A large group of family, friends and colleagues have come together to fundraise in memory of my young son Max, who sadly passed away in his sleep due to a sudden heart arrhythmia linked with Dravet Syndrome. Max was 22 months and lived life literally to the Max !

Max was a perfectly normal little boy who was walking, talking and enjoying life. Max had a genetic form of epilepsy which he probably would have outgrown and seizures only came through when he was under the weather. Max's seizures were tonic clonic, (full body seizures where he would lose consciousness) and in a child of his age these seizures were difficult to control with some critical short stays in the Poole General Hospital Children's High Dependency Unit. The doctors and nursers who looked after Max are wonderful.

Please join us for one or two of our scheduled events, your support would be greatly appreciated. If you would like to help or sponsor us, we would be delighted, please get in touch. Our Calendar of Events can be seen if you click on the tab above.

Thank you for your support and thank you for having a look at our site,

Max's Mummy, Gail