Posts Tagged ‘university’

How Will They Know What I Need?: Disability Services in Post Secondary

Written by on September 11th, 2014 – 5 Comments

Being in post-secondary can be a very stressful time – so trying to figure out to manoeuver one’s MS diagnosis at the same time can make it even more difficult, especially if a flare-up hits at an inopportune time.

Luckily there are many services available to post-secondary students available at universities but at times it can be difficult to try to figure out where and how to get said services.

On September 20th, the Multiple Sclerosis Society is hosting an event titled “How will they know what I need? Accessing disability services post-secondary” at York University. Students with MS and their families are invited to participate as different services are talked about by staff.

I’ll also be speaking at it briefly about my experience in post-secondary with disability services and navigating the system.

I invite you all to this orientation and lunch. I’d love to see you all there.

Register for the event here: http://mssociety.ca/toronto/events.htm#postdisablility

Student Leadership and Multiple Sclerosis

Written by on November 12th, 2013 – 4 Comments

A big part of who I am is the fact that I am a university student. Especially since I live on residence, work three different positions on campus and I’m a full-time student, my university career is my entire life. I even want to work in higher education when I’m older.

However, at the beginning of my journey of living with MS, I didn’t know if that was in the cards for me. I knew I had to avoid stress, but I live off being busy. I call myself a professional busy bee. So how was I supposed to avoid stress, while maintaining the lifestyle I loved and thrived off of?

My philosophy on student leadership needed to be change. Now it is one that has been touted by many: You’re a person first, a student second, and a leader after. I can only be a student leader, and involved in so many things if I’m a student, and I’m putting my academics first. So that needs to be the focus after I’m making sure to take care of myself.

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Start of Something New

Written by on June 11th, 2013 – 8 Comments

Hi there! My name is Juan, and this is my first post, so I should probably introduce myself. I’m very excited to be part of this initiative as it has served as great aid and help to me since I’ve been diagnosed. You see, I was diagnosed with MS in July 2012, so it hasn’t even been a year since I’ve known that I’m living with MS. The time that I’ve seen my neurologist, shorter, and the amount of time that I have been going through treatment for it, even shorter. I’m relatively new to this community, and so, as part of the Internet Generation, I was instantly drawn to the blogosphere that revolves around MS. The someoneonelikeme.ca (et commemoi.ca) has served to bring comfort and put my mind at ease knowing that I wasn’t the only young person with MS.

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