At the beginning of the pandemic, the National Deaf Children’s Society had to quickly adapt to a new environment and move much of their support online – ensuring families were still able to communicate with their deaf child was a priority. So, during the first lockdown they launched a...
The National Deaf Children’s Society is dedicated to creating a world without barriers for deaf children and young people. We work to overcome the social and educational barriers that hold deaf children back, by: helping families give the best possible support to their deaf child every step of the...
As part of Treacher Collins Syndrome, Maia has bilateral microtia atresia. This means both of her ears are underdeveloped, with no ear canal openings, and this contributes to her conductive hearing loss. Mum, Josie, explains some of the problems that this can cause teenager Maia, in daily life. “A...
Supporting a deaf child and their family will often involve a face-to-face support session, meetings with a Teacher of the Deaf and getting together with other families in the same situation to share experiences. The COVID-19 lockdown meant all of these services were put on hold, further increasing the...