These are stories shared by SCN8A parents who have opened up to share some of the most challenging and scary parts of having a child with or losing a child to SCN8A-Related Epilepsy.
By sharing these stories, we hope to make it clear to decision makers the constant fear we live in and the pain our children endure without targeted treatments.
The Toll on Our Children and Families
Click on the collage to hear each family's story.
“At 13 months Jake was seizing uncontrollably. Nothing could stop them and we were told to be prepared to lose him… 2-3 months later we were told Jake had an SCN8A mutation and we should try all the sodium channel drugs. They provided some help where we could go a day without a seizure…but one day without a seizure is not life…Watching your child suffer endlessly is not life…the endless drugs that I had to give him to stop seizing caused such detrimental side effects …that were often worse than the seizures…I was at a place where my son was suffering every minute of his life that I had to let him go. No parent should ever have to choose that.
That is why new medicines must be in place. I’m asking you to help us – to help children like my son – to help the future children. I never want another mother to live what I lived. I never want another child to have to endure what my child did.”
- Britani, Jake's mother -
Jake passed away at age 3 in 2016.
“This is Connor’s kitchen and Connor’s medicine cabinet. No 10-year-old should need their entire cabinet in the kitchen for medications. But when you have difficult to treat epilepsy, you do…We implore you to invest in an areas giving Connor a specific medication for SCN8A.
- Krista, Connor’s mother -
Connor is 10 years old and lives in Virginia.
“Our children are dying. Our children are dying from this disease. This is a terrible life-sucking disease. It sucks the life out of our children. Our children are suffering. Our children are dying. Our children are seizing. Our children are in pain. Our children’s stomachs don’t empty out. My son can’t run and play with his brothers and sisters. Something needs to be done. I don’t know what research or what medicine, but we need to have a cure. I am begging whoever is listening to this to please work your hardest at finding something for our children.”
- Tammy, Liam's mother -
Liam is 6 years old and lives in Michigan.
"We spent a majority of the first two and a half years in and out of the hospital, sometimes twice a day and sometimes a week at a time, countless ambulance rides and airlifts. No child should have to endure a life like this."
- Alisha, Clayton's mother -
Clayton is 6 years old and lives in California.
“He filled our lives with joy. He made us smile. My children do smile without him, we do, but we are not the same. There’s a giant piece of us all missing…This is a tough mutation and a tough disease. I really hope there are medications out there than can treat the actual channel and not just the symptoms. And that there are better outcomes.”
- Elizabeth, Declan's mother -
Declan passed away at age 6 in 2018.
“I envision telling his sister that Elliott’s gone. It scares the heck out of me. But he’s so fragile that there’s a distinct reality that it could happen to him – at any moment. A lot of children with SCN8A are dying and we definitely need treatments. We desperately need life-altering treatments that will not just get rid of the seizures but will help our children to grow and prosper. And live a life that is more than just lying on a bed, lying on a mat, getting fed through a tube. He deserves more. All our children deserve more.”
- Gabi, Elliott's mother -
Elliott is 7 years old and lives in
If you have any questions or would like to be in touch with us, please contact Gabi at email@example.com.