- About us
- What we do
-
Living with episodic ataxia
When we last wrote about Jade, now 15, she was eight and loved playing the recorder, horse riding, dance...
16 June 2021
Ataxia UK
-
Online signing success
At the beginning of the pandemic, the National Deaf Children’s Society had to quickly adapt to a new environment...
16 June 2021
National Deaf Children's Society
-
Acorns Children’s Hospice 20/21 review
Acorns Children’s Hospice is the UK’s largest children’s hospice charity, measured by the number of children and families we...
16 June 2021
Childlife Info
-
National Deaf Children’s Society 20/21 review
The National Deaf Children’s Society is dedicated to creating a world without barriers for deaf children and young people....
16 June 2021
Childlife Info
-
Ataxia UK 20/21 review
The ataxias are a set of life-limiting neurological conditions that disrupts the messages sent from our brains to our...
16 June 2021
Childlife Info
-
National Children’s Bureau 20/21 review
The National Children’s Bureau brings people together to bring about the best for the UK’s children and young people....
03 June 2021
Childlife Info
-
Returning to Fundraising
In March 2020, we ceased all our face-to-face fundraising in residential and retail locations, in line with the requirements...
03 January 2021
Childlife Info
-
Maia’s microtia
As part of Treacher Collins Syndrome, Maia has bilateral microtia atresia. This means both of her ears are underdeveloped,...
15 December 2020
National Deaf Children's Society
Latest update categories
- What we do
