Virtual Santa Fun Run 2020
Take part in the south's jolliest fun run virtually!
19th December 2020, Your local area!
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.
Read Evie's 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.
Read Eva's StoryYour donations will make a difference this Christmas
£34.50 could allow our care team to take a child around Naomi House on our magical Christmas journey.
£78 could fund an hour of vital care, sibling support and counselling from our Family Support Team.
£231 could fund a whole day of expert nursing care this Christmas.
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.
Naomi & Jack’s Big Mexican Night In
Join us for an evening of incredible food, brilliant games, live music and bundles of fun with our Big Mexican Night In!
26th November 2020, Your home!
Make Your Will 2020
Get involved in our 2020 Make Your Will campaign to support Naomi House & Jacksplace! Create a new Will or update your existing Will in return for a donation to your local children's hospice.
7th September 2020, At your chosen location
Family Stories
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.
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.
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.
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.
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.