nervous system. I know this is very difficult to hear, but things are progressing more quickly than we first thought.’
I look at him. ‘Things?’
He shifts on his chair. ‘You’ve moved further along the line, Tessa.’
There’s a big window behind his desk, and out of it I can see the tops of two trees. I can see their branches, their drying leaves, and a bit of sky.
‘How much further along the line have I moved?’
‘I can only ask you how you’re feeling, Tessa. Are you more tired, or nauseous? Do you have any leg pain?’
‘A bit.’
‘I can’t judge it, but I’d encourage you to do the things you want to do.’
He has some slides with him to prove the point, passes them round like holiday snaps, pointing out little splashes of darkness, lesions, sticky blasts floating loose. It’s as if a child with a brush and too much enthusiasm has been set free with a tin of black paint inside me.
Dad’s trying unsuccessfully not to cry. ‘What happens now?’ he asks, and big silent tears fall out of his eyes and plonk onto his lap. The doctor hands him a tissue.
Outside the window, the first rain of the day spatters against the glass. A leaf caught by a gust of wind rips, then flares red and gold as it falls.
The doctor says, ‘Tessa may respond to intensive intrathecal medication. I would suggest methotrexate and hydrocortisone for four weeks. If it’s successful, her symptoms should improve and we can continue with a maintenance programme.’
The doctor keeps talking and Dad keeps listening, but I stop hearing any of it.
It’s really going to happen. They said it would, but this is quicker than anyone thought. I really won’t ever go back to school. Not ever. I’ll never be famous or leave anything worthwhile behind. I’ll never go to college or have a job. I won’t see my brother grow up. I won’t travel, never earn money, never drive, never fall in love or leave home or get my own house.
It’s really, really true.
A thought stabs up, growing from my toes and ripping through me, until it stifles everything else and becomes the only thing I’m thinking. It fills me up, like a silent scream. I’ve been ill for so long, puffed up and sick, with patchy skin, flaky fingernails, disappearing hair and a feeling of nausea that permeates to my bones. It’s not fair. I don’t want to die like this, not before I’ve even lived properly. It seems so clear to me. I feel almost hopeful, which is mad. I want to live before I die. It’s the only thing that makes sense.
That’s when the room comes sharply back into focus.
The doctor’s going on about drug trials now, how they probably won’t help me, but might help others. Dad’s still quietly crying, and I stare out the window and wonder why the light seems to be fading so quickly. How late is it? How long have we been sitting here? I look at my watch – three thirty and the day is almost ending. It’s October. All those kids recently returned to classrooms with new bags and pencil cases will be looking forward to half term already. How quickly it goes. Halloween soon, then firework night. Christmas. Spring. Easter. Then there’s my birthday in May. I’ll be seventeen.
How long can I stave it off? I don’t know. All I know is that I have two choices – stay wrapped in blankets and get on with dying, or get the list back together and get on with living.
Ten
Dad says, ‘Hey, you’re up!’ Then he notices the mini-dress I’m wearing and his lips tighten. ‘Let me guess. You’re seeing Zoey?’
‘Anything wrong with that?’
He pushes my vitamins to me across the kitchen table. ‘Don’t forget these.’ Usually he brings them up on a tray, but he won’t have to bother today. You’d think that’d make him happy, but he just sits there watching me swallow pill after pill.
Vitamin E helps the body recover from post-irradiation anaemia. Vitamin A counters the effects radiation has on the intestine. Slippery elm replaces