cancer

Saturday Afternoon

~ Naomi ~ Leave a comment

It’s Saturday afternoon and my Mum, Dad and brother are sat downstairs watching TV. After a few days of rain and a lot of days of grey, summer seems to have returned. The sun is shining, the birds are singing, it’s hot, there’s a nice breeze flowing through and a hum of lawnmowers in the air.

A year ago Mum would have been out in the garden tending to the vegetable patch. If she wasn’t there, she’d have been at her friend’s, playing their saxophones, baking something in our kitchen, or sitting outside with a book and a cold drink. She might have been doing the weekly shop, changing all the sheets or de-cluttering the kitchen. Whatever it was, it would have involved being on her feet, being busy, and not stopping until this evening. We probably wouldn’t have been allowed to be sat down either.

In fact on a day like today, around this time, my Mum would probably have come in from the garden, wiped her muddy hands on her gardening trousers, told my brother it was a beautiful day outside and he should get off the computer and join her out there, and gone to get a drink before heading out again (most likely dragging my brother with her). The door to the garden would remain open all day and the house would feel light and airy.

Today, the door to the garden is firmly shut and three faces stare at the TV screen. The sound of dramatic music can be heard throughout the house. None of us have ventured anywhere near the vegetable patch, we haven’t heard the saxophone in months, Dad has done the weekly shop so there are different foods in the fridge from what we were used to, and the kitchen remains somewhat cluttered.

This frustrates me. I want to walk into the lounge and shake everybody and tell them to get up and get outside and shout about what a beautiful day it is. I want to kick-start our family into moving again. Into having lunch before 2pm and getting up before lunchtime. This is not who we are and it is not what we do; we are active and engaged and busy all of the time.

Mum might not be able to do much but surely she can at least take her book outside?! (I asked Dad about this and it would involve taking her chair outside and be as much effort for Mum as walking half a street and she can only probably walk one street so realistically this isn’t so possible). Dad isn’t cancer-ridden, so surely he can do stuff? But he wants to spend Mum’s waking hours with Mum, which I guess makes perfect sense.

As for my brother, he’s young, fit and healthy, he should be doing stuff with his summer. Starting projects he’ll never finish, visiting friends, pretending to do his summer homework. I’ve thought about it though, and in a year’s time, he probably won’t be able to sit and watch TV with Mum. In fact, he probably won’t be able to in a few months/weeks. So maybe it’s okay for him to sit there with her, and maybe it’s what he needs.

And me? I’m desperately resisting this way of life, terrified that once I fall in I’ll never get out. I’m spending my summer working, revising and project-ing. I’m running every morning to get me out of the house and just keep my body moving. I’m cleaning every surface I can see (or as my Dad calls it, ‘drinking bleach’) and throwing away anything ‘unnecessary’ in my life. I bake and bake and bake and then drag my poor brother into the kitchen to do some more baking. I’m going into overdrive; a whirlwind of uni work, housework and paid work, before crashing into bed each night, absolutely exhausted.

None of us know what we’re doing. We’re all swimming in a cancer-ridden life, hoping that we won’t regret each decision we make. We are all trying to cobble together lives of ‘spending time with Mum’ and ‘carrying on as normal’, but often it’s like trying to join two pieces together from two different jigsaws. Thinking about all of this leaves me feeling frustrated, angry and upset. So I’m going to go and put that energy into making my bathroom as clean as it’s ever been. I hope you all have lovely Saturdays wherever you are, and if you’re able to, please make sure you get outside and enjoy the sunshine, even if it’s just for five minutes.

 

I Miss Our House Being Noisy

~ Naomi ~ 1 Comment

I’m privileged enough to have had a wonderfully happy house throughout my childhood and upbringing. It’s almost always been filled with activity, music, laughter and conversation. Barely a weekend would go by when we didn’t either have someone over, or visit someone’s house, and seeing friends of my brothers or parents who I didn’t know, sat in our kitchen or lounge, was an everyday occurrence. Mum played her saxophone (or foghorn, depending who you asked), Dad would play the piano, as would my brother, my other brother, my Mum and I would dance around the kitchen to Caro Emerald whilst baking and cooking. It was certainly never quiet.

Even a year ago, you’d never have known that Mum had terminal cancer. As a palliative medicine consultant, she was working pretty much full time with people who were at the end of their lives. She didn’t look like a cancer patient. She was on hormone treatment at the time, and her hair had grown back from the chemo she’d had during her first bout of cancer just 18 months before. We’d both get up on a morning while the male members of our family were still asleep, have breakfast, chat, and head our separate ways to work. On evenings we’d both return; tired but still keeping up with any household chores that hadn’t been attended to during the day (or asking other members of our family to do them). At weekends, we’d visit people or have people over. The house would be filled with laughter and chatter.

Not anymore. When I get up on a morning now, everyone is still asleep. I get up in silence, creep around the house getting ready for my run before returning, showering, and getting ready for work as quietly as possible. I walk through the door on an evening now and I see and hear nobody. It’s silent. Sometimes I’ll get a “hello” from my brother who’s revising in the office, welcoming me home, but that’s about it. I’ll walk through the house towards the bottom of the stairs and there’s no music coming from the lounge (which is now my parent’s second bedroom, from when Mum couldn’t get upstairs). I normally pop my head into the living room to greet Mum who will be sat in her chair watching TV; she doesn’t always hear me come in. Dad’s often sat in there, too. Upstairs will be my other brother, headphones on, watching something or listening to music. He used to spend his evenings on the computer in the living room, talking to us all, and I’m not sure when that changed – though I think that’s probably a teenager thing and may well be the most normal thing around here at the moment.

It feels like Mum is fading into her chair. I know that the whole dying-and-coming-back-to-life thing was clearly going to affect her, and you’re never quite sure how that will translate. But Mum’s always been so active and so sociable. People do come round to see her, but my brother and I can’t remember the last time she left our house/garden. Also, for someone who’s always been early to bed, early to rise (and told us off if we’ve been to bed late and got up late!), she now sleeps for around 15 hours a day; going to bed really late and getting up around midday most days.

I suppose change isn’t uncommon for someone with a terminal disease, but I underestimated the extent to which it would affect our family and our house. Mum getting up late means everyone else gets up late. The lack of Mum tidying up means nobody really tidies up. Her being less active means we’re all less active. Being at home feels like wading through treacle, everything just slows down. It feels harder to revise, harder to get up on a morning, harder to get dressed. Everything feels slow and drawn out.

Even though I’m not a superfan of Harry Potter, the best way I can think to describe it is like there’s a ‘Dementor’ living with us. Entering the house, I feel smothered and devoid of energy; filled with an overwhelming sense that something is wrong. I feel uneasy, unsure, anxious and depressed. The last couple of days, all I’ve felt like doing is crying.

I don’t feel able to write a positive post this week. I feel quite low – it’s tiring trying to stay on top of everything, and some mornings I just do not want to get out of bed. When I’m at home, I do my best to stay busy, to clean, tidy and bake when I’m not revising, and to spend time with my family as much as I can. At work I throw all the energy and love I have at the kids I look after. I’m incredibly lucky to have friends who are organising things with me so I have stuff to look forward to, because that’s something I sorely need right now. I’m thankful for all those people who are looking out for me, and recognise more than ever how precious and comforting small and normal things, from my brothers making fun of me to the constant struggle to locate the garage key, can be in the midst of all of this.

Featured: http://www.huffingtonpost.co.uk/naomibarrow/i-miss-our-house-being-noisy_b_7935278.html

Podcast

~ Naomi ~ Leave a comment

I recorded a podcast a few weeks ago with podium.me who work hard to share the voices of those under 25.

It’s now been published and you can find it here.

It’s basically just me having a chat with Beth, one of their journalists, about having a parent with terminal cancer.

Terminal Cancer Might Be Taking My Mum’s Body, But It Will Never Take My Mum

~ Naomi ~ 1 Comment

A few weeks ago, I was pottering around York, as I often do. I went into a gift-type shop (there are loads of them in York – you know the type I mean). I was looking for something specific , so was taking my time looking at each display when I saw a sign which read ‘the best Mums make the best Grandmas’.

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It hit me like a punch to the stomach and I had to leave the shop before I melted into a puddle of tears on the floor. As I paced around town, attempting not to cry, I couldn’t help feeling angry at the injustice of cancer in general, and Mum’s in particular. My Mum is awesome and would make an incredible Grandma. She’d love it, too. In the past few weeks she’s knitted three baby cardigans so that if/when my brothers and I have children, we would each have something for them ‘from Grandma’.

Almost every day at the moment, I see something that Mum’s not going to have, or be able to do, and it makes me want to cry. It could be going on a trip to Tesco and realising she probably won’t do that with us again, seeing graduation photos on Facebook with a parent proudly standing either side of their offspring, or coming out of my driving theory test and thinking about what we’d be doing if Mum was well (going to Starbucks for a Frappuccino and people-watching before heading to Primark for a bit of a splurdge.

People often say that ‘they can’t believe how well you’re handling this’, ‘you’re all doing so well’ or ‘I’d never know from your Facebook posts what’s really going on’. I don’t mind this because on the whole; we are managing well, and my Facebook is not a shrine to my Mum’s illness because I’m still living my life. But it doesn’t mean that I never feel angry at the injustice of it all and just want to punch a wall.

Over summer, I am a nanny to two wonderful boys. They’re seven and five and I’ve looked after them every school holiday for two years – it’s the best job I can imagine having at this stage in my life and is both fun and rewarding in equal measures. We baked a lemon cake yesterday (at their request!), and then today, we cycled to the park, pushed a big swing pretended we were in James’ Bond whilst spinning on a spinny thing, and fell about on the grass. I started thinking about all of this kind of stuff again.

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Knowing the boys as long as I have, and spending so much time with them every school holiday, means that we have a fairly solid relationship. I hug them, they hug me, we play fight, laugh, joke, and enjoy each other’s company. They’re not my children (despite many museum workers calling me ‘Mum’ in the past), but they’re good practice for if I ever have my own.

Baking is something my Mum taught me as a child. She spent hours teaching me how to use a mixer, how to break eggs, and how to remember various recipes. Teaching the boys how to bake is a joy, and they get better each time we do it – they’re pretty good at it now, and love it just as much as I did at their age. Going to the park is something my parents and I did a lot as when I was a child. They must have spent hours pushing me on swings and helping me conquer climbing frames.

My entire attitude towards children and the skills that I pass onto them come from my experiences and upbringing, and especially from my parents. My Mum probably won’t be there in person if I ever have kids – I probably won’t be able to beg her for some childcare favours when I need some sleep. But so much of my Mum is in me, and has shaped who I am, that in some small way she will be there – and that’s something that cancer can never take away.

Each time I let one of the children lick out the mixing bowl, they receive some of my Mum’s baking passion. Whenever they fly high on a swing, they’re experiencing some of Mum’s joy through my own love of parks. Whenever they’re making stuff, I hope they’ll experience some of Mum’s patience for my various crafting endeavours, something I do my best to remember when I have to iron countless Hama bead creations, or make multiple loom band animals.

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Cancer might be taking my Mum’s body, but it will never take my Mum. It will never take all the things she taught me (not to mention other people), the impact she’s leaving in the medical world, or the impression she’s made on everyone she’s ever met. Cancer can’t take her love for me and my brothers, her pride in what we achieve, or her hopes and dreams for our futures. Cancer can’t destroy the memories I have of her and our family, of holidays, hill climbing and funny voices when we read bedtime stories as kids.

Cancer makes no sense on an emotional level, and I don’t think it’s something I will ever truly understand. But, when I find myself on my bum in the middle of a park having lost a play fight with two adorable boys – I know that my Mum, her attitude of always getting ‘stuck in’ and her willingness to do anything with the three of us, however silly it might make her look, will always be with me.

Featured: http://www.huffingtonpost.co.uk/naomibarrow/terminal-cancer_b_7899680.html

Hope Is a Special but Fragile Thing

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I actively avoid thinking about the future most of the time. Part of this is because it sends me into a blinding panic of attempting to work out how I will ever get a job and afford a house and a cat (yes, it’s an essential item) and change lightbulbs and work out how to pay bills and all that terrifying “adult” stuff. I reckon these are fairly common worries for people my age… but the main reason I avoid thinking about the future is because Mum won’t be there, and why would I want to imagine or think about a life without my Mum?

This complete mental block about the future has been making life a little difficult lately. I can think a couple of days ahead, and I can put things in my diary a couple of weeks in advance if I know I’ll be able to cancel if I have to, but that’s about it. Try to imagine what it’s like to be unable to think about the future. Firm summer holiday plans are out of the question, and anything further than that is impossible: vague plans for Christmas, career or promotion ideas, dreams of living in another part of the country… Thinking about these things is a luxury that, for now, I don’t have.

It makes it hard to make good decisions daily. Only when you stop thinking about the future do you realise how much keeping it in mind affects your daily decisions. Eating healthily, exercising daily, going to bed on time, revising for an exam; in making all of these decisions, we factor in the future. If I knew I had no future beyond today, I’d probably stay up late and eat a tonne of chocolate… I definitely wouldn’t bother revising.

On Saturday, I went down to London for a session with Team v – a programme which takes 100 young people from around the country and works with them over nine months to lead three social action campaigns. I have been on the Team v programme since August 2012 (just before Mum was diagnosed the first time), starting out as a leader, and eventually graduating to be a senior mentor. This programme is the only thing which has been a constant in my life since Mum’s original diagnosis. The circumstances of my education, job, friends and family have all changed, but this has always been there and the people I have met through it are amazing.

Unfortunately, the programme is coming to an end this summer, the funding is ending. For me, and many others, this is a huge loss. In the same way that I don’t think about a future without Mum, I’ve been trying not to think of a future without Team v.

I’ve had times in the past three years when I’ve felt completely hopeless. Mum’s been ill and things have seemed dark, but because of Team v, I have stood up and spoken to a room of 100 young people excited about changing the world… it has lifted me up, and given me hope. When Mum was in hospital in February, I got a surprise bunch of flowers and a card from my Team v family, showing me that even though my friends are scattered around the country, they care about me, they’re there for me, and they understand. We have a strong bond spanning the length and breadth of the country, and despite the programme ending, that will always remain.

This Saturday, we were consolidating what we’d learned over the years we’ve been involved in the programme. We did activities which involved thinking about our own personal strengths, and speaking about the strengths and personal qualities of others. The first part of this is immensely difficult for me – like many of us, I can easily see positive qualities in others, but I struggle to see or articulate my own.

I left the day absolutely exhausted, but happy. I’m going to miss this programme so much, it’s made an incredible difference to my life (something I will write more about on my personal blog sometime over the next few weeks). But even though there will be no more leaders coming through Team v, no physical office space, and no staff working on it, it’s not disappearing completely. It will always be in my heart and in the hearts of those who’ve been involved in it. I will never forget the things I’ve learned or the people I’ve met through it. Furthermore, there are around 350 young people around the country who’ve been through the programme and who are going to continue to make a difference in their communities, and that gives me hope.

Being back with these people on Saturday gave me hope for the future for the first time in a very long time. It reminded me that though it may be a life without my Mum, there is a life waiting for me. Whatever happens outside of me, I am still me and I can still achieve amazing things. Hope and gratitude are so fragile, but so important. I am grateful for the brilliant people around me who lift me up, inspire me to hope for the future, and be the best version of myself that I can be.

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Some of the Team v mentors, never missing the opportunity to dress up or take a selfie.

Featured: http://www.huffingtonpost.co.uk/naomibarrow/cancer-hope_b_7736224.html

Cancer: An Organised Person’s Worst Nightmare

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It’s that time of year again when everyone seems to be planning something. Plans for summer, post-graduation, jobs and housing… plans of moving away, plans of coming back; talk about travel to far-flung and interesting places. Everyone is beginning to look towards the future, planning what they want to do, what’s achievable and in many cases, what they can afford. People are signing new rent contracts, starting new jobs or internships, and there’s a general buzz of change in the air.

Ever since Mum’s diagnosis, we have tried to keep life as normal as possible and on the whole, I think we’re doing a pretty good job. One thing that we constantly struggle with though, is planning. Despite what books and movies say, cancer is not linear or predictable, and Mum’s has often proven even less predictable than most. You can’t plot it on a graph, and doctors can’t tell you exactly how long you have left to live – at least that’s our experience of it. One week Mum can show no warning signs at all; the next week her immune system, weakened by chemo, might fail to stop a common cold resulting in a hospital admission for a week being pumped full of antibiotics.

A few weeks ago, Dad was trying to give our extended family numbers of how many of us would be able to attend the family holiday in late August. I’m easy – I have an almost full time summer job and it’s over the university resit period (I’m taking one of my exams then as I couldn’t catch up all the work in time after missing lectures when Mum was in hospital), so I can’t go. My youngest brother and Dad are going. My other brother has prioritised Christian camp over family, apparently. As for Mum… we don’t know whether she will be with us then. We don’t know if she will be fit to travel then (if she’s not then Dad won’t go either, nor will my brother). She might be absolutely fine and happy to join them all at that point. So there we go, anywhere between 0 and 3 of us might attend that week. Imagine how hard that is for financing and planning the holiday!

For me, the lack of ability to plan is one of the hardest things with this cancer situation. I’m someone who likes things to be organised and planned. I live by my diary, own a ‘to do’ list book and print timetables to plan other things. I have friends who are doing internships and travelling this summer and every week the careers people email me with #YouNeedWorkExperience stuff. I love my job and wouldn’t change it for the world, but I didn’t feel I had the option to get an internship this summer for fear that Mum would go into hospital and I’d have to let them down. I don’t feel able to book a trip away for a week in case Mum deteriorates and I’m not there. Everything that I’m planning has to have a back-up plan for if I have to head home.

My last year of university is coming up and people are beginning to think about jobs, masters degrees, grad schemes, you name it. I’m looking at the next year and thinking that I hope Mum doesn’t deteriorate around an important deadline. I hope I can get through third year without mitigating circumstances and that I can graduate at the same time as my friends. I’m thinking that once I have (hopefully) graduated, I need to get a job (or further study) somewhere around here because this is where my support system is and Mum’s either likely to be very poorly or not with us this time next year, so I’m going to need those people around me.

The worst bit of all of this is that I find myself wishing that it was all over. That I could just get back to ‘normal’ life and be able to move on. But then I remember that this only ends one way: Mum dies.

As hard as this is, at least Mum is still here. At least I can still ask her for advice when I’m stuck and give her a hug when I’m struggling. At least, for now, she’s still at the end of a phone or an email. At least my Mum is still here to help me through it.

Featured: http://www.huffingtonpost.co.uk/naomibarrow/cancer-an-organised-persons-worst-nightmare_b_7690034.html

Crying Is Not Weak

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On Sunday, I ran the Race for Life with a few friends. It was great, the atmosphere was fantastic, we raised a good amount of money, and Mum was there to watch us go (something we could never have imagined a few months ago).

Sunday evening came along and I began to struggle with the reality of Mum’s condition again. While I’m at uni, I’m in a bit of a bubble. Yes, I know Mum’s ill, and that never goes away. I’m always waiting for the phone to ring and not a day goes by when I don’t think about it; but I’m shielded from many of the day-to-day impacts that cancer has on Mum and home and family life. Being at home is different – I have no choice but to confront it; she has limited mobility, she is more tired, and she is visibly unwell.

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When I got back to uni this Sunday, the pictures of the race began to appear on Facebook. There are some absolutely lovely photographs, capturing lots of really special memories. However, when I loaded them in my photo editor, they came up alongside one from last year’s race. Mum looked like any other 50-something year old woman. She’s standing next to me, taller than me, and we’re both smiling and laughing at the camera. This year we’re still smiling and laughing, but Mum’s in her wheelchair, has lost weight and is rocking the post-chemo hair (it will be the next in thing in Vogue, just you watch…). It’s horrible to see someone you love deteriorate so starkly before your eyes like that, and understandably, I’ve been feeling slightly more fragile than usual for the past few days as a result.

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I’m trying to accept that it’s okay to be upset, that it’s okay to cry. To most it would seem a fairly natural reaction to cry when someone you love is dying. I remember the Monday after I found out Mum’s diagnosis, I saw someone from the uni welfare team and they asked me why I wasn’t crying (I shrugged whilst mentally responding that I was on a new record of 4 hours no crying since finding out Mum’s diagnosis and would happily cry again if that would please him). Logically, I know that crying is okay and that it is a normal reaction to death, illness, and anything else difficult in life, but sometimes I find it difficult to do.

I don’t think I’m alone in this. I think many of us struggle to cry or to show we’re upset. We feel like other will see it as a sign of weakness. I think we often judge ourselves if we cry and view ourselves as weak – I know I do. But I’m slowly learning that crying, or being upset, is not a sign of weakness – they are simply emotions like any other. They are natural human reactions to difficult situations. Everyone has times when they are upset, when they cry, when they completely break down and sob into their pillow. Every single human on this planet has cried at some point in their lives. Not only is that normal, but it’s completely okay. These difficult emotions deserve to be felt, and hard as it is to sit with them and experience them, it is important and healthy to do so.

I don’t think we should be ashamed of being sad or upset. I’m not saying we should cry all the time (that would be highly unproductive and a bit weird), but when we need to, and when the time is right, I don’t think we should be afraid to just let it out – whether it’s with a friend, with a teddy, on your own, or watching the final episode of Gilmore Girls one more time because it’s just too perfect. Crying is not weak; it’s simply a release of the built-up, difficult emotions that you’ve been holding onto for too long.

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Featured: http://www.huffingtonpost.co.uk/naomibarrow/crying-is-not-weak_b_7607958.html

Race for Life 2015

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On Sunday, I’m taking part in the Harrogate 5k Race for Life with four of my friends as ‘Team Fiona’, named after my Mum. These lovely people have stuck by me since Mum’s diagnosis providing listening ears, a comfy sofa and unlimited hugs. Each of us has our own reasons for taking part so here’s a quick post to share with you all why this race is important to us.

RFLBBeth: I’m taking part in the Race for Life for Cancer Research UK to raise as much as possible for this amazing charity. In the UK, one in two people born after 1960 will get cancer during their lifetime. I’m not great at maths, but that’s half of us. In the 1970s, only a quarter of people survived cancer. Today, more than half will survive for at least ten years all due to excellent research funded by charities like Cancer Research UK. Let’s make sure this progress continues!!

RFLGGrace: I’m taking part in the race for life for two very special people I know who are currently battling cancer, Fiona and Graham. Such events raise awareness and much needed funds, uniting the nation in the battle against cancer. I will feel proud to run the race for these two incredible people and hope that our efforts will one day help to eliminate this devastating disease.

RFLHHarri: I’ve known the Barrow family all of my life. Naomi and I have been friends since we were weeks old, so I can’t remember a time without her, and Fiona, in my life. It’s very important to me to run this race to prove to Fiona that I can do it. I also want to raise money so that Cancer Research can keep researching treatments and less people die from cancer in future.

RFLNNaomi: I ran the race for life with Grace last year and it was awesome. I wasn’t sure that Mum would still be with us for the race this year, but she is and that’s even better! Whilst running this race is not going to ‘cure’ Mum, it makes me feel like I’m doing something in what can often seem like a hopeless situation. I hope that raising money for Cancer Research, will enable them to continue their work, so less people receive the devastating news that someone they love is going to die from cancer.
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Sarah: The reason I’m running is because there’s no reason not to. It’s such an amazing experience to know that the money you raise WILL help people. I’ve never been involved in a charitable cause where the support for it is so unified before. Everyone is affected by cancer; directly or indirectly. So there’s no reason not to support the cause. But I want to live in a world where cancer is rare, not expected and not just accepted as what happens.

Now that you know why we’re doing this, please consider sponsoring one (or all!) of us for the race this Sunday. Any donation, big or small, helps Cancer Research to continue their incredible work. For our individual fundraising pages, please click our names. Our team page is here. You can also donate to my page by texting ‘RFLN94 £[amount]’ to 70070.

Carers Are Hidden Heroes

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Carers Are Hidden Heroes

At the moment, there seem to be a lot of days and weeks dedicated to raising awareness of various issues (or celebrating donuts), encouraging people to share their stories and tag their friends. But how much awareness can be raised before it all fizzles into a blur of “share this”, “read that” and “use this obscure hashtag please”?

This week is carers week. I think it’s important to highlight this because carers are amazing. They are hidden heroes who care for loved ones day and night, often without a break or a holiday away from these responsibilities.

There are almost seven million carers in the UK of all ages, genders and ethnicities and that number is rising: at some point in their life, three in five people are likely to be a carer. Currently, about 700,000 of these carers are young people – children and teenagers who are caring for a parent, sibling or someone else every single day. Though many of these children wouldn’t wish to lose this responsibility entirely, because they love the person they’re caring for, it can mean that they lose aspects of their childhood; time that should be spent playing with friends or being a kid is spent instead shouldering more responsibility than any adult could reasonably ask of a child.

You can’t tell that someone is a carer by looking. They often go unnoticed, quietly getting on with things. Many might not even recognise themselves as carers, so their friends and family are almost certainly not going to pick up on it. Despite the lack of recognition, they carry on every single day; administering medication, completing personal care, cooking, washing, cleaning, and more. All of these things would cost a fortune if a care worker had to be employed to do them, but carers do them every day with no regular wage (apart from potentially some carer’s allowance). Unlike a paid worker, there’s no annual leave, no bank holidays, and no TOIL. Carers save our country huge amounts of money by simply loving and caring for a family member or friend.

My Dad is a carer – he cares for Mum. We’re lucky in that Mum is relatively independent at the moment, she can do most things herself. But she still needs help here and there, and that’s where Dad comes in. Sometimes I imagine Mum finds it difficult to accept this help, because she’s always been incredibly independent – imagine how frustrating it must be to realise that the simple things you’ve done yourself for your whole life, the smaller things you really take for granted, you now can’t do without help.

I wouldn’t class myself as a carer; I’m at university, so the only person I’m really looking after is me. I do worry about Mum, I keep in touch with everyone at home as best I can, and I’m forever waiting for the dreaded phone call, but I don’t have any regular caring responsibilities.

When I’m home I try to help where I can: walk behind Mum when she’s walking up the stairs, help her to reach things, cook and clean, other bits and bobs like that. But I don’t see it as an ‘extra’ or ‘caring’ responsibility; I see it as part of family life. I imagine many people who are carers feel the same and that is why they so often go unnoticed.

Keep your eyes open this week (and beyond). If you know someone who is a carer, or you think someone you know might be a carer, make contact with them. It’s hard to maintain friendships when your life revolves around medication charts and routine meal times. Invite them round for coffee, or go round to theirs. Ring them for a chat, drop them a Facebook message. Don’t go overboard by any means, just initiate contact. It doesn’t cost anything but will mean the world to someone who is tirelessly caring for someone they love.

Carers are incredible, they really are. They are hidden, hardworking and humble. Please try and notice them this week. Please reach out to them. If anyone deserves an hour of your time, it’s them.

Featured: http://www.huffingtonpost.co.uk/naomibarrow/carers-week_b_7536544.html

Making Difficult Decisions

~ Naomi ~ Leave a comment

University is about more than just a degree. It’s about making friends, trying new things, and becoming independent. Personally, I love it. It’s given me a chance to escape from my teeny-tiny village (you can’t walk down the street without every man and his dog knowing about it the next day), and brought some fantastic opportunities. A major part of it for me has been about moving away from home. I’d taken a gap year prior to uni where I stayed at home working for various charities, and as much as I enjoyed it, I was looking forward to spreading my wings and having a chance to indulge in some self-discovery.

Despite some homesickness, I only went home a few times during the first term of my first year. By Christmas, I was more than ready for some TLC and a break from washing up but going into second term, I was determined to be more independent, go home less, and rely on my parents less. Then Mum was diagnosed, and that changed.

Half of me desperately wants to be a ‘normal’ student. To abandon my parents, make stupid mistakes and stay up too late most nights. I want to join my friends on nights out, spend weekends exploring the city and forget about my life back home.

The other half of me is different. At the time of diagnosis, Mum had somewhere between four weeks and four years to live (I know in movies they always have a definite length, but that’s not how it is in real life). My friends will probably have their parents waiting for them when they graduate. They can forget their Mum’s birthday, lob some flowers in their general direction a week later, and hope that makes up for it. If they get pregnant, they can reach for their Mum every time something freaks them out. Once their family has grown, they can visit with the grandchildren, using their parents as free babysitters (it’s cheeky, but it’s allowed, right?).

But for me it’s different. Mum probably won’t still be here when I graduate. She will probably die whilst I’m still at uni. I have to cram twenty or thirty years of visits into twenty or thirty days/weeks/months. I have to ask all my questions now; predict what I might want to know in years to come. Each birthday might be Mum’s last, so rather than forget it I want to make it special.

Should I continue to be as independent as possible and stay away from home, or should I return most weekends and spend time with my Mum? Should I spend my evenings binging on TV shows with my friends until 2am or making memories with my family? Will I regret not spending more time with Mum when she dies… or will I regret not spending more time at uni when I graduate?

There is no right or wrong answer to this. There isn’t a guidebook. There’s nobody to tell you what to do. Uni is different from school where you come home and see your Mum each night. It’s not like work where you’re home evenings and weekends (and even if you have your own house you can probably drive and visit your parents). University is an all-encompassing bubble and (for most) a once in a lifetime experience.

Every day I question my decisions and most nights I worry about whether I’m getting it ‘right’. Currently, I spend most of my time at uni, but speak to Mum on a regular basis. I go to her when I need advice or have a stupid question, and being able to do that is so wonderfully special. When I see her I cherish those moments and we take tonnes of photos.

Nothing is permanent in life and I’m lucky to have the chance to prepare for my Mum’s death where many don’t. That doesn’t make it any easier, but it’s something I have to be thankful for. Every day we all have to make decisions; some are bigger than others. I just hope I’m making the ‘right’ ones.

Featured: http://www.huffingtonpost.co.uk/naomibarrow/terminal-cancer-planning_b_7467058.html