Children’s Additional Needs Network
These swimming sessions take place in a Hydrotherapy pool which is warm, airy and welcoming. This pool is fully accessible with a hoist and the session is staffed with two qualified life guards. Confident swimmers aged 8+ may enter the pool alone but must be…
Rotherham
Service Description Come and try the fully inclusive sport of Boccia! Session 1 of 4 in Jan-Apr block. We encourage youngsters to come to all 4 sessions if possible if they’re interested in a competitive pathway and/or building on their playing skills …
Barnsley Doncaster Rotherham Sheffield
Tree of Hope is a children’s charity that supports families to raise vital funds for specialist care, not available through the NHS, for their sick and disabled children. Fundraising under the banner of a registered charity enables families to claim gift aid, receive corporate donations and match funding, as well as providing donor reassurance.
61-63 Camden Road Tunbridge Wells Kent TN1 2QE
Yorkshire Sport Foundation is a National Lottery funded charity working across the nine districts of South Yorkshire and West Yorkshire, and part of a network of England-wide Active Partnerships. We believe in the power of movement, physical activity and sport to change people’s lives, bring us together and tackle inequalities. We want as many people as possible to enjoy all the benefits being active can bring.
Nepshaw Lane South, Morley, West Yorkshire. LS27 7JQ
One of our main aims is to support children with a limb difference and their families. This could be simply chatting in our closed group, linking people with others in the same situation and providing the opportunity for our children to meet other limb different children at Activity days and parties to realise that they aren’t alone. We support families, raise awareness of LD, create 3D printed aids, visiting schools and linking with other charities and universities doing research. We provide all our services free of charge.
9 Shepherd Way Royston Barnsley S714fx
SWAN UK is the only dedicated support network for families of children with undiagnosed genetic conditions. Approximately 6,000 children are born in the UK each year with a syndrome without a name – a genetic condition so rare that it is often impossible to diagnose. Without a diagnosis it can be difficult to access basic information and support. We have information leaflets below which are available to download. We are developing leaflets in further languages and these will also be available to download once they are completed. If you can’t find the answer to your question in the resources below or would like to make an enquiry please email: info@undiagnosed.org.uk. Our animation called ‘Ellie’s story’ explains what it means to have an undiagnosed genetic condition and how SWAN UK helps. Click the link to find out more: bit.ly/elliesstory We offer 24/7 information and support through our online forums for registered members. If you would like to become a SWAN UK member please email: joinus@undiagnosed.org.uk or click here to find out more. Don’t forget to check out our news section and join our mailing list too.
Genetic Alliance UK SWAN UK CAN Mezzanine 49-51 East Road London N1 6AH
Accessibility Tools
