The Brain Tumour Charity Lifeline


The Brain Tumour Charity

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My name is Tom Daley,

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and this is my dad, Rob.

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He was my biggest supporter,

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the driving force behind my career,

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there at every event, cheering me on.

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But most of all, he was my best friend.

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In 2011, my family's world came crashing down.

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Dad had been diagnosed with a brain tumour five years earlier,

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but, despite having successful surgery,

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he was told it had come back and the prognosis was bleak.

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Always the fighter,

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he vowed he would make it to the Olympic Games in 2012.

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It wasn't to be.

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Dad lost his battle in May 2011,

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when he was just 40 years old.

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Losing a parent at any age is absolutely devastating.

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You can feel like you've nowhere to turn.

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But the Brain Tumour Charity were an incredible support

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for me and my family during one of the toughest times in our lives,

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and I'm so proud to say that they've supported thousands of people

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around Britain who've been through the same thing as my family.

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Right, let's go. Come on, then.

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I am definitely a busy person.

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When I'm not out dancing,

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then I'm out walking with my dog, Skye.

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Angela is 27 years old, and six years ago,

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she received life-changing news.

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I was in my final year of uni when one night,

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I was just lying in bed and suddenly had this immediate,

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excruciating headache. Just, like, bang.

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You know, out of nowhere.

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I was saying, "Help, something's wrong, but I don't know what."

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So we rang the NHS number

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and they said it was likely a migraine

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but they were going to send an ambulance, just in case.

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Feeling reassured her symptoms were probably stress-related,

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Angela went along to a local hospital to be checked over.

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But as time went on, she began to feel worse.

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I was surrounded by seven doctors, all around my bed.

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And one of them held my hand and said,

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"OK, we've looked at the CT scan

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"and we've realised that you're having a brain haemorrhage."

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And from there, they realised that I had a slow-growing brain tumour.

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And then the doctor said, "In our opinion,

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"the best thing to do would be just to leave it because

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"there'd be far more risks to opening you up and having surgery."

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So I had five years of MRI scans,

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until 2015, when the scan showed

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that it was actually beginning to grow again.

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And at that point, my neurosurgeon said, "Now we need to operate."

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I'd gone from being, you know, Miss Independent

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and travelling here, there and everywhere with my job

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to suddenly not even being able to wash my own hair or put my socks on.

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Having six months off after my surgery, it really gave me

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some time to kind of think about things

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and think about the potential symptoms of the past.

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When I was 14, I struggled a lot with weight and I was very nauseous.

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Looking back now, I know that nausea is one of the signs and symptoms.

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Potentially, that was maybe a symptom of the brain tumour.

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The symptoms associated with brain tumours can be

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so easily mistaken with those of other illnesses.

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To tackle this,

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the Brain Tumour Charity launched a campaign called HeadSmart,

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which aims to raise awareness of the common symptoms

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of brain tumours in babies, children and teenagers.

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Since it began, the average time to diagnose childhood tumours

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has been halved from more than 13 weeks to just six and a half.

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And it was because of HeadSmart that Rosie was able to get

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her son, Daniel, treated quickly.

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Daniel was about three when he first became unwell.

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Prior to that, he'd been a very happy, cheerful little boy.

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And it was in the Easter of 2014

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that his personality started to change.

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He began to have tantrums, being quite grumpy.

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I dismissed most of the changes as either, "It's just a little bug,"

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or "He's just growing up,"

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or "It's just him being a normal little boy."

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He really started then to become physically unwell,

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and vomiting in the morning on waking.

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I didn't think anything of it at that time,

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and it was when he vomited again in the morning,

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and that's when I remembered the HeadSmart card

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that I'd seen previously, which made me think about

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the symptoms of a brain tumour.

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You always have it in your head, "Maybe I'm overreacting,

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"but I do really need to take him to the doctor

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"and get him checked out, really."

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And at that point, the doctor said they that would refer him,

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and obviously, that really worried Rosie, when they said that.

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I just really stressed all the symptoms that I knew

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he was showing, and I knew from the HeadSmart campaign.

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And they immediately sent him for a CT scan.

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I think it was half an hour later

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they sat us down and told us what it was.

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And I went from being, trying to be the,

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"Oh, it's all going to be fine," to being a complete wreck.

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I was a mess.

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Daniel's tumour was the size of an adult's fist

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and had caused a build-up of fluid on his brain.

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The doctors had to rush him into surgery within hours

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to remove the growth.

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Your job as a parent is to protect your kids from anything

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that might come along in their life and hurt them.

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And it's just that realisation of knowing

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that you're helpless in this situation,

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there isn't anything you can do to make it better for them.

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The early diagnosis of brain tumours can save lives

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and prevent serious disability.

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Daniel's story is proof that HeadSmart has helped people

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to spot the signs and get their children the treatment they need.

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And now, the charity wants to do more.

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Here at Edinburgh University, Dr Paul Brennan is heading up

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pioneering research funded by the Brain Tumour Charity.

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We know the HeadSmart campaign has been a great success.

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We're hoping to be able to achieve the same impact for adults

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with brain tumours, and the funding from the Brain Tumour Charity

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is going to help us to achieve that.

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We're using patient data from across the UK to really understand

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the spectrum of the problem of early diagnosis.

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We like to see a time in the future when patients can be confident

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that when they go to their general practitioner

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or to the hospital with symptoms,

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that those people who are most likely to have brain tumours

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have the investigations as quickly as possible,

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and that that leads to earlier treatments

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and hopefully better outcomes.

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I can say without a shadow of a doubt,

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if it wasn't for the fact that I'd seen the HeadSmart card,

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Daniel wouldn't be running around, playing with his sisters now.

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They saved our little boy's life, and if they didn't do what they did,

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Daniel probably wouldn't be here now.

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Daniel's latest appointment, we were told that his scan was great, it was

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all clear again, they're happy the tumour's not going to come back.

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So he has basically been given the all clear, really.

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I'm so glad that my mum knew about HeadSmart,

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and they made me better.

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Keen to help others after her own experience, Angela has become

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a staunch campaigner for HeadSmart along with her friend, Natalie,

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and together, they hand out cards to local pharmacies and opticians.

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We got some up-to-date HeadSmart cards.

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We actually met at a support group for young people going

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through things like brain tumours.

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We kind of became friends and became a force for fundraising

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and awareness raising, as well.

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These are aimed at...

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These HeadSmart cards have saved, so many lives already

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and I just get so important to get the message out there

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and also to stop other people going through the same as what

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me and Angela went through.

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You never know who's going to be at the receiving end of the card

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and what the impact would be.

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Over 100,000 people in Britain live with a brain tumour.

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And, speaking from first-hand experience, it's devastating.

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But together, we can defeat the disease.

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With your help, we can fund vital research, reduce diagnosis times,

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and one day, stop families from wondering, what if?

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My dad couldn't be saved,

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but there are people out there like Angela and Daniel who can.

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Please help this great charity and donate now.

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To give by phone, call...

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Calls are free from mobiles and landlines.

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Texts cost £10 plus your standard network message charge,

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and the whole £10 goes to the Brain Tumour Charity.

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For full terms and conditions,

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or to make a donation online, visit the Lifeline website.

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Or, if you would like to post a donation,

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please make your cheque payable to the Brain Tumour Charity

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and send it to...

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..writing "The Brain Tumour Charity" on the back of the envelope.

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Thank you so much.

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