Mia
Due to her missing parts of her brain she has many seizures
periodically throughout the day. Her seizures are kept under
control by the drug vigabratin. She also has optic displasia,
which spikes spontaneous fevers due to her abnormal thermostat which
is controlled by the hypothalamus in the brain. She sweats
from her feet and not her head, because of the brain disorder and the effects
it has on her hypothalamus gland. She has a gastrostomy tube to feed
her through her stomach and requires frequent suctioning throughout the
day. Mia also goes into occasional crying spells where it is very difficult
to stop her from crying. Sometimes she cries for days on end and all the
mother can do is rock her and hold her. Its at these times that she plays
classical music to soothe Mia She calms down somewhat listening to classical
and nature sounds. She loves to listen to the music, it seems
to soothe her pain away and calm her down when nothing else will.
Mia’s life expectancy is day to day. She
lives in a beautiful, loving foster home where she receives all of the
love she so justly deserves. Despite all of the frightening information
given to her family before she came to live with them, Mia is still fighting.
Fighting every day to take another breath. Fighting to stay alive. She
truly is a miracle baby.
Mia's health is very unpredictable. She is
often sent to the hospital suffering life and death situations.
She was just recently discharged from the hospital after suffering
from grand mal seizures and respiratory distress. Once again mom
and dad watch her fight for her right to stay alive. Then after days of
prayers she miraculously comes home to her familiar surroundings to be
loved and comforted by mom and dad. Again defying all odds,
she stares up at her parents with her big eyes as if to say its okay. I
did it again. I’m home again. She is such a precious child. Doctors again
tell the family to take her home and enjoy what little time they
have left with Mia.
She is our angel, “Mia” comes from that. She has
inner and outer strengths beyond comprehension. Every minute we have
with her we cherish. She has taught us how precious life is. She
has shown the family what courage is. Mia cannot speak words but
she most definitely communicates with her eyes, actions and sounds.
Mia is surrounded by people who love her. She has 5 siblings ages ranging from 2-17. From the youngest to oldest their names are, Shanley Hope, Ryan, Allen, Jennifer, and Sheri. She is also blessed with two very loving parents, Laurel and Darcy. Parents who some days survive on 3-4 hours of sleep a night caring for all their children. They also have a 2 year old who is experiencing seizures and have to cope with the terrible two’s syndrome. All in all, one big loving family who do their best to make their house into the best home that these children could ever have.
Mia is a very special child with very special parents.
If you wish to send a card to Mia please address it to the following address:Mia H.
70 C Mountjoy St. N.
Suite 315
Timmins Ont.
P4N-4V7
Canada