Care for Cancer is committed to supporting local people and their families who have been affected by cancer, by providing information and advice, quality practical services and support, in a friendly and caring environment, by dedicated staff and volunteers. visit careforcancer.co.uk
The Elimination of Leukaemia Fund (ELF) raises funds to advance the treatment and cure of leukaemia and related blood cancers. Each year in the UK over 21,500 people contract a blood cancer. Today 80% of children with leukaemia and 50% of adults under 65 years, are cured.
Independent Cancer Patients' Voice is a patient advocate group led by patients for patients. We bring the views and experience of cancer patients, their family and carers, to the cancer research community. We believe that clinical research and practice will benefit more patients more quickly if people affected by cancer are partners with clinicians and healthcare professionals, rather than passive recipients of healthcare.
Thank you for visiting our profile page on MyDonate. Please donate to support our cause. Charity No: 3640937
Het Rett syndroom heeft een incidentie van 1 op de 10.000 tot 23.000 geboren meisjes, het is extreem zeldzaam bij jongens. Het is beschreven bij alle rassen en etnische groepen. In Nederland zijn op dit moment ruim 250 meisjes met het Rett syndroom bekend. Het is een ontwikkelingsstoornis van het zenuwstelsel; met name de hersenstam. De symptomen treden op na en periode van ogenschijnlijk normale ontwikkeling, vanaf een leeftijd van 6-18 maanden. De ontwikkeling vertraagd en een periode van verlies van motorische vaardigheid en communicatie volgt, met in vrijwel alle gevallen volledig verlies van spraak en loopvermogen. In deze periode ontstaat vaak onregelmatigheid in de ademhaling. Na deze regressie volgt een stabielere periode, waarin apraxie (het onvermogen te handelen), epilepsie en scoliose meer een rol gaan spelen. In deze periode kan verbetering van motoriek en communicatie bereikt worden. Uiteindelijk kan de mobiliteit terugvallen als gevolg van spierzwakte, stijfheid en toenemende scoliose. De ernst van de beperkingen kan variëren, waarbij de intensiteit van de symptomen per individu moeilijk te voorspellen is. De gemiddelde levensverwachting wordt verwacht boven de 40 jaar te zijn, hoewel dit door het relatief korte bestaan van de diagnose niet met zekerheid bekend is. Overal waar we Rett-meisjes/vrouwen schrijven, worden ook Rett-jongens/mannen bedoeld.
One Clear Vision is the leading international charity working for people with Degenerative Vitreous Syndrome (causing severe eye floaters): raising awareness and promoting a better understanding through fundraising, providing information and support to sufferers and collaborating with eye specialists and researchers to help achieve clear sight for everyone affected.
Regeneration is a small UK charity for people affected by ataxia, their families, carers and health/social care professionals working on their behalf. Working in partnership with the Somerset and Essex ataxia centres, we help people to live with the effects of their condition 'Today' by providing care, support and information services. We also look to the 'Future' by funding scientific and medical research as well as supporting and undertaking research into supportive treatments.
A regional cancer centre treating over 5,000 patients a year, Mount Vernon provides patients with specialist radiotherapy and local chemotherapy services. Through its partnership with the Royal Marsden and Institute of Cancer Research, it is also one of the leading cancer centres in the UK when it comes to researching new potential treatments. We have the first CyberKnife in the NHS. It delivers a high-dose radiation to tumours with pin-point accuracy, giving us more treatment options for our patients, especially those with cancers that are hard to treat or where existing treatment options may have run out. Please click here to find out more about the CyberKnife. The Mount Vernon Cancer Centre is located in Northwood, Middlesex and supports hospitals in Hertfordshire, North West London and parts of the Thames Valley. Please click here to find out how to get to Mount Vernon and here to find out more about the facilities available to patients and their visitors.
The Wayne Howard Trust, is a small, local, registered charity based in Southampton, which gives advice and support to acquired brain injured patients and their relatives. The Charity’s main objective is as follows; "The relief of persons who have suffered a brain injury, their families and carers, particularly but not exclusively by the provision of advice and information, financial assistance for the purchase or hire of specialist equipment or treatment and the establishment of neurological treatment and rehabilitation clinic." We have some runners taking part in the Porstmouth 'Colour Me Happy' Fun Run on Sunday June 30th. Visit our event page 'The Wayne Howard Trust Runners 2014' to find out more and sponsor them. Visit our Fundraising Page.... http://uk.virginmoneygiving.com/fundraiser-web/fundraiser/showFundraiserPage.action?userUrl=waynehowardtrust12&faId=469046&isTeam=true
The Shepherd’s Purse is our bursary fund and used solely to support residents who are funded by the local authority. The Home is run on a ‘not for profit’ basis with a strong ethos of caring for any elderly person in need residential nursing care. We strongly believe that the elderly deserve the best care we can provide and that they should be treated with dignity and respect at the end of their lives. A fee is set each year by the Board which will allow us to break even financially whilst providing good quality, attentive care in a homely setting. Local Authority funding is now unrealistically low and falls well below this ‘break even’ fee. Without the support of the bursary many residents would not be able to live at Green Pastures. We don’t want to turn anyone away because of funding. The Shepherd’s Purse Fund helps us to keep our doors open to everyone. This year we need to raise £30,000 and we anticipate the need increasing now year by year. All the money we receive via Virgin Money Giving will go into the Shepherd’s Purse fund and be used to support needy residents.
Melanoma Action and Support Scotland is a charity ran by patients for patients. Our focus is on supporting anyone who has received a diagnosis of melanoma or skin cancer, helping them through the difficult times they may be facing. Raising awareness of skin cancer is also a top priority.
Cancer Focus Northern Irelandis your local cancer champion, here to help you and your family if you have cancer. We’ll help your community take positive steps to a healthier life, to lower your risk of cancer, and we aredetermined to bring a more hopeful future by working for better public policies and funding ground-breaking research.
The Breath of Life Foundation is a UK registered charity (1122160), formerly known as Lanka Osteopathic Centre for Children. It was founded in 2005 to help children and families recover from the devastation caused by the tsunami of the previous year through osteopathic treatments. Having achieved its initial objective, the foundation continues to help, support and reach out to vulnerable children in Sri Lanka through paediatric osteopathy and education programs.
The Robbie Elliott Foundation was setup in 2012 by former Newcastle United defender Robbie Elliott. Robbie has been keen to focus his efforts on raising money for charities involved in the research & treatment of cancer after relatives & friends found themselves affected by the disease.
Mitre Trust is a Charity based at Musgrave Park Hospital, Belfast. It aims to raise funds to improve patient services and to fund new developments at Musgrave, the regional centre for Orthopaedics and rehabilitation in Northern Ireland. Funds raised go directly into providing state of the art equiptment and facilities.
Chernobyl Children Cancer Care Cardiff (The 5Cs) is a small, non denominational, non political Cardiff based charity that is officially twinned with the Belarusian Childrens Hospice in Minsk, Belarus.
The Everest Marathon is a 26.2 mile high altitude mountain marathon held every 2 years in Nepal, which requires endurance and stamina. Participants raise money for the Everest Marathon Fund which supports water, health and educational projects in rural Nepal. Profits from the race organisation also benefit the Fund.
Promise Nepal is dedicated to the elimination of leprosy from Nepal and surrounding endemic areas. We enable Nepali medical professionals to cure, care and help leprosy-affected people rebuild their lives and become self-supporting. Foremost, each patient is treated with dignity, love and respect.
Thank you for visiting our profile page on MyDonate.Our purpose is to generate discussion and share information about Tick and other vector-borne illnesses;from the fields of human and animal medicine, Tick-borne diseases are a major health hazard to humans and animals. There is limited knowledge of the extent and severity of tick-borne diseases by the general public and health care professionals. Vis-a-Vis Vector Infection Symposiums are designed to help medical practitioners, healthcare agencies and the public understand more about tick-borne diseases.Our approach is two-fold:To help share information about tick and other vector-borne illnesses we bring together UK and international researchers and practitioners from the fields of human and animal medicine. The funding generated by Vis-a-Vis, which is a not-for-profit charity, goes towards the organising events and continuing medical research and intervention in this increasingly important area of healthcare.By working together to raise awareness, diagnosis, and treatment we can improve both the lives and the life chances of vector infection patients and their carers. Charity No: 1165099 Find out more Website http://www.visavissymposiums.org/ Facebook https://www.facebook.com/VisaVisSymposiums Twitter https://twitter.com/VISSymposiums
helps young children and teenagers while suffering with long term illness. cancer,and to create a more relaxed area for teenagers and young children while in hospital. to send families for day trips. to donate memory boxes.
The Windlesham Foundation comprises of three funds: a bursary fund, a hardship fund and a capital development fund. Please go to www.windlesham.com/windlesham-foundation for more information
The mission of Infant Clubfoot Appeal (ICA), set up in 2010 by Harley Street Consultant Dr Charlotte Hawkins, is to improve the life chances of children suffering from Club Foot, a birth defect that is readily cured.
The Leeds Teaching Hospitals Charitable Foundation is launching a new Brain Research Appeal in January 2014 to raise £2million by 2015. The fundraising appeal will create a world-class Yorkshire Brain Research Centre to help tackle life-limiting brain conditions, including Parkinson’s disease, epilepsy, multiple sclerosis and dementia. Currently 1 in 6 adults suffer from diseases of the brain and there is an expectation that with an ageing population brain conditions will be a ticking time bomb. Professor Selby who helped write the case for the new Yorkshire Brain Research Centre said, “As the population gets older, there will be a significant increase in brain conditions in Yorkshire in the near future. To have a centre of excellence for brain research at Leeds means that patients do not have to travel out of the County. The Centre will conduct research for patient benefit and will help Yorkshire scientists find new treatments and drug therapies as well as conduct clinical trials.” Dr Helen Ford, Consultant Neurologist said “This is an exciting time for brain research with many new discoveries in treatments for neurological conditions. The Yorkshire Brain Research Centre will help attract the very best clinicians from around the world to train and study at Leeds and grow a strong neurosciences community for the benefit of patients in Yorkshire and beyond.” The Yorkshire Brain Research Centre will mean we will have better diagnosis, better treatment and better outcomes for patients in Yorkshire.
Alzheimer's and Related Disorders Society of India-ARDSI, is a National organisation dedicated to the cause of people suffering from Alzhiemer's disease and other Dementias since 1993. ARDSI through its 20 chapters enables short and long term care services, awareness, carers training and research.
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.