Give Hope. Change Lives. Honor Ryan

Give Hope. Change Lives. Honor Ryan campaign photo, 1 of 3Give Hope. Change Lives. Honor Ryan campaign photo, 1 of 3

6 donors
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$3,330 raised of $10K CAD

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Give Hope. Change Lives. Honor Ryan

Give Hope. Change Lives. Honor Ryan

0% complete

$3,330 raised of $10K CAD

6 donations
Donation protected
Help us advance Tourette Syndrome research, education, awareness, and advocacy.

The Ryan Lawrence Tourette Syndrome Foundation was created in loving memory of Ryan Lawrence, a young man who lived with Tourette Syndrome and whose life continues to inspire our mission.

Tourette Syndrome is a neurological condition that affects individuals and families around the world. Too often, those living with Tourette Syndrome face misunderstanding, stigma, and challenges accessing appropriate support and treatment.

We believe every person with Tourette Syndrome deserves to be understood, accepted, and supported.

Your generosity helps us continue important work, including:
  • Supporting Tourette Syndrome research.
  • Creating educational resources for individuals, families, teachers, and healthcare professionals.
  • Sharing conversations with internationally recognized Tourette Syndrome specialists through our Movers & Shakers interview series.
  • Producing Ryan's Tic Chronicles, an animated educational series inspired by Ryan's experiences.
  • Raising awareness, reducing stigma, and supporting scholarship opportunities.

Whether your gift is $25, $50, $100, or another amount, your support helps us continue our mission.

What began as a father's desire to honour his son has become a commitment to helping others. Ryan's life may have been far too short, but his legacy continues through the people we support, the awareness we raise, and the progress we help make possible.

Please donate today and share this campaign with your family and friends.

From our family to yours, thank you for helping us turn love into lasting change.

Ryan Lawrence Tourette Syndrome Foundation
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Ryan Lawrence Tourette's Syndrome Foundation
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