The Cure GM1 Catalyst


Thank you so much for being part of our Giving Tuesday campaign.

FUNDRAISING


Thanks to your generous participation, we received $39,084 in donations including matching funds. Your support means everything to us and the families affected by GM1. This funding is crucial for:

Additional funding can help to expand our xCures natural history pilot to include more participants, providing invaluable data. Our advocacy efforts continue to keep drug development moving forward. We continue to work to launch new initiatives to explore potential treatments, offering hope to children and their families.

Because of you, we’re one step closer to these breakthroughs. We cannot thank you enough for standing with us in this critical effort. Together, we’re not just raising funds – we’re creating hope and changing the future of GM1.


Silhouette of a child raising a hand under a vivid fireworks show lights up the night sky.

Let’s finish the year strong!


Rare Pediatric Disease Priority Review Voucher Program Status

The Rare Pediatric Disease Priority Review Voucher Program has still not been renewed past December 20, 2024. Stay updated on the latest developments. Read more >

Meanwhile, H.R. 7384, the “Creating Hope Reauthorization Act,” would amend the date by which the drug must be designated as a rare pediatric disease drug to September 30, 2028, and the date by which the application must be approved to September 30, 2030. This bill was introduced in the House and referred to the Energy and Commerce Committee’s Subcommittee on Health.

If the rare pediatric disease PRV program is not reauthorized, eligibility to receive a voucher will be limited to products that receive rare pediatric disease designation by December 20, 2024, and are approved by September 30, 2026.

Action Alert: Contact your Senator today to ensure the “Creating Hope Reauthorization Act” passes before December 20th, 2024!


Take Action Here>

Share Your Holiday Spirit with the GM1 Community

COMMUNITY & ENGAGEMENT

As the year wraps up, we’re spreading awareness and recognizing our global community, and we’d love for you to be part of it! Share a high-resolution holiday photo of your family or children, along with a meaningful holiday quote. Please note that all submissions will be shared publicly within our community. Submit your holiday quote using this form: Holiday Quote Form.



Sweet Iris Day Was December 3rd

December 3rd was Sweet Iris Day, a day dedicated to raising awareness for GM1 gangliosidosis. This special day was proclaimed by our mayor in honor of Iris, who, at just 9 years old, inspired our community with her strength and spirit. Join us as we shine a light on GM1 awareness and advocacy.



Christine Represents Cure GM1 at the Ultragenyx Rare Disease Bootcamp

Christine attended the Ultragenyx Rare Disease Bootcamp on November 12th and 13th, connecting with a dedicated community of advocates working to develop new treatments for rare diseases. While Cure GM1 has been tirelessly fighting this battle for years, staying connected with advancements in technology and expanding our network is essential to driving progress and hope for our families.

Read More>


Worldwide Candle Lighting Ceremony  On December 8, 2024, at 7:00 pm local time, candles will be lit around the world to honor the memory of children gone too soon. The annual Worldwide Candle Lighting (WCL), organized by The Compassionate Friends, is now the largest mass candle-lighting event globally. 

Learn more>

Love Letters to Our Angels

COMMUNITY & ENGAGEMENT

“There is no foot too small that it cannot leave an imprint on this world.” – Unknown
“Luís Gabriel lived among us for 3 years and 23 days and will live in me as long as I live. There is no way to measure how much we learned from him in these 3 years. A love so pure, a look into the soul, as if we could contemplate God in your eyes. Forever my eternal Beloved Son Luís Gabriel. I hope from the bottom of my heart that one day this disease will be cured and treated, so that other families are not torn apart by it.”
DEAR Luís Gabriel
CHILD
“God’s visiting our lives! That’s what you were to us, Tetê. We always knew it would be for a short time, we always knew that you were Christ Wounded himself visiting us. You were born ready for Heaven. God gave us a daughter more worthy of Heaven than of Earth. We cared, we loved you, we gave you back! Your deep, pure eyes will always be recorded in my heart and soul. I wish I had done more, I could have done more, but time doesn’t come back. The longing seems to crush my heart, the pain is suffocating!”
DEAR Tetê
CHILD
“With you we experienced the greatest joy and the greatest suffering, but we understood that you came to leave an incredibly large mark on your short life.”
DEAR Alejandro
CHILD
Matthew 19:14 – Then Jesus said, “Leave the little children alone, and don’t try to keep them from coming to me, because the kingdom of heaven belongs to such as these.” You taught me the purest love I could feel, thank you for choosing me as your mommy.”
DEAR Pedro
CHILD

Use the code FUNDRAISECGM1 at checkout to receive a special discount on your purchases. Plus, 15% of your purchase will be donated to charity. It’s a simple way to give back while shopping for beautiful, high-quality products. Every purchase helps make a difference for those affected by GM1 gangliosidosis.

Visit Minted.Com to support Cure GM1