It’s been a long time since I’ve had a chance to write a blog post. Between work, family, and finding time for adequate sleep, blogging has (temporarily) gone to the wayside. However, it’s never too long before I’m reminded of the omnipotence of epilepsy both in my life and the world around us.
Last week I accepted two new patients into my general pediatrics practice with intractable epilepsy. The mother of one young girl with Lennox Gastaut Syndrome brought pictures taken of her daughter during infancy. The bright-eyed toddler with an open mouthed grin in the picture acutely defied the image of the now 8-year-old non-verbal and minimally interactive young lady reclined in a wheelchair. The same day, I met a three-year-old boy with a genetic syndrome and subsequent seizures. I smiled as he toddled around the exam room and touched everything within reach to explore his environment. Still, as I typed in his medication list and reviewed his history of past hospitalizations, I worried about how his recurrent prolonged seizures would affect his development. Time can only tell how each child will endure their significant challenges.
Earlier this month, I had an article published in Epilepsia, the journal of the International League Against Epilepsy, discussing what it’s like to navigate life as both a professional and patient with epilepsy. You can see that article here:
And later this month, I am looking forward to participating in an event sponsored by Madison Friends of CURE and Joey’s Song (see the past post about Joey here) If you’re in the Madison area and would like to participate in a great event to raise awareness about epilepsy, please click on the link below:
In the meantime, to those of you who don’t live with epilepsy or have a loved one with seizures, thank you for opening your heart and mind to understanding this incredibly common but still stigmatized disease. And to those who intimately understand what it means to live with seizures, God bless and let’s continue to raise awareness and find a cure.