Caring without burning out: How smarter workload strategies for (multiple sclerosis) nurses can safeguard qualitative care in European healthcare systems

20/10/2025
MS Nurse PRO Community
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Context

Over 1 million Europeans live with Multiple Sclerosis (MS), most diagnosed in their 20s and 30s. MS is a chronic disease of the central nervous system, causing symptoms such as fatigue, vision and motor problems, cognitive changes, and difficulties with speech, mobility, and bladder function.

  • 80% of people with MS are unemployed within 10–15 years of diagnosis.
  • 40–60% reduce social and leisure activities, especially in advanced stages.
  • There is no cure, but modern therapies and rehabilitation can delay disability and improve quality of life, work participation, and wellbeing.


Specialised nurses are essential to make therapies effective. They are the workforce ensuring:

  • monitoring MS drug treatment efficacy,
  • managing complex symptoms and side effects,
  • providing comprehensive patient education and
  • supporting diagnostics procedures. 


In 2024, MS Nurse PROfessional launched a survey to collect insights on the workload management of nurses caring for people with MS*.

Find the abstract below:

BACKGROUND: MS Nurse PROfessional is an educational program designed to support nurses caring for people with multiple sclerosis (PwMS), serving as a platform to increase knowledge and share expertise. As part of advocating to improve working conditions, MS Nurse PROfessional conducted a survey to describe workload practices of nurses in Europe caring for PwMS, and survey their opinions on potential solutions to address tasks currently left undone.

METHODS: The online survey included questions around demographics, professional background, and workload management. It was made available in ten languages to MS Nurse PROfessional community members and other MS nurses.

RESULTS: 108 nurses from 15 countries were included. 74% (n=78) of respondents have a caseload >300 PwMS per year, which equates to a mean average caseload of 516 PwMS per MS nurse. The majority of nurses (69%) spend between 30 minutes and 3 hours on each consultation, including follow-up tasks. Nurses dedicate most time to treatment and symptom management. Work left undone due to time constraints includes clinical trials, social benefits advice, team consulting, psychological interventions/support, and paperwork completion. Over half of nurses surveyed have limited administrative support. Findings indicate that the nursing community is advocating for an increase in the number of nurse colleagues, increased access to psychological support for the PwMS, the ability for nurses to refer to a multidisciplinary care team and the ability to independently prescribe certain medications.

CONCLUSIONS: This survey of nurses caring for PwMS provides useful insights into current workload practices and awareness of their improved management.

In short, the findings reveal alarming trends

  • An average caseload of 516 patients per nurse, far above the recommended level;
  • Widespread unfinished clinical and psychosocial work, largely due to excessive administrative burden and lack of integrated care;
  • Strong consensus among MS nurses on the need for systemic change: more specialised staff, integrated and multidisciplinary care teams, streamlined processes, and referral authority.  

 

*Find additional information here.

A multinational survey on the workload of nurses caring for people with multiple sclerosis in Europe

Take a look at our draft journal article that has been submitted for publication.
A multinational survey on the workload of nurses caring for people with multiple sclerosis in Europe

Presenting at ECTRIMS

As part of advocating for improved conditions, we presented our study in the ECTRIMS 2024 e-poster session.


This year, we were able to display our poster during the ECTRIMS 2025 printed poster session

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Poster Workload management of nurses caring for people with multiple sclerosis

Poster Workload management of nurses caring for people with multiple sclerosis

Read about the current workload practices of neuroscience nurses in Europe that care for PwMS, and their opinions on potential solutions to address unfinished tasks.

Our next steps

Building on this momentum, we recently held an online policy meeting featuring Member of European Parliament Katrina Konecna (CZ), substitute to the Committee on Public Health, Ber Oomen, Executive Director of the European Specialist Nurses Organisation, and Noreen Barker (UK), MS Consultant Nurse, and are preparing the next key session, a live meeting at the European Parliament. The objective of these sessions is to bring together European and national politicians, policymakers, and healthcare stakeholders to share with them our survey findings, present our evidence-based policy recommendations, and discuss how smarter workload strategies for (multiple sclerosis) nurses can safeguard qualitative care in European healthcare systems.


Click here to access our online policy meeting report!

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Advocacy leaflet: Workload Management of Nurses Caring for People with Multiple Sclerosis

Advocacy leaflet: Workload Management of Nurses Caring for People with Multiple Sclerosis

Our advocacy leaflet highlights our findings into clear, actionable recommendations for policymakers and healthcare leaders. Explore the key messages that can transform MS care.

Our concrete, evidence-based recommendations

1. More specialised nurses caring for PwMS (incl. digital skills)​

  • We need more secondary school students to pursue a career in nursing and more available positions for them to study
  • We need affordable and accessible advanced training following the nursing degree on neuroscience nursing and this should include multiple sclerosis
  • We need affordable and accessible continued medical education opportunities for nurses on multiple sclerosis treatment and care
  • We need affordable and accessible trainings on digital skills for neuroscience nurses


2. Access to psychologist, physiotherapist, occupational therapist, social worker for PwMS​

  • We need reimbursement schemes that enable PwMS to be referred in an affordable manner to allied healthcare workers
  • We need these HCP to be available (sufficient in number) and accessible (in-person or virtually) for PwMS


3. Access to and a central role for nurses within the multi-disciplinary team (MDT) and ability to independently refer​

  • Any nurse getting in contact with a PwMS should be part of a multi-disciplinary care team, working in the same electronic patient health record (ePHR).
  • Nurses that have advanced training in multiple sclerosis treatment and care should be the person that keeps the overview of the treatment and care provision to the PwMS (It is: monitoring from the healthcare provider’s point of view the clinical care pathway of the PwMS).
  • Nurses that have advanced training in multiple sclerosis treatment and care should be able to independently refer a PwMS to a psychologist, physiotherapist, occupational therapist or social worker.


4. Less and more efficient paperwork & streamlined administration utilising digital technology

  • Projects should be implemented that map the current admin burden on nurses and other care workers with the objective to reduce it by 25% by 2030.
  • Any nurse should have access to in-person or remote administrative support
  • Nurses should have access to effective digital tools that make any administrative work more efficient (e.g. note taking, updating ePHRs, …)
  • PwMS should remain owner of their own health data and should have access to an ePHR that allows them to see their clinical care pathway, including upcoming appointments (and ability to reschedule), test results and contact details of their care team. 


5. Nurse independent prescriber qualification is available*

  • Nurses that have advanced training in multiple sclerosis treatment and care should be granted the authority to prescribe certain medications related to multiple sclerosis symptom management. 

* We acknowledge that in many healthcare systems, this requires an evolution of the legal and training framework.

How can YOU contribute

We have launched a call for contributions, inviting MS nurse and patient to share their testimonials to support us in advancing our recommendations. 

I want to contribute as a nurse!

I want to contribute as an MS patient!

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We want to confront the systemic challenges faced in multiple sclerosis (MS) care and to present concrete recommendations that can both improve patient outcomes and enhance nurses’ working conditions.

Join us in shaping that future!

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