WAKING up and slowly opening her eyes, Abi Burton gazed around the hospital room.
Staring back at the England star were the desperately worried faces of her as she wondered what on earth had happened to her.
Back in 2022, Abi, 25, was put in a medically induced coma by doctors for almost a month after what they thought could be a episode caused by .
But after numerous tests, it turned out to be something even more sinister – a deadly brain-eating disease that made her extremely aggressive – even causing her to lash out at her parents.
It left her unable to walk and suffering from severe memory loss as she battled to make it back onto the rugby pitch.
Abi, who was called up to the England national women’s rugby union team in January this year, shares her shocking story with The Sun.
‘I was numb’
I had no clue. I knew I was in the hospital but I didn’t really feel anything, I was numb.
It was summer 2022, and unbeknownst to me I had been lying in a medically induced for almost a month.
With zero memory of what had happened, I could only listen in total disbelief as my parents explained what had led to me waking up 25 days later and 44lbs (20kg) lighter.
My mum, Sarah, told me that when doctors decided they wanted to put me in a medically induced coma, she wasn’t there, and my poor dad Danny had to make that decision alone.
He confessed to me that he carried the weight of that decision every day, feeling like if I hadn’t woken up he would have killed me.
I heard how they had kept the extent of how ill I was hidden from my two younger brothers, twins Joe and Oliver, 23, and carried the worry themselves, just trying to keep the family together.
As soon as I woke up, I was in floods of tears, and we all held hands together. They did not leave my side.
Prior to all this I had been struggling for a long time, not feeling like myself and battling with my mental health.
I started to feel different in May 2022.
I am a bubbly person, but I started to not want to spend time with friends, and I just felt sad most of the time.
A psychologist I went to see for some answers thought I had and I was put on the antidepressant in June.
I was desperate to feel like my old self again, but days later I had a fitting seizure at the dinner table that lasted for six minutes.
‘I was sectioned’
Horrified, my mum called an ambulance and I was rushed to A&E.
I was desperate to know what was wrong with me, and at first, doctors thought maybe the had caused it.
After that, I suddenly went from a very timid person to having manic and aggressive behaviour.
I punched my mum in the face with my phone, I pulled spindles off the stairs, and tried to hit people with them.
I had got out of the ward and rugby tackled three people and had to be sedated
Abi BurtonEngland rugby star
Doctors came to the conclusion I had -induced due to my job as an player and the high-pressure environment I was in, gearing up for the .
I kept displaying aggressive behaviour towards anyone who would come near me.
I kicked nurses in the hospital and put one of them out of work for a few days.
I even picked up knives and got into full-on physical fights with my parents – who were devastated and worried sick.
I had two more frightening before I was eventually sectioned at the hospital under section two, which means all your rights are taken from you.
I couldn’t function. Normal daily tasks like going outside for a walk or taking food from the fridge felt impossible.
I continued having seizures, both twitchy facial ones and seizures where I completely blanked out.
It was only while I was sectioned that a blood test revealed I had autoimmune , which occurs when the body’s immune system mistakenly attacks the brain.
‘Completely baffled’
By this point in July, I was so poorly and too agitated for treatment, doctors told my dad I had to be put into a medically induced coma.
Originally, it was supposed to be four days, so they could treat me, but it became a lot longer.
And that is what had led me to finally waking up three and a half weeks later, with no idea at all of what had happened.
One of the main symptoms of encephalitis is that you lose all memory, and it was a lot to wake up and find out how differently I had behaved as a person.
I pride myself on first impressions really mattering.
Then I discovered a lot of people had met me for the first time and I was trying to hurt them because I thought they were trying to hurt me.
I still carry a lot of guilt around, especially towards my parents having to go through all of that. And I don’t remember any of it.
I was shocked when people I thought I had met for the first time in the hospital told me stories about how I had pushed them out of the way.
“Oh, you look so much better than last time I saw you,”; a security guard I didn’t recognise said to me.
Completely baffled, I asked my mum what he meant and she told me I had got out of the ward and rugby tackled three people and had to be sedated.
Hearing that was just so shocking, I could never imagine doing anything like it.
On the pitch, I’m an aggressive character. But off it, I’m quite a gentle giant.
It just did not sound like me at all and it was so hard to comprehend that this had happened.
‘An absolute journey’
Waking up, I thought I could do anything. And with three weeks away, I was certain I could still take part – even though I couldn’t even walk to the toilet on my own.
I turned purple on an bike and my went through the roof.
Still, I was very optimistic and said: “I will be OK in three weeks.”; My mum firmly answered: “No you will not.”;
Of course, I wasn’t able to compete, but from a rugby point of view, I’ve been able to get back to playing internationally, which is everything I had hoped for when I woke up.
From a cognitive point of view, having to adapt my life into something different has been an absolute journey.
Today, I am a bit slower and I forget what I have told people.
The ordeal has changed my perspective on life in general.
It sucks when you’re not selected for a tournament. It sucks when you get injured.
But actually, I just have to tell myself, at least I’m not dying again.
In the past, not getting chosen for tournaments or getting injured used to feel like the end of the world, and I would think: “I’m never going to come back from this.”;
But now, as long as I’m healthy and happy and my friends and family are too, then that’s all I can ask for.
I’ve faced the reality that I might never play rugby again and it now allows me to enjoy it a lot more, rather than put so much pressure on it and my teammates.
My closest friends are in the seventh squad and they were with me through it all, and they were some of the first people to see me when I woke up.
They’ve supported me throughout this entire journey and will continue to support me, even though it was difficult for them at the time.
The staff made the decision not to tell any of the girls that I was in a coma while it was the and I was absent.
My mum didn’t want them to know either because she didn’t want it to affect the tournament.
But they knew there was something not quite right – and ultimately, it has brought us closer as a squad.
‘Never give up’
One of our family mottos is, ‘Never give up’, which I’ve got tattooed on my foot.
I am proud I was able to go back to to graduate in exercise science in March 2024, and that happened so quickly because of my family.
One of the main things I want to say to everyone is – allow yourself to rely on the people that love you, because there will be people who love you.
Sometimes you might not feel it, but the people who support you and the people who love you will be the people who carry you through those times.
It’s all about being able to lean on those people.
Now, aged 25, it doesn’t feel like it even happened to me.Even though it spanned over a period of four month, I can’t really comprehend it even happened.
I look back at photos from that period and it literally feels like a distant dream.
If you’re experiencing similar feelings, please go to your GP. Don’t ignore it.
And if you have seizures, you are within your rights to get someone to look at you. Make sure you seek help.
