Katie Price’s Son Harvey Begins Weight-Loss Jab Treatment: “It’s Life-Changing — He’s at Risk of a Heart Attack”

LONDON — Television personality Katie Price has revealed that her eldest son, Harvey Price, 22, will begin a new course of medical weight-loss injections in a desperate bid to improve his health and overall quality of life.

Harvey, who weighs approximately 28 stone, lives with several complex health conditions including Prader–Willi syndrome, autism, septo-optic dysplasia, learning disabilities, and visual impairment. Katie, 46, shared that after years of struggling with traditional diets and lifestyle changes, doctors have approved the use of an Ozempic-style injection to help control his appetite and reduce his weight.

“It’s really, really serious and life-changing for Harvey,” the mother of five told reporters. “He’s at risk of a heart attack, and because of his condition, he’s not getting any smaller.”

A Mother’s Desperate Fight to Save Her Son

Katie Price has long been open about the challenges of raising Harvey, her first child, whom she shares with former footballer Dwight Yorke. Harvey was born with Prader–Willi syndrome (PWS), a rare genetic disorder that affects one in every 10,000 to 30,000 births worldwide.

Among the most distressing symptoms of PWS is an insatiable appetite, often leading to severe weight gain and related health complications. The condition also affects metabolism and muscle tone, making weight management extremely difficult, even with strict diets and supervision.

Katie has spent years trying to help her son maintain a healthy lifestyle through diet, activity, and structured care plans, but the challenges have persisted. “We’ve tried everything — nutritionists, exercise routines, different therapies — but with Harvey’s condition, nothing works long-term,” she explained. “He just doesn’t get that feeling of being full. It’s heartbreaking.”

What Are Ozempic-Style Jabs?

The new medical intervention that Harvey is beginning involves a semaglutide-based injection, similar to the medication marketed as Ozempic or Wegovy. Originally developed to treat Type 2 diabetes, semaglutide helps regulate blood sugar levels and can significantly reduce appetite.

In recent years, these injections have gained global attention for their effectiveness in supporting weight loss in patients with obesity or metabolic disorders. However, doctors emphasize that such treatments must be closely monitored, especially in patients with complex medical histories like Harvey’s.

Katie confirmed that Harvey’s medical team carefully reviewed the decision before starting the treatment. “His doctors agreed that this was our next step,” she said. “It’s not about vanity — it’s about saving his life.”

Living With Prader–Willi Syndrome

According to the NHS, Prader–Willi syndrome is a genetic condition caused by an abnormality on chromosome 15. It leads to a wide range of symptoms including poor muscle tone, hormonal imbalances, learning difficulties, and a constant, uncontrollable hunger.

Because of these challenges, people with PWS are at high risk of obesity-related health issues such as heart disease, type 2 diabetes, and sleep apnea.

For families like the Prices, the disorder is a constant battle. “You can’t take your eyes off him for a second,” Katie explained in a past interview. “If there’s food around, he’ll find it. I have to lock the cupboards and fridge at home.”

Despite the daily difficulties, she has always spoken about Harvey’s joyful personality and sense of humor. “He’s the kindest, funniest boy,” she said. “But the world doesn’t always understand him.”

Life After Fame and Family Focus

Harvey now lives in residential care, where he receives full-time support and therapy tailored to his needs. The move was a difficult but necessary decision for Katie, who has frequently shared her emotional struggle with letting her son live independently while ensuring his safety.

Still, she visits regularly and remains deeply involved in his life. “He’s thriving in his college environment, but his weight has always been a shadow over everything,” she said. “This new treatment gives us hope — real hope — that we can help him live a longer, healthier life.”

Public Support and Awareness

Fans and supporters have flooded social media with messages of encouragement for the Price family since the announcement. Many praised Katie for her openness and advocacy for children with disabilities and complex medical needs.

Advocacy groups for Prader–Willi syndrome have also commended the Price family for raising awareness about the condition. “What Katie has done for public understanding of PWS cannot be overstated,” said a spokesperson for the Prader–Willi Syndrome Association UK. “Families like hers face enormous daily challenges, and it’s important that people see both the love and the difficulty involved.”

A Hopeful Step Forward

For Katie, this next chapter represents both fear and optimism. “It’s really scary as a mum to try something new,” she admitted. “But doing nothing isn’t an option. I just want him to have the best life possible.”

As Harvey begins his new treatment, doctors will monitor his response closely. While the journey ahead will be challenging, his mother’s determination remains unshakable.

“He’s my first baby,” Katie said softly. “I’ll never stop fighting for him — no matter what.”