Vanessa Dale - by Vanessa's mother, Janie
July 6, 2005
Our lives have just recently been struck with tragedy as well. My baby girl
Vanessa was diagnosed at 2 months old with DCM (Dilated Cardiomyopathy) and
her struggle for life ended on April 7, 2005. She was only 4 months old but it
seems as if she had shared a lifetime with us.
While we miss our little angel Vanessa more than we could
possibly express
in a letter; My husband and I realize that we must choose to either envelop
ourselves in self-pity and shy from the world, or latch on to the deeper
meaning and a better understanding of the frailty of life on Earth and to
embrace even more the remaining moments we have. Due to the support of friends
and family, we have clearly chosen the latter and are looking for ways to add
meaning and purpose not only to Vanessa's life, but to ours as well. That
being said, we joined the Children's Cardiomyopathy Foundation (childrenscardiomyopathy.org)
and we are dedicated to helping uncover causes and cures for cardiomyopathy in
children.
I have read all the great things The Chad Foundation has done and I applaud
your great efforts. Your fundraising programs and the Free Echo screenings you
have provided for young athletes is amazing. You are going to save lives that
would of never known there was anything wrong until it was too late.
That being said, I would also like to put my energy into organizing a Free
echo-screening for children in my area. I live in Houston, TX and I am in
close contact with the Texas Children's Hospital Cardiologists which I hope
will join me in my efforts.