To relieve persons in need suffering from multiple sclerosis and other related conditions in Ipswich and the surrounding area through support and services.
Erb's Palsy Group offers advice and information on the injury Erb's Palsy/Obstectric Brachial Plexus Paralysis. We do this by giving support to parents, adults and children, putting parents in contact with each other, newsletters and information leaflets and also holding annual events for families.
Simone Cowland Trust was founded in 2006 to raise funds for Cystic Fibrosis sufferers and particularly those at the Royal Brompaton and Harefield Foulis ward. Our aim is to help the day to day lives of those suffering with CF a little easier.
Road Victims Trust support of road victims is provided by a team of highly skilled counselling volunteers and staff. The principles and ethos of the RVT reflect a primary and compelling aspiration to provide personal support to all those affected by the trauma caused by serious road collisions.
The Waterberg Welfare Society provides help and support to those individuals infected and affected by HIV/AIDS in the Waterberg, Limpopo Province, South Africa.
Me too & Co helps children and young people with additional needs, including Down syndrome, ASD, hearing or visual impairment, cerebral palsy, developmental delay and rare syndromes. We offer opportunities for play and development and provide information and emotional support for families.
Starfish Greathearts Foundations supports children who have been orphaned or made vulnerable by the HIV/AIDS pandemic in Southern Africa. Starfish believes in bringing life, hope and opportunity to these children…helping each child, one child at a time.
Small Steps, provides vital assistance for children with special needs aged 0-4 years. It teaches parents of children with cerebral palsy, and other forms of motor and sensory impairment, how to help their child develop basic skills. No government funding is available for such deserving children.
The Turner Syndrome Support Society is a national charity caring for the needs of those with Turner syndrome throughout the UK, offering support and information to girls and adult women with TS, their families and friends. The Society also enjoys a good relationship with medical and other specialists to promote a good basis for education and uderstanding of the management of TS.
The Rainbow Centre is Fareham based charity that provides Conductive Education to children with Cerebral Palsy, adults with MS, Parkinson’s and Stroke & Head Injury sufferers. CE focus's on emotional, social, cognitive and physical development with aims to improve the individuals quality of life.
Since 1954 Epilepsy Scotland has provided advice, information, support and services for people in Scotland who have epilepsy, their families and carers. We are a lifeline for people who need information and advice, training and literature. Call our freephone helpline on 0808 800 2200.
CMV Action is a UK organisation of parents and volunteers, who have come together to support families and raise public awareness of congenital Cytomegalovirus - one of the most common cause of birth defects in the UK. We offer advice, support and friendship to anyone affected by congenital CMV.
HOPE For Autism supports children aged 3-20years with autism and their parents/carers who reside in North Lanarkshire, by offering a range of services and childrens' activities, 6 days a week at the HOPE Centre in Airdrie.
The Foundation is an information and resource centre for those wishing to learn about dyspraxia. It operates a telephone helpline and produces information and literature for parents and professionals. It organises conferences and events to promote greater understanding and supports those affected through a network of groups around the UK.
The MTV Staying Alive Foundation fights HIV the smart way by supporting innovative prevention programs on the ground and broadcasting original content to help spread awareness around the world.
The Craighalbert Centre's services and facilities are exclusively funded by donations, and would not exist without the generous support of our donors. Services supported by fundraising include the Siblings Group, the hydrotherapy pool and the Centre’s provision for children under the age of two.
Thank you for visiting Burning Nights CRPS Support charity's profile page!Burning Nights CRPS Support is a registered UK charity specifically aimed at raising awareness for a not well understood chronic neuropathic condition; Complex Regional Pain Syndrome (CRPS). We also help and support to all those affected by this condition, not only the sufferers but their family, friends, loved ones and carers.We provide regular a local support group currently in Manchester but we are wanting to expand these support groups to other areas of the UK. We have an information helpline as well as a 24/7 online community forum, an annual conference with professional speakers and social media. Complex Regional Pain Syndrome (CRPS) formerly Reflex Sympathetic Dystrophy is a poorly understood condition which affects approx 1 in 3,800 people in the UK & worldwide. CRPS can cause a person to experience persistent, severe and debilitating pain. The condition may develop after an injury, surgery, stroke or heart attack, but the pain is out of proportion with the severity of the initial injury. The cause of CRPS isn’t clearly understood & awareness in the UK is low.With low awareness & understanding of CRPS both globally & in the UK, it is vital that a support system is in place for those who suffer from this condition. We offer detailed information & support for sufferers, loved ones, carers, friends & families.We aim to improve the quality of life for sufferers, carers, families & friends. Increasing knowledge of CRPS on a global & national scale in the UK is a necessity. Please donate to support our cause and let us help those affected by this debilitating condition. Charity No: 1166522 Find out more Website http://www.burningnightscrps.org/ Facebook https://www.facebook.com/chronicpainCRPS Twitter https://twitter.com/BNightsCRPS YouTube Please click here to visit our YouTube page
We work with our organisations that support our beneficiaries, that support patient with kidney disease to provide them with items that will improve the renal patients quality of life and we work with Welsh Kidney Patients Association to support welfare applications.
ADD-vance supports families of children who have ADHD and/or Autism through personal support groups and telephone helpline, consultations and coaching in the home as well as training and consultancy to schools and other professionals. A parent says "When it feels like every door has shut and you feel confused, upset and on your own, ADD-vance is there in person and on the phone to listen, advise, support and open another door"
Chester MS Support Centre offers practical support, therapies and helpful strategies to manage the symptoms of MS as effectively as possible in a happy, supportive and understanding environment. Individuals are encouraged to take a positive attitude towards the management of their symptoms, allowing them to take control of their lives with MS, rather than MS controlling them.
TM Society provides information and support to over 1200 TM sufferers, carers and families in UK. TM Society also supports people with other rare auto-immune neurological conditions eg ADEM and NMO (Devic's Disease). TM Society is affiliated to worldwide TM Association.
The Butterfly Trust provides support to people with Cystic Fibrosis. This life limiting condition causes chronis lung disease and digestive problems. People with Cystic Fibrosis require intensive, exhausting and expensive treatment administrered at home. Our services improve quality of life by alleviating the physical, emotional and financial burden of care.
Headway Jersey supports islanders and their families, who are living with a brain injury. Our Headway Centre provides an environment and services which enable members to learn new skills, gain confidence and coping strategies to deal with everyday situations that most people take for granted.
The Hotcourses Foundation was set up in 2004 to help fund the education of children in the developing world whose access to education was limited or non-existent. Its objective is to make a measurable, tangible difference to the lives of children in some of the poorest parts of the world. Initially it has focused on AIDS-orphans in Kenya and HIV positive young adults in Uganda.