Corey

In 1999, our first-born Corey died from Niemann-Pick Type A Disease, a severe and currently incurable neurodegenerative disorder. Corey was 2 1/2 years old when he passed away.  While the years have passed, and time has been of help, it is still a challenge to comprehend this loss.

My hope is that by sharing our story it will stress the importance of genetic testing and awareness and to spare others the same grief and pain that we have endured.  By doing so, this will help create an understanding of the importance of genetic testing coupled with genetic counseling, research, and education.

I will never forget the frightening moment when Jim and I were told that Corey was diagnosed with this terminal disease.  We were told that Corey would have – at best – 3 years to live and he would never reach any milestones…. that he would never talk, sit-up walk or say I love you.  The news was cruel and impossible then and still is today.

At the time of my pregnancy, I was only tested prenatally for Tay Sachs disease.  I was not made aware of any other screening options.  I certainly was not tested for Niemann-Pick disease and had no idea I was a carrier of the gene.  Further, we did not know my husband was a carrier as well.  I had a normal pregnancy and like most young parents, our expectation was that we would give birth to a healthy, thriving baby.  Corey, at birth, seemed to be all those things.  Complications arose shortly and we were back and forth from doctor to doctor from the time Corey was 3 months old until we were led to Dr. Desnick and his team at Mt. Sinai Hospital in NYC where he then was conclusively diagnosed at 6 months old.

In honor of Corey, it is our personal mission to educate the public on genetic testing options and on further advancements of research and education.

Over the past 25 years The Genetic Disease Foundation (GDF) has accelerated the effort to help this fight against these devastating diseases and importance of genetic testing, awareness, and research. I am proud and thrilled to share the progress.  We have come a long way and it is incredible to think how we are making a difference and we can affect other people’s lives in a way mine and my husbands were not.  We have choices and know that carrier couples have options.