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Christie DeSouza photo de profil

Christie DeSouza

Peel-Halton MS Walk

Encouragez-moi!

Lar and I are enormously honoured to raise funds to end MS.  Contributing to this battle adds to the greater body of research into so many other auto-immune conditions as well.  MS is close to our hearts because of a dear friend who has lived with MS for over 30 years.  In our participation with the MS Walk, other friends have let us know that they, too, live with this unpredictable and dangerous disease.  The progress research has made is so encouraging.  We thank you for being part of the cure by your generous donations through the years!

Since the 2022 fundraising page didn't go live until mid-February, I'd like to thank those who have already donated directly to the MS Society for Lar's avatars.  Although your donations in January and the first half of February aren't listed here, know that the over $2800 you have given has been enormously appreciated by us, and more importantly, those who live with MS in Canada.


Canadians have one of the highest rates of MS in the world, and on average, 11 Canadians are diagnosed with this unpredictable illness every day. We don’t know what causes MS, and we don’t have a cure. Yet.

I am participating in MS Walk because I want to support the world’s leading researchers discover the cause, treatments and cure for MS. Leading-edge research and support programs have improved the quality of life for people affected by MS. 

When you make a donation to my fundraising, you are helping continue this incredible work.

Thank you for supporting our MS Walk community. We wouldn’t be where we are today without your support.

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