Thank you for visiting our profile page on MyDonate.This charity is set up to help people who are currently going through treatment for cancer or have a family member going through treatment for cancer and are finding everyday bills a struggle. Please donate to support our cause. All monies raised go directly to helping people with the financial costs that having cancer can have on a family, bills like gas, electric, fuel, parking costs etc. It's the unforeseen costs no-one thinks about. Charity No: 1165956 Find out more Website http://www.costofcancer.org.uk
We are a children's cancer charity, supporting children, young people and their families suffering through cancer, with financial support. We cannot always improve the quantity of a child's life, but we can do everything we can to try to improve the quality of their life.
DaBKA aims to help and support renal (kidney) patients in our local area from pre-dialysis though to transplant. We offer local patients blood pressure monitors, fistula wristbands and organise social events. Please see dabka.org.uk for further information. Thanks for your support.
Cancer Bridge is the only holistic cancer support centre in the north of England, for patients, partners, family and carers. It offers FREE support, counselling, complementary therapies and nutritional advice to all affected with cancer. It sees over 700 clients each month and is funded entirely by donations and charitable giving. Just £50 helps someone have a therapy.
This fund is been set up in memory of Dr Fiona Dolan, formerly specialist registrar in Ophthalmology, Glasgow who died, aged 36. It funds a cause close to Fiona's heart - enabling Ophthalmology colleagues to perform cataract operations and restore sight to people of all ages in developing countries.
The Laila Milly Foundation was set up in 2010 by Maya & Steve McCormack after their daughter Laila was born with a rare neurological condition. Sadly Laila passed away a day before her 1st birthday. Her parents are raising money to open a day centre for children with severe & complex health needs.
ROHHAD is a rare life threatening and life limiting condition affecting Children worldwide. The Charity mission is to - Fund and promote research leading to a new understanding of and treatments for ROHHAD, one day leading to a cure. We also offer support to those affected and raise vital awareness
The Chelsea Burley Trust was Created after our daughter Chelsea was diagnosed with a brain tumour in November 2012 and is still fighting now. We want to help by raising as much money as we can to help with the much needed research into brain tumours. We also aim to give the other oncology patients of Stoke the opportunity to have some fun by funding days out and to make the oncology day room and ward a more comfortable place to be as the patients and their families do spend a great lot of time there for treatment.
BBKA works to support bees and beekeepers. The honey bee is under continuing threats from Varroa Mite, disease and lack of forage. We invest in honey bee health research, provide educational resources on honey bees & their environmental importance and support beekeepers in the beekeeping craft.
The Cornwall Down's Syndrome Support Group is run by parents to help families affected by Down's syndrome living in Cornwall. We offer families a chance to meet, socialise and share information, friendship and support. We organise fun days out, trips away and challenging fund raising activities.
Reach for Health is a rehabilitation centre helping people recover from Strokes, Brain Injury, Heart Problems, Cancer, Joint Replacement and many other disabling conditions.
Stiff Man Syndrome was the name assigned to the condition when first identified in the 1950s by Moersch and Woltman in the USA. In recent years, in the modern world of PC, the condition has also become known as Stiff Person Syndrome. SMS or SPS does not appear to differentiate between sex, colour, or creed, although UK evidence tends to suggest women are more likely to fall victim to SMS. SMS is a neurological condition believed to be of auto-immune origin. It is unique among neurological diagnoses due to its lack of significant similarity to any other neurological diseases. Although rare, once observed it is quite unforgettable. Because of its rarity, many neurologists and GPs are not aware of the condition. In most cases, the first symptoms are insidious and victims are often initially misdiagnosed with depression. The onset is most frequent between the third and fourth decades of life. Liz Blows, who set up the UK and Ireland Support Group in 1998, began presenting symptoms in 1990 but it wasn’t until three years later that it became clear something was seriously wrong and she set off in search of a diagnosis that eventually came in 1997. She began the support group with just five members to champion the cause of this little known and misunderstood disease. Today, there are more than 100 members in the group and she remains passionate about raising awareness in both the public and medical sectors.
The Gary Barton Memorial Trust was created in memory of Gary Barton who died aged 45 years, from Cancer of Unknown Primary. Gary expressed that irrespective of the outcome of his journey that the staff should be recognised for the care and dedication they had shown to him during his illness. The Trust supports the two wards who cared for Gary during his illness, Talbot Butler Ward at Northampton General Hospital and Cawthorne Ward at Danetre Hospital in Daventry. The Gary Barton Memorial Trust goals are to relieve sickness and preserve the health of cancer patients of Talbot Butler Ward and palliative care patients of Cawthorne Ward. By providing and assisting in the provision of equipment, facilities and support services as well as advancing the education of cancer to the general public. All of The Gary Barton Memorial Trust fundraising events aim to include an element of fun to them, to represent the fun loving character of Gary.
Fighting for Sight was established in 2001 to protect the vision of the people in Scotland. It has already raised money to build a dedicated research Centre, adjacent to the Eye Clinic at ARI and now the charity continues to raise money to provide education, rehabilitation, equipment and research.
The Mayor chooses the charities they will support each year and the monies raised during the mayoral year go entirely towards the nominated charities. This year the Mayor is raising funds for Rose Road Association, Saints Foundation and Southampton Air Cadets.
The XLP Research Trust promotes and funds medical research into a potential cure for XLP, a rare always life taking genetic disease that affects only boys. The charity also acts as a support hub for families affected by XLP worldwide and looks to raise the awareness of this awful disease.
CLEFT aims to research the unanswered problems in improving care for children born with cleft lip and palate. We aim to push the boundaries of conventional treatment by funding research into improving operating techniques and by looking at the underlying reasons for cleft deformities.
The Danny Porter Foundation provides donations and grants to other charities and bodies providing research, support, care and equipment to people suffering from cancer and / or requiring neurological surgery. Through this support we hope to help with the journey that cancer patients have to undergo, help to advance the quest to cure cancer and help keep up with the very latest advances in neurological care. The Foundation will also share Dannys experience. It will not provide advice on treatment, opinion on research or methods - that is not our place. What it will do is share some of the feelings he experienced so that hopefully people in similar situations will know that what they are feeling is not unusual. It will also demonstrate that there is a full life to be enjoyed following major surgery of this type. We aim to give hope, support and reassurance to people in similar positions through the telling of Dans story.
The Northern Ireland Kidney Research Fund is a totally voluntary organisation which exists to support local research and treatment into kidney and associated diseases with an aim to finding a cure and ultimately the means of preventing such diseases.
ME Research UK commissions and funds high-quality scientific (biomedical) investigation into the causes, consequences and treatment of the myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), a debilitating illness which affects approximately 200,000 people in the UK alone but which is not well understood nor, in many cases, properly recognised. In addition, we have a mission to "Energise ME Research" globally by raising awareness of the illness through the production of high-quality reviews and reports.
The Masonic Samaritan Fund supports Freemasons and their dependants. Grants are available for eligible applicants who have a diagnosed medical, dental, respite or mobility need and, faced with a long wait via the NHS or Local Authority, are unable to afford their own private treatment or care.
The Stoke Mandeville National Spinal Charity is working hard to raise essential funds to help patients with spinal injuries. We are focused on a fund raising project for a new £2m sports facility dedicated to patients. Please support our wonderful London to Paris riders by donating here...
The Marie Curie Research Wing at Mount Vernon Cancer Centre is an internationally-renowned institution for cancer research, including radiotherapy and new drug treatments. It comprises of several teams which specialise in different cancers; including breast, prostate/bladder and head and neck.
Down Syndrome Liverpool (DSL) is a registered Charity based in the City of Liverpool, (charity no.1097276) run by Parent and Carer Trustees of people with Down syndrome. DSL aims to support parents, carers and families affected by Down syndrome, seeking to enhance the lives of people with Down's.
A charity devoted to improving the lives of teenagers and young adults with cancer and supporting young musicians.