Sunday, November 16, 2014

Aislinn's Treasures Over the Moon

October is one of my favorite months of the year.  The weather allows us to be out and about because it is not too hot or cold.    Fall break allows us freedom to come and go without the worry of homework.  

This October unfolded many goodies!   At the beginning of the month, Aislinn’s private insurance pediatrician, Hospitalist at Children’s Hospital, and a social worker made a house call.  Yes, a house call in this day and age.  It was a two hour meeting to identify our wishes for Aislinn.  You might know this as the "end of life discussion" or "the quality of life talk".   I always struggle with this subject.  I did appreciate being in the comfort of my own home.  It was a supportive conversation.  I think I surprised my guests when I laid out "the plan" and described my support system.  Yep, the plan includes hospice at home, list of happy songs, and a video. It will be a celebration of her ascending into Heaven into the arms of her Irish Grandma Sharon and Swedish Grandparents Florence and Roy!  We might just release butterflies to fill the sky with the same vibrant colors that Aislinn brought to this world!



October brought a blessing of communication from three families each with a child living with a diseased GRIN1 gene.   Interestingly they are all girls.  These families span from Vermont, Pennsylvania, and Sweden.  How cool is it that my blogs for Miracles for Mito have brought these wonderful families in our lives to share our trials and tribulations?  Way cool I say!  I cannot tell you how happy I am to have a connection with other families with the same rare gene mutation!

Aislinn had so much fun at Bison Park!  Wellness and perfect weather helped make the below cheerful memories of playing in the swing and laughter with her big sister!   Maybe someday Aislinn will have a swing of her own in our backyard!
  

  

  

For the first time in years, Aislinn was able to go to the Boo at the Zoo in Denver.  Lions, tiger and bears oooohhhh a baby giraffe!   She and her big sister were diva vampires who had a great time scaring up some fun!  
       
  


Over the past 18 months, Aislinn has struggled with daily seizures and status epilepticus requiring multiple hospitalizations.   Countless medication have been gvein such as Zonismide, Rufinamide, and Clonazepam which brought temporary relief or none at all. October brought some promising news about Aislinn’s seizures.   Imagine having fewer seizures in a day or month or year.  Could this be a reality for her?  I hope so! This news shot me over the moon because there maybe  seizure releif or reduction on the horizon!        

          
*Photo by S. Milto

Much love,
Michelle D.  Voss-Shelley

(Mom to eight year old Aislinn with a GRIN1 mutation)


Saturday, November 1, 2014

Rockstar Connections

Without context, a piece of information is just a dot.  It floats in your brain with a lot of other dots and doesn’t mean a damn thing. Knowledge is information-in-context…connecting the dots.-Michael Ventura

The above quote recently resonated in Aislinn’s world when I learned my blogs for Miracles for Mito had traveled across the pond. To my surprise, it was a doctor in the United Kingdom that had seen my blogs!  How cool is that!?! 

With much excitement I began corresponding with Dr. Fry, an established genetic specialist from the Institute of Medical Genetics at the University Hospital of Wales. He has been doing research into the genetic basis of childhood disease since 2004.  He was interested in Aislinn’s confirmed GRIN1 mutation and possibly including her medical data in a paper that could consolidate what is known about GRIN1. 

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Believing in my heart that power is knowledge, more connections were made with the fabulous Children's Hospital Colorado genetics team who identified her GRIN1 mutation and Emory University where her mutation is being studied.    I felt it would be beneficial to the medical community at large, and for other families recently diagnosed (or searching for a diagnosis) of GRIN 1 defect to have a collaboration of as many specialists as possible.  These connected dots have profound possibilities.  Who knows what might come out of these newly connected dots?


I am very grateful that Dr. Fry reached out to me, and I wish to continue down this path for two main reasons:
1) More minds, the better.  Anything we can do to mitigate the symptoms and increase the quality of life is most welcome.
2) To “blaze the trail” for current or future families afflicted with this defect.

Someone pinch me because sharing Aislinn’s journey through blogs has been healing. Knowing that her struggles have created an interest for those in the medical field and across the world is more than I could have ever asked from God or the Universe!   I am honored to have been contacted by him and others.


Aislinn is on this earth for a reason, hers is to be the guiding light and trail blazer for others to better treatment and hopefully a future cure.  In her own rite, she is a Rockstar!  She says so herself!


Much love,
Michelle D.  Voss-Shelley, APA
(Mom to eight year old Aislinn with a GRIN1 mutation)


* Image per http://news.bbcimg.co.uk/media/images/68963000/jpg/_68963038_hosp.jpg