Decoding Dravet Blog

As the Dravet syndrome patient community approaches the possibility of ASO and gene therapy advancements, DSF acknowledges the importance of proactive planning to ensure seamless patient access and insurance coverage when these treatments become available. This year, we launched our latest initiative, our Legislative Advocacy Program, aimed at ensuring that the concerns of our community […]

I became involved with the Dravet Syndrome Foundation (DSF) to find a sense of control where there was none. Being active and trying to be part of a solution became a driving force for me. Grace was diagnosed with Dravet syndrome (DS) a couple of months after her first birthday and I felt shock, sadness,

“How is Cora doing?” is a typical question we get after our 4 year old daughter has had a seizure. It is a socially acceptable and appropriate question to ask a parent who has a medically complex kid. I wish I could say as the parent of that medically complex kid that the answer is

At this year’s conference, we honored five individuals whose dedication and active participation in our mission are helping to drive advancements in the field of Dravet syndrome. Continue reading to discover more about this year’s recipients and the impact they are making for the Dravet syndrome community. Impact & Legacy Award – Theron (Ted) Odlaug,

This year commemorates the 15th anniversary of DSF! We eagerly anticipate celebrating the initial 15 years of our impactful journey with you throughout 2024, sharing the highlights of what our community has accomplished through DSF: 15 years of funding groundbreaking research.  15 years of connecting and supporting families. 15 years of raising awareness of Dravet

This June, take action. Do your part (big or small) to give the Dravet syndrome community the recognition it deserves during Dravet Syndrome Awareness Month.   Like & Share our Posts: Get connected with us on our social media channels so you can like and share our posts throughout June. Spread Awareness on Social Media: This

DSF hosts monthly online sessions to offer caregivers the opportunity to connect and engage with peers, to support one another, as well as to ask questions of DSF and its staff. We know that exposure to stories, insights, and information sharing is particularly helpful when you are caring for someone with Dravet syndrome. Chat &