The Cute Syndrome Foundation: SCN8A Support, Awareness, and Research
  • Home
  • About
    • About SCN8A
    • About Us
    • Partner Organizations
    • Volunteers
    • Annual Report
  • Families
    • Join our SCN8A Community
    • Connor James Smith Patient Assistance Grant
    • Educational Videos >
      • Annual Gathering Event Recordings
      • Cheers to a Good Life
      • Clinical Trial Readiness Series
      • Family and Researcher Roundtable Series
      • Meaningful Change Series
    • Resources >
      • Caregiver Support
      • Reference Guide
      • Shareable Graphics
    • CUTE Connections Grant
    • SCN8A Warriors
    • Virtual Memory Wall
  • Events
    • Annual SCN8A Clinician, Researcher, and Family Gathering >
      • CUTIES Awards
      • Speakers
    • Researcher Roundtable
    • Awareness Day
    • Layla: The Festival of Mark Making
    • Virtual 5k
  • Research
    • Clinical Trials
    • Research Grants
    • SCN8A Registry
  • Donate
  • Contact
  • Blog
  • Shop

How You Can Help

Picture
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.
CREATE A FACEBOOK FUNDRAISER

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.
SIGN UP FOR IGIVE

Purchase TCSF Merchandise

We currently offer three different ways to purchase merchandise: our Annual Gathering t-shirt campaign in the Fall; our Annual Awareness Day t-shirt campaign in the Spring; and our online TCSF 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.

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.
Picture
Picture
Picture
Past Annual Reports

Past PCDH19 Efforts

​Privacy Policy

The Cute Syndrome Foundation

PO Box 842 Ozark, MO 65721​
The Cute Syndrome is registered as a tax-exempt organization under IRS section 501(c)(3).
​
Our tax identification number is: 46-2699066.

© The Cute Syndrome Foundation, All rights reserved
Picture
Picture
Picture
Picture
  • Home
  • About
    • About SCN8A
    • About Us
    • Partner Organizations
    • Volunteers
    • Annual Report
  • Families
    • Join our SCN8A Community
    • Connor James Smith Patient Assistance Grant
    • Educational Videos >
      • Annual Gathering Event Recordings
      • Cheers to a Good Life
      • Clinical Trial Readiness Series
      • Family and Researcher Roundtable Series
      • Meaningful Change Series
    • Resources >
      • Caregiver Support
      • Reference Guide
      • Shareable Graphics
    • CUTE Connections Grant
    • SCN8A Warriors
    • Virtual Memory Wall
  • Events
    • Annual SCN8A Clinician, Researcher, and Family Gathering >
      • CUTIES Awards
      • Speakers
    • Researcher Roundtable
    • Awareness Day
    • Layla: The Festival of Mark Making
    • Virtual 5k
  • Research
    • Clinical Trials
    • Research Grants
    • SCN8A Registry
  • Donate
  • Contact
  • Blog
  • Shop