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MNDAWA

Tax Appeal 2025

Support person-centred care for WA families affected by MND

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I am sharing my story to help people understand that MND can affect people of all ages and how important it is to raise money for the Motor Neurone Disease Association of WA, which has done so much for us all.

It all started back in December 2022, my son complained of his finger “getting stuck”, but like most mums would, I brushed it off as too much gaming and nothing to worry about. When it didn’t improve, we saw a neurologist in August 2023, then in March 2024 my greatest fear was realised and we heard the words, “we are going to treat this as motor neurone disease.”

Everything happened so fast from there, it was overwhelming, and for the first nine months, I felt like a zombie. Going through the motions and meeting new health professionals every day was hard for my son, who is just a teenager dealing with everything that comes with growing up.

It’s hard to think about all the things he isn’t going to get to do, like go to university, get married and have children. These are dreams that mums have for their kids, but my son’s future looks very different.

I can’t fix my son, and that’s hard. No one prepares you for this. When do I talk to him about the future, about what’s going to happen to him, about his funeral? How do you ever come to terms with something like this?

What I can do though, is raise awareness and funds for MNDAWA. Through them, we have a community. We would be lost without the Association, which has provided so much for us as a family.

They have guided me and allowed me to continue being a mum by alleviating some of the stress and explaining what we are to expect. They connect us with the health professionals we need, and they have stopped us from feeling alone in all of this.

Please support the Association to continue to provide person-centred care and support for families just like mine.

“They help me keep showing up as a mum.”

My name is Sarah, and I’m a single mum living with Motor Neurone Disease.

As a parent, I carry a certain weight, managing routines, emotions, and the everyday life stuff that happens when you have children. When MND entered my world, I didn’t just worry about what was happening to me. I worried about how I could keep showing up for my kids.

That’s when the Motor Neurone Disease Association of WA (MNDAWA) became a lifeline.

Real Support, When It’s Needed Most

They’ve been there in the quiet moments, when the medical news is overwhelming, when I’m unsure what questions to ask, or when I just need someone to listen who truly understands what this disease does to a person and a family.

They’ve helped me make sense of what’s ahead and made sure I don’t have to face any of it alone.

MNDAWA’s support isn’t just clinical. It’s personal. It’s human.
They check in. They follow up. They remember my children’s names. They understand what it means to still be a mum when everything in your life is shifting beneath you.

Thanks to them, I’ve had someone by my side to help me plan, to connect me with the right people, and to simply listen on the days I feel like I’m falling apart.

Why MNDAWA Needs You

That kind of support is priceless, but it’s only possible because of people like you.

MNDAWA relies on community donations to continue delivering person-centred support and specialist care to families just like mine across Western Australia. Every dollar helps them reach more people navigating the fear, uncertainty, and heartbreak of MND.

Please Help Today

While I’m here, I’ll do everything I can to raise awareness and funds for MNDAWA. And I ask you to please do what you can, too.


💙  Because no one facing MND should ever feel alone, and thanks to your support, they won’t have to. MNDAWA are my umbrella in the rain.

With gratitude,
Sarah

MND has taken so much from us. But thanks to Motor Neurone Disease WA, we haven’t faced it alone.

My husband, Todd, was always strong. He was a Police dog handler, active, capable, someone who looked after others for a living. He also loved running. That’s how most people knew him: always moving, always doing, always giving.

 

So, when he was diagnosed with Motor Neurone Disease at just 50, it was hard to believe. Todd had already lost his mum to MND, so we knew what this disease could do. But nothing prepares you for hearing that diagnosis of your life partner.

 Since the first symptom onset, Todd's progression has been rapid. For him, it started in his lower limbs and has travelled up his body. Within 10 months, he was in a wheelchair permanently, and so began the dramatic loss of independence. As he loses more of his upper body strength and his respiratory system is compromised, the greater his reliance is on me.

"The speed at which Todd has been robbed of his mobility and independence is staggering.

Within the space of a year, he has gone from running and cycling for hours to now just having enough strength to control his electric wheelchair."

IMAGE: © WEST AUSTRALIAN NEWSPAPERS LIMITED

But being a wife isn’t all I am. I’m also a mum.

 Raising our daughters through this, supporting them, helping them process their emotions, making sure they feel seen and heard, is just as important as supporting Todd. We’re all trying to stay strong for each other.

Some days, that’s easier than others. It’s not always simple to juggle the needs of our family, but making sure Todd feels included, valued, and respected while also being there for our girls, that’s just what families do. This is what love looks like.

That’s why the Motor Neurone Disease Association of WA has been so important to us. They were there from the beginning, helping us understand the disease, answering questions, checking in, and offering support tailored to us.

More than anything, they made sure we never felt alone.

They also introduced me to other people who are living through this too, other wives, husbands, and family members who understand the emotional rollercoaster, the practical challenges, the quiet grief that comes with slowly losing someone you love while they’re still beside you. That sense of community has meant so much.

 

Knowing we’re not doing this alone, that we’re part of a wider MND family, gives me strength on the harder days. It reminds me that even in this, there is kindness, compassion and connection.

That’s why I hope you’ll support MNDAWA this tax time.

 

Every person facing MND, and every family walking alongside them, deserves the support we’ve received. Your donation helps provide equipment, expert guidance, emotional care, and connection. It helps ensure that no one has to navigate this cruel disease by themselves.

You might not be able to stop MND. But you can help make sure people like us feel supported, understood and cared for.

Please give before 30 June. Your donation is tax-deductible, and it helps give something MND can’t take away: support, dignity, and hope.


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