2017 Team Caleb Shirts

This year, we're going blue and yellow... Down syndrome awareness colors! Sizes and prices can be found if you scroll past the following images!

 

Moisture-wicking tee (Sport-Tek 100% cationic polyester interlock)

Available in the following unisex sizes:

Adult: XS-4XL

Youth : XS(4), S(6-8), M(10-12), L(14-16), XL(18-20)

$15.00/each

Moisture-wicking racerback tank (Sport-Tek 100% cationic polyester interlock)

Available in the following sizes:

Ladies XS-4XL

$15.00/each

Cotton tee (Bella+Canvas 100% combed/ringspun cotton)

Available in the following sizes (unisex):

Adult: XS-4XL

Youth: Small, Medium, Large

$12.00/each

Infant/toddler tee (Rabbit Skins 100% cotton)

Available in the following sizes:

6mo, 12mo, 18mo, 2T, 3T, 4T, 5/6, 7

These sizes tend to run small.

$10.00/each

Add $5/order if you need it shipped.

Please let us know which style/size you'd like. You can pay with cash, check, PayPal or Venmo. If you want to use PayPal or Venmo, send me an email or comment below. Shirt orders are due Sunday, Aug 20th.

Shirts should be ready for delivery on early-mid September.

One Minute Monday

It’s been a while since I posted a “Five Minute Friday”, because it seems a free five minutes can be hard to find some days. So I’m going to do a super quick “one minute Monday” just to share a few things that are on my mind.

-        Our pastor is out of town this month, so we’re having some guest preachers each week. Senator James Lankford (a member of our church) preached the past two Sundays on the topic of stress. He spoke about Jesus’ time at the Last Supper as he prepared himself and his disciples for his eventual death. Both sermons were so good. I wish I could tell you more about what he said and what I learned, but the clock’s ticking. You can listen to the sermons here. http://qsbc.org/resources/sermons/

-         

-        Caleb had his thyroid levels checked last week. He has a history of “dysfunctional thyroid”, which means his TSH and T4 levels don’t seem to be in sync. This time, his TSH was elevated but his T4 was totally fine. There seems to be some confusion about whether or not to treat it. He has taken Synthroid for periods of time twice and has been off of medication for the last year. We’re going to recheck his labs next month and then figure out if we need to start treating it again. I would love to avoid having him on a daily Rx, but we’ll do it if we need to. In the meantime, I’m researching ways to help those thyroid levels naturally. We already avoid soy products, because we’ve been told soy can negatively affect thyroid function.

I typed quickly and still went over my one minute… oops! 

Mild Sleep Apnea

I know I've mentioned some of this here already, but here's a little update. Caleb had a sleep study done back in December. We learned that he had "borderline severe obstructive sleep apnea", and his ENT recommended that Caleb have a tonsillectomy/adenoidectomy to help open up his airway. He had that procedure in March, and then Brad took him for a second sleep study in June. We had an appointment with the ENT yesterday and went over the results. His sleep apnea improved 2.5 times! While that's so good, he still has mild sleep apnea. Nothing needs to be done about it now, and we will do another sleep study in a year.

World Down Syndrome Day - March 21st

This Tuesday, (3/21) is World Down Syndrome Day! 3/21 is to represent the three copies of the 21st chromosome! Here are some ways you can show your support of people with Down syndrome...

- Wear yellow and blue (Down syndrome awareness colors)
- Wear mismatched crazy socks... https://worlddownsyndromeday.org/lots-of-socks
- Or my favorite... wear your Team Caleb shirt!

Post your photos on Facebook, Instagram or Twitter! #teamcaleb #wdsd2017

Another Five Minute Friday

And the five minutes starts now...

We're now on post-op day 10. Caleb is starting to show some improvement. He's drinking more and willing to take a few bites of soft foods every now and then. He also seems happier throughout the day and sleeping a little better at night, so I think the pain is starting to go away.

We're wrapping up Spring Break here. The boys were off from school and MDO (not that Caleb would've felt like being at school this week anyway). Brad and I still needed to work, so family watched the boys for us while I worked on Monday and Wednesday. Brad and I are tag-teaming today. I'm working this morning, and Brad is working this afternoon.

I have a couple fun things planned for this weekend. I'm going to a baby shower for a friend tomorrow. Her first child, a son, was born in October 2015. He had a congenital heart defect and only lived three days. Now she's expecting another precious little boy, and he's due on Easter Sunday. I'm so excited to celebrate with her tomorrow. And then on Sunday, I'm running the Go Girl half marathon here in OKC!

Time's up!

One Week Post-Op

It's been one week since Caleb's tonsillectomy/adenoidectomy. I'm exhausted, and I'm sure Caleb would tell you that he's hungry. To catch you up to speed since my last post...

Caleb was discharged from the hospital the morning after his surgery. While that was the plan going into the surgery and even right after, I was surprised they discharged him. I didn't feel like he was drinking/eating well enough yet. The attending physician (who I liked and remembered from when Tyler was at the same hospital for RSV a couple years ago) said that kids who are "borderline doing well" usually do better at home. He was discharged with instructions to give Tylenol/Motrin every 3 hours for the first 24 hours and then as needed after that. He also had a Rx for three days' worth of a steroid and a Rx for a tetracaine lollipop. We were told not to let him drink from a straw for 10 days, because sucking on a straw could loosen the scabs in his throat and cause pain. We were also told to keep him on a diet of liquids and soft foods for 10 days.

I reluctantly took him home, and the hard work began. Caleb didn't want anything in/near his mouth. No drinks, no food, no medicine, and he hated having to be woken up during the night for his Tylenol/Motrin. I told Brad that I felt like I was reenacting a scene from "24" whenever I had to give him medicine. By Monday, we were concerned about how little he was drinking and were starting to worry that he might get dehydrated if something didn't change soon. Brad called the ENT's office and spoke with the nurse. She spoke with someone else (not sure if it was the ENT or the PA), and they agreed to let Caleb start using a straw. There was still the risk of the straw causing some scabs to come off, but they'd rather that happen than Caleb get dehydrated and need IV fluids.

Now that he's drinking from a straw, his fluid intake has increased a little. We also got some chewable Tylenol and Motrin, and he seems happier taking that than the liquid medicines. The jury's still out on the tetracaine lollipop. He doesn't like it, and it's another "24"-like moment whenever I try to give it to him. He seems pretty happy during the day now, but the nights are still tough on him. We're praying that he'll start sleeping better at night soon and that his desire to eat/drink will continue to increase. We've been told that the recovery period is about 10 days, so I'm hopeful that we'll see some big improvement by the weekend.

Sleep Apnea

At Caleb's four year well-check in October, the pediatrician and I went line-by-line through the AAP guide for children with Down syndrome. One of the things mentioned is sleep issues, and the AAP recommends a sleep study by the age of four. Caleb hadn't had one yet, so the pediatrician ordered one. I took him to the sleep clinic at the local childrens hospital in December. That was a rough night, but he slept enough that they were able to get some good data. From that sleep study, we learned that he has sleep apnea. We also learned that there are basically two types of events that indicate the severity of sleep apnea. Apnea is a suspension or pause in breathing...thank goodness, Caleb didn't have any apnea events. He did have several hypopnea events though. Hypopnea is a overly shallow breathing and/or low respiratory rate. Caleb's ENT recommended Caleb have his tonsils and adenoids removed, so that leads us to today!

Caleb's tonsils and adenoids weren't particularly enlarged, but the ENT said that would be the first (and easiest) thing to try to help remedy the sleep apnea. While in the OR today, the ENT used a scope to watch Caleb's airway as he fell asleep. He didn't see any obstructions, but he said Caleb's airway is incredibly narrow. Getting the tonsils and adenoids out should make some room in that airway and help him breathe easier. He also checked Caleb's ears and put a new tube in his right ear. The tube in his left ear was still in position and open. 

Caleb did great waking up from anesthesia. He seemed comfortable and content watching a movie on his Kindle. About an hour later, we moved to a room on the pediatrics floor. Caleb took a good nap, Tyler came by for a visit, and then Caleb ate a decent dinner (soup, pudding, mashed potatoes, more pudding, yogurt and milk). Brad and Tyler went home a little while ago, so now Caleb and I are getting settled in for the evening and will hopefully go to bed before long. Assuming everything goes okay tonight, the plan is to go home tomorrow morning. Caleb will do another sleep study in a few months to see if today's surgery took care of the sleep apnea.