…

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…

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…

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…

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…

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…

The government of Canada soon will provide new income benefits designed to help Canadians living with a disability — including people with multiple sclerosis (MS). Applauded by MS Canada, a nonprofit that actively advocated for these benefits, the announcement follows the passing of the Canada Disability Benefit Act,…

To address knowledge gaps and avoid duplicate efforts in the lab and in trials, 10 multiple sclerosis (MS) organizations from around the world have committed to a single global research strategy to find a cure for the progressive neurodegenerative disorder. The nonprofits, with headquarters in countries ranging from the…

The National Multiple Sclerosis Society (NMSS) has earned a shoutout from the digital fundraising platform DonorDrive for being recognized as one of the top 30 peer-to-peer fundraising programs in the U.S. by the Peer-to-Peer Professional Forum. MS Canada also made the list for the top…

Jonathan Allenger, diagnosed with multiple sclerosis (MS) a decade ago, is planning to bike more than 6,000 kilometers (3,700 miles) across Canada to raise awareness and CA$1 million for MS research and patient support services. Proceeds from the journey — set to begin on May 7 and conclude by…

The Multiple Sclerosis Association of America (MSAA) is holding its ninth annual Improving Lives Benefit to spotlight inspirational members of the multiple sclerosis (MS) community. This year’s fundraisers feature an in-person reception in Philadelphia on May 3 and a “Together at Home” virtual reception on May 18,…

Photo courtesy of Lindsey Holcomb Day 24 of 31 This is Lindsey Holcomb’s story: My daughters were both preschoolers when I was diagnosed with relapsing-remitting multiple sclerosis (RRMS). It took well over a decade to find an answer to the myriad symptoms that had come and…

The U.S. Equal Employment Opportunity Commission has approved a class settlement overhauling a decades-old medical clearance system that led to illegal discrimination in the U.S. Foreign Service against people with mental health conditions or other disabilities, such as multiple sclerosis (MS). The class settlement, signed in December,…

A new podcast series called “A Campbell Never Quits” is telling the life story of Tyler Campbell, a patient advocate who was diagnosed with multiple sclerosis (MS) during his junior year at college. “The podcast aims to appeal to sports fans, people living with MS, and anyone who appreciates…

Aiming to promote equitable access to multiple sclerosis (MS) treatments worldwide, an international MS alliance is asking that three disease-modifying therapies (DMTs) be added to the World Health Organization’s (WHO) list of essential medicines. Inclusion on the WHO list is considered an important if “initial” step in assuring that helpful treatments…

You may not have heard of Judy Heumann, who died March 4 at the age of 75. Although she’s not directly connected to the multiple sclerosis (MS) community, you should know about her. Everyone who lives with a disability owes her a great deal. At just 18 months old,…

Have you ever heard of an ABLE savings account? I hadn’t until a couple weeks ago. The acronym stands for the Achieving a Better Life Experience Act, a law passed by the U.S. Congress in 2014. It created special savings accounts that allow disabled Americans, including people with…

“I Am Not The Doctor For You” is the title of a shocking new study published earlier this month in the journal Health Affairs. It reports that a number of doctors acknowledged being uncomfortable with treating people with a disability. The study was conceived of by Lisa Iezzoni,…

“I thought it would never happen to me.” I’ve lost count of the number of times I’ve heard someone utter that phrase during my four decades in the news media. Last week, it happened to me. About three years ago, my wife and I bought a condo as a…

The newest recipients of the MS Australia incubator grants will seek novel ways to prevent and treat multiple sclerosis (MS) and explore the prevalence and incidence of the neurodegenerative disorder in different parts of the country. One scientist will use the funding to explore disease risk factors — and…

When Sarah Garcia was diagnosed with the relapsing-remitting form of multiple sclerosis (MS) at age 13, she didn’t know any other young Latino women with the neurodegenerative disorder. Garcia grew up in a tight-knit Hispanic community in Socorro, Texas, near El Paso. Most of her doctors were white,…

For the second year, the communications and software company Windstream is supporting the National Veterans Wheelchair Games, touted as the world’s largest annual wheelchair sports event exclusively for military veterans. The event is for all U.S. veterans with a spinal cord injury, amputation, multiple sclerosis (MS), or other…

The Multiple Sclerosis Society of Canada has opened MS Bike, an annual cycling event to raise awareness and funds for research and services that make the difference for the more than 90,000 Canadians living with multiple sclerosis (MS). Conducted in an entirely virtual format due to COVID-19 in 2020…

It’s a decision most of us with a chronic illness have to make sooner or later: When do we disclose our illness, and to whom, and how do we do it? Thirty-one-year-old Katie Coleman faced that decision not long ago. Coleman has stage 4 kidney cancer, and, in April, she…