Author Archives: Mary Chapman

‘No Surprises Act’ Aims to Rein In Out-of-network Billing in US

Under rules in the No Surprises Act, insured patients people in the U.S., including those with multiple sclerosis, should no longer receive unexpected medical bills for emergency care or for treatment from out-of-network providers at facilities in their network. The act, which became effective on Jan. 1, prohibits…

New Podcast Focuses on Improving Self-image, Reclaiming Confidence

A new podcast series hosted and produced by cultural expert Jess Weiner aims to help girls, non-binary individuals, and women, with their confidence. The target audience includes those with physical disorders, such as multiple sclerosis (MS), that may affect their self-image. Called “Dominant Stories with Jess Weiner,” the 12-episode…

Musical About Mother Cabrini the Work of NY Playwright With MS

A musical about the life of St. Frances Xavier Cabrini, the Italian-born Roman Catholic nun known as Mother Cabrini to the many immigrants in New York she served in the late 19th and early 20th centuries, tells Cabrini’s story through the eyes of a 13-year-old girl with multiple sclerosis (MS)…

Submissions Now Open for 2022 MSAA Art Showcase

The Multiple Sclerosis Association of America (MSAA) is calling for submissions for its 2022 MSAA Art Showcase, an initiative that celebrates the work of artists who have multiple sclerosis (MS). The showcase, which began in 2009, gives MS patients in the U.S. the opportunity to share their…

Canadians Urged to ‘Take Action for MS’

As the federal election looms in Canada, a nation that has one of the world’s highest rates of multiple sclerosis (MS), the MS Society of Canada is urging patients and advocates to inform candidates about issues of importance to the MS community. The letter-writing and social media campaign,…

OM1 Launches MS Registry for Use in Research, Trial Planning

OM1, a technology company focused on chronic conditions, announced that it has launched a multiple sclerosis (MS) registry to generate data that may ultimately be used to improve care and develop treatments for the disease. The OM1 registry is being touted as the largest, most representative MS…

Advocates ‘Roll’ on Capitol Hill for Disability Rights

In an effort to make sure those with spinal cord injuries and disorders (SCI/D) are included in disability legislation, the United Spinal Association and some 200 advocates recently gathered virtually for this year’s “Roll on Capitol Hill.” The annual event, in which advocates met with lawmakers, gives organization members…

$1M Gift Will Expand Adventure-based Healing Program

A $1 million gift from Velocity Global will help expand First Descents, an adventure program for young adults living with multiple sclerosis (MS) or other serious chronic conditions. The money will go toward program development and is expected to help First Descents reach 1,000 MS patients over…

Canada’s MS Walk Returns for Awareness Month

The Multiple Sclerosis Society of Canada‘s (MSSC) MS Walk fundraiser is still on for this month — May is MS Awareness Month in Canada — although in an altered form due to the pandemic. The annual nationwide community-driven event raises funds and MS awareness to help battle the…

MSAA Hosts First Virtual ‘Improving Lives Benefit’ on May 13

Despite the current challenging times, the Multiple Sclerosis Association of America (MSAA) will host its annual Improving Lives Benefit this year, albeit virtually. The May 13 event will spotlight the nonprofit organization’s community efforts over more than 50 years. The affair will be hosted by multiple sclerosis (MS)…

One-third of Patients in the UK Hid MS Status, Poll Finds

An MS Society survey found that about one-third of people with multiple sclerosis (MS) in the U.K. have kept their condition hidden from their partner, family members, employer, or work colleagues. To help mark MS Awareness Week, observed in the U.K. April 19–25, the nonprofit organization released…

MS Run the US 3,260-mile Relay Keeps Going Despite Pandemic

The pandemic notwithstanding, MS Run the US has fielded 18 runners — including eight with multiple sclerosis (MS) — to traverse the United States to raise awareness and funds to support MS research and to aid those living with disability caused by the neurodegenerative disease. The organization’s Ultra…

Foot Drop Device Earns Innovation Challenge Prize

As winner of the Lyfebulb and Bristol Myers Squibb Innovation Challenge in multiple sclerosis (MS), Evolution Devices will use the $25,000 in prize money to further develop a smart stimulation therapy that seeks to improve patient mobility. The innovative electrical device under development by Pierluigi Mantovani, co-founder…

It’s March – Make Time for MS Awareness

Note: This story was updated March 8, 2021, to note that tickets for MSAA’s Virtual Art Tour are still available for purchase.  Activities are underway to mark Multiple Sclerosis Awareness Month, set aside each year to call attention to the neurodegenerative disorder estimated to affect almost 1 million U.S.

MSAA Asks Patients to Take Survey Into Opinions on Clinical Trials

People with multiple sclerosis (MS) are encouraged to complete a survey aimed at understanding the experiences and expectations of those with a chronic illness who have either participated in a clinical trial or may in the future. The questionnaire was created by Kayentis, an electronic solutions company, in…

New $100M Program Aims to Improve Diversity in Clinical Trials

A new $100-million program aims to improve the diversity of participants in U.S. clinical trials with the ultimate goal of achieving better health outcomes and parity in care for underserved patient populations. The initiative seeks to extend the reach of clinical studies to underserved populations in the nation’s urban and rural…

Innovation Challenge Seeks Solutions From Entrepreneurs in MS Community

A $25,000 contest is inviting entrepreneurs who have multiple sclerosis (MS), or take care of someone with MS, to pitch their non-therapeutic solutions for people with the neurodegenerative disorder. The virtual Innovation Challenge, which takes place in March 2021, is part of a collaboration between patient-powered platform Lyfebulb…

BMS, Dragonfly Working on Immune System-targeting Therapies for MS

Dragonfly Therapeutics and Bristol Myers Squibb (BMS) announced an expanded partnership focused on discovering and developing treatment candidates for multiple sclerosis (MS) and neuroinflammation targets. The companies have been working together in therapy research and development for cancer and autoimmune diseases using Dragonfly’s proprietary immunotherapy targeting…

$7.2M NIH Grant Supports Study of MS Diagnostic Biomarker

The National Institutes of Health (NIH) awarded a $7.2 million grant to a team led by Cleveland Clinic researchers that will study whether a new biomarker might more accurately diagnose multiple sclerosis (MS). Grant money will support a study in 400 adults suspected of having MS to determine if the…

Dancing Doodle

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