It seems like every time I check out at a store, someone asks for a donation to a charity. Homeless pets, people with disabilities (really - that's how they phrased it), cancer, you name it. It's like a gift with purchase, only it's going to someone else. I actually admire this approach, even if it's a bit overwhelming to be asked every time. I usually end up giving some small amount - it's barely noticeable to me, but if everyone does it the donations really add up.
It came as no surprise to me a couple of weeks ago when the cashier at Borders asked if I wanted to donate a book. They were collecting books for kids at Children's National Medical Center and Inova Fairfax Hospital for Children. This was a really easy sell. I am a sucker for books and A has been spending time with specialists at both hospitals. I even got to choose which book I wanted to donate. I was happy to make that donation, but a little skeptical because BUMD's cashier didn't ask him to donate (we always check out separately so we can each use coupons). I eventually shrugged it off and figured that Borders is a good business - surely someone got to enjoy those books.
Just over a week later, I got my answer. We were in Borders (again) when A had to go to the bathroom. I took her in and she decided that we should share a stall. She's six and relishes her independence, so this doesn't happen much anymore. As I was helping her, I realized that the pee in the toilet was pink. Now, she's known as the "Reigning Queen of Pink, Duchess of Fluff, and High Protector of Barbies", but this was taking her pink-love a bit too far. We headed back home in a bit of a tizzy and I made her pee in a cup so I could see for sure. Again, pink/red pee. I put in a call to her primary care, who told me to call her nephrologist, who told me to take her into the ER. Yeah, Happy Mother's Day to me. It wasn't like BUMD could take her - he doesn't do girl part stuff or needles if he can help it.
We went to Fairfax Hospital, where we stood in line for a few minutes before signing in. After waiting for a few more minutes, we were called back to the kids' triage area. From there, we were escorted to the kids ER. They found a small gown for her and then showed us to a room with a bed, rocking chair, a small TV, and the usual ER stuff. A was particularly delighted by having a gown that fit her. We keep ending up at facilities that serve mostly adults and have no child-size gown. She always looks like she's wearing a kimono. She told the nurse that she walked like a penguin in those gowns. She cracks me up.
Once she was in the gown she had to pee in their cup (and yes - I brought the pink pee with me). Of course, now her pee was clear. It figures. They tested it while she was seen by nurses and doctors. In between those exams, she got to watch TV in bed - what a treat for her! The child life specialist stopped in to introduce herself and asked if there was anything she could do to help. She then excused herself and came back with a selection of books. She told us that they had been donated to the hospital and that A could choose one to keep. Ah ha! Well, that answered my question.
Eventually, it was determined that A didn't have an infection. We were sent home and advised to see the nephrologist that week. We saw her on Tuesday. She sent A for a renal ultrasound, where they found a kidney stone. It should be no big deal, but it does explain the hematuria and perhaps the stomach cramps. We'll be keeping a close eye on things, since she only has the one kidney.
Overall, the visit to the ER was one of the best doctor's visits I've experienced. The staff was excellent, the facilities were nice, and everything went smoothly. We were home in less than two hours. Of course, the main reason is that A is not very sick. I'm exceptionally grateful for that.
We have a lot of appreciation for our good health these days. A's godmother also spent Mother's Day in the hospital with her son, who is our godson. Devin was diagnosed with Aplastic Anemia in January. He entered Duke University Hospital in February and had a stem cell transplant in March. Yesterday, he was released from the hospital. He'll continue to be seen as an outpatient for a few months while they monitor his recovery. I am so, so thankful that he's doing so well. He is a fighter and we're so proud of him. We're also thankful that his parents have been taking such good care of him. They are exceptional people. A child (sorry - teenager) could not hope to have better advocates. If I can be half as good as them, my kids will be lucky. BUMD is going down to see them this weekend. We're excited that this moment has come. It's been a long winter and spring for them, but summer's definitely coming.
Scrooge With Hives
1 week ago
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