I last wrote about James in May. As expected, it’s taken three weeks into the school term and I’m writing about him again. That’s not surprising considering the last five posts have mostly centred around his school life.
Tuesday, 6 October 2026
Monday, 18 May 2026
Parenting James: Learning Again, Living With Trauma, and What the Diagnosis Really Means
James has been with his new tutor for three weeks. We didn’t know how it would go. He spent the weekend before the first session begging me to cancel it. His anxiety was through the roof. He didn’t want to go back to anything that looked or sounded like school.
We didn’t cancel. We adjusted. We started at 10am instead of 9.30am so he had space to breathe. That shift made the difference. He met G. They talked. They found a rhythm and lesson interests. She explained that learning didn’t have to be at a table, actively involving worksheets, or be the rigid routine that broke him. They could go out, explore, and learn in the world. Whatever sparked his interest. Lessons, resources, and routines all built around him.
Friday, 24 April 2026
Parenting James: The Long Awaited ASD and ADHD Diagnosis
James has always been bright, funny, creative, expressive, mischievous, troublesome and mouthy, but “different”. He never needed fixing. He just needed micromanaging. He was never purposefully naughty, despite often finding himself in trouble. For the school, it was always labelled as behavioural.
As an ex-teacher, qualified in child development and psychology, and someone who knows our son’s true character, I knew there was an underlying cause outside of behavioural issues. Nevertheless, a question mark always hovered above him.
That was until this month.
Wednesday, 1 April 2026
Why I’m Seeking an ASD Assessment
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Having a disability like mine means I understand my body well. My brain, however, is a different story.
A map was drawn in 2012. In 2011 everything collapsed. My disability diagnosis changed. My marriage and my work ended. My community disappeared. Debt followed. Drinking increased, a lot.
Then 2012 arrived.
Thursday, 10 September 2020
A Positive Start
Friday, 25 October 2019
It stops with me!
It wasn’t long before we knew we were expecting William that we found out that my health condition had been misdiagnosed.
I had gone 12 years with a misdiagnosed condition; I now had Facioscapulohumeral Muscular Dystrophy.
A genetic condition that would eat away at my muscles.
Monday, 6 April 2015
James' Stammer - 'Making Meaning'
Thursday, 12 March 2015
William's rare mouth!
Wednesday, 11 February 2015
Review - Head Lice - Hedrin
Tuesday, 10 February 2015
Head Lice - Frequently asked Questions
Head Lice
Whilst we went over the Christmas holidays both boys were nit free. They had been treated and we're checked and 'treated' one extra time to make sure.
3 weeks in and James, and subsequently William, has them again.
Sadly this happens to children when they're having day to day contact in settings with other children their age.
I was lucky enough, off of the back of a previous post to receive an email from the pharmaceutical company Hedrin offering me some products to review; what fantastic timing, well at least from my point of view.







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