Samantha Dickson Brain Tumour Trust funds scientific and clinical research into childhood and adult brain tumours, and offers support and information to patients and their carers. We have been working to improve understanding, diagnosis and treatment of brain tumours since the charity was set up in 1996 by Samantha's parents, Neil and Angela Dickson. We now spend around £1.3 million per year on brain tumour research and support, making us the largest brain tumour charity in the UK.
Mobile phones and wireless communication technology is used with almost no precautionary advice. The purpose of the RRT is to uncover and communicate the facts concerning electro-magnetic radiation on our and our children’s health, whilst trying to raise funding to research conditions such as electrosensitivity, EMFs and cancer etc.
With his personal charity Alberto Contador aims to promote the awareness and prevention of strokes. Additionally, he champions the cause of promoting public health and well-being through cycling. Visit http://charity.saxo for more information.
Remedi provides funds for medical research projects in the UK which result in new rehabilitation procedures, improved medical equipment, services and facilities which dramatically improve the quality of life for babies, children and adults and make the journey from illness or disability back to a normal life a reality.
Katharine Dormandy Trust For Haemophilia And Allied Disorders
As part of the Betsi Cadwaladr University Health Board charities The Ron Smith Cancer Appeal supports the North Wales Cancer Treatment Centre and raises money for equipment, training etc. All appeal workers, both lay and medical, are entirely unpaid volunteers. Every penny raised helps directly.
The appeal is raising £100,000 towards a £1.2 million project by Macmillan Cancer Relief at the Royal Berkshire Hospital to refurbish and extend the Berkshire Cancer Centre and support three Macmillan nurses and a Macmillan psychologist. The project will also help people with cancer who are in financial difficulty.
The Anna Trust raises funds to finance medical research into adult Cystic Fibrosis carried out at Southampton University Hospital.
The Trust raises funds in memory of Ciaran, who suffered from a genetic skin disorder called Keratitis-Ichthyosis-Deafness Syndrome (“KID syndrome”). The Trust aims to help people with similar conditions, as well as supporting research and promoting awareness about the difficulties of living with the multiple disabilities of blindness, deafness and skin disorders.
The Centre for Complementary Care offers support, information and treatment for the relief of sickness, pain, fear and sorrow. We aim to treat everyone at the point of need, regardless of ability to pay. To support this work, we raise money in the community and from charitable sources.
The Community Cancer Centre mission statement is:- “To enhance the quality of life for anyone affected by cancer” Patient, Carer & their family as a Drop In Centre We provide FREE: Become a CCC friend and contribute a minimum of £12 a year. This is will support CCC to continue it's much needed services to everyone who is affected by cancer. Fundraising:
ISARC NI is the first Sarcoidosis Support Group established in Northern Ireland. We exist to help suffers & their families get quality information on this common but unpublicised condition and a provide forum to receive support. Sarcoidosis (sar-koy-DO-sis) is a disease of unknown cause that leads to inflammation. This disease affects your body’s organs. Normally, your immune system defends your body against foreign or harmful substances. For example, it sends special cells to protect organs that are in danger. These cells release chemicals that recruit other cells to isolate and destroy the harmful substance. Inflammation occurs during this process. Once the harmful substance is gone, the cells and the inflammation go away. In people who have sarcoidosis, the inflammation doesn't go away. Instead, some of the immune system cells cluster to form lumps called granulomas (gran-yu-LO-mas) in various organs in your body. Sarcoidosis can affect any organ in your body. However, it's more likely to affect some organs than others. The disease usually starts in the lungs, skin, and/or lymph nodes (especially the lymph nodes in your chest). Also, the disease often affects the eyes and liver. Although less common, sarcoidosis can affect the heart and brain, leading to serious complications. If many granulomas form in an organ, they can affect how the organ works. This can cause signs and symptoms. Signs and symptoms vary depending on which organs are affected. Many people who have sarcoidosis have no signs or symptoms or mild ones. Lofgren's syndrome is a classic set of signs and symptoms that is typical in some people who have sarcoidosis. Lofgren's syndrome may cause fever, enlarged lymph nodes, arthritis (usually in the ankles), and/or erythema nodosum (er-ih-THE-ma no-DO-sum). Erythema nodosum is a rash of red or reddish-purple bumps on your ankles and shins. The rash may be warm and tender to the touch. Treatment for sarcoidosis varies depending on which organs are affected. Your doctor may prescribe topical treatments and/or medicines to treat the disease. Not everyone who has sarcoidosis needs treatment. The outlook for sarcoidosis varies. Many people recover from the disease with few or no long-term problems. More than half of the people who have sarcoidosis have remission within 3 years of diagnosis. “Remission” means the disease isn't active, but it can return. Two-thirds of people who have the disease have remission within 10 years of diagnosis. People who have Lofgren's syndrome usually have remission. Relapse (return of the disease) 1 or more years after remission occurs in less than 5 percent of patients. Sarcoidosis leads to organ damage in about one-third of the people diagnosed with the disease. Damage may occur over many years and involve more than one organ. Rarely, sarcoidosis can be fatal. Death usually is the result of problems with the lungs, heart, or brain. Poor outcomes are more likely in people who have advanced disease and show little improvement from treatment. Certain people are at higher risk for poor outcomes from chronic (long-term) sarcoidosis. This includes people who have lung scarring, heart or brain complications, or lupus pernio (LU-pus PUR-ne-o). Lupus pernio is a serious skin condition that sarcoidosis may cause. Research is ongoing for new and better treatments for sarcoidosis.
MAARA, or the Midlands Asthma and Allergy Research Association as we are also known, is a registered charity based in the East Midlands. We were founded in 1968 by Dr Harry Morrow Brown to undertake and fund research into the causes of asthma and allergy.
We aim to increase public awareness about head, neck and mouth cancer so that people can spot early signs of a problem resulting in a quicker diagnosis and treatment plan.
Camp Quality UK is a non-profit organisation that is committed to giving children with cancer and leukaemia repeated opportunities to enjoy a positive, fun and inspiring childhood through quality recreational, play and creative activity programs. For over 20 years, we have given children with cancer the same opportunities their peer group take for granted. We exist not just to give hope, but to challenge, inspire and, above all, bring some much-needed fun and laughter into their lives.
Hypothalamic Hamartoma Uncontrolled Gelastic Seizures - United Kingdom (HHUGS-UK) is a charity which aims to provide support and information to people and families affected by hypothalamic hamartoma (HH). It aims to promote awareness about the HH condition, its complexities and effective treatment among the public and health professionals. To actively support and promote the right of HH sufferers to recieve proper treatment, care, education and social acceptance. To assist and encourage research into the causes, effects, treatment and management of hypothalmic hamartoma.
Moston Care Foundation is a charity established to provide support to caring charities and organisations through financial grants. The Foundation has a particular focus on UK elderly, children and cancer care charities. We will support a number of charities including Maggies Cancer Care Centres, CHAS and Carers Trust. The Foundation will raise funds through organising cycling and related events. The first events are a London to Paris sponsored cycle ride and a cycle ride from London to Marrakech by the founders.
The supply, support and promotion of treatments, cures, research and equipment, to help people suffering from cancer, debilitating diseases and disabilities.
The 22Crew is the only registered charity supporting 22q DS in the UK run exclusively by parents of children with the syndrome. We are thus completely motivated to ensure our members interests come first. 22q Deletion Syndrome is one of the most commonly occurring chromosome deletions, yet few know about it. We want that to change! Our Mission Funding research and providing social, educational and medical support for all those affected by 22q Deletion Syndrome.
Supporting Men with Prostate Cancer and Their Families in Dorset, Hampshire and Sussex
Our charity was set up to honour my son Andrew who was killed in a cycling incident in Edinburgh early 2012. The aims of the Trust are We are also participating in the Scottish Parliament Cross Party Group on cycling and are delighted to be associated with Pedal on Parliament. Funds raised will be used to support innovative new cycling initiatives in Scotland. Ian McNicoll
The charity was formed to facilitate the following objective: The relief of sickness and the protection of health by the support and funding of medical research in all branches of oncology, in particular (but without prejudice to the generality of the foregoing) research in myeloma, to the intent that the useful results of such research can be disseminated for the public benefit, the support of research in the field of oncology, and the dissemination of the results of that research, through publications and lectures
ROBOCAP is a charity aimed at providing "Robotics Assisted Surgery" in the Three Shires of Gloucestershire, Herefordshire and South Worcestershire. We are aiming to purchase and hand over to the Three Shires NHS Cancer Network a state of the art robotic surgery system which will be used to improve(primarily, but not exclusively) cancer patient surgery. The system will shorten surgical procedures, reduce hospitalisation periods and improve patient outcomes.