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FamilieSCN2a

The official site for families of children with SCN2a mutations of epilepsy.

http://www.scn2a.org/

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FamilieSCN2a | scn2a.org Reviews
<META>
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The official site for families of children with SCN2a mutations of epilepsy.
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KEYWORDS
1 BFNIS
2 LG
3 Lennox Gastaut
4 MPEI
5 Othahara syndrome
6 autism
7 dilantin
8 epilepsy
9 genetic
10 genetic epilepsy
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FamilieSCN2a | scn2a.org Reviews

https://scn2a.org

The official site for families of children with SCN2a mutations of epilepsy.

LINKS TO THIS WEBSITE

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Home

http://www.bensbunch.com/home.html

FamilieSCN2a Foundation Donation Page. Welcome Back Ben's Bunch! ALL HANDS ON DECK! The FamilieSCN2a Foundation is hosting the first ever 5K Color Dash to raise funds for research to find a cure for SCN2a. The event will be local for all of you awesome Ben's Bunch supporters to come and share this special day with us. There will be loads of fun activities for those of all ages and athletic ability! Did I mention the food vendors? Please register today and share with all your friends and family.

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Families with SCN2A - Special Parent Connections

http://www.specialparentconnections.com/familiescn2aorg.html

FAMILIEScn2a is an organization created by parents of children diagnosed with epilepsy as a result of a mutation in the SCN2a gene. Our goal is to find a cure for our kids. You are not alone! If you or your child(ren) have been diagnosed with a gene mutation of SCN2A, please know there are other families out here that want to connect with you and help support you on your journey. Please click on the web site link in the button above to visit the FAMILIEScn2a.org web site. Create a free website.

specialparentconnections.com specialparentconnections.com

SCN2A - Special Parent Connections

http://www.specialparentconnections.com/scn2a.html

Emily's Official Diagnosis - SCN2A Missense Gene Mutation. Emily's results were this: the gene where the mutation occurred is at SCN2A. It is considered Autosomal dominant. Meaning if Emily has children she will have a 50% chance of passing this gene onto one or more of her own children. It is considered Characterized. Which simply means this mutation IS associated with epilepsy. Her protein change is a p.G882E. And her Nucleotide Change is c.2645G A. Not from either parent. Her Alteration. Emily's speci...

bensbunch.com bensbunch.com

What Now?

http://www.bensbunch.com/what-now-.html

Friday evening, after a day and a half of failed induction that led to a C-section, we welcomed a healthy, beautiful and big baby boy into our family. Benjamin was 8.9 lbs., 21 inches long and perfect in every way. Everyone said he was the cutest baby in the nursery, and biased as we all may be, I truly believe he was! When they finally laid my baby in my arms, I whispered in his ear, I have been waiting for you my whole life. I was in love. I learned that our support group is huge, and absolutely devote...

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Gallery

http://www.bensbunch.com/gallery.html

bensbunch.com bensbunch.com

My Story

http://www.bensbunch.com/my-story.html

Hi My name is Ben and I am 4 years old. If you have met me, you know that I am the sweetest, most loving and affectionate little boy in the world! I have a smile that makes people's hearts smile back. My favorite toys, besides my mom and dad, are things that light up or spin. I am also super into music and have more rhythm than a jazz band! Some things I am really good at are, snuggling, kissing, eating goldfish, climbing everything and winning over anyone that crosses my path! It is not all bad though&#...

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