Breaking News: With heavy hearts, we announce the passing of a sweet angel

The parents of Ryleigh Hillcoat-Bee, a three-year-old who tragically succumbed to a rare illness, are outraged upon discovering that their daughter’s life could have been preserved.

Ryleigh suffered from rhabdomyolysis, a condition characterized by the breakdown of muscle tissue. The complications arising from this illness, which affects approximately one in 200,000 individuals in the UK, ultimately led to her untimely death.

Coroner Alan Wilson, overseeing the case in Blackpool and Fylde, determined that the medical team responsible for her care had failed to recognize critical warning signs prior to her discharge from the hospital after a five-day stay.

The opportunity to further investigate her lack of movement was lost before Ryleigh was sent home, and she passed away three months later.

It was imperative for the physicians to consider that the deterioration of her health could be linked to a neuromuscular disorder. During her admission to Blackpool Victoria Hospital, tests indicated abnormal blood results, including “extraordinarily high” levels of Creatine Kinase, which likely pointed to muscle damage or disease. Nevertheless, the medical staff concluded that she was suffering from either hepatitis or a chest infection, despite her exhibiting signs of fatigue, lethargy, and weakness.

Coroner Wilson has indicated that he will seek evidence from the doctors who treated Ryleigh at Blackpool Teaching Hospitals NHS Trust.

Diane Rostron, a medical malpractice attorney, stated, “The hospital was given clear advice… to seek specialist consultation from a neuromuscular expert.” She asserts that had the hospital engaged a specialist, they could have accurately diagnosed rhabdomyolysis and informed the family, allowing them to explore further treatment options.

We extend our heartfelt condolences for the loss of Ryleigh Hillcoat-Bee and wish her family the peace they rightfully deserve. May she rest in peace.