Authors
Roz Kalb , Psychologist & Brian Hutchinson , Physical Therapist
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17 May 2026 | ~06:39 Engagement Time
The term “Social Prescribing” may be relatively new, but the concept has been integral to comprehensive MS care for decades. As healthcare professionals working with people affected by MS and their care partners since the 1980s, we have emphasized the importance and value of incorporating wellness – physical, social, emotional, intellectual, vocational, and spiritual – into neurologic care. Attention to the health and wellbeing of everyone in the family affected by a chronic illness like MS requires not only a multidisciplinary healthcare team, but linkages with community resources and services that support and reinforce individual and family wellbeing.
In the past, coordination of care with community resources was done primarily by social workers with a thorough understanding of the individual and family’s needs and familiarity with the community in which they lived. Today, the explosion of community and online resources and the complexity of MS care have given rise to a range of “social prescribers” who help connect individuals with local community services as well as national and online resources. Social prescribers include:
In 2023, the Surgeon General declared isolation and loneliness as an epidemic. Although this report was released in 2023, the data cited for the epidemic pre-dates the COVID-19 pandemic, which only served to increase that isolation.
Recent research tells us that social connections are declining in this country in a variety of ways. Social connection is determined by:
In general, social networks are getting smaller, participation is decreasing, and fewer people feel attached to – or supported by – their community. In other words, opportunities to feel connected and supported are increasingly few and far between.
It’s important to remember, however, that social connection isn’t static. It changes over time as various life events, including illness, job transitions, relationship changes, and changes in location, among others, come into play. Social prescribing offers a means to support people through life transitions and identify resources that help them navigate challenges in ways that support rather than diminish their social connections.
The research has shown that social isolation and loneliness increase the risk for chronic disease and premature death while also increasing economic costs to individuals, communities, and society. Efforts to increase social connection will reduce these risks while providing resources, connection, and support in the process. Social prescribing programs demonstrate improvements in mental health, social engagement, and lifestyle behaviors, as well as better health system outcomes.
In addition, social connectedness often occurs in concert with activities that promote other aspects of wellness. For example:
All of these activities promote health and wellness interventions while decreasing social isolation.
Neurology providers, including neurologists, nurse practitioners, and physician assistants are limited in their role as social prescribers by three key factors:
Comprehensive MS care (whether provided at a single center or by care providers in the community) requires a multidisciplinary team of clinicians who can address symptom management as well as the physical, emotional, social, intellectual, and spiritual aspects of wellness.
Social prescribing can and should be integrated into an overall comprehensive care plan for people with MS and their support partners. It increases the ability of people affected by MS to connect with others with similar concerns, get answers to their questions, and access essential wellness resources while enjoying a critical community of mutual support. The bottom line is that social prescribing focuses on activities that people report wanting as part of their overall comprehensive care – which means that social prescribing is an essential adjunct to the neurologic care a person is receiving.
So how can MS providers become better social prescribers?
The answer is for them to point their patients in the direction of resources that already exist for this purpose. And all of us can help them do that.
Together, we can work to make social prescribing an integral part of MS care for the benefit of people with MS and their care partners.
If you are looking for ways to connect and engage with others living with MS, or with agencies, organizations, and other local or on-line resources, reach out to:
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