CWCF was set up in 1998 by Ursula & Chris Downton with Kirsty & James Denny. Now with the help of other friends and family we still go out having fun raising funds to grant wishes to local children and their families who have had or are suffering from cancer that live in East Sussex, Brighton & Hove
Anna's Hope assists in the rehabilitation of children and young people who have suffered from a brain tumour or who have had brain surgery . It also will fund research into the causes , treatment and cure of childhood brain tumours
Donations support a wide range of charitable and health related activities benefiting both patients and staff within the Trust. The Trust relies on the kindness and generosity of many individuals, groups and companies who donate their time and money for this purpose.
The Lynda Jackson Macmillan Centre provides support and information to people affected by cancer. Based at Mount Vernon Cancer Centre in Northwood, the LJMC's services include a drop-in centre, telephone helpline, counselling, complementary therapies and benefits advice. The LJMC responds to more than 35,000 requests for help each year and we are extremely grateful to everyone who raises money to enable us to meet these requests. Thank you. The LJMC is an integral part of Mount Vernon Cancer Centre and a fund within the charity East & North Hertfordshire NHS Trust Charitable Fund, reg. no 1053338
The Ups of Downs was formed in January 2006 in Leamington Spa, Warwickshire to provide a forum for children with Down syndrome and their families to meet on a regular basis. We run weekly sessions for pre-school children and fortnightly sports clubs for infant age children. Our driving ethos is to empower parents to give their child with Down syndrome every opportunity to develop, flourish and achieve, by providing each parent with the knowledge, confidence, ability and resources.
The University of Lincoln is a leading teaching and research institution. We make a difference through education, ground-breaking research and outreach activities. Our excellence extends across all disciplines and your donation will impact people across the globe. Thank you for your support.
Making a difference to patients and staff at the Yorkshire Heart Centre at Leeds General Infirmary A message from the Chairman Take Heart was founded in 1989 and since then has raised over three million pounds to fund both major and minor projects. We are committed to giving care and comfort to patients and their families at the Yorkshire Heart Centre at Leeds General Infirmary and St James Hospital and its Units within the Leeds Teaching Hospitals NHS Trust. We endeavour to ensure that patients and their families enjoy the very best of comfort within the Yorkshire Heart Centre at what can be a very stressful time. The charity is run entirely on a voluntary basis,so the vast majority of funds go directly to the projects for which they are intended. If you can help us continue our work, we would be more than grateful. Why not join us for a one time membership fee of £1.50? Details on our website at www.takeheart.net. Thanks for reading. Colin Pullan, MBE
Odyssey is a charity which enhances the quality of life for people with cancer through imaginative programmes of challenging and dramatic activities using the outdoors.
Our mission is to make blood cancer sufferers able to receive more effective treatment in the future. We are willing to fight blood cancer regardless of how long it might take.
The ME Trust is working towards the day when all those suffering from Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME) have access to the best resources for diagnosis, treatment and care to enable early and full recovery. CFS/ME is an umbrella term for a neurological disease or spectrum of diseases. People who are severely affected can be bed-bound and in severe pain for many years. Common symptoms include extreme exhaustion, muscle and joint pain, noise and light sensitivities, cognitive impairment and digestive problems. The ME Trust is the only charity in the UK that is focused on providing life-transforming patient care for people suffering from this debilitating illness. A quarter of a million people in the UK suffer from CFS/ME. There is no cure for CFS/ME and there has been a lack of adequate support for the majority of people with the disease. Many who need hospital care or specialist referrral are left at home without the help they so badly need.NHS in-patient care for people with CFS/ME is almost non-existent. Private medical insurance typically does not cover the illness. The ME Trust is working in association with Burrswood Hospital to provide care specifically adapted to each patients needs. Burrswood has almost 20 years experience of helping CFS/ME patients and offers the highest levels of both clinical and compassionate care. Your kind contribution will help the ME Trust transform the lives of people with CFS/ME. Thank you so much for your support.
The Duchenne Research Fund has the vision that, through our work, a cure will be found for Duchenne Muscular Dystrophy (DMD). The Duchenne Research Fund, formerly know as The GM Trust, was established in May 2007 to identify and fund research into finding a cure for this devastating disease.
About SOFT UK SOFT UK provides information and support at all stages following a prenatal diagnosis of Trisomy 13 or Trisomy 18 - whether a family decides to terminate the pregnancy early or allow it to continue. SOFT supports those caring for a baby or child with these conditions (often living with multiple and profound disabilites), and families if a bereavement occurs. As a membership organisation, families can share their experiences through the SOFT UK website, members' magazine and annual members' events. SOFT offers support to all members of the family, including siblings of the affected child, for as long as required. At the heart of SOFT UK is the belief that no family should have to cope alone and that offering an opportunity to share experiences can reduce feelings of isolation commonly felt by members of families affected by these rare conditions. Thank you so much to everyone involved with raising funds for SOFT UK - click on the links below to find out more about just a number of these kind people. Or visit the fundraising section of the SOFT UK website. The Steve Ruston and Matthew Breakwell will be running the "Bolt the Holt" half marathon on 5th April to raise money for Diabetes UK and SOFT UK. April Ritchie will be running the 2014 Virgin London Marathon for SOFT UK. Good luck April! On the 17th November 2013 Amy Fall will be doing a bungee jump to raise money for SOFT. Sian Kelly will be running the 2013 Lloyds TSB Cardiff Half Marathon on 6th October 2013. Martin McLaughlin will be taking part in the Great Scottish Half Marathon on 6th October. Martin is raising money for 2 great causes - Cancer Support Scotland and SOFT UK - in memory of Paul and Ben. On the 15th of September Neil Hindle ran the Bupa Great North Run. Neil has raised £660 so far and is still accepting donations for SOFT UK. Caroline and Sean Watts ran the Bristol Half Marathon on 15 September in memory of their daughter Cerys. They are still accepting donations for SOFT UK, Jessie May Trust and Chidren's Hospice South West. Jason Tomkins is taking part in several cycle rides throughout the year to raise funds in memory of his precious Nephew Oliver. Jonathan Worth is fundraising in memory of Amelia Rose. Steve Pilkington ran the Torbay Half Marathon in June 2013 in a time of 1:58:05. More than £600 raised so far.... Visit the SOFT UK Website for
Our charity is dedicated to raising money for research into the causes, prevention, diagnosis and treatment of childhood cancer, which affects 1 in 600 children. Since 1991 we've raised £2m of start-up funding for new research, enabling scientists to eventually attract national funding.
The Healing Foundation is a national fundraising charity championing the cause of people living with disfigurement and visible loss of function, by funding research into pioneering surgical and psychological healing techniques. Through research, we also raise awareness about the cause and provide information about the sources of support.
Wings for Life is dedicated to finding a cure for spinal cord injury and funds world class scientific research & clinical trials aimed at accelerating progress towards this. 100% of your donation goes directly to research as the charity’s founders cover all administrative costs.
The Buckinghamshire Hospitals NHS Trust Charitable Funds supports Amersham, Stoke Mandeville and Wycombe hospitals. It uses donations and other funds to donate medical or other equipment, fund research and training & improve the environment for patients, visitors and staff.
Just imagine, living with your family in an isolated fishing village with no dentists, a high sugar diet , no toothbrushes and no fluoride tooth paste. You don't need to be a dentist to imagine the consequences, but the dental neglect shocks even the most experienced of this group of national dentists and their team. Abscesses, pain and distress, parents of these children in Morocco are no different to any other around the world, they want their children helping.Maybe a little pebble in a big pond but three years ago a group of dentists from around the UK came together to form the Dental Maverick charity to provide dental care in remote areas of the world Expanding significantly in 2012,the Mavericks numbered a team of 15, including 8 clinicians and their support staff of dental nurses and admin staff. Excited at the prospect of providing restorative fillings for the first time to complement the inevitable extraction work load the Mavericks met up in Southern Spain for the ferry journey to Morocco. Laden with a tremendous range of clinical equipment donated by incredible dental company generosity and public donation, dental care we take for granted headed for a North Africa desperate for the services of this western team.
Luna's Little Stars was set up after the devastating loss of our beautiful little girl Luna to a brain tumour. We send children with terminal brain tumours to Disneyland Paris and families looking for lifesaving treatment abroad by funding their trip to meet Dr's and discuss any available options.
The Ellen MacArthur Trust takes young people aged between 8-18 sailing to help them regain their confidence, on their way to recovery from cancer, leukaemia and other serious illness. Sailing is perfect for these children; it gives them a chance to test themselves in a safe and supportive environment. Simply the experience of going out on the water for the first time is an adventure. Each child has the challenge of helping sail the yachts throughout the voyage and takes part in all aspects of the trip from sailing the yacht to the washing up! The children come from all over the country, including Northern Ireland, London, Essex, Sheffield, Dorset, Wiltshire, Hertfordshire, Hampshire, Kent, Nottingham & Ellen’s birthplace, Derbyshire.
BUST (Breast Cancer Unit Support Trust) is a Bristol based charity founded by patients for patients to support the work of the Southmead Hospital Breast Care Centre. Since 1991, BUST has spent £750,000 on equipment and resources to support innovation in diagnosis and treatment of breast disease.
500 people die every year in the North East from Urological Cancers and many more suffer unwanted after effects without appropriate support. These cancers are testicular, prostate, bladder, kidney and penile, they are some of the most curable cancers if detected early enough. UCAN continue to raise funds to highlight awareness of the signs and symptoms of urological cancers and to support sufferers through provision of Scotland's only urological cancer support centre based on Ward 44 at Aberdeen royal Infirmary.
We are the Fylde Coast Head and Neck Cancer Support Group. The group was set up because of difficulty a lot of people have with swallowing and provides information and support for both patients and their carers. We need your donations or fund raising events. Please help us to help others!
Logan’s Fund are a children’s cancer charity who operate Scotland wide and aim to provide anything that will give a cause for optimism or an alternative focus away from hospital and beyond the treatment they are going through for any child and their family affected by cancer. Our philosophy is to try and win back some of the childhood lost to time in hospital. We want to give your child's horizon a sprinkling of magic dust.
The British Polio Fellowship supports people in the UK who have had polio by providing: Information on all aspects of living with polio A variety of support networks Information about the management and treatment of the late effects of polio (Post Polio Syndrome) Campaigns on polio and disability-related issues
Postural Tachycardia Syndrome (PoTS) can be a life altering and debilitating chronic health condition. The simple act of standing can be a challenge for people with PoTS as their body is unable to adjust to the pull of gravity when upright. PoTS is characterised by orthostatic intolerance (the development of symptoms when upright that are relieved by lying down). Symptoms include headaches, fatigue, palpitations, sweating, nausea, fainting and dizziness and are associated with an increase in heart rate from the lying to upright position of greater than 30 beats per minute (40 in teenagers) or a heart rate of greater than 120 beats per minute within 10 minutes of standing.PoTS UK aims to :• To support patients in obtaining a diagnosis and treatment.• Provide evidence based information to patients, carers and heath-care workers.• Facilitate mutual support via a Facebook forum.• Co-ordinate research projects• Promote awareness• Raise funds to support these aims.