5 People who will Love Superhero Joey’s World

I don’t know about you, but I am tired of looking around and seeing scared, frustrated parents. Parents who just want to better understand their child’s Epilepsy diagnosis. So many are struggling with the unknown of their child’s diagnosis. There just isn’t a solid resource center to help them find more information on understanding their child and the future, so I decided to build this blog! Let me explain the what’s, why’s, and how’s, right now:

• If you are a parent (especially a mom, since I am that too), you’ll want to visit my blog!
• If you are looking for a place to better understand what your doctor is telling you at your child’s last appointment, you’ll want to visit my blog!
• Looking for someone who shares your feeling, frustrations, and gets “your” situation? Yup, visit my blog!
• Are you are a teacher looking for some good resources to share with your classroom about Epilepsy? Visit my blog! (PS, I would love to visit your classroom to share more about my book, via online, or if your around the Minnesota area, I could make an appearance in your classroom! [Visit my webpage for more information: http://www.amandaskoupublishing.com])
• Are you a doctor looking for ways to share more information with your patients? Visit my blog! (My book was written for that in mind! I hope all doctors who have patients with Epilepsy have access to my book one day, as an extra resource for their diagnosis.)

****I however, will NOT give out medical advice. I am NOT a doctor, or educated as one. The ultimate decision, should be between you and your child’s doctor on your child’s medical needs.****

This blog site is where I will share my knowledge, feelings, frustrations, and life as a mom. With two sons who have Epilepsy, I have done extensive research of my own. In fact, have written a children’s book about Epilepsy called Superhero Joey (check out my website for more information by clicking on the highlighted Superhero Joey above).

In conclusion, if you are someone wanting to feel first hand what it’s like as a mom of children with Epilepsy, feel free to browse around my blog page. Its an emotional blog, but so are we as parents going through life with a child with a uncurable (so far) disease. Please leave a comment and join this blog page! Thanks so much for stopping by!