I wanted to give an update on my son's diagnosis in case it might help someone else.
Nov 2013 my son had his first seizure. Complex partial. Middle of the day. It was preceded by a tiring weekend trip and accidental gluten exposure during our travels. He was diagnosed with BRE after an EEG that...
hi everyone,
I haven't posted in a long time, but I do spend time reading here. I actually thought we were out of the woods with seizures. Early this year my son, now 19 months, was having regular seizures. sometimes 2 to 3 in a day. I started to notice a connection to diet and seizures and had...
I'm curious if anyone who has tried the gluten-free diet has noticed improvement in neurological symptoms other than seizure activity.
I've seen reduction or elimination of a number of symptoms since going GF: yawning, memory & concentration problems, an intense need to sleep about an hour...
Here's a very interesting article from Gluten Free Society.
http://www.glutenfreesociety.org/gluten-free-society-blog/gluten-leaky-brain-and-epilepsy-seizures/
Hello, all! I'm not sure if I'm using this correctly, it's my first time on any type of forum. To start off, I'm 21 and living in Chicago. I thought my seizures were a part of my past so I could move out of my parents house and start a fresh chapter, but I guess they threw a curve ball and came...
Hi all,
I am back on this website to hopefully to help others get through the tough times that we experienced. This website was definitely helpful to us.
Our daughter, Stella, developed absence seizures about 2 months before her 5th birthday. Within a week, we had figured out from our own...
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