DONATE
DONATE

Shamrock Shuffle

Join us for the Shamrock Shuffle and Run for A-Rare-Ness! ☘️

Join the Movement. Make a Difference.

Exclusive Combined Sponsorship Opportunity

🌟 Act Fast! Limited-Time Sponsorship Offer Ends February 28, 2025 🌟
Sponsor both the Shamrock Shuffle and the Run for A-Rare-Ness and Wiffle for a Cure to maximize your impact while gaining double the visibility!

  • Recognition at both events
  • Reach over 800+ attendees at Run for A-Rare-Ness alone
  • Be a champion for MPS1 families and rare disease awareness
View Sponsorship Flyer | Become a Sponsor
 
Standard Sponsorship Opportunities:

Prefer to sponsor one event? Choose from the options below:

🌈 Shamrock Shuffle – March 15, 2025

  • A family-friendly race bringing the community together for a great cause.
View Sponsorship Flyer | Become a Sponsor

🏃‍♂️ Run for A-Rare-Ness and Wiffle for a Cure – May 3, 2025

  • A one-of-a-kind fun, run, and Wiffle Ball tournament supporting MPS1 families.
Become a Sponsor

 

Why Your Support Matters

MPS1 is more than just a rare disease – it’s a relentless thief, stealing childhoods, moments of joy, and the hope every family deserves. But together, we can change the story. Every dollar raised through these events fuels life-changing initiatives:

  • Empowering Families: Helping families impacted by MPS1 with travel and accommodations so they can find connection and community at our events.
  • Driving Research: Accelerating the search for a cure and better treatments that bring hope to every family facing this diagnosis.
  • Enhancing Lives: Providing tools like iPads to give children a voice, fostering their ability to connect and thrive despite the challenges they face.

 

When you sponsor, donate, or participate, you’re not just funding a cause – you’re restoring hope and making life brighter for children and families who need it most.

Register for the Events
 
Let’s Make 2025 a Year of Hope and Action

Your support helps us continue our mission to raise awareness for MPS1 and bring hope to families impacted by this rare and progressive disease. Together, we can make a lasting impact.

Have questions or need more information?
Contact us at info@kennedyladd.org