Welcome to the Grace Nolan foundation!
The Grace Nolan Foundation is a non profit organisation and registered charity formed by Michael and June Nolan in November 1999, and was inspired by the short but ebullient life of their daughter Grace, who died, aged 9, from Hereditary Hemorrhagic Telangiectasia (HHT).
This website was established by the Grace Nolan Foundation in November 2003. The site is a non-medical web publication, and it's main purpose is to seek support for the Foundation and it's ideals, and to highlight it's fundraising activities and products. These, in turn, assist the Foundation in achieving it's objectives.
This website also endeavours to create awareness of HHT,by providing an "online gateway" to medical information, news and events, while also inviting those with HHT and their families to get involved in supporting the Foundation and to help us make a difference in improving their lives and the lives of their children.
News & events
27/02/2013 - 13:00
The Grace Nolan foundation letter Competition has extended its closing date to March 21st 2013. Please click here if you would like to download the competition form.