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Kate's Story

 

Tell me about your experience with multiple sclerosis.

I was diagnosed with MS in July 2002. As the loss of feeling started in my left foot and worked its way up to numb and bind the left side of my body, I realized something was horribly wrong. I have relapsing-remitting MS and have been fairly fortunate over the years. This unpredictable disease has decided to leave my left side alone and hang out with my right foot and leg.

I have adapted my life style to accommodate this disease but it has not ruled over me and my family. Actually, thanks to MS I have taken on a healthier lifestyle even though I am still learning how to pay closer attention to fatigue. It is a sneaky little side effect that can be quite debilitating. I consider myself very lucky, I have family, friends and an employer who have learned and understand the unpredictable nature of this disease. They do not identify me through MS but they do understand and will accommodate when needed. To them I am wife, mom, daughter and friend. Not Kate with MS.

I am excited to think of the future day when no one else will be diagnosed with MS. And I truly believe that I will see that day in my lifetime.

 

Profile of an MS Champion

2009 in Ontario marks the launch of the MS Champions program. This is an opportunity for participants who live with MS to voluntarily identify themselves to show the different faces of MS: this is Kate’s story.

 

How long have you participated for?

I have volunteered for two years and this will be my third year cycling, making this my five year anniversary with the Grand Bend to London Tour.


Why did you first get involved?

My husband and friends decided to do more for MS and started training for the Grand Bend to London ride. I was at a stage where I thought I couldn’t ride, so I volunteered. I was one of those people who got up at 6 am to help out at the registration tables. I then worked my way to UWO and helped at one of the tables handing out ribbons and stars. It was overwhelming to hear the stories of the cyclists. I met some cyclists who have MS and I started to think…’if they can do it, why can’t I?’

I started eating better, took off those pounds that had easily accumulated over the years and then started training for the ride. The RONA MS Bike Tour turned me around. So now I have become a MS cyclist and I will ride as long as I can. I am expecting that old age will turn me into a volunteer again and not this disease.


What does it mean to you to know that so many people participate in events like the RONA MS Bike Tour to raise funds to help end MS?

It is so clear to me that this horrible disease touches so many people. Friends, family and loved ones ride in the RONA MS Bike Tour to say enough is enough…this disease has to end. It is overwhelming to see the number of people who participate in the ride. This tells us all that the number of people affected by MS is equally overwhelming.

The research dollars are so important to help End MS and every rider and volunteer shares this common goal. The RONA MS Bike Tour means that we will all be part of changing the future of MS.


What does being an MS Champion mean to you?

Being an MS Champion means that I can adapt to what has been forced on me! As others have said and I will copy them …I have MS but it does not have me!

MS is a cruel and unpredictable disease that alters so many lives in so many different ways. I am overwhelmed and humbled at the number of people that ride and raise money to end MS.

As an MS Champion, I also get to say “thank you”. I am able to use Disease Modifying Therapies and have access to a wonderful MS Clinic. And it all comes from research dollars raised by previous and current riders.

I hope that I can put a face to the disease and help others who are living everyday with MS.


What are you most excited about for the upcoming tour?

First off, I can’t wait for Lori Anne (Lori Anne McNulty, Senior Manager, Fundraising Events) to lose the cow-boy hat because we will be the biggest ride in Canada!!!! Think of it…more cyclists…more donors…more research dollars. It all adds up to end MS!

The tour is absolutely the best weekend of the summer. All these people come together and participate in the greatest team I have ever been a part of. The team consists of crazy riders and crazy volunteers where every rest stop is filled with fun, laughter and food! Mmmmm….really good food!

 

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Our Mission :
To be a leader in finding a cure for multiple sclerosis and enabling people affected by MS to enhance their quality of life.
 

Ontario Division
Multiple Sclerosis Society of Canada
175 Bloor Street E., Suite 700, North Tower
Toronto, Ontario M4W 3R8


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