Winchester Half Marathon 2022
Join Team Naomi for the Winchester Half Marathon!
25th September 2022, Winchester
Bonnie's Story
Bonnie was born with severe brain damage and her mum was told to take her baby home and keep her happy. They didn’t expect her to live longer than a month. That was 30 years ago. This is Bonnie's Story.
Read Bonnie's Story
Emma's Story
My husband Simon and I had so many plans and dreams for our new little family. We’d imagined all those special moments with our child, so when Dr Kate said, “We can make Christmas happen for you,” that’s when we knew we had to go.
Read Emma's StoryHow your donation will make a difference
£31 could fund an hour of vital nursing care for a seriously ill child or young adult
£52 could fund a magical sensory room session at Naomi House
£150 could allow a child or young adult to get out of their wheelchair for a while for a dip in our hydrotherapy pool
Keep in touch with Naomi & Jack
Find out more about the amazing difference Naomi House & Jacksplace makes every day. Keep up to date with our work and find out how you can support seriously ill children and young adults across the south.
Keep in touch with Naomi & Jack
View All Events
Featured Events
Do something amazing this year - take on a challenge to support your local hospices for children and young adults.
Santa Fun Run 2022
Take part in the south's jolliest fun run this festive season at Winchester or Salisbury
4th December 2022, Winchester
Family Stories
Archie's Story
After a difficult birth, Archie was born with severe brain damage, causing quadriplegic cerebral palsy, epilepsy and blindness. Archie is a funny, cheeky boy with a contagious smile. This is his story.
Faith's Story
Faith has Dravet syndrome, a rare form of epilepsy that has a wide range of traits such as autism, ataxia, learning difficulties, speech delay and mobility problems. In her story, her parents talk about the importance of respite.
Hector's Story
When Jessica was pregnant, the couple found out that baby Hector had trisomy 18. Most babies with this condition die before or shortly after being born. This is Hector's story.
Ollie's Story
Ollie was born with Alternating Hemiplegia of Childhood, meaning any muscle in his body can become paralysed at any time. Ollie is a happy, cheeky boy that smiles constantly, loves people and loves life. This is his story.
Amelia's Story
As a result of difficulties at birth, baby Amelia had severe brain damage, cerebral palsy, four limb quadriplegia, blindness and very severe epilepsy. This is her story, told bravely by mum, Debbie.
Lucy's Story
In this story, Lucy tells us all about family life with congenital muscular dystrophy and how Jacksplace has given her independence and freedom when she needed it most. Also included is a poem Lucy wrote about Jacksplace.
Ethan's Story
At the age of just 14 months, little Ethan was diagnosed with a brain tumour. He spent the next nine months in hospital, and many of those in intensive care. This is his story.
Evie's Story
Evie had a progressive neurological disorder known as Labrune syndrome. She visited Naomi House since the age of 7 for respite care. Her condition caused a gradual deterioration in her health and sadly, in June 2020, she passed away at the age of just 12. This is her story.
Eva's Story
Eva has Rett syndrome, a rare genetic disorder which affects brain development, resulting in mental and physical disability. Eva has a very big heart with a lot of love to give. This is her story.