The Cute Syndrome Foundation: SCN8A Support, Awareness, and Research
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Call for Abstracts for the 6th Annual SCN8A Clinician, Researcher, and Family Gathering

9/2/2020

1 Comment

 
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2020 has been quite a year. I know we are all disappointed about not being able to all be together in person for our 6th Annual SCN8A Clinician, Researcher, and Family Gathering  in December. However, with the help of John Schreiber, Manoj Patel, and TCSF's volunteer team, we are planning a virtual Gathering so that we can convene as a community to share our work and updates from the last year. The Gathering is tentatively scheduled for Dec 4.
The Gathering platform will require a slightly different approach. We will also be piloting a new approach for sharing research--we invite all of you to submit abstracts for consideration for a panel discussion at our main professionals and families event as well as in-platform poster sessions. 

Abstract Submission Information:
1. We are requesting abstracts detailing your SCN8A-related research. This is a great opportunity to share your recent scientific work and observations on SCN8A with the SCN8A community.
2. Abstracts should be 300 words or less (yes, please feel free to use your AES abstracts!)
3. Submit to me at [email protected] by September 30th, 2020 

Looking forward to "seeing" all of you in December!
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1 Comment
Charter Tunisie link
6/23/2023 05:30:23 pm

Thanks forr a great read

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The Cute Syndrome is registered as a tax-exempt organization under IRS section 501(c)(3).
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  • 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