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    Looking at the Stars

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      Writing this book has made me realise that this is just the beginning. I don’t know how long I have on this earth, but I can promise you one thing: I’m going to make every day count. I want to travel the world and watch the Knicks play in New York, see a show at Caesars Palace in Vegas, try out surfing in Hawaii and go to the Paralympics to cheer on my peers. I want to learn how big charities become global and I want to beat KSI at FIFA. I want to have new experiences and help change the way people view disability everywhere. My illness gave me the ability to understand and help others, so that’s exactly what I’m going to do. Life may have dealt me a challenging hand, but I’m not ready to fold yet. I’m proud of my disability and, for the first time in my life, I finally feel like I’m living.

      ACKNOWLEDGEMENTS

      I WOULD LIKE TO SAY a special thank you to my mum, Emma Hine, and my sisters Chloe and Jessica. Their lives changed forever the day I was diagnosed with a brain tumour, but instead of feeling sorry for me or themselves, they helped me to fight, and encouraged me to follow my dreams. They sat for hours and hours during the process of writing this book, helping me to remember things. I couldn’t have done it without them.

      Special thanks also go to the Sophie Hicks Agency and Bonnier Publishing for believing in me and giving me this opportunity to share my story with the world. I was a big gamble, as I can’t read or write very well; but with the help of the amazing Charlotte Abrahams, I’ve done it. Charlotte sat on the end of a Skype call or phone and listened to my voice memos for so many hours I lost count; she was brilliant at rearranging our meetings at short notice around my seizures, and always noticing when I was tired and needed to stop. It must have been challenging working with me and around my illness, but she did, and it’s meant that my book has become a reality.

      In addition, I would like to thank the following people for their valued contribution to my book: Nan and Grandad Bicheno, Uncle Richard, Mike, Stephen, Alan and Auntie Marie, Callum Austin, Saffron Barnes and Izzy Colville, Elton John, Kid Ink, Tha Alumni Clothing, Nick Grimshaw, KSI, Jennie Jacques, BBC Breakfast, Radio 1 and O2.

      I would also like to thank the following who have helped me on my journey. Without them, I wouldn’t be here to write my book:

      Great Ormond Street Hospital

      Dr Varadkar

      Emma Ninnis

      Queen Alexandra Hospital Portsmouth

      Southampton General Hospital, especially children’s neurosurgery

      Mr Sparrow

      Dr Whitney

      Chrissy Ward

      Mandy, Kate, Shona and the amazing team at children’s neuro

      My healthcare workers, especially Matt Stevens

      Roslyn Ferguson

      Solent Mobility Centre

      Tech21

      Mark Smith and The Car Finance Company

      ActionCOACH

      Giant Leap Photography

      Manic Stage Productions

      Hotel Chocolat

      The Digital Awards

      Young Epilepsy

      Philip Haynes

      Leon Legge

      Marks and Spencer

      No Isolation and the AV1

      CBBC

      CTVC, especially Leonie, Will, Georgia and Emily

      Portsmouth City Council

      Portsmouth Guildhall

      Poken

      Medtronic Foundation

      Audrey, Jacob and team

      O2 and Mark Evans for believing in me, the amazing GoThinkBig team – Bill, Tracey, Kerry, Craig, Alex and Lilly – and the gang at the Think Big Hub

      Ajit Sharma, Elliott Lenton, Chris Buggie and Adrian Cunliffe from O2 Wifi for helping me meet Kid Ink

      Gary Lockwood and 24/7 Fitness for supporting Friend Finder and always being there for me.

      And finally, thanks to everyone who has attended a Friend Finder event. We couldn’t have done it without you!

      I was 17 months old when I had brain surgery to remove a tumour – I call this scar my shark bite!

      You can just see the drain coming out of my brain. My mum never left my side in hospital.

      Surgery probably saved my life, but it’s hard looking at someone so young in bandages.

      Me and Mum fundraising at the Mini Great South Run. I think I make a cool Superman (lol).

      Having my seizures monitored in Southampton General Hospital around the time that my epilepsy started.

      The Friend Finder Official logo.

      The Friend Finder team. From left to right: Eden, Billy, Jasmine, Eddie, Jess, Hannah, me, George and Callum on the floor.

      Me and Nick Grimshaw on stage at Wembley in front of 10,000 screaming teenagers – one of the best moments of my life!

      Appearing on the BBC Breakfast sofa to talk about Friend Finder was a crazy experience. Everyone was really lovely.

      What can I say? The man himself, Kid Ink, with Jess (left), me and Chloe.

      With Radio 1 DJ Scott Mills, who’s wearing a Friend Finder wristband, backstage at Wembley. How cool is that!

      Talking live on Nick Grimshaw’s Radio 1 show. Nick’s making me laugh!

      Me and Mum at the Digital Leaders 100 Awards dinner where Friend Finder won Mobile Innovation of the Year.

      Prince William was very kind and inspiring when I met him with the other Radio 1 Teen Heroes at Kensington Palace.

      At the palace with William and Kate, Radio 1 DJs and my fellow finalists. What a photo!

      An image from an epilepsy awareness campaign for Young Epilepsy and River Island. I felt privileged to do it.

      With my new stormtrooper friend at the Royal Albert Hall for the Star Wars premiere. I felt like a celebrity on the red carpet.

     

     

     



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