This is Lauren
She has Noonan Syndrome. She is still perfect.
Lauren has quite a list of characteristics. She looks a bit different
and her heart has defects. Her growth is slow, her muscles have low tone
and her joints are overly flexible. She has digestive issues, hearing
problems, skeletal deformities and the potential for significant heart
failure later on.
These complications, and more, are tied to Noonan Syndrome.
It’s a part of her, but it is not WHO she is.
She is Lauren and she is just perfect.
Who Are We?
Living in Guelph, ON we are Robyn,
Kevin, Roman and Lauren. I (Robyn) spent many years in the advertising
industry managing the web department for a boutique firm in downtown Toronto.
Kevin is an audio engineer working on televisions shows like "Pitchin' In" and "Chopped". Roman, two years older than Lauren, is her amazing
To get in touch, send us an email,
join the Facebook group or give us a call (519.341.8991). We'd love to hear from
Why Another Website?
It is our intention that this site be a resource for people
and parents whose lives are touched, influenced or absorbed by Noonan
Syndrome. That it be the site we needed when Lauren’s syndrome was diagnosed.
We firmly believe Lauren has been given to us for a reason. If one person
or family’s journey can be eased through our sharing of experiences then
we are beginning to understand our purpose.