Your hospice stories

For Dylan Kay, his regular visits to Jigsaw mean that he can meet new people and make new friends. The youngster from Langholm in Dumfries and Galloway has quadriplegia cerebral palsy which means he has no movement in all four of his limbs as well as being cortically visually impaired.

Caring for a child with complex health needs can be a daunting experience for most parents, but for Wendy Arnot being supported by Jigsaw, Cumbria’s Children’s Hospice has allowed her and her family not to feel alone.

Heather’s son Robbie, 24, attends Jigsaw. Here Heather explains Robbie's love for the place and the break it provides for the family.

For more than a decade, Jigsaw was a home from home for Jordan Mossom and his family. Jordan lived with Duchenne Muscular Dystrophy and before passing away he worked extremely hard to raise awareness of his condition which is characterized by muscle degeneration and weakness.

Blake Penny’s favourite place to visit is Jigsaw, Cumbria’s Children’s Hospice – with his mum saying she never sees him as happy as when he’s there being cared for.

Helen’s son Jack, 11, has a metabolic disorder called NKH, he uses a wheelchair, has seizures and is tube fed.

Adam has been attending Jigsaw for more than 14 years and has a number of life-limiting conditions. The Jigsaw team has been hailed as a "lifeline" for Adam and his family who say they don't know where they'd be without their support.

Max has a genetic duplication called 5p13 duplication syndrome which was discovered after he started showing seizures when he was 11 months old, has been supported by the dedicated Jigsaw staff since he was around four years old.

Jacob Mortimer was diagnosed with a rare brain tumour when he was just six months old and sadly died a few months later. While his short life was filled with love and care, Jigsaw, Cumbria’s Children’s Hospice was able to support Jacob and his family through the toughest of times.