New to SharingOurDays -- E. is for Epilepsy

Here's a great one from Paula Apodaca about her life with Epilepsy:

http://epilepsy-paula.blogspot.com/index.html

Here's how she describes her blog:

There are social barriers that keep people with E. out of normalized life. I want to talk about these things, so my blog isn't about treatments or surgical techniques. To me, it's more important to talk about E. with an emphasis on the experiential, social and cultural elements of epilepsy, in place of the medicalized jargon we have all been subjected to.