CHILD HEALTH INTERNATIONAL (CHI) works to help greatly improve the care and treatment of children with the life threatening condition, cystic fibrosis in countries where provision for the disease is less developed than in the U.K. by sending U.K. specialist medical teams to provide know-how on all aspects of treatment.
The International Costello Syndrome Support Group provides support and information for the familes affected by this very rare, life-limiting genetic syndrome. It provides information to medical professionals in order to assist in research for potential treatments and assists families by sharing information and providing emotional and practical support
The RLHKPA assists persons suffering from kidney disease who are patients of The Royal London & St. Bartholomews Hospitals, & associated renal units. Also, it helps family of such renal patients, as defined above, who are in necessitous circomstances.
Charity for Kids aim is to help sick/terminally-ill children by improving their current quality of life around Hastings Bexhill and Battle We of course want to help everybody we can but funds are very limited therefore we will focus on areas in which we can make the biggest difference
Established by Clarke’s parents in 1996 when 10-year old Clarke Lister died suddenly of a brain haemorrhage. We promote and assist research into causes and treatment of brain haemorrhage and share the useful results for public benefit, as well as providing support services for families affected by brain haemorrhage
we raise funds and awareness for cri du chat syndrome and help to bring families affected together at support meetings and regional events we also support a local community school who educate children with genetic disorders please see our website for more information
It provides support and information for parents, familes and carers and raises awareness of the syndrome amongst the medical profession. Actively involved in raising funds to promote and provide research into the Syndrome. Organises annual Conference and forwards bi-annual newsletters
The George Coller Memorial Fund is a national children's asthma charity, which was set up in 1999 in memory of little George Coller who tragically passed away to this debilitating condition when he was just 3 1/2 years old. Our aims are to provide adequate asthma care, support, help & advice in the hope that no other child will die as a result of asthma. We do this by placing George Coller asthma nurses in hospitals and clinics, help families in their homes and we are currently working on an asthma training programme which will be free of charge to all schools and childrens organisations across the U.K.
Our main focus is the treatment & development of new medicines for Neglected Tropical Diseases (NTDs),which affect over 1.4 billion people worldwide especially women & children.For every 50p raised, we can treat a child in Sub Saharan Africa against 7 of the most common NTDs such as Bilharzia.
Asthma and Allergy Foundation is dedicated to improving the quality of life and health for people living with asthma. Every day, two or more people needlessly loose their lives to an asthma attack. With your support, we can help people with asthma live longer, healthier and productive lives.
Deafness Research UK is a national charity which is committed to securing radical improvements in the prevention, diagnosis and treatment of deafness and other hearing impairments such as tinnitus.
We seek to raise funds to increase awareness of Sudden Adult Death Syndrome (SADS). We have a defibrillator donation scheme in Northern Ireland and welcome the opportunity to educate the public about SADS. Together we can save lives.
Tree of Hope offers hope to the families of sick children in the UK who need specialist medical surgery, treatment, therapy and equipment in order to free them from suffering, giving a better quality to their young lives. England & Wales 1043092 Scotland SCO4261 http://www.treeofhope.org.uk
The Leah Wilby Foundation was set up in 2011 in memory of Leah who died after a 7 year cancer battle with neuroblastoma aged just 15. It provides free holiday accommodation for children with cancer and their families at Leah's Lounge static caravan based at Haven Seashore Great Yarmouth.
ME North East delivers support, help, understanding and information to all people with ME/CFS their families and carers. We empower people to make informed choices and work in partnership with statutory services to enable access to services. We support research into the cause and cure of this disease.
The Andi Bull Cancer Trust is a registered charity which was formed to assist individuals aged 13-25 who are fighting cancer. The aim is to help provide young people with a link between the isolated world of hospital and the outside world. The money raised/donated to the ABC trust will be used to help young people take their minds off cancer.
We take cancer patients registered with a GP in Bonnybridge or Denny to hospital treatments and appointments free. They are collected from their homes, taken straight to the hospital and brought home. A friend or relative can go with them.Our drivers ‘provide valuable company and reassurance.
To offer support to other families affected by Worster-Drought Syndrome.To raise awareness with professional workers and other interested individuals. To Support and promotion of any research into Worster-Drought Syndrome
Thank you for visiting our profile page on MyDonate.WW2 Escape Lines Memorial SocietyRegistered Charity No: 1148116The WW2 Escape Lines Memorial Society is dedicated to the ‘helpers’, escapers and evaders who either organised or used the escape lines of mainland Europe during WW2. Our membership is made up of former WW2 ‘helpers’, escapers and evaders, their families and friends, historians, researchers, and others who are interested in our aims.
Let's Talk About Mouth Cancer to improve the prognosis of Mouth Cancer through early detection.
“We are a patient-led support group; men with prostate cancer helping other men with prostate cancer.”
We are a national charity whose aims are to assist as many children as possible by means of small grants given directly to the families of poorly and terminal ill children suffering from a wide variety of illnesses ranging from Cancer, Leukaemia, Proteus syndrome etc. We also support their families that have the trauma of diagnosis; it is often long a journey through the treatment bringing the worry the financial stress. Every day 10 families are told that their child has cancer. Diagnosis often comes as a terrible shock. Treatment usually starts straightaway and can last up to three years. We are funded only by the generosity of the public; we operate by keeping overheads to a bare minimum. We make a donation directly to the family. We are inundated with requests for help, each as deserving as the next and nearly all of our appeals are via social workers or medical professionals. Give today, help a child tomorrow Thankyou
The principal objects of the charity are to undertake, promote, develop and encourage research into diseases of the kidney and urinary tract and research into the treatment of such diseases. In principle, the charity agrees to support training posts in the three fields of Transplantation, Urology and Nephrology, providing that these posts are formulated into specific research projects.
Empowering people living with rare parathyroid conditions. We are the UK's only charity for adults and children living with a rare parathyroid condition, particularly hypoparathyroidism (or hypopara) which can be genetic or caused by surgery. Living with a long term rare disease can be challenging so we offer support and provide information to patients and health professionals. We engage in research, raise awareness and bring people together. Please donate to support our cause. Find out more Website http://www.hypopara.org.uk Facebook https://www.facebook.com/hypopara.uk Twitter https://twitter.com/HypoparaUK Flickr https://www.flickr.com/photos/hypopara_uk/