Elisa Blasi

Elisa

Introduction

“You are no different than anyone else,” was a phrase Elisa Blasi consistently heard growing up as she struggled to understand her non-verbal Learning Disability. It took many experiences of struggling and rebuilding for Elisa to find her voice and understand her own learning style. Elisa became the fist female Ambassador of the Learning Disability Association of York-Simcoe. Her journbey with us started in 2012.

However her journey as an champion for those diagnosed with a learning disability started much earlier when Elisa was diagnosed with a learning disability herself.

Her goal is to provide a platform for all types of learners to feel comfortable in voicing their own academic needs.

Elisa graduated from York University with Honors in Psychology. She attributes her success in school to the resiliency she has developed as a person with a disability that impacts her learning process. After graduating University Elisa became an Assistive Technology Consultant for students in York Region; this allowed Elisa to interact one on one with students within the LD community and the teachers that support them.

After 3 years in the field, Elisa became a Training Specialist at an Environmental, Health, Safety, and Quality software company in Toronto. Being a Training Specialist, Elisa works to understand new software configurations for companies and then travels around the world to train clients at head offices. Regardless of the career Elisa has been in, she has always advocated for the LD community.

For her work with the organization in 2016 Elisa was bestowed the Very Important Person's Award from for her commitment to supporting different types of learners finding their own voice!

Read My Story...

I was lucky because I had extremely supportive and encouraging parents. My parents were the type who looked at the learning skills on a report card before the grades. They would spend their summers trying new ways to break down my roadblocks and create a learning style that I could thrive in. What was most important about those summers was not only all the things we learned about myself, but also the message my parents sent me through their efforts. They showed me that I can and will learn and that they were not going to give up on me.

Making friends seemed to be very complex in my childhood. I often became the “funny friend” to draw attention away from my disability. It did not take long for me to realize that the struggles I was facing were not the same as my friends’. When most girls were reading Cosmo Girl for tips on “what to wear on a date,” I was trying to find the answers to “how to pretend that you are able to read a menu on a date”.  In essence, most of my elementary school years were spent wondering when I was going to grow out of my Learning Disability.

Once high school hit I did not want anything to do with the special education department. I made it very clear that I was not to be called down during class, and would not be using my laptop or any other tools that would enhance my learning. I did not want other students to know I was different. By the end of grade ten my grades were barely passing and I was instructed to rethink the classes I was to take the next year. They made it obvious to me that these grades would not gain me acceptance into a university. But I was not going to let that happen.

What happened next was really a build up to that moment when I realized that I was the only person who couldtake control of my disability. All the struggles I had up to that point fueled the fire that pushed me to want to do better and give everything I could offer. I no longer wanted to coast and think of my disability as something I would grow out ofI wanted to own it.

 I have learned that my disability sets me apart from other people and this is something that can be celebrated and seen as an advantage. This is not to say that I no longer struggle. I will always be faced with situations where I must learn how to adapt. However, through my past efforts I no longer see a failure as the end result, but rather an opportunity to refine my style and come at it in a different way. The way you view your Learning Disability makes all the difference.

Voices of LDAYR group

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