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Tag: Manchester childrens cancer research

Proton Beam Therapy project gets funding for second year

The Children’s Cancer Research Fund is funding a second year of a vital research project investigating the biology of protons used in Proton Beam Therapy (PBT) to treat sarcomas in children. This will bring the grant total for this project to £140,000. Here lead researcher, Dr Amy Chadwick, and Research Associate, Dr Emma Biglin, tell […]

Promising results for new blood test to detect Ewing Sarcoma

Ewing sarcoma

Promising results for new blood test to detect Ewing Sarcoma Over the past two years, Friends of Rosie has funded a £145,000 research project into the use of a revolutionary new blood test to diagnose Ewing Sarcoma, a rare type of bone cancer in children. Now complete, this pioneering new research has shown promising initial […]

A Christmas party to remember

On Saturday 9 December we joined forces with three other fantastic children’s cancer charities to host a special Christmas party for the children of Ward 86 at The Royal Manchester Children’s Hospital.  It was a truly wonderful day, not only because it gave the children and their families some time away from the ward to […]

Local charities join forces for children’s cancer ward Christmas party

Friends of Rosie has joined forces with three other Manchester children’s cancer charities to create a special Christmas party for children currently undergoing cancer treatment on Ward 86, the oncology ward at The Royal Manchester Children’s Hospital. The Friends of Rosie Children’s Cancer Research Fund, Milly’s Smiles, Holly’s Hearts, and The Joshua Tree Foundation have […]

Calling all volunteers

Kym Green

As a small, volunteer-led charity, we are always looking for the volunteer support of willing and skilled individuals who want to give back. There are lots of ways to volunteer your time and effort that will make a huge difference to children with cancer. These include: Administrative support Marketing & PR support Graphic design Video […]

Easter raffles underway

Easter eggs

Huge thanks to everyone hosting Easter raffles for Friends of Rosie this year and to Slatterys Chocolatiers in Whitefield for providing the delicious Easter eggs and hampers. Let’s hope we raise lots for children’s cancer research this Easter to really make a difference. We’ll keep you posted after Easter to share how much we’ve raised […]

Pioneering research for children with head & neck cancers

facial disfiguration

Over the past 12 months, Friends of Rosie has funded research at The University of Manchester looking at ways to decrease the risk of facial disfiguration in children with cancers in the head and neck. Dr Marianne Aznar and her team have been looking at how we could enable ‘smarter’ radiation treatments, leading to a […]

Could a blood test diagnose Ewing Sarcoma?

blood test

Friends of Rosie has joined forces with another like-minded charity, Megan’s Rose of Hope, to fund research into the use of a revolutionary new blood test to diagnose Ewing Sarcoma, a rare type of bone cancer. In 1 in 4 children or young people with Ewing Sarcoma there is little chance of survival because the […]

Double your donations!

Big Give Christmas Challenge

Donate during our Big Give Christmas Challenge and your donation will be doubled! We’re very excited to let you know that Friends of Rosie has been selected to participate in the Big Give Christmas Challenge 2022, the UK’s largest match funding campaign. Last year, thanks to generous supporters like you, the campaign raised over £22 […]

Become a Parent Trustee

parent trustee

Would you like to become a Parent Trustee and make a difference in early-stage children’s cancer research? When 5-year-old Rosie was diagnosed with cancer her parents were told there was no cure. When she died, they asked what they could do to prevent such tragedies. The doctors told her parents the only answer was research. […]

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Nancy Dykes

Nancy Dykes

Nancy, 11, was diagnosed with rhabdomyosarcoma when she was just 2 years old. She was treated with Proton Beam Therapy (PBT) in Germany but unfortunately relapsed less than a year later. The family were then sent to Germany for a second round of PBT. Although treatment helped to cure Nancy’s cancer, she has been left with lots of lasting effects which will require ongoing treatment throughout her life. Here Nancy and her mum, Antonia, share their story in the hope it will help others, raise awareness, and raise more money for children’s cancer research.

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Prof John Hickman

Prof John Hickman

Why I am a Trustee of CCRF
 
I am a relative of the Larkin family and knew Rosie Larkin ( Friends of Rosie, now CCRF) when she had and then died of neuroblastoma, aged six. At that time, I was a scientist and professor at Manchester University, actively working on the problem of why some cancers do not die despite intensive and toxic therapies.  Seeing Rosie during her unsuccessful therapy and then attending her funeral, besides being emotional, drove me to double down on my own research as well as to support the Charity as best I could as a cancer researcher. I spent over a decade as the Chairman of the Scientific Advisory Board of the CCRF, when the Board moulded policies to ensure that funds raised for research into childhood cancers were distributed only to clinicians and researchers who had the brightest ideas that could impact of cancer medicine for children.
 
My role on the Board
 
As a Trustee,  I hope that my many decades of experience in cancer research and medicine can help the CCRF determine where best the funds that are raised can be invested in cutting edge research and medicine. I am also keen that the CCRF brings together UK and international experts in science and cancer medicine to brainstorm on how best to advance the treatment of childhood cancers.
 
My Background
 
I was a Professor of Pharmacology at Manchester University, working on drug resistance in cancer. I then moved to Paris, where I still live, to head cancer drug discovery at a French pharmaceutical company (Servier). I then headed an EU consortium for six years that brought together researchers from the pharmaceutical industry, universities and biotechnology companies, from all over Europe and the UK, to improve cancer drug discovery. I continue to be active in cancer health policy, publishing in the medical literature.
Katrina

Katrina London

Why I am a Trustee of CCRF

I have spent my professional career representing individuals and families affected by the devastating asbestos-related cancer, mesothelioma, which has no cure and for which there are only a limited number of palliative treatments available on the NHS.

I joined CCRF because I wanted to bring my understanding of the need to raise awareness of less well known cancers and passion for the need to secure improved funding for research to children facing a cancer diagnosis.

My role on the Board

I am responsible for oversight of our collaboration agreements with other charities to co-fund research into cures and treatments for childhood cancers. I also manage our challenge events and help with community fundraising. 

My Background

I am a Senior Associate at Irwin Mitchell LLP and specialise in Asbestos Disease Litigation, acting on behalf of victims of asbestos related diseases and their families.  Over the years, I have undertaken a number of fundraising challenges to raise money for cancer research, including a 1000 mile cycle ride from Glasgow to Southampton.   

Carla

Carla Nuttall

Why I’m a Trustee of CCRF
 
I became a trustee of the Children’s Cancer Research Fund because I believe every child deserves the chance to grow up healthy and with everything to look forward to in life. Like many people, I’ve seen the impact cancer can have on families and I wanted to do something that could make a real difference. This started through my work as an ambassador for Cyclists Fighting Cancer, which supported young people and their families in finding strength, confidence, and joy through movement.
 
That experience shaped my understanding of the challenges families face and the importance of community-led support – but crucially, the clear need for that to go hand-in-hand with targeted research and long-term solutions.
 
This is why I’m so passionate about the work CCRF does and proud to contribute to a cause that gives children and their families, the greatest chance of living a life without limits.
 
My Role on the Board
 
I support CCRF’s mission by bringing my experience in brand, marketing, and communications to the board. My focus is on helping CCRF tell its story in a way that resonates with people – whether that’s families, researchers, donors, or the wider public. I work alongside an incredible team to strengthen CCRF’s voice, build trust, and grow awareness so that more children and families can benefit from the breakthroughs we’re helping to fund.
 
My Background
 
I’m the Executive Director of Corporate Affairs and Marketing for The Growth Company, a social enterprise dedicated to helping people, businesses, and places to thrive through its market-leading insight, employment, skills and business support.
My passion is to help the organisations I work with to communicate with clarity, purpose, and integrity. That’s why I’ve spent my career in strategic communications supporting organisations that want to make a positive difference – CCRF could not fit my sense of purpose any better.