Posts Tagged ‘college’

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

The Never Ending Battle With MS, My Weight and My Laziness

Written by on June 24th, 2014 – 3 Comments

I bIMG_0051ought a new shirt earlier this month. It says “I’m not lazy – I’m physically conservative.” I tend to be on the lazier side – y’know little things like not wanting to get out of bed to answer a phone, stretching as far off my couch to reach my computer without actually getting up, frequently choosing the escalator over stairs.

But I’ve always been active – when I was younger I was in swimming lessons, and my mom would try to get me involved in basketball and soccer (that didn’t stick.) For 8 years I was enrolled in Karate, and that gave me a chance to exercise and get off my couch. I loved it, and even though it’s taken a back seat to my academics and volunteer work, I 100% intend on returning to it.

And my mom always made sure I was a healthy eater – lots of fresh fruit and veggies, homecooked meals as often as possible, limits on the amount of cookies and pop I could have.

But despite that, I’ve never been the healthiest person. I probably like McDonald’s a little too much, and may have some self control issues when a pizza or chocolate is placed in front of me.

However that all changed when I was diagnosed with Multiple Sclerosis. I realized that I needed to become more aware of my body, my health and really take control of it. This realization was by no means an instant one. I was diagnosed in July 2012, but it wasn’t until May 2013 that I realized how important it was.

Living on campus, and not having my mom looking over my shoulder led to me not being physically active… at all, and making poor choices about my diet. This led to me getting completely out of shape, and gaining a lot of weight.

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