Epilepsy Blog Relay: Kat takes on temporal lobe epilepsy
Kat takes on living with temporal lobe epilepsy from a personal perspective
Kat takes on living with temporal lobe epilepsy from a personal perspective
Our wedding was perfect, we said the vows, danced to some favorite songs, and enjoyed our ranch dressing fountain. Just a month later, I had a tonic clonic seizure. It was the first one in over a decade, and the first one my husband has had to witness.
Reflecting on my life with epilepsy, I remember the medications and how they made me feel, the hospital stays, and the many, many doctor appointments. This Mother’s Day, it’s time for a special thanks to my mom who was there through it all. Looking back on the early days When I … Read More
Once a month, I plan to bring to light an incredible news story and how it relates to all of us affected by epilepsy. For starters, just last week in Texas, an organization had its very first harvest of medical marijuana.
When I calculate the cost of each medication I take, I could be paying over $1000 per month to manage my epilepsy if I did not have insurance to help.
The future of healthcare in the United States has become frightening and scary for our family since three of my four family members have epilepsy.
Those working on the new healthcare bill that doesn’t cover preexisting conditions must NOT have any loved ones who are affected by one.
Over 20 years ago, I told my neurologist that before menstruation, my number of seizures increased. I had never been told (or read) my monthly cycle could be a trigger, but my gut feeling said it was. My doctor assured me that menstruation was not a trigger and the increase in my … Read More