News & blogs
The latest news and thinking about migraine
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Statement on the Universal Credit and Personal Independence Payment (PIP) Bill
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Statement on the NHS Ten-Year Plan
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What does the UK’s biggest neurology survey tell us about living with migraine
By Rob Music, Chief Executive, The Migraine Trust
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What’s going on with changes to disability benefits and what does it mean for people with migraine?
By: Andrea Quinn, Senior Communications Officer
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“I feel so angry and sad when I think of how much less stressful things could have been if I’d had support in school”
Madison shares her experience of migraine in education
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The Migraine Trust welcomes two new trustees
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Better migraine care: The potential for strengthened care in pharmacies
By: Rob Music, Chief Executive of The Migraine Trust
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Better migraine care: The pivotal role of GPs
By: Rob Music, Chief Executive of The Migraine Trust
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Living with migraine as a trans person
This blog looks at some of the key challenges involved in living with migraine as a trans person.
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“When I’m in a cycle of attacks, the headache from the last one is still there when the next starts”
You don’t just get over an attack when it finishes, it literally feels like a hangover
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‘Migraine has impacted pretty much every aspect of my life’: women share their experiences
Three women, Charlotte, Abigail, and Emily, tell us about their experience of migraine and how it has affected their careers, social lives, relationships and families.
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Runny noses, mind blanks and tummy troubles: symptoms you may not have realised were linked to migraine
By: Andrea Quinn, Senior Communications Officer
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