Living with secondary progressive multiple sclerosis can be very costly, both financially and emotionally.
The study found that people with secondary progressive multiple sclerosis (pwSPMS) face high costs each year, averaging about €41,500. More than half of these costs are indirect, meaning they come from lost work and support needed at home, like help with chores. Many patients also require medical care and support services, with almost 70% using primary care and around 50% needing help in rehab centers. The study showed that older patients with more severe symptoms have higher costs, which can add to their stress. This information highlights how SPMS impacts not just health, but also finances and everyday life.
MS patients should care about these findings because they show the real financial burden of living with SPMS, which can affect their quality of life. Caregivers can better understand the challenges their loved ones face and prepare for the support they may need. Healthcare providers can use this information to advocate for better resources and support systems for their patients. Policymakers should take note, as these findings suggest a need for improved care pathways and financial assistance. Understanding these costs can help patients and families plan for the future and seek necessary support.
The study has some limitations, such as being based on data from only 34 hospitals and not including all potential costs. This means the actual burden of SPMS might be even higher than reported. It’s important for patients to discuss their specific situations with healthcare providers to understand their unique costs and needs.
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Read MoreWhether you’ve recently been diagnosed with Multiple Sclerosis (MS) or are seeking to broaden your understanding of this complex, neurodegenerative disease, navigating the latest research can feel overwhelming. Studies published in respected medical journals like BMC health services research often range from early-stage, exploratory work to advanced clinical trials. These evidence-based findings help shape new disease-modifying therapies, guide symptom management techniques, and deepen our knowledge of MS progression.
However, not all research is created equal. Some clinical research studies may have smaller sample sizes, evolving methodologies, or limitations that warrant careful interpretation. For a more comprehensive, accurate understanding, we recommend reviewing the original source material—accessible via the More Details section above—and consulting with healthcare professionals who specialize in MS care.
By presenting a wide range of MS-focused studies—spanning cutting-edge treatments, emerging therapies, and established best practices—we aim to empower patients, caregivers, and clinicians to stay informed and make well-informed decisions when managing Multiple Sclerosis.