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Eli's Journey with Epilepsy | Updates and information for our family and friends

Updates and information for our family and friends

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Eli's Journey with Epilepsy | Updates and information for our family and friends | elisepilepsy.wordpress.com Reviews

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Updates and information for our family and friends

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1 YEAR SEIZURE FREE!! | Eli's Journey with Epilepsy

https://elisepilepsy.wordpress.com/2015/04/19/1-year-seizure-free

Eli's Journey with Epilepsy. Updates and information for our family and friends. Almost 2 years seizure free! 1 YEAR SEIZURE FREE! April 19, 2015. I hate to even write this post because I don’t want to jinx anything, but we are 1 year seizure free! On his developmental front, his language continues to improve. He is using about 5-10 words now to communicate with us! Https:/ www.facebook.com/tracy.luckhardt/videos/vb.601441044/10152727102991045/? He actually participated in Easter Egg hunts this year!

2

Normal(ish) Brain! | Eli's Journey with Epilepsy

https://elisepilepsy.wordpress.com/2015/02/21/normalish-brain

Eli's Journey with Epilepsy. Updates and information for our family and friends. 1 YEAR SEIZURE FREE! February 21, 2015. Well, it has been 10 months since our little man had part of his brain removed, and he is doing amazing! His EEG is normal and looks great. No spiking, no abnormal discharges, yay! I also wanted to post because since my last post, Eli has had a word explosion! All in all, just really great news. My little man amazes me so much. He has been through so much and just really takes ...Fill ...

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Our Story | Eli's Journey with Epilepsy

https://elisepilepsy.wordpress.com/our-story

Eli's Journey with Epilepsy. Updates and information for our family and friends. Little man is much happier now and overall appears to be in a better mood, even though there has been no change in his seizures. Leave a Reply Cancel reply. Enter your comment here. Fill in your details below or click an icon to log in:. Address never made public). You are commenting using your WordPress.com account. ( Log Out. You are commenting using your Twitter account. ( Log Out. Notify me of new comments via email.

4

trluckhardt | Eli's Journey with Epilepsy

https://elisepilepsy.wordpress.com/author/trluckhardt

Eli's Journey with Epilepsy. Updates and information for our family and friends. Almost 2 years seizure free! February 16, 2016. I have been meaning to update this blog for a while. Our little man has been doing sooooo well! We have come so far from the continuous, generalized spiking and epileptic discharges that were there 22 months ago. Now, unless we see any seizure activity, we don’t have to do anymore routine EEGs…eek! Some pics of his growth over the last year:. Turning 3 in October 2015! I hate t...

5

Normal EEG | Eli's Journey with Epilepsy

https://elisepilepsy.wordpress.com/2014/08/23/normal-eeg/comment-page-1

Eli's Journey with Epilepsy. Updates and information for our family and friends. Hope for 2015 →. August 23, 2014. It has also been determined that he DOES NOT have Tuberous Sclerosis (YAY! They did genetic testing on his cortical tuber, and it was negative. That along with the fact that he only had 1 tuber and absolutely no other findings suggestive of tuberous sclerosis means that he likely doesn’t have it. The geneticist did not feel we need to do anymore testing or follow up! Hope for 2015 →.

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Savanna’s Story | Savanna's Journey

https://savannalininger.wordpress.com/savannas-story

Infantile Spasms. Partial Epilepsy. Surgical Treatment. ASD. Skip to primary content. Updated December 4, 2014. I knew big news was forthcoming when Rebecca visited my office unannounced. Yes, we both wanted to have more children. But with Tristan a month away from turning 3 and Brandon 6 months old, we were just starting to find our way again. There before me was my beautiful wife not speaking and showing me an ultrasound picture clearly indicating 2 embryo sacs! I Think Something is Wrong? The second d...

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kenlininger | Savanna's Journey

https://savannalininger.wordpress.com/author/kenlininger

Infantile Spasms. Partial Epilepsy. Surgical Treatment. ASD. Skip to primary content. Skip to secondary content. Parent of Savanna, author of the blogs, husband to Rebecca, learning about all things epilepsy and autism. A Bucket of Flowers. April 1, 2016. It’s just a bucket of wild flowers from the pipeline behind our house. But, it is a bucket Savanna decided on her own to fill with flowers to give to Mommy on Easter Sunday. That was not the plan! But, I must say, many of them turned out great. She rece...

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Eli's Journey with Epilepsy | Updates and information for our family and friends

Eli's Journey with Epilepsy. Updates and information for our family and friends. Almost 2 years seizure free! February 16, 2016. I have been meaning to update this blog for a while. Our little man has been doing sooooo well! We have come so far from the continuous, generalized spiking and epileptic discharges that were there 22 months ago. Now, unless we see any seizure activity, we don’t have to do anymore routine EEGs…eek! Some pics of his growth over the last year:. Turning 3 in October 2015! I hate t...

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