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.
Jesse was diagnosed with Anaplastic Large Cell Lymphoma just after his ninth birthday. After spending over six and half years in remission, Jesse relapsed and had to have more treatment. We hear from Jesse who talks about the impact cancer […]
Manchester are off to the Royal Albert Hall to see One Republic, this short film shows us their day including a meet and greet with a few celebs!!!
Luke was diagnosed with Desmoplastic small-round-cell tumour, a rare cancer. After various surgeries and months of chemo and radiation he’s been in remission for 4 months. A big racing car fan, Luke is enjoying the post hospital life and getting on […]
Filmed and edited by Tom through jimmyteens.tv media training programme. Tom was in his final year at university when he noticed swelling on one of his testicles. Tom put off visiting a GP originally as he didn’t want anything to […]
Andrew is officially two years out of treatment a day he and his Doctors thought might not happen. Today, Andrew finally got rid of his port-a-cath which has made Andrew feel like he is finally free from his cancer treatment. […]
New Mum, Naomi was diagnosed last November with a rare form of cervical cancer. Naomi found out that she had cancer when she had a C section after the birth of her first child. During her 5 months of chemotherapy, […]
Jordan is back! We catch up with Jordan in hospital who is having his 16th transfusion and see the preparations for Jordan’s upcoming radiotherapy. Jordan also speaks about how he and his parents recently moved house to Brisbane which has […]
It’s been seven years since Katie was first diagnosed with CML, Katie discusses why she feels it’s important to remember her cancerversary and talks about her upcoming big decision, whether to try a new chemotherapy drug which understandably Katie has […]