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Loving Luke

My husband, Dan and I have 2 sons. Ben is 6 years old. Luke was born March 17, 2010. Luke has a rare genetic condition MPPH (Megalencephaly Polymicrogyria Polydactyly Hydrocephalus) Syndrome and epilepsy. This blog is to help keep friends and family updated and also to hopefully find other parents/families who have experience with polymicrogyria and MPPH.

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Loving Luke | lovingluke1.blogspot.com Reviews
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My husband, Dan and I have 2 sons. Ben is 6 years old. Luke was born March 17, 2010. Luke has a rare genetic condition MPPH (Megalencephaly Polymicrogyria Polydactyly Hydrocephalus) Syndrome and epilepsy. This blog is to help keep friends and family updated and also to hopefully find other parents/families who have experience with polymicrogyria and MPPH.
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1 loving luke
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6 share to twitter
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9 hunkered down
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loving luke,posted by,4 comments,email this,blogthis,share to twitter,share to facebook,share to pinterest,hunkered down,working on homework,3 comments,epilepsy,mpph,mpph syndrome,polylmicrogyria,seizures,neurologist appointment with,both boys oy,so great
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Loving Luke | lovingluke1.blogspot.com Reviews

https://lovingluke1.blogspot.com

My husband, Dan and I have 2 sons. Ben is 6 years old. Luke was born March 17, 2010. Luke has a rare genetic condition MPPH (Megalencephaly Polymicrogyria Polydactyly Hydrocephalus) Syndrome and epilepsy. This blog is to help keep friends and family updated and also to hopefully find other parents/families who have experience with polymicrogyria and MPPH.

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lovingluke1.blogspot.com lovingluke1.blogspot.com
1

Loving Luke: Christmas in June and July!

http://lovingluke1.blogspot.com/2014/07/christmas-in-june-and-july.html

My husband, Dan and I have 2 sons. Ben is 6 years old. Luke was born March 17, 2010. Luke has a rare genetic condition MPPH (Megalencephaly Polymicrogyria Polydactyly Hydrocephalus) Syndrome and epilepsy. This blog is to help keep friends and family updated and also to hopefully find other parents/families who have experience with polymicrogyria and MPPH. Thursday, July 3, 2014. Christmas in June and July! Sooo much great stuff to update and so little time! Well, first of all, it takes for-ev-er! Second ...

2

Loving Luke: March 2015

http://lovingluke1.blogspot.com/2015_03_01_archive.html

My husband, Dan and I have 2 sons. Ben is 6 years old. Luke was born March 17, 2010. Luke has a rare genetic condition MPPH (Megalencephaly Polymicrogyria Polydactyly Hydrocephalus) Syndrome and epilepsy. This blog is to help keep friends and family updated and also to hopefully find other parents/families who have experience with polymicrogyria and MPPH. Monday, March 16, 2015. Happy St. Patrick’s Day and Happy Birthday, Luke! Luke is really excited about his birthday this year. On the weekends and when...

3

Loving Luke: April 2014

http://lovingluke1.blogspot.com/2014_04_01_archive.html

My husband, Dan and I have 2 sons. Ben is 6 years old. Luke was born March 17, 2010. Luke has a rare genetic condition MPPH (Megalencephaly Polymicrogyria Polydactyly Hydrocephalus) Syndrome and epilepsy. This blog is to help keep friends and family updated and also to hopefully find other parents/families who have experience with polymicrogyria and MPPH. Thursday, April 17, 2014. He's totally skipping just playing and going straight to sleepovers! He's turning into such a nut. Subscribe to: Posts (Atom).

4

Loving Luke: Summer 2015!!!

http://lovingluke1.blogspot.com/2015/06/summer-2015.html

My husband, Dan and I have 2 sons. Ben is 6 years old. Luke was born March 17, 2010. Luke has a rare genetic condition MPPH (Megalencephaly Polymicrogyria Polydactyly Hydrocephalus) Syndrome and epilepsy. This blog is to help keep friends and family updated and also to hopefully find other parents/families who have experience with polymicrogyria and MPPH. Tuesday, June 23, 2015. Nurse Leah, Ms. Birner, Mrs. Walker. Mrs Mayer and Luke. Exciting stuff.Luke is learning to write his name! All By. Himself!

5

Loving Luke: The Big Five!

http://lovingluke1.blogspot.com/2015/03/the-big-five_16.html

My husband, Dan and I have 2 sons. Ben is 6 years old. Luke was born March 17, 2010. Luke has a rare genetic condition MPPH (Megalencephaly Polymicrogyria Polydactyly Hydrocephalus) Syndrome and epilepsy. This blog is to help keep friends and family updated and also to hopefully find other parents/families who have experience with polymicrogyria and MPPH. Monday, March 16, 2015. Happy St. Patrick’s Day and Happy Birthday, Luke! Luke is really excited about his birthday this year. On the weekends and when...

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Caring for Callie: How it all went down

http://calliebloggie.blogspot.com/2011/01/how-it-all-went-down.html

A mommy's journal about her very special baby girl. Wednesday, February 2, 2011. How it all went down. I remember thinking this seemed like an over-reaction, but okay. I called Allen at work to let him know and got the kids together. Believe it or not, this was our first trip to the ER. I don't know how it is possible that we had a nearly 4 year old boy and never spent time in the ER, but I guess we were lucky (until this point). This is Callie just before she was diagnosed. When things were perfect.

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Caring for Callie: March 2014

http://calliebloggie.blogspot.com/2014_03_01_archive.html

A mommy's journal about her very special baby girl. Friday, March 7, 2014. We have had quite a winter here in Northern Virginia! By the standards of my friends farther north, it has been nothing, but VA is not very good at dealing with cold weather and snow removal. We live in the more densely populated eastern part of our county and often get snow days due to the conditions of the roads in the more rural western region. The other day was our 13th snow day! Callie did great in the snow this year!

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Caring for Callie: April 2014

http://calliebloggie.blogspot.com/2014_04_01_archive.html

A mommy's journal about her very special baby girl. Sunday, April 20, 2014. Subscribe to: Posts (Atom). This is a mommy's journal about her very special baby girl. Callie has a rare neurological disorder called bilateral perisylvian polymicrogyria (PMG). She has also experienced infantile spasms and has been diagnosed as failure to thrive. Callie currently battles seizures, eosinophilic esophagitis (EoE) and apraxia of speech, and has a G tube. Life on Mystery Lane. Didn't See It Coming.

calliebloggie.blogspot.com calliebloggie.blogspot.com

Caring for Callie: Trampoline

http://calliebloggie.blogspot.com/2012/09/trampoline.html

A mommy's journal about her very special baby girl. Monday, September 24, 2012. Thank you for the trampoline, Miss Angela! It brought tears to my eyes too. So sweet to see her doing so well. On September 24, 2012 at 7:45 PM said. Such a big, strong girl! On November 8, 2012 at 1:25 PM said. I just love this! So proud of her:)! Subscribe to: Post Comments (Atom). If you would like to read from the beginning, here is how it all went down. Life on Mystery Lane. Didn't See It Coming. Pieces of the Reeses.

calliebloggie.blogspot.com calliebloggie.blogspot.com

Caring for Callie: Apraxia Awareness Day

http://calliebloggie.blogspot.com/2013/05/apraxia-awareness-day.html

A mommy's journal about her very special baby girl. Tuesday, May 14, 2013. Today is Apraxia Awareness Day! Apraxia is among the most severe speech and communication problems in children. Affected children have difficulty planning and producing the precise, highly refined and specific series of movements of the tongue, lips, jaw, and palate that are necessary to produce clear, intelligible speech. I recently joined a Facebook Group for parents of children with apraxia which has over 10,000 members!

calliebloggie.blogspot.com calliebloggie.blogspot.com

Caring for Callie: September 2013

http://calliebloggie.blogspot.com/2013_09_01_archive.html

A mommy's journal about her very special baby girl. Thursday, September 19, 2013. Callie started her second year of special ed preschool at our home elementary school. I really like the fact that she and Owen are in the same location and their classrooms are right down the hall from each other. This year Callie is in an afternoon class five days a week. A big yellow school bus picks her up and drops her off right in front our our home. She loves it! Can you believe how grown up she looks in this picture?

calliebloggie.blogspot.com calliebloggie.blogspot.com

Caring for Callie: Callie at 3

http://calliebloggie.blogspot.com/2012/12/callie-at-3.html

A mommy's journal about her very special baby girl. Friday, December 7, 2012. I can't believe our baby girl turned 3 this past month. Like I did 6 months ago. I thought it would be good to recap where she is in different areas. Stats: Callie is now just over 35 inches tall (10%) and weighs 28 pounds (25%). Her BMI is 50%, which really great. Gross motor skills: As you know, Callie started walking. Although her gait remains abnormal. Her legs still hyper-extend when she does not have her AFOs. Was correct...

calliebloggie.blogspot.com calliebloggie.blogspot.com

Caring for Callie: October 2013

http://calliebloggie.blogspot.com/2013_10_01_archive.html

A mommy's journal about her very special baby girl. Thursday, October 31, 2013. Happy Halloween from Princess Callie! Wednesday, October 9, 2013. Subscribe to: Posts (Atom). If you would like to read from the beginning, here is how it all went down. Life on Mystery Lane. Didn't See It Coming. Pieces of the Reeses. Upped the dose again. 21 Days of AAC Challenge: 2016. Fighting Monsters with Rubber Swords. There was an error in this gadget. Flower Image by Dapino.

calliebloggie.blogspot.com calliebloggie.blogspot.com

Caring for Callie: Return of Seizures

http://calliebloggie.blogspot.com/2013/10/return-of-seizures.html

A mommy's journal about her very special baby girl. Wednesday, October 9, 2013. On October 15, 2013 at 10:51 PM said. Im so sorry to hear about the return of the seizures. I just hate them so much. Luke did really well on Keppra for quite awhile w/ no side effects. Big hugs to you and Callie. Mel. Subscribe to: Post Comments (Atom). If you would like to read from the beginning, here is how it all went down. Life on Mystery Lane. Didn't See It Coming. Pieces of the Reeses. Upped the dose again.

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Loving Luke

My husband, Dan and I have 2 sons. Ben is 6 years old. Luke was born March 17, 2010. Luke has a rare genetic condition MPPH (Megalencephaly Polymicrogyria Polydactyly Hydrocephalus) Syndrome and epilepsy. This blog is to help keep friends and family updated and also to hopefully find other parents/families who have experience with polymicrogyria and MPPH. Sunday, December 13, 2015. It's never as easy as I think it's going to be. We ended up taking the whole week plus a bonus weekend! While he was seizing...

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