The Cute Syndrome Foundation
PO Box 842 Ozark, MO 65721
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 are fighting for the future of children with these disorders. We cannot do this without your support!
Please consider making a donation to The Cute Syndrome via PayPal below, or contact Kacie for more information. Donations are tax deductible as allowed by law. TCSF’s tax identification number is 46-2699066.
Make a Financial Donation
Making a financial donation is one of the most important ways you can help. We are a 100% volunteer-run organization, which means 100% of your donation goes toward fighting SCN8A.
Currently, you can donate via Facebook and PayPal. *Please note that Facebook does not deduct a fee from your donation, so 100% of your donation comes to us. PayPal does deduct a percentage.
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 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.
Sign Up for AmazonSmile
Sign up for AmazonSmile and choose The Cute Syndrome Foundation as your charity of choice. Amazon will donate a percentage of all eligible purchases to us.
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
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.
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.
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.