About the DIS THE DIS movement
At Dis the Dis we aim to challenge the perceived negativity that comes with being labelled Disabled. It can impact on peoples’ perceptions of being incapable, another negatively prefixed category.
While some people don’t see the term ‘disabled’ as a negative, a great many people living with disability do and that’s why we think we should Dis the Dis ~ Take the DIS out of disABILITY.
DIS THE DIS connections
These are the groups that helped start the movement and continue to support us.
DIS THE DIS podcasts
Join Alessia as she interviews people in the community to talk about Dis the Dis, their experiences, stories and more.
Buy some merchandise, take a selfie!
Support the movement!
All profits from the sale of our merchandise go to support the movement
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The speech that started a movement
……. and in November of 2023, the movement was started
We need to spread the message to TAKE THE DIS OUT OF DISABILITY.
Layla Raposo-Melo
Linda, Director, Garderie Reve D’enfance Verdun
Message from visitors ….
I have had the honour of working with Alessia during her stage in grooming, she started off as such a shy girl and I got to watch her step out of her shell and become a strong and confident grooming assistant! She slowly but surely worked on stepping out of her comfort zone . I am so proud to see how she has grown from this experience, how she went from being afraid to fully blowing drying a large dog on her own without any fear ! I know that if she keeps pushing herself out of her comfort zone and always reaching for new goals she will not only achieve everything that she puts her mind to but she will be unstoppable !
Gabriella from COMMUNITY GAB
Hey Alessia
I think the PODCAST was incredible - I loved hearing the background of how dis the dis came to life and all that you've had to overcome to get to where you are now. I also feel inspired by the key message of perseverance. You said something about working extra hard on what you're good at and that resonated me. I feel strongly that your gift is speaking to others and sharing this message of dissing the dis. You are fully leading a movement 😍 I am 100% sure that you will be publishing your book some day soon and speaking on many more stages to come...
Super excited about Dis the Dis! Go Alessia!
Marley from motionball Ottawa
“Give them credit for something because they are trying their absolute best!.” ~ Alessia ~
DIS THE DIS Podcast
Alessia speaks with Steven Atme, Summit graduate and success story.
Steven Atme is a musician on the spectrum. From being scared of everything to living his very best life. He is an inspiration to us all. Enjoy!
Visit the New DIS THE DIS Marketplace!
Buy some merchandise to Support the movement!
AND THEN ……
Take a selfie with your DIS THE DIS merch.
“We are honest and hard working” ~ Alessia ~
Awesome: Daughter teams up with family on advocacy venture. by Olivia Integlia
(Scroll over the text)
Alessia Iglio has achieved far more than most her age. At just 21 years old, she is the executive director and co-founder of Dis the Dis, a movement focused on changing the discourse around disability.
Iglio’s track to success did not come without its challenges. At just 20 months, she was diagnosed with developmental coordination disorder, or dyspraxia, a neurodevelop- mental condition causing a global delay and impaired coordination in motor skills, such as tying laces or writing.
“Alessia goes from A to C to get to B, whereas other people just go from A to B,” explained Angie Spatari, Alessia’s mother. “But in the end, she gets there. Everything she tries [...] she manages to conquer.”
Iglio first got the idea for the Dis the Dis movement while she was a student at Summit School. In 2022, she was selected among her peers to make a speech during the annual Awaken the Potential golf tournament.
Iglio thought of ways she could inspire the crowd. Having been bullied for her disability at a previous school, she wanted to talk to her audience about the negative language often used towards the special needs community.
It was then that her mother gave her the idea to create a poster with the “Dis” in disability crossed out, alongside other negative words used to classify people with disabilities.
“This three-letter word is so negative,” said Iglio, “Even though [someone] has a dis- ability, it doesn’t mean they can’t do it. It’s just going to take them longer to do it.”
She could not have predicted what happened next. “I made the poster, I told [the crowd] what it was about, and they were going crazy about it [...] I was very sur- prised because I made a room of full-grown men cry.”
Just like that, the Dis the Dis movement was born. Iglio, with the help of her parents, then decided to create a website where she sells merchandise and spreads her message around the world.
Spatari said her daughter has always been strong-willed and has always had grandiose ambitions. She thinks back to when Iglio first began taking swimming lessons. Despite doctors discouraging her from the sport due to sensory issues, she pursued it anyway.
“The neurologist always said, ‘I’m glad you didn’t listen to me,’” said Spatari. “She cried, and she cried, but we didn’t give up [...] and now she’s a fish. It’s the same thing with skating.”
Iglio’s ambitions are ever-growing. Currently, she is a student at the English Montreal School Board’s Wagar Adult Education Centre, where she is pursuing culinary education. She hopes to inspire others to equally pursue their passions despite any hurdles they may face.
“If you wake up and you say, ‘Today, I’m going to give it all I got, even if I’m really low,’ then you’re still doing your best, and I’m very proud of you just even getting out of bed because it’s a tough position for people with and without disabilities.”
She also aspires to expand the Dis the Dis movement. “I’m hoping to write a book about it and do a speaking tour at the Bell Centre,” said Iglio, “I want to show [every- one] that you could also take the Dis out a disability.”
For more information: www.disthedis.org.
Video created by
Jesse Heffring, Director of Development at Summit School,
and his students for the Summit school SCERT event in 2024
In 2025, The cerebral palsy association of Quebec reached out to us to request an interview with Alessia to speak about her movement.
Interview with Guy Baillargeon of Téléhandicap
“We will help you more than you will help us!.” ~ Alessia ~
Click tfor more information
2025 Wager Adult Education
Alessia was asked to speak to her schoolmates. First ever Q&A followed & Alessia was amazing. This was to be her best speech.
Thank-You to our sponsors
These are the groups that helped start the movement and continue to support us.