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We are the UK’s eating disorder charity.
- SEND Local Offer
- Early Help
The National Deaf Children’s Society is the UK’s leading childhood deafness charity. We’re here for every deaf child who needs us, no matter what their level or type of deafness or how they communicate. We’re also here for their parents and carers, extended family members and the professionals who w
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You can call, text or email our Freephone Helpline, Monday to Thursday,
Phone: 0808 800 8880
Text: 0786 002 2888 (SMS)
Website: ndcs.org.uk/helplinecontact
Live chat: ndcs.org.uk/livechat
SignVideo: ndcs.signvideo.net
Our website has all the information families of deaf children and deaf young people need to make informed choices, find deaf-friendly services,learn from other families and access support. Go to ndcs.org.uk.
The Buzz is our website for deaf children and young people aged 8 to 18. It’s packed with information, support and real stories from other deaf young people, and all content is available in English and BSL. Check out the Buzz at buzz.org.uk.
We offer a wide range of family events, both online and in-person. Our events are a great way to connect with other parents and families, grow your knowledge and learn from experts.
We also work with deaf young people through our interactive workshops, digital events and webinars, supporting them to develop their knowledge, skills and confidence.
Local deaf children’s societies are support groups run by parents and carers. They’re located all over the UK and offer support and advice as well as a range of activities.
We also have an online forum - Your Community - where you can connect with other parents and carers, get tips, ask questions and share experiences.
Our Technology Test Drive loan service gives families and deaf children and young people the chance to try out products, such as vibrating alarm clocks and radio aids.
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We are the UK’s eating disorder charity.
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The hub for those working with bereaved children, young people and their families across the UK.
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The National Organisation for FASD is dedicated to supporting people with Fetal Alcohol Spectrum Disorder (FASD), their families and communities. It promotes education for professionals and public awareness about the risks of alcohol consumption during pregnancy.