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Creatively Speaking

The Smallest, Bravest Walk-a-thon
There was once a dreadfully wicked hobgoblin who decided to make a looking glass that would reflect everything that was good and beautiful in such a way that it would look dreadful or at least not very important. When you look in it, you would not be able to see any of the good or the beautiful in yourself or the world. If there was anything that a person was ashamed of or wanted to hide, you could be sure that this would be just the thing that the looking glass emphasized.

After the glass was finished, the hobgoblin's assistants carried it up to the heavens. They hoped that perhaps God himself would look into it! But as they reached the heavens, a great invisible force stopped them and they dropped the dreadful looking glass. And as it fell, it broke into millions of pieces.

Each of the pieces was hardly as large as a grain of sand, and they flew all over the world. If anyone got a bit of glass in his eye there it stayed, and then he would see everything as ugly or distressing. Everything good would look stupid...

Adapted from "The Snow Queen,"
By Hans Christian Andersen


When I first came up with the idea for the first Forward Face Walk for Awareness of Facial Difference, I hoped that through the walk we could start gathering up the pieces of shattered glass from the hobgoblin's mirror and toss them away where they could do no further harm. Someday, I hope, through education and awareness that individuals peering into a looking glass will see themselves as well as people with facial differences as good and beautiful people. A lofty goal, worth striving to achieve, especially for those of us who grew up with or have a child with a facial difference due to a craniofacial condition.

Even though craniofacial conditions and their often resulting facial differences are not that rare, the general public knows relatively little about them.

Forward Face through its lifetime has helped many children and families cope with the emotional and social issues of growing up with a facial difference.

In the autumn of 2003, when the Forward Face education committee was trying to think of ways to promote social awareness of facial differences, I put forth an idea I had been thinking about for a while.

" Why don't we have a walk," I asked. "What better way to be recognized then to put ourselves right out there on the street for people to see."

Dina, a new Forward Face board member, was also born with a craniofacial condition. We had met many years ago in 1980, when I was conducting a series of workshops to help teens cope with the issues of growing up with a facial difference. Eleven at the time, Dina was shy and quiet. Dina 's mother had hoped the workshop would help Dina become more outgoing. Dina only came to one workshop and I never saw her again until a few years ago when we met up at a Forward Face function.

It seemed liked fate had hooked us up again to plan the walk.

Once underway, Dina and I soon realized we had no idea how to start planning a walk. What do you do? We did the easy part. We picked the date and place, Sunday October 3, 2004. The walk would take place on the Hudson River Park walkway on the West Side of Manhattan along the Hudson River. We started gathering information on how to plan a walk and were alarmed to find out that the planning should start a year before the walk is to take place. We had started planning in May for a walk we wanted to execute in October of the same year.

With a few phone calls we learned that we needed a walk permit. We held our breath after applying for the permit. Had we applied too late? What would we do if we had? Finally we got our permit. EXHALE!

What Dina and I lacked in knowledge and experience we made up in determination and enthusiasm.

As we planned the walk, Dina and I meshed into quite a team. We had no conflicts, only contrasts. We talked almost every day about small issues and at times, what seemed like insurmountable problems.

In the early part of July 2004, Forward Face was suddenly left without an executive director. Up until then Dina and I had huddled under the protective umbrella of the director's knowledge in planning events. Now we were on our own.

After hearing the news, we went to an outdoor caf≥ in Manhattan not far from the Forward Face office. We sat there wondering if we could do this by ourselves.

" Hanna is going to be so disappointed if we can't pull this off," said Dina
Hanna is Dina's niece, who at the time was six.

" Why is Hanna going to be disappointed," I asked.

" She wants to walk," Dina said. "She wants to help make people aware of facial difference."

Dina had always been open and honest about her facial condition to her niece and nephews. She wanted them to learn at a young age not to be afraid of people who are different. And Hanna sure did learn. She wanted to walk for the cause. Hanna proves that with knowledge and awareness, children can embrace difference.

I have always believed that when you are faced with a dilemma an answer is provided for you, so when God whispers, I listen. And he whispered through Hanna. I knew we had to go on.

" Dina," I said. We are going to get this done. We are going to do it for Hanna."
From then on neither of us could afford to doubt our ability to organize the walk. Hanna depended on us.

Sunday, October 3, 2004, we couldn't have asked for a better day, a pristine day with a clear blue sky without a speck of white in sight. The day of the walk had finally arrived and everything was in place. As the walk drew closer, the Forward Face board and office staff provided us with plenty of support, and extra hands.

About an hour before the walk started, I rode down to the finish line with a couple of other Forward Face board members to make sure everything was in place. When we returned back to the start area, all we could see was a mass of baby blue T-shirts.

Dina came up to me and said, "You are not going to believe this, we have close to 100 walkers."

Shortly after the walk was underway, I turned around to gaze at the almost one hundred people, those with craniofacial conditions, their families, friends, Forward Face supporters, and Hanna all wearing T-shirts saying: WE BELIEVE IN THE GIFT OF FACIAL DIFFERENCE.


By Christine Karlsson