Showing blog posts tagged with: cancer

Shana tova

by Hilla Duka - View comments

Applehoneypot6_fotor

This week was the Jewish new year, Rosh Hashanah, and though I don’t normally fuss much unless my dad’s around, this time it felt important to celebrate. It also happened to coincide with me being half way through treatments, also worth celebrating. It’s a whole new year, 5775, and I hope so much that it will be a sweet year, a year of better news, than last year. As is traditional, we dipped our apples in honey, and I might have prayed more fervently than usual for a sweet, happy year for all of us.

 

Rosh Hashanah is followed by ten days of atonement, and though I’m not religious, these days have always held a special place in my heart, mainly because they make so much sense to me. The days that follow new years is a time for reflection, looking back on the year that passed, on your actions. It’s holding yourself accountable for the mistakes you’ve made, and apologising to the people you’ve mistreated. The idea is that god enters the names of those who will live on new years, but gives people these ten days to change his decision. If you’ve atoned, repent, and done good deeds, he can still change his mind and put your name down for the year to come. Needless to say, this year the holiday holds a new meaning to me.

 

So these past few days, I’ve spent looking inwards, trying a bit harder than other times to align who I want to be with who I am, how I want to act and think and behave. I’ve changed so much in the past few months, it’s sometimes hard to even recognise myself.

 

Thankfully I’m now past the most horrific days of treatment no 5, my strength returning, my head clearing, and the nausea gone for this time. I luxuriate in the energy returning to my body, in the fact that I can do math in my head once again, and that I can follow a conversation from start to finish once more. Everybody always says it’s the small things that matters - who knew they were right? My heart fills with gratitude when I think that I will have almost two weeks of feeling this well before it’s time for my next round.

 

It seems my reaction to the chemo is different for each time, strangely enough. This time, I felt affected almost as soon as I left the hospital, my head drowsy and drugged, my body weak and toxic. Usually so far, day one and two have been fairly easy on me, but this time I was quite broken down. Day Three, the dreaded Day Three, came and went, and perhaps because I was already so affected, it didn’t seem like the worst Day Three I’ve gone through.

 

I try to take some comfort in knowing that I’m half way now - I’ve managed five treatments and I’ve another five to go. I still haven’t heard of anyone receiving as many as ten rounds of chemo, the maximum I’ve heard of are six. When I consider how much these five turns have altered me, it does leave me a bit fearful of what I’ve ahead of me. How much will the next five treatments take, how will they change me? What kind of person will I be when at last I’ve done all ten courses?

 

And as one always does at the beginning of a new year I’ve made an effort to be extra healthy. I’ve started to make super icky drinks, ones with celery, cale and beetroots and stuff in them, and I do feel like I have way more energy now than before. It might just be the fact that my blood counts are better, or maybe the drinks really do help. In any case I’ll keep drinking them, anything I can do to help my body have the best possible chance to fight. And ironically, physically I feel better now than I have all year, even way before I got the diagnosis.


One of the best things anyone told me since I found out was “Accept the diagnosis, not the prognosis”. I try to live by that, though it’s sometimes harder than other times. On the one hand, it makes perfect sense - I don’t feel like I’m sick, and I know that I’m strong, so why shouldn’t I be different? On the other hand, it’s very hard to ignore when you read how long people with my kind of cancer lives. And while on one hand you have to stay positive, you also have to get used to idea of dying, to try to wrap your head around it. It’s a balance hard to perfect, how much to believe and stay positive, and how much to accept. I’ve promised myself to try to let these thoughts be while we’re away, to simply enjoy the moment, and not think too much. I don’t know how well I’ll be able to do it, but I will at least try to only be present in the moment, to create some happy memories for all of us.


This life of mine

by Hilla Duka - View comments

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When I was a teenager, I suffered from hypnophobia: as bedtime approached, I was sure that I would die in my sleep. It didn’t worry me so much, I don’t think I’ve ever really been afraid to die, but leaving people mourning me worried me, and so I did the only rational thing my brain could come up with (well, as rational as one is capable of being as a teenager) - I refused to go to sleep. Certain in the knowledge that if I was not sleeping, I couldn’t die in my sleep, I roamed our home at night, trying desperately to stay awake, and then unfailingly falling asleep somewhere really strange - on my windowsill, at the bottom of my parents bed, at our kitchen table - anywhere that wasn’t my bed would at least be less dangerous, I felt.

 

My parents weren’t too happy to have a teen ghoul roaming the house in the small hours of the night, and tried everything - punishing me, bribing me… Actually, they tried pretty much everything except for asking me why I wasn’t sleeping. Eventually, I just gave up. I figured if I couldn’t make anyone understand this very real threat to me, why should I be bothered myself? And so I went to sleep, still sure that I would die in my sleep, but no longer concerned with those I would leave behind. Today, I’m not a teenager anymore, I don’t have hypnophobia, and I can never stop being concerned for those I leave behind. My fears are no longer the illogical machinations of a teenage mind, but very, very real. But then, so is my determination to fight. To survive, for as long as I can, and as well as I can.

 

As my children went through their fear-of-death phase, I calmly and surely told them not to worry about it yet, that it would be many years yet, before they were touched by death, and by that time they would have all the tools needed to deal with it. I told them about how my grandmother had died, old and tired of life, and how we had spoke before her death, her calmly assuring me she was ready for this and telling me not to worry. And how, even though I was sad, I had been ok with it. She was 88 when she was diagnosed with pancreatic cancer, and I didn’t want her to suffer. Her husband and almost all of her siblings and friends had already died, and she explained that she was fine with following them. And my kids calmed down, feeling sure that no death was imminent, that they were safe.

 

But I am not 88. I have not had the time to raise my children, to see them grow up into wonderful new adults, maybe forming new families themselves, finding their passions in life, their place. I want to be there for that. I need to be there. I am not ok with dying. Even though cancer has ravaged my body, leaving it in some places broken, and even though chemo is sometimes hell and has changed and taken so much from me, I still want this life. Even though there are days when I can hardly even get out of bed, days when sadness at the unfairness of it all consumes me, even though there is pain and aches and worries, I still want this life.

 

So I fight. I fight by trying to take as good care of my body as I can, trying to stay emotionally connected - to allow the hard thoughts as well as the good, positive ones. I fight by not allowing the effects of the cancer or the chemo to limit me too much, by doing things anyway. I fight by enjoying the here-and-now, counting all the things I’m grateful for in the day as I go to sleep. I fight by waking up in the morning and not focusing on where it hurts, but on the fact that I am alive, and happy to be so.

 

I fight to stay with my kids, with my husband, in this body, this life of mine. I know that I can only do this for so long, and eventually I have done all I can, and I can only hope that by that time, someone else has done all that they could and come up with a cure, or a new way to prolong my life. Quite like Piglet in that chapter with all the rain in Winnie the Pooh, when he’s tossed the bottle and knows he’s done all he could to save himself, and now it’s up to someone else. That’s not a likeness I would have ever thought to make - comparing myself to Piglet.

 

I will not be happy with five more years or ten - I want more. And if I am greedy and that is wrong, then it is only because of this: I love my life, my family, my boys, much too much to be ok with leaving.

 

Booked!

by Hilla Duka - View comments

Holiday

This past week has been so rough, physically and mentally. Physically mainly because of the different tests I’ve had to undergo for my halftime evaluation, and in part because I chose to participate in life. I went to vote, and I deliberately wanted to do it on the election day (even though it meant standing in line for ages). I don’t know how many more times I’ll get to go and vote, so I wanted to do it properly. I went bowling with the kids, and after much persuasion I actually did some bowling myself (the last time was in my teens, I ended up dropping the ball and someone was hit in the head...) My fingers and my hands hurt for the rest of the day and then some, but it was worth it to do something fun with the kids (they all love bowling).

 

Mentally, because I’ve been waiting for my half term results. I got them today, and I’ve been a nervous wreck waiting for them. Imagine if you got the result of all of your university exams in one day, and then multiply it by some factor - it’s not just a university exam at stake here, but my whole life, my whole future.

 

My head was in complete and utter turmoil, but it turned out to be good news. The ultrasound didn’t produce much - as the tumour is lobular it’s spread in a very spidery way, making it very hard to tell if it’s shrinking or not. The mammography results weren’t back yet, but my doctor was more than pleased when she examined the breast - much smaller, almost as small as the healthy one!

 

My blood tests showed that I was producing blood by myself, at least some of what I need, which is a good sign that the metastases in the bone marrow are receding, even if my blood values where lower now and I’ll probably need a blood transfusion on Friday when I have my next round of chemo. And my lymph nodes were almost normal in size! So, all in all, really good news. The best bit was that there was no new metastases, and the fluid in my right lung that had been there before had gone away.


To celebrate, I’ve booked tickets for the holiday that Heidi and all the lovely people who contributed enabled me to go on through the fundraising campaign! A week of sun, bathing, drinks and ice cream with all my boys - the kids are going to love it! And I will too. And it’s just two weeks away! It’s been hard settling on a date - basically I’m in no condition to do anything for the first week after treatment, and then comes four days when I’m extremely sensitive to infection - not a good time to be on a plane. And after that I have about ten good days, before it’s time for another round, so it had to be on October first. Thankfully, I found a great trip on
Fritidsresor. I’ll be home a day before the 6th treatment, and we leave just as soon as I stop being so sensitive to infection after my next round - perfect! It will be just perfect.

 

 

The picture is borrowed from Fritidsresor, of the hotel we'll be staying at


The art of living

by Hilla Duka - View comments

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In June 2014, my life changed forever. I finally got to see a doctor who took all my strange symptoms seriously, examined my breast and my swollen lymph nodes, and who answered me gently, but made it clear that cancer was a real risk. The next day, after I had left some blood samples, a doctor called me and ordered me to go to the emergency to get a blood transfusion. As my doctor’s office and the emergency didn’t have the same data system, my doctor’s office had faxed my papers, and as I signed in to the emergency room, I was given those papers, to give to the doctor I would see. Naturally I checked them, and from the statement and values it was clear to me that I had cancer. The next day, I was told that it had spread to my lymph nodes, and a week later that it was also found in my skeleton and bone marrow, meaning that it was stage four cancer, with no way of ever being cured from it.

 

Since then, so much of what it is that I’m coming to terms with, is a question of learning how to live with death as a part of life. This is not something we’re forced to do in this day and age, and learning how to is alien and stressing and strange. My reality is that the best I can hope for is that my body can manage all ten chemos now, and that the cancer cells can't, and then… Well, yes, then it’s the question of what then. Basically, after that, it’s living with death around the corner. Even if (or when) I manage to get through all ten treatments, and they give me the amazing news that they can find No Evidence of Disease (NED), the rest of my life will be spent worrying about some lump I’m feeling or a pain in the side or whatnot. I’ll go on checkups, and when I get all clear and they tell me they can’t find anything, I’ll celebrate. And then the next day I’ll start worrying about the next checkup, the next lump, until one day they tell me they can find new spreadings. Coming to terms with this kind of future is taxing and difficult and horrific, and is not something I would wish upon anyone.

 

I’ve done my fair share of trying to negotiate with this unarmed weapon pointing at me, hell - I’ve probably done most peoples share of that. I will willingly, gladly, accept this future as long as there is a future and it’s long, but simply accepting it isn’t the same as understanding what it will mean. It’s a bit like when parents tell someone who doesn’t have kids that they’re tired, and that person goes ‘Yeah, I totally understand’. They don’t, because you can’t unless you’ve been there. It’s not that they don’t want to understand, it’s just that unless you’ve stood there with the baby that just won't stop screaming unless you carry it and rock it at exactly the right pace, while you’re legs are aching and you’re ready to fall asleep standing up, indeed walking around, for the fifth night in a row, you really can’t get it. I think it’s the same now. It’s like I’m standing on one side looking into this thing that will hopefully be my future, and trying hard to accept it and understand what it will be like, only I can’t really understand it yet, because I’m not living through it yet. Almost, but not really yet. One leg is there, and the other is still standing in chemo-reality.

 

But as they say, hope is the last thing that leaves you, and as humans we must have something, that is just maybe out of reach but not entirely, to hope for. And as I’m not religious I can’t really hope for salvation or heaven, and I’m not really interested in eternal peace anyway. The only thing I can hope for is more time, more future. So it stands to reason that a lot of the machinations of my brain will therefore investigate what kind of future I can hope for, if all goes well. It turns out, even in the best outcome of this I have to accept death, as part of my new life.

 

Ironically, I’m actually way better at living since I found out I’m dying. I mean, not right now, and in some sense we’re all dying, but you get the idea. I’m so much better at life, when life also involves death. I’m better at embracing my feelings, I’m better at being grateful, I’m more conscious of the sort of thoughts I allow into my head, and whether they’re worthy thoughts or not. I’m better at enjoying the here-and-now moments, and I’m so much more grateful. Before, I had a good job, decent money and great friends and family, and while I did appreciate every bit of it, I think in some ways I felt entitled to it. It was due to me, as a result of who I was, of what I did.

 

Now, as I’ve struggled to understand how wholly unfair life actually is and that there really isn’t anything you can do about it, whether or not I deserve something is completely unimportant, because you don’t actually get the things you deserve. In comes the gratitude. Yes, I may have cancer and it will change everything about my day to day life and my future, and my death, and it’s not fair in any way, but it’s just part of the portion I’ve been served. I’ve also been given incredible kids, a wonderful husband, loving family and friends, great opportunities to do amazing things… The list goes on and on.


I’ve had to give up basically everything that I was, everything that I thought defined me, but in return I’ve gotten something back. It may not be a fair bargain, but I’m so not left empty-handed in this. If the price I’m paying for living is a life with death as a participant, I’m ok with that.


Dreaming away

by Hilla Duka - View comments

Dream-holiday

When the worries and fears of the next checkup, or just of life as it is these days, threaten to overtake me, I have a new weapon. I dream myself away. To after the doctor’s appointment, when she’ll have given me the news that I’m doing fantastically, that the results are better than they had dared to hope for. To a holiday in the sun, playing with the kids. The more real the worry, the more real I make the dream.

 

Yesterday it was time for the half time checkup I’ve been dreading and hoping for for months now. The checkup itself was done quickly and more or less painlessly (they just insert a needle and at one point give you contrast fluid through that), just lying down and then you get moved back and forth through a huge machine with a round hole. The day before that was the blood sample which will tell me if my all-time high of 112 was a fluke, or if my body really is producing blood on its own again (which would mean the cancer cells in my bone marrow are fewer), and tomorrow its time for another mammogram. And for all I’m willing my body to have done well, there really isn’t anything more to do but wait for the results.

 

So, I start dreaming away, to a holiday in the sun with my family. My lovely friend Heidi started a fund-raising when I got diagnosed, to send me away on a dream holiday. The fund-raising went through the roof, and it means I will get to take the kids on their first holiday in years.  I’ve some red tape to get through first, like getting OK to going on holiday while I’m still on sick-leave (Sweden has loads of rules on stuff like that), but my oncologist cleared me for travelling, just to go somewhere “safe and practical” as she phrased it.

 

So now I’m looking at holidays - the kind of chartered ones with preferably all-inclusive and pools and beach just around the corner. The kind I never would have looked at before having kids, and that always seemed too expensive or over-the-top once I did. This summer, I think, in the end turned out to be a good one for the kids. Thanks to the car we could go to fun places we didn’t really go to before, and all of us, Ilir, my brother and my dad, made an effort to take them out as much as possible, so that they could go swimming, or go to the really fun park across town. But we couldn’t go away, at that point. Everything about the diagnose was still so new, so raw, so dangerous. The year before that I had time off in the summer, but no money to take them anywhere, and the year before that I worked all summer, so they’ve really waited long enough for this. We all need this, I think. For one week, just to get away from it all, the morning stress and the homework that needs to be done and the constant, constant worrying…

 

Now, when I start to worry about the result and what it will show and I realise that it’s just one of those improductive worries, I start to think about our holiday instead. I know we will have an amazing time once we get there, and for that I’m so very, very grateful. But even before that, just now, it’s doing me a world of good to just have this to dream away to, as a counteract to those worries that will just lead me nowhere. I just start dreaming away to a place where I’m lying by the pool sipping goldfish-bowl-sized drinks and watching the kids splash around in the water. This trip will be another thing that I hope they can remember for the rest of their lives, something we did together as a family.

 

I’m so, so grateful to everyone who helped the fundraising become such a success. Thank you so much, for caring, sharing, contributing. And a massive thank you to Heidi, who as always knows how to make stuff happen!

The image above is borrowed from fritidsresor


Perfect imperfections

by Hilla Duka - View comments

Hillabald

As crazy as it sounds, I don’t think I’ve ever been happier with myself and my body than now. Now, when it’s being pumped full of toxins, when my head is bald and my skin is freckled to the max, three of my nails have darkened and are threatening to come off completely, and my eyebrows and eyelashes are gone. Now is when I love it the most.

 

I’ve always had a weird relationship to my body. Though sadly, this relationship should perhaps be described as normal. Most of my friends have the same one with their bodies. I’ve hated that I’m so short, wishing desperately for just ten more centimetres, preferably straight to my legs. Or just as desperately wishing for ten less kilos, or better yet twenty. I developed anorexia and bulimia pretty much as soon as I hit my teens, and even though I came out of it by the end of my teens, the mindset remained. I adored skinny girls, and I hated my curves. I would curse my body for being built so sturdy, for the muscles and fat that would never go away. Now, I’m so very grateful for them. Had I been one of those super skinny girls, there’s no way I would have been able to take ten rounds of chemo.

 

I’ll not pretend like I enjoy seeing my own scalp when I look in the mirror, or the strange, lashless eyes that look back at me, but I love my body for working so hard to get through this. And I feel connected to it in a way that’s very new to me. Before, my body was the means to achieve a goal. It was my transportation, not part of the real me. Now, I feel like I’ve taken possession of it in a brand new way.

 

My dad told me of how, when my grandmother learned she had cancer she had raged ‘How could my body betray me like this?’ but I look at it very differently. I feel as though it was the disconnection between my self, my personality or soul or what have you, and my body, that allowed the cancer to creep in. And, if I’m lucky, connecting the two together again will be what will let it heal.

 

I caused this, at least in some sense. Or at the very least, my negligence to my own health and my body meant that I didn’t see the small signs something was terribly wrong. A lack of respect for my body meant I didn’t take it seriously enough. I didn’t check my breasts very regularly. I didn’t know all the things to look for when you do. And, when I noticed there was a difference between my two breasts, I didn’t think it was the breast with the tumour that was the problem - that one was looking perky and nice. No, was I looking at the healthy one, wondering why that one had decided to go dog-eared on me. I didn’t think of myself as a vain person, but if I had looked at my body without vanity, maybe some concern for these changes would have prompted me to look into all this sooner? We’ll never know.

 

Recently, I changed my profile picture on Facebook. It’s a small bloody thing, but it was big to me. I removed the picture of me laughing on our office terrace, my long hair taking up half the picture, and instead uploaded one of myself with no hair. The one that’s over this post in fact. I used my long hair to hide behind. I wanted to hide my apple cheeks and my double chins and my sadly sloping eyes. Being bald lets you hide nothing. But being loved makes you bold, and for me, it has allowed me to show myself and see myself as I really am, these days. Bald head and all.

 

Going through chemo is really, really rough on the body. I’m now on my fourth treatment, and physically, it’s extremely taxing. If you’re not well-read on the effects of chemo, the basic idea is that since we have no way of actually targeting cancer cells, we just pump the whole body full of toxins, that strike at every single part of your body, hoping that it will also hit the cancer cells. Of course it’s a bit more complicated than that, but that’s pretty much the gist of it. It especially hits the fast-growing cells, like hair, skin, blood, mouth and stomach, but long term use (I will be on chemo for about eight months) will affect the heart, kidneys, lung, and nervous system. To some extent it already is, and I can feel that. It’s somewhat ironic that one of the things I was mourning when I found out I had cancer was the fact that I wouldn’t get to be a little old lady, and now that’s exactly what I feel like - an old lady with bad joints, a heart that races at times, knees and hands that won’t function the way they used to… But throughout all of this, I’m so proud of my body, I’m so thankful for how hard it’s working, to cope with the chemo and to fight the cancer in my body.

 

Cancer is not a gift, and no one should make the mistake of thinking I’m happy for what I’m going through, but it has changed me for the better in many ways, and how well I am now connected to my body, how proud I am of it, how much I love my life, even when so much has been taken from it - these are just a few of the positive changes I’ve had in my life in the past three months.

 

Squandering the day

by Hilla Duka - View comments

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There’s no beating around the bush with it - not working is really hard for me. Work has always been such a big part of my life, when I was a stay at home mum it drove me insane, and then I had babies and toddlers all over the house. It drove me so much round the bend, I ended up starting my own company during Milos infancy. Needless to say, it’s been more than a little difficult learning to be on sick leave. And as basically all of my friends work full time and have careers of their own, when we meet up, the question always comes up - Really, what do you do all day??

 

Honestly, not much, but maybe more than one would expect. I say good bye to the kids and Ilir in the morning (he gets them up and dressed and fed since I’m still not a morning person - that much hasn’t changed), and then I clean up the house. I’ve usually cleared it a bit at night, but somehow the morning rituals seem to just completely clutter the house again. I reason that if I can start the day by getting it nice looking around me, I’ll have started on a good note, and it will bode well for the day to come. It’s become a bit of an obsession - I reason that the day I die will not start with me cleaning and making all the beds, so if I do this every day, I’ll ward off the grim reaper, or something to that extent. Plus, since I’m now spending so much time at home, it only makes sense to keep my surroundings nice and tidy. As a result, our home has never looked nicer.

 

I usually make time for unpleasantness during the day, be they planned or out of the blue. As I’ve written several times before, I need to make room for the horrible thoughts less they consume me, so (I know this will shock anyone who knows me), I do some guided meditations, and let all the sadness come out. Better that than the alternative - panic attacks. I can honestly say that I’ve never cried this much in my entire life, and that includes the pregnancies with their hormonal roller coaster rides.

 

I try to learn stuff, I have a long to-do list with stuff that I want to learn how to do for this site, but basically anything I didn't know will do. Today I learned that if you don’t have eyelashes or eyebrows, you really shouldn’t just put soap on your face and leave it there for a bit. It will sort of just slope down into your eyes. Bet you didn’t know that?

 

I read a lot. Like, loads. Biographies mainly, but since my attention span sometimes, depending on where I am in treatment, is that of a goldfish, I often just resort to social media… I know, it’s sad. I’ve taken to putting on music when I’m alone around the house, not really the things I used to listen to, but mainly Chopin. It’s kind of soothing and doesn’t really demand very much from me, and it’s still not boring. I'm basically like this little old lady walking around with stiff joints fluffing pillows and listening to classical music. But with wine. 

 

The thing is, I don’t really have that much energy. So if I manage to go out to meet someone for lunch, or go for a walk or fix some snacks for when the kids get home, for me that’s a good day, a day of accomplishment. Life has become so very small. And as I try to remind myself, my main job right now is to go through treatment and take care of myself as much as I can. Well, I try to remind myself. It's probably a good thing people around me do it too.