Miss Mira: Clean Slate and Bad 80's Cartoons

Tuesday, March 20, 2007

Clean Slate and Bad 80's Cartoons

Mira is now completely off of the Felbatol and all Sarah and I can say is good riddance. Certainly, it was worth a shot to help in gaining some seizure control, but the side affects far outweighed any benefit, which frankly, there weren't any benefits. She was on it for only a week and it was awful for everyone, especially Mira.

She is now taking multi-vitamins and an omega supplement only, which we started a few days after the Felbatol was out of her system. She is taking two packets of Rainbow Light (not to be confused with Rainbow Bright) and taking one packet of Coromega-3 Fatty Acid supplements daily. She is getting additional Vitamin E and B12 as well. So far, her daily seizure count has 'stabilized' to a certain degree. We have been seeing a few tonics in the morning, but nothing in the afternoon.

Sarah is enjoying some time in Illinois with her sister this week (it's spring break for the kids) and Daddy is at home turning the house into a bachelor pit. Nothing beats the smell of sweaty boots and leftover pizza on the living room floor. Just kidding, I don't leave my boots on the floor.

Thanks to the Flora family for taking everyone in for the week!

No comments:

Post a Comment

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