Beyond medication: A tiny device making a big difference
A tiny device called AspireSR offers a little hope to Rachael, diagnosed with the rare Aicardi Syndrome, and her parents.… Read More
A tiny device called AspireSR offers a little hope to Rachael, diagnosed with the rare Aicardi Syndrome, and her parents.… Read More
I was recently invited to be the guest host on h360 LIVE, which is Healtheo360’s live talk show. The show was fun and I thought you might want to take a look. … Read More
I am pleased to introduce you to Emily. She approached Living Well With Epilepsy and asked if we would do a post on Project EpiBear. I encourage you to take a moment to learn more about this young woman who is taking on epilepsy one bear at a time. – Jessica Keenan … Read More
This summer my family took a vacation at Hunter Mountain thanks to the generosity of some very good friends. It was our first vacation in a few years. The trip was not only relaxing, but it gave me the chance to try pushing the limits of my epilepsy in ways that surprised … Read More
On this Father’s Day I would like to take a minute to publicly say thank you for all my dad has done for me. Here are a few photos to show how dad has always gone above and beyond for me and the rest of my family. Dad has always been concerned … Read More
If you missed the broadcast, check out the recording of Jessica Keenan Smith, founder of Living Well With Epilepsy, as she talks about epilepsy on WHYY.… Read More
This personal story was contributed by Debbie Fincher, mom to Noel and Board Chair and Founder of the Angel Wings Foundation, an organization which is creating a new housing model for people living with epilepsy in need of long term support. … Read More
We are now looking for someone to cover the Epilepsy Mommy column. You could be a mom living with epilepsy or a mom to a child with epilepsy. … Read More