The Migraine Trust

March for Migraine 2024

Lisa McIrvine

Lisa McIrvine

My Story

I have suffered from migraines for many, many years since I was 11. I get migraine with aura which usually starts with my vision going then I feel numb on the left side of my body, sometimes it can affect my speech then the pain starts. After a sleep in a dark room, I can still feel pain & extremely tired. I want people to be aware that a migraine is much, much more than a headache.  I'm hoping by taking part in March for Migraine it will help raise awareness.

The Migraine Trust is dedicated to helping people affected by migraine. We are the only UK migraine charity providing information and support, campaigning for awareness and change, and funding and promoting research. 

One in seven people in the UK live with migraine, and this complex and debilitating neurological disorder significantly affects their lives. We have been leading and bringing the migraine community together to change this since 1965.

Every year over two million people visit our website and thousands contact our helplines for information and support on all aspects of migraine and for help in managing it at work, in education, and in accessing healthcare.

We campaign for increased awareness and understanding of migraine, and national policy change to improve the lives of people who get it.

265%

Funded

  • Target
    £200
  • Raised so far
    £530
  • Number of donors
    40

My Story

I have suffered from migraines for many, many years since I was 11. I get migraine with aura which usually starts with my vision going then I feel numb on the left side of my body, sometimes it can affect my speech then the pain starts. After a sleep in a dark room, I can still feel pain & extremely tired. I want people to be aware that a migraine is much, much more than a headache.  I'm hoping by taking part in March for Migraine it will help raise awareness.

The Migraine Trust is dedicated to helping people affected by migraine. We are the only UK migraine charity providing information and support, campaigning for awareness and change, and funding and promoting research. 

One in seven people in the UK live with migraine, and this complex and debilitating neurological disorder significantly affects their lives. We have been leading and bringing the migraine community together to change this since 1965.

Every year over two million people visit our website and thousands contact our helplines for information and support on all aspects of migraine and for help in managing it at work, in education, and in accessing healthcare.

We campaign for increased awareness and understanding of migraine, and national policy change to improve the lives of people who get it.

Lisa McIrvine is fundraising towards