2,300 children rely on Skylarks to help support them on their special journey. Being born with a rare syndrome, having a disability or additional need due to autism, Down's syndrome, speech/hearing/visual loss, anything that's not neuro typical, for our many 0-25 year old's life can be incredibly challenging. Their young lives need as much as they can to develop their potential, be heard, understood, meet others where they can share, be themselves, connect, have fun without being judged or alienated.

Skylarks are working hard to help develop programmes for the next stage of their life where they're given the opportunity to thrive through access to work.

We're here for the parent carers and whole families too supporting everyone as the pandemic has impacted routines and had a big impact on their wellbeing.

Skylarks sessions went online at the start of lockdown to keep contact with familiar friendly faces and engaging them with their favourite classes and useful sessions. This helps their self confidence, learning and being part of our special and unique community.

Our fundraising is ever more vital to support our beneficiaries.

Skylarks receive no government funding and solely rely on donations we need to ensure that for youngsters like Rosie (who has a chromosomal syndrome) and who says "it would be a disaster" without Skylarks in her life, that we're here to support her.