Three days ago, while browsing on
channelcincinnati.com, I came upon
http://www.desserich.org/, which
journalizes the story of a beautiful little girl named Elena Rosemary
Desserich, who was diagnosed with a rare form of brain cancer. Elena passed away on Saturday, August 11
th, 2007, just nine months after being diagnosed. She was only six years old.
I have read every word of the journal (which is written by her parents), beginning to end, and viewed every picture of Elena’s journey. I feel like I cried a tear for every single word written in that journal.
Bawled is actually more like it. My emotions caught me by surprise because I’m not usually a crier.
I never met this little girl or her family, but I was heartbroken to see the life of this bright-eyed, loving little girl, who was not much older than my own elder daughter (and seems to be very similar to her in temperament and style), so devastated by this disease and ultimately cut way too short. It shook me to the core. I shared the site with my husband, and he, too, could not tear himself from this family’s story or hold back his own tears.
When I first began to read their story, I was overwhelmed with feelings of sadness, disbelief, and sympathy. Then my emotions quickly turned to anger. I was angry that something so devastating could strike a child, without rhyme or reason. A beautiful, loving, innocent child. She was robbed of her future, of life’s full journey, before it had even began. Her parents, her little sister, and all those close to her, they were just
robbed. Robbed of the gift of Elena. She
wasn’t even my daughter and I just felt so angry about that. Why?
Because it’s so damn unfair.
But another reason might be a bit selfish: the
Desserich family remind me so much of my own. They have two daughters, Elena and her little sister Grace. And in appearance, age, and interests, the girls remind me so much of my daughters. And of course it reminds me that this could just as easily happen to me, my family,
anyone. Cancer does not discriminate. And I think if I were in that situation, being the control freak that I am, I would be so angry because I would feel like there was nothing I could do about it.
But that’s where I would be wrong. The
Desserich family
is doing something about it. They are keeping Elena alive in so many ways every single day, including sharing their journal and story with people like me. They are bringing awareness about pediatric brain cancer through
The Cure Starts Now charity, helping other families fight the fight against this devastating disease.
I have not quite been the same since discovering the
Desserichs, and I want to thank them for that. Because of Elena I no longer rush through bedtime stories at night. I hug my girls a little longer, listen to them more intently, play with them with my full attention. I try to cherish every second. Elena has reminded me that the physical life is precious, uncertain, and fleeting. A gift. A beautiful gift that Elena, even at her tender age, never took for granted.
But the
Desserichs have also reminded me that
every life should be cherished. Not just those in my own personal world. The
Desserichs didn’t stop caring after Elena left this life on August 11
th. I’ll be participating in the first annual
The Cure Starts Now Walk-a-thon on September 30
th. For more information, visit
http://www.thecurestartsnow.org/