Some South Yorkshire CANN Organisations
The Eden Dora Trust for children with Encephalitis was formed specifically to offer support to children and their families affected by Encephalitis and childhood Acquired Brain Injuries through support, information, education and research. We support children in hospital with Encephalitis and families after hospital discharge, advice on re-integration to school, different forms of rehabilitation, along with working on an Acquired Brain Injury schools award and much much more including raising awareness and funding research into the causes, diagnoses & treatments of Encephalitis/A.B.I; We hold study days & fund training workshops for families, teachers and health care professionals involved with the ongoing care and rehabilitation of children affected by Acquired brain injury and this life changing illness. Helping children and their families feel less isolated, different, misunderstood and alone. The Eden Dora Trust works with the help of their extensive advisory panel and is the only charity in the UK dedicated solely to children who suffer from Encephalitis, that anyone can get, at any time. Our Mission SPEAK: Support – for those affected by Encephalitis to find out about what help is available and how they can access it. Provision – of funding to support further research into the causes, symptoms and potential cures for Encephalitis Education – funding essential training for those […]
The Eden Dora Trust for Children with Encephalitis
Caudwell Children is a registered charity that provides emotional and practical support to disabled children and their families. Our Services Include: Autism Service – ASD Assessments, OT Sensory Pathway Assessments, Workshops for parents and children aged 4 -11 years. Family Support – Families with support, signposting and information at the point of diagnosis or during treatment. Equipment – Funding towards Mobility, sensory and specialist sports equipment. Treatment – Funding towards vital treatments that can dramatically change or save a child’s life. Therapy – Access to therapy programmes for children with cerebral palsy, brain injuries and other associated conditions Supported Breaks – Teaching practical life skills through activity programmes, family trips and accredited courses. Caudwell International Children’s Centre (CICC).
CICC, Caudwell Children. Innovation Way, Keele Science & Innovation Park, Newcastle Under Lyme ST5 5NT
Irwin Mitchell is proud to be a member of SY CANN. If your child lives with a disability or has suffered from a serious injury or illness, the emotional and physical impact can be life-changing. We understand how concerned you may be about the level of care and support your child has had or is currently receiving and can offer help and legal advice. We believe that all families should have access to legal support and we are able to offer guidance on the following: Disability and Educational Rights Education, Health and Care Plans Medical Law and Negligence Protecting Your Child’s Future including wills and trusts Court of Protection Personal Injury Trusts Anna has 20 years of experience specialising in medical negligence claims and helping families through the process. She has worked with families on a significant number of complex cases, including birth injury, brain injury, cerebral palsy cases and amputation cases. Contacting a lawyer may feel daunting but if you want to find out more about your options, please do get in touch for a free initial chat. If you wish to take forward a legal case we will always explore funding options available to you and your family.
2 Millsands, Sheffield, S3 8DT
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: firstname.lastname@example.org. 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: email@example.com 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