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	<title>Maternal Dementia</title>
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	<description>Thoughts from what&#039;s left of my brain</description>
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		<title>Driving Lessons</title>
		<link>http://maternal-dementia.com/2018/07/30/driving-lessons/</link>
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		<pubDate>Mon, 30 Jul 2018 15:26:32 +0000</pubDate>
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					<description><![CDATA[The tutorial Buddy-roo was receiving seemed to last forever. I wanted to go back to reading – I was in one of those books so nourishing you hate to put it down but you discipline yourself to do so anyway because you want it to last – but I waited because I wanted to witness her departure.  Symbolic, somehow, that first moment that portends her inevitable independence.  Brake lights.  Ignition.  Slowly the car slipped forward, on to the road.  She got the clutch right the first time.  Then I heard the switch to 2nd gear.  Nice, Buddy-roo.  Drive away.]]></description>
										<content:encoded><![CDATA[<p>They walked toward the car, the two of them, long-legged.  <a href="http://maternal-dementia.com/the-cast/#Buddy-roo">Buddy-roo</a> opened the door to the driver’s side of the car, <a href="http://maternal-dementia.com/the-cast/">De-facto</a>, the passenger’s.   I didn’t move from my chair in the sun, relishing the state of leisure I only experience here at the <a href="http://maternal-dementia.com/2011/04/22/country-rhythm/">country house</a>.  I looked up from my book to watch them.  The engine started.  Then turned off.  Brake light on.  Off again. He must have been talking her through all the dials on the dashboard, the steps of starting a car.  Testing the clutch.  The brakes.  I’m glad she will learn to drive with a standard.  There is a joy to driving a manual shift, controlling the gears, racing the car at your pace, something unknown to a generation of drivers taught on automatics, let alone self-driving cars.  Will my children’s children never need to drive themselves?  Will my children have children?  Will I ever see them at the wheel of a car, if there even is a wheel anymore?<br />
<a href="http://maternal-dementia.com/2018/07/30/driving-lessons/drive_away_3/" rel="attachment wp-att-21677"><img fetchpriority="high" decoding="async" src="http://maternal-dementia.com/wp-content/uploads/2018/07/drive_away_3.png" alt="drive_away_3" width="201" height="267" class="alignright size-medium wp-image-21677" /></a></p>
<p>The tutorial Buddy-roo was receiving seemed to last forever. I wanted to go back to reading – I was in one of those books so nourishing you hate to put it down but you discipline yourself to do so anyway because you want it to last – but I waited because I wanted to witness her departure.  Symbolic, somehow, that first moment that portends her inevitable independence.  Brake lights.  Ignition.  Slowly the car slipped forward, on to the road.  She got the clutch right the first time.  Then I heard the switch to 2nd gear.  Nice, Buddy-roo.  Drive away.</p>
<p>They are full-blown teenagers.  Buddy-roo is fourteen.  <a href="http://maternal-dementia.com/the-cast/#Short-pants">Short-pants</a> just turned seventeen last week.  It was my 15th <a href="http://maternal-dementia.com/2010/07/03/fiesta/">fiesta</a>, and I dutifully left Pamplona on the day before her birthday, as I do every year, to celebrate it with her.  Once it pained me to leave my drunken friends before the massive party was finished – they had two more days of delirium.  Lately, I’m ready to shed my whites and leave the boom-boom-boom, to <a href="http://maternal-dementia.com/2009/07/16/red-right-return/">return</a> to the family, and to the country house, and to the rhythms of our every July.</p>
<p>They aren’t as rotten as we suspected, our teenage girls. When they were little, when I started writing this blog, De-facto and I would whisper across our pillows about how sweet and adorable they were, and how before you know it they’d be rotten teenagers.    </p>
<p><em>Before you know it</em> – starts the mantra of parental advice we’ve heard from everyone.  When they were babies people would tell us to enjoy them while we could, <em>before you know it</em> they’ll grow up.  When they were toddlers, unsolicited counsel from anyone and everyone: Enjoy it, <em>before you know it</em> they’ll be all grown up. Just last month, learning that Short-pants is taking SATs, a friend asked if I was ready for her to go away to college. &#8220;<em>Before you know it</em>, you&#8217;ll have an empty nest.&#8221;</p>
<p>But I am not afraid of this dreaded empty nest. I&#8217;m more curious about what happens to them when they grow up and go away.  Of course I will miss them, their affection, their laughter, their company.  But there will be so many things I will get to do again.  I look forward to fewer interruptions. My work these days takes me to interesting and exotic places, from which I am always compelled to return quickly.  When I am gone for more than two weeks, something shifts in the household.  It’s too long for a mother to be gone. They need some point of contact with me. It’s the same when De-Facto is on a trip that lasts longer than a fortnight. They get restless, short-fused. <a href="http://maternal-dementia.com/2018/07/30/driving-lessons/gaudi_window/" rel="attachment wp-att-21684"><img decoding="async" src="http://maternal-dementia.com/wp-content/uploads/2018/07/gaudi_window.jpg" alt="gaudi_window" width="202" height="268" class="alignleft size-full wp-image-21684" /></a> Not to mention being the only parent for too long takes its toll.  It is much nicer to share the responsibilities. You know, you can say things like, “ask your father.” </p>
<p>I realize, too, that blogging through their childhood – until recently at least – kept me very present.  I noticed things about them, paid attention to capture detail.  I wrote down the things they said and did, recorded their everyday stories.  Their childhoods have not passed too quickly.  I’ve slowed them down by observing, living it twice by writing it down.</p>
<p>These days it’s so very interesting, what they talk about, what they’re discovering,  who they’re becoming.  One daughter stays close, stands at the foot of the bed, lingering, silently soliciting more contact.  We play cards, words games. We read books side-by-side. We read a book together, taking turns reading aloud to each other.  She has a few friends, but cares to see them only at school.  She’s a homebody, preferring to pass her time at home with her father and me.  Or alone in her room, reading or listening to science podcasts.</p>
<p>The other daughter craves our attention no less, but on her own terms.  She wants us to seek her out, to do what she loves to do.  To talk about Minecraft, or her favorite YouTubers, or the obsessive crush she has on a K-pop star.  I’m glad that she wants to tell me about all of it, careful to be authentic in my appreciation.  I remember, when I was a teenager, the sharp edge of a patronizing adult. That <em>you-kids-these-days</em> chuckle in response to something that was important to me. The things that she is interested in are important, to her, and the only way I will keep her trust, keep her talking to me about the other things that will become important to her, and to me, is to keep listening, and listening with interest. Though sometimes that is hard to do.  </p>
<p>The day I turned sixteen I went to the DMV to take my written test to get a learner’s permit.  My sister took me out for my first drive, and like my girls I started on back roads in the country, less traveled.  I wove back and forth across the center line, unfamiliar with the touch of the steering wheel.  That summer I took a Driver’s Ed class.  The teacher, an amiable man who grunted more than he spoke, guided me through to my driving test.  Once I had my license I’d drive whenever I could.  If my mother ran out of milk, I’d offer to drive to the store to get more, taking the longer route, making a swing <a href="http://maternal-dementia.com/2018/07/30/driving-lessons/driving_around/" rel="attachment wp-att-21687"><img decoding="async" src="http://maternal-dementia.com/wp-content/uploads/2018/07/driving_around.jpg" alt="driving_around" width="267" height="201" class="alignright size-full wp-image-21687" /></a>around the extra blocks of our small town, looking for friends, or for that guy I wasn’t supposed to like – he was always in his car, it seemed.  He’d pass and dip his head, a sultry greeting.</p>
<p>Driving meant I could go someplace alone, un-chaperoned, un-tethered.  It was one step toward being my own person with my own life. In the summer, especially, I remember sliding into the car, the vinyl seats hot from the sun burning my thighs, bare because my cut-offs were way too short.  I’d crank up the radio, singing along to Thin Lizzy’s <a href="https://www.youtube.com/watch?v=SGZqDzb__bw">Boys are Back in Town</a>, cruise down the steep curvy hill from my house to the lake road, slowing to the speed limit on the stretch of road into town – speed trap, my father had warned me.  I&#8217;d pick up my girlfriends, and then we’d simply drive around. In circles. Four or five girls in the car. We’d stop at a park for a while, sit on the picnic tables. Then drive some more.  Stop at the pizza joint on the corner. Drive some more. Pass people we knew. Tell stories. Even in the safe circles that knotted us around the 10 blocks of our downtown, we were on our own. We were out. Without parents and older siblings. We were free.</p>
<p>Later, it was Short-pants&#8217; turn to take the wheel.  She is older, more practiced &#8211; De-facto started teaching her to drive last summer &#8211; but more cautious. She needs less explanation to start. Brake lights. The car starts.  The car idles. She revs the engine, too hard, lurches forward. Stalls. Starts again.  Idles. Try again, Short-pants. The car glides forward. No lurching this time, just a smooth departure down the lane.  I hear her shift into 2nd, as she pulls out of sight. They’ll drive a kilometer or so and he’ll make her stop.  Use reverse, bring the car around.  Every day a bit more confidence.   There are (mandatory in Europe) <a href="http://maternal-dementia.com/2018/07/30/driving-lessons/girl_with_glee/" rel="attachment wp-att-21689"><img loading="lazy" decoding="async" src="http://maternal-dementia.com/wp-content/uploads/2018/07/girl_with_glee.jpg" alt="girl_with_glee" width="203" height="267" class="alignleft size-full wp-image-21689" /></a> driving classes ahead and tests to pass, but <em>before you know it</em>, she’ll be driving on her own, and driving away.  And Buddy-roo won’t be far behind her.</p>
<p>And me, well, I’ll stand at the side of the road and wave. I will miss them both. But I&#8217;ll wish for them the freedom to stretch beyond the borders of our family, to carve out, for themselves, the next steps of their lives.  I&#8217;ll wish for them all the freedom they need. And then, maybe, I’ll get mine, too.</p>
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		<title>Explaining the Loss</title>
		<link>http://maternal-dementia.com/2016/11/14/explaining-the-loss/</link>
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		<pubDate>Mon, 14 Nov 2016 07:48:13 +0000</pubDate>
				<guid isPermaLink="false">http://maternal-dementia.com/?p=21613</guid>

					<description><![CDATA[She was hunched over her computer, sitting cross-legged on the floor when I pushed open the heavy door to Short-pants&#8216; bedroom. Fully dressed, ready for school, her purse already draped over her shoulder as though she might need to jump up and sprint out the door at a moment&#8217;s notice, her head moved back and [&#8230;]]]></description>
										<content:encoded><![CDATA[<p>She was hunched over her computer, sitting cross-legged on the floor when I pushed open the heavy door to <a href="http://maternal-dementia.com/the-cast/#Short-pants">Short-pants</a>&#8216; bedroom.  Fully dressed, ready for school, her purse already draped over her shoulder as though she might need to jump up and sprint out the door at a moment&#8217;s notice, her head moved back and forth as she read from her screen.</p>
<p>&#8220;He&#8217;s <em>winning</em>,&#8221; she said, &#8220;how can he be ahead?&#8221;</p>
<p><a href="http://maternal-dementia.com/the-cast/">De-facto</a> sat on her bed, his hand on her shoulder. I crouched behind her and wrapped my arms around her so I could whisper the news I&#8217;d come to tell her.</p>
<p>&#8220;It looks like he&#8217;s going to win.&#8221;  </p>
<p>The reality of that &#8211; the thing we all thought was impossible &#8211; hung in the air over us. It was 6:45 am, the CNN commentators &#8211; we&#8217;d been up all night with them &#8211; were scrutinizing the counties of Michigan and Wisconsin, and though the race had not yet been called in Mr. Trump&#8217;s favor, the data did not look good.<a href="http://maternal-dementia.com/2016/11/14/explaining-the-loss/broken_ideas/" rel="attachment wp-att-21633"><img loading="lazy" decoding="async" src="http://maternal-dementia.com/wp-content/uploads/2016/11/broken_ideas.jpg" alt="broken_ideas" width="255" height="200" class="alignright size-full wp-image-21633" /></a></p>
<p>Short-pants bent over her screen, her shoulders heaving, letting out her signature moan, a forlorn wail of grief and disappointment.  </p>
<p>&#8220;But, what about women&#8217;s rights? And minorities? The environment? The Supreme Court?&#8221;</p>
<p>I didn&#8217;t have an answer.  I myself was numb with disbelief at how the red and blue graph lines had criss-crossed and grown in opposite directions, a possibility that <a href="http://fivethirtyeight.com/" target="_blank">Nate Silver</a> never ruled out but that I hoped was an impossibility. Even over the weekend, when the polls had tightened, I just couldn&#8217;t believe that it could happen.  Not in my America.  We wouldn&#8217;t elect an impulsive, vulgar bully to the highest office in the land, would we?</p>
<p>Absent any authentic words to re-assure her, I simply rubbed her back and kissed the crown of her head. </p>
<p>She began to sob.</p>
<p>When I pushed myself up from the floor and pattered across the hall into <a href="http://maternal-dementia.com/the-cast/#Buddy-roo">Buddy-roo</a>&#8216;s room, it was still dark, just a hint of dawn&#8217;s early light squeezing through the shutters of her window.  She lay motionless in bed; I crawled in to spoon behind her.  </p>
<p>&#8220;What happened?&#8221; she mumbled, half asleep.  </p>
<p>I didn&#8217;t answer right away, I wanted to take in the peace of the morning cuddle for an extra beat before spoiling her day.  </p>
<p>&#8220;Hillary?&#8221; she said. </p>
<p>&#8220;I&#8217;m afraid Trump has pulled ahead, and will probably be the president.&#8221;</p>
<p>She&#8217;s a lazy riser, Buddy-roo. It takes several nudges, hugs, shoulder rubs and calls-up-the-stairway to be sure she gets out of bed every morning. This time, though, she jerked around and threw off her comforter. </p>
<p>&#8220;You&#8217;re joking, right?&#8221;</p>
<p>I shook my head to answer. She turned back and buried her head in her pillow.  </p>
<p>~  ~  ~</p>
<p>The girls took an active interest in the election over the course of the summer.  It was hard not to, the media circus that was our election spilled over into Europe.  Plus we spent nearly a month in the United States in August, news about the Clinton-Trump <a href="http://maternal-dementia.com/2016/11/14/explaining-the-loss/red_white_striped/" rel="attachment wp-att-21631"><img loading="lazy" decoding="async" src="http://maternal-dementia.com/wp-content/uploads/2016/11/red_white_striped.jpg" alt="red_white_striped" width="200" height="267" class="alignright size-full wp-image-21631" /></a>race was inescapable.  These last weeks I was fairly addicted to my various news feeds; by osmosis they had to pick it up on their radar.  </p>
<p>De-facto and I lean left, and as long as we&#8217;ve known each other (20 years now) we&#8217;ve favored the same candidates. Still, we try our best to inform our daughters about politics without indoctrinating them.  I know it&#8217;s impossible for any parent to hide their bias, and perhaps it is a parental right to pass on  political values. But I&#8217;ve felt it was important to try to set an example: to speak respectfully, not to be vulgar, dismissive or to demonize the other party&#8217;s candidate. That was much harder to do this time around, I&#8217;m sure I couldn&#8217;t mask my truest fears about Mr. Trump&#8217;s character, which from where I sit, was hard to paint in any kind of neutral light. Still, days before the election when Buddy-roo stated emphatically that she <em>hated</em> Trump, I corrected her.  She could dislike his ideas but hating him, personally, was not the answer. I suspect my attempt wasn&#8217;t very authentic, it was hard to hide my disgust given how he insulted women, minorities, veterans, and the disabled. His cavalier discourse brought out the worst in all of us &#8211; on <em>both</em> sides of the ballot. </p>
<p>~ ~ ~</p>
<p>I really want to be a good loser, to take the long view. I want to <a href="https://www.washingtonpost.com/news/monkey-cage/wp/2016/11/11/hate-trump-if-you-want-but-hume-says-that-democracy-requires-respecting-the-winners-legitimacy/" target="_blank">respect the democratic process</a>.  I&#8217;ve been reading about the <a href="http://www.npr.org/2016/11/10/501505527/trump-is-another-republican-striking-a-blow-for-the-way-things-used-to-be" target="_blank">pendulum swings</a> of politics, how it&#8217;s <a href="http://waitbutwhy.com/2016/11/its-going-to-be-okay.html" target="_blank">going to be okay</a>. (Or <a href="http://waitbutwhy.com/2016/11/its-going-to-be-okay-follow-up.html" target="_blank">maybe it&#8217;s not</a> all that okay.)  I&#8217;ve even been willing to explore how Trump could be <a href="http://www.nytimes.com/interactive/projects/cp/opinion/election-night-2016" target="_blank">a good president</a> after all.  I&#8217;ve tried to take solace from conciliatory posts <a href="https://medium.com/@missjenny/to-my-friends-and-family-who-voted-for-trump-fb89e4d37873#.qdiktquwf" target="_blank">asking for respect</a> between sides. Though it&#8217;s hard to imagine this when a scan of the nation&#8217;s <a href="http://graphics.wsj.com/blue-feed-red-feed/" target="_blank">Facebook feeds</a> shows how polarized we are.  I&#8217;m incensed by the images of <a href="https://twitter.com/i/moments/796417517157830656" target="_blank">racists emboldened</a> by Trump&#8217;s election. And just as angry when <a href="http://edition.cnn.com/2016/11/11/politics/trump-supporters-react-street-protests/" target="_blank">anti-Trump protestors have turned violent</a>, too.  </p>
<p>The meme that tires me out the most is the one about being sore losers. It&#8217;s so much more than that.  It&#8217;s fear. If Romney had beaten Obama four years ago, I&#8217;d have been discouraged and concerned, but I wouldn&#8217;t have been <em>frightened</em>. I was angry about many of the actions of the Bush administration, but I wasn&#8217;t <em>afraid</em> of him.  I am scared of what will happen to the rule of law in our country with Mr. Trump as president. I can&#8217;t even fathom what this administration will be like to anyone who disagrees with him.</p>
<p>To be blunt, I&#8217;m lost. I&#8217;ve written before about how <a href="http://maternal-dementia.com/2010/09/22/in-between/" target="_blank">I like being other</a>, living between cultures, understanding the codes but at the same time, escaping them.  What I know, now, is that I no longer understand the codes of my home country. I don&#8217;t know how to explain to my daughters, who still identify as <a href="http://maternal-dementia.com/2016/11/14/explaining-the-loss/ask_yourself/" rel="attachment wp-att-21640"><img loading="lazy" decoding="async" src="http://maternal-dementia.com/wp-content/uploads/2016/11/ask_yourself.jpg" alt="ask_yourself" width="200" height="265" class="alignleft size-full wp-image-21640" /></a>American despite never living there, when they ask what this means to their future.  Even if they never set foot in the states again, they worry about the ripple effect, around the world, of a Trump presidency. </p>
<p>My daughters are worried and afraid. I am worried and afraid.  And when they ask me how a man like that could be president of the United States, I have no answer.</p>
<p>How to explain that the party I identify with, a party that I truly believed was trying to do good things for our country and for the world, <a href="https://theintercept.com/2016/11/09/democrats-trump-and-the-ongoing-dangerous-refusal-to-learn-the-lesson-of-brexit/" target="_blank">misunderstood or ignored</a> the suffering and disgruntlement of the large portion of Americans who voted for Trump, or didn&#8217;t vote at all? How discouraging that so many people felt so <a href="https://hbr.org/2016/11/what-so-many-people-dont-get-about-the-u-s-working-class" target="_blank">abandoned and ignored</a> that Trump was the candidate they chose. For their sake, I hope they haven&#8217;t been conned.  Women, minorities, gays, lesbians, non-Christians &#8211; and our environment &#8211; are all going to pay the price for this decision. If rural, red America ends up getting shafted by Mr. Trump, too, if his promises to <a href="https://www.washingtonpost.com/blogs/right-turn/wp/2016/11/14/drain-the-swamp/" target="_blank">drain the swamp</a> of elite lobbyists and cronies turns out to be campaign-speak and nothing more, we will have given up all our progress for absolutely nothing.  But maybe that&#8217;s what it will take &#8211; being in the same boat of suffering and misery &#8211; to get America to work together again.  </p>
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		<title>The Joyride</title>
		<link>http://maternal-dementia.com/2016/07/18/the-joyride/</link>
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		<pubDate>Mon, 18 Jul 2016 21:15:58 +0000</pubDate>
				<guid isPermaLink="false">http://maternal-dementia.com/?p=21589</guid>

					<description><![CDATA[I sliced peaches into a bowl of vanilla ice-cream while Buddy-roo scrolled through the options in my computer’s movie folder. It had been an ideal summer day at the country house: bike rides down the lane with Winston running joyously beside us, a little bit of yard work, trimming grapes and pulling ivy off the [&#8230;]]]></description>
										<content:encoded><![CDATA[<p>I sliced peaches into a bowl of vanilla ice-cream while <a href="http://maternal-dementia.com/the-cast/#Buddy-roo">Buddy-roo</a> scrolled through the options in my computer’s movie folder.  It had been an ideal summer day at the <a href="http://maternal-dementia.com/2011/04/22/country-rhythm/">country house</a>: bike rides down the lane with Winston running joyously beside us, a little bit of yard work, trimming grapes and pulling ivy off the walls of the stone house, <a href="http://maternal-dementia.com/the-cast/">De-facto</a> making progress on a construction project in the <em>bergerie</em>.  A late afternoon trip to the lake with sailing and swimming, followed by an <em>apéro</em> on the back terrace, then burgers and chicken from the grill with a chilled pale rosé. As soon as the sun set – and it sets late at this time of the year – we’d planned to gather around my computer to watch a movie. Buddy-roo, our media-kid, had been begging for one all day, and was sustained through the outdoorsy activity only by the promise of a movie after sunset.  It was between <em>Guardians of the Galaxy</em> and <em>Malificent</em>, in her mind.  I was lobbying for <em>The Way Way Back</em>, when I heard De-facto shouting from outside.  I ran out to see him doubled over, just down the road. He motioned to me, urgently.</p>
<p>&#8220;Winston’s dead.”  His voice strained.  &#8220;A car. He ran into the road.  Wouldn’t come when I called.”  His chest was heaving, his face anguished.  I held his hands; they were shaking.<br />
<a href="http://maternal-dementia.com/2016/07/18/the-joyride/black_heart/" rel="attachment wp-att-21594"><img loading="lazy" decoding="async" src="http://maternal-dementia.com/wp-content/uploads/2016/07/black_heart.jpg" alt="black_heart" width="200" height="267" class="alignright size-full wp-image-21594" /></a><br />
&#8220;I heard the sound. When he was hit.  It was awful.&#8221;  </p>
<p>“But where is he?”  I needed to see Winston, lifeless, to believe it.</p>
<p>That was the worst – or the weirdest – part.  De-facto couldn’t find the dog. They’d been at the edge of a track road that runs into a main road behind our house, a road on which cars speed by.   Winston can be cheeky, but he usually minds us when call him to head back home.  This time he’d dashed into the road and stood there, his head was probably extended upwards sniffing at something in the air.  De-facto heard the car coming and yelled to Winston to get out of the road.  Though he didn’t see it happen – the tall field grass was in the way – De-facto heard clearly the sound of car meeting dog.  He’d cried out,&#8221;Nooooo!&#8221; but we did didn’t hear him, crowded around our kitchen island contemplating movie titles, 300 meters away.</p>
<p>De-facto ran to the road, expecting to find the mangled body of our beloved dog.  There was nothing there.  No evidence of an accident.  No broken plastic pieces from a car.  No blood, no hair.  No dog.  He looked in the ditches, but no sign of Winston.  That’s when he ran back to the house, when he called me to come outside.</p>
<p>By now the rest of the family joined us. Buddy-roo saw De-facto holding my hand, his head bowed, and noticed the absence of our dog and collapsed in the road.  <a href="http://maternal-dementia.com/the-cast/#Short-pants">Short-pants</a> and my <a href="http://maternal-dementia.com/the-cast/#Mother-in-love">mother-in-love</a> hugged each other, shocked at the news.  </p>
<p>“We’ve got to find him.” De-facto’s anguish commanded us to the task. He started barking orders, which we all accepted dutifully. He and Buddy-roo drove off in the direction that the car had been going, to see if they could find Winston or its driver.  I ran down to the spot in the road where the accident occurred to search again for his body. </p>
<p>I couldn’t piece it together, everything went into a spin.  He couldn&#8217;t be gone. I pictured Winston’s empty basket, the bed he sleeps and his food and water bowls; how we’d look at them <a href="http://maternal-dementia.com/2016/07/18/the-joyride/dog_pulls_me/" rel="attachment wp-att-21596"><img loading="lazy" decoding="async" src="http://maternal-dementia.com/wp-content/uploads/2016/07/dog_pulls_me.jpg" alt="dog_pulls_me" width="199" height="267" class="alignleft size-full wp-image-21596" /></a>tomorrow, empty, and how we’d grieve.  We haven’t had him in our lives even two years.  It took half of that time for him to get to know us, to let go whatever fear he carried with him from his life prior to us bringing him home from the rescue center. For more than a year, he was even standoffish, a dog that only loved us loving him.  It was until very recently that I had the feeling he had actually started to love us back. </p>
<p>We’d become a family with a dog.  And now – way too soon – our dog was gone.</p>
<p>There was nothing on either shoulder of the road. I scoured the ditches for a red-haired body with its blue harness.  Maybe the impact had thrown him away from the road into the thick of bushes and trees.  I was about to head home and change out of my sundress and flip-flops into long pants and boots in order to search in the weeds and briars beyond the ditches, when I saw De-facto, in our car, driving toward me.  </p>
<p>“He’s alive!”  He stopped the car.  “Get in!”</p>
<p>We rushed back to the village – at least a 1.5 km distance – where I saw Buddy-roo standing with a young couple, staring at the front of their car.  De-facto pulled in beside them; I didn’t wait for the car to stop before jumping out.  There was Winston.  Neatly wedged into the front grill of the car, his paws hanging out comfortably, his head moving from side-to-side.  He panted and blinked, like nothing was the matter.  He did not bark.  He did not whimper.   He looked only slightly relieved to see us after his little joyride.</p>
<p>The couple in the car had already called the pompiers, and though De-facto wanted to take the bumper apart and free Winston immediately, we persuaded him to wait.  There was no blood, and Winston did not appear to be in pain, but who knew what kind of internal injuries he might have suffered.  They would have tools to extract him carefully from the grill of the car and avoid further injury.<br />
<a href="http://maternal-dementia.com/2016/07/18/the-joyride/winston_joyride/" rel="attachment wp-att-21600"><img loading="lazy" decoding="async" src="http://maternal-dementia.com/wp-content/uploads/2016/07/Winston_joyride-300x203.jpg" alt="Winston_joyride" width="500" height="339" class="aligncenter size-medium wp-image-21600" srcset="http://maternal-dementia.com/wp-content/uploads/2016/07/Winston_joyride-300x203.jpg 300w, http://maternal-dementia.com/wp-content/uploads/2016/07/Winston_joyride.jpg 400w" sizes="auto, (max-width: 500px) 100vw, 500px" /></a><br />
It was probably only 15 or 20 minutes, but if felt like hours before the firemen arrived. They probably did exactly what De-facto wanted to do, dismantled the bumper and stretched open the grill where Winston had been squeezed in.  Winston stepped out, like slipping out of a train berth, and even stood up on the sidewalk for several moments before collapsing. There was not one cut on him.  No external marks or bruises.  All bones appeared to be straight.  No blood, anywhere.</p>
<p>I’m still not sure why the driver of the car didn’t pull over sooner, why he drove past several turn-offs and driveways and continued all the way to the village.  Winston must have had the ride of his life, a full front bumper view of a French country road for nearly 2 km.  </p>
<p>The pompiers helped us locate a veterinarian, who, even at 10:00 on a Saturday night, opened his office to attend to Winston.  After a thorough physical examination and a series of X-rays, Winston appears to have suffered only 2 cracked ribs and some mild internal swelling.  He’s on anti-inflammation medicine now.  He’s moving a bit slower, as you’d expect, but he walks, and even trots a little.  He still manages to be underfoot, sitting in exactly the spot you want to stand, in front of the very cupboard you need to access, or just at the base of the refrigerator at the moment you want to open it. Not only is he alive, he&#8217;s his old self.</p>
<p>If things come in threes, then I’ve used up two of the three miracles I&#8217;m allotted in this life.  A dozen years ago we almost lost Short-pants and even the doctors called her recovery a miracle. Searching the ditches for Winston’s body, I was transported back to those brutal days when we didn’t know if Short-pants would make it or not, standing on the threshold of grief, wondering if we’d have to enter its dark room.  The pain of almost losing our dog reminds me of the pain of almost losing our child, which puts me in touch with the pain of so many people this year who <em>did</em> lose someone they loved: in Paris, Istanbul, San Bernadino, Orlando, Dallas, Baton Rouge, just last week in Nice, and dozens of other places that don’t get enough media attention but merit our mindfulness as well. There&#8217;s so much loss in the world, it&#8217;s hard to hold on to hope.<br />
<a href="http://maternal-dementia.com/2016/07/18/the-joyride/winston_on_white/" rel="attachment wp-att-21603"><img loading="lazy" decoding="async" src="http://maternal-dementia.com/wp-content/uploads/2016/07/Winston_on_white.jpg" alt="Winston_on_white" width="261" height="198" class="alignright size-full wp-image-21603" /></a><br />
Short-pants felt terrible because, as she put it, she loves Winston the least in the family.  It was a wake-up call to her, thinking he might be gone, to appreciate him more.  Near-misses like this can be gifts, it’s true, to remind us to appreciate the present and the people – and animals – who are here for us to love right now, in this moment.  We don’t know when they will be swept away from us. (Even if it’s if only for a few moments, in the grill of a stranger’s car.) Seizing the joy of the day is how we avoid regrets.</p>
<p>Yesterday Buddy-roo and I took Winston back to the vet for a <em>controle</em> to check that everything is okay.  He’s been vomiting repeatedly and the vet took another X-ray to look at his internal organs.  There’s some additional inflammation in his stomach and esophagus that’s causing it, and we hope the medicine will kick in soon and he’ll start eating normally again. </p>
<p>While he was getting his X-ray, Buddy-roo and I sat together in the waiting room, running through the events – and the rollercoaster of emotions – of the previous 24 hours.  We keep going through it in our heads, again and again, what happened, what could have happened, what didn’t happen.  We’ve all been shaking our heads, doing a dance between disbelief and relief.  I’m exhausted from the rapid cycle through so many emotions in such a short span of time.</p>
<p>Buddy-roo reached over, took my hand and caressed it.</p>
<p>“Mama,” she said, her voice pitched perfectly between laughing and crying, “tonight, can we just <em>watch</em> a movie, rather than <em>living</em> it?”</p>
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		<title>Watching Out</title>
		<link>http://maternal-dementia.com/2016/06/23/watching-out/</link>
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		<pubDate>Thu, 23 Jun 2016 15:49:19 +0000</pubDate>
				<guid isPermaLink="false">http://maternal-dementia.com/?p=21512</guid>

					<description><![CDATA[I always imagined that it would get easier as they got older. Of course there'd be some teenage rebellion - the passage of separation - which we'd have to take in stride. But in general, they'd need me less, right? It turns out it's not at all easier, and they don't need less from me. It's not as physically demanding to have a 12 and a 14 year-old as it was to have two toddlers two years apart, but it's mentally taxing.  The crisis of the day -- and often there's more than one -- requires a thoughtful response.  You cannot switch to auto-pilot parenting when with adolescent girls. Every thing matters. Every word matters. You have to pay attention. Especially if you're miles from home.]]></description>
										<content:encoded><![CDATA[<p>The air was hot and thick, moist, confronting me as I stepped out of the airplane.  I marched up the jet-way, headlong into smells I&#8217;d never smelled before but recognized right away. Smells raw and pungent, like the dank smell of dirt, the scent of people who eat and wash differently, the smell of untamed industry and much less regulated pollution. The smell of a city.  Not just any city, a city in Africa. <a href="http://maternal-dementia.com/2016/06/23/watching-out/mean_eye_on_you/" rel="attachment wp-att-21538"><img loading="lazy" decoding="async" src="http://maternal-dementia.com/wp-content/uploads/2016/06/mean_eye_on_you.jpg" alt="mean_eye_on_you" width="200" height="267" class="alignright size-full wp-image-21538" /></a></p>
<p>&#8220;Did they scare you with stories about Nigeria?&#8221; one of the participants of my workshop asked.  </p>
<p>They had. I&#8217;d been warned.  Nigeria is not a place you go lightly and nobody would have criticized me for refusing the assignment. The kidnapping of schoolgirls by Boko Haram was in the north – a good distance from Lagos in the south where I was going – yet a very troubling occurrence, one that remains unsettled.  Nigeria is well known for its corruption, but also its violence and crime. This was not a place to wander about with naive curiosity.  You have to watch out.</p>
<p>Still, I had a spring in my step. Traveling to new places is always an adventure, even if you have to exercise an extra dose of caution. Or maybe because of that.</p>
<p>~  ~  ~</p>
<p>My work is changing.  I&#8217;ve always traveled to do it, since I started running workshops two decades ago. Originally it was in the domain of marketing and business, later with academics and scientists – still a primary customer.  In the last year, though, I&#8217;ve been working to introduce our methodology to the sector of economic development.  As a result, I&#8217;ve been traveling to countries in Africa: South Africa, Cote d&#8217;Ivoire and Nigeria. Or to Asia, last week I ran a workshop in Thailand. And there’s a project in the works for Mexican assignment next fall. </p>
<p>I&#8217;ve been dreaming of doing this kind of work and now I&#8217;m starting up a new venture to realize it. I have the enthusiastic support of the colleagues, but at the moment the lion&#8217;s share of the work falls on me: strategy, marketing, selling, managing projects and delivering programs. It&#8217;s all terribly interesting, satisfying, and potentially very important work. But it does result in way too much to do in any given day.  </p>
<p>As the work piles up in front of me, sometimes so high that I can&#8217;t see over it, I have to sharpen my peripheral vision to keep an eye on my daughters. They are becoming more and more self-sufficient in practical ways: walking themselves to school, attending (mostly) to their own homework assignments, managing their wardrobes, making decisions about activities <a href="http://maternal-dementia.com/2016/06/23/watching-out/teenagers/" rel="attachment wp-att-21554"><img loading="lazy" decoding="async" src="http://maternal-dementia.com/wp-content/uploads/2016/06/teenagers.jpg" alt="teenagers" width="200" height="267" class="alignright size-full wp-image-21554" /></a>and friends. It&#8217;s easy to think they&#8217;re over the hump, on their way to adulthood. They might be on their way, but they&#8217;re not there yet. They have <a href="http://www.nimh.nih.gov/health/publications/the-teen-brain-still-under-construction/index.shtml" target="_blank">teenage brains</a>. They may appear to be adults. But they are imposters. </p>
<p>They have become, <a href="http://maternal-dementia.com/the-cast/#Short-pants">Short-pants</a> and <a href="http://maternal-dementia.com/the-cast/#Buddy-roo">Buddy-roo</a>, suffering teenagers. Suffering is too strong a word. They are both too lucky to suffer. Lucky to have a safe home, to be consistently loved.  Lucky to go to school and to imagine a wide range of professional choices in their future. Lucky to have opportunities to travel, to receive their most desired gifts every Christmas and birthday. Lucky to have their own iPads and smart phones. Still, they suffer the things that teenage girls must unfortunately endure, passing through this disconcerting phase, painful and poignant, dabbling in the awkward art of self discovery while navigating the perilous social minefields of adolescence. These are the things that cause their very vocal, or sometimes very quiet, suffering. These are the things to watch out for.</p>
<p>I always imagined that it would get easier as they got older. Of course there&#8217;d be some teenage rebellion &#8211; the passage of separation &#8211; which we&#8217;d have to take in stride. But in general, they&#8217;d need me less, right? It turns out it&#8217;s not at all easier, and they don&#8217;t need less from me. It&#8217;s not as physically demanding to have a 12 and a 14 year-old as it was to have two toddlers two years apart, but it&#8217;s mentally taxing. The crisis of the day &#8211; and often there&#8217;s more than one &#8211; requires a thoughtful response, one that is empathetic but not over-indulgent, one that soothes them as the same time prods them towards taking responsibility for their thoughts, actions and feelings. You cannot switch to auto-pilot parenting when with adolescent girls. Every thing matters. Every word matters. You have to pay attention. Especially if you&#8217;re miles from home.</p>
<p>~  ~  ~</p>
<p>I lived in Hong Kong for almost a year, more than 20 years ago. It wasn&#8217;t the best year of my life. The job that I&#8217;d come for wasn&#8217;t the one I found when I arrived. The man who was my partner, proved not to be. My adventurer-self pretended it was fine, tried to make the best of it. But inside I was spiraling down, cursing my choices. What saved me?  My creativity training. Tired of the feeling stuck at a dead-end, I gave myself an assignment. I opened a notebook and wrote without stopping &#8211; a stream-of-consciousness brain-dump of words &#8211; allowing myself the fantasy of what would be the ideal way of life if things weren&#8217;t in the rut they were in. I wrote eight pages.<a href="http://maternal-dementia.com/2016/06/23/watching-out/you_are_here-2/" rel="attachment wp-att-21542"><img loading="lazy" decoding="async" src="http://maternal-dementia.com/wp-content/uploads/2016/06/you_are_here.jpg" alt="you_are_here" width="200" height="267" class="alignleft size-full wp-image-21542" /></a></p>
<p>Fifteen years later, I found that notebook, packed away in a box of my things that&#8217;d been stored in my mother&#8217;s basement. I was stunned to read what I&#8217;d written; the description of what I&#8217;d hoped my life would be like was almost exactly what it had become. Living in a European city, traveling, working with creativity, with a network of international colleagues with whom there&#8217;s respect and rapport.  It only fell short in that my travels weren’t quite as exotic as I’d fantasized. But that was six years ago. Look where I get to go, now.  </p>
<p>It&#8217;s not that those pages became a blueprint, a strategic path I deliberately followed. I wrote them, put them away and didn&#8217;t look at them again until years later. Some might say I&#8217;d released an intention for an ideal future and the choices I made, subsequently, reflected the vision I&#8217;d scribbled down. If so, they were choices made at a subconscious level. In retrospect my career path may look coherent, but it was haphazard in the making.</p>
<p>One thing that was noticeably absent from those prophetic pages: children. I hadn&#8217;t factored them in. It wasn&#8217;t that I didn&#8217;t want any, they just weren&#8217;t in the picture. I didn&#8217;t have a vision for what it would be like to have kids, let alone how&#8217;d it all fit in with the life I dreamed of for myself.  It still surprises me. I look at them, all long and lanky, and I think, how on earth did that happen?  </p>
<p>~  ~  ~</p>
<p>It&#8217;s easy to see the cracks in my parenting. For everything I&#8217;ve done well, there&#8217;s something I could have done better. A bit stricter on this.  Maybe more indulgent on that.  More consistent across the board.  More present.  More plugged-in. I can already bullet-point the earful of grief their therapists will hear from them.  I know I just have to ride it out, until they&#8217;re in their forties, which is about the time I think most people forgive their parents for not being perfect.</p>
<p>They hate, most of all, when I go away on a trip. Short-pants marches around chanting, &#8220;<em>No se puede ir</em>,&#8221; when she sees me preparing my suitcase. Buddy-roo hurls herself theatrically on to the couch. &#8220;Why must you go away? Why can&#8217;t you work like <em>normal</em> parents?&#8221; <a href="http://maternal-dementia.com/2016/06/23/watching-out/exclamation/" rel="attachment wp-att-21531"><img loading="lazy" decoding="async" src="http://maternal-dementia.com/wp-content/uploads/2016/06/exclamation.jpg" alt="exclamation" width="200" height="268" class="alignright size-full wp-image-21531" /></a></p>
<p>But I <em>love</em> it when I go away. I love getting up in the dark for a 5:45 am taxi. I love airports. I love walking down the jetway, the long tunnel to somewhere else. I love the outbound journey, infused with anticipation. I like the homeward trip, too, with its promise of the comfort of my own pillow and the reunion with my family. I count on the fact that even if they&#8217;re mad that I&#8217;ve left, they&#8217;ve forgiven me by the time I get home. </p>
<p>I know there are things I miss &#8211; maybe important things &#8211; working as I do, being away for a week or two at a time. And even when I&#8217;m home: I burrow into my computer screen, or prattle away on back-to-back conference calls that kick off just as the girls get home from school. I tell myself it means I&#8217;m not helicoptering around them, but rather, watching out for them from afar, out of their hair, leaving them to learn to sort things out on their own. Not all things, but some things.  I guess we&#8217;ll only know if it&#8217;s enough guidance when we see how they survive these treacherous teenage years. But that&#8217;s why the work I do, and the travel it brings, is so important to me. It might be the key to how I survive their teenage years, too. </p>
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		<title>Time for Christmas</title>
		<link>http://maternal-dementia.com/2015/12/23/time-for-christmas/</link>
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		<pubDate>Wed, 23 Dec 2015 09:02:55 +0000</pubDate>
				<guid isPermaLink="false">http://maternal-dementia.com/?p=21466</guid>

					<description><![CDATA[And then there's Christmas. The time of year for spirited joy and treasuring family traditions. Time-honored traditions that take a lot of time. It's a holiday that's the hardest on moms, even if dads play along. Or maybe it just hits *me* the hardest. Me and my mother, who used to get all wound up at Christmas and I never understood why until I was the one buying, wrapping, baking and planning. Though nobody's holding a gun to my head to bake 4 dozen ginger-bread men and 8 dozen Christmas cut-outs (that's what the recipe makes) every year. ]]></description>
										<content:encoded><![CDATA[<p>I’ve lost ten hours of my life to that bank. Ten hours I didn’t have to spare.  Hours of fussing with the new on-line interface that won’t connect, or calling help-lines and being put on hold. Hours standing in line at a branch office, the only one that deals with my problem, a problem that can be addressed at only one desk, the one with six people waiting in front of it. I will lose at least three more hours opening a new account in a different bank, and trotting down to the previous one and attempting to withdraw all my funds.  I suppose it will eventually get sorted and in the context of all the other horrible things that are happening in the world, this is a luxurious problem. But I’ll never get those hours back. <a href="http://maternal-dementia.com/wp-content/uploads/2015/12/clocks_times_three.jpg"><img loading="lazy" decoding="async" src="http://maternal-dementia.com/wp-content/uploads/2015/12/clocks_times_three.jpg" alt="clocks_times_three" width="200" height="266" class="alignright size-full wp-image-21470"/></a></p>
<p>It’s not a time when I can be generous with hours. An array of projects lie unfolded before me, marked by a mosaic of bright Post-it notes on the wall above my desk or Skype calls inked in my calendar. All of these need time and take time.  Each one of them something important or at least fascinating to me, none I would be prepared to discard.  Yet all of them, all at once, fill up the hours of the day, and quickly.</p>
<p>I have so many things I want to write. Website updates and posts about all those interesting projects.  A book to finish editing (for work).  A book to finish writing (for myself). So there’s no pleasure in the time spent on bank interfaces that won’t work, or calling our internet service provider about the strange undulation of our allegedly high speed, high quality fibre optic wifi, or hunting down viruses that have snuck into my computer, or scheduling doctor’s appointments I should have made weeks ago.</p>
<p>The girls, of course, need time from me, now more than ever.  <a href="http://maternal-dementia.com/the-cast/#Short-pants">Short-pants</a> is carrying the stress of her schoolwork.  Always conscientious about homework, she manages it without assistance, but lately you can see the burden of the workload – it increases in intensity and volume every year &#8212; taking its toll on her.  Each week, her introverted self gets depleted by Thursday. She explodes in anger or bursts into tears at the drop of a hat.  Especially when it’s her sister who drops it.</p>
<p>Her sister, who is going through her own existential crisis, spiraling down into dark thoughts. Don’t laugh: I remember going through this myself when I was <a href="http://maternal-dementia.com/the-cast/#Buddy-roo">Buddy-roo</a>’s age, conjuring up weird fantasies about what would happen if I was dead. Never enough to make it happen, but wondering about it, which leads to wondering about why are we here anyway, and for Buddy-roo, pondering what’s the point, especially if she doesn’t have a iPhone like all her friends?</p>
<p>The only antidote to their various bouts of teenage angst &#8211; both legitimate and dramatic &#8211; is time. Time spent sitting on the couch beside them, listening, chatting, or just being there and doing nothing at all.  Time when I step away from the computer and give them my full attention.  Time when they get to feel like they are the most important thing on my to-do list.<br />
<a href="http://maternal-dementia.com/wp-content/uploads/2015/12/santas_elf.jpg"><img loading="lazy" decoding="async" src="http://maternal-dementia.com/wp-content/uploads/2015/12/santas_elf.jpg" alt="santas_elf" width="200" height="267" class="alignleft size-full wp-image-21473"/></a><br />
And then there&#8217;s Christmas. The time of year for spirited joy and treasured family traditions. Time-honored traditions that take a lot of time. It&#8217;s a holiday that&#8217;s <a href="http://maternal-dementia.com/2009/12/24/mere-noel/">hardest on moms</a>, even if dads play along. Or maybe it just hits <em>me</em> the hardest. Me and my mother, who used to get all wound up at Christmas and I never understood why until <em>I</em> was the one buying, wrapping, baking and planning. Though nobody&#8217;s holding a gun to my head to bake 4 dozen ginger-bread men and 8 dozen Christmas cut-outs (because that&#8217;s what the recipe makes) every year.</p>
<p>&#8220;Because it&#8217;s your tradition,&#8221; <a href="http://maternal-dementia.com/the-cast/">De-facto</a> says, when, wincing at my sore shoulders, I ask myself out loud why I do this every year.</p>
<p>I do know why. The girls love it. They jump up and down at the mention of the seasonal baking. Now they&#8217;re old enough to really help &#8211; as opposed to when they were toddlers, when their &#8220;help&#8221; had a short attention span &#8211; and they do their share by mixing the ingredients to make the dough, rolling it flat and cutting out the angels and stars and fir trees and Santas.  They know how to add the food coloring to the sugar, and how to sprinkle it on the cookies while the icing is still soft. That&#8217;s time well spent, and spent together, but it makes me long for a time when I was the one standing on the stool watching my mother read from her recipe card while she blended the ingredients with her <a href="https://www.flickr.com/photos/suzannesf/4879844688" target="_blank">foley fork</a>, admonishing me, with affection, not to eat too much of the raw dough.</p>
<p>Because for me &#8211; and I know I say this every year &#8211; Christmas isn&#8217;t entirely joyful. It&#8217;s a time when I miss all those people who used to come together for the holidays, whose collective presence seated around my parents&#8217; living room was the most comforting thing in the world. Christmas makes me want to regress to an earlier time, a time when <em>I</em> was the one marveling at the tree and its trimmings and shaking the decorated packages beneath it, when my only responsibility was playing the elf who distributed the gifts as we sat around and opened them one-by-one, and maybe setting the table or drying a few dishes after Christmas dinner. I long for those days when the hours between now and Christmas morning seemed an eternity, when time couldn&#8217;t move fast enough. If only we could put those restless, protracted hours in the bank when we&#8217;re young and impatient, and withdraw them later, when we&#8217;d appreciate them so much more. (Santa, can I open <em>that</em> account for Christmas?)</p>
<p>In the meantime, the speed of how we experience time is variable but (mostly) out of our control. There&#8217;s nothing to do but take in this moment now: Buddy-roo squatting before the Christmas tree, <a href="http://maternal-dementia.com/wp-content/uploads/2015/12/keep_out.jpg"><img loading="lazy" decoding="async" src="http://maternal-dementia.com/wp-content/uploads/2015/12/keep_out.jpg" alt="keep_out" width="260" height="200" class="alignright size-full wp-image-21491"/></a>bemoaning how many days there are still before Christmas while I put a &#8220;keep out&#8221; sign on my office door and scramble to finish wrapping presents. This is what she will remember, and some day she will long for it. That&#8217;s the most enduring gift I can give those girls, a string of Christmases to remember fondly, even if the memory is always a little bit bittersweet.</p>
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		<title>Under Attack</title>
		<link>http://maternal-dementia.com/2015/11/15/under-attack/</link>
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		<pubDate>Sun, 15 Nov 2015 20:08:25 +0000</pubDate>
				<guid isPermaLink="false">http://maternal-dementia.com/?p=21430</guid>

					<description><![CDATA[It’s remarkable how a network of friends reaches out to support one another at a time like this. I was desperately texting my Parisian friends on Friday night, unable to get to sleep until I’d heard from them that they were safe. Saturday morning I woke to a full inbox myself, messages from friends who weren't aware that we'd moved to Barcelona, or who know I often go back to Paris and that we have many close friends there who might have been hurt. It made my heart grow. In the midst of this horrible tragedy, little pockets of kindness make all the difference.]]></description>
										<content:encoded><![CDATA[<p>I am not done with Paris. That conclusion I came to just over a week ago, when I was there on a last minute trip, a quick overnight visit provoked by an administrative errand. Usually I pack my schedule with lunches, drinks and dinners, taking advantage of the time on the ground to catch up with Parisian friends. This last trip I organized very few appointments. I&#8217;ve a lot of work at the moment and I didn&#8217;t <a href="http://maternal-dementia.com/wp-content/uploads/2015/11/metro_sign.jpg"><img loading="lazy" decoding="async" src="http://maternal-dementia.com/wp-content/uploads/2015/11/metro_sign.jpg" alt="metro_sign" width="200" height="266" class="alignright size-full wp-image-21439" /></a>want to orchestrate every minute of my visit. I wanted to be in Paris with a bit of time on my hands. The way it used to be. Just being there.</p>
<p>Standing in line to board the flight, I cringed at the weather forecast: chilly, cloudy with showers. This was one of the main reasons for relocating to Barcelona. We craved a warmer, sunnier climate. The cold and gray of Paris can wear you out. But luck was with me, the forecast was inaccurate. The Paris weather was milder than predicted and the sun had only a few clouds to hide behind. Walking across the <em>Pont Notre-Dame</em> to the <em>Prefecture</em> for my appointment &#8211; one that had been assigned to me so I had no choice but to make the last minute trip &#8211; I took in the majestic vista of Paris&#8217; bridges arching over the Seine, and all the familiar landmarks, <em>Notre Dame</em>, the <em>Louvre</em>, the <em>Conciergerie</em>.  No matter how many times I make the walk between the left and right banks, I am still struck by the stunning beauty of the city.  Second only to the friendly upstate New York village where I grew up, this is the place that feels most like home. It was home, for eighteen years of my life.</p>
<p>~  ~  ~</p>
<p>Our try-a-year-in-Barcelona turned into two years (one was not enough to really get a full experience of the city and culture) which then turned into three years (it takes more than two years to feel at home) and who knows, now, how long we will stay.  We&#8217;re set up comfortably, in a roomy apartment, walking distance to the school, a mere block away from a forested mountain that leads to a track where we love to run, bike and walk the dog. New friends aren&#8217;t as intimate or familiar as those we knew in Paris, but there is potential. I am not unhappy in Barcelona. Our life is lovely. But it isn&#8217;t what my life was in Paris. And I do miss that life.</p>
<p><a href="http://maternal-dementia.com/the-cast/">De-facto</a> was out playing basketball on Friday night and <a href="http://maternal-dementia.com/the-cast/#Short-pants">Short-pants</a> and <a href="http://maternal-dementia.com/the-cast/#Buddy-roo">Buddy-roo</a> and I heaped ourselves together on the couch with Winston to watch the an episode of our latest favorite Netflix series. It was a text message from a faraway friend that alerted me to the attacks that were unfolding in Paris. I plugged into news coverage of <a href="http://www.liberation.fr/france/2015/11/13/fusillade-dans-le-10e-arrondissement-de-paris_1413313" target="_blank">Liberation</a> and the <a href="http://www.bbc.co.uk/news/world-europe-34814203" target="_blank">BBC</a> and <a href="http://america.aljazeera.com/articles/2015/11/13/shooting-explosion-reported-in-paris.html" target="_blank">Al Jazeera</a>. I scanned my Facebook feed to see which Parisian friends were online and sharing updates &#8211; partly to hear<a href="http://maternal-dementia.com/wp-content/uploads/2015/11/paris_runs.jpg"><img loading="lazy" decoding="async" src="http://maternal-dementia.com/wp-content/uploads/2015/11/paris_runs.jpg" alt="paris_runs" width="200" height="267" class="alignleft size-full wp-image-21441" /></a> their perspective, mostly to confirm they hadn&#8217;t been caught in the mayhem.  </p>
<p>It was hard to go to sleep and harder still to wake up in the morning to the tally of dead and injured and the stark images of a vibrant city shut down by terror and bloodshed. When Short-pants delivered my coffee &#8211; a Saturday morning luxury &#8211; I pulled her into bed with me for a morning hug. It made me think of the days just after 9/11 when we were glued to the TV, the altar for our grieving. I was breastfeeding Short-pants &#8211; she was only two months old &#8211; and while I watched the news, I&#8217;d glance down at her little mouth seriously at work taking in nourishment, her tiny fists banging against me and wonder what kind of world we&#8217;d brought her into. Now, fourteen years later, I held her (considerably) taller body in a long embrace and wondered, again, what kind of world she was inheriting. How will this ever go away?</p>
<p>~  ~  ~  </p>
<p>It’s remarkable how a network of friends reaches out to support one another at a time like this. I was desperately texting my Parisian friends on Friday night, unable to get to sleep until I’d heard from them that they were safe. Saturday morning I woke to a full inbox myself, messages from friends who weren&#8217;t aware that we&#8217;d moved to Barcelona, or who know I often go back to Paris and that we have many close friends there who might have been hurt. It made my heart grow. In the midst of this horrible tragedy, little pockets of kindness make all the difference. </p>
<p>Later, at lunch, I asked the girls what they thought about what happened in Paris the night before. They both had the same first instinct: to ask <em>why</em> someone would want to kill so many people with such violent attacks. I struggled to respond.  How to convey the complexity of such a convoluted reasoning &#8211; the perfect storm of anger, hate, disenfranchisement and indoctrination?  How to share my indignation, my fear, my grief, but without fueling their prejudice and creating the fear and hatred that only perpetuates a cycle of terrorism? How to tell them the truth without scaring the bejeezus out of them?  I always tell them, &#8220;Be smart, not scared,&#8221; when it comes to dealing with danger.  But is that enough to keep them safe from this kind of arbitrary violence?  <a href="http://maternal-dementia.com/wp-content/uploads/2015/11/go_paris.jpg"><img loading="lazy" decoding="async" src="http://maternal-dementia.com/wp-content/uploads/2015/11/go_paris.jpg" alt="go_paris" width="260" height="200" class="alignright size-full wp-image-21450" /></a></p>
<p>I am relieved that my family and I are safely away in Barcelona, that we weren&#8217;t subject to the immediate fright of it, the menace of proximity to such a massacre.  And yet a part of me is aching to be there in Paris, now, to witness for myself what has happened, to be there not only in spirit but in person, showing my solidarity with some of my dearest friends and with the city that was my home for so long, and in my heart, still is. </p>
<p>But are we really safer here? Any European city – any city at all – might be subject to the same terror as Paris. There&#8217;s nothing to do but return to our routines, taking it all in stride, just like we numbly take off our shoes and place our liquids in plain view at airport security, running through the motions of protecting ourselves from a mid-air terror, when simply sitting at a café with friends can be just as deadly. How do I explain <em>that</em> to my daughters?</p>
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