It exists to help Renal Patients in Tayside with all aspects of treatment and day to day living, with dialysis or transplant
Set up by a pancreatic cancer survivor, we aim to improve survival for pancreatic cancer by focusing on early diagnosis. We raise awareness among the public and medical communities, fund research to improve early diagnosis, provide information for patients and educational courses for clinicians.
Cheshire Down's Syndrome Support Group run family events, meetings, and training sessions across the Cheshire Community. Its aim is to unlock the potential of it's children by raising awareness of Down's Syndrome, providing support to new parents, and providing best practice education and resources.
We are a friendly group providing support to individuals and families whose lives are touched by downs syndrome. In addition to giving support and advice to families with new babies and young children on a one to one basis we have a number of fun family regular meets and events Our roots go back to 2004 but gained registered charity status in 2010. The concentration of our activities centre around Cheltenham and we currently offer support to families throughout the Gloucestershire and Cotswold area. You can take as little or as much as you want from Cotswold Downs Syndrome Group and hopefully meet some long lasting friends along the way.
Batten disease is a group of rare, progressive neurodegenerative, genetic metabolic diseases that occur in children & adults worldwide. The BDFA's Vision is to be the central point of excellence in the UK for supporting affected families funding research into a potential cure.
CES occurs when the 'Cauda Equina' nerves at the bottom of the spine are damaged, often by trauma or disc prolapse, which can result in a devastating disability. We are the only registered UK charity which offers support to those affected by CES and works to raise awareness of the condition.
The mission of the Coffin-Lowry Syndrome Foundation (CLSF) is to provide information and support for families, caregivers, relatives, educators and medical professionals affected by, or working with, individuals diagnosed with Coffin-Lowry Syndrome. CLSF seeks to become a visible group in the medical, scientific, educational and professional communities in order to facilitate referrals of newly diagnosed individuals, and to encourage medical and behavioral research in order to improve methods of social integration of CLS individuals.
Supports research, care and communications initiatives. To date, HDF has funded and supported projects by MNDA, Cancer Research and Crisis. The HD Foundation was established in 2015 by Hayes Davidson Founder, Alan Davidson.
Cardigan Cancer Care is a local charity covering the town and local area of Cardigan.Based in Cardigan we have been serving the town and district as a care and support group for patients and families who have someone suffering with cancer for almost 20 years.We offer a listening ear and offer strictly confidential emotional support and friendship during times of stress for the patient or their family.We can provide practical assistance in the home, where necessary, to enhance the patient’s mobility and comfort together with financial assistance to make life easier.We can help with petrol costs and advise on transport to hospital appointments when there is no car available. A great deal of our resources goes into transporting patients for treatment which can be a great burden both financially and practically for sufferers.All requests are dealt with almost immediately and all monies raised quickly go back into the community.We rely on the generosity of local people both through the donations we receive and the amazing fundraising tasks that are performed.
Providing palliative care for cancer sufferers in North and East of Sri Lanka
The Hibbs Lupus Trust improves the lives of people affected by lupus. We are a dedicated team of volunteers whose own lives have been affected by lupus. Visit our website or call our free helpline on 0800 633 5118. Raising awareness is a way of life.
Bowel Cancer West is dedicated to promoting research in the diagnosis and treatment of bowel cancer; education and training of the public and health professionals who care for bowel cancer patients across the westcountry area.
Helping Families by raising funds to help children that need life changing treatment
The SR Foundation supports cancer awareness, research and treatment, with a focus on young people and cancers of the digestive system. The charity was established in memory of Savvas Regas.
There are at least three epilepsy-related deaths a day in the UK. The majority are Sudden Unexpected Death in Epilepsy (SUDEP). We care for the bereaved and work with families and professionals to make change. Using research and awareness, we strive to get the answers that will save lives.
Thank you for visiting our profile page on MyDonate. The charity was formed with the express purpose of meeting the demand for a coordinated public cord blood registry to meet the current unmet need for stem cells transplants in the UK.Precious Cells Miracle is developing a model that will facilitate the release of high-quality cord blood stem cell units to the NHS and other hospitals around the world, allowing more and more people to access and benefit from stem cell therapies.
The Swinfen Charitable Trust was started 1998, with the aim of assisting poor, sick and disabled people in the developing world. The Trust's policy is to do this by establishing telemedicine links, using high quality digital cameras and email, between hospitals in the developing world and medical specialists worldwide, who generously give their advice on diagnosis and recommend treatment free of charge.
We offer support and practical help to patients, families, carers and friends of those diagnosed with the genetic condition Alpha-1 Antitrypsin Deficiency.
The only Registered UK charity dedicated to getting good medical research underway to help children with Trisomy 21. (Down's syndrome). Check out www.dsrf-uk.org for more info! Thanks for visiting!
The Ichthyosis Support Group (ISG) is a small user led charity, run almost entirely by volunteers affected by ichthyosis to create a supportive network of sufferers, parents and medical professionals. The charity strives to raise awareness of the condition and the ISG amongst medics and the public.
Neurocare raises money to buy equipment for the Neurosciences Department at the Hallamshire Hospital, Sheffield. Neurocare funds equipment for patients with head injury, brain tumours, strokes, cancers of the nervous system and those suffering from neurological disease.
‘The Karen Trust’ mission is to design, build & open a dedicated retreat house in the UK for terminally ill cancer sufferers. It will be a place where cancer sufferers can stay with their loved ones to indulge themselves in the tranquillity & peace of the English Countryside - www.thekarentrust.org
A SMALL BUT ESSENTIALCARING CHARITY THAT HELP CHILDREN WITH LEUKAEMIA AND OTHER CANCERS COPE WITH THE TRAUMA OF TREATMENT AND THE AFTER EFFECTS BY PROVIDING GIFTS AND HOLIDAYS FOR THE WHOLE FAMILY ONCE TREATMENT IS OVER AND ANY THING ELSE WE CAN HELP OR SUPPORT WITH