Migraine stories

People affected by migraine share their personal experience

The migraine stories shared below aim to show the real impact of living with migraine, whilst also offering support and comfort to others affected by this debilitating but often misunderstood condition. Each person’s experience of living with migraine will be different – from the symptoms to frequency and severity of attacks, to the treatments used and the impact on work, family and social life.


“I will always be grateful to them for their kind and generous treatment of me.”

Read Alison’s story >


“I remember being very frightened, I thought I was having a stroke”

Read Gordon’s story >


“I still try to live every moment to the fullest and experience everything I can.”

Read Nicholas’ story >


“Migraines are invisible and that’s why no one understands”

Read Emily’s story >


“I can only hope that there is a magic solution out there in the near future”

Read Gary’s story >


“I struggled greatly with university thanks to migraine”

Read Louise’s story >


“Dear Migraine, I feel it’s time to write to you. You have been a part of my life for so long”

Read Amanda’s story >


“I ended up in the emergency department with slurred speech and weakness”

Read Richard’s story >


“Over the years it has affected work, relationships and confidence”

Read Sally’s story >


“I found that people just did not understand or even care”

Read Carol’s story >

Photo of the Dawson familyDawson Family

“Heartbreakingly for our three children, the headache free days are rare”

Read the Dawson Family’s story >


“I increasingly feel that I have not been able to fulfill my potential”

Read Elizabeth’s story >


“My face, mouth and leg starts to tingle and become numb”

Read Matt’s story >


“I was diagnosed with chronic daily migraine, trigeminal neuralgia and hemicrania continua”

Read Rebecca’s story >

Photo of TonyTony

“My vision was disappearing, disappearing, disappearing”

Read Tony’s story >

Migraine stories: KarenKaren

“Over the years my migraine patterns have changed, as have I”

Read Karen’s story >

Photo of SarahSarah

“Migraines only became a problem for me in my 50s”

Read Sarah’s story >

Photo of ClaireClaire

“I started to experience visual disturbances”

Read Claire’s story >

Head and shoulders graphicPaul

“It is with some trepidation that I share my story”

Read Paul’s story >

Photo of PatriciaPatricia

“I had pain down the left side of my head and face and could not think clearly”

Read Patricia’s story >


“Since I was nine years old I’ve suffered from hemiplegic migraines”

Read Rebekah’s story >


“Then the headaches set in and things got really bad”

Read Jeff’s story >

Head and shoulders graphicKaty

“I was caught completely off guard with the volume of pain”

Read Katy’s story >


“I have been retired from the Police Force after 14 years of service”

Read Jill’s story >


“I lost all confidence in going out. As a mum I felt completely useless”

Read Gemma’s story >

Migraine stories: HollyHolly

“I became so petrified of my migraines”

Read Holly’s story >


“I curl up in a ball most nights in such severe pain I’m crying”

Read Lewis’s story >


“I was diagnosed with basilar migraines about eight years ago”

Read Sharron’s story >

Migraine stories: ChristinaChristina

“I was so worried I’d be fired”

Read Christina’s story >

Migraine stories: GrahamGraham

“One of the hard things to deal with is how other people react to my migraines”

Read Graham’s story >

Migraine stories: LindaLinda

“I’m the bog standard classic without aura”

Read Linda’s story >


“If you get migraine, or are a care giver for someone who is, just remember that you are not alone”

Read Clare’s story >


“My first migraine occurred three days after the accident”

Read Tim’s story >