Epilepsy Blog Relay: Help from an epilepsy support group
Early on, Soo’s family would not use the word epilepsy in their home. Now, she is an advocate and makes the most of her local epilepsy support group.… Read More
Early on, Soo’s family would not use the word epilepsy in their home. Now, she is an advocate and makes the most of her local epilepsy support group.… Read More
Amber shares her story of brain surgery and brain tumor related epilepsy. She shares her struggle to find hope and create a life despite her challenges.… Read More
FDA offers renewed hope for families facing rare disease with the launch of the Accelerating Rare disease Cures (ARC) Program… Read More
Chantal has been battling epilepsy for 19 years with the help of VNS. She shares a recent letter to her epilepsy.… Read More
Karen on brain surgery for epilepsy: My life was going well, epilepsy didn’t stop me doing anything and I thought why take the chance?… Read More
After 38 years of secrecy, Alison is now shedding light on epilepsy by sharing information and being open about her condition.… Read More
Accepting epilepsy as a part of my everyday life only happened when I felt the slightest bit of control and ownership over this new obstacle.… Read More
When warmer weather rolls around I begin to wonder does hot weather affect epilepsy? Well, turns out I wasn’t the only one wondering.… Read More