Miss Mira: Baby Day Photography

Saturday, March 5, 2011

Baby Day Photography

Mira's former therapist and friend Shannon Lockwood at IDC came in to our house this past week to document our family, as a sort of 'day in the life' through candid pictures. They turned out to be nothing short of amazing. As somebody who really appreciates a good photo eye, I think the images she took are incredible. Our pictures are on the March 4th, 2011 blog post here on her website. With so many images to choose from, we have our work cut out for us in which ones we want to have framed. We cannot thank her enough for taking such great shots.

Shannon also compiled a video of all the images in this video:

2 comments:

Reagan Leigh said...: Neat pictures! I can't believe how big your little guy is now!! He SO reminds me of Mira! How is Mira doing? Is she still having seizures? She's gotten so big too! I can NOT believe you guys don't have a wheelchair lift on your van! That's a lot of work for mom!! I don't think I'd have it in me! As of now, Reagan's 36lbs and we're still just using a stroller with her, but eventually we'll have to take the plunge and I'm not sure how we'll do it!; March 5, 2011 at 10:54 AM
Sophie's Story by Elaine said...: Absolutely BEAUTIFUL pictures.; March 8, 2011 at 1:33 PM

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Mira's Brief Story

Mira was diagnosed with Infantile Spasms (I.S.) in September 2005. Since her diagnosis is part of larger picture of issues, including developmental delay, and hypsarrhythmia, Mira was originally diagnosed with West Syndrome.

Hypsarrhythmia represents a completely chaotic and disorganized EEG background pattern consisting of high amplitude slow waves and spikes that are asynchronous, non-rhythmic, and variable in duration. The common combination of seizures/spasms, developmental delay, and hypsarrhythmia constitutes the form of infantile epilepsy, West syndrome.

Since Mira has what is described as a catastrophic epilepsy and has multiple seizure types, she has also been diagnosed with Atypical Dravet Syndrome (SMEI), Lennox-Gastaut Syndrome (LGS), and at even Atypical Rett Syndrome. While a host of early genetic testing failed to find a typical mutation, deletion, or mosaicism in the typical genetic markers for these syndromes, it does not rule out other possible associated genetic markers that have yet to be discovered. Mira has also been tested for a series of other random genetic syndromes, through partial genome sequencing and a few individual microarrays.

In 2015, a heterozygous mutation of TPP1 was found through a genetic epilepsy panel. We do not have a definitive answer as to whether this mutation (associated with NCL - Neuronal Ceroid Lipofuscinosis) is relevant to Mira's diagnosis.

Mira has tried nearly every anti-seizure medication, finding brief 'success' with Lyrica, her 14th medication. Mira was seizure free* for about 6 months in late 2007 and into early 2008.

*(Her EEG never improved during this period, which means that she was still clinically having seizures and that the Lyrica was simply masking the symptoms. Visible seizures slowly surfaced after about 5 1/2 months of being on Lyrica.)

She received weekly OT/PT, vision, feeding, aqua, and group therapy up until 2011. She now receives PT/OT and other therapies through the school district. Mira also did hippotherapy for the summer in 2008 as well.

For Mira's longer story, please visit the January 2007 Archive. For an explanation on this blog, visit the January 2, 2017 post.

Medications Tried - in Chronological Order