Unpacking the Brain Backpack, AKA, “What grade did my kid just get?!?!?”

My kiddo is smart.

I’m not saying he’s like, “genius-savant-off-the-charts” smart, but the kid can keep up conversations with people three times his age. Half the time, when he’s in trouble, he can skillfully debate with my on a level that leaves me shaking my head (and he definitely keeps me on my toes). I’m not looking forward to the teen years, let me tell you.

He’s quick-witted, easily distracted, and possibly OCD when he gets on a topic of choice. He may have a slight dose of ADD, but as long as he continues to maintain acceptable levels of self-control, I’m not going to look at getting a formal diagnosis. The investment into keeping him in a small, faith-based school means that he’s getting a lot of one-on-one relationships and education, so we’re able to maintain independence as parents when it comes to our child’s unique personality (Unpopular opinion: When your kid is 1 in a class of 24, with 1 teacher, and they have a lot of energy/thoughts/need to express all of the above, the teacher can’t possibly give them the space they need to do that, without affecting the other kids. Kids then fall behind, because they’re not getting what they need and they’re in an impossible environment. It’s hard on the teacher, the child, and the parents, and many times, parents are told they need to get their kids “under control.” The conditioning has become to get your child a formal diagnosis, an Individual Educational Plan, medication in many situations, counseling, and an asterisk that they are “different” or somehow not on a level that’s even with their peers. I feel like this would be the path we’d be facing in public school. I’m not saying it’s good or bad, but I am saying that it’s not for us. Small classes, individual attention, a solid curriculum, and most importantly, a foundation of faith, is the education I grew up with and is the education we chose for our child. I understand it is not for everyone—I’m not here to pass judgment, and am in no way saying that all kids are treated the same, or should expect to be. I will definitely say that I’m a huge advocate for Christian education, and that if you ever have any questions about it, I’m more than happy to answer to the best of my abilities. I went to Christian schools from Kindergarten through my Bachelor’s degree, and my son is now in his 4th year of Christian education, so I feel like I’ve got a pretty good grasp on the good, the bad, and the scary.). My son’s teachers have all celebrated Jericho’s strengths and have challenged his rough edges; I don’t always agree with them, but I will always support them (and when I don’t agree, I reach out to them to clarify my questions, and they ALWAYS respond with kindness).

Second Grade is challenging my son. I have to say that I don’t believe it’s challenging his intelligence as much as it’s challenging his patience and his focus (and looking back, I wish I would have realized the same things about myself as I faced my own academic issues). He gets the facts straight for his classes, but then doesn’t exhibit the focus he needs in order to recall those facts. He doesn’t want to slow down enough to have legible handwriting for his answer to count as correct.  This has led to a number of discussions (many ending in tears) about, “Jericho, what is the point of knowing the answer if you won’t take the time to write it neatly enough to be read? You KNOW this stuff!!!” I find myself getting frustrated. I don’t want to go the route that devolves into hurting feelings, or making him feel like he’s “less than.” It can be challenging to convert, “DO better!!!” to, “Hey, you’re awesome, and you’re enough…and you’re also way smarter than a “B,” so slow down and do the job.”

I want him to understand that he is more than capable, and that it’s WORTH IT to slow down and to do it right…

But what does he hear???

It’s very difficult for me to stop, refocus my words, and to clarify both my intention and my love for him. I look at his little face when he’s turned in a “Bad” grade, and I know he’s beating himself up for it more than I ever could.

When we’ve had remote learning, he’s told me, “I don’t WANT to do the work with you!!  You expect me to be PERFECT!!!!!!!”

It’s not true, but oh, how that hurt my heart to hear. I still want to cry when I think about it—have I failed him, in pushing him towards his potential? Or do I keep pressing in? 

I’m not inclined to accept mediocrity when I know he has the ability to excel, but at what cost?

“You’re not here to be his friend,” I remind myself on an almost-daily basis. I love him too much to let him take the easy way out, even when it’s hard for me to stand my ground.

Now, don’t get me wrong—I’m not Tiger-Momming it over here. I consistently tell him that I want to see that he’s TRIED. If he tries and he gets a “C,” I’m totally okay with that—but I want him to TRY. That’s what matters to me, more than letters. Speaking of “C,” last night, he brought home a “C” on a science test.

I about fell over….the words escaped my mouth before I could stop them” “What in the world?!?  A C?!?!”

Cue the tears.

He cried, and he wailed, and he yelled, and he had a Total. Meltdown. David was working upstairs, and he came down to see what torture I had inflicted in the household, to warrant such a racket.

I hadn’t said a word, other than my initial shock. You see, the night before that test, Jericho had recited almost word-for-word, the entire Study Guide. He knew it all. When I went to bed the night before, I just knew he was going to kill that science test, and maintain his GPA (yes, we talk about it in the Second Grade). He knew all of this stuff, and for him to bring home a “C” was a genuine shock to me.

He cried his little eyes out while sitting on my lap. I shushed him, told him it was okay, and quietly said that I just wanted to unpack what happened (I never raised my voice, if you’re wondering). He kept yelling. It took a while to calm him down and to focus, but once he did, I told him this story:

“Your brain—sometimes, your brain is full of cats in paper sacks. It’s nearly impossible to get your thoughts wrangled together and to focus through to find what you need, right?

Jericho, think of your brain like your Backpack. Say you’re going to Grammy’s house, and you need socks. You throw them into your backpack, first thing…and they sink to the bottom, as everything does when you throw it into the backpack, first.

As the day goes on, more things go into the backpack: Shoes, pajamas, stuffed animals…everything goes into the backpack, on top of everything else….

But you need your socks….and they’re at the bottom of the backpack….So what do you do?”

“You dump the backpack out and you find them.”

“Exactly. So, you sort through everything to find what you need, right?

It’s the same thing for your Brain. Think of your Brain as your Backpack:

You see, you KNEW all of the answers to that science test. You had it!  But things happened….maybe a video game, or a TV show. Maybe you put a puzzle together that you were excited about, or you had a really great recess. All of those were things that went into your Brain Backpack, on TOP of the science stuff you knew so well, the night before.

So when the science test started, you needed to take a few deep breaths, focus, and really concentrate on sorting through all of the “other” stuff in your Brain Backpack, and find the answers you knew in the bottom of the bag—THEN you can pull the answers out, and write everything down as you know it.”

I don’t know if this mental picture will help him on his next test, but I know that as parents, our responsibility to encourage him towards excellence while protecting his self-esteem is very important to me. I never want him to feel like HE is not enough, even when his efforts are lacking. I’m grateful that he’s first of all, in a classroom, and secondly, surrounded by educators who are on the same page as David & I are, in lovingly pushing him towards his potential while giving him space to learn. It’s a delicate, balance and one that I am very challenged by.

Parenting isn’t for the faint of heart, and it’s not for those who aren’t willing to look at tear-filled eyes and still stand their ground (in love). I’m not his friend; I love him so much more than that….and I’m so grateful for my spirited, smart, hilarious little mini. He’s a good kid.

This video by The Holderness Family basically sums up our lives right now, and I couldn’t agree more!!!!!!!!!

Side note—Since my last post, we got a dog! Say “hello” to Noodle the Mutt—she’s about 5 months old, and she & Jericho are still getting used to each other, so that comes with its own set of challenges. I never wanted a small dog, and David never wanted a rescue or a mutt….Noodle happily meets all three of those “nevers” and we couldn’t love her more.

“Nothing Breaks Like A Heart…AKA, “[Don’t] Take Another Little Piece of My Heart Now Baby”

Waaaaaay back when I was born, my mother was told that I had a slight heart murmur that I would most likely grow out of. I did.

In college, too much stress + bad food choices + lack of sleep + tooooooo much caffeine = Cardiac Arrhythmia, which eventually resolved. Everything was juuuuuust fine….

Until it wasn’t.

In 2006, I became pregnant with my first child. As a first-time mom, my complaints of, “Hey, I really can’t breathe too well,” and “Um, Doc? I can’t get enough breath support to sing,” were written off as new-mom, “well, what do you expect? You have a human pressing on your diaphragm,” rhetoric and explained away (I’m just a woman, Mr. Doctor. What do I know?).

2 months before I was due, I started seeing double, having migraines, and throwing up. Basic science diagnosed me with severe preeclampsia, and do you know what the “cure” for preeclampsia is? Delivery. So, my daughter was delivered 6 weeks early, and I was “gonna be just fine, ma’am,” said Mr. Third-Generation-I-Know-Everything OB-GYN….

Until it wasn’t.

2 days after I delivered, I couldn’t breathe…coughing and choking on top of a C-section incision is no fun. My sister ran for help, my mother prayed in tongues at the top of her lungs, and the nurses (who were in the middle of changing shifts, as of course, I have fantastic timing) & doctors realized I was in severe congestive heart failure. Over 20 pounds of fluid were drained out of my heart and lungs in the next 24 hours, and I went in for the fight of-and-for my life….while also trying to be a new mom to a premature infant.

Peripartum cardiomyopathy with congestive heart failure and pulmonary hypertension became the noose of a diagnosis that hung around my neck for the next 6 years as I went from specialist-to-specialist, trying to find a cardiologist that would both “fix” me, and would work with me as I wanted to try to have another child.

Once the heart has been blown up in CHF (my left ventricle was three times the size of the rest of my heart. I like to call it, “Grinch Syndrome.”), it tends to sort of hang around like a balloon that’s been overstretched. It’s kinda gross, if you think about it. My heart was literally broken in every possible way….by my body, by grief, by everything.

Image result for grinch's small heart grew

So, I had a few years of echocardiograms, medications, etc., until I found a doctor at Missouri Baptist that ordered more tests and found that my heart issues, outside of blood pressure, had miraculously resolved. I didn’t have any of the long-term problems they expected me to have, and we went on to have Jericho with the help of infectious disease specialists, cardiologists, perinatologists, and a whoooooole lotta grace from God….but it wasn’t without consequences.

As expected, even with a strict regiment of really miserable medications, I went into heart failure towards the end of my pregnancy with Jericho, and was rewarded with a lengthy hospital stay. After delivery, and after promising to never try to have any other children, I have a continued medication regiment that I’ve stayed on, and will be on for the rest of my life. I have my son; I have ZERO regrets.

The meds work great! Most of them are the same ones I’ve been on since 2006, with very few side effects, and with positive results. My CHF numbers stay low (the key number is the ejection fraction for the left ventricle. I’ve been under 10% before. My current numbers are around 40-50%, which is almost normal). My weight has been a challenge (particularly in the post-thyroid world), but has stayed in the same general area since my first pregnancy (give or take 40#. I gain, I lose, I gain, etc.), and my blood pressure stays under control with medication…it’s all working, which is crucial.

SO, why am I telling this story? Why does it matter? It matters, because YOU matter. 1 in 3 women in America are dealing with some sort of heart disease–that’s more than all other cancers, combined: https://www.goredforwomen.org/en/about-heart-disease-in-women

Per the Go Red for Women campaign, “80 percent of cardiac and stroke events may be prevented with education and action.” That’s what we can do. That’s what I can do–I can share my story, and maybe help others to become aware of the resources, the signs and symptoms, and the protocols that can help them understand heart disease more clearly. Knowing is the first step of prevention, right?

Today, my heart is functioning pretty darn well. In fact, I really don’t think about it very often, which is awesome when you consider that at one point, it was ALL I thought about…I couldn’t go up the stairs in my own home without feeling like I was going to pass out! I don’t have any limitations from cardiac issues, and I don’t worry about it…but I AM very conscious of it, and of paying attention to it when something seems “off.” I had some episodes last year of almost passing out. I wanted to ignore them, but I know better, so I called my cardiologist. Turns out, my blood pressure medication needed a simple adjustment….it was nothing complicated, and a simple phone call, and listening to my body, made all of the difference.

Take care of your heart, people. It really is the engine that drives you…and we all know that if the engine is broken, you’re not going anywhere. Love your heart….Live Fierce…and Go Red for Women!!!