Scarlett AVM warrior

Scarlett AVM warrior AVM arteriovenous malformation survivor and Child Stroke survivor

Follow my journey to recovery 💕

https://gofund.me/c315567c

16/02/2026

Scarlett AVM warrior story in the The Mirror 💕
15/02/2026

Scarlett AVM warrior story in the The Mirror 💕

When Laura Stockley’s mobile rang in the supermarket on a Friday afternoon, she assumed it was the call every parent half expects. đŸ“±

Her daughter Scarlett had been at her gymnastics class, so Laura thought she might have fallen and broken a bone.

“When they told me she was having a seizure. I just went into a state of panic,” said Laura, 41. 💔

Laura abandoned the shopping trolley and headed straight for the car.

By the time Laura arrived, Scarlett was unresponsive.

The ambulance crew suspected a serious brain injury and they rushed her to their local hospital in Hastings.

Scarlett was a normal, healthy nine-year-old girl, so the family were floored when scans revealed a massive brain bleed caused by a previously undetected arteriovenous malformation, known as an AVM.

“It’s basically a tangulation of blood vessels in your brain, which you’re born with. You don’t know you have one until it’s too late. We could all have one. It’s like a ticking time bomb,” says Laura. 🧠

Scarlett was rushed to King’s College Hospital in London and within hours, surgeons told her parents they had to operate to save Scarlett’s life.

“They told me if they didn’t do the surgery, she wouldn’t make it through the night”, Laura says.

Scarlett went into theatre at 10pm, was out by 3am.

Less than 48 hours later, she began seizing again as swelling caused dangerous pressure in her brain.

She underwent a craniotomy and spent more than two weeks in intensive care.

“After she came round, they were weaning her off her drugs just to see if she even recognised us,” Laura said.

“They didn’t know how brain damaged she was. We were just holding our breath. At first you’re begging ‘please survive this’. Then you’re pleading ‘please don’t be brain dead’. Then you’re thinking ‘she can’t be in a wheelchair for the rest of her life’.”

Scarlett had effectively suffered a stroke. She couldn’t talk, walk or eat. She had to relearn basic skills through rehabilitation on the ward.

Doctors later confirmed she had been left with left-sided hemiplegia and hemiplegic cerebral palsy, which means her left arm will only ever be a supporting arm.

“But, Scarlett being Scarlett, she’s determined to prove them wrong,” Laura said. Laura spent months in hospital with Lee looking after Grace at home. Five months after the initial bleed, Scarlett was discharged, but her surgical wound wouldn’t heal.

On Scarlett’s 10th birthday, Laura and her husband Lee returned to King’s College Hospital. “The screw was physically coming out of her head,” Laura said. Scarlett had developed a severe skull infection and surgeons removed a section of bone, leaving Scarlett without part of her skull for more than three months.

“You could physically see her head pulsating all the time. She had to wear a white helmet, as if she was to fall or knock it, there was no protection there. She hated that!”

Scarlett has now had nine surgeries. She’s had plates fitted, skin grafts and has spent long periods on antibiotics, and there are likely to be more operations ahead.

Laura said: “Believe it or not, she’s the strongest she’s ever been. She’s such a positive force. Anywhere she goes, she just lights up the room. In hospital they said, she is a perfect patient. She never complained. She just got on with it.”

But her physiotherapy is expensive. Laura has totted up the cost to be ÂŁ16,000 a year, which the family have paid for through crowdfunding.

Through King’s College Hospital, Laura learned about NeuroKinex, a specialist centre in Crawley for people with neurological injuries, and the family now makes a three-hour round trip twice a week from Hastings.

Laura has given up her job at her parents’ pub to take care of Scarlett and Lee, a self-employed carpenter, has had to keep the household going.

“It felt like we became single parents,” Laura said. “Grace still needed looking after. And I literally did not leave Scarlett’s side.”

Scarlett missed the final term of Year 4, all of Year 5, and most of Year 6.

She has only recently returned to school for three hours a day.

While still in hospital, Scarlett was offered help from children’s charity Rays of Sunshine, which grants the wishes of seriously ill children. ❀

They secured Scarlett an invite to the film premier of Wicked in November 2025.

Laura and Scarlett were in tears when they received the call back in October and they attended with Grace and her Grandmother Maureen.

“She’ll remember it for the rest of her life, and we still talk about it all the time,” Laura said.

Now, nearly two years on, specialist therapy has made a difference.

Laura said: “They’ve said she won’t make a full recovery. But I can’t help thinking she will. I’ve got to think that way. She believes in herself so much. When I look at photos of how she was to how she is now, it just breaks my heart. But she’s lucky to be with us and we are so lucky to have her."

14/02/2026
Look at this beauty đŸ„° Scarlett's incredible story is featured in OK online! A truly lovely representation. You'll need t...
13/02/2026

Look at this beauty đŸ„° Scarlett's incredible story is featured in OK online! A truly lovely representation. You'll need to ask for her autograph soon! 😉

05/02/2026

Scarlett began her upper limb rehabilitation programme at the Evelina Children’s Hospital at the end of January 2026. Although it was originally due to start in January 2025 her setbacks meant it began a year later. From the outset, the programme was structured around clear, goal-oriented milestones to be achieved over six weeks.

Her goals were ambitious: to eat pancakes using a knife and fork, to put on her trainers while wearing her AFO, and to independently manage her school T-shirt. If progress allowed, she would also attempt to tie her shoelaces.

What none of us could have predicted was just how quickly Scarlett would rise to the challenge.

By the end of her very first session, she had already managed to put on a school top. By the end of week one, she could independently put on and take off school tops and even tighter clothing. By the end of week two, she was confidently putting on her shoe with her AFO.

Last Monday 2nd Feb, the therapy team suggested she try tying her shoelaces — something that once felt a long way off. After a day off, this is now her third attempt.

As her mum, I couldn’t be prouder. Her determination, resilience, and sheer will to keep going leave me in awe every single day. She doesn’t just meet challenges — she meets them head-on and quietly proves how strong she really is. Scarlett truly blows my mind.

Keep going swetheart, we are behind you every step of the way đŸ„°

04/02/2026

Scarlett returns to Hastings gymnastics club after recovering from brain bleed

It was so wonderful to visit and see Scarlett AVM warrior friends and teachers. It made her realise how much she misses ...
04/02/2026

It was so wonderful to visit and see Scarlett AVM warrior friends and teachers. It made her realise how much she misses gymnastics....watch this space she is more determined than ever to return đŸ’ȘđŸ€žâ€â™€ïž

Scarlett, a young gymnast, has made a heartwarming return to her local club for the first time since suffering a devastating brain bleed on May 31, 2024.

02/02/2026

🎁 Part 4: Scarlett’s Deal or No Deal – 11th Birthday Special THE FINAL

After the worst 10th birthday (having emergency neuro surgery), Scarlett deserves all the surprises in the world.
This game got VERY exciting

Everyone was shouting

But the real question is

did she take the deal
 or go for the mystery box?!

02/02/2026

🎁 Part 3: Scarlett’s Deal or No Deal – 11th Birthday Special

Things are getting serious now!
More boxes opened, bigger decisions

January has been busy
Mostly filled with rehabilitation, hard work, and making wonderful memories.It’s Scarlett’s birthd...
01/02/2026

January has been busy


Mostly filled with rehabilitation, hard work, and making wonderful memories.

It’s Scarlett’s birthday month, and after her 10th birthday ended with emergency neuro surgery, we decided this year deserved to be extra special and make the whole month about celebrating her, and treating her sister of course!

You deserve it, sweetheart.
Here’s to hoping this year continues just like this – full of smiles, strength, and magic ✹💗

01/02/2026

🎁 Part 2: Scarlett’s Deal or No Deal – 11th Birthday Special

Its starting to get exciting 😆 Grace is being the perfect host đŸ„°

Address

Hastings

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