The EPDA is the only European Parkinson’s disease umbrella organisation. We represent national Parkinson’s organisations in 36 countries across Europe and advocate for the rights and needs of more than 1.2 million people with Parkinson’s and their families. Our vision is to enable all people with Parkinson’s to live a full life while supporting the search for a cure. Our mission: to become the leading voice for Parkinson’s in Europe by providing innovative leadership, information and resources to all Parkinson’s stakeholders
Orthopaedic Research UK is a charitable organisation which funds high quality research into orthopaedic science
We’re a non-profit organisation for the public benefit and assistance of young adults in Herefordshire & Shropshire, aged 19-30, with a life limiting cancer diagnosis. We are an official supporter of Severn Hospice and will continue to support them through fundraising.
EMAT is an Aberdeen-based charity which has been working in Pakistan for over a decade, primarily in the prevention & treatment of eye disease.
The 2Simple Trust helps families of children suffering from neuroblastoma. Help is given by the provision of financial assistance for treatment and other needs as well as the funding of research into the disease. This work will shortly be transferred to a new charity set up specifically for the purpose and called The Neuroblastoma Children’s Cancer Alliance.
The Phoenix International Charity is an independent initiative, raising funds for worthy causes in the UK and across the globe. In addition to supporting nominated charities on a corporate level through the sale of Phoenix Christmas cards, Phoenix Traders run their own initiatives to help raise money for many causes.
Friends of the Beatson was established in 1995 with the aim of providing practical comfort and support for Beatson patients. It has recently merged with The Beatson Oncology Fund to form the Beatson Cancer Charity
Joshua's Wish provides a helping hand for children diagnosed with terminal cancer, and their families. It was created by Sarah Cornelius-Price on September 5, 1998, named after her son Joshua who died in 1998 aged seven after a two year battle with Desmoplastic Round Cell Tumour of the abdomen.
Ice Cool Kids is a local charity raising money to teach groups of local special needs children skiing, both in this country and abroad. These children have a variety of conditions some of which are life limiting. Our aim is to allow these very special children the opportunity to experience an activity from which they would normally be excluded. Participating in this therapeutic activity not only allows them to fulfil a dream but also brings a huge sense of fun, enjoyment and achievement. Skiing helps promote co-ordination, balance, movement control and general health and well being. It enables the children to develop their functional abilities and to reach their full potential, so improving their independence and quality of life. All of these children have special needs and sadly there is no cure for many of the conditions they have, but all will benefit from this chance to develop themselves, it will give them the opportunity to reach for their dreams http://icecoolkids.homestead.com/index.html
FDUK is a UK based charity to help support sufferers of Familial Dysautonomia and their families. One of the charitys main aims is to raise awareness in the community of FD as well as educate and help those with the condition. However, the condition is very rare and the charity is small and based in North London meaning many people around the country are unaware of it. The fear that the charity has is that there maybe people with the condition that are being diagnosed incorrectly and not receiving the correct treatment. The condition Familial dysautonomia (FD, used to be known as Riley Day syndrome) is a disorder of the autonomic nervous system which affects the sensory, sympathetic and some parasympathetic neurons in the autonomic and sensory nervous system resulting in variable symptoms including: insensitivity to pain, inability to produce tears, development delay, frequent lung infection caused by reflux or poor swallowing and labile blood pressure (episodic hypertension and postural hypotension). The charity Familial Dysautonomia United Kingdom (FDUK) is a charity set up to help support sufferers of FD and their families. Formally known as DSGB, the charity strives to raise awareness of the condition in the community. Its aim is also to raise money to fund individual medical needs and requirements, as well as to pay for specialised doctors in the condition to come to London to hold clinics to assess the FD sufferers and guide UK doctors in their specialised expertise. The charity is always looking for ways to spread awareness or raise money to support the sufferers. If you are able to help with either of these, please contact the group admin and they will be able to direct you.
The “Kieran Mess Foundation” was set up in memory of our beloved son Kieran,Kieran was diagnosed with a benign brain tumour in 1999.During December 2005 Kieran’s health deteriorated,sadly he passed way on 10th Feb 2006 aged 10.We provide additional quality of life to children with Brain Tumours.
Patients diagnosed with acute leukaemia can often feel isolated and lonely and want to reach out. Despite the incredible support their families and friends bring, many desperately want to talk to someone, who, through their own experience, knows exactly what it is like to walk in their shoes, someone who has been where they, themselves, are now. The Bpositive Patient Support Group is a beacon of moral support for acute leukaemia patients, their families and their friends; a network of people who understand, through first-hand experience themselves, and are there to offer them support in any way they can.
Amyotrophic lateral sclerosis (ALS), or motor neurone disease (MND), is a muscle wasting condition that affects individuals and those who care for them across the world. ALS/MND progresses rapidly; average life expectancy is estimated to be 2-5 years. Currently, there is no known cause or cure. It is estimated that over 400,000 people are living with ALS/MND worldwide! To help people with the disease, groups of people have come together to form associations. The International Alliance of ALS/MND Associations was founded in 1992 to provide an international community for individual ALS/MND associations from around the world. Our vision is to engage with our members, prospective members and other organisations to share resources globally, advance awareness and support people with ALS/MND worldwide.
Thank you for visiting our profile page on MyDonate. Para-Monte is a charity set up by the Savories in dedication to Adam. To raise awareness of altitude illnesses as well as highlighting safe travel to altitude.
Founded by Ex-Watchdog presenter and bowel cancer survivor Lynn Faulds Wood. We help to investigate every stage of the patient’s journey - from prevention and screening to palliative care - to help save lives from bowel cancer and to improve the quality of life of those going through the journey
Medical Assistance Sierra Leone was established in 2003 with the aim of supporting access to health care and urgent medical treatment for communities and individuals in Sierra Leone. Sierra Leone is the poorest country in the world (UNDP 2004), with high infant mortality and globally the worst maternal mortality rates. Sierra Leone's health infrastructure clearly requires support at all levels. However there are specific strategic areas where an input of resources can be expected to begin to save lives, improve health and well-being and better enable individuals to meet the vast development challenges facing their families and communities. MASL focuses on three areas of work longterm: Reducing maternal mortality. About 2% of women die in childbirth, largely due to lack of services to manage emergency obstetric care, harmful traditional practices, inadequately trained staff, a weak referral system and high hospital-patient costs. Reducing child mortality. A study by the government and UNICEF revealed that 1 out of 4 children die before their fifth birthday. Children are dying from easily treatable illnesses like malaria, which accounts for up to 65% of such deaths, diarrohea, measles and complications associated with malnutrition. Low cost, well-targeted interventions can save lives. Facilitating access to treatment for those with rare and specialist medical conditions, who face no prospect of getting treatment in Sierra Leone. Currently this includes support to spinal surgery patients, developing the first epilepsy service in Sierra Leone with UK consultants and plastic surgery support to burns patients. MASL works with others to raise awareness of the key health and development issues facing communities in Sierra Leone - and to generate interest and support in meeting the health needs of the country. We have virtually no UK overheads and employ one Coordinator in Sierra Leone, who liaises with and supports local partners and carries out a monitoring and evaluation function.
The Mayor of Croydon for her Mayoral year 2014/15 is supporting two charities which are Macmillan Cancer Support and Age UK Croydon.
The Conveyancing Foundation has been established to help conveyancers raise funds for their chosen charities. Over the years, our Free Legal Fee Competition has raised over £300,000.00 for charity.
Our team of therapists provides free complementary treatment to children and young people with a range of disabilities, health problems and special needs. the focus is on treatments that are either not available to children on the NHS or affordable to their families in the private sector.
The Institute of Cancer Research (ICR) is one of the world's top cancer research organisations as well as being the home of the Everyman male cancer campaign. With the ICR working in all areas of cancer research from genetics through to drug development, its male cancer campaign, Everyman, focuses specifically on raising awareness and funds for research into prostate and testicular cancer. For further information about the work of the ICR and Everyman, please visit their brand new JustGiving profile pages at:
Meningitis UK merged with the Meningitis Trust this year to become Meningitis Now. We exist to save lives and rebuild futures by funding research, raising awareness and providing support. If you would like any further information, please do get in touch using the contact details below.
Thank you for visiting the Sole Bay Care Fund page on MyDonate.
W4CR aims to promote cancer awareness and raise money for cancer research, education and support. Sunrise Sunset 2013 on June 15th is W4CR's big annual fun and fund raising event. Since 2009 W4CR has been able to distribute more than £150,000, see www.W4CR.org for details.