Care That’s Personalized for You

Receiving a diagnosis of multiple sclerosis can be frightening. I know firsthand—I was diagnosed in 2013 shortly after I turned 29. I worried about my future and mourned for my past.

The disease comes in several forms with many manifestations. Much like our varied symptoms, people living with MS embark on different journeys. But while our individual experiences may be unique, there are similar underlying needs and conversations that must be had.

The Patient-Centered Outcomes Research Institute (PCORI) is working to learn more about individualized health care by way of six research studies on the four following topics:

Would You Rather

Recently, I began an aggressive disease-modifying therapy (DMT) after new active lesions popped up on an MRI. With the potential for daunting side effects ahead, escalating my treatment was scary and the process, taxing. But I know that all treatments mix risks and benefits. We ask ourselves, “What can I endure now to give myself a better quality of life later?” It’s a real-life game of “would you rather…”

With so much at stake, it’s important to understand whether using stronger treatments early after diagnosis will prevent or delay the worsening of symptoms, or whether we should wait to use aggressive treatment until after our MS has progressed. Two PCORI funded studies, one at the Cleveland Clinic Foundation and the other at Johns Hopkins University, are comparing these treatment strategies.

Results from these studies may mean that patients in the future won’t be in my situation, wondering what would have happened if I had started aggressive therapy sooner.

To Treat or Not to (Continue to) Treat

Most people with MS begin taking DMTs in the early stages of the disease, as research shows that’s when the treatments are most effective. But research has also shown that relapses and the appearance of new lesions decrease as we get older, and that DMTs are less effective at treating MS in its later phases.

So, could it be safe to stop taking DMTs later in life?

A project at the University of Colorado Denver asks whether patients age 55 and older who haven’t had a relapse or change in a brain scan for five years can stop taking DMTs without their MS worsening. It’s learning whether those who continue DMTs have a difference in quality of life and in symptom progression compared with those who stop.

I’ve chosen to discontinue DMTs for periods of time in the past, and while it was freeing to get a break from pills or injections, I couldn’t shake the fear that I had opened a door to more damage or disability.

But opposing questions arise, too: Is it worth the cost, risk, and toll on our bodies to continue DMTs as our MS progresses?

I’m not thrilled about the idea of taking a DMT forever, but I’m also not sure how I would respond if my doctor advised me to stop. Would I feel like I was giving up? Would I feel relieved? What if the disease started to progress again after a quiet period? Research into the safety and effectiveness of this option could help me decide.

Miles to Go Before We Sleep

Fatigue is my worst, most consistent symptom. It’s also the most common symptom experienced by people with MS. I have to decline invitations and miss out on social activities. I sometimes rely heavily on my husband to do the bulk of household chores. I struggle to help others understand what MS fatigue feels like.

There are no approved medicines to treat MS-related fatigue, but doctors often prescribe  amantadine, modafinil, and methylphenidate, which have been approved to treat other health problems. A Johns Hopkins University study is comparing each of these medicines to see which works best to treat MS-related fatigue.

But PCORI is not just about comparing pharmaceuticals. They are also supporting research comparing other approaches to fatigue, and this study looks at whether exercise programs delivered over the internet are as effective for increasing physical activity by people with MS as in-person programs.

Managing fatigue is a tricky endeavor, so having an evidence-based way to help us decide how to do so will be very helpful!

Somebody to Lean On

Depression is an often-overlooked symptom linked to the underlying disease process, and also can be a side effect of some DMTs. Financial struggles, feeling like a burden to family and caregivers, and uncertainty over future health and quality of life can make this struggle harder.

Evidence-backed physical and behavioral treatments for depression exist, but many MS patients either don’t know about them or don’t have access to them. A study at the University of Washington asks if a collaborative care approach can help control depression and chronic pain and improve overall quality of life. In the approach being tested, a nurse, supervised by physicians, psychiatrists, and psychologists, coordinates and provides treatment for depression as guided by individuals’ goals and preferences.

I’ve struggled with MS-related depression, and while I’ve never experienced collaborative care, I can imagine its benefits. There’s a stigma attached to depression that we need to work through. We shouldn’t feel shame for struggling.

But MS doesn’t have to be all negative. Life doesn’t end here.

Each of these studies raises questions that are often neglected or uncomfortable to consider. No matter what patients’ views are on these topics, my hope is they plant seeds for more assertive self-advocacy. I encourage people living with MS to speak to their specialists and share their thoughts and concerns.

Be heard.

To read more about PCORI research in MS, visit Momentum magazine.

This article was authored by Cat Stappas and originally published on the National Multiple Sclerosis Society’s blog,, on March 22, 2018. 

2 thoughts on “Care That’s Personalized for You

  1. I always love your articles. They make me feel better. I have wondered if I would have been like this if I had been able to start DMT much earlier. I had started having symptoms in my 20’s and things weren’t so bad as I got older so I was able to do all sorts of activities, as well as extensive travel. All of a sudden things went bad. Just as I turned 60, I was diagnosed with MS. I was on Tysabri for nine years, lost my insurance, and that was real trouble – I had a massive relapse. It took me a long time to just get out of bed and I hate pushing a walker around. I also hater the idea that my husband has to do all the housework and I feel so helpless .

    Liked by 1 person

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