We recognize that there are a number of causes competing for your attention and support.​ What sets us apart is that TCSF has been able to accomplish an amazing amount in a short period of time by strategically funding only the most promising and innovative SCN8A research. We cannot do this without your support!
*Processing fees and tips to GiveButter are 100% optional. Processing fees cover our credit card processing costs, so more of your donation goes to our mission. Tips go directly to GiveButter to keep their fundraising platform free for nonprofits like TCSF.

Make a Financial Donation

Making a financial donation is one of the most important ways you can help. Because of the generosity of our supporters, TCSF is able to fund cutting-edge research that brings hope and the potential for better treatments and provide valuable resources for our families living with SCN8A.
Donations are tax deductible as allowed by law. TCSF’s tax identification number is 46-2699066.
Mailing Address:
The Cute Syndrome Foundation
PO Box 842 Ozark, MO 65721​

Other Ways to Help

Follow Us on Social Media

Learn about the families affected by SCN8A, and stay up to date on our events and progress by following us on Facebook, Instagram, and Youtube.

Create a Facebook Fundraiser

Creating a birthday fundraiser (or just because!) on Facebook is a great way to raise awareness and funds for TCSF. Just click the button below to begin! You can also sign into your account, select "fundraisers", click "select non-profit", and search for The Cute Syndrome Foundation. Then add a goal, timeline, and info about why you are raising money. We will be mailed a check automatically after the fundraiser ends.

Use iGive.com

Shop at over 2,000 stores through iGive.com or the iGive app and a percentage of your purchase will be donated to The Cute Syndrome Foundation! Create a free account and select The Cute Syndrome Foundation as your cause to get started.

Purchase TCSF Merchandise

We currently offer three different ways to purchase merchandise: our Annual Gathering t-shirt booster campaign in the Fall; our Annual Awareness Day t-shirt booster campaign in the Spring; and our online TCSF home & apparel shop that is open year round. A portion of proceeds from each sale comes back to TCSF. Follow us on social media to see our Annual Gathering and Awareness day shirt sales.

Buy a SCN8A Ornament

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What better way to spread awareness to family and friends than by purchasing SCN8A items to give for birthdays and holidays? Lacey Juroske, whose daughter Sadie has SCN8A, started an ETSY shop called DandLImpressions, where she sells hand stamped SCN8A items which make a great gift! Not only are you spreading awareness, but 20% of sales are donated to TCSF with every purchase.

Volunteer

It doesn't matter whether you have experience as a non-profit volunteer, plenty of time to spare, or a specific set of skills, as long as you've got a desire to help then we could use you! Contact Shelley for more info.

Spread Awareness

Please help us reach as many people as possible by sharing our information with friends, family, clinicians, researchers—anyone you can! Also, take some time to learn about SCN8A and Epilepsy first aid, and share what you learn!

We have various graphics available to make sharing easy, or you can share our posts on Facebook, Instagram, or LinkedIn. Sharing about TCSF and SCN8A on social media is one of the easiest ways to spread awareness to a large audience.