FAQ

Frequently asked questions

Everything you need to know about My MS Path.

What do I actually get at the end?

At the end of your check-in, you get an instant summary across six areas of MS: mobility, fatigue, cognition, vision, mood, and daily activities. Each area is scored so you can see where things feel stable and where changes are most noticeable. You can save your summary to your account, view it alongside previous check-ins, and share it with your healthcare team when it is useful.

How is this different from other MS questionnaires?

Most MS questionnaires focus on a single domain or are designed for clinical use. My MS Path is built for patients. It covers six areas of MS in one short check-in, gives you a patient-friendly summary straight away, and is designed to help you reflect on what has changed over the last 6 months — not just record data for a clinician.

Will this help me at my next appointment?

Yes. My MS Path is designed to help you arrive at appointments with a clearer picture of what has changed. Instead of trying to remember the last 6 months on the spot, you already have a structured summary ready to refer to or share. Many people find it most useful to complete a check-in shortly before an appointment.

Can I save my results and come back to them later?

Yes. Creating a free account lets you save each check-in and build a record over time. You can view your history, track how things have changed between check-ins, and share or print a summary when it is useful.

What MS types does My MS Path cover?

My MS Path is not tied to one specific type of MS. It is designed to help you reflect on more prolonged or ongoing changes that may be happening over time, which can be relevant across different types of MS. The check-in focuses on what you have experienced over the last 6 months, making it useful for anyone who wants to keep a clearer record of how things have been.

Can a carer or family member fill it in on my behalf?

My MS Path is designed to reflect the experience of the person living with MS, but support from a carer or family member can be very helpful. They may notice changes you have not picked up on, or help you remember things that have happened over the last 6 months.

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