Neuroblastoma is a rare aggressive childhood cancer. About 100 children are diagnosed in the UK each year. The Society works exclusively for these children in raising funds for British research into the disease, and offering information and support to families affected by neuroblastoma.
The Fund has over 1100 funds for the benefit of patients and staff in the Grampian area. Each hospital, ward, department and speciality has its own individual fund and provides enhanced patient care together with extra facilities and opportunities not available from government funding.
The Histiocytosis Research Trust funds scientific research into uncovering the causes of Langerhan's Cell Histiocytosis and Haemophagocytic Lymphohistiocytosis as well as seeking to ensure early diagnosis, effective treatment and a cure. We also aim to support patients and their families.
We help everyone to prevent and recover from cancer through Breast Cancer Partnership, Children's Cancer Recovery Project & our umbrella services. We understand people need immediate support & give cancer patients and their families financial security, hope and valued advice when they need it most.
The Marfan Trust was set up in 1988, to support medical research into the cause and prevention of Marfan syndrome. All funds raised are put towards various research studies and informing patients and medical staff about appropriate care. Our research work covers the whole of the United Kingdom and the Marfan Trust is the only charity in the UK that primarily supports research into Marfan syndrome. If you would like us to promote your event on our website / Facebook or Twitter pages, or all three, please email us. Please send us your name, link to your Virgin Money Giving page, a short paragraph about what you are doing and why and a picture you would like us to use. We will happily promote your event.Thank you very much for your continued support.The Marfan Trust
ME Research UK funds high-quality biomedical investigation into the causes and treatment of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). This illness affects approximately 200,000 people in the UK but is neither well understood nor, in many cases, properly recognised.
EHERCC supports EHE rare cancer patients, raises funds for critical research, and promotes EHE awareness. We help those with EHE while funding research to understand and ultimately defeat EHE, because people with rare cancers should not feel forgotten. We are determined to ensure they are not.
Alder Hey Children's Charity raises funds to support the hospital's pioneering work and aims to improve the quality of life for not only the 270,000 children and young people we see each year but through innovations and research, the quality of life for children across the world.
Devastating the lives of 250,000 people in the UK, M.E. is a disabling and chronic illness. Action for M.E. provides support and information for those touched by M.E., and campaigns for better services and invests in research to ultimately find a cure.
CRIS Cancer Foundation is an independent non-profit organisation dedicated to the promotion and development of research to eliminate cancer. We believe that science is the only weapon that can beat cancer. CRIS Cancer Foundation focuses on the types of cancer that have fewer resources or more difficulty in obtaining financing. By funding research in the scientific community we believe that we can make a notable improvement in the understanding of the biological mechanisms of cancer. We are hopeful that this will allow us to develop new medicines and treatment plans capable of overcoming this fatal disease, so that it can be managed and ultimately eliminated. CRIS Cancer Objectives: Invest in cutting edge cancer research projects Fund research for rare and underfunded forms of cancer Fund translational projects to get new REAL treatments Share research findings CRIS Cancer Foundation is currently funding three research projects. One translational haematological research unit in 12 Octubre hospital in Madrid, and two paediatric oncology project, one guidebook giving recommendations for child pain management to help in their treatment whilst suffering from cancer. The final research project is research in Natural Killer Cell therapy in child oncology cases.
The mission of Foundation for Prader-Willi Research UK (FPWR UK) is to eliminate the challenges of Prader-Willi Syndrome through the advancement of research. High quality research will lead to more effective treatments and an eventual cure for this disorder. FPWR UK was founded in 2010 by parents of children with Prader-Willi Syndrome.
The Robin Cancer Trust aims to raise awareness for Germ Cell Cancers, including both Testicular and Ovarian Cancer, in 16-35 year olds. Your continued support is invaluable to our cause and we greatly appreciate your donations. Thank you.
We seek to promote the care of cancer patients, their families and friends by providing emotional support through both complementary and talking therapies
Jessica Robson was diagnosed with alveolar sarcoma cancer on the 1st of November 2010 aged 14 after finding a slight lump in her left thigh on a holiday in August the same year. After a hard 3 and half year battle with cancer she passed away peacefully in her sleep in the early morning of the 16th of May 2014 aged 18. Jess always loved raising money and with all the fund raising she has done in the past 3 years, as a family we have raised over £28,000 for a number of charities. Jess loved when people brought presents in for Christmas and Easter eggs in for the patients. We (Jessica's sister and parents) are keeping Jessica's inspiration alive by keeping her fundraising going but now in her name. We have set up the charity 'JESSICA'S SARCOMA AWARENESS', in the memory of Jess, the money we will raise will go 25% to teenage cancer trust (a charity closest to Jessica's heart) 25% to Sarcoma UK (as jess always wanted to help beat cancer) and the other 50% will stay in the charity which I will then work out money to be able to make up presents for the other children in hospital fighting this awful disease. For example, Easter, Christmas and so on and financing days out for the patients and their families. Jessica was never selfish, always smiling and never gave up. She never deserved this awful disease but I want Jessica's spirits to live on.
Short Bowel Survivor & Friends are a children's Charity set up by parents/carers of children with the potentially life threatening condition Short Bowel Syndrome (SBS) Our Mission is to: Children suffering with SBS need surgery immediately or soon after birth if they are to survive. They are fed intravenously through a catheter or central line which leaves them vunerable to serious line infections. These children will inevitably return to hospital for further surgery and treatment throughout their young lives.
The Grace Kelly Ladybird Trust was set up in memory of Grace Elizabeth Kelly who passed away at the age of just 4 1/4 from a rare aggressive tumour on her kidney called a Malignant Rhabdoid Tumour. She went from being a happy, healthy school girl to passing away within 3 weeks. The Grace Kelly Ladybird Trust for research into rare solid tumours of childhood, including malignant rhabdoid tumours is working to provide grants and funding for research into these tumours. We are also working to improve awareness of childhood cancer and the symptoms children may present with. Childhood cancer affects 1 in every 285 children before their 20th birthday. It is also the biggest medical cause of death of children in the UK. Despite this fact, research is massively underfunded. We are fighting to change this. We are working to save lives to fulfill Grace's wish of helping others.
The Bodie Hodges Foundation was inspired by the loss of our 10 month old son who became an organ donation hero when he saved the lives of four babies. We aim to raise £150,000 to buy a holiday home for families bereaved of a child. We promote awareness of the Organ Donor Register
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We will become Scotland’s leading University celebrated internationally for the quality of our graduates and the impact of our research.
ALD Life is a patient support group for patients and families affected by Adrenoleukodystrophy (ALD) - a rare genetic disorder that affects mainly young boys aged 4 to 10. At present, there isn't cure for ALD and death usually occurs within a few years. Help us today to give hope for tomorrow.
We provide children whose parent/s are undergoing cancer treatment with some recreational activities during this time. We work with the families to provide some activities the children can go off and do with another family member whist their parent are resting and recovering.
The Psoriasis Association is the leading national charity working for people with psoriasis. We provide information, advice and support via a comprehensive website, email and telephone helpline to people who have psoriasis or whose lives are affected by it. We aim to raise awareness of the condition that affects 2-3% of the population. The Psoriasis Association also funds research into the causes, treatment and care of psoriasis.
CARE FOR CASUALTIES APPPEAL - The funds raised from this appeal are dedicated to support the immediate, medium and long term care of Rifles' Casualties.If you would like to make a donation or fundraise for this cause, please would you also contact our Appeal coordinator at [email protected] so that we can keep in touch with you and support you. Thank you!
Milly's Smiles provides Welcome Bags for children who have been newly diagnosed with a cancer related illness. The bag contains lots of items that will help them through the first frightening weeks of their journey.