Always on
This project successfully funded on 9th February 2026, you can still support them with a donation.
This project successfully funded on 9th February 2026, you can still support them with a donation.
Baby Aiyla is in critical condition and needs urgent life-saving treatment. Please help us save her — your support can keep her alive
Nine-month-old Baby Aiyla was born with eyes full of light and a smile that could melt a heart.
But today, behind that innocent smile hides a silent battle — one that no child should ever face.
Aiyla has been diagnosed with Spinal Muscular Atrophy (SMA Type 1) — one of the most aggressive and heartbreaking genetic diseases in infants.
It slowly weakens the muscles, steals the ability to move, swallow, and eventually even breathe.
The doctors said words that shattered her parents’ world:
“Without treatment, she won’t survive.”
Her mother breaks down every night, holding Aiyla close to her chest, afraid that one day she might not wake up to her baby’s tiny heartbeat.
Her father sits silently beside her crib, watching every breath, terrified of the day those breaths may stop.
Their world has turned into a race against time, and the clock is ticking mercilessly.
But there is hope
A life-saving treatment called Zolgensma can stop SMA from progressing and give Aiyla a chance at life.
The impossible part?
The treatment costs £600,000.
Her parents have sold everything they had. They borrowed money, emptied their savings, and knocked on every possible door.
But no matter how much they try, the amount is beyond what any ordinary family can ever gather alone.
Time is not on their side. The treatment is most effective before Aiyla turns one.
Every passing day reduces her chances.
Every sleepless night reminds her parents that they are running out of time.
When I met Baby Aiyla, I saw a child whose body is weak — but whose spirit is incredibly strong.
She still tries to smile through the pain.
She still reaches out with her tiny fingers, as if asking the world not to give up on her.
No child who fights this hard deserves to lose their life because of money.
I am Sharif, a very close friend of Aiyla’s family, and I have stepped forward to help them in this desperate fight.
I have seen their heartbreak, sleepless nights, and endless struggle — and I could not stand by without doing something.
This campaign is a desperate plea
Not from an organization, not from strangers — but from a mother and father who are fighting with everything they have to save their only child.
They cannot do this alone. But together, we can.
If 60,000 people give £10…
If 6,000 people give £100…
We can save her life.
Your donation — whether £10 or £100 — could be the pound that gives Aiyla:
• Her first birthday
• Her first steps
• Her first words
• Her future
And if you cannot donate, please share this campaign. One share could reach the person who saves her life.
💛 Why Your Support Matters
Every minute matters for Baby Aiyla.
Without urgent access to Zolgensma, her condition will continue to worsen, affecting her ability to breathe, move, and survive.
Your support is not just a donation — it is a chance for her to live.
Your help gives her:
• A chance to receive life-saving treatment
• The possibility to celebrate her first birthday
• The hope of a future filled with milestones she deserves
You are not just helping a child — you are helping save a future.
💛 Use of Funds
Every pound will be used transparently for Aiyla’s treatment and essential care:
• Zolgensma Gene Therapy
• Hospital & Specialist Care: Pre/post treatment monitoring, evaluations
• Travel & Medical Transport (if needed)
• Medical Equipment & Ongoing Support
• Emergency Contingency: Unforeseen medical needs
Thank you for giving Aiyla a chance to live.
Organized by: Sharif
— Trusted family friend and coordinator supporting Aiyla’s parents during this medical emergency.
Funding method
Keep what you raise – this project will receive all pledges made