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The nausea, the pain and the mental strain placed over the 19-year-old became too much. She sat in the hospital bathroom, holding herself close, alone yet crowded by excessive thoughts. She lifted her phone and started to record.

“This is so dreadful… this is terrible, this is something I have to do, and I know I’ll get through, it’s just, this is my life for the next four to six months,” she shares. “Day four, it sucks.”

I met up with Emili months after COVID-19’s claustrophobic isolation. The tight wrap of her arms reminded me greatly of the fragility of life. After many months of lockdown, I noticed how her hair had changed. No longer was it a thick shade of dark brown but now it waved lightly over her pale cheeks. Its reflective light brown was highlighted by her wide smile, matching her cosmically brown eyes. Her face lit up the room with a rare positivity, yet her voice was croaky – alluding to the reality of her treatments.

In 2020, 19-year-old Emili Milosevska was diagnosed with Stage 4 Hodgkin Lymphoma. Over many months of chemotherapy, Emili has won the battle against the tumour that called her lung home. Emili’s outlook on life remained positive throughout, relying on a number of tools to help restrict chemos intense blow. As the chemo progressed and the negative thoughts shrouded, Emili embraced humour to ward off their ugly heads.

Her Experience

In late 2016, a 15-year-old Emili experienced a nasty, recurring cough. It got worse, and doctors diagnosed her with asthma, but the puffers never helped rid of the asthma attacks.

“The thing is they did the scans… but they diagnosed it wrong,” Emili said.

Then last year the physical pain started. Doctors scoured for an answer, and after the years of suffering, she finally received the news that a large tumour had been discovered. After learning the news, the joy-filled Emili decided to give the tumour a name in an effort to de-emphasise the defeatist grip it would hold over her life. Rob began to press against her nerves, causing such immense affliction. The pain was overwhelming and exhausting. Rob was an unwanted foe, thus began the demanding and debilitating process of chemotherapy.

Her Resilience

The first 14 days of her first chemotherapy cycle brought many challenges. Doctors attempted to find medications that could be taken home so Emili could continue her treatments in the comfort of her abode. This process, however, was difficult. The medication caused a number of problems that Emili was not equipped to handle.

“I remember that I was hallucinating. I was sitting in bed; I couldn’t move I was so high.” Emili said.

With a hallucinating spell cast over her, she noticed a nurse who attempted to kidnap her. She cried out in horror and began to hyperventilate. The nurse, in fact, had no plan to kidnap Emili, only wishing to continue the work in which they started. In actual fact, Emili had taken medication, anxiety medication, meant to generate a calming effect. However, the opposite occurred.

As the second round of chemotherapy approached, fear tied Emili down. Memories of the first cycle and the torment 11 days spent in hospital had, ate away at her nerves. But her strength and resilience allowed her to face the wall of anxiety as she danced her way into TikTok.

@emilimilosevskaI’m so bored haha. ##foryourpage ##feauture ##fyp ##shakira ##dance ##hipsdonttlie

♬ Hips Dont Lie by Shakira – goalsounds

“You know how positive I am, how crazy, so this process was a lot easier for that, because of my mentality.”

Emili still had a long way to go, not only having to experience the dread of chemo, but she also had to endure gut-wrenching fertility treatments. The thought of children had previously occurred to Emili in passing conversations with friends. She never wanted to go through the horror that is childbirth, so she often thought of adoption. In spite of this, she still had the option to conceive a child of her own.

One night, however, whilst at a friend’s party, she found herself crying in a kitchen, isolated the crowds and absorbed in a phone call that changed everything. The treatments didn’t work, the option was no more.

What do I tell my future husband about kids, how do I bring that up?”

When speaking of this night, I saw a comfort in her eyes. The knowledge that adoption is still an option allowed positivity to take over her young mind. She sat and spoke of her future Gary and the ways in which adoption could be spoken about. Funnily enough her humour began to reveal itself during the disheartening conversation, as the name Gary did not only belong to her future imagined husband but belonged to her hospital IV pole.

Emili’s individualistic experience with chemotherapy was one of positivity and resilience. For Emili she was able to scare cancer off in only two months. She told herself that even though the road was long and coarse, cancer was not going to be the end. 

Her Family

On day four of the first cycle Emili found herself trapped, surrounded by claustrophobic dark thoughts. Split-second conceptualisations of demise began to plague her once pragmatic mind. It was bad. She asked herself, is life worth this treatment? She continued to reflect on family and close friends who became main channel of positivity and assistance throughout.

Whilst we sat eating Emili could not stop talking about the love that continues to grow for her family in which her strength stemmed.

“I feel like it’s harder for the family and friends then it is for the person… I had to go through there’s nothing you can do, but other people have to see me go through that experience.”

With the prescribed medications altering Emili’s hormones, she began to have breakdowns. The strength of her parents shone through during the most difficult of times. A Mum who helped her daughter in showers where the water became a feared enemy of long, transparent glass. When she found herself in compromised positions unable to muster up the strength, her father became her muscles.

During hospital chemotherapy sessions, her father embraced Emili’s style of dry, sarcastic humour, as he began to laugh and joke with doctors.

“Would you give her another bag (of chemo),” he asked the doctor, only to be met with a confused expression.

“Why?” the doctor replied.

“Because she won’t shut up,” he laughed.

Even when retelling the story over coffee, laughter caused Emili’s eyes filled to the brim with tears.

It goes a long way to show just how parents will act when their child is sick, craving to create a smile no matter what. Trying to provide comfort when the idea of such is hard to imagine.

Her Faith

The first cruel cycle led her to want to give up. On the fourth day of an unbearable 11 days in hospital, she sat in the bathroom crying. This became a significant factor in shaping Emili’s idea of hospital, now never wanting to go back. A breakdown was had alone. Emili’s physical and mental state ready to give up. She let it out, standing there unable to convince herself that she could do this alone. Even with the comfort provided by doctors and family, Emili turned to her faith.

 

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My Hair Journey ❤ . One of the hardest parts about this camcer journey is losing a piece of yourself. I went from being a sick person to looking like one but it made me so humbly confident in my other features that I think this was meant to happen. Not only for the hair but this whole journey, to show my strength and turn me into this confident strong person I never knew I could be. . I lived with this disease for so long and I had no idea. Get checked and not only checked, if you don’t feel right push. Because I did and they still mistreated me, till I was finally diagnosed and on the way to healthy. . My tumour has shrunk significantly so to that I say #fuckcancer and I’m going to play with my new hair while I get healthy 🤣❤. Hodgkins Lymphoma stage 4 whoo?? . #lymphoma #hodgkinlymphoma #cancer #cancersucks #hair #wigs #wig

A post shared by Emili Milosevska (@emili_milosevska) on

“I’m giving you my life God, you want to take it away, you want to use it, you want to abuse it, do whatever, but this is in your control now. I’ll be here for the ride and you do whatever you want to do.”

It wasn’t until the journey home days later where Emili sensed a change. The hardest and most draining part of the first cycle was coming to an end and a shift was felt. The pain and exhaustion began to drift slowly away as her father began to drive further from the hospital. Her life was no longer in her control.

Knowing God held her life, she sat back to await the next chapter of her story. It caused her to shift from dark thoughts and the rollercoaster of emotions began to calm. The sense of a higher power taking control over her life allowed the weight on her shoulders to decrease.

From this Emili started to sing again, play music again. She sat in the bathroom singing, not crying. From here things began to look up and as she sat in that car, reminiscing of the days in hospital, the pain that began to fade and her mood began to change.

“You did listen, you son of a gun,”

This Christmas marks the fourth anniversary since 7 year old Jarvis was diagnosed with cancer. Make a Wish foundation has been valuable in offering joy, hope and the chance to feel like a regular kid, for many children like Jarvis.

#WorstChristmasEver

It was only a couple of days before Christmas 2014 when Jarvis’ parents took him to the doctor for blood tests. He’d been feeling out of sorts, lethargic and falling asleep all the time, and they’d noticed bruises on his legs that weren’t healing.

Just two hours later, their GP rang and told them to go straight to the hospital where the team from Ward 3B were waiting. While their instincts told them something was wrong, the truth came crashing down as they arrived and saw the sign – Ward 3B was the children’s cancer ward.

At just four years old, Jarvis was diagnosed with Acute Lymphoblastic Leukaemia, a type of cancer that affects the blood and bone marrow.

The diagnosis came on Christmas Eve, and Jarvis started chemotherapy the same day.

For the whole family – Jo, Ben, Jarvis and his two little brothers – it quickly became the most desperate Christmas ever.

Every parent’s worst nightmare

Jo and Ben did their best to stay strong for their three boys – with their youngest just 16 weeks old at the time. However, Ben remembers feeling completely overwhelmed: “I was just walking through the ward, pushing the pram with the other kids, and it was all just a bit of a blur.”

In the months that followed, Jarvis began an intense course of medical treatment including daily chemotherapy and high dose steroids. However, the life-saving regime took a huge toll on his health, leaving him listless and often withdrawn. He gained around 40 percent of his body weight due to the steroids and was almost unrecognisable. His muscles also weakened to the point that his parents had to carry Jarvis between his bed at home and the hospital.

As Jo remembers, Jarvis hated going in for treatment. “He’d be crying and saying ‘please, don’t take me….’ He was old enough to know what was coming.”

Over the next three and a half years of treatment, Jarvis missed out on many of the things other kids might take for granted – from school and swimming lessons to birthday parties and playgrounds.

During this incredibly tough time, Jo and Ben felt they had to ‘bubble wrap’ their son.

His incredible wish

Through cancer support groups, Jo and Ben heard about Make-A-Wish® Australia and applied for a wish mid-2017. As a keen reader, Jarvis wished for a very special treehouse, much like the one in his favourite book, The 13-Story Treehouse.

As the #WishForce team quickly discovered, Jarvis’ treehouse had to be somewhere a young boy could escape his day-to-day cares, enjoy some quiet time, and let his imagination roam free. Of course, it also needed a veranda, a rock-climbing wall and its very own flying fox!

Construction began earlier this year, with Jarvis watching on excitedly as his vision came to life.

Today, visitors to the family’s home will find a two-storey treehouse taking pride of place in the backyard – with a good-natured seven-year-old playing with his brothers and friends inside.

Jarvis is now doing his best to put the years of cancer treatment behind him – and while it will be five more years of regular blood tests before he’s completely in the clear – thankfully, his chances of a full recovery are strong.

For Jo and Ben, the impact of their son’s wish journey is clear – it has allowed him to become ‘a regular kid’ again.

“Experiences like this give everyone hope and give kids who’ve missed out and faced a lot of adversity a bit of happiness. That’s very special – and so important,” says Ben.
Bake-A-Wish for kids like Jarvis

Each year, thousands of Australian children are diagnosed with a life-threatening illness. For their families and the kids themselves, life is put on hold while they learn to cope with and in the best cases, beat their illness.

Which is why a wish is so important – with the power to calm, distract and inspire sick kids at the time they need it most.

You can help bring more incredible wishes to life in 2019 by joining Make-A-Wish Australia’s largest ongoing fundraising campaign, ‘Bake A Wish’.

It’s a piece of cake, and whether you choose to arrange a dinner party with family and friends or an afternoon tea – every dollar raised means more unique and life-changing wishes coming true for sick kids like Jarvis.

Visit www.bakeawish.org.au or call 1800 032 260 to find out more, pledge your support and access your free fundraising toolkit.