The Cute Syndrome Foundation: SCN8A Epilepsy Support, Awareness, and Research
  • Home
  • About
    • About SCN8A
    • About Us
    • Partner Organizations
    • Volunteers
    • Sponsors
    • 2021 Annual Report
  • Families
    • Caregiver Support
    • Join our SCN8A Community
    • SCN8A Warriors
    • Educational Videos
    • Reference Guide
    • Resources
    • Shareable Graphics
  • Events
    • Annual SCN8A Clinician, Researcher, and Family Gathering
    • Researcher Roundtable
    • Awareness Day
  • Research
    • Clinical Trials
    • Research Grants
    • SCN8A Registry
  • Donate
  • Contact
  • Blog
  • Shop

Shareable Graphics & Resources​

Images may be saved and used to spread awareness. The Cute Syndrome Foundation logo may be used when raising awareness, but anything for profit using the logo must be approved by TCSF. Please do not use the SCN8A Epilepsy heart separate from the rest of the logo as it is The Cute Syndrome Foundation's logo.

The Cute Syndrome Foundation Brochure

Print your own!
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2022 International SCN8A Awareness Day Map

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2022 Faces of SCN8A Banner

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Printable SCN8A Info Cards

Business Card size
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Facebook Profile Frames

AWARENESS DAY CANVA TEMPLATE
Facebook no longer supports profile frames, however we have created Canva templates that you can add your own photo to and upload to Facebook. Canva accounts are free to create. To make your profile photo:
  1. Open the template
  2. Click "uploads" on the left and upload your photo
  3. Drag it into the Awareness Day frame you want to use
  4. Click "share", then "download"
  5. Select the page number of the frame you used
  6. Click "download"
  7. Upload your new profile photo to Facebook!
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).
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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
    • 2021 Annual Report
  • Families
    • Caregiver Support
    • Join our SCN8A Community
    • SCN8A Warriors
    • Educational Videos
    • Reference Guide
    • Resources
    • Shareable Graphics
  • Events
    • Annual SCN8A Clinician, Researcher, and Family Gathering
    • Researcher Roundtable
    • Awareness Day
  • Research
    • Clinical Trials
    • Research Grants
    • SCN8A Registry
  • Donate
  • Contact
  • Blog
  • Shop