Bone Cancer Research Trust

BCRT funds research into primary bone cancer, in particular, osteosarcoma, Ewing's sarcoma, chondrosarcoma, chordoma, spindle cell sarcoma, and adamantinoma.

BCRT was initially a parents' group started in September 2004. Five families who had lost children to osteosarcoma and wanted to see more research carried out into this rare cancer to hopefully improve the outcome for future sufferers were brought together.

The parents' group increased with the addition of families, including one from Ireland, whose children had battled against another primary bone cancer, Ewing sarcoma. Expanding the group helped to unite skills and enthusiasm as well as funds already raised. The families pooled money totalling £176,000 to start the charity and fund the first pieces of research.

The Bone Cancer Research Trust became a registered charity in March 2006 and by September 2006, the first two successful applications for research grants had been accepted.

The Cancer Research Trust's website, provides information about the charity's activities including details of past and present research being funded by the charity; primary bone cancer information, information for Health Care Professionals, a patient's forum, stories of people's bone cancer journeys, and social media links.

The charity normally puts out two research calls per year. To date the charity has funded 83 projects totalling £3.9 million.

The families who formed the charity had major concerns regarding the lack of reliable information available. Little detailed information resources were available in the UK or the internet as a whole.

Alongside research funding, information provision is now one of the charities activities. The Bone Cancer Research Trust provides information (online and printed) on primary bone cancers for patients, their families, the general public, media and health care professionals. Currently there is detailed information on osteosarcoma, Ewing sarcoma and chondrosarcoma and a glossary/ medical dictionary.

The Bone Cancer Research Trust has an annual "Awareness Week" (in October).[2][3][4][5]

During Awareness Week various activities are carried out by the charity's supporters with the main campaign being "Bake a Cake for Bone Cancer". Another highlight is the annual Patients' and Supporters' Conference, which brings together patients and parents with the many different professionals whose work affects the lives of those who find themselves with a diagnosis of bone cancer.[6][7]

The work of the Bone Cancer Research Trust is almost entirely funded by the public. The charity raises money through donations, community fundraising events, retail and legacies. Fundraising events are commonly tagged on social media using #TeamBones.

The Bone Cancer Research Trust produces a twice yearly newsletter entitled "United".

The Bone Cancer Research Trust has National Institute for Health Research (NIHR) Partner status. The charity also works closely with The Teenage Cancer Trust and the Information Standard.

BCRT governance is provided by a Board of Trustees. The current chairman is Andrew Lewis (patient parent). The deputy chairman is Roger Paul (patient parent). The remaining Board consists of Gill Johnstone (founder and patient parent), Sarah Dawson (patient parent), Mr Jonathan Stevenson (consultant orthopaedic surgeon), Malcolm Matthews (patient parent), Professor Bernadette Brennan (consultant paediatric oncologist), Hannah Millington (former patient), Arlene Eves (former patient), Dr Darrell Green (research active molecular biologist and geneticist), Professor Alison Gartland (research active molecular and cell biologist) and Damian Harper (former patient).

Sam Waley-Cohen

James Corden, Diane-Louise Jordan, Paterson Joseph, Piers Morgan, Amanda Holden, Ben Shephard, Aled Jones

• Cancer in the United Kingdom

• The Bone Cancer Research Trust
• Teenage Cancer Trust
• Irish Cancer Society