Daniel’s story
Hi I’m Daniel. I am now 33 years old and was diagnosed with Acute Lymphoblastic Leukaemia (ALL) when I was three years old in December
Hi I’m Daniel. I am now 33 years old and was diagnosed with Acute Lymphoblastic Leukaemia (ALL) when I was three years old in December
Come along to a lovely charity Christmas concert hosted by the fabulous Altrincham Concert Orchestra and you’ll be supporting vital childhood cancer research. The event
Kendra Haigh started this year with a goal of staying alcohol-free for as much of 2018 as she could. Her aim: to help raise money
We give our sincerest thanks to the late Mrs Mary Smith of Paisley, and her family, for her extremely generous legacy donation of £12,805. This
This year, we have once again partnered with Charity Cards for our charity Christmas cards. Although it’s only just October, thoughts are already turning to
Friends of Rosie is now registered with AmazonSmile. This means that, when you shop with AmazonSmile, you can now donate and help us raise more
We’re delighted to announce the appointment of a new Parent Trustee, Katie Cutler, to join our Board of Trustees. Katie’s son Arthur, from Bolton, was
Max Edwards, aged 9, from Prestwich was inspired to fundraise for childhood cancer and breast cancer research after his grandmother’s battle with the disease. The
Huge thanks to Jo Richardson and Lee Wood who have chosen to do a Sober October in support of childhood cancer research. Says Jo, “As
© 2025 Children’s Cancer Research Fund | Charity No. 1046278 | Website by ATTAIN.
Lorna is Senior Research Fellow & Patient Engagement Lead at the CCLG TYA Research Centre. She is also a Director at the University College London Hospitals NHS Foundation Trust.
Lorna is an internationally recognised leader in teenage and young adult oncology, with 20 years’ research experience across academic, industry, clinical and healthcare settings. She has led a diverse research and development portfolio. Her expertise includes early diagnosis and detection, research and innovation, inequalities in access to care and research, and patient engagement. A member of the Department of Health and Social Care Children’s and Young Persons Advisory Task Force, Lorna chairs national multi-stakeholder and patient initiatives and is an invited keynote speaker, media contributor and parliamentary presenter.
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.
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.
