This video features Philip Hojgaard-Olsen in the process of achieving his Bronze Duke of Ed
Fun Stuff
Stories on Boccia, wheelchair sports, accessible sports venues, etc
Accessible NYC or Japan, essential equipment, adventure tales
Netflix, accessible stadiums and arenas, pop concert reviews, etc.
Fun, silly or even educational. Podcasts from people with NMCs.
From craft to scrapbooking to gaming, or other fun activities to do in your downtime.
Sport & Rec
My name is Michael and I’m 57 years old. I have Myotonic Dystrophy type 1
Jamieson Leeson and Dan Michel have a couple of things in common. Firstly, they were
“In March I went disabled surfing for people with disabilities. It was not competitive. The
Fletcher Ball is 7 years old and has a rare form of Congenital Muscular Dystrophy.
Hi, I’m Jaxon and I am 13 years old. Years ago, my mum and I
Getting together with your mates and playing sport is a very Australian thing. From backyard
My journey with Boccia began when I was introduced to the sport as a 15-year-old
Growing up as a kid in Australia, many of us dream of the chance to
“Mind Over Muscle” is a biographical short film by the late Peter Dalrymple, chronicling his
Travel
UK couple Karla and Stephen aim to show that camping, caravanning and motorhoming is a
Accessible Travel Guru Cory Lee interviews Angela Coate of All Access Disneyland – her own
Jamie, his family and his trusty Luggie Super motor scooter travelled to South East Asia
Accessible hire vehicles Disability Hire Vehicles in Mulgrave, Sydney Integrity Car Sales and Rentals in:
Disability should not stop you from experiencing the joy and benefits of travel. Accessible travel
My name is Michael and I’m 57 years old. I have Myotonic Dystrophy type 1
My name is Scott Green, I’m 19 and I completed the Diploma of Travel and
The last few years have been quite stressful for my family and one contributing factor
Day 7 After 6 nights exploring the gorgeous Upper West Side we checked out of
Day 1 After a fairly pleasant 5 hour flight we experienced disorganised chaos at Newark
What NDIS Funding Has Meant for Me My name is Sarah. I was diagnosed with
Jamie, his family and his trusty Luggie Super motor scooter travelled to Japan for 3
Just a quick bio – I’m 43, I have Duchenne Muscular Dystrophy, I use NIV
Presenters at the 2016 Building for the Future Conference, Kate Thomas and Philip Hojgaard-Olsen, participants
This American video features a group of friends who love travelling together, and decided to
When Jaxon Taylor went on holiday to Bali with his family he wrote a blog
Philip Hojgaard-Olsen is a 19 year old Australian whose biggest dream is to move out
Entertainment
When booking accessible seating for concerts, theatre shows, sporting events and other shows, you will
Dr Phil interviews 17 year old Jake and his Mum about not letting Duchenne Muscular
Drama The Theory of Everything The Theory of Everything is a thoughtful study on the
Andrew Duffy is an English comedian and aspiring actor, who also happens to live with
“Lives in Action” is a short documentary made inclusively, both in front of, and behind
Meet EllieDP, an aspiring fashionista living with SMA in the UK. With thanks to Barcroft
Podcasts
Passions & Pastimes
This video features Philip Hojgaard-Olsen in the process of achieving his Bronze Duke of Ed
Dr Phil interviews 17 year old Jake and his Mum about not letting Duchenne Muscular
Awesome Australian disability advocate Carly Finlay reviews US YouTube sensation Shane Burcaw’s autobiographical, humorous read
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