Spunk

I'm all about anniversaries. And on Tuesday, I celebrated one: the two-month anniversary of a sideline sprint that ended with me crawling off the soccer field, my left Achilles tendon partially torn like a piece of frayed rope. 61 days later, my Achilles spent its "anniversary" feeling just about as worthless as it did the moment it tore.

These unfortunate circumstances are partly my fault, I know. There's no use in denying it - I'm a bad patient. After all, my doctor did tell me to wear my walking boot at all times unless I'm fully engaged in my usual fetal position in bed for a too-short night's sleep. But the boot's hot. It's a pain to take on and off. It's not the best summer fashion statement - I keep thinking I should decorate it with miniature leis and little pink umbrellas and other fun things that make me think of cute sandals and tropical islands and activities best done bootless. And, it's not water sports-friendly. I spent this past weekend at my aunt and uncle's house on beautiful Smith Mountain Lake in Virginia. Getting from the house to their dock in a beautiful, quiet little cove with a full view of the mountain itself requires navigating 86 unevenly-sized wooden steps. My uncle, a surgeon, was horrified at my lack of compliance with doctor's orders - first when I attempted to come down those steps barefooted and crutch-less and then later, when I came down the steps a second time, still barefooted but this time on crutches, only to ditch the crutches as soon as I reached the bottom step.

One reason I'm a bad patient is that I am extremely prone to cabin fever. I cherish those fleeting moments in which I have nothing to do and can simply sit still and breathe, but when I'm forced to sit still, it drives me crazy.

The second reason I'm a bad patient is that I'm just plain stubborn. Sometimes, when instructions don't suit me, and I'm the only one who stands to lose, I just don't follow them.

I'm stubborn about Batten disease. Some people have asked me, and my mom, why we're still fighting this damn monster. It's winning the fight right now and has been all along, so why are we still throwing punches?

I'll tell you why we're still fighting. We haven't been knocked out yet, that's why. We may have bloody lips and swollen eyes and busted noses, but we're still standing, and we've managed to get in a lot of good licks on Batten, too. There are still people out there who haven't heard Taylor's story. There are still people out there who, given the opportunity, would be inspired to fight beside us - for one battle or maybe the whole war. I learned that this spring; I spoke publicly on behalf of Taylor's Tale on six different occasions, and every time, at least one perfect stranger came up to me afterward wiping away "I want to help" tears. And, most importantly, there's still a lot of kids who need us to keep fighting. We won't find the answer in time to save all of them - maybe not even my own sister. I know that. Believe me, I've known it for a long time.

But just as my family's still standing, my sister's still smiling. When Taylor was little, we called her "spunky," which really meant she was stubborn as hell but so damn cute that "spunky" just fit better.

Keep throwing those punches, Batten. Eventually, the fight will end, and you'll be lying on the ground, and we'll be standing. We'll be covered in blood, and we'll struggle to keep our balance, but we'll still be on our own two feet. Because we're too spunky to take "no cure" for an answer.

In spunk we trust.

Batten Disease Awareness Weekend

How did you first hear about Batten disease?

Nearly five years ago, I was sitting at my desk on a Charlotte hospital campus when I heard that awful phrase for the first time. I was writing a press release when my mother called to tell me through tears that a geneticist had just told her and my dad that my seven-year-old little sister was going to die.

I wish I'd never heard of Batten disease. I wish I could wrap my brain around the idea that one single defective gene out of the estimated 20,000-30,000 we humans have can cause all of the terrible things that are a part of Batten disease. But a large part of me is glad that I can't always wrap my brain around the truth that all of those terrible things are happening or will happen to my little sister, now 12. Because it's during those moments of truth that I'm engulfed by feelings of helplessness and despair.

I'm proud of all that Taylor's Tale has done to advance the search for a cure. Nearly $300,000 and many stories later, we're much closer than we were on the day of that fateful phone call. More than that, however, I'm proud of my family for how they've faced this monster each day with nothing but hate for it and love for each other. And most of all, I'm proud of my sister for never losing her beautiful spirit - even in those moments when the twisted demon of a disease is at its strongest.

Today marks the beginning of Batten Disease Awareness Weekend, so I have a small favor to ask: over the next few days, please make a point to share Taylor's Tale with everyone you know. Scientists are very close to finding an answer for infantile Batten disease, but that answer will never reach the children who so desperately need it unless more people know about it. Batten disease is anonymous in the eyes of much of the world, and that has to change. Then, and only then, will we witness a miracle worthy of the courage that lives in each and every one of these children.

The Raindrops Danced

Tonight, throughout most of the 30 minutes I spent chained to a recumbent bike at the gym, my eyes darted from the Kindle in my lap to the darkening sky through the windows - layers upon layers of deep blueberry blue and blackberry purple, like a frosted layer cake left out in the sun on a humid day. As I hobbled out the front door some time later, the orthopaedic boot that has been my fashion statement for the past month holding my busted Achilles together like Scotch tape, the front desk attendant told me to stay dry.

As luck would have it, the first warm, fat drops of rain fell from that layer cake sky just as I walked out into the balmy night.

Normally, I would have sprinted the 50 feet to my car. I don't like to get wet. My husband routinely teases me about my love for the outdoors and, conversely, my distaste for rain unless I'm safely out of it. Just two days ago, he watched with a smile from the door of the chapel where our friends were about to be married as I limped unevenly across the parking lot, my left foot in the boot and my right foot in a three-inch heel, a slippery pashmina slung over my shoulders and the world's largest golf umbrella clasped in both hands.

As I pulled out of the gym parking lot, I received an unexpected visit from a decade-old memory of an afternoon at my grandparents' house in Wake Forest. In the pictures that played on the projector screen in my mind, Grandma Kathryn chases an overalled-toddler version of Taylor around the front yard under a gray sky. Taylor manages to avoid our grandmother's outstretched arms, only to be scooped up by John when she rounds the corner and runs right through his hiding place. He turns her upside down and tickles her, then sets her on her feet. And the game begins all over again.

A soft breeze rolls over the tops of the trees - a warning for rain. As the first drops cascade out of the sky and onto our waiting faces, I run for cover. Taylor runs to the porch and tugs at the handle of an umbrella three times her size. John takes the umbrella from her, opens it and wraps her tiny fingers around the shaft. Her cherub face breaks into a grin, and she takes off down the winding path to our grandmother's garden, singing in the rain.

I smiled as I remembered this very real moment - a testament to my little sister's ability to find beauty in every drop of rain. The image of Taylor skipping down that garden path reminded me of words spoken by Cindy Smith, a courageous mother who lost her son to the same disease that threatens to take my little sister away from me forever.

"Life is not waiting for the storm to pass. It's learning to dance in the rain."

As the spring rain poured from the sky, I rolled down my window. The raindrops danced on my outstretched arm as a smile danced across my face and love filled my heart.

Run Toward the Light

I have a confession to make: saving my sister will not be easy. This is not a new revelation on my part. In fact, no one in our family ever claimed that our mission to save children like Taylor would be a piece of cake. Some days (many, in fact), we search for the answers in a pitch black world, with seemingly no hope to light our way. But we must never stop searching. We must continue this journey - if not by sight, then by faith.

Sometimes, I let several weeks pass between blog posts. If I'm not writing, I'm searching. Searching for what? God only knows. Hope? Salvation? Happiness? Eventually, I find my words. Often, they drift toward running.

I cannot run at the moment. I tore my Achilles playing soccer three weeks ago - the culmination of a less severe injury that originally occurred two days before I ran a 10-mile road race in Taylor's honor. So I run in my mind - on cool, damp sand by the sea as the sun sinks behind a low cloud, or a field of wildflowers in a high mountain meadow - but never the unforgiving pavement.

Charlotte Benson, the mother of a child with Batten disease, is not a runner. But Charlotte understands the difference between a sprint and a test of endurance. She understands that our shared battle is a test of the latter. She knows that often in our long race to defeat this monster, we must run in the dark. 

I am injured, and Charlotte is not a runner. We have never met. And yet, we are running together - through the deepest, blackest darkness that is Batten disease, buoyed by our faith and the incredible gift of each other and the sick children we love.

Thank you, Charlotte, for your beautiful words. On their wings, I'll run toward the light for another day.

Run to the Sun, by Charlotte Benson

A year ago, Lance Thompson, our good friend and avid runner, came to us with an idea to organize a 100-mile overnight relay run to raise money for the Foundation. Admittedly, I’m not a runner, and my first reaction was, “Who in the world is going to want to do that?!!” But as the idea evolved, and he shared his vision of a race whose course would meander under the starlit sky of the Texas countryside and culminate at a stunning destination at sunrise, I began to understand. Now, less than two weeks away, that vision will become a reality on May 14 when 30 teams of eight people each will compete by running a rugged Hill Country 96-mile course starting at Mount Bonnell and ending in the dawn light at Enchanted Rock. Members of each team will follow the route together in a van to support their runner and cheer him on as he steps onto the course alone to face his own unique challenge in the dark. Lance wanted the participants to experience first-hand the physical darkness and challenges that a child who is blinded by Batten Disease faces. It has been transformative to watch Lance’s ambitious dream become a reality and I am struck by how incredibly this race also mirrors our own life, and so perfectly mimics the mission of the Beyond Batten Disease Foundation. I love the way God inspires us only later to reveal His full intention.

As parents of a child with a terminal illness, there are so many unanswered questions. This not only is a race against time to find a treatment or a cure for our own daughter, but it’s a journey through the dark, facing the fear of running alone, and not knowing what obstacles and challenges lie ahead. The verse that continually comes to mind and is such a great source of comfort is 2 Corinthians 5:7, “For we walk by faith, not by sight.”

Our foundation was built by our family, our friends, and our community, all of whom have shared their talents, their gifts and their resolve to achieve the same goal. We have set out to accomplish something that has never been done before……..to eradicate Batten Disease and 600 other rare diseases through our carrier screening test. It’s a journey where friends and community follow us closely and offer support and encouragement. It’s a journey where everyone brings their talent and strength and sews them together to form an unbreakable bond: a resolve to commit, to endure, and to finish what we’ve set out to do.

This race is not a sprint. It is an endurance event that requires the commitment and support of a team. There is an African proverb that says, “If you want to go fast, go alone. If you want to go far, go with others.” God has provided for us with the incredible gift of our community, our “team,” which perseveres. These runners do not face the challenge of this course alone; our foundation does not face the challenge of Batten Disease alone. We are a team.

And best of all, we have charted a course. We are not simply running in the dark, aimlessly wandering from hopelessness, to fear, and despair; we are running to the sun, to the light, to the hope, to the dawn of a new day where Batten Disease no longer exists: our own Enchanted Rock. For light emerges from the darkness and morning is born from the womb of night.

Visit Charlotte's Blog

The Meanest Mother in the World

Growing up, I thought I had the meanest mother in the world.

My friends' mothers did most of the work on their science fair projects, but I had to do almost all of the work on mine. One year, I tested different brands of store-bought popcorn for their popping prowess. On a gorgeous Saturday afternoon, my mother made me sit at the kitchen table counting hundreds of popped and unpopped kernels while my friends played outside.

In elementary and middle school, I hated wearing dresses and got nervous around boys, but my sixth grade year, my mother forced me to participate in Teen Cotillion. On Wednesday nights, instead of building forts in the woods or going to Charlotte Hornets games with my dad, I had to put on a skirt and go to a middle school gym to learn how to do the waltz and the shag and the electric slide and hold hands with boys.

For more than a decade, my mother dragged me to piano lessons once a week, and the other six days, she made me practice for at least 45 minutes, setting the timer on the oven so I couldn't cheat. While other kids got to play fun music from movie soundtracks and chart-topping albums, I had to play the classics. And while lots of kids got away with just playing in the annual recital, I had to play in all of the competitions, too. I got a 'superior,' the best score, every single competition in every single year - all but one. That time, I got an 'excellent,' the second best score, and on the way home, my mother told me I didn't play to my potential.

Some of my friends bought pizza in the school cafeteria five days a week, but my mother sent me to school with thermoses of chicken noodle soup and apple slices and peanut butter sandwiches with the crust still attached.

A lot of my friends' rooms looked like war zones, but my mother made me clean my room and took away privileges if I didn't. She used to follow me around with the vacuum cleaner and got mad when I wore my muddy soccer cleats into the kitchen.

Most of my high school friends had midnight (or later) curfews, but my mother forced me to be home by 10:30. During my sophomore year, on the night before I turned 16, I went to the senior follies production at school with my junior and senior friends, and one of them insisted that we celebrate my birthday at midnight. I walked in the door of my house at 12:25, almost two hours after curfew. My mother grounded me.

None of my friends' parents pressured them about their grades like my mother pressured me. The first semester of my freshman year of high school, I got my first-ever 'C,' in English. My teacher told my parents that I got the 'C' because I didn't apply myself, so my mother took away my Cliffs Notes, threatened to hire a tutor and insisted on reading my take-home papers before I turned them in. I never got another 'C' again; that spring, I took the state writing test and got the highest score in the school, and seven years later, I graduated from college with an English degree.

Many of my soccer teammates' moms came to every single game - even the weekend-long tournaments out of the state - and waited in the parking lot after practice so they could yell at the coaches about their daughter's playing time. My mother never came to practice, never yelled at my coaches and never even came to many games. She was too busy being president of the Junior League or serving on some other board to give kids with handicaps or from less fortunate families a chance to believe. And while my teammates' mothers helped them research college soccer programs and athletic scholarship opportunities, my mother told me to go to the best school, even if I had to walk on the team or, worse yet, never got a chance to play on the varsity.

When I became extremely homesick at the beginning of my freshman year of college, my mother wouldn't let me move home to go to the school my boyfriend attended. She told me that if I didn't like my school, I could go somewhere else, but I couldn't come home.

When I told my mother my boyfriend and I wanted to spend the summer after my graduation driving across the country, she told me no. Instead, she made me get a PR internship at a local ad agency while I figured out what I wanted to do with my life, since my original plan to be a starving artist didn't solve the issue of getting me off my parents' payroll. That internship led to the career I have today. And when I wanted to get married after I earned my undergrad degree but before my husband finished his, she convinced me to wait until he was halfway through grad school.

Finally, after years of waiting, my wedding day was the happiest of my life. That day, I stood in front of 75 of our closest family and friends and toasted my father and my mother for giving me everything a daughter ever could ask for.

Since that day, I've seen my mother torn apart by the disease that shattered our family the same day we learned of its existence for the first time - just one month after my wedding. I've watched her fight for my sister, Taylor, like her own life depended on it - and maybe it does. I've watched her demand the best of the people who have a chance to give kids with Batten disease a future, just like she used to demand the best out of me. I've seen her at her most desperate, and in those moments, I've tried (often in vain) to be the rock for her that she's always been for me - even though I used to be too naive to see it.

I love my sister, but I'm not only fighting for her. I'm fighting for my mother - the greatest mother in the world. Because that's what she always did for me.

Mother's Day isn't until two weeks from Sunday, but my mother deserves to be honored 365 days a year. Happy Mother's Day, Mom. I love you!

Digging Deep

I managed this self-portrait before dawn
the morning of the race.

As promised, following are my results from the 2011 Tar Heel 10 Miler, run on the campus of UNC and the streets of Chapel Hill on a misty Saturday morning before the sun ever broke through the clouds.

Time: 1:25:27
Pace: 8:35/mile
Laurel Hill time: 7:35
Place: 734 out of 2,189 overall; 267 out of 1,252 females; 60 out of 200 females ages 25-29

I began the race on Stadium Dr. with a nasty head cold, an injured Achilles (pulled in a soccer game two days prior) and maybe an hour of sleep (worried I'd sleep through my 5 a.m. alarm, I never quite made it to dreamland).

Around mile marker 2, I felt a burning sensation in the ball of my left foot. It never went away, forcing me to change the way I run (more naturally a sprinter than a distance runner, I run entire road races on my toes). Hours later, I'd discover the source of the pain - an enormous blood blister.

Near mile marker 5, the pain in my Achilles relented, blissfully replaced by a runner's high.

A few miles later, I called my parents from the course just to check in. Their voices gave me the boost I'd need just moments later.

Soon after we said goodbye, I reached Laurel Hill - the most difficult part of the race, featuring a 200-foot vertical climb over the course of a mile. By then, my lack of sleep had caught up with me. But when I crossed the first timing mat, I pushed myself, getting as close to a sprint as my body permitted. Each time my ruined feet hit the pavement, I heard my little sister's laugh, and I dug deeper. I crossed the second timing mat at the top of Laurel Hill 7 minutes and 35 seconds after crossing the first - meaning I'd run the most challenging mile a minute faster than my average mile pace.

Soon afterward, I heard the music at the finish line as I rounded a bend. And when I reached the final straightaway, as in every race, I pulled out one more sprint for "T."

I ran the 2011 Tar Heel 10 Miler 12 minutes faster than in 2010, so tonight, true to my word, I'll make a $60 donation to our Miles to a Miracle campaign. But more importantly, I'll never stop running. In fact, I got back out on the track tonight, ready to tackle the next race for Taylor. Laurel Hill has nothing on the mountain we have yet to climb. But I believe.

Please consider making a gift of your own to help Taylor's Tale cross the finish line of the ultimate race: the race to save the lives of children like my little sister. Give Now

Still Standing

It's been one of those weeks for me. They come along every once in awhile. My tears are threatening an uprising.

I cried all the time back in 2006, when we learned Taylor has infantile Batten disease. One early evening I started crying without warning as I stood at my kitchen counter making macaroni and cheese, listening to music and watching the sun tuck into the clouds behind the trees in my backyard. I sank down to the floor and stayed there with my back against the dishwasher and my bare feet on the cold tile floor as hot tears soaked my shirt and my shoulders shook. I didn't know what made me cry at that moment, and I didn't know how to stop. So I just cried until I didn't have any tears left.

After a 5K fundraiser one cool, rainy Saturday morning the following spring, I held the hand of a boy with juvenile Batten for 30 minutes. I knew Seth wouldn't have seen my tears, but I still held them in until after I'd walked away. And as soon as I did, that was it for me. I took my mom by the arm, and we found my car and drove home. I climbed the stairs to my bonus room, closed the blinds and slept on the couch for five solid hours. And I NEVER sleep during the day.

Somewhere along the way, my life before Batten disease (B.B.D.) dropped out of sight in the rear-view mirror. I cried less and less. Mostly I stayed angry. I'm still angry, which is good in a way because it makes me want to fight like hell. Sadness doesn't get me anywhere. Lately I'm feeling worn down, so the sadness is back. When I feel it creep into the corners of my eyes, I run if possible. I love to run for many reasons, one of which is that it makes me feel powerful. Each time my ruined feet and ankles pound against the pavement, I beat back the tide.

Mostly, it's working. I cry very little, but when I do - it's epic.

I don't know where I am or how I got here. If you've lived my story, you understand the source of my doubts.

Originally this line said that I don't know how I'm still standing, but I deleted it. Because I DO know.

I'm standing because of my family. Tragedy generally does one of two things to relationships: tear them apart or super-glue them together. Tragedy sucks, but it's still been my super-glue. I love being in the same room as the people I love, and I'd walk through fire for them.

I'm standing because of the amazing human beings I've met since being thrust into the world of Batten disease. My hero at the moment is Noah Coughlan, who's running across the nation for children like Taylor - almost 2,500 miles in just over four months. I'm truly honored that Noah's offered to share the pavement with me when he reaches Florida in July.

I'm standing because of my sister - my hero for the ages. She has the most evil, unfathomable disease on the face of the earth; it belongs in hell. She can't see, and she can't always say what she's thinking. But today she gave an awesome presentation on Moby Dick. Tonight she helped me push our cart through the grocery store - while singing a Bee Gees song. And for the first time all day, I really laughed.

Most of all, I'm standing because of faith. This past Christmas, a dear friend gave me a necklace with these words:

"FAITH is the strength by which a shattered world shall emerge into the light."  - Helen Keller

With the passing of each day, Taylor's survival falls somewhere farther away from logic. But as long as I'm surrounded by angels, I'll believe.