What it is, in plain words

Motor neurone disease (MND), also called ALS, affects the nerves that control the muscles we move on purpose — for walking, gripping, speaking, swallowing, and breathing. Over time these muscles get weaker, and everyday actions become harder. It affects each person differently, and at a different pace.

MND asks a great deal of the person living with it and of those who care for them. Alongside the practical changes come real feelings — grief, worry, and moments of strength. All of that deserves space and support.

The kinds of experiences people track

A gentle record can help you and your team keep pace with change and plan ahead. People and carers often note:

  • Movement — walking, balance, grip, and tiredness.
  • Speech and swallowing — clarity, eating, drinking, and any coughing.
  • Breathing comfort, especially lying down or at night.
  • Sleep, energy, and pain.
  • What is getting harder, and what support or equipment helps.
  • Mood, worries, and moments that bring comfort.

How Lantern helps

Lantern is a calm space to capture these changes in your own words, at your own pace, so slow shifts are not lost between appointments. A partner or carer can help add notes too. Over time your entries form a clearer picture to guide conversations and decisions.

Your MND team may use their own measures to follow the condition — for example the ALS Functional Rating Scale – Revised (ALSFRS-R), which looks at everyday abilities. Lantern lets you note the names of the tools your team uses so you can talk about the same things. Lantern does not carry them out, fill them in, or score your abilities — that is your clinician's role. Lantern simply helps you bring a clear, honest account to your care.

A gentle note

Lantern is a companion, not a doctor. It does not diagnose MND, measure your muscles, or tell you what your symptoms mean. Your MND team, GP, and specialist nurses lead your care and are there to support you and your family. If breathing, swallowing, or safety are a concern, contact them promptly, or seek urgent help if it is severe.

Bring your Motor neurone disease (MND / ALS) experience to your next appointment

Capture symptoms, notes and recognised questionnaires in Lantern, then export a clear summary to share.