You Can Say No, But...

When you go through the foster licensing process, there is a special form you have to fill in. It is just a long, long, long checklist of diagnoses and descriptions. You have to say yes or no to each on that list.  My husband and I have filled it in three separate times. 

It is a little like a game. We sit staring at one another as the social worker reads each item on the list. The game is trying to answer the same as your partner.  Not really, our rule is that if one says no, then the answer is no, but still. 

It isn't actually a game, but trying to be playful takes the ick off the process. It feels so wrong rejecting unknown kids based on the things that oughtn't define them. At the same time, it is an important step in the process. First, it compels careful consideration (Accidental alliteration! score!) by the prospective family. You have to talk about what you're willing and able to do. 

When we lived in a teeny apartment, a wheelchair was not an option, so we needed to say no. My husband and I have taken ASL classes and love the language, so we said yes to children who were deaf or hard of hearing. We had two aging dogs, so cruelty to animals was a no-go for us. ADHD and dyslexia are in the water we drink, so those were easy yeses for us, too. If you don't think you can do it, you should say no, because these kids coming from hard places need to be welcomed.

So, you do the icky list. It's rough, but get through it and take it seriously (while you're having fun) and say your no. It matters...until it doesn't.

Yep, that's the catch. Just like with biological kids, there is a lot out of our control with foster and adopted kids. Life happens. And people living in dinky apartments sometimes end up needing to use wheelchairs.

We made our list this time around, too. There are things we said no to that are now part of our lives. The difference is that we aren't talking about abstract experiences or diagnoses. They are our little girls and there is no backing out now--and we wouldn't dream of it.

March: 2023

So, in March '22, we were living the dream. We were doing whatever we wanted to. I was looking for a different job, and trying to find a way to fit in at church, but life was easy--except for the unending illnesses we kept contracting from sick preschoolers. In the eight months I worked there, I had Covid twice, Bronchitis three times, flu, colds, pink eye... It would have been laughable had laughing not triggered breathless coughing fits.

If we fast forward to March '23, the list of changes in our lives was long! My daughter moved into her first apartment, oof! I earned a Master of Science degree in Learning Experience Design and Educational Technology. I got a new job (called The Best Job in The World--outside raising kids) working at a preschool a mile from my home as a 3s teacher two mornings a week, a 4s Assistant one morning a week, and a PreK teacher every afternoon. 

I need to pause to say how serious I am about it being the Best Job Ever. That PreK class was phenomenal! My boss was the most supportive and encouraging boss I'd ever had. And my coworkers? I've never met an entire crew of people so wholly dedicated to loving and teaching children. The board (fewer accolades there, tbh) had just approved opening a Kindergarten class for the following year, so my boss and I were dreaming and brainstorming curriculum, advertising, and schedules. So fun!

Oh, and I need to add another little change to the list of happenings from '22 to '23. We got licensed for foster care and were adjusting to doubling our household with three—THREE—little girls! What?!? How did that happen? We were done. Foster care had shredded our hearts. We were in retirement and nearly empty nesters. We were going to travel. I got a cool degree that I could use to do anything. We were dancing.

Well, I will tell you. Roe v Wade was overturned. The church we were attending had a guest speaker who said there was a difference between being pro-birth and pro-life. Being pro-birth was not enough.  To be pro-life, we needed to meet people as they were living through difficult times, "from womb to tomb." 

There could possibly be an uptick in unwanted babies born. It is an awful thing to be unwanted. My husband was deeply moved and announced that afternoon that if God allowed it, we were going to adopt so we could be a home where kids would know they were wanted. Wow! 

So here we were in March, planning a massive uptick in my commitment to work while fostering three little girls we desperately wanted to adopt. In March, we had gotten word that perhaps they would go back to their first parents. I was an emotional wreck. We never intended to actually foster again.  We wanted only adoptable kids. The girls themselves had heavy burdens of trauma, delays, and needs. Caring for one was more than a full-time job. Three? Fugedaboutit.

What a March!

Doctor Update

 In case you were wondering, I have an update on our therapy referral. Guess what? We're wait-listed because the therapist is on maternity leave til May.  

So, there we go.

Going to the Doctor

 We made it through three well-child visits! As a side note, when the office called to make the appointments, I misunderstood her and thought she wanted to set up wild-child visits. I thought it was a great term and told her so, asking how she knew how appropriate it was. It is NOT what she said. 

Some of our past visits were fiasco-adjacent. I hoped to establish a solidly positive session to create a frame of reference for what a doctor visit COULD be. We talked about expectations, did some role-playing, and equipped them with the times they could ask to hold a hand, sit on a lap, or say no.

And we did it! My girls are watching Dora as I type this and I want to exclaim, "Lo hicimos!" We left the building with three smiling little girls and two gushing-with-praise parents!

We need to make vision appointments, because it is time, but also as a first step to investigating headaches in one girl. There is a good possibility that they will all need glasses, so we'll need to keep monitoring that.

One girl had a rough visit with an insensitive tech a while back, so she was very nervous.  On another side note, the medical staff we have encountered since getting the girls have all been wonderful.  Most are good at speaking in code above the girls' heads to discuss possibly scary or triggering topics.  All are positive and supportive of adoptions. And they are really terrific with the girls.

Anyhow, the one wonky tech left my girl feeling really scared about going, but after all the prep and the amazing primary we see, she did really well.  Our daughter allowed for the exam and test, so...triumph! 

We have a referral to OT.  We have confirmations on other diagnoses and support for our chosen treatments. And we have a plan for behavior that can't be diagnosed yet. Everyone was on board with avoiding shots to keep things positive, so... triumph again!

We have one little miss who has struggled massively with past visits who did very well and said no when she needed to to certain procedures. But she is triggered, so we will spend hours snuggling, affirming, and watching to see her through whatever is going on in her mind and body that she can't articulate yet.

I have to make myself not cry whenever I go to the doctor with them.  It is overwhelming for me.  I love them. Even with a wildly successful visit as this, the tears threaten. I am proud of their bravery and growth. I grieve the gaps in my knowledge. I grieve the brokenness still evident.  And I am hopeful and thankful that we can do this with the help of a team.

I trust God is never surprised by any of this and is always present.  I go through this life ignorant of so much. But I know a God who knows.  He is enough.  I'm thankful that even though I am failing and stumbling, God is bigger than it all--including my flaws and stubbornness.

I Started Writing This, But Saw Something Shiny

Here we are on day two of looking at some of the issues we have encountered with any of our five kids.  If there were a poster family for ADHD, we might be it.  You should see me trying to write this post!

Starting with my parents, there is not one in my family of origin or current family whom ADHD hasn’t given a big fat squeeze! When you are raised by and with people who have ADHD, it is like water to a fish: I just don’t know any differently. Doesn’t it take your family four hours to leave the house? I thought everyone had trouble with being on time, remembering why they are where they are, knowing they are forgetting something, and having no idea how long any particular task takes. I thought spaghetti-like conversations were the mark of being female because there are so few men in my family.  I thought losing things like keys, wallets, and important papers was common for everyone. I never examined why everyone I am related to is always procrastinating, thriving on self-imposed deadlines, and swinging from hyper-focused to being incapable of finishing anything.  I didn’t know I had ADHD. And then I moved 2000 miles away.

Separated from my ultra-ADHD family members, I started to see myself in a new light.  Flitting from one topic to another during conversation, or one task to another didn’t look so normal. Suddenly, my behavior—and my daughter’s exasperation—finally clued me in that I might share this diagnosis.

And guess what? ALL FIVE of our children have signs of attention deficit.  God chose so well for us!  This is one we know and embrace! When we homeschooled our son, I read to him while he did flips or hung upside down on the couch. Observers doubted his comprehension or retention.  How could anyone pick up on my words with that much activity?  We lovers of people with ADHD know that the truth is that if all his attention went to holding still, he would have none left over for listening. And today you will always find him with little Lego figures in his pocket so he can fidget whenever he needs to.

We can make these accommodations for all our children.  It is a perk of homeschooling to arrange the day to help our kids be successful, turning something like ADHD into an asset!  We alternate active and quiet activities and provide ‘busy hands’ when there is a need to be more still.  The girls illustrate what I read, play with fidgets, sit on inflated textured pillows so they can wiggle in a smaller space, or snuggle under weighted blankets.

Outside of school, we watch their faces and body language to see when we need to intervene before they run into a virtual wall.  We have breathing games to help them slow their brains down. Charts are around the house to help the girls stay on track with various routines. And big, active, or heavy movement is worked into every day.

It took me three and a half hours to write this. I distracted myself. Four daughters took turns interrupting me with their needs.  My husband came and went. And I distracted myself.  By the way, my little series may be interrupted by other posts because focusing on one theme is difficult for this gal!