For 47 years kids have been taking part in the MS Readathon and helping families with MS and neurological conditions not feel alone.
CHRIS AND HIS SON TEDDY
Chris, Mel and son Teddy have been living with the realities of multiple sclerosis for nearly two decades, ever since Chris was diagnosed at just 20 years old.
Now 39, Chris continues to face the unpredictable nature of MS with resilience, using a walking stick and motorised chair as needed, but never losing the strength, love, and hope that bind their family.
Their son Teddy, who turns four this June, is already a dedicated participant, proudly reading each year
"to help people like Daddy"
For their family, the MS Readathon is more than a fundraiser—it’s a cherished tradition, a symbol of connection, and a source of purpose.
This year, they will once again read with love and courage, and are grateful for everyone who reads alongside them.
DEANNA - DIGANOSED AT 17years old
As a child, Deanna enthusiastically took part in the MS Readathon, loving that reading could help others.
When Deanna was diagnosed with MS at 17, it was the first thing that came to mind—
THE MS READATHON REMINDED DEANNA THAT MS MATTERED AND MADE HER FEEL LESS ALONE
Deanna's lifelong love of storytelling, especially in children’s books, has inspired Deanna's support for the MS Readathon. Deanna believes the MS Readathon sparks imagination, empathy, and a sense of community in young readers.
It's Ollie & Poppy here & our mum has MS
Mum says MS is like a mouse nibbling at the electric cables connecting her brain and body.
There are thousands of people living with MS in Australia. And our family does lots of things to try and help them. . . We’ve done the MS Walk and the MS Fun Run in Melbourne…but our FAVOURITE thing is the MS Readathon!
Mum used to do the MS Readathon when she was little, and now we all do it together as a family!
By joining us in the MS Readathon this year, you can help people like our mum.
TATE AND SOPHIA ARE DOING IT FOR MUM
Rachel is the mum of two beautiful children, Tate and Sophia and has had MS for 18 years. Because of her MS, Rachel experiences fatigue, vertigo, numbness, and other challenges.
Rachel and her husband are so grateful for the help their family receives through MS Queensland thanks to wonderful supporters like you!
“I'M ABLE TO DO SO MANY THINGS I WAS TOLD I'D NEVER BE ABLE TO DO... I OWE SO MUCH OF THIS TO MY AMAZING FRIENDS, FAMILY AND THE MS TEAM”, says Rachel.
LIANA READS FOR FRIENDS AND FAMILY WITH MS!
We have family and friends that have MS and this is why I know it is so important to read as many books as I can and raise lots of money to help others.
It is so much fun reading books. I read 40 books.
You can read almost anywhere . . . . in the car, while shopping, on the tram, at restaurants and in bed. I even read while I am waiting for my swimming lessons.
IF EVERYONE DOES A LITTLE BIT, IT CAN MAKE A BIG DIFFERENCE
Hi, I am Belle, and this is Theo!
My mum was diagnosed with MS just after her and daddy got married!Last year we had an empty bookcase. We put all the books we read in it and my mum would video my updates.
MS Readathon supports people living with MS in every state and territory of Australia.
'I LOVE READING, AND IT'S NICE TO HELP LOTS OF FAMILIES....'
