This film is about how people make decisions about treatments when they have a child with rhabdomyosarcoma, a type of soft tissue cancer. We’ll hear from Professor Bob Phillips of the University of York and Leeds Children’s Hospital, one of the researchers […]
Leeds Children’s Hospital TV This film will explain what mucositis is, how it may affect you and what photobiomodulation can do to help reduce the symptoms. if you would like more information and meet the team that made this film […]
In this film we hear from young people who use the day room on Ward 94 at St James’s while on treatment there.
Each month Maddi will be starting some much-needed conversations about cancer and our mental health. She’ll be joined by someone different who will bring their own story and thoughts to the chat. We’re all busy, but we can all make […]
Ryan’s Journey continues as he takes a trip to Italy with a new contract.
Febrile neutropenia is a common and potentially life-threatening complication of cancer treatment. It’s managed by admission to hospital, and giving powerful antibiotics. We know that for 4 out of 5 young people, the temperature wasn’t a severe infection, and we […]
One minute pharmacists series continues with Chris explanation of the protective effect of calcium folinate against Methotrexate.
Stephanie, Lily and Ella instantly connected when they met on their Trust trip. They learned new skills, made lots of friends and most importantly had fun. Interested in coming on a Trust trip? Find out more here –https://www.ellenmacarthurcancertrust.org/our-trips/first-time-
All films related to Cerebellar Mutism. You may find this website helpful www.posteriorfossasociety.org
The Ellen MacArthur Cancer Trust has launched its ’12 Years, 12 Stories’ video series with the help of Tom Roberts, 22, from Ripley, Derby, a budding videographer who has sailed with the Trust as both a young person with cancer […]
Stephanie, Lily and Ella instantly connected when they met on their Trust trip. They learned new skills, made lots of friends and most importantly had fun. Interested in coming on a Trust trip? Find out more here. Emmie was diagnosed […]
Positivity and optimism is the best cure to the loneliness and isolation young people feel after treatment. As the young people explain in this video a weight is lifted off your shoulders by being around people who understand. The support […]
For many young people, picking up from where they left off before cancer just isn’t possible. So, when treatment ends our work begins. We support young people aged 8-17 and 18-24(ish) to rebuild confidence through sailing and adventure.
The My Voice Vlog Series is an opportunity to share what’s on your mind. The community is here to listen. You can talk about anything at all relating to your experience and your perspective. Email hello@teencanceramerica.org or upload your own […]
There are a lot of different approaches that healthcare professionals take to address their AYA patients, but here are some of the most common issues that AYAs have with the way healthcare professionals talk to AYAs Teen Cancer America partners […]
C101 and C102 are a series of films to use as a teaching aid.
Filmed and edited by Alfie himself who was diagnosed with Acute Lymphoblastic Leukaemia back in February 2011. Alfie talks about the issues surrounding getting a cancer diagnosis as a young person, how the cancer treatment he received impacted on his […]
Meet Lauren who has been diagnosed with Papillary Thyroid Cancer. Initially Lauren was misdiagnosed after finding a lump on her neck, but as the lump grew Lauren went back to her GP who gave her a two week cancer referral. […]
Amazingly written poem by Anie who takes us through various cancer experiences in such an unique, beautifully put way.
We asked our filmmakers “What advice would you give to a young person newly diagnosed with cancer?” who were on hand to give newly diagnosed patients some excellent top tips from their experiences. To watch each filmmaker’s individual advice in […]