After a normal pregnancy and birth, Cole and Holly could’ve never imagined that their son Carter would be diagnosed with a rare disease that only one in 300,000 people are diagnosed with, but that was their reality. After giving birth to Carter in Prince Albert, SK, they received devastating news from their pediatrician.

“The next thing we know, the pediatrician is coming in telling us that he seems to have a skin condition and we were both in shock. She then said that the Jim Pattison Children’s Hospital (JPCH) is on their way with an ambulance to come and pick him up,” said Holly as she recalled her experience after giving birth to Carter.

Carter was transferred from Prince Albert to the Neonatal Intensive Care Unit (NICU) at JPCH just a mere two hours after his birth and was diagnosed with lamellar ichthyosis, a rare skin disease. When a child is born with lamellar ichthyosis, they are encased in a collodion membrane. Once that membrane has shed, the newborn is left with plate-like scales. Those affected by this disease, like Carter, are prone to dehydration, a decreased ability to sweat, increased sensitivity to heat, and ectropion eyes where Carter’s eyelids will turn outwards when the skin becomes too tight.

“He’s my whole life. Like I wake up and it’s Carter. Everything I do is for him,” explained Holly.

Holly, Cole, and Carter travel to Saskatoon from Prince Albert for appointments every four to six months so that Carter can have his ears cleaned at JPCH, which involves Carter receiving general anesthesia.

Although Carter’s condition will never go away, it was their time in the NICU at JPCH and the follow-ups with their team that will allow Carter to live life to the fullest. In order to manage Carter’s condition, he requires two lengthy baths of at least 40 minutes in a specialized tub every day, eye drops and ear drops at night to ensure they stay moisturized, and plenty of lotion. As Carter’s gotten older, Holly and Cole also need to monitor his temperature closely and he typically wears a cooling vest to keep him from overheating. He’s at a high risk for heat stroke, so the family avoids venturing out when it’s warmer than 22 °C.

But for Holly and Cole, it’s worth it. 

“The children’s hospital saved his life because without it, we may not have him here with us today,” said Cole.

$600 raised of $10,000 goal.

This fundraiser is now complete, but you can always support the Jim Pattison Children's Hospital Foundation by making a donation.

Miracle Story Sponsor

BECOME A MONTHLY DONOR, JOIN THE SUNSHINE MAKER CLUB

Sunshine Maker Club Logo

Sunshine Maker Club is a meaningful way to donate via pre-authorized payments of $20 or more on the 15th of every month. It’s an easy way to spread your generosity throughout the year!

Sunshine Maker Club Logo