Family among thousands priced out of life-changing medication

Jade Hlucshniow faced a heartbreaking decision—selling her home to afford the necessary treatment for her daughter, whose severe skin condition had severely impacted her childhood.

Seven-year-old Ruby was engulfed by eczema so severe that it dominated the family’s everyday life.

“Watching her suffer was unbearable. She would tear her skin apart, and there was nothing we could do to stop it,” her mum, Jade, told nine.com.au.
Jade said that before her daughter had access to proper treatment, life was a living “nightmare.” (Supplied)

“The nights were unbearable,” Jade recalled. “I’ll never forget the sound of her cries—pleading for relief—as we stood by, powerless to ease her suffering.”

Before Ruby received the right treatment, Jade described their existence as a relentless “nightmare.”

Ruby’s condition forced her to miss school, and she lost her appetite, becoming too self-conscious to venture outside.

“She constantly feared the judgmental stares of others,” Jade explained.

The Hlucshniow family considered selling their home to afford a medication available to millions for only $25. (Supplied)

When the family heard about Dupixent, a treatment Jade describes as a “miracle” injection, the hope came with a brutal price tag: about $1600 a month.

“We found ourselves going over everything – what we could cut from our expenses, how we could earn more money, what we could sell – just to try and make this treatment an option,” explained.

“I can honestly say we would have gone as far as selling our house.”

Ruby gained compassionate access to the drug a year and a half ago, and according to her mum, has become “a different child.”

“I can’t put into words the overwhelming relief we felt in that moment…for the first time in so long, we could finally breathe again.”

Dupilumab, sold under the brand name Dupixent, blocks the pathways in the immune system that drive inflammation. (Supplied)

Now, families who cannot afford the same treatment want the Federal Government to take immediate action by subsidising Dupixent through the PBS for children under 12.

The drug is already available on the Pharmaceutical Benefits Scheme for Australians aged 12 and over, but younger children are excluded without special access.

National charity Eczema Support Australia is spearheading the SOS for Kids with Eczema campaign to advocate for PBS funding of Dupixent for children aged six months to 11 years.
Access to Dupixent meant Ruby could have her face painted for the first time. (Supplied)

Managing director Melanie Funk is urging for improved access to treatments, saying the current lack of funding leaves thousands of families suffering unnecessarily.

“Families of young Australian children with severe eczema are at a breaking point, unable to afford a medicine that can change lives,” she said.

If listed on the PBS, the cost would be slashed from $1600 to about $25 a month.

Eczema affects approximately three million Australians, including one-in-three children aged six years or younger.

Dr Li-Chuen Wong, from the Australasian College of Dermatologists, said severe cases could be debilitating for young children, causing relentless itching, skin infections and sleep disruption.

Eczema affects approximately three million Australians, including one-in-three children aged six years or younger. (Supplied)

“In the worst cases, children are in constant discomfort and unable to function normally, and the impact on families is profound,” she said.

That was the harrowing reality for the Hlucshniow family – a stark contrast to Ruby’s life today, where she can finally enjoy the same experiences as other seven-year-olds.

“She joins in sports, participates in all school activities, and no longer has to sit on the sidelines. She goes to birthday parties – something she used to avoid – and has become such a social butterfly. It’s been incredible to watch.”

“These might seem like small things, but for Ruby, they mean everything,” Jade said.

A spokesperson for the Department of Health, Disability and Ageing told nine.com.au that the pharmaceutical company responsible for dupilumab in Australia has not provided the required documentation for the PBS listing to progress. 

The Pharmaceutical Benefits Advisory Committee will consider an updated proposal at its July 2026 meeting.

NEVER MISS A STORY: Get your breaking news and exclusive stories first by following us across all platforms.

Leave a Reply

Your email address will not be published. Required fields are marked *

You May Also Like
Iranian protesters reveal plan to disrupt New Zealand opening game

Iranian Protesters Unveil Plan to Target New Zealand’s Opening Game

Iran’s opening World Cup match against New Zealand on Monday night is…
Iran faces protests in US ahead of tense World Cup opener

Iran Confronts U.S. Protests Ahead of High-Stakes World Cup Opener

Iran forward Mehdi Taremi has criticized FIFA, saying the national team has…
Gold Coast builder Levi Hilton (pictured) went viral after posting a video of the moment he burst in on former girlfriend Jessica Te Huia and his 19-year-old son, Lorenzo Hilton

Dad Who Filmed 19-Year-Old Son in Bed With His Ex Has Troubled Past and Family Tragedy, Report Says

He recently became an internet sensation after sharing footage of himself confronting…
Iran's players train in Anatalya, Turkey, ahead of the World Cup in an attempt to build up their fitness. The nation’s domestic football league has been suspended since February due to US and Israeli air strikes.

Why Iran’s World Cup Run Left Its Fanbase Deeply Divided

Iran’s path to the World Cup has been punishingly difficult, with the…
A protester holds a sign with a portrait of the son of the last shah of Iran, Reza Pahlavi, as people demonstrate against the Iranian regime outside Los Angeles Stadium

Iran’s World Cup Opener Faces Fan Protest as Supporters Plan Anthem Boos and Stadium Demonstration

Demonstrators started assembling ahead of Iran’s opening World Cup fixture against New…