Our Families — Childcan

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Handling the Unexpected: Lauren’s Story

Handling the Unexpected: Lauren’s Story

During the otherwise normal summer of 2019, Lauren’s family noticed that she wasn’t her usual energetic four-year-old self. She was always up for playing and wasn’t afraid to go for a tumble, but she had some excessive and unexplained bruises, particularly on her legs, as well as a pale complexion. Her mom, Liz, was concerned and felt it best to take her to the doctor to get checked. Her mother’s intuition proved to be right.

The next day, Lauren’s dad, Rick, was at work when Liz relayed the unforgettable news: Lauren’s doctor had called and told the family to get to Children’s Hospital as soon as possible—there was a very good chance that Lauren had leukemia.

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You Will Get Through It: Jan Pavol's Story

You Will Get Through It: Jan Pavol's Story

Last February, I started to have these headaches, mostly at the front of my head and at my temples. Our pediatrician thought it might be sinus headaches, but recommended a CT, just to be safe. We went to the ER and had the scan.

Point-blank, the doctor there told us, “Good thing that you came; you have a cerebellar tumour.” I went into a sort of shock; I don’t even remember what happened right after hearing this news.

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Not Alone in This Fight: Lachlan's Story

Not Alone in This Fight: Lachlan's Story

For most of us, 2020 will be known as the year of COVID. The year that we stopped shaking hands and started wearing masks, that schools, businesses and even borders closed. 2020 was certainly a year that our way of life changed and a year that most would like to forget. This could not be any more of an understatement for Lachlan’s family.

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A Story of Courage: Dax’s Story

A Story of Courage: Dax’s Story

Dax’s story began towards the end of April 2020, when his parents noticed the shells of his ears were crimson red. His Fitbit was reading an accelerated heartbeat of 130 beats per minute, but his blood pressure was extremely low. Dax was prescribed antibiotics and told to wait four or five days to see if any changes occurred.

That lasted two days. At 2 am the morning of May 9th, 2020, Dax woke up with his face completely swollen, crimson in colour, and having difficulty breathing.

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Easing a Difficult Journey: Johnny's Story

Easing a Difficult Journey: Johnny's Story

Johnny’s mom, Jessica, remembers August 5, 2020 as the day their world was flipped upside down. “Our son woke up completely yellow with blue lips,” she recalls. “He couldn’t walk and had a fever.” Johnny was admitted to the Pediatric Critical Care Unit, and three days later, the diagnosis was made.

Johnny was five years old when he was diagnosed with B cell ALL.

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Finding Ways to Cope: Laura's Story

Finding Ways to Cope: Laura's Story

October 27th, 2020 was supposed to be a day of celebration. Laura’s older brother, Phillip, was turning six. The cake was decorated and tacos - a favourite of both the kids - were on the menu. Instead, October 27, 2020 was the day that Laura was diagnosed with PH+ ALL - Acute Lymphoblastic Leukemia - at just two years old. From that day on, the family knew their lives would never be the same.

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A Network of Support: Jamie's Story

A Network of Support: Jamie's Story

In 2016, Jamie was diagnosed with leukemia.

“I refer to it as the ‘Best Club You Never Wanted to Belong To’,” explains Jamie’s mom. “All of those families go through the same kind of pain, and mental anguish, and emotional and physical exhaustion. You can relate to those families and those parents on a completely different level than you can with anybody else.”

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I Always Saw My Little Girl: Layla’s Story

I Always Saw My Little Girl: Layla’s Story

One morning, Layla woke up with her eye closing shut. Trying not to panic, her family took Layla immediately to the ER. An MRI revealed that there was a mass on her right side, just below her brain.

Once admitted to LHSC’s Children’s Hospital, a myriad of tests and procedures confirmed that Layla had Stage 4 Orbital Embryonal Rhabdomyosarcoma, a highly malignant, soft-tissue tumour.

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A Radiant Smile and a Positive Attitude: Brianna’s Story

A Radiant Smile and a Positive Attitude: Brianna’s Story

On July 13, Brianna found a lump on the inside of her left thigh. Bloodwork was done at their local hospital’s ER, with the family returning the next day for an x-ray and ultrasound. The following morning they were on their way to Children’s Hospital to meet with a paediatric oncologist, not really knowing what was happening. They were given the news that Brianna more than likely had cancer and tests began.

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Bright Notes Among the Darkest Days: Justin’s Story

Bright Notes Among the Darkest Days: Justin’s Story

Justin and his family had just returned from a vacation on Manitoulin Island. A musician, 17-year-old Justin had a weekend of playing ahead of him when he started to feel, as he describes it, “off”. His mom, Lorraine, decided a visit to the clinic was in order, hoping that blood tests would offer an answer to their concerns. Bloodwork and x-rays taken, Justin and his family awaited the results. The call came at 9:00 o’clock that evening.

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A True Angel: Brooklyn's Story

A True Angel: Brooklyn's Story

On September 9th, 2017, one week into the new school year, a large lump was found in Brooklyn’s left forearm. Her family made a trip to the local hospital’s emergency department, where they immediately did x-rays and an ultrasound. On October 25th, Brooklyn was diagnosed with Alveolar Rhabdomyosarcoma, a very aggressive rare cancer, in her arm and a spot in her lung.

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Definition of a Hero: Celina's Story

Definition of a Hero: Celina's Story

Celina is the true definition of a hero, especially to her parents, George and Krystal. She had never once been sick or even had so much as a fever. Not until September 18, 2017. After that, their world was forever changed.

On October 10th, 2017, at only 10 months old, Celina was diagnosed with a very aggressive, malignant brain tumour.

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Part of the Childcan Family: Kolby's Story

Part of the Childcan Family: Kolby's Story

The symptoms leading up to Kolby’s diagnosis – individually – all seemed minor. His energy was low, although only really noticeable when he was playing hockey. Kolby had always loved hockey and, in the two months prior to the diagnosis, he didn’t seem to enjoy it, just going out and skating around. He began to have headaches and even fell asleep in class one day. His parents knew something wasn’t right, but were at a loss as to how to proceed.

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Always Knowing What to Say: Keiran's Story

Always Knowing What to Say: Keiran's Story

Keiran lights up everyone around him, especially his parents, Liz and Jeff. At three years old, he tries his best to keep up with his older sister, Rebecca - sometimes falling behind, but never quitting! With a love of dinosaurs, movies, pizza and superheroes, he is an energetic little brother. But, just over a year ago, the family’s life changed dramatically after a pediatric cancer diagnosis.

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