The tapestry of the life of a medically complex family

Archive for the ‘Medicine’ Category

Reliance

Today my son spent hours off oxygen when he should have been on it. A nurse forgot. The nurse switched him from a portable tank back to the recently filled liquid tank and forgot to turn on the Liter flow.

I watched him have a higher than normal respiratory rate. I watched him play lying down. I watched him develop black circles under his eyes during dinner- yet I never second-guessed the nurse’s competence in following doctor’s orders.

I made the assumption that the nurse had turned the oxygen ON when his tubing was attached to the tank. I looked for reason’s beyond what would have been my first instinct had I been home alone and been responsible for providing him oxygen. Such a competent nurse made a simple mistake. And tonight my son pays. He struggles to maintain sats above the ordered minimum & requires oxygen to supplement his fatigued ability to breathe strongly enough. Again my son pays for the mistakes of others.

And I live the guilt.

Activity Tolerance

Yesterday we went for our second music group with our pulmonologist and other NICU graduates. The pulmo spoke about being aware of our kids respiratory baselines & to pay attention to their activity tolerance and share that info with he & our other docs. I have long been aware that my children have increased fatigue & reduced activity tolerance-especially Trachboy. Yesterday into today illustrated this more than ever to me.

All 3 kiddos were gotten up a bit early, fed & readied for a day out. We drove to our children’s hospital, about an hour away, then I put the twins in the stroller and wheeled them into the room used for the group. Trachboy was only off oxygen about 35 min in the early morning for nebs to be delivered, otherwise he was attached to a 1/2Lpm flow on portable and home tanks. At the class, he showed clear evidence of “stress” by being 100% physically withdrawn & having an elevated breathing rate (RR) of about 35 while seated.

After 1.5 hours of sitting theer, we went a few blocks away to “visit” a friend staying in a hospital residence while her son heals from heart & trach surgery. While there, he walked indoors, was off oxygen to use the bathroom (2min), and we sat on the front porch to eat lunch- for him 7oz of peanut butter milk. He sat there maybe an hour, while his sisters got to march back & forth on the porch after finishing a pretty full picnic lunch. Although it was in the mid-40s & eating is hard for him, there was no real exertion in our trip. He rode home attached to oxygen as well.

When we got home, his activity level was okay, maybe a little subdued, but he played after a neb, the Vest & snack, for the 2 hours until dinner. Dinner of 2-3T of stew took an HOUR- usu a sign of fatigue. After dinner, we essentially brush teeth, toilet, sometimes read books (if we haven’t read a lot earlier) and tuck in for night nebs before sleep. Trachboy sang me the good night song with a tight, soft volume voice (compared to usual). He then almost immediately fell asleep during the first neb and slept through morning nebs given later than usual (about 14 hrs of straight sleep). He also only satted in the mid-90s (94-95) throughout the night on 1/2Lpm (usually rebounds to 99/100 by 11p or so). Is simply riding in a car and sitting in a group too much for him?

A “Group” Activity

Today we rose early for a Saturday. We ran nebs early; we ran Vest CPT early; we finished breakfast at the time we typically BEGIN… I got a shower and took the time to straighten out the girls’ hairdos.

Clean & hair & dressed for the day

They looked GREAT!

 

Then we drove through Starbucks so Momma could get a coffee before driving the hour plus to our children’s hospital to join a music class run by our pulmonologist for ex-preemie NICU grads. We got there after the presentation & chat time [oops!] but in time to be seated before the music began.

At the start all 3 kids stared, unmoving, at the musician leading the group. They were older and more reserved than any other of the attendees- it’s been about 3 years since they have been in a group of children in a community setting. This particular setting is designed for kids to come when they are HEALTHY only, once a month. It is designed to be for kids younger than mine, but certainly my kids fit the group dynamics with their lack of experience in the setting. By the end, the girls were trying to sing a bit and playing musical instruments along with the singer. Tav even chose an instrument to hold while staring- for him, stellar participation.

My kids’ pulmonologist recommended we attend- and he is encouraging us to continue coming. He runs the group on a Saturday and my kids have spoken of little else since we got home. Looks like we may have to get started earlier so we arrive in time for his talk next month. I am so thankful to have caring and devoted doctors on my kids’ team who go above and beyond to address their needs as “whole children” who need special consideration when it comes to being in a group.

the Evolution of Saturday Morning

My oldest child is 18. I remember Saturday morning with him: a time of lounging together, sleeping in, Saturday morning cartoons… It was the morning we ate at the diner, got out to the park, met friends for hiking excursions…

Now Saturday “morning” typically begins as a continuation of Friday evening. Getting to bed before Tavish completes his first “barrel roll performance” is impractical. I typically stay awake and occupy myself with the computer or TV or laundry until just about 1a.m. before settling in to my first nap of the night. Overnight “morning” continues as I am startled awake by an oximeter alarm, or a breath that sounds off, or the crashing of knees into the metal siderails of the medical cribs. On & off, I steal sleep in 2-3 hour increments until true Saturday morning begins.

Gone are the Saturday morning snuggles, the invasion of my bed by young children to gently awaken me. Today’s Saturday mornings begin with a startle to awake and realizing that the morning neb treatments must begin or the feeding schedule will be so off we will miss an essential 200-300 calories for the day. Typically I shut off oximeters and then the mist compressors. Together the twins and I stretch our arms to the side, close our eyes, and mark the “moment of silence” before the mechanical deluge begins anew with nebulizer compressors running the first of 2 morning nebs. As the first neb runs, I get Keva from her room or the nearby cushion on the nights she “rooms in” in our “ward”. She gets to the bathroom as I try to make my coffee so I can complete all the rest of the morning tasks which keep my kids breathing well-enough to enjoy some of the day.

It has been quite an evolution from the morning of rest, of “refresh”, to the morning of “assess, neb, toilet, meds, nutrition, assess, repeat”.  The most difficult part of the transition? There no longer IS a “refresh”…

A Quiet Week

This week is a “quiet week” – 4 days no nursing & only 2 doctor appointments, 1 for each twin. O sure, the doctor appts we are going to are genetics (results) and an ECHO with cardiology follow-up, but it’s only 2 trips in- and one of them I will have a nurse.

Maybe its just that the next 46 hours are covered with nursing. Maybe it’s that place of denial where a parent needs to live to get through the stress of waiting for testing to see if your 5 year old is suffering from pulmonary hypertension… Maybe. But this is my quiet week.

Cool!

The evaporative cooling vests turned out to be amazing. “Activated” with some cool water, they kept Tav & Adrien cool enough to ride their balance bikes on the bike path for 20 minutes before resting- in 85 degree F heat. SO happy we have a tool to help with this. The fearsome 3some had a GREAT time.

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