Get Lilia Movin'

Get Lilia Movin' Lilia is a lovely little girl who, after being deprived of oxygen for 27 minutes at birth, has cerebral palsy. A lovely little girl called Lilia…. # # #

Lilia is inspiring in how she always strives to be her best. Lilia is working towards independence and a fulfilling life of possibilities. Lilia was born on the 10th October 2013 after a very very long wait of 41 weeks and six days. She was overdue by 13 days but the pregnancy had been all things lovely and her parents, Amy and Liam, were extremely excited to meet their first baby. After a straigh

tforward pregnancy and labour Lilia was born quickly after her heartbeat was lost by the midwife. The emergency cord was pulled by a shocked and distraught Liam and the amazing doctors came at lighting speed. The baby was taken away into the emergency room and resuscitated for 9.5 minutes. The beautiful baby had come back from the dead, her determination being a sign of things to come. Lilia had been deprived of oxygen for approximately 28 minutes and was pronounced HIE Grade 2. Amy and Liam saw their baby for the first time after 30 minutes and only for a few seconds before she was taken to the NICU to be ‘cooled’ to just above hyperthermic temperature. Lilia lived for the next hour, and the next, and by 5 hours later she was breathing by herself. She was cooled for the next 3 days. Amy finally held her baby for the first time on her 5th day. After 72 hours everyone waited for a whole day to see if the baby would survive being ‘warmed’ back to normal temperature. Lilia has seizures during her first week of life but she did surprise us all and continued to live. Amy and Liam were told that the chance of brain damage was probable but to what extent would be unknown. Lilia began to miss milestones from an early age. She did not put her hands to her mouth, roll over, sit up, and the list goes on. At 5 months old Amy and Liam were told that Lilia had Quadriplegic Cerebral Palsy (affecting all of her limbs and body). However, one thing she did do was SMILE. She smiles all the time. She laughs lots (except when she is doing her physio!). She loves to play but does become frustrated when she finds this difficult. Lilia has many appointments with her Physiotherapist, Occupational therapist and the speech and language therapist. In addition she attends a charity therapy centre every few months to track her progress and learn new physio techniques which the NHS do not always have the time to do. Amy was told that Lilia would never walk. Nobody truly knows if this is the case but we are determined to give her the best chance possible. Lilia loves to be around her friends, family and those she considers her 'framily', and she desperately wants to join in with everything. Amy and Liam are committed to her having as many experiences as possible in her life, and not missing out on anything due to her condition. This is why they would like to raise money for a specially designed trike. These cost anywhere from £1000 - £6000 as they are specially adapted. Lilia would also benefit hugely from a new therapy called ‘Therasuit’ therapy which is currently happening in America. This is a 3 weeks course of daily 4 hour therapy while wearing a space suit, as well as oxygen therapy to help heal the brain. This will cost in the region of £15,000 so the fund raising has now begun. We know Lilia is one of the luckiest little girls ever as she has so many amazing, lovely, thoughtful people in life….you know who you are…we love you. Thank you so much!!!

08/07/2025
14/06/2025
Posting late as usual…because…well, life is soooo incredibly busy! May half term 2025 Lilia completed week 9 Swimlab! Sh...
14/06/2025

Posting late as usual…because…well, life is soooo incredibly busy!

May half term 2025 Lilia completed week 9 Swimlab! She’s a competent swimmer now and we couldn’t be prouder of her. She puts in 100% effort at all times, even when she’s not feeling it! Her determination is something to be admired!

Lilia worked hard out of the pool on controlling her dystonic movements, we got some exercises to do in the morning to ‘wake up’ her body and help get to control those extra long limbs when her dystonia kicks in. Her dystonia seems to ramp up every time she grows. She has DBS (brain stimulation which was inserted into her brain) but we are still trying different settings to find the optimum frequency) which helps but it isn’t a miracle.

Lilia worked hard with her Momma and Poppa watching this time. So grateful they found the time and funds to be able to come and watch Lilia working hard!

Lilia also worked on keeping her head out of the water (dystonia again) when she did length after length on her back! For a child with this level of physical disability to swim unaided is just incredible! We’re beyond grateful to Paul, Kris and all of the Swim Lab International team!! At the end of our first week we had the pleasures of seeing that CEO and Lilia’s swim coach won the European CEO of the year by Forbes! So grateful to the attitudes Paul has around ‘no limits’! Huge congratulations to you Paul and thank you so much to you!

We met some old friends and made new ones! Honestly Swimlab have given us so much..it’s not just the swimming! 🙏🏻

Back to Swimlab in October! Let’s see what else this girl CAN do!! 💙💙💙

18/05/2025

Some beautiful, profound and real words here by a good friend Carl Arla!

By Carl Ara

They say “needs”
and forget the people.
They write reports
and miss the dreams.

They call them different
and assume it means “less.”
But they’ve never seen
what we see every day.

This is not a pity piece.
This is power.
This is protest
with paint on its hands,
with maths sheets in its bag,
with soil under its nails
and stars in its vision.

You think support means soft.
But support is steel.
The kind you lean on
when the world won't bend.
The kind that listens
without trying to fix
what was never broken.

These students don’t need saving.
They need space.
They need access - not excuses.
They need ramps, not reasons.
They need lessons that speak
to who they are
not who you expect them to be.

We don’t all follow the same path.

They know resilience
like most people know routine.
Daily battles fought
behind quiet eyes,
behind a keyboard,
behind a communication device
or a body moving through
a world that wasn’t built for them.

And yet -
they move.
They create.
They cook.
They write.
They plant life and grow it.
They make the digital world brighter.

They show up,
when half the world
is too busy looking away.

You want to know ability?
Watch a student who’s been told “no”
every day of their life,
say “yes” to trying again.

You want to know joy?
See someone light up
when the world stops underestimating them
for just long enough
to notice they’ve been shining all along.

They are not your burden.
They are not your feel-good story.
They are not a box to tick
on your policy form.

They are students.
Humans.
With unfiltered kindness,
with the sharpest humour,
with empathy in volumes
this world’s forgotten how to hold.

So don’t tell them to dream small
Support them to dream big.
You can’t picture their future.
They’ve been building it
while you were busy writing them off.

They don’t need your pity.
They need your respect.
They don’t need less.
They need equity.
They don’t need to change.
The system does.

And in the meantime,
while the world catches up,
they’ll keep going.
Louder.
Brighter.
Bolder.
Beaming proof
that different
was never less.

I did it!! 1 hour 58 mins and 59 seconds (I think). Posting 5 days later but if it’s not on here it never happened, righ...
28/03/2025

I did it!! 1 hour 58 mins and 59 seconds (I think). Posting 5 days later but if it’s not on here it never happened, right?!

I’m so grateful for everyone who has taken the time to sponsor me for a cause very very close to my heart! It means the world to see all of the kind kind donations from so many gorgeous people I know! Not only for the money they’ve given, but for the time and effort it takes to put all your details in to even donate haha!

I thought I’d give my lovely friends and wonderful people I’ve crossed paths with, one last chance to get a lovely, little dopamine hit from doing something for others! Come on guys…I’m almost at my target of £1000 for the incredible Paces and all the work they do to give opportunities to children and adults with motor disorders, such as cerebral palsy.

Start your Friday off well…give a £5er to get this to its target and feel the huge sense of being a part of something bigger! Happy weekend everyone! You’re all lovely ❤️

The incredible PACES Sheffield are an independent school giving education, hope, oppor… Amy Fynn needs your support for Raising money for the incredible PACES

PACES school of conductive education is a place where we were given so much hope when nobody else was prepared to! They ...
22/03/2025

PACES school of conductive education is a place where we were given so much hope when nobody else was prepared to! They are so incredible…so much so that after 6 years of mainstream school our not so little Lilia is hoping to return for her next chapter of secondary eduction.

In order to enable this incredible school to give children with physical disabilities opportunities to do fun, brilliant things and experience some of life’s great adventures just like all children should, they rely on charitable donations!

It is for this reason that I am running Sheffield half marathon this Sunday 23rd March. As I run this beautiful route I will be thinking about what a privilege it is that I get to move my body like this. I’ll be thinking of all of all the challenges my daughter, Lilia, (and many others) faces every single day!!

If you can spare a £5er please use this link to enable these kids and young people do all the things!! So much appreciated!

The incredible PACES Sheffield are an independent school giving education, hope, oppor… Amy Fynn needs your support for Raising money for the incredible PACES

This not so little princess had her hair cut off a few weeks ago to donate to the ‘The little princess trust’. Lilia had...
25/01/2025

This not so little princess had her hair cut off a few weeks ago to donate to the ‘The little princess trust’. Lilia had been growing her hair to make it long enough to donate for a while now. All donations of hair go to children facing cancer so that they can have a wig to make things a teeny tiny bit easier. Lilia really wanted to donate her hair to this amazing cause. Here is a link to Lilia’s fundraising which pays for her hair to made into a wig for a little boy or girl going through something heartbreaking and unimaginable. The funds go directly to the charity and any tiny donation would be so gratefully received! Thank you so much!

Do you want to join me in making a difference? I'm raising money in … Amy Fynn needs your support for Lilia chopped her hair and she’s hoping to pass it on ❤️

October 2024 update…Is it too late to post about Lilia’s achievements in October 2024…life got in the way and as my list...
02/01/2025

October 2024 update…Is it too late to post about Lilia’s achievements in October 2024…life got in the way and as my list got longer I didn’t manage to report on this.

Swimlab no.8 for Lilia! As always she surprised us with her continued resilience and determination. I always wonder if these traits would have been hers anyway or if the cards she was dealt have meant she has had to learn to be these things!

She worked her body hard and after 5 months since her last Swimlab she got back into the water with her incredible coach Paul and swam 25 meter lengths like she’d never been away. Paul was concentrating lots of her arms and she did some incredible strength work (which I’ve since seen the Chestefield players do in the gym, might I add 🤣) and impressed us all with how her grip has gotten so much stronger. Using her arms is always so difficult as coordinating your body when you have quad dystonic CP (affecting all limbs and muscles, even those inside your body) is immensely difficult as your body moves when you don’t want it to and stays still when you do want it to move. The concentration involved is mind blowing for the majority of us. Lilia has a left arm weakness and so lifting her left arm high up to do back stroke arms (Lilia can swim on her back 25 meters unaided - incredible for someone who uses a powerchair full time - but arms are always difficult) is hard work.

The most amazing progress to report this time is that Lilia had the experience of a ‘pool side’ coach! Paul was so confident in Lilia’s ability in the pool that she did some swimming with Paul on the pool side! Swimlab’s tag line is just so true…’there are no limits’ 💙💙💙

As always, she gave it her all…after some bribery from Paul (he had an excellent bride 😜❤️❤️❤️) she stopped her jokey complaining on day one, she had the most amazing fun, as did we all. We met some incredible families and the siblings together was just such a beautiful time! We made life long friends!

Can’t wait to get back in 2025 and see what this brings ❤️❤️❤️

22/10/2024

Doing so well on day 3 Swim Lab International This is so hard yet your determination shines through here! You’re incredible Lilia!! And so are you Swimlab!

Squeezing this in before Lilia embarks on her next therapy trip! Lilia spent almost all of April in Austin, Texas workin...
25/05/2024

Squeezing this in before Lilia embarks on her next therapy trip! Lilia spent almost all of April in Austin, Texas working so very hard to keep her body in its best shape. Her sisters were there everyday with her cheering her on and making those therapy days as fun as possible!

Lilia has come home with a louder voice (this time we got to do speech which we’ve never done before), more strength in her legs which makes weight bearing and transfers so much easier for her and us, a huge improvement in her range of movement which means her body move more easily, even things like sitting her in her chair is much easier. Lilia has had less pain and after getting over the jet lag and fatigue from working so hard every day for 3 weeks (equivalent of a 5 hour gym session every day for 3 weeks for us) she’s been on top form!

We’re committed to keeping Lilia in the best shape she can be. We’ve got to remember the ‘use it or loose it’ phrase and keep this at the forefront of our minds.

As always, Lilia you astound us with your resilience and determination, and you inspire me to always try harder. Also, Napa Austin, you are incredible!

16/04/2024

This is someone else’s great words on why we use private therapies and why we have to!

16/04/2024

Big loud voice coming on amazingly after 7 days of amazing speech therapy at NapaCentre Austin! We underestimate the power of using our voice! She’s so proud of herself being able to get her name out like this and has even gone around some of kids here practising saying it to people she isn’t familiar with!! Amazing!

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Derbyshire

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