Sue is married with two grown up children and lives in the Midlands. Her youngest was diagnosed with Kawasaki Disease in 1992. Initially she searched for any information throughout the world (before the internet!) Managed to find some and wondered if others were going through the same ordeal. She got in touch with Contact A Family, where she ultimately met with the co-founders of the group.
Her role in KSSG
Sue manages and is involved in the day to day running of the helpline and keeps up to date with any Kawasaki DIsease updates worldwide. She was instrumental in helping to set up the first Kawasaki Clinic in the UK. Sue has been involved with several published medical papers.
On a lighter note, she was once asked for a quote on an article to do with Kawasaki Disease in a UK newspaper and on searching the net, this quote was found translated into nearly half the worlds languages!
Nicky is married with three grown up children and lives in the South East of England. She works as a full time PA. Her youngest was diagnosed with Kawasaki Disease in 1993. Initially using local media she searched for other parents, resulting in 12 contacting her. One of these contacts was instrumental in putting her in touch with Contact A Family where she met the other co-founders of the Support Group.
Her role in KSSG
Nicky is primarily involved with the financial side of the group, general administration, social media maintenance and fundraising support. She was instrumental in organising the Family Day in 1996, where Panorama filmed for a programme on Kawasaki Disease, aired in November 1996.
Nicky & Sue are Co-Founders of the KSSG in the UK. Some credit for setting up the group must go to the third original member, Zaen.