SickKids Fundraisers in the Community

Secondary text about the current campaign goes here.

A photo of Simon smiling during a check-up at SickKids

SIMON'S STORY

Simon’s parents worried about the challenges their son would face because of his serious food allergies. But thanks to a supervised allergy study at SickKids, Simon can now tolerate minor exposures. To his family, this means freedom.

SickKids patient Rehan as a baby with his mom holding him

MEET REHAN

Born with esophagus, kidney and heart conditions, Rehan spent his first four months at SickKids and continues to be treated there. “SickKids is a great place,” says mom Seema. “I’m so grateful to everyone who cared for our family.."

Give for Tala

Tala’s rare liver disease means she’ll need lifelong medical care. But her parents are grateful for SickKids, and for the staff who treat them like family. Tala loves her doctors and nurses and wants to be a nurse herself when she grows up.

SickKids patient Tala sitting on her hospital bed with stuffed animals.

MEET TALA

SickKids patient Marky smiling at home, wearing red pyjamas.

Meet our patients: Marky

Marky was diagnosed with a rare form of leukemia and underwent CAR-T cell therapy at SickKids: a ground-breaking treatment that harnessed his own cells to fight his cancer. Thanks to SickKids research and care, today Marky is doing well.

SickKids patient Maxen, smiles at the camera for his first day of school

MEET MAXEN

Maxen was born with a heart defect and other serious health conditions. He had open-heart surgery at four days old: the first of many. Thanks to SickKids, today Maxen is thriving, and can take part in his favourite activities, like karate.

Noah smiling when she was a baby with a headband that features a flower

MEET NOAH

Eight major surgeries during her first seven months – that’s the snapshot version of Noah’s SickKids story. SickKids surgeons were able to fix her heart, and save her life. Thanks to donor support, we’ll be able to tell more stories like Noah’s.

A photo of SickKids Patient Ately smiling in a hospital room

ATLEY'S STORY

For Atley, precision healthcare meant using genome sequencing to diagnose a potentially deadly heart condition, Brugada syndrome. Now, doctors can monitor Atley before any serious issues occur – and today, he’s doing well.

Atley, 8, Brugada Syndrome patient

Atley and his family are living proof of the power of Precision Child Health. Genomic sequencing revealed Atley’s rare heart condition, only discovered in families when someone dies. Because of this, they found Atley’s dad had the same condition. Now they both have pacemakers. His dad also had an internal defibrillator implanted. Monthly donor support is helping create more success stories like this.

GIVE FOR ATLEY

Atley has Brugada syndrome – a rare heart condition that his doctors monitor via his pacemaker. However, Atley’s diagnosis doesn’t hold him back from just being a kid: he loves superheroes, trying new foods and is learning the ukulele.

What does the sign up process look like

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Step 1

Fill out the contact info on the tablet

Step 2

Speak to the verification call centre

Step 3

Confirm sign up and receive confirmation

“SickKids means so much to our family. Maddie has been through so much with several hospital stays. Our only reassurance as a family was that we were at the best place with the best people looking after her.”

Julia and Cam

SickKids parents

“Without the hard work and expertise of every doctor, nurse, therapist, radiologist and so many more, we would not have our son. We feel privileged and beyond grateful to call SickKids our hospital.”

Subrina and Janathan

SickKids Parents

“I won’t bring my child to any other hospital, and I’ll never move far away from SickKids. The staff are so friendly. They all know and love Maya and it feels like family when we are there.”

Jason and Annette

SickKids Parents

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