So last week A had a fairly short-lived stomach virus. She was fever-free by Saturday afternoon but on Monday her return to school also included a return of her fever. Throughout the week she maintained about a 100-degree fever. We took her to the doctor (not her regular pediatrician) on Wednesday because her cough had worsened significantly, her congestion and runny nose were terrible, her ear was draining and on and on. Her teacher and a friend in her class had recently been diagnosed with an upper respiratory infection so, even though we had a pediatric pulmonology appointment scheduled for today, we thought it best to take her in. I won't say this was a wasted trip entirely but we certainly didn't get many answers. The physician suggested that her left ear seemed infected and she could not see the tube. Her right ear tube also could not be seen but she noted that there was a white ball that she could not decipher. She suggested it might be an odd ball of wax, a foreign object, or a cholesteatoma. So, we are going to the ENT this upcoming Tuesday morning. How lucky--3 physician visits in 7 days. I will admit that by Wednesday night I was feeling neither hopeful nor optimistic about my life or my career (after rushing to teach directly after the doctor's appointment, I got a call from Chad that I needed to come home because he had come down with the stomach virus! seriously! this is our life right now). The doctor didn't really have an answer for the cough worsening but thought it could be "her usual junk" (that seriously was a quote) or a cold. She also had lost a pound since December. This isn't necessarily cause for concern; it's just worth noting. We were given a 3-day course of antibiotics (mostly for the EI). Unfortunately, nothing has really changed since then in terms of her symptoms.
She absolutely hated the chest x-ray last May so I was feeling a bit of trepidation about how she would do today. The radiology department was outstanding, though. They were so gentle and patient and explained what they were doing and validated that it was scary for her. She did cry but she pulled it together pretty quickly once she was finished (it was also so much faster than when we had the x-ray done last year). She wasn't completely won over by the sticker (Tinkerbell) but the bubbles with a princess ballerina on top made her smile once she calmed down.
Unfortunately we had to go from radiology down to the lab for blood work. While she greatly enjoyed the waiting room (complete with a Cozy Coupe, train table, tons of animals and toys), she knew what was up once we got into the lab room. They explained that they would first do a Lidocaine jet injection (J-tip) which "shouldn't hurt" but made a scary noise (it is aptly named!) to numb the area. Poor thing was pretty afraid even before the J-Tip but she really lost it when it made the pop/hiss sound. Unfortunately, once they inserted the needle, they discovered that the J-Tip had blown the vein. This meant re-prep which gave us a chance to pick her back up and try to console her but she really was too far gone. We felt awful laying her back on the table for them to try again on her other arm. They had some trouble getting blood at first (she may have my tiny, deep, rolling veins...) but fortunately it worked the second time. Chad and I both have been surprised at how well we do with vaccines. Neither of us has ever cried when she got a shot. However, it was all I could do to keep it together today. I am not sure I'll ever forget the look on her face. I made myself maintain eye contact with her as I tried to support her and explain what was happening. Sometimes being a parent is just so hard. I know most parents go through this at one time or another but man. It stinks. It also really made us think about those kids with severe illnesses who are having blood drawn frequently. My heart truly goes out to them and their parents.
The good news is that once we got in the car, she immediately fell asleep (even before we left the parking garage). We were able to go pick up aunt Amber (yay!) from the airport and get all turned around and lost on the way to the Irish restaurant where we had lunch (and our driving around allowed her to get a slightly longer nap so that was a perk of Tulsa construction confusion).
So, to follow back to the original thought/title of this blog--I have some hope that this new plan will work and am generally optimistic that things will get better. It definitely is a process though. When we were leaving the office we felt pretty good. Once getting home, though, we realized what we already truly knew--a different inhaler and more allergy medicine may not work. But we will try to remain optimistic. In the meantime, we are also making plans/thinking about what we would need in order to pull up our carpet and put down hardwood floor to decrease environmental allergens. I am guessing that will be awhile from now but fortunately we have a couple of people who have volunteered to help install it once we purchase it. Chad's allergies have been much worse since moving to Oklahoma (mine have stayed comparably yucky across multiple state lines) so he wonders if this is part of her issues (Stillwater is situated between OKC and Tulsa, two of the worst cities for allergies and asthma). Silly Oklahoma.
No comments:
Post a Comment