2021 Parliamentary reception hosted by Michael Gove MP
Postponed until June 2022. In March 2021 Michael Gove MP will host a Parliamentary Reception at the House of Commons for Harry’s HAT. The aim of the event is to officially launch the work of the charity and to highlight why the UK needs to increase spending on hydrocephalus research. We are currently organising the […]
Twilight Runway Challenge
Harry’s HAT have been chosen as a charity partner for the Twilight Runway Challenge. The rescheduled event is taking place on the 26th of September 2020 at the famous Blackbushe Airport in Hampshire. Sign up here.
Michaela
Hydrocephalus sounds as though it could be an ancient Greek hero, up there with the likes of Hercules or Achilles. Michaela explains…
Karen
A journey that started back in 2013, when Karen was 23 and living in Birmingham. One day she knew something wasn’t right.
Rachel
Rachel starts her story at her 20 week scan. At 39.5 weeks Rhys is born and we find out all about their hydrocephalus story.
Jenny
Jenny writes about Jethro’s journey and how, at 5 weeks old, they discovered sunsetting eyes was a symptom of hydrocephalus.
Myrna
Myrna writes about her experience from 20 weeks into her pregnancy, and why she believes in miracles.
Non
Non has a different story but one which resonates closely with parents whose children have additional needs.
Nichole
A slightly different Hydrocephalus story from the Whitacre family, from small town Ohio, USA.