A mum forced to say her "final goodbyes" to her sick child five times is overjoyed after hearing him saying "mum" for the first time in eight months.
Georgia Eaton, 36, was told "countless" times that her teenage son wasn't going to "make it" after he was diagnosed with a rare auto immune disease, encephalitis - a rare neurological condition causing inflammation of the brain and intense spasms.
Her son, James, 14, first became unwell with a high temperature and bursts of dizziness in December 2021. After multiple trips to seek medical help, his local GP was stumped, and his symptoms continued.
READ MORE: Baby found dead in bathroom 'five days' after mum died
Just weeks later, in January 2022, Georgia walked into James' room, at their home in Ellesmere Port, Cheshire, to find him bleeding from the mouth with "blue lips and vacant eyes". The schoolboy was rushed to the Countess of Chester Hospital in an ambulance where he was put on life-support.
An MRI scan revealed James had a collapsed lung, sepsis and a chest infection - but despite this, doctors were still unable to pinpoint a diagnosis. After one hour, worried medics transferred him to ICU at Alder Hey Children's Hospital, Liverpool.
Over the next month, Georgia was forced to watch as her son took multiple turns for the worse until he was finally diagnosed with encephalitis - a rare neurological condition causing inflammation of the brain.
Doctors pumped James with a cocktail of medication, including steroids, a specialised ketogenic diet and a therapeutic plasma exchange. But despite this, his health continued to falter and on March 20 his heart stopped and he was rushed back to critical care.
Thankfully James is now on the mend, over eight months after first falling sick, after a board of doctors approved a steroid treatment - never before trialled on children. Georgia is now overjoyed at hearing her son say "mum" again for the first time in nearly a year.
The mum-of-two said: ""I never thought I would ever hear my son call me 'mum' again. I collapsed to the floor, I had waited so long to hear James' voice again."
Georgia - who is also mum to Alfie, 11 - continued: "I thought my son was gone so many times. I was devastated, I was trying to wrap my head around what was going on, but I was just numb."
When the family saw James for the first time in the ICU, Georgia said: "I didn't recognise him." After two weeks on life-support, James struggled to recover and showed no signs of responsiveness.
Georgia said: "Watching my son battle for his life while all I could do was look on was the most painful experience I've ever been through. He was on and off life-support, and we still had no idea what was the matter with him.
''It was terrifying and frustrating. Thankfully in February he got a diagnosis. 'I had no idea what he had, I wasn’t a doctor, but I knew my son was poorly.
"It was bittersweet, I was relieved that we finally had it, but it was so serious, I didn't know if my boy could beat it."
James started showing signs of improvement until his heart stopped beating and medics were forced to rush him back into critical care in February 2022. After he had been in hospital for four months, doctors arranged a consultation with Georgia and her mum, Debbie, 51, to discuss a new treatment that might possibly save James' life.
Georgia said: "We had no more options. I had to do whatever it took to save my son."
The treatment called anakinra involved James being injected three times a day for six months to reduce inflammation on the brain. On June 20, Georgia was told the treatment had been successful and James was finally out of danger.
Georgia said: ''In June he said my name and that's when I really started to have hope again, it was amazing. James has been home a few weeks now and it's just something we were never sure would happen.
''I'm so grateful to everyone who helped him. 'He can call out for me whenever he wants now, it's the best sound ever.''
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