Google Hangout on raising special needs kids Check out my conversation with blogger Lisa Thornbury (Forever in Mom Genes) and Katrina Carefoot who blogs at Fickle Feline about the challenges and joys of raising children with special needs hosted by iVillage.ca. It was a great exchange of ideas and experiences.
Deane’s weight is so far below the curve on a standard growth chart that it is unmeasurable. No wonder the dietitian is giving me ultimatums. It is very distressing when the doctor points to a spot inches below the sweeping curve of normal weight for 14 year olds. But what I’ve found out on our … Continue reading
When I talk to someone I’ve just met about Deane, I don’t use the phrase cerebral palsy. In fact, unless it is important, I don’t even mention that he is disabled. This has led to some awkward situations, but I’m willing to risk that to avoid labelling Deane. I’m afraid that if I say “My … Continue reading
Flipping channels the other night, we came across the documentary Hot Coffee. The premise of the movie is that the U.S. justice system has been distorted by big business reaction to the well-known case of the 83-year-old woman who sued McDonald’s after received third degree burns a spilled coffee. The documentary sites four stories as … Continue reading
In her blog about special needs children for Today’s Parent, Anchel Krishna describes receiving her daughter’s cerebral palsy diagnosis in a very straight forward, calm manner: And that’s when the fog came in, and all I could think about was not crying in front of the doctor…. Then she proceeded to tell us that she … Continue reading
I don’t consider us a disabled family. Don’t get me wrong, my son has cerebral palsy spastic quadriplegia and is developmentally delayed so, technically, we are a family with a disability. Certainly that’s how the many people view us. I’m not going to say that “disabled” is a mindset. There are many things my son … Continue reading