by Gabbie Nadeau | Oct 17, 2018 | Uncategorized
Dr. Haaland is currently the President of the CdLS Foundation Board of Directors What is something about CdLS or the Foundation that people might not know, but should? Many families recognize the Foundation for one or two things, since that’s what they call the...
by Gabbie Nadeau | Oct 17, 2018 | Uncategorized
When you think about your child’s care team, you probably think about their teachers, grandparents, therapists and medical care professionals. You may also think about the staff at the CdLS Foundation as part of this team. However, there is one care team member...
by Gabbie Nadeau | Oct 17, 2018 | In Memoriam
A lot of people think that it requires a distinctive or special type of family to raise a child with special needs but that’s far from the truth. In all actuality, it is that child that creates the “special” family. I know this is true because Nikki was that child for...
by Gabbie Nadeau | Oct 17, 2018 | In Memoriam
Our son Andrew, like so many other CdLS children had multiple physical and cognitive challenges to deal with in his life. As he got older, keeping him safe became a 24×7 job. Managing his life, was a time consuming, logistically complicated, and sometimes...
by Gabbie Nadeau | Oct 17, 2018 | In Memoriam
Jeremiah was a little guy so full of life and energy and charisma. He charmed everyone, leaving a lasting impression on every single person he came in contact with. When Mick and I first met Jeremiah, our lives were changed forever as we were immediately spell bound...
Recent Comments