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Young Leo with growth hormone deficiency finds inspiration in Lionel Messi's story

From ABC Australia · () English

Translated from English, summarized and contextualized by DistantNews.

At a glance

In-depth Sources not specified Context piece
  • Six-year-old Leo Slattery, who has growth hormone deficiency, finds inspiration in the story of Lionel Messi, who also had the condition.
  • Leo's parents found the Australian medical system supportive, contrasting with online accounts of struggles in the US.
  • The treatment for Leo's condition involves nightly synthetic growth hormone injections, with a weekly option now available.

For six-year-old Leo Slattery, the story of Lionel Messi is more than just a bedtime tale; it's a source of inspiration. Like his famous namesake, Leo also lives with growth hormone deficiency, a condition where the pituitary gland produces insufficient growth hormone. His parents, Liam and Mia Slattery, discovered Leo's diagnosis when he was three.

We used to read that story to our Leo. He got diagnosed with growth hormone deficiency when he was three.

โ€” Liam SlatteryLeo's father, Liam Slattery, explains how the story of Lionel Messi inspired his son.

"We used to read that story to our Leo. He got diagnosed with growth hormone deficiency when he was three," Liam Slattery told the ABC. "It was a positive story to put towards him that, 'hey, yeah, he's got the same thing as you'."

The Slatterys found the Australian medical system to be a lifeline. After initial concerns about Leo's growth, they navigated a path through GPs, pediatricians, and finally an endocrinologist. Despite initial doubts from a doctor about Leo's presentation, thorough testing led to the correct diagnosis.

It was a positive story to put towards him that, 'hey, yeah, he's got the same thing as you'.

โ€” Liam SlatteryLiam Slattery describes the impact of Lionel Messi's story on his son Leo, who has growth hormone deficiency.

This experience contrasted sharply with stories Mia encountered in online support groups from the United States. "Hearing stories of where they have to fight tooth and nail with insurance companies and doctors to try and get their child diagnosed," Liam recounted. He noted that in the US, treatment costs can run into thousands of dollars if not covered by insurance, with one initial treatment costing $2,500. In Australia, however, Leo's treatment was covered by the Pharmaceutical Benefits Scheme (PBS), with the Slatterys paying only $60. "We paid $60 because it was covered under PBS. So yeah, very thankful that we do have that system in Australia," Liam said.

Then once they reach towards the end of growth, they get reassessed to see if they are still deficient in growth hormone.

โ€” Dr. Peter SimmDr. Peter Simm, a pediatric endocrinologist, discusses the ongoing assessment for growth hormone deficiency treatment.

Treatment for growth hormone deficiency typically involves nightly injections of synthetic growth hormone until the end of puberty. Dr. Peter Simm, a pediatric endocrinologist at the Royal Children's Hospital in Melbourne, mentioned that a weekly dose is now also available. Patients are reassessed near the end of puberty to determine if adult treatment is necessary, as growth hormone has functions beyond just promoting growth.

Hearing stories of where they have to fight tooth and nail with insurance companies and doctors to try and get their child diagnosed.

โ€” Liam SlatteryLiam Slattery contrasts the ease of diagnosis and treatment in Australia with the struggles faced by families in the US.
DistantNews Editorial

Originally published by ABC Australia in English. Translated, summarized, and contextualized by our editorial team with added local perspective. Read our editorial standards.