LABI (TONY LA BIANCA) HAS (MND)

Hi my name is Carmen and I am HELPING LABI and his FAMILY fund raise money to SUPPORT his FIGHT with ( MND ) Motor Neuron Disease that he has been dealing with for over 2 years now! His medical expences, eg: Medication, Treatment, Home Modifications, Cares are all extra unepected expenses.

LABI needs around the clock care which is mainly provided by his elder sister Mary! Who also suffers from her own medical conditions. All your Support is greatly appreciated!

There is no CURE for MND

Thank you!

https://www.mndawa.asn.au/

Hi I am Tony’s daughter Carissa and would like to share my dad’s story.

In February 2025, our beloved dad, Tony, was officially diagnosed with Motor Neurone Disease (MND) a devastating, progressive neurological condition that currently has no cure. While the diagnosis came last year, the symptoms began quietly in August 2023, slowly and silently stealing parts of his independence before anyone truly understood what was happening.

Tony is 70 years old, a proud and strong man who lived life fully and independently. Today, he requires assistance with almost every basic task from eating and dressing to getting in and out of bed. The muscles in his arms have been the most affected, leaving him with less than 10% mobility. He can only walk a few metres at a time with full assistance, and he relies entirely on his electric wheelchair for mobility.

He now lives with his 74-year-old sister, Mary, who is also his full-time carer. Together, they do their best with very minimal support, navigating each day with strength, love, and resilience. Tony cannot be left alone, and Mary provides round-the-clock care—including helping him through the night with his breathing mask, lifting, repositioning, and basic comfort.

They currently receive just nine hours of government respite care spread over three days a week. While myself and Carmen do as much as we can, staying overnight, helping when our work and families allow, it’s not enough. Mary is running on little sleep, physically and emotionally stretched, and we’re deeply concerned for both her wellbeing and our dad’s comfort.

We are reaching out with this GoFundMe to raise support for Tony’s ongoing care.

Our goal is to keep him at home, surrounded by love, where he feels safe and at peace. Funds raised will help us provide:

• A night nurse or additional carers to give Mary much-needed rest and support.

• Physiotherapy, remedial massage, and cold therapy to help with muscle pain and overall comfort.

• Medical equipment upgrades, including breathable mask attachments and cushions to reduce discomfort and a bed.

• Out-of-pocket medication costs, as not all MND treatments are covered.

• A modified vehicle, so Tony can continue to enjoy outings and remain connected to the world outside his home.

MND takes so much, from mobility to independence, from the person diagnosed to the family who stands by them every day. But what it can’t take is love, dignity, and the desire to make each day count.

We are doing everything we can to give Tony the best quality of life in the time we have. Your donation, no matter how small, will make a meaningful difference in helping us ease his suffering, keeping him home for as long as we can and support those who care for him every single day.

From the bottom of our hearts, thank you.