The Cute Syndrome Foundation: SCN8A Epilepsy Support, Awareness, and Research
  • Home
  • About
    • About SCN8A
    • About Us
    • Partner Organizations
    • Volunteers
    • Sponsors
    • 2019 Annual Report
  • Families
    • Join our SCN8A Community
    • SCN8A Warriors
    • Reference Guide
    • Shareable Resources
    • Family Meetup Grant Application
  • Events
    • 2020 Annual Gathering
    • Annual SCN8A Clinician, Researcher, and Family Gathering
    • Researcher Roundtable
    • Awareness Day
  • Research
    • Research Grants
    • SCN8A Registry
  • Donate
    • How You Can Help
    • SCN8A Awareness Gifts
  • Contact
  • Gathering Family Portal
    • 2020 Annual Gathering >
      • Video Page
    • 2019 Annual Gathering >
      • Day 1 Agenda
      • Day 2 Agenda
      • Presentations
      • Speakers
      • Video Page
    • SCN8A Lexicon
  • Blog
  • Shop

How You Can Help

We recognize that there are a number of causes competing for your attention and support.
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​What sets us apart is that The Cute Syndrome Foundation 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.


And we cannot do this without your support! So, please consider making a donation to The Cute Syndrome via PayPal or contact Hillary for more information. ​​​

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.

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.

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!

Add a TCSF Facebook Frame to your profile picture!
To find all past & current frames:
  • Go to facebook.com/profilepicframes.​
  • Search for our frames by entering The Cute Syndrome.
  • Choose the frame you want to use from the results.
  • Click "Use as Profile Picture".
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Past Annual Reports

Past PCDH19 Efforts

​Privacy Policy

​Annual SCN8A Family Gathering Portal
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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
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  • Home
  • About
    • About SCN8A
    • About Us
    • Partner Organizations
    • Volunteers
    • Sponsors
    • 2019 Annual Report
  • Families
    • Join our SCN8A Community
    • SCN8A Warriors
    • Reference Guide
    • Shareable Resources
    • Family Meetup Grant Application
  • Events
    • 2020 Annual Gathering
    • Annual SCN8A Clinician, Researcher, and Family Gathering
    • Researcher Roundtable
    • Awareness Day
  • Research
    • Research Grants
    • SCN8A Registry
  • Donate
    • How You Can Help
    • SCN8A Awareness Gifts
  • Contact
  • Gathering Family Portal
    • 2020 Annual Gathering >
      • Video Page
    • 2019 Annual Gathering >
      • Day 1 Agenda
      • Day 2 Agenda
      • Presentations
      • Speakers
      • Video Page
    • SCN8A Lexicon
  • Blog
  • Shop