Save our daughter Arzoi - A Race Against Time

Our hearts are shattered, and we are turning to you—kind strangers, friends, and

compassionate souls—for help.

On January 19, 2025, our beautiful baby girl Arzoi came into this world, bringing us endless love and joy. But just days later, our happiness turned to devastation. Arzoi is diagnosed with Spinal Muscular Atrophy (SMA) Type 1—a cruel genetic disease that weakens her muscles, steals her ability to move, eat, and eventually breathe.

Without treatment, SMA is fatal. Most babies with SMA Type 1 do not live past their

second birthday. Watching our daughter slowly lose the ability to move, swallow, and

breathe on her own is an unbearable thought—but we have a chance to change her fate.

Zolgensma – The Only Chance to Save Arzoi

There is a ground-breaking gene therapy called Zolgensma, a one-time treatment that can stop SMA in its tracks. It could mean the difference between life and loss, between a future filled with possibilities and one filled with pain.

But this miracle treatment comes with an unimaginable cost—$3 million AUD

approximately- We are not eligible for getting it through Medicare and our

Insurance won’t cover it. We don’t have the funds and we are running out of time.

Why Your Help Matters.

Every single day without treatment means more irreversible damage. The earlier Arzoi receives Zolgensma, the better her chance at a healthy, happy life. But we can’t do this alone.

We are asking for your kindness, your generosity, and your belief in the power of community. No donation is too small. Every dollar brings us closer to saving our baby girl.

Even if you can’t donate, please share Arzoi’s story. Spreading the word could reach

someone who can help.

Time is Against Us, But Love Can Win

Arzoi is too little to fight this battle alone. But together, we can give her the future she deserves.

Please donate, share, and be a part of Arzoi's miracle.

A Helpless Father & Family.