For Families

The inspiration for this site was a desire to provide families with a better scientific understanding of our children's disorder(s), tools for improving the quality of healthcare, and with critical information from other families and medical professionals with first-hand experiences with SCN8A.

Dr. Hammer

SCN8A-related Information

Resources for Families
dna1

Know What to Ask

Questions to ask your doctor if your child is diagnosed with an SCN8A gene variant.

dna2

Doctor Directory

Find neurologists and epileptologists familiar with SCN8A-related disorders.

dna3

SCN8A Registry

To advance SCN8A research, we're working to document the first 1,000 cases of gene variants and their impact. Families are encouraged to contribute, doctors and researchers are encouraged to review and learn from our variant and phenotype databases.

Events Schedule

Feb

09

International SCN8A Awareness Day

Dec

01 - 05

American Epilepsy Society Meeting

More Resources

your stories

YOUR STORIES

 

Share your stories with SCN8A community.

general questions

MEDICATION

 

A list of medications with a goal of controlling seizures.

Doctor Directory

DIRECTORY

 

Find your nearest doctor.

Donate

DONATION

 

Help us grow!


This page was last modified on: 11/29/2017 1:04:33 AM