How we’re doing
Access our latest accounts and see where our money goes
Annual Review for 2021
Our Annual Review looks at what we did in 2021, why we did it, and the impact it had, and you can download it below.
At the end of every financial year (February to January) the Trustees produce a report and audited accounts for The Migraine Trust. This is available to read in the following summer from the Charity Commission website as well as being available to download below.
Where our money comes from
We are a charity and our income is mainly based on donations from people, which is a mixture of direct donations, fundraising for us, or leaving money in their Will. We are very grateful for these donations as they enable us to continue our work in helping people with migraine.
We also receive money from trusts and foundations, pharmaceutical and device sponsorship, investment income, and finance services provided to headache charities. Here is a breakdown of that income for the financial year 2020-21.
£664,753 - Total income 2020/21
Where our money goes
We keep administration costs to a minimum.
For every £1 that we spend, 84p goes on charitable expenditure.
All donations and money raised in support of The Migraine Trust helps the charity to carry out work towards three main aims.
A large part of our work focuses on improving access to good quality information about migraine, increasing awareness and understanding, and increasing the ability of sufferers to make informed decisions.
We produce and distribute evidence-based information and facilitate discussion about migraine. To achieve this we:
- provide an Information Service
- provide an Advocacy Service
- organise ‘Managing Your Migraine’ information events
- and further share information through outreach events, our popular website, social media and regular ebulletins.
We carry out policy and campaigning work that aims to position migraine as a serious public health issue. We engage with employers, education providers, the health sector, parliamentarians and relevant bodies in order to challenge misunderstandings and promote good practice.
Since 1965 we have sought to understand migraine better so that we can improve treatment and management and, ultimately, find a cure. We champion migraine research and are the only charity actively funding such research in leading UK academic institutions.
In order to strengthen the migraine knowledge base, we promote the dissemination of research results and support people working in the field of neurology and headache by, for example, hosting a biennial meeting called MTIS (Migraine Trust International Symposium).
Through lobbying government, funders and the health sector we promote investment in research to further improve our understanding of migraine.
Here is a breakdown of our spending for the financial year 2020-21.