I was in AZ last weekend to participate in an event for TGen’s Center for Rare Childhood Disorders  and the Wylder Nation Foundation.  The event consisted of a tour of TGen’s research facility followed by a dinner with the employees…
I was in AZ last weekend to participate in an event for TGen’s Center for Rare Childhood Disorders  and the Wylder Nation Foundation.  The event consisted of a tour of TGen’s research facility followed by a dinner with the employees…
This April, I will be running in the Boston Marathon raising awareness for Rare Diseases, a cause that I am very passionate about. In a previous blog post, my patient partner Emma and I shared our story of how we…
On Monday, April 15th, 2013, my husband and I ran the 117th Boston Marathon while I was 14 weeks pregnant. Six months later, we welcomed to the world a beautiful baby girl that we named Emerson. She joined her two…
Meet Shauna – Rothmund-Thomson Syndrome How do I describe my own child? Obviously a little on the bias side, but here goes! Shauna is a blessing that came into our lives 9 years ago! She is extremely inquisitive and I…
So it begins the start before the start of the 2014 Boston Marathon. It is an honor to be part of the Genzyme Boston Marathon Team, an honor to run on behalf of this organization, all the patient partners, and for the national organization of rare diseases in support of a life-saving/life-changing cause.
The following is a story that Jessi and I worked on for Genzyme’s intranet, to share our community’s story with everyone at our company. We thought our blog readers may like to read it, too. As you’ll see, it is…
[David and Cian are traveling from Waterford Ireland to run the Boston Marathon for their patient partners Ryan and Ethan.] Ryan and Ethan Caulfield McCormack from Tramore, Co.Waterford, were recently diagnosed with Adrenoleukodystrophy (ALD). Â ALD, is a deadly genetic disease…
Life has a way of being unpredictable.  It would be wonderful if we could always choose the road we want to go down, but sometimes it is chosen for you.  Thus was the case when my daughter was diagnosed with…
For those of you that don’t know me, my name is Kristin. I’m an avid runner, a patient living with a rare disorder called Homocystinuria (HCU), and I’m beyond thrilled to be part of this year’s Boston Marathon Team! I can’t believe in…
A story told by Julie about Ben and his hurdles living with Congenital hyperinsulinism and how Congenital hyperinsulinism International (CHI) began Ben with his sister Hannah  Ben with his Mom…
Recent Comments