Motherhood
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A Forbearance That Far Outstrips My Own.

By: Jen Shoop

Ed. note: This morning, I am republishing a modestly-edited version of an essay I initially released in 2021. I have been reflecting a lot on parenting my way through my daughter’s eye condition, especially after we were able to take a break from patching for several months, only to discover that she needed to resume the treatment. The transition back has been rough. My six year old is full of questions, self-conscious enough to be mortified at the idea of wearing a patch in company (thereby dramatically reducing the contexts in which we can apply the patch), and capable of astonishing recalcitrance. (Fellow mothers of strong-willed girls will agree: I know I will one day cherish and admire these traits as my girl takes on womanhood with conviction and pluck, but my goodness, does it make these early years challenge.) There are still weeks where we must reason with her every single evening in order to coax her into compliance. To be sure, this is a small test, as far as health goes, and I know many Magpies have children with much more severe, complex, and demanding ailments, disorders, and differing abilities. One of the great outcomes of helping my daughter through her amblyopia has been a greater sensitivity for those parents, who are often invisibly carrying the weight of the world on their shoulders. You are real-life superheroes, and I see you.

*****

My daughter has amblyopia, a sight disorder in which the brain fails to process inputs from one eye and over time favors the other. It is treatable when caught early, as it was at her 18-month checkup as a baby girl, and has meant that she has worn an eye patch for five hours nearly every single day for the past few years, and will continue to do so until the age of seven.

It is difficult to inspire a two-year-old who feels she sees much better without an eye patch to comply with the treatment. It is similarly difficult to motivate a three-year-old who wants to know why no one else is wearing an eye patch to persist in her occlusion therapy. At the age of four, however, the treatment is so engrained in her daily existence that she will bring the patch to us in the morning, the picture of saintly acceptance. One way or the other, we have made it to this point, largely relying on an alchemy of consistency, M&M bribery, and various short-lived empathy tactics, including patching each and every one of her dolls and stuffed animals. There have been mornings Mr. Magpie and I have worn an eye patch in solidarity. There have been books about eye patches purchased. There have been patches with loud and funky prints on them ordered. There have been energetic celebrations every afternoon at 1 p.m., when the patch comes off. We call them “M&M parties,” and we all drop what we are doing and dance wildly around the room, shouting: “M&M party, M&M party, M&M party for Emmy-Lu! M&M party, M&M party, M&M party JUST FOR YOU!” These have become such a mainstay in the rhythm of our family life that several of my siblings know the lyrics and intonation and, on the occasion they are present for the 1 p.m. taking-off-of-the-patch, will also gyrate exaggeratedly in celebration, anointing her in song and support, and mini will beam from the center of the living room, thriving on the attention.

My daughter’s condition has opened my heart in surprising ways. At first, I felt a clinching, flinty angst towards anyone who dared gape at her patch, let alone comment upon it. I remember taking mini to a restaurant for lunch one morning, just the two of us, and a diner at a neighboring table invited herself into our universe with needling questions: “What’s going on with her eye? Will she be OK?” I batted these questions away with nodding, brisk replies delivered through a plastered-on smile, pretending to busy myself with the diaper bag to encourage the woman to return to her own affairs. When she asked about how the patch was impacting my daughter’s depth perception, I just about lost my mind. My rancor did not stem from vanity or a will for privacy. It was triggered by an inborn defense mechanism in service of my girl: I did not want anyone, anywhere to make her feel different or less than or impaired. I did not want her to experience a self-consciousness born of othering. I had the impractical parenting instinct to cocoon her from the prying eyes and unfeeling queries that seemed to follow us everywhere. I was quick to anger.

Time has sanded down the edges. I understand now that many people are well-intentioned or benignly curious, and I can’t expect them to behave as I wish they would. I appreciate that very few parents have thought through a sensitive way to respond to their own children pointing at my daughter and asking: “Why does she have a bandaid on her eye?” I can now laugh a bit at the time a visiting priest at my parish halted the entrance procession at Church one Sunday morning to pause with solicitude at our pew: “God bless this child,” he said, gravely, issuing the sign of the cross over her tiny form, I’m sure assuming that she had lost an eye. Afterward, the parishioners in our pew bobbed their heads in our direction, brows furrowed in dramatic displays of concern. At the time I remember shrinking from the attention, drawing my girl to chest, kissing the top of her head. Now I can look back on that moment as a mildly humorous, well-intentioned misunderstanding.

Young children are often curious about the patch but not unkind. They may crane their necks to get a better look at her colorfully-printed patches, or stand a few feet from her face staring in open-mouthed inquisitiveness, but it has never, thankfully, turned cruel. When asked about the patch, sometimes parents at the playground will say: “Oh, that’s her superhero patch! She has super strength!” or “She’s a cool pirate!” or “What a fun accessory!” I understand the desire to transform the device into something playful, but we remain dedicated to the bare-bones, unfussy truth: “The patch helps make her eye stronger.” We came to this phrase after fumbling through countless interactions that ultimately led us to productive parenting conversations that would spool late into the night. In this way, her occlusion therapy invited us to make a conscious commitment to speaking the simple truth to our children in this case and countless others.

Mini’s condition has made me feel deeply for parents who care for children with more severe or permanent ailments or disabilities. I have experienced a tiny fraction of what they face. How exhausting for them to constantly contend with unwelcome comments and stares, especially on the heels of the added responsibilities of caring for a child with special needs. I have made it my business to interact with those parents with particular care — opening doors or helping a wheel out of a divot when the situation warrants it with a wordless friendliness that is designed to avoid the shape of pity, but mainly going out of my way to afford them privacy and normalcy. The patch has also, I believe, helped us cultivate in our children empathy for those who are unwell or differently abled. When we see people with corrective or assistive devices, whether helmets or orthopedic braces, the patch provides an easy reference point: “You know how you wear the patch to help strengthen your eye?…”

Mainly though —

I am humbled not so much by the disorder, or by the many learnings and awarenesses it has borne, but by the quiet and uncomplaining grace of my beautiful daughter as she has toddled, walked, then run and skipped and hop-scotched, through life wearing an eye patch. Wearing one out of solidarity for only a fraction of a morning was dizzying, frustrating, and disorienting, and I could not wait to tear it off. My daughter, by contrast, submits frictionlessly to her treatment every single morning, even when the patch makes it difficult to judge depth perception at the playground or leaves her off-balance when focusing on toys with small parts for too long. I have not written about her condition for the last two and a half years out of respect for her privacy. But yesterday, I was watching her sprint down the sidewalk in front of her school with her friends, a radiant and wide-open smile on her face, her arms stretched out like wings as she kept pace with peers who do not have to go through their days with one eye covered, and I thought — well damn it, this girl deserves to be praised. I will shout it from the mountaintops!

Awhile ago, a reader shared a personal mantra: “I can do hard things.” Ever since, I have issued this affirmation to my daughter in moments of hesitation or fear: “You can do hard things,” I whisper. And while it can’t hurt to reiterate, the truth is, she needn’t be told. If anything, watching her move through the first years of her life with forbearance that far outstrips my own has been her way of telling me: “Mama, we can do hard things.”

Post-Scripts.

+Oh man, motherhood is an elegant and lopsided dance: “…These unremarkable details are the fabric of my motherhood.  Nothing dramatic or over-the-top about them–they are, simply, the silent devotions of a mother to her child, the self-same ones practiced by women in rural India and northern Ireland and the southernmost tip of Argentina.  But just beyond these quiet minutaie lies a hot, fierce love, which occasionally bubbles up into elbows-out protectiveness, or sentimental sobs, or an outburst of kisses that leaves mini writhing out of my reach.”

+Parenting feels like living with a heart rent in too many directions.

+Time is a thief.

+On making it through several months of the pandemic without childcare, while recovering from COVID myself.

Shopping Break.

+I have been wearing this striped mohair coatigan all week. It is SO warm and I love the swingy shape and unexpected stripes. I especially like layering over a turtleneck in solid navy (I wore this one) or stripes (I wore a past season version of this one).

+OMG. These under-$100 strappy pointed toe heels are a dead ringer for Miu Miu. SO GOOD. I’m tempted…

+Love the Agolde 90s pinch waists — I own in a lighter wash (run TTS but had to have like a foot hemmed off) — especially in this fab black wash.

+So, I finally got my hands on the Clarins Cryro-Flash Mask people have been raving about and it is excellent. I specifically love the way it shrinks pores and leaves skin glassy-clear-smooth. Clarins is so legit. I also LOVE their v-facial de-puffing mask — I’ve been using it for years now, and it is incredible. It really has a chiseling effect — I didn’t even know my face can look puffy before I started using this. Both are going to be beauty cabinet staples for me for a long time to come. If you want to start with one, I’d still rec the v-facial. It is transformative. I love to put it on before a night out.

+We just bought our children these electric toothbrushes on the rec of our pediatric dentist. We use these timers so that they brush for an appropriate length of time. For some reason, they LOVE the timers.

+This knit dress from Boden is SO good. Also love this one, especially in the navy.

+Loving Madewell’s Emmett series of pants — these cords and these garment-dyed pants are SO good. Heads up that you can get 20% off sitewide at Madewell with code LTK20 now through Sunday. All my top picks here.

+LOVE this head-to-toe Thanksgiving/Pumpkin/Fall look for a little boy. Janie and Jack does a good job styling outfits from head to toe like this if you’re ever in a rush/bind and just can’t take the time to assemble a full outfit for a special occasion, family portrait, etc.

+Undertaking some closet organization this weekend. Our coat closet had become a disaster of overflowing baskets of gloves/hats/etc, and it was impossible to find anything. I ordered these stackable wire bins after lengthy research because I wanted a solution where my children could each have their own “section” but we wouldn’t need to physically lift any lids / bins / etc to access. I also bought these for Mr. Magpie and my bulkier winter scarves, and will keep on the shelf above the hanging rack. In general, I find wire/mesh/see-through options like these helpful or I totally forget what’s where.

+While we’re talking clothing storage, this pack of cedar blocks/balls/etc is such a great purchase. You can hang in your coat closet, throw in garment bags, toss in sweater bins, etc. Cedar deters moths and moisturre and preserves clothes / keeps them nicely scented.

+Love the tortoise pattern on these shades.

+This velvet mini is fab.

+We don’t use nonstick pans in our home (Mr. Magpie has theories about this — achieving fond, etc), but if we did, I love the look of these.

If you want more Magpie, you can subscribe to my Magpie Email Digest for a weekly roundup of top essays, musings, conversations, and finds.

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Jenna
Jenna
1 year ago

Jen – I was just browsing Time’s list of the best inventions of the year and saw this – https://luminopia.com/about-us. You may already be aware, and I’m not sure how accessible this is, but wanted to pass it along. Thanks as always for sharing so much of your motherhood experience with us and reminding us that we’re not alone on the most trying days.

Brooke
Brooke
1 year ago

I needed this this morning as I sit in a hospital waiting room with the news my sons chronic autoimmune disease is not improved. He has eosinophilic esophagitis and despite eliminating the top 9 allergens from his diet we are now moving on to twice a day steroids in hopes it improves. We’re depleted. Thanks for your kindness and a moment of feeling seen this morning.

LeahK
LeahK
1 year ago

Beautiful. Thank you for sharing this. You can do hard things. Bravo!

Jeff Lepper
Jeff Lepper
1 year ago

Hi Jen, I read the above about Emory’s eye patch and it so resonated with me. Two of my granddaughters have had eye issues, operations, patches, etc. All is well now as one is 21 and one is 13. Those patches really do work and they are so cute now! But your straightforward approach, your humor, your deep love, your sensitivity, were so awe inspiring that I felt I had to touch base with you and tell you how much this meant to me. Love, Jeff

Rachel
Rachel
3 years ago

I just wanted to say thanks for deciding to share the factual side of your daughters condition and offering a script for how to explain it to kids and adults. I came to your blog looking for ways to handle a quarantine with kids…and left with a new understanding of one of the reasons kids might use eye patches, plus how to explain it factually and simply to my own sons. I totally understand and admire your decision to protect your daughters privacy, but it’s also a kind and generous act to inform others….so thank you : ) !

MK
MK
3 years ago

Coming to this so late, but oh my, what a beautiful post! It has left me teary-eyed like so many others who have commented before me. You are an incredible mother and Mini is so lucky to have you. I’m also in awe of her strength in navigating her condition so gracefully, at such a young age. It’s very moving, even to a total stranger! Sending her (and you) my love and hopes that in time, her amblyopia will become less of an issue. xxx

P.S. I love the image of the 1pm M&M parties! How sweet, and how special for her (and all of you!)

Mia
Mia
3 years ago

Oh Jen! I was tearing up reading this. I love that photo of your mini. What a strong, joyful, and resilient little girl you have! (And what strong and resilient parents she has too!)

I know it feels so hard finding out something is atypical in your child… I remember at my 20-week anatomy ultrasound when I found out my baby’s kidney was not growing well and I bawled right there in the doctor’s office. They monitored her from then on closely, and while she does have a kidney condition for which we see a nephrologist and urologist annually, she is otherwise healthy (knock on wood). At any rate, kids are amazing little humans — they (and we) can definitely do hard things!

I don’t know if this sounds strange coming from a stranger on the Internet, but you and Mr. Magpie sound like such wonderful parents. You seem to bring out the best in each other and in your kids!

Continue rocking that eye patch, mini!

Kristen
Kristen
3 years ago

Oh, this is such a genuinely lovely tribute to Mini’s fortitude and resilience and adaptability. So beautiful. As someone noted above, what an incredible team you two make.

Also, this made me feel seen and validated in my experience of parenting my 1 year old son who has a somewhat prominent hemangioma on his scalp. We’re fortunate in that it will fade and ultimately disappear over time but I do find myself bristling a bit when other kids point it out or ask about it. I think that desire to protect our children from feeling any sense of otherness or exclusion is so innate in us as mothers, even if the questions or comments from others are ultimately benign. Thank you for sharing with us.

Alexandra
Alexandra
3 years ago

This is so lovely and such a testament to both of you! It reminds me of this post- I found it really interesting hearing an adult’s perspective looking back on her childhood wearing an eye patch.
xx
https://cupofjo.com/2015/07/courtney-klein-beauty-tips-storq-maternity/

Mary
Mary
3 years ago

You are an incredible mother and an inspiration! Thank you for sharing.

Katie
Katie
3 years ago

I love love love this post! What a beautiful tribute to your sweet girl and a testament to you as a mom.

My older son, William, is the exact same age as Emory and has intermittent alternating esotropia. He just had strabismus surgery less than two weeks and Dr. Vike Vicente here in DC is INCREDIBLE. I cannot say enough good things about him and wanted to pass along in case you needed a new pediatric ophthalmologist when you move. Happy to chat offline as well – just email me! Xo

Elisse
3 years ago
Reply to  Katie

I worked with Dr. Vicente when I was a medical student in DC! He is such a great doctor and amazing with kids. I I also definitely credit him for helping me get into my residency program. Highly recommend him.

Cynthia Coleman
Cynthia Coleman
3 years ago

My daughter also wore a patch. She’s a beautiful 28 year old now.

Rachel Parrish
Rachel Parrish
3 years ago

Also wanted to add – my 4 year old son Teddy has a “best friend” at school who wears glasses. He has asked Santa for glasses for the past two years and constantly talks about how cool it is that his friend has different colored glasses. 🙂

Rachel Parrish
Rachel Parrish
3 years ago

This made me tear up (and I’ve kind of lost the ability to cry, so no small feat!”)

Thank God for good pediatricians

What a strong sweet girl. What a strong brave mom you are.

Thank you for sharing

Brooke
Brooke
3 years ago

Reading this gave me a lump in my throat. I’m grateful you shared this. I, too , have wondered at the balance of sharing and protecting privacy when it comes to my daughter’s ADHD diagnosis and it calls to mind a recent FB post by another friend who wrote about her son’s journey to a hearing aid and added, “I write this to share with other parents who may be on a similar journey–let me know if I can help.” It felt like a gift to her community, her willingness to be a bit vulnerable in sharing her story and in doing so be a resource for other parents. This essay made me feel the same!

Elisse
3 years ago

Thank you for sharing this beautifully written essay. I’m an ophthalmologist in training and I noticed some of your past instagram posts with your daughter in glasses and remember being mildly curious if she had amblyopia but of course didn’t want to ask. This essay really helped me see things from the perspective of her, and you as her parent – it is easy for us as doctors to say “wear a patch every day” but so much harder in reality. Big hats off to you and her for your strength and resilience during this process. Loved reading some of the other comments too about people who had success with the patching. And I absolutely love that picture of your daughter; she looks so joyful!

Cristina
Cristina
3 years ago
Reply to  Elisse

I loved your reply.

Elisse
3 years ago
Reply to  Elisse

Wow, thank you for the book rec! What a great idea. I will definitely keep that in mind for my future patients!

Kristin
3 years ago

Aww, hugs to you and hugs to that brave smart girl! My little one (almost 4) patches every day for exotropia and we’re getting glasses next week. I’m dealing with mom guilt even though I KNOW we started treating in time, but isn’t it amazing how these little girls have the strength to handle it? Even after the bribes and the crying and the sneaking into a corner to take the patch off, they do it. You’re a great mom. Maybe the mini magpies can start a Preschool Patch Posse when you move to DC. They’d be inspiring!

marge
marge
3 years ago

So inspiring, thank you for sharing! I have the same condition as your daughter and had to wear an eye patch over my eye when I was her age (I’m now 22 and it does not impact my day to day at all). I think it will bring you comfort to know that I had completely forgotten about that situation early in my life until I read your post this morning. Someday mini will only vaguely recall the details of this experience but the resilience she is developing will improve her approach to every challenge she encounters going forward. Like I said, I vaguely recall the nuances of my eye patch regiment- but the parts of the experience that stand out in my mind is my interactions with my parents during those times. The help and love you are giving Mini during this experience will illuminate your profound love for her more than any words could convey. That is the part of this she will remember. Sending you both love and strength!! You are such a great Mom

Cynthia
Cynthia
3 years ago

So well said! Your words conveyed everything so eloquently. You and your daughter are stronger together. Love is so powerful!
Stares and odd glances are unfortunately a part of our world! Early on I caught myself staring back (loud and hard) as if to say, how do you like it when I stare at you. Time has calmed me down, but I wish more parents would take opportunities when they present themselves to teach helpful lessons on disabilities. It’s not a life anyone wants, but some are blessed with it.

Katherine
Katherine
3 years ago

Jen, this is such a beautiful tribute to your daughter and to you as her mother! You two make a formidable team. It made me want to call my mom and thank her too!

Molly
Molly
3 years ago

My (now not-so-little) brother was patched daily for a few hours each day until he was about 4 when his “lazy eye” wasn’t getting any better and a new dr realized he instead had a condition that could only be reversed through surgery. All is well now, and he’s 17 with no eye issues. I’m so impressed by Mini’s resilience with and submission to something that just has to be a part of her life – a good lesson for us all.

Also – this was a great reminder that even in this world of everything being online, you never *really* know what people can be going through or dealing with until you know. It’s so easy to take acquaintances and friends social media presences for the whole story when in reality it’s just a fraction.

PS – that picture!!! SO adorable!

Stephanie
Stephanie
3 years ago

Oh, so glad to hear this was caught early and is treatable! I so relate to the singing/dancing/bribery/etc to get small children to willingly participate in their treatment. Our girl is in remission now, but her neuroblastoma was diagnosed at about the same age that mini’s condition was. Such babies!! We never really had to deal with stranger’s comments though…her scars are mostly hidden by clothes and even though you could see her chest port and feeding tube through her bathing suit no one ever mentioned it. And she was so little when she lost her hair that maybe she looked like a toddler who haven’t gotten her hair yet? Anyway, glad we dodged those uncomfortable interactions. She has been such a champ throughout. She definitely pulled us grownups through the ordeal with her cheery disposition. She still has several scans per year and since she’s more opinionated (ha) about things now, I’m feeling grateful that she was so little when we were in the thick of it.

Thanks for sharing this!! We can all do hard things…even things that seem like the worst, most impossible things. We are strong for our children and they are strong for us, even when they’re too little to know it!

Stephanie
Stephanie
3 years ago
Reply to  Stephanie

P. S. Forgot to mention another commonality here…her cancer was caught because of her eyes. My husband noticed a VERY slight droop on one eyelid, and that (in combination with the fact that as a baby sometimes half of her face would flush randomly – even though that had not happened for months at the time we noticed the droopy eyelid) sent us off on a round of eye appointments and an MRI which found the tumor. It was on a nerve that controls the eyelid and pupils. Since her (SUCCESSFUL!!!) surgery, her left pupil will always be larger and her left eyelid is still a teeny bit droopy but not noticeable if you aren’t looking for it.

Jacqueline
3 years ago

My 10 year old niece has strabismus. You are so brave to share this. I love the way you write, and this is the most authentic piece I have ever read by you. Thank you for celebrating your daughter’s bravery by being brave in what you post. It will echo goodness and understanding through the community you have built!

Claire
3 years ago

Oh, this was so eloquently said! My daughter will be born with a heart condition requiring surgery and I’ve felt similarly fiercely (pre-emptively, I’m my case) protective, even bristly, and simultaneously more tender towards families facing far worse. I love the photo at the top — the very picture of joyous resilience!

Cristina
Cristina
3 years ago
Reply to  Claire

I love that – joyous resilience.

Joyce
Joyce
3 years ago

Jen! My youngest sister wore an eyepatch for years. (The treatment worked!) In hindsight, especially now as a parent, I am so impressed with my mother’s tenacity to establish it as a daily routine. I remember some screaming battles, rude stranger questions, etc. But now (20 plus years since I last saw my sister in a patch) it mostly feels like a testament to my mother’s care for her children. Thank you for this essay as it encourages me to consider my sister’s perspective as well.

Leslie
Leslie
3 years ago

My daughter who is now 9 has refractive amblyopia and quite an aggressive prescription. She patched for years too. It was a looong slog but made a huge difference. One thing we found that helped was maze books, it helped her vision a lot especially during patch time. Also we did the fabric patch over the glasses which was much more comfortable for her skin than the adhesive ones, found on Amazon or Etsy. She’s doing great though!! I know this road is tough.

Barbara
Barbara
3 years ago

Beautifully said! And that photograph-beyond adorable!

Courtney
Courtney
3 years ago

Thank you for deciding to share this, and pictures of your precious kids on the blog! My daughter has strabismus and has been wearing bifocal glasses since 2 years old, and I can relate to every single word you so eloquently wrote. We are so grateful we caught it early as well, and are amazed at our girl’s resiliency like Emory! All the mom feels on this one. You’re doing a great job!

Colleen
Colleen
3 years ago

Beautifully written and so touching. I continue to learn daily from my three boys who are 21,20 and 17. I am in awe of their grit and resilience, especially my 17 year old who has CP and is wheelchair bound. He is the happiest, well adjusted teenager. He is an active member of his high school and diligently preparing for his AP History exam……he encourages me to do hard things everyday.

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