Patient Contributor

Laura McKee

Migraine Patient Stories

Laura is a former primary school teacher, blogger, poet, and jeweler living in Sussex, United Kingdom. She is a positive-thinking mom of two teenage boys and is happily married to Joel.

Overview

Living With Condition
10 Years
Published
5 Articles
Location
Sussex, United Kingdom

Laura's History with the Condition

Laura is a chronic “migraineur” who sadly had to give up her 14-and-a-half-year teaching career after developing a debilitating brain condition in 2014. Looking for a purpose, she pursued her life-long love of writing and started her blog, "Strength of Tears."

Over time, Laura's blog evolved into raising awareness of disabilities, chronic illness's impact on family life, and the effects on mental health.

Laura also runs a Twitter account, which shares advice and articles from charities, researchers, and other bloggers worldwide.

Always keeping busy, Laura also started her own business, “Paprika Jewellery & Accessories,” after she began making jewelry as a distraction from her pain. In her spare time, she writes poetry to explore her own mental health and well-being.

Laura writes about using positive thinking so she and her family can live their best lives. She hopes to inspire others to find their own sense of purpose.

Laura says:

"At 36, I was diagnosed with chronic migraine, and a headache specialist confirmed that I'd been living with undiagnosed migraine since puberty.

"In 2014, I had what I thought was a migraine attack, but the pain was constant for weeks. Nothing my neurologists tried helped.

"I noticed some new symptoms a few months later and found a specialist ENT surgeon in Cambridge. He diagnosed Idiopathic Intracranial Hypertension (IIH), a rare and incurable brain condition.

"When my neurologists found out, they refused to treat me, even for migraines, as they disagreed with the diagnosis.

"My symptoms are atypical and similar to my worst migraines, but I knew the difference. My condition deteriorated quickly, but I was too late for the Cambridge team's medical trial and had to wait 18 months for treatment.

"I felt like I'd been left by the wayside. Eventually, my GP diagnosed me with depression and anxiety. The situation was tough on my husband and sons, who became my primary carers.

"Despite some improvement, my conditions are still debilitating. My cognitive function has improved, but I need mobility aids, such as a stair lift and wheelchair, because of my poor balance.

"I have a carer come in daily, and they've become part of the family team! We support each other's mental well-being and ensure every day is filled with love and laughter."

The information presented is solely for educational purposes, not as specific advice for the evaluation, management, or treatment of any condition.

NPS-ALL-NP-00929 April 2023

Published Articles

“That's Not My Name”: 10 Disability Terms I Hate
6 mins
article
Laura McKee

“That's Not My Name”: 10 Disability Terms I Hate

Migraine and Brain Fog: 15 Tips to Beat the Brain Fuzz
10 mins
article
Laura McKee

Migraine and Brain Fog: 15 Tips to Beat the Brain Fuzz

How My Children Feel about Family Life with a Chronically Ill Parent
12 mins
article
Laura McKee

How My Children Feel about Family Life with a Chronically Ill Parent

Coming to Terms with Chronic Illness as a Family
10 mins
article
Laura McKee

Coming to Terms with Chronic Illness as a Family

Chronic Illness and the Pandemic: How Did Some of Us Cope?
10 mins
article
Laura McKee

Chronic Illness and the Pandemic: How Did Some of Us Cope?