I love that mug!
On the human side, for the most part my doctors have been great. During my first pregnancy, I had a bunch of residents doing most of my exams and it scared me sometimes when we had repro conversations and they asked me about endocrine pathways and said that they were never taught in depth about reproductive endocrinology... I hope they really mean they don't remember much of repro endo.
Once my kiddo was born, I feel lucky that most of her doctors have been very pro parent advocacy. Some have made a point of giving the lecture that our kiddos (children with Down Syndrome) don't just not read the texts, they rip out whole chapters and say they don't apply. Our job as parents, in this case, is to know more than the doctor about DS and about our kid. If the doc suggests something that doesn't feel right, speak up. And it's not a matter of us knowing more or less than each other, but we, as parents, specialize in Down Syndrome and read up on it continuously, versus the doctor likely will have less than 1 in 600 patients with an extra chromosome and (in the words of 1 doc) "they sometimes act (medically) like a whole different species."
But a good parent won't dismiss the words of the doctor for google. They will question and have a conversation and together, the 2 will try to find an answer that works best for this child.