A family with Apert Syndrome launch 'Elijah's Hope' to support families of disabled children in UK's South West

Kaddy Thomas has created Elijah's Hope CIC, named after her seven-year-old son Elijah. The aim of the CIC is to help and support families within the South West of the UK facing challenges due to illness. Kaddy says: 

'I am passionate about supporting children, young people and their families who have disabilities.' 

Both Kaddy and Elijah suffer from Apert Syndrome, a congenital disorder characterised by deformities of the skull, face, hands and feet. Whilst Kaddy lives a mostly healthy life herself, Elijah is wheelchair-bound following an infection aged one, which left him severely brain damaged. 

The CIC launches on March 24, Elijah's eighth birthday, and will offer information packs and newsletters about disabled services, as well as luncheon clubs for parents and children, peer support, and workshops for families. 

To find out more call Kaddy on 01275 269359 (UK)