Weekly Grace 1

Taking the lead from Rachel, I thought I’d try doing Grace in Small Things. Realistically I can probably only do it weekly, but it’s a start, and it’s a nice way to be appreciative of the smaller things that can get lost in the shuffle of everyday life.

1. Long weekends. Even though we just started a new semester, I am so looking forward to the upcoming three-day weekend. More time to hang with Baby Girl, to work on the book, and to prepare for next week’s classes.

2. Time Machine. I love this back-up feature on my Mac. It takes the thinking out of it for me, and means I always have a recent version of all my work saved.

3. Pho. Baby Girl and I are both a bit under the weather, and the thought of steaming, fragrant Vietnamese broth (cooled off a bit for her, of course!) is lovely.

4. Hand-me downs. Baby Girl has a lot of just-older cousins, and we’ve been lucky to get so many bags of beautiful clothes. It’s much colder than it has been, and I pulled out a great winter coat for her today that is brand new to her. Love! Plus, it’s always neat to see her in things I remember my nieces wearing—lots of good memories.

5. Libraries. Our town has a wonderful, spacious, vibrant library. We just started a weekly Story time there this month, and it’s been a lot of fun hanging out after and looking through all the books. It’s a good way to while away a winter morning, and to socialize with other babies the same age.

Have a great weekend!

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On the Working, Parenting, and Chronic Illness (Take 2)

Spring semester starts tomorrow.

My syllabi and rosters are printed, my lesson plans are set, my work clothes are ready and my bag is packed. A meticulously detailed schedule for completing my book revisions during the semester is open on a Stickie note on desktop, and my January Google calendar is updated with deadlines, reminders, Mother Goose Story time, playgroups, and meetings.

I spent last night making a huge batch of homemade chicken vegetable soup for lunch for my girl, and several dinners’ worth of a roasted vegetables/turkey/GF pasta dish for her, with extra to freeze.

I always start the new semester with such good intentions of getting it all done, of sticking to the very detailed schedule. I know going in it probably won’t happen, but I’m learning to prioritize so that the most important tasks get the best of me.

A few months ago I wrote a post on working, parenting, and chronic illness and promised a follow-up on the more practical aspects of getting it all done. The fact that it took me about three months to do so should tell you I don’t have a ton of credibility in that department right now, but here’s what I’ve been doing when I haven’t been blogging.

For the most basic stuff, let’s start with the fact I make lists—daily, weekly, and monthly. I can’t go to sleep without my to do list for the following day set.

It is really important to me that my daughter eat healthy, whole foods—no junk food, no processed food, no baby food—so I spend a lot of time on the weekends (Saturday or Sunday night, usually) making a bunch of different meals (homemade stock/soups, pastas, risotto, roasted vegetables, stir fry, etc.) I put a lot of them in the freezer so that if we don’t all eat together before her bedtime, or we’re out doing an activity and then we have to squeeze chest PT in right around dinnertime, I always have something healthy and flavorful for her. She adores spicy and sour foods, and her favorite right now is hummus—she loves it so much we’re going to try and make our own next weekend so we can add extra spice to it.

I take advantage of any available work time. For example, her naptime is automatically my work time, seven days a week. (Not housework time, but writing, editing, or evaluating student papers, etc.) She goes to bed around 7:30pm, so typically six nights a week I plan to work at least a few hours between her bedtime and mine.

I am a lot more flexible with my notions of when things should get done. Laundry? I fold it at 11pm, when I’ve closed my laptop and unwind with The Daily Show. If I happen to be home for an extra hour in the morning and know I will be busy late in the day, I’ll throw a bunch of chicken pieces in the oven while I make my morning coffee. (Not appetizing, but I might as well use the time while I have it.)

Like pretty much all of us, I multitask—but I’ve gotten a little better about having more discretion about what things are appropriate for that. Cleaning the kitchen or cooking dinner while returning a phone call is one thing. Trying to conduct an interview while juggling projectile vomit or doing a bottle feed never worked out that well for me.

For better or worse, I have a sort of tunnel vision, particularly during the academic year. I don’t expect free time, and I don’t want to squander any time, either. I usually know I will need to work at least one weekend night, and I am okay with it because it is more stressful for me to have things outstanding than it is to just get it done. This time when she is young won’t last forever, and I don’t want to miss any of it. When the deadlines and the course work and the chest PT and the appointments and the laundry and the scheduled-ness begins to feel like there is never a single moment to just be, I know that the hard stuff is temporary, too.

And well worth it. (What is that famous quote? “I never said it would be easy; I only said it would be worth it?” I’m a fan.)

But there are some things I am going to try to do better this semester. I mentioned wanting to be more presentin more aspects of my life. I am hoping to bring home less work from campus (physically and mentally) by using office hours more productively. I’m going to try going into campus much earlier in the morning to work on the book then, so I meet my revisions deadline. I am going to try and keep my laptop upstairs in my office more, so that when I finish at night I am truly done and whatever I am doing—talking with my husband, watching something on DVR, etc—gets my full attention. Little things, but hopefully things that will make me feel like I have more space to just be.

I know a lot of this is obvious stuff, but somehow putting it down gives me more accountability. What about you? What things do you do to manage working, parenting, and chronic illness? What strategies have helped you be more present, or helped you save time?

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On New Year’s

Happy New Year!

I didn’t write a 2011-in-review post, but I do think my first post of 2012 will cover that anyway.

Just before New Year’s last year, I wrote that 2010 was the year of the baby, and all that entailed.

Looking back, I’d have to say that 2011 was the year of figuring out where to place everything else in my life, since my baby comes first.

I remember writing Bring It, 2011 , so vividly. I was sitting at our breakfast bar late at night, and I could see my reflection in the kitchen window as I hunched over my laptop. I was days away from starting my first full-time semester, though I’d gone back to work on a more flexible schedule a few weeks after she was born. I wrote how my biggest concern was figuring out how to balance it all—a young infant, a job, a book, health needs, family health needs, etc.

I wrote about working and chronic illness, and discussed another huge change in our lives—my husband’s company, The Well Fed Dog.

I savored every morningspent with my giggling, wriggling little baby, who quickly became a a signing, walking, talking, exploring, pointing, dancing, chair-climbing, fork-wielding toddler. No matter what else was going on, how many stresses and anxieties, obligations and expectations the year presented, as long as she was okay, nothing else mattered.

And as the year progressed, and after some successes and some misfires, I came to the conclusion that sometimes, balance isn’t possible and knowing how to prioritize is much more important than that ever-elusive notion of balance.

I’ve come a long way since that night a year ago when I was nervous about making all of this work. When I think about what I want for 2012—for my daughter, for myself, for my family, for the rest of the roles in my life—I want to be as present as possible.

Sure, I have more concrete goals: finish my book revisions by February 1; implement some new strategies in my courses; be more consistent in attending playdates and playgroups with my daughter; getting back to more regular group classes at the gym; keeping in better touch with friends, etc.

But the larger theme that ties all of those smaller threads together is being present. It is something I have done well with my daughter—each day, the time I spend with her is hers, whether we’re playing in her room, at music class, or at a playgroup. No laptop, no television, no scrolling through Facebook updates on my phone. The time with her is precious and hard-fought, and she deserves the best of me.

When I’m in the classroom my students are my focus, and when I read their work, I give it my full attention. I’ve started using the full screen option in the latest Word version, which blacks out my desktop and browser windows and allows me to look only at my words when I’m working on my book.

But now I want to focus on harnessing that in other areas of my life. I find myself doing work while getting my haircut, or glued to my laptop till midnight while my husband sits on the other couch watching “our” shows, answering my phone while sending e-mail, and other things less minor and more ridiculous. All of this is to say, it’s the next natural step in an effort towards the prioritization I wrote about in 2011—if I am going to do something, then I need to focus in on that one thing (or person, or interaction), and be fully present.

(And that means being more present in this blog space, too.)

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On Holiday Wishes

Another edition of the ChronicBabe blog carnival will be out soon, and it’s about holiday wishes when you live with chronic illness. Jenni Prokpy asks, “What are you asking Santa for? What do you wish for the people who care for you? What wishes have already been fulfilled this holiday season?”

Where to start?

In so many ways, I have everything I need and want: I will wake up on Christmas morning with a happy, healthy toddler who greets every day with joy.

But that doesn’t make for much of a blog post, does it?

For people struggling with infertility, which is even more difficult and heartbreaking this time of year, I wish for them a path to building the family they dream of that is as smooth and expedient as possible.

For the babies and families spending the holidays in the NICU, I wish for them that they surpass all the odds they face and are soon able go home, and that they have compassionate caregivers and supportive friends and family until that happens.

For people living with chronic pain, I wish for them relief, physically and emotionally, and substantive distractions if relief is not possible.

For patients living with chronic illness, I wish for them a sense of acceptance that does not mean resignation, and a sense of balance that tends to their bodies and still nourishes their minds.

For the people who love, care for, and often live with people with chronic illness, I wish for them that they truly know how appreciative we are of their efforts, and that they give themselves permission to take a break.

For parents caring of sick children in particular, I wish for them the grit to advocate, the strength to defer when necessary, and (some) solace in knowing that what might hurt right now often helps their children long-term.

For the doctors and researchers working on rare diseases, mine and so many others, I wish for them continued ingenuity, persistence, and necessary funding.

And for my daughter, among so many hopes and wishes, I wish for her that she experiences as much joy from life as she brings into it.

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On Why I Write

Sharon at Bed, Body & Beyond is hosting the next Patients For a Moment blog carnival and asks us to consider why we write.

I’ve posted about writing often here, and how the questions of
public lives versus private lives and storytelling
get more complicated the longer we write.

But since it is such a fundamental part of my life, as well as a fundamental part of my experience as a patient, it’s a question worth exploring further.

First, there’s the obvious. I write because as an author, editor, and an academic who teaches writing, it is my job.

I started writing this blog because I knew there must be other people like me out there, young adults living with chronic illness, and I wanted to find them. I’d always been the sick kid, the sick teenager, the sick twenty-something, and while I knew I might never meet someone with my rare set of diseases in real life, I knew wasn’t alone. And I knew that whether we’d been sick our whole lives or were recently diagnosed, whether our illnesses were life-threatening or life-altering, our individual symptom differences paled in comparison to the universals we struggled with: acceptance, denial, balance, guilt, etc.

I keep writing this blog because as my own journey has evolved from being a single graduate student to becoming a married person, an author, and a mother, I continue to learn and be inspired by those I find on similar paths, facing similar challenges. Careers, infertility, chronic illness, parenthood, patient-hood—the perspectives I encounter on all of this from readers and from other blogs are often invaluable.

I wrote Life Disrupted for similar reasons: I wanted to capture the experience of living with chronic illness as young adults. I am writing my second book because I started asking lots of questions about the evolution of chronic illness in American society that I didn’t know the answers to, and I realized I had to keep digging. (Still digging, but getting close to the end!)

But more simply, I write because it is what I have always done, for as long as I have memories. I write to process, I write to clarify, I write to learn.

As a sick child, I wrote because it was something I could do no matter how bad I felt or how many nights I was in the hospital. I wrote because I loved to read, and books kept me both distracted from illness and connected to something beyond myself. I wrote because I couldn’t always run or play, and I wrote because the voice I discovered in writing gave me an identity beyond that of the sick one. It gave me self-esteem and confidence when my body betrayed me over and over. I don’t know that I’d have gone to Georgetown, or interned at Washingtonpost.com, or done a lot of the things being a teenage and college-aged writer allowed me to do had writing not already been such an integral part of my self-concept.

I have no doubt I’d still be a writer even I hadn’t spent my whole life as a patient. It’s the way I make sense of my world, it is my instinct at every turn. But I wouldn’t have needed writing the way I did so often through the years, and I don’t know that I would appreciate its ability to build community and connect people the way I do. Writing is an extricable part of my personal life, but I’m fortunate that having a career based on writing isn’t just good for my spirit. Writing allows me to have a successful professional life despite my health issues, and though I didn’t consciously set out on this path for those reasons all those years ago, I am grateful to be here.

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On Gratitude

Two years ago, I wrote about being grateful for the knowledge that comes with a celiac diagnosis, and more than that, for the simple gift of being present at Thanksgiving, instead of being in the hospital.

Last year, I wrote about being grateful for the amazing blessing of my newborn baby girl, and for all the dedicated health care professionals, advanced technology, and support that allowed both of us to make it. I also wrote about how complicated an emotion gratitude can be when to comes to serious illness.

Here we are, twelve months later.

Motherhood. In the best way possible, it throws all the pieces of you up in the air and when they settle back down to the ground, they are forever rearranged. Family illness, work, writing a Book, (and yes, that’s a capital “B” in my head)—in ways less luminous and more wearying, they also throw up the pieces of me, the pieces that make up us, and reconfigure them all.

And here I am, a year since my last gratitude post, a year removed from the immediacy of birth and the physicality of newborn-hood. A year removed from the decision to re-structure the whole book, and now some 85,000 words in a new direction. A year and six classes and multiple committees removed from the end of maternity leave. A year of negotiations and boundaries and compromises that accompany being a mother and a daughter, a patient and a caregiver.

Amid so many changes, I am at extremes (as usual).

I find myself grateful for the smaller details, noticing them in more vivid technicolor than the pale backdrop of daily life: a chuckle over the monitor; an unsolicited hug. An unexpectedly light commute that means I am home earlier to play; unseasonably warm weather that means one more day at the playground. Putting on my headphones and squeezing in some revision hours; finishing the very last paper of a deluge. Making time to try a new recipe; eating dinner in the dining room together because that makes a Wednesday night something better than. The magic of a Thursday night, when the meat of the week is behind me. Coffee with a friend. A clean house.

And the much bigger stuff: To witness my husband take a risk and follow his dream, so that when he tells our daughter to do that some day, it will not ring hollow. To able to work on a book that explores questions I didn’t know the answers to, because really what more can a nonfiction writer ask for?

And the biggest thing of all, the thing that is immeasurable, the thing that still makes me catch my breath in the grocery store aisle and smile to myself when I think of a certain smile: grateful to be somebody’s mother, grateful to be her mother.

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On Inspiration

Aviva at Sick Momma is hosting the next edition of Patients For a Moment. In her prompt, she asks,

“So what do you do to get yourself out of the doldrums when you fall into a funk? What (or who) inspires you and gives you hope? Where have you found inspiration when you weren’t even looking for it? How do you keep on keeping on when your pain is high and your fatigue is even higher?”

When I try to think of the big picture concepts here, I get a little bogged down. There are so many things I could say, and I end up staring at a blank screen, precious moments of time slipping away. More just write, already and less perseverating, shall we?

Honestly, I’m just not in the right zone to write specifically about illness right now. I’m in a tunnel of baby-deadlines-more deadlines-caffeine and focused on getting through the day, and getting enough done that I can get to sleep. Like it or not, good for me or not, there isn’t a lot of mental space left to think about or process anything related to illness, even when its immediacy and urgency wakes me up at 3am.

So, I thought about the stories and thoughts that have inspired me this week, the things that make me stop and pause as a writer, a professor, a mother, a citizen, and, yes, a patient, too. I’m not in the doldrums of illness, but I am definitely in a place where a few good reminders about perspective, trust, curiosity, and discovery are nourishing.

–Have you read the eulogy for Steve Jobs written by his sister? It’s a rich, personable portrait of a man whose vision is a force in many our lives, and it’s also a beautiful look at love, creativity, and passion. His last words were, “Oh wow. Oh wow. Oh wow.” Pretty powerful.

–As the owner of two rescue dogs with sad pasts, I am always moved by stories of redemption and hope. I cam across this emotional article about abuse, trauma, trust, and resiliency for both a dog and her owner. While the animal’s abuse haunts me, the way both have been able to re-build their lives and trust unconditionally are truly inspirational to me. Living in the moment and letting go of pain, frustration, anger, and doubt are never easy, but this really brings to light what is possible when we do.

–I have always felt pretty fortunate to teach the classes I do (writing in the health sciences). My students have been and are passionate about their future careers as health care providers, are they are intellectually curious and engaged, and as a professor and a patient, they me feel just that much more hopeful about the future. Patients would be lucky to have some of these students as their doctors, nurses, pharmacists, and PTs. Every semester, reading their research papers and seeing the inspired issues they delve into makes me appreciate this more.

–Watching this little girl of mine grow from a baby into a walking-talking-signing-laughing-teasing-bike-riding toddler is, quite simply, amazing. No matter what else is going on in my day, in my body, in the world in general, watching her develop, experience new things, and approach life with an independent, open spirit is the essence of inspiring. Every day is a new opportunity to learn, to grow, and to build on what was already there, and that’s a lesson that helps everyone, I think.

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On Priorities

So I’m now a year into this whole balancing motherhood-working-illness thing. I originally planned to write this post, the first in a two-part series, three weeks ago, and yet here I am. There’s a lesson there for anyone tempted enough to write about balance:

It doesn’t really exist.

Reflecting on the whole baby/book/job/illnesses/family illness/new business scenario—and while my particular brand of hectic may differ from yours, the point is, we’re all managing a lot of moving parts—I think it’s more accurate to say that striving to prioritize is much more useful than striving for balance. Something will always have to give, and the real lesson is learning how to be okay with that.

My daughter, my family unit, come first. Whatever else I have going on immediately fall into place behind her needs and what is best for her and by extension, what is best for our family. That priority is at the heart of the
constant negotiations
that come with a non-traditional full-time work situation (part on campus, part from home). The amount of time I spend with her every day and the flexibility I have to do things with her make up for the challenges involved in squeezing a lot of that work in late at night, early in the morning, and on weekends—without hesitation.

It is worth it, it is indescribably worth it; it is just not easy.

But it’s not supposed to be.

It is easy to prioritize when things operate as we assume they will, when we can plan out our schedule and depend on our productivity. Parenting and chronic illness do not subscribe to predictability.

The really rough patches, the weeks where nothing goes according to plan and illness throws everything out of whack, have been the most illuminating. Times when I am sick and Baby Girl is sick and she needs to go the doctor and I need to go to the doctor and students papers are piling up as quickly as the laundry is and the book revisions are haunting me, when I am worried about her and rocking her and cursing my own stupid infections for making me cough just when her little eyes closed and I startle her awake, are when I have the most clarity:

There will always be papers, and they will eventually get graded. The revisions will get done, just like somehow, some way, the draft got done. The extended family obligations and illness obligations will settle out. The laundry and the dishes and the editing and the phone calls will all get done. The most important thing I can do, that I will ever do, is be there in this moment, physically and mentally. I kiss her damp forehead and whisper in her ear that there is nowhere else I’d rather be.

I have dropped a lot of balls this year. I have missed deadlines (and quite epically, too), I have canceled plans and forgotten tasks. I’ve made promises I haven’t always been able to keep, I’ve disappointed people who have wanted more from me than I physically give. I’ve climbed the stairs at 11pm with coffee in hand, ready to pull a long night in front of the computer, and I’ve put hot coffee in the refrigerator and creamer in the microwave. At points I’ve moved so far from any sort of balance that it is laughable.

But I’ve learned to be okay with that, because I think that my current lack of balance means I am prioritizing as I should. Right now, what matters most (baby and husband, family, students, book, my health) depends on me knowing when to pull back from everything else: when to say no, when to put up boundaries, and when to say all I can do is my best and really believe that is good enough.

A long time ago I saw this quote on Penelope Trunk’s blog: One thing at a time. Most important thing first. Start now. I may have even blogged about that line before. Honestly, I repeat it to myself often, and I find that it’s knowing how to judge what are the most important things and letting go of the white noise that is the key.

While a lot has slipped through the cracks, what I’ve gotten in exchange is incomparable.

(And because I want this writing to be more of a priority again, I am holding myself accountable: next up, the second piece in this series about all the pragmatic stuff that helps keep life in motion. A happy baby who sleeps great, an extremely hands-on husband, and a whole group of people who love this child, support this book, and care about my family? That helps!)

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On Priorities (and balance)

So I’m now a year into this whole balancing motherhood-working-illness thing. I originally planned to write this post, the first in a two-part series, three weeks ago, and yet here I am. There’s a lesson there for anyone tempted enough to write about balance:

It doesn’t really exist.

Reflecting on the whole baby/book/job/illnesses/family illness/new business scenario—and while my particular brand of hectic may differ from yours, the point is, we’re all managing a lot of moving parts—I think it’s more accurate to say that striving to prioritize is much more useful than striving for balance. Something will always have to give, and the real lesson is learning how to be okay with that.

My daughter, my family unit, come first. Whatever else I have going on immediately fall into place behind her needs and what is best for her and by extension, what is best for our family. That priority is at the heart of the
constant negotiations
that come a non-traditional full-time work situation (part on campus, part from home). The amount of time I spend with her every day and the flexibility I have to do things with her make up for the challenges involved in squeezing a lot of that work in late at night, early in the morning, and on weekends—without hesitation.

It is worth it, it is indescribably worth it; it is just not easy. But it’s not supposed to be, and I had no expectation that it would be.

It is easy to prioritize when things operate as we assume they will, when we can plan out our schedule and depend on our productivity. Parenting and illness do not subscribe to predictability. The really rough patches, the weeks where nothing goes according to plan and illness throws everything out of whack, have been the most illuminating. Times I am sick and Baby Girl is sick and she needs to go the doctor and I need to go to the doctor and students papers are piling up as quickly as the laundry is and the book revisions are haunting me, when I am worried about her and rocking her and cursing my own stupid infections for making me cough just when her little eyes closed and I startle her awake, are when I have the most clarity:

There will always be papers, and they will eventually get graded. The revisions will get done, just like somehow, some way, the draft got done. The family obligations and illness obligations will settle out. The laundry and the dishes and the editing and the phone calls will all get done. The most important thing I can do, that I will ever do, is be there in this moment, physically and mentally. I kiss her damp forehead and whisper in her ear that there is nowhere else I’d rather be.

I have dropped a lot of balls this year. I have missed deadlines (and quite epically, too), I have canceled plans and forgotten tasks. I’ve made promises I haven’t always been able to keep, I’ve disappointed people who have wanted more from me than I physically give. I’ve climbed the stairs at 11pm with coffee in hand, ready to pull a long night in front of the computer, and I’ve put hot coffee in the refrigerator and creamer in the microwave. At points I’ve moved so far from any sort of balance that it is laughable.

But I’ve learned to be okay with that, because I think that my current lack of balance means I am prioritizing as I should. Right now, what matters most (baby and husband, family, students, book, and oh yeah, my health) depends on me knowing when to pull back from everything else: when to say no, when to put up boundaries, and when to say all I can do is my best and really believe that is good enough.

A long time ago I saw this quote on Penelope Trunk’s blog: One thing at a time. Most important thing first. Start now.I may have even blogged about that line here before. Honestly, I repeat it to myself often, and I find that it’s knowing how to judge what are the most important things and letting go of the white noise that is the key.

While a lot has slipped through the cracks, what I’ve gotten in exchange is incomparable.

(Because I want this space to be more of a priority again, I am holding myself accountable: next up, the second piece in this series about all the pragmatic stuff that helps keep life in motion. A happy baby who sleeps great, an extremely hands-on husband, and a whole group of people who love this child, support this book, and care about my family? That helps!)

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Baby Talk

I joke that our daughter needs an intervention. Really, the child is obsessed with Baby Signing Time.

Haven’t heard of these DVDs of the oh-so-grating musical score? I hadn’t either, until a few mothers whose blogs I read started raving about them. I know some parents in real life who taught their babies sign language, and I’d read a few articles that talked about its benefits for babies, but I didn’t take really take the plunge with Baby Signing Time until Baby Girl was about 10 months old.

Now, we have a baby who will point at the TV and sign “please,” and if we don’t put it on, she points to the remote as if to say, “Listen, all you need to do turn it on. I’ll take it from here.” Sometimes, I swear she hardly blinks she is so intent on watching. It’s hilarious, but also? It’s a bit much, and from what I’ve read on other blogs, the obsession is fairly universal among the baby set.

To backtrack a bit, we did teach her a couple of the most basic signs at about 6 months—“more,” “all done,” and “cup,” and she caught on pretty quickly. Her sitter knows a ton of signs, and has been great about reinforcing them. But then she started saying a word or two, and then a few more, and our rudimentary signing slipped to the wayside because we were so caught up in hearing her words. And we got a bit lazy about it.

At around 8 months, it really hit me how much of the world she was absorbing, how much babies in general absorb, and just how much was going on in that little mind of hers—she recognized colors, could find hidden toys when asked, etc. Though she was saying a handful of words, I really wanted to find the right way to tap into what else she understood.

“We just need to ask her the right questions,” I said to my pediatrician, marveling at how amazing the experience of watching a little human emerge really is. Perhaps signing was one way for us to do that?

I hesitated at first, not because I wasn’t sure about signing but because I wasn’t wild about the thought of her watching a DVD (yes, we’ve read the American Academy of Pediatrics’ guidelines on infants and television, and we don’t disagree.) But the DVDs are short, and one of us sits and watches and signs along with her, so it’s an interactive thing. (And this explains why I currently have “One shoe, two shoes,” on repeat in my head right now.)

Between what we’ve learned from signing along with her and all the signs her sitter knows and uses, in the past month or so she has really become versatile with her signing. We didn’t realize how much of it translated until she moved past signing things on request. Last week, we said our dogs’ names in passing and she signed “dog.” She will now sign “please” and then indicate what she’s asking for, instead of needing us to ask her to say please after she’s pointed at something. It’s so neat to see her use signs in the appropriate context.

Someone asked me if I was worried signing would stunt her vocabulary development, which is a reasonable question. I’m not, since she says a lot, and since she hears the terms for so many things over and over when she learns the signs for them. In fact, from what I’ve read, signing can enhance vocabulary.

But from a purely day to day perspective, it makes communicating so much easier. She has a way to express the things she can’t yet say, and it’s a blast having meaningful interaction with her where we know she knows what we’re asking. It wasn’t something I set out to do when she was born, but I am happy we stumbled into it. If nothing else, it’s made me really stop and appreciate just how cool it is to witness a baby growing up and learning about his or her world.

Have any of you out there tried signing with your kids? Do you have any insights for those who may have heard about teaching babies to sign but aren’t sure it’s for them?

(And yes, I know this is a chronic illness blog. Stay tuned for some posts of that persuasion soon!)

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