The last of the night photos. This is the Evans Center, where the COM, Nursing School and Visual Arts department is located. I may have already mentioned this place. It is a very interesting building and it’s especially cool at night. I’m beginning to get a little more used to it, though I do still miss Fisher Hall.
Today Ashley, Boston & I headed into Manteo, which sits on Roanoke Island. I’ve spoke of Boston before and her having Cystic Fibrosis (CF) and how I had watched her and experienced some of the trials her family faces. Since moving to NC I think its safe to say its been a good move forward for Boston. Today though, today I experienced a joy or rather funny side of this. CF produces a lot of phlegm and its super important that its coughed out. So Ashley and Josh have taught Boston to spit it up in a Kleenex or if outdoors, in the bushes. While walking down the sidewalks of Manteo, Boston gets to coughing pretty good, an older couple walks by with a look as if to say, “Why have that sick child in public”. Just as were passing by them Boston leans over in the bushes and spits an awesome amount of mucus. Ashley starts to congratulate her and asks for a high five….all the while I’m watching the horrified looks on peoples faces, as they’ve watched this petite beautiful girl bend over and spit in the shrubs with an overly excited mother.
She’s not sick. She’s a fighter. She’s not misbehaved, rather making her lungs healthier. She’s not a horrible parent, but a mom who has sat up many sleepless nights praying for a hour of peaceful sleep for her coughing baby girl.