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.
Time for a quick history lesson on all things JTV Cancer Support and find out why we were originally called jimmyteens.tv!
Rebecca tells us about the five signs of cancer which are persistent/unexplained pain, lump (bumps or swelling), significant weight loss, extreme tiredness or changes to a mole. Rebecca also talks about how important it is to visit your GP if […]
Brain tumour patient Peter talks about how his body image issues have affected him throughout his life including through his cancer diagnosis. Peter talks honestly about how he’s tried to take control of food as he feels like he can’t control other […]
Shelbee chats about her cancer and talks about what her plans were before her cancer diagnosis, Shelbee also fills us in on what she plans to do now after treatment.