Making a difference - One Individual at a time

The RGF – Making a Difference to Max and his Family.

We recently received an inspiring update from Max’s mum, Liane, updating the RGF and all our supporters, on his progress.

Liane said: “I just want to say thank you again. Every time I see Max like this all settled at his appointments (see photo) I think of you guys and feel so grateful – The iPad has been an absolute godsend.”

Last year, the RGF granted Max an iPad to use during his treatments to keep him stimulated; an effective distraction through watching his favourite tv programmes and videos and playing games to while away the time.

RGF trustee, David Cant said: “Three-year-old Max has a Glioneuronal brain tumour and had 85% removed in March 2023, only for the tumour to start growing again in June 2024. Max is now on oral medication that he takes every 12 hours, and his treatment also involves numerous hospital appointments for blood tests to monitor his progress. Max has a scan in February, and I know we’re all joining his family in praying it will be good news. Liane assures me that Max has few side effects and is a little warrior.”

Thanks to your support, the RGF continues to make a difference to many young people across the UK, and Max is the perfect example of what that means!