This blog is dedicated to our sweet lil angel, Liam Riley Howe.
Liam has been diagnosed with Neuronal Migration Disorder, a rare condition, which has left him fighting for his life.
Meet Liam
Tuesday, March 2, 2010
He's Home!!!
Great news! Liam arrived home to his own little crib today! They are all very happy to be out of the hospital! Now, through a little time, things will get back to normal and Liam will continue his healing process and grow up to be a cute little boy!
1 comment:
Anonymous
said...
My name is Aaron Maurer. My daughter Marissa was also born with a seizure disorder and had seizures from the age of 2 months old. She was a fighter and was so very full of life. We too spent many of Days at UNM and in Phoenix trying to get some sort of answers all in the while she still was in pain. Doctors only want to prescibe more meds, the Cary Tingley Center in ABQ, NM was the best place for Marissa's treatment. She lost her battle on June 15th 2009 just before her 3rd Birthday. I would like for Jeff or Heather to give me a call to just talk. I know these times are tough but it does help when there has been someone who has already walked in those shoes. May God Bless Liam and your family. I am in Farmington, NM. Sincerely, Aaron Maurer 505-215-3932
1 comment:
My name is Aaron Maurer. My daughter Marissa was also born with a seizure disorder and had seizures from the age of 2 months old. She was a fighter and was so very full of life. We too spent many of Days at UNM and in Phoenix trying to get some sort of answers all in the while she still was in pain. Doctors only want to prescibe more meds, the Cary Tingley Center in ABQ, NM was the best place for Marissa's treatment. She lost her battle on June 15th 2009 just before her 3rd Birthday. I would like for Jeff or Heather to give me a call to just talk. I know these times are tough but it does help when there has been someone who has already walked in those shoes. May God Bless Liam and your family.
I am in Farmington, NM.
Sincerely, Aaron Maurer 505-215-3932
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