What is Mother’s Day to these groups? I may have missed some categories, but in general this is what I have observed:
Married women with children
Single women with children
Women with special needs children
Single women without children
Married women without children
Women who have lost children through tragedy: war, accident, illness, other circumstances
Women who have lost mothers
Women who don’t want children
Women who can’t have children but want them
Looking at this list, I know what it’s like to:
be married with a child
have a (relatively high functioning) special needs child
want another child but unable to have one (yet)
be single until the age of 36 until marriage stabilized my life enough to have children
This is my life experience so far, and I admit my empathy is limited to women who fit into these categories. Some fit neatly, for some the lines are blurred. I do my best to understand that, too.
I know women who:
are single with children
are single without children
have special needs children across a very broad spectrum
have lost children through tragedy
have lost mothers
don’t want children
can’t have children but want them
Every Mother’s Day I think about these women. What are their struggles? How do they cope? Is this holiday something they even care about, or is it just another day? It seems the world praises mothers as women who have children, but I’ve always felt strongly that to be a mother you do not have to have children. I’ve always cringed at that part of that (cultural/societal) definition of motherhood; I’ve always felt to side with those who may fall in the shadows of the child bearers.
Not that child bearers shouldn’t be standing tall, because they totally should. Raising children is never easy, and devoted moms everywhere should be extremely proud of their hard work. My mom is wonderful. She sacrificed and taught and nurtured and scolded and guided me to learn really important lessons about life. I will always be grateful for everything she’s done and is doing for me.
I know many wonderful women who qualify as “super moms,” because they’re doing it all. They overcome all obstacles; they push aside excuses. They bend the universe around their will. These women have determination and passion, and I know they have their own trials and internal conflicts, but to me they are unstoppable. I admire them, because I know they also have to be super tired all the time.
But you guys. YOU. GUYS. I probably know even more women who deeply suffer when Mother’s Day comes around. It seems they feel a lot of traditional moms look down on them. They feel inferior, less than; their divinities/self-worths don’t measure up because of their different life experiences. Feeling this way, year after year — or even every day for some — is really hard.
If we don’t dedicate this day only to women with children, are we dismissing them? Is this their one day to feel better than the women without children? To say, “I’m so much more like Christ now because I have children”? Is motherhood the only thing that matters to our (eternal) happiness?
Wouldn’t the womanly and motherly thing to do is to include and love women for their differences and experiences, no matter what they are?
Every ten years or so a good thought graces my soul, and four years ago on Mother’s Day I posted this on Facebook, and it still holds up:
As women are all descended from Eve, we all should remember our nobility as Mothers of All Living. Our stewardship, however we currently define it in our lives, is divine.
Happy Mother’s Day.
To my glorious mom, happy Mother’s Day. To all mamas everywhere, happy Mother’s Day. But especially to my dear women friends who face pain, loss, and sadness, and live with heartbreak: at the very least, you have nurtured and guided me and helped me heal in profound ways. If that isn’t being a mother, I don’t know what is. Happy Mother’s Day to you.
This post was written 10 April 2018, but I’m backdating it to Z’s birthday, 8 April.
Almost three months ago, you and I got sick with fevers, headaches, and congestion. You and I went to the doctor to see if we had the flu. The doctor sent us somewhere else to get a nasal swab to determine the flu. I’m not sure why he or any of the nurses in the office couldn’t swab us. I still might be a little bitter about it.
The doctor’s office wasn’t entirely clear on where we were supposed to get the swabs: do we get them at the hospital, or at one of the affiliated clinics near the hospital? I should have asked for clarification; part of our long day was that I should have gotten better directions.
We stopped by the hospital first. When we were checking in, the intake lady heard you coughing, handed me a mask, and instructed me to put it on your face. This wasn’t going to happen. I knew you weren’t going to keep the mask on. You sat on the floor, keeping mostly quiet, being very good for a sick 3-year-old.
The intake lady heard you cough again, and she reminded me to put the mask on your face. I didn’t do it, because that was a battle I chose not to fight: I’d rather you quiet than struggle to keep a mask on your face. She double checked our insurance and told us a flu swab wasn’t covered. I was irritated. My head was throbbing. I remember half-heartedly asking about the insurance, and the intake lady answered something. I took your hand and quietly walked away.
We eventually found the place where someone would be able to give us the flu test. We ended up both negative. That was a relief, but we’d spent a lot of the day driving around, feeling like absolute junk. I’m so sorry for dragging you all over Orem and Provo that day.
We both tested negative that grey January day, but I can’t stop thinking about my lingering negative attitude about that experience, especially at the hospital. What I wanted was not to have to explain why you wouldn’t wear the mask. What I resented was the assumption that you would wear a mask at all. Maybe the intake lady trusted that moms know the best approach for putting a mask on their children, since no “normal” sick child would cooperate wearing a mask. I didn’t know how to say I was clueless. What I wanted was an acknowledgement–at least from this healthcare institution, in a state that has a higher population of autistic children–or some sort of effort to accommodate, a simple “if your child has sensory issues, then [here’s an alternative].” That can’t be too much to expect at a hospital that probably sees hundreds of children every day.
But guess what? I figured it out. When we were at another waiting room, the receptionist asked me to take masks for both me and you. You started coughing, and I held a mask up to your mouth. Every time you coughed, I covered your mouth with the mask, and you were actually ok with it. I was so grateful for this!
Dadda and I have been your parents for four years now, and we’re still figuring it out. I’m still learning patience, but I’ve appreciated the process of learning to see the world through your eyes. I love how you’re never in a rush. How you give in to adult-perceived distractions, when you’re just enjoying your surroundings. How you run your hands over all surfaces. How sometimes you exercise your curiosity by sticking your tongue on things (which often grosses me out). How you run and laugh and sing–and spin, of course. How you verbalize your feelings even though you don’t have as many words as you’d like.
You’re working on getting more words, though. More skills, more coordination. More understanding. A greater attention span and focus. You’ve developed a liking for coloring and puzzles. You can sit with these activities for at least an hour sometimes. Your teachers have been so impressed with you over the past year. When you began preschool, you weren’t able to sit still, and you had no words. Now look what you can do!
We’ve taught you to repeat simple phrases like, “I’m cool” and “I’m smart”; Lola has taught you, “I’m beautiful,” and on your birthday you’ve been able to repeat, “I’m four.” Four. We can’t believe it.
You are adorable, and everyone loves you. Friends and family, definitely. It’s a little weird when strangers smile at you while we’re out or traveling, but most of the time you’re oblivious and could give zero cares. I need to find a way to live more like you.
It can be so hard being a kid sometimes. So many rules, so many boundaries. It’s been hard for me to reconcile your supposed limitations with your potential. Just thinking of your immense potential makes my heart full. But to you, you don’t have any limitations, other than your parents’ occasional inability to understand what you want or need. Such understanding often requires words. Which you are acquiring more of every single day. Your language–both jabbering and intelligible words–has expanded our minds and blessed our hearts in so many ways, made us better parents. We’re learning as we go. Just like you, we’re figuring it out. We try our hardest to open up the world to you. No limits, baby girl. No more assumptions.
We have you as our daughter, and you have brought us more than we could ever imagine. More love. More happiness. More life.
Valentine’s Day is a colossally dumb holiday. Like a lot of “holidays,” much of Valentine’s Day’s finds meaning in how much you can spend. Supposedly we’re celebrating love and Cupid and being together. That’s nice. There’s chocolate and flowers and restaurants and jewelry. I like that singles call it “Singles Awareness Day”, and that girlfriends go out for Galentine’s. That’s fun.
This commercially dedicated day is framed in a way to appear the only day in a whole year to declare love. Or make some grand gesture of love. You don’t want to miss your chance. But it does seem to be the only day people will wait in line for hours at a decent (or even crappy) restaurant. New couples may get to see an ugly, dark side of their dates as lines stand still; seasoned couples may wonder why they didn’t stay home and cuddle in front of the television. Hello, it’s the Olympics! What’s more romantic than watching people at their peak athleticism and talking about how we’re so much cuter and stronger and, better yet, way more comfortable in our jammies? We (I) do love Johnny Weir and Tara Lipinski, who may be the best commentators of any event in the history of humankind.
But it’s only coincidence the 2018 Winter Olympics overlap with Valentine’s day. And that the Winter Games only comes around once every four years, and Dumb Valentine’s Day (yes, that’s the name of the entire proper noun) is every year.
It’s possible not to celebrate Dumb Valentine’s Day, to make that very deliberate choice, but this is also dumb. If I’m being completely honest with myself, despite this holiday being overhyped and spendy and chaotic and commercial and exclusionary, I actually quite love it. Mostly because my love loves it. Reilly really gets into giving me flowers and chocolate and a perfectly written card. And we have fun giving Z little chocolates. I enjoy this overt expression of his deep and abiding love. Throughout the year he does so many little things to support me and brighten my day. Like laundry: for me, folding clothes ranks below going to the dentist, but Reilly speeds through washing and folding loads of laundry without a single complaint. That’s pretty hot, and just thinking about it makes me wanna …
I don’t necessarily expect a sweeping flourish for Valentine’s Day, but I certainly relish the moments where he puts forth a greater effort beyond his daily, loving actions.
We’ve learned not to go out on Dumb Valentine’s Day itself. We might go out sometime this week, but tonight, people be crazy, so we’re staying in. Besides, I like the idea of spending a quiet evening with my family, of celebrating our love doing something non-sparkly. That’s plenty special.
I love hanging out with my family. It doesn’t even matter what we’re doing: Driving without having a place to go (sorry, environment!), watching TV, eating, sitting around. We don’t even have to be talking. It’s nice to read in the living room near (it doesn’t even have to be next to!) my honeyman, while Z plays or reads or spins around.
In true, self-contradicting, Dumb Valentine’s Day fashion, to demonstrate my love for my family, I have a somewhat grand gesture of my own. (Insert evil laugh here.)
I have been listening to Lorde’s first album–PURE HEROINE–a lot lately. Something about the second song really catches my ear, and it was on repeat for hours at a time, several days in a row. It’s a cute little song called “400 Lux,” and it’s about young love realizing it’s evolved into something deep and real. The couple in the song don’t have to be going anywhere to feel like they’re doing something together. They don’t feel unpredictable and uncertain anymore; their love is stable.
I love these roads where the houses don’t change
Where we can talk like there’s something to say
I’m glad that we stopped kissing the tar on the highway
We move in the tree streets
I’d like it if you stayed
That’s where I feel we are.
Many of my guilty pleasures are often cheesy and awkward things that sometimes cross over into being uncomfortable. I like Hallmark and Lifetime movies. I like movies about animals getting lost so they talk to each other telepathically and find their way home. I have a feeling that I would really like This Is Us. Anyway, I edited together some footage of our family hanging out with “400 Lux” as the soundtrack. Dirty windows, cracked lenses, the works. The result is a cheesy, awkward, and possibly uncomfortable video that I hope you (try to) enjoy. I love our little dog and our growing daughter and my always-super-hot husband.
2017 has challenged us in so many ways. It has strained our rights as human beings, divided us from friends and family, tested faith, broken individuals seemingly past repair. It has taken my family down stressful paths. Although we have been blessed with quality time and other graces, others have suffered deeply, and often silently.
Some time during the summer someone from church asked me to help out with organizing potato dishes for funerals. Cheesy potatoes are important to any post-funeral luncheon. People gather after saying goodbye to their loved ones and find comfort in sharing food with those who also love the dearly and recently departed. Their emotional needs are met through one of their most primal needs, by eating something delicious, something made with love.
Cheesy potatoes are only one aspect of the meal, but it’s a favorite among mourners. Lots of starch, and lots of cheese. Those elements in that combination are meant to fire off certain neurons that translate to comfort, which tries to coexist with the burden of grief.
After receiving this assignment, a few months passed, and no funerals had been planned. The first half of the year had been replete with passings-away, but I was not yet part of the funeral meal committee. Then the last Sunday of October the lady who extended the assignment remarked how quiet it had been, and I thought to myself that this was a good thing. I wasn’t opposed to doing the work, but I was glad that people hadn’t experienced that kind of heartache in our ward, at least for a few months.
Go figure the moment someone mentions how a thing hasn’t happened, the thing happens shortly after that. Later that week our ward received an email about the passing of someone from our ward. I researched the person and found out that he had suffered from depression. His beautiful obituary profoundly saddened me. Usually during these times I feel the most helpless, but this time I could actually do something. Never had potatoes seemed more vital. If the other parts of the luncheon failed, cheesy potatoes had to prevail.
I had a list of sisters in the ward who were willing to make the cheesy potatoes. It was my job to call these ladies to see who would be available to provide the potatoes that weekend. I came up with a spreadsheet and kept track of responses and commitments, which would also help with future funerals. Here, I deleted names for privacy:
The sisters who were able to help that weekend were very kind. I had never really been an active part of this kind of effort, and their love and solemn treatment of this responsibility humbled me.
The ladies made their dishes and dropped them off at the church the morning of the funeral. It wasn’t until the following Sunday morning at church that I found out the funeral had gone well, that the food was delicious, that the family was grateful for all the help and support. I had imagined everyone eating and sharing stories and feeling a degree of unity that only comes with grief over a mutual friend and family member. Potatoes were all I could do—and I didn’t even cook them but just called people on a list—but for this moment, they mattered.
I have several close friends whose lives are entangled with depression and anxiety. They navigate their brain chemistry and the changing seasons and pollution and other circumstances with medication and therapy and exercise and hanging out with loved ones. It’s not easy for them, fighting the grey. But they are brilliant and creative and so passionate about the earth and humankind. They are the best readers and writers and experiencers of life; they are musical and endlessly curious and know all the best cusswords (and usages). I am so honored to know them.
Reilly’s mom has had every excuse to spiral into depression, yet she pushes through with such determination. And a smile. And enduring positivity. She’s coming up on her first full year of bi-weekly cycles of chemotherapy for stage IV metastatic colon cancer. It’s hard to imagine her daily hardship of increasing weakness and regular wooziness, but she has kept busy with work and doing as much as she can. She’s had excellent care with amazing doctors, and she knows she is surrounded by so many people who love her. Everyone faithing her well seems to be making a difference. Her strength amazes me.
She and her family have seen a pet cross the Rainbow Bridge this past month. A Chocolate Labrador Retriever, Maya was a boisterous and carefree and previously big dog, until diabetes caused drastic weight loss, blindness, then finally loss of use of her hind legs. No one likes to hear the vet say what the best course of action is to minimize suffering, even though it makes the most sense and really is the most humane for the dog. It’s painful saying goodbye to a pet, especially after almost ten years of companionship.
This year Alzheimer’s, dementia, Parkinson’s, and other ailments have ambushed or harrowed loved ones’ journeys.
My mom broke four toes when she slipped from an elliptical machine. But she hasn’t slowed down. This is both annoying and endearing at the same time. I love her for that.
Friends in Florida and in/near Texas or with family in Puerto Rico endured hurricanes and are trying to repair their lives.
Friends who married their high school sweethearts nearly 20 years ago have gotten divorced.
Other friends are enduring similar trials and heartache.
Earthquakes. Fires. Volcanoes. Shootings. Tax cuts. Health insurance. Church. #metoo.
How do people find comfort? What helps them in their agony and despair?
Z’s diagnosis was not as much of a bombshell as the anticipation of her diagnosis. This expectancy involved asking myself (after wondering what I did wrong) how I would handle this situation, what our “new normal” would be, how we would teach our innocent, nonreader of emotions to defend herself against monsters and assholes, among a plethora of other questions. But once we obtained a diagnosis, a wealth of resources became available, I found out several families are in our ward who have children with autism, and Z’s ABA therapy has helped her little personality emerge in ways that that weren’t obvious even six months ago. We have received an outpouring of support and love from so many caring people. You know who you are, and we are infinitely grateful. Thank you for your acceptance, kindness, and generosity.
This past year I have looked forward to Sunday dinners in Payson and Saturday donuts with my family. Family visiting from Florida. It has been nice to go on occasional movie dates with my perfect husband. To travel, to take long breaks and relax in our home. It has been rejuvenating to hang out and eat pizza with friends and discuss actions for lessening the hate in this world. Like a good nap or fresh air.
I have enjoyed picking apples and peaches and trying to make pies and making toffee and brownies and other little goodies to share. But I have also found calmness in literally tearing down walls (maybe figuratively, too?) and building shelves and painting and caulking. I have nurtured new friendships. I have explored more good music, movies, books, and television. I have discovered Twin Peaks while rediscovering the treadmill. My heart pumping, blood flowing, and sweat dripping are sometimes all I want out of life. It feels so good.
I have marched.
Contacted my senators and representatives.
We have also relished hosting a quarterly lecture series in our home, where we listened to speakers/friends talk about a variety of subjects: Satire (Reilly), the Poison Control Center (Reilly’s sister, Amber), Horror and the Family (Jon Smith), and Fan Studies (Melissa Beattie). What an exciting reason to gather with friends!
Yes, there’s a shload of darkness and nonsense in the world right now, and we make it through one day at a time. Probably more like an hour—or even a minute—at a time. Sometimes at the end of the day things don’t look brighter. We’re still sad or confused or hurt. It is ok to feel this way. And sometimes all we want to do is pull the covers over our heads and cry. It is ok to do this.
It is ok to bring this version of ourselves into 2018, because 2017 was ruthless. Pick your best cussword. You know: it’s complicated. I may spend the first part (or majority) of the New Year swimming in my covers, trying to find/push away sunlight and coming up for air/holding my breath.
This supply of oxygen, though, the most significant mercy that came out of 2017, was that many of us took the time to listen to each other. Even though we have disagreed on many fronts, a greater striving for understanding has risen from our immediate social circles, communities, and the world. This has sustained a hope I will always cling to.
I want to keep listening to you. I want to bolster the comfort and love of real friendship between us. I want to be there, to be the equivalent of cheesy potatoes for you. Something full of love.
Or I could just make cheesy potatoes. And hug you with them. In 2018, and in years to come.
In the past months since the last blog post, a couple of experiences have lingered in my memory. These remind me just how different human beings are, and in terms of behavior among “normal” individuals, there is also a broad spectrum to navigate. And how we respond to these people reveals more about ourselves than they.
The first experience comes secondhand. Reilly came home one day the middle of last month and recounted he and Z had taken Sia to the vet for her booster shots. They were in the waiting room, and Z was spinning in place and jabbering happily. An older woman was watching her and asking her questions, and Z wasn’t answering, because as a 3-year-old, spinning and jabbering are far more important. But Z did stop spinning, and the lady asked her a question. Z answered with more jabbering, which made the lady turn to Reilly and ask if she knows real words. She wasn’t mean about it, and Reilly explained that Z has autism and delayed speech. The lady then replied that her daughter is a special education teacher in an elementary school and asked Reilly if he knew her. Z attends pre-school in a different district, so it’s not likely that we would have run into this lady’s daughter. Nevertheless, this was a short, but cordial conversation, and I was glad to hear how accepting the lady seemed of Z’s circumstances.
The second situation happened about a month ago. I was observing a group being talked to by an important person in a certain industry. He was telling the group how essential they were to the overall vision, that he was pleased with how their colleagues in other offices were looking to adopt this group’s production model. He told the group that they were special, “not special ed, but special.” Some of the people in this group laughed. I did not. I was disappointed that a person that people respected would make a joke like this. I don’t know if I was particularly sensitive because of my new closeness to the special needs world, but I also wondered why people are still making fun of others who happen to be different.
Yeah, broad spectrum. I’m generally accepting of most decent and well-intentioned people. And sometimes I say things that may be insensitive to others’ circumstances. And yes, I do want to protect our daughter, but I know she’ll have to face the world to live her own life. And if I struggle reading people at times, I just wonder where on the autism spectrum is Z’s ability to discern emotions in other people. How much will we be able to teach her, to prepare her to handle interactions with complete cussheads?
On a sort of similar note, Z has been through two weeks so far of ABA sessions with a tutor. The interventionist (the tutor’s supervisor) says Z’s learning really fast and likes to push her with different challenges. Z now has a little toolbox of word approximations, so that when we ask her, “What do you want?” she can say, “dee” (candy), “boo-boo” (bubbles), “chih” (chips), “chee” (cheese), “kha” (drink), “koo-eeh” (cookie), “doh” (donut), “side” (outside), a maybe a few other little words. You can tell that food is a major motivator for her. She’s become a better imitator, she waves and says, “bye-bye-bye-bye-bye,” and she can say “mama” and “da-yee” when prompted.
This is so exciting and reassuring. Our little communicator. We love her.
Happy third birthday, my love! I’ve spent the past few weeks thinking of what to write you for your birthday. I thought I could plan something elaborate and fun and recap the last year of your life with a flourish, because your third birthday is a really big deal. The planning didn’t go so well, but I’ll still reminisce this past year with you. You have grown so much, and the world anticipates all the new things you have yet to discover.
Dadda and I worry about you all the time. We’ll keep worrying about you as the world continues to open up to you. That’s what parents do. We wonder how you’ll play with other kids, communicate your wants and needs. You do express yourself well; all it takes is one look at your irresistible face, and we can tell what you’re feeling.
You want to be independent so badly. You’ll climb the countertops to get what you want. If you need help with it, you’ll bring it to us, at which time we realize you’ve climbed the countertop, which is a big no-no. But you’re stubborn and persistent. These characteristics will ultimately prove valuable to you in this world, if you use them the right way.
Lola and Poppy are in town to celebrate your birthday, and you’re so eager to show them how much you know. Just last night you led Lola to the bathroom, where you brought the iPad, then brought the stool to the toilet, put your potty seat on the toilet and had Lola help you with your pants. You then sat on the toilet and went potty. Lola was so very impressed.
Only recently have you started opening the refrigerator to retrieve one of your favorite foods, yogurt. You’re getting stronger and more resourceful, and if there’s a way to do something without our help, you’ll figure it out.
A few months ago, we bought a house with a back yard and lots of space to play. You seem to enjoy it. You’ve found your little niches where you love to play, but it seems that you can fall asleep anywhere, which is so convenient.
For some reason, you’ve gotten a lot more energetic as you’ve gotten closer to 3. You run, skip, jump, and dance so much more. Jumping on the couch, jumping on the bed. Running from one room to another. Going down your slide while watching one of your favorite movies. Climbing the fence, throwing rocks. Spinning and spinning wherever you are. You’ve also gotten a lot more curious in your old age, and it’s so much harder to keep up with you.
You’re also putting a lot more stuff in your mouth that isn’t supposed to go there. Just the other day I barely saw you eat a giant booger before I could do anything about it. It really grossed me out, and we need to do better at catching you eating prohibited things. We actually need to be better at teaching you not to eat those things. Ah, parenting. Thanks so much for your patience, little one.
We love how you’re participating more at school (daycare). We love how excited you get when you want to show us something. We love how often you sing and how you recognize the songs we sing to you. We love that you like watching music videos, how Beyonce’s “Single Ladies” and ‘NSync’s “Bye, Bye, Bye” are among your top favorites lately.
So much is happening in the world. So much legitimately weird stuff. You’re oblivious to most of it, but we do want to teach you how to navigate all the weirdness in a constructive way. We want to teach you how to give beauty and goodness to the world. I know you’re only three, but you’re actually already three. You’re growing too fast. I would like to stop time just for a little bit, just for today, to really sit back and enjoy remembering the past three years with you.
We’re having a party for you today: balloons, yummy food, family and friends. Toys and clothes and everyone cherishing your life. We hope you like it. Thank you for bringing us so much joy, for teaching us, for making us love more deeply and way beyond what we originally thought our abilities were.
This next year will be very exciting, and we cannot wait to live it with you.