Multiple sclerosis - information for teachers

Multiple sclerosis (MS) is a common neurological condition affecting around 100,000 adults in the UK, but it is rare in childhood – and particularly rare in children under 12. Specialist care for these children and young people is therefore crucial and Great Ormond Street Hospital (GOSH) has an established Neuroimmunology Centre to manage young people with MS and similar conditions. MS is a lifelong condition, which at present cannot be cured, but for which disease modifying drugs are available. These drugs can significantly alter its course and improve long-term outcomes.

The nerves in the body and central nervous system – that is, the brain and spine – are covered by a fatty protective sheath known as myelin. This myelin allows the electrical impulses to be transmitted quickly and easily from the brain to the muscles. Sometimes, this fatty covering can be damaged – we call this “demyelination”. This then interferes with the normal messages being sent from the brain and/or spinal cord.

MS varies from person to person and so the symptoms experienced will be different for different young people. The symptoms experienced by one person will also be different at different times. Below are some of the common areas of difficulties you may see in school.

Children and young people diagnosed with MS may miss school for a number of reasons.

• They may be required to attend a number of hospital appointments.
• Periods of relapse may lead to further time off, particularly if a hospital admission is required.
• On-going difficulties such as fatigue may also impact upon attendance.

As MS affects the brain and eye sight, there can be an effect on a person’s short-term memory, their ability to work with information quickly or academic work at school.

Young people with MS may experience walking difficulties, difficulty with balance or co-ordination, or muscle weakness. They may also experience different sensations such as numbness or tingling in the hands or feet. In school, this may lead to difficulty moving around a large site, problems with writing or difficulty accessing the usual programme of physical education.

Problems with vision can include blurred or double vision or temporary loss of sight in one or both eyes. Within the school setting this may lead to difficulty seeing a board at the front of class or reading notes written in small print.

Children and young people with MS often experience significant fatigue. This can have a very substantial impact on day to day life and as a result, on education. It may make continuing a full-time timetable very challenging, impact upon attendance, or affect a young person’s ability to concentrate and participate fully.

The emotional or psychological impact of being diagnosed with and managing a life-long condition is well recognised. Children and young people diagnosed with MS may experience a wide range of emotions in relation to their diagnosis. They may express a wide range of feelings within the school setting, such as anxiety, sadness or anger. At different points in their journey from diagnosis children, young people and families may find additional support in relation to this helpful.

Each child or young person diagnosed with MS will have their own individual support needs and these are very likely to change over time.

One of the challenges facing those diagnosed with MS is that, for most children and young people, the condition is relapsing-remitting in nature. This means that they will experience episodes of relapse, where symptoms occur or increase and additional treatment may be required. Symptoms will then remit, reducing in severity or going away completely.

Teachers have a really important role in understanding and responding to this, so that support can be offered in a way that meets each child’s changing needs.

Below are some suggestions relating to some of the common difficulties we know that children and young people can experience.

It may be helpful to plan in advance for how time off school will be managed. It may help for a young person to have a mentor or allocated staff member in school as a main contact point. This can be useful in ensuring someone holds an overview of the amount of work missed and can help the young person to develop a realistic plan for completion.

For some of our patients we refer for a comprehensive neuropsychological assessment at some stage of their care, however this does not apply to all.

If you have significant concerns about the progress of a patient with MS please get in contact with us. It may also be helpful that you refer them to the educational psychologist allocated to your school to understand the support that may be required to facilitate their educational progress.

Children experiencing motor symptoms or difficulties may require adaptations such as extra time to move around school, access to lockers, or text books in each room to prevent the need to carry heavy bags. Some children may also find that their motor symptoms make it difficult to take notes during lessons and at these times may require copies of notes to be provided.

Occupational therapists or physiotherapists may be involved in supporting a young person with MS and may make specific suggestions relevant to the school setting.

Children experiencing visual symptoms may need to adjust where they sit in the classroom in order to see the board, or require enlarged copies of notes or handouts.

Within the school setting, it may be helpful to plan with a young person how to manage their fatigue and use the energy they have in the most useful way. Helpful strategies can include taking steps to plan activity, prioritising the most important activities and pacing activities in a manageable way with breaks and rest planned in if needed. For some children and young people with MS, it may not be possible to maintain a full timetable. Some may need to reduce the number of subjects studied at GCSE or A-level through careful discussion with their family and school team.

In recognition of the psychological aspects of life-long illness, all of the children and young people seen at GOSH have the opportunity to meet with the paediatric psychology service. They can access this service by asking their consultant or CNS for a referral. Alternatively, referrals may be made to appropriate local services. It may be helpful to think with a child and their family about what support they are currently getting, what they may find useful within school specifically and to discuss accessing additional services where needed.