On April 13th Madelynn had her first neonatal follow-up clinic. We met with a pediatrician, a neurologist, a speech therapist, a physical therapist, and a audiologist. We also had a student NP shadow us for the day. I am all for letting students come along and learn because some day they will be helping families just like ours in the NICU.
I digress. We met with each specialist individually so it was a lot of repeating Maddie's history. For the most part everyone was pleased with Madelynn's progress. The one concern they seemed to share was her head shape. I explained this was because PCMC neglected to turn her as IMC diligently did. They all suggested she get a helmet.
The pediatrician was the first one who saw Maddie, and stressed her out so bad it was hard for the other specialists to examine her as she was either still trying to organize herself or she had fallen asleep.
The neurologist brought up Madelynn's MRI from February 1st, and thought there may be something wrong with her pituitary gland (something PCMC neglected to tell us). He sent orders to Riverton to have her blood work done to make sure she does not have a thyroid problem. As he spoke he looked me up and down and I told him I don't have a thyroid problem, I'm just fat.
Her next appointment will be when she is six-months adjusted age. Some time in June or July I'd imagine. Hopefully Jeremy will be able to go to this one.