Face the Press without Stress

There’s no publicity like FREE publicity, especially if you run a small business on a small budget.

Right now I’m the media manager and PR-advisor to “Music for MS,” a benefit concert organized by and featuring my wife.

It’s my job to drum up as much media interest for this event as possible, and fill up the venue on February 26th by word of mouth and other means.

Every glossy flyer or multicolored poster we would print or ad we’d have to buy, would mean less money for the cause (the National Multiple Sclerosis Society), so I’m not doing that. Instead, I’m mobilizing the local press and I’m using social media to reach out to the community. It saves tons of paper which makes it eco-friendly.

The official campaign began yesterday, and so far we’ve already landed two interviews. This is where things get serious. Anyone can write a glorious press release, but not everyone does well on radio, television or in the papers. I know what I’m talking about because I have trained hundreds of people to get ready to meet the press.

One of the first things my students would always complain about is the focus of the media: Why do they only cover sensational stories? Why has the news become so superficial? Why don’t they come to me for a story? What they’re really saying is this: “Paul, you’re a journalist. I’m interesting and you should interview me!”

My knee-jerk response would be: “No you’re not, and why should I?” But of course I’d keep that to myself. Here’s what I’d say instead:

1. You have to have a hook to be heard.

If your name is Kim Kardashian or Paris Hilton, you don’t have to do anything special to attract the attention of millions. In fact, that would be your only accomplishment: being famous for being famous. Mere mortals such as you and me have to give the news media a good REASON why they’d want to come to us. A hook. Preferably with fresh bait.

News is the report of an event that is:

  • recent
  • unusual
  • previously unknown and
  • interesting and relevant to a great number of people

Let me add something to that definition: If there’s nobody to cover it, it’s not news. Fortunately or unfortunately, these days, all we need is one idiot with an iPhone.

Secondly, news is news if conglomerates like Rupert Murdoch’s News Corporation or Bertelsmann AG decide we should learn about it.

Third, news is news if the corporate sponsors (or other powers that be) feel it does not undermine their interests. (click here for an example)

Fourth: the more local the outlet, the lower the bar for what is deemed to be newsworthy.

Let’s assume you’re a voice-over professional hoping to attract some interest from the local papers. You’ve just completed another audio book. That’s something recent, but is it news?

Well, it depends on how unusual the book is and how many people would be interested in it. If we are talking about the audio version of Hitler’s secret diaries that were thought to be lost, you might have a story, but I don’t think this type of publicity would do your career any good. Which brings me to my next point.

2. You have to have a clear objective.

What do you ideally want to happen as a result of the media attention you hope to generate? Unless you’re hungry for recognition, an interview is just a means to an end.

In the case of my concert, the overall goal is to raise money and awareness for the fight to find a cure for Multiple Sclerosis, a chronic, mysterious and often misunderstood disease of the central nervous system. In order to accomplish that I need as many people as possible to come to the concert. This gives me a way to measure the success of my campaign.

Please note: what you hope to accomplish and what the journalist wishes to accomplish, might be two very different things!

If you don’t know what you want to get out of the interview, don’t do it. Just because you can, doesn’t mean you have to. It’s better to wait for the perfect opportunity than to waste a mediocre one.

If you do have an objective in mind, it’s time to go to the next step:

3. You have to craft a compelling core message.

If you could summarize what you’d like to get across in one or two sentences, what would it be? Let me put it in another way: If at the end of the interview people would only remember one thing, one powerful image or one great idea, what would you want that to be?

That should become the heart of your message, and it is your mission to get it across no matter what.

In the age of information overload, it is harder and harder to cut through the clutter and be heard. People scan the news and rarely look past the headlines or sound bites, so give them headlines and sound bites. You’ll survive.

I don’t care if you think it’s shallow or giving in to sensationalism. Should you get the chance to reach thousands, if not millions of people, don’t waste it by being boring. It’s regrettable to be forgettable.

A sound bite is usually not something you’ll come up with when the intimidating cameras are rolling and you’re staring into the hot, blinding studio lights. Do not count on your magic talent for improvisation. You can’t wing it.

4. You have to be prepared.

Well, well… isn’t that a given? Of course you need to give it some thought. Or is it better to be spontaneous and ‘in the moment’? You don’t want to look too rehearsed, do you?

Here’s my take on that.

One of the biggest mistakes I’ve seen people make is not preparing for an interview. They’ve literally said to me: “But I’m the expert. You can throw any question at me any time. I don’t need interview training.”

Just because you’re an expert doesn’t mean you’ll do well during an interview. Readers, listeners, viewers… they all hate pompous know-it-alls that talk over people’s heads.

I have seen great thinkers, captains of industry and even bishops nearly faint because they couldn’t handle the pressure of the simplest unexpected question.

They approached a 2-minute interview as if they were delivering a half-hour sermon, and when time was up, they had said nothing of significance. Of course they’d blame the network for not giving them enough air time.

Everyone who’s ever been interviewed will agree with me: When you’re in the hot seat, time as we know it does not exist. In the stress and excitement of the moment, people forget the simples of things such as their middle names and the phone number of the organization they’ve come to promote.

Here’s the good news: it doesn’t have to be that way. In the next installment I’ll tell you what you need to know before you meet the press.

Meanwhile, have you ever been interviewed?

What lessons did you learn?

Paul Strikwerda ©2012
www.nethervoice.com
Be sweet. Please retweet.

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The Seven Deadly Words

No matter how tightly you run your ship, not everything will always go according to plan. That’s life. What matters is how you deal with setbacks, mistakes and mess-ups.

Whether you run a one-person operation or you employ over 33,000 people worldwide, if you don’t go out of your way to treat your customers as if they’re the most important asset to your business, you’re playing Russian roulette with your reputation. This week, US Airways completely dropped the ball.

Before I tell you what happened, there’s something you should know.

My wife has Multiple Sclerosis (MS), an incurable chronic disease of the central nervous system.

Symptoms differ from person to person, and can include muscle weakness, spasms, numbness, coordination and balance issues, problems in speech and swallowing, bowel and bladder difficulties, visual problems and fatigue.

We don’t yet know what causes MS, but we do know that MS symptoms can be triggered by physical exertion, overstimulation, temperature changes and stress.

Now think about the joys of modern day air travel. Who doesn’t feel overstimulated, stressed and fatigued after a day of going in and out of airplanes? Even if you don’t have MS, it can wipe you out.

Since my wife was diagnosed, we have learned to pace ourselves. Take our flight to Fort Lauderdale. My wife was invited to speak and perform at an MS gathering (she’s a flutist), and we were scheduled to arrive in the early afternoon. That way she would have plenty of rest to be ready for her appearance the next day.

Unfortunately, our first flight to Philadelphia was delayed by thirty minutes. When we were in the air, the flight attendant assured us that we would make our connecting flight to Florida, as long as we’d alert personnel on the ground who were supposed to be waiting with a wheelchair. They would need to let the gate know that we were on our way, and that the doors of the plane had to be kept open.

That morning we learned three lessons:

1. Don’t expect employees of the same airline using the same computer system to communicate with one another, let alone pay any attention to instructions.

When we arrived there was no wheelchair, a scene that would repeat itself at different times at different gates and different airports. As one of the pursers remarked: “The guys responsible for getting you off the plane are usually chatting or playing with their cell phones. We almost always have to get them.” And as we were waiting, time was ticking away.

2. Never trust or act upon the advice of one employee.

We asked four different people involved in ground transportation to notify the gate that we were coming. Some told us they couldn’t do that. Others shouted “Later!” and never did.

In order to get to the gate, my wife had to jump into an electric car, onto a shuttle bus and into a wheelchair that took her to another electric car. For fit and able-bodied people this is no big deal, but if you have MS it is an ordeal.

3. People are oblivious of their environment.

If you’ve been at an airport lately, you might have noticed a strange phenomenon. Almost everybody is connected to some kind of portable device, which completely disconnects them from reality. They’re all in their little bubble, totally unaware of, or seemingly uninterested in the rest of the world.

This becomes obvious when you’re in one of those electric cars used to transport passengers from gate to gate. Don’t expect people parading the aisles of the terminals to step aside. They don’t see the car coming. They don’t hear it beep. They don’t hear the driver shout. And when the car finally manages to pass by, people look peeved because they were almost run over.

Meanwhile, the passengers inside are holding on for dear life as they try to balance their bodies while keeping their luggage from falling off. The jerky movements of the car as it is attempting to avoid human roadblocks, are enough to make a healthy person seasick. Believe me, by the time we arrived at our gate, my wife wasn’t doing so well.

That’s why it was a huge relief to see that the plane was still there. As I was taking our luggage off the car, the woman at the US Airways desk looked at me and said in a stern voice: “Sir, this gate is closed. The plane is leaving.”

I said to her: “Did anybody notify you that we were on our way?” “No,” she answered. “Any chance we could still get on board?” I asked. We really need to catch that flight.” “Sir,” she said in an annoyed tone,  “I told you that this gate is closed. We do not keep planes waiting.”

I told her that I’d been on many flights that had left a few minutes late so as to accommodate passengers coming in from other flights.

The woman at the counter looked at me as if I had just murdered her baby. Then she said these seven deadly words:

“THERE’S NOTHING I CAN DO FOR YOU.”

There and then I learned my fourth lesson:

4. Body language is far more powerful than any word in the Oxford Dictionary of Current English.

“What are we to do?” I asked the unhelpful employee. “Go to Customer Service,” she said. “They will get you on the next flight.”

When our car took off again, the driver asked: “When you landed in Philadelphia, did you let the people on the ground know you had to catch this flight?” I told her we did. “Well,” she said, “There’s absolutely no reason why you should have missed it.”

As we approached the Customer Service desk, my wife had to get into another wheelchair. I could tell she was exhausted.

“Yes?” said the woman behind the counter. As I explained what had happened, I learned a few more lessons from the US Airways book of customer treatment:

5. Never give a customer your full attention. You have far better things to do. Keep on staring at your computer screen and continue typing.

6. It’s not important that you understand the customer. The customer needs to understand you.

7. No matter what happens, do not show any signs of empathy.

“So, you arrived late at your gate,” concluded the customer service rep. “Boarding time was over. Let me see when the next flight leaves.”

“But the flight attendant assured us we would make it,” my wife replied.

“She should never have told you that,” the rep said.

8. When things go wrong, blame someone else.

“We asked four people on the ground to make a call to the gate and no one could be bothered,” my wife continued.

“Sir, what are their names?” the rep wanted to know.

I looked at my wife who appeared to be fading fast.

“We were in a hurry to catch this flight,” I explained. “There was no time to write down people’s names. The driver of the electric car told me the gate could have been kept open a little longer.”

“She should never have said that,” retorted the rep. “Your next flight leaves in six hours.”

“But I have a medical condition,” said my wife. “I can’t wait that long. What do you suggest we do?”

“Sir,” said the rep, “I suggest you go to the gate and wait just like all the other passengers.”

THERE’S NOTHING I CAN DO FOR YOU.”

9. Ignore people in wheelchairs. Always talk to the caregiver.

At that point I was really getting ticked off. My wife was treated as if as she didn’t exist and I asked the rep to include her in the conversation.

“I have MS,” my wife continued. “I need to lay down. The right side of my face is already numb. I can’t see properly. I’ve lost my sense of balance and I’m having trouble swallowing.”

“Is there a place we could go to,” I tried. “A quiet place where she can put her feet up and close her eyes. A first-class lounge perhaps?”

“There are Minute Suites at the airport,” the rep said.

“That sounds like a solution,” I said. “Could you get us a room?”

“We could get you there, but we wouldn’t pay for it,” the rep answered. “It’s $30 per hour.”

“Look,” I said as I was getting increasingly frustrated, “it wasn’t our fault we missed this flight. In what way can US Airways accommodate us for what happened? I shouldn’t have to pay $30 per hour out of pocket.”

“Sir,” the rep responded, “you can always file a complaint and send us the bill, but I can practically guarantee you that we won’t pay for it. You missed that flight. THERE’S NOTHING I CAN DO FOR YOU.”

At that point I asked to speak to her manager.

When he arrived, my wife could hardly hold her head up and parts of her face were twitching. “I can barely swallow,” she said. “If I don’t lie down now, things will only get worse. Your employee said there was nothing she could do for us.”

The manager looked at me and said: “Sir, your wife is obviously upset. Could I talk to you alone for a moment?”

“Absolutely not,” I responded. “We are a team and we’d like to know what you can do to help us. We’re stranded for six hours and my wife needs to rest because she has MS. The longer we wait, the worse it gets. I don’t feel we should have to pay for accommodation. It’s not our fault we missed that plane.”

“Sir,” said the manager, “US Airways has no arrangements with any hotels and we can’t put you up at our lounge. That would be more expensive than these Minute Suites and we’re not paying for that. If I were to offer that to you, I would get fired. Now, do you want to get me fired?”

That did it for me. I snapped.

“All I want is a quiet space for my wife while we wait, and I’d like US Airways to pick up the tab. You turn this around and make it about you losing your job? This is not about you. This is about my wife.”

I stopped for a moment and looked at him. “The stress of having to deal with your customer service -or lack thereof- is triggering all of my wife’s symptoms. Can’t you see that? Are you sure you don’t have anything to offer to us?”

He said: “We did. We booked you on another flight and we told you about the Minute Suites. Other than that, THERE’S NOTHING I CAN DO FOR YOU. You have to be reasonable. I need your name and email address so I can file a report.”

Eventually, we ended up going to a Minute Suite and the organization that had invited my wife to speak, agreed to pay for a couple of hours.

Two hours later, when I stepped out for a moment, I saw the US Airways customer service rep drop off two meal vouchers for us. They were ten dollars each.

Our connecting flight to Fort Lauderdale was delayed as well, and as usual, there was no wheelchair waiting for us at the gate in Florida, even though I had specifically and repeatedly reminded ground personnel to make arrangements. After another half hour wait for the car service, we finally arrived at the hotel around 10:30 PM, 14 hours after we had left our home.

Stepping out of the car, it was as if we had entered a different world. Staff at the Mariott warmly welcomed us with a smile, and did everything they could to make our stay as pleasant as possible.

The next day I did some research on airlines and customer service. It turned out that Forbes-contributor Steve Denning had had a similar experience:

“The US Airways gentleman on telephone was the quintessential unhelpful bureaucrat from Hell. He was following rules and doing what he had been told was the right thing to do and saving money for the airline in the short run. The only problem for US Airways that his behavior was rapidly turning me into a vocal detractor of US Airways—someone who would tell the world how badly I was being treated.
The agent whom I met at customer service was trying hard, and was being very helpful and pleasant about it, but she was hemmed in by company policies that prevented her from delighting me:

• No system to deal with a recurring problem: The airline has no provision to deal with the obvious and recurring problem of people who don’t make their connection because of flight delays. Instead the problem is dumped on the passenger to solve, by waiting in a long queue, increasing the level of frustration.

Denning continues:

“Over the last two decades, there has been an epochal shift in the balance of power from seller to buyer. Today the customer has options and access to good information, can avoid companies whose principal objective is taking money from our wallets and putting in their own. As a result, companies whose primary goal is to make money are vanishing off the face of the planet, ever more rapidly. Studies show that the life expectancy of firms in the Fortune 500 is down from around 75 years to less than 15 years, and fast approaching five years.

(…) The future belongs to firms like Apple, Amazon and Salesforce.com which are dedicated to delighting us. It is some consolation that companies that do not delight us will not be with us much longer.”

As I was reading his words, my mind wandered back to that dreadful day at the airport. Like Denning, we had noticed that some people still seemed to care about the customer. I particularly remember that young guy whose shift had ended but he still insisted on helping my wife get to a room where she could rest. Or the lady back home at Allentown International Airport. She was there with a chair and she stayed with us until we were picked up.

As I said in the beginning: not everything always goes according to plan. When something goes wrong:

  • Acknowledge it.
  • Show some empathy.
  • Listen actively.
  • Understand first. Then be understood.
  • Be accountable.
  • Seek solutions.
  • Don’t make matters worse.
  • Make them right.

It’s a well-known fact that if a person has a great experience, they will tell only a few people. However, if that same person has had a bad experience, they will most likely tell 30 to 40 people.

Whether you run a one-person business or a global corporation, the reputation of your brand rests on the number of positive interactions your customers have with you.

Adopt the attitude that is central to the way the Walt Disney Company consistently delights its customers. When something goes wrong, here’s what they say to their employees:

10. It may not be your fault, but it is your problem. Do whatever you have to do to fix it.

How’s that, compared to: THERE’S NOTHING I CAN DO FOR YOU.

Paul Strikwerda ©2012
www.nethervoice.com

PS Have you had similar experiences? What is your number 1 customer service tip you’d like to share below?

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DRUNK and LAZY

The rumors started a few years ago. It all began when they had seen her struggle to get to the car. It was not a pretty sight.

Swaying from one side to the other, Jennifer stopped to take a breath and regain her balance. Her brain was telling her body to walk upright, with that strong, steady gait she had always been so proud of. But somehow, that message didn’t reach her muscles because she kept on waddling like a duck.

As she looked down, she realized how uneven the sidewalk was. Every tile that was sticking out turned it into an obstacle course.

She stopped again and looked at her neighbor’s porch. A shadow quickly moved away from the front window.

When she finally reached the car, she had to hold on to it, to stay on her feet. Jennifer opened the door and swung herself into the driver’s seat. When she drove away, she already felt exhausted, and the day had barely begun. She wondered how well she would do at the audition.

NEIGHBORS
The people next door were old school. They didn’t say much, and when they did, it was usually behind her back. Much of the world was a mystery to them, and yet, they acted as if they knew everything.

For one, they thought that Jennifer was lazy, because she hardly ever left for work in the morning. They had no idea that Jennifer had a state of the art voice-over home studio equipped with ISDN and SourceConnect.

Secondly, they were pretty sure that Jennifer was faking a handicap. One day, they had seen her walking with a cane. The next day, she seemed to be totally fine. Besides, she looked great. Sick people usually don’t look that good.

Perhaps Jennifer was feigning disability to get money from the government. How else could she afford the mortgage? After all, she had no job and people abuse the system all the time.

The neighbors also knew something else: Jennifer liked a drink or two… or three. That would explain the swaying and the stumbling on the sidewalk. In short: Jennifer was a jobless, lazy drunk who shouldn’t even be driving. She should be ashamed of herself!

THE STAGGERING TRUTH
This week is MS Awareness week, and like many other people who suffer from multiple sclerosis, Jennifer was gearing up for the annual Walk MS event in May. She needed sponsors for the walk and she decided to stay close to home. Jennifer loved to bake and had an idea: she would go door-to-door with her delicious home-made cookies and raise funds for the event.

As the oven was heating up, she thought back to the last meeting of her support group. That night, they had discussed the many misconceptions surrounding MS.

Larry, the facilitator, warned everybody:

“When it comes to a chronic illness like MS, if it’s not visible, it does not exist. In other words: as long as you’re not in a wheelchair, people tend to think that you must be doing alright.

Some folks think that MS is the result of a poor diet or negative thinking. In other words: you’re basically doing it to yourself. Eating healthy and an optimistic attitude alone could solve the problem. Wouldn’t that be lovely?

As you know, many MS symptoms are silent; different people have different symptoms and some of them come and go. There’s poor coordination, fatigue, vertigo, visual disturbances, tremors, spasticity, weakness, slurred speech, unstable walking, sensitivity to heat… do I need to go on?”

POLLING THE PEOPLE
“When they surveyed people in the UK about MS last year, almost half of the respondents couldn’t name a single symptom. Others believed that MS was contagious or inherited and almost always fatal. None of that is true. Mind you, the people that were interviewed were from a cross-section of the population. They weren’t exactly uneducated.

So, on top of suffering from a nearly invisible autoimmune disease, people with MS also suffer from these myths and misconceptions.”

At that point, Carlos interjected. He had been a flight attendant for many years, until MS had him grounded.

“I always tell people: Even though I have this disease, it’s not who I am. I’m still the same person. I don’t want your sympathy. I want your understanding.”

SPONSORS NEEDED
While Jennifer was making her cookie dough, I thought of the things I could do raise money and awareness. I decided that it was time to re-launch my campaign for the Walk. It’s called “Giving a voice to MS”. This is how it works.

There must be people who’d love to have their favorite poem or short story read by a professional narrator. Well, when you make a donation to my Walk MS-team, you can send me a short script and I’ll record it for you as my way of saying “Thank You”. You can donate from anywhere in the world. For now, my campaign is geared toward the general public, but I’m willing to consider corporate sponsorships for more substantial gifts.

This year, my goal is more ambitious than ever: I want to raise at least $1500 for the fight to find a cure. Here’s where things stand. My campaign started at the end of last year, and thanks to the generosity of one colleague, I managed to raise 25 dollars.

Every amount counts, but I really need to step it up if I want to come close to my target. Please click on the MS-banner on the right, for details. Even if you don’t need me to record something for you, you can still make a donation!

FEELING IT
Have you ever wondered what it feels like to have MS? Singer-songwriter Kristie Salerno Kent was officially diagnosed in November 1999. She made a short film about living with MS. Please take a few moments to watch it. I think you’ll like her approach. Depending on your computer, you might have to turn the volume up a little:

DOOR-TO-DOOR
Let’s pick up Jennifer’s story where we left off. Her scrumptious chocolate chip cookies were ready and wrapped with an orange ribbon. Within the hour, she had sold almost her entire batch to the people on her block, and there was only one house left: the neighbors. On her last legs, she rang the doorbell.

“What’s up with you?” asked the neighbor. “It looks like you were hit by a truck.”

“Oh well,” said Jennifer. “It’s the fatigue. I’ve been going door-to-door to sell these cookies for the MS Walk…”

“I know exactly what you mean,” interrupted the neighbor. I get tired too. We all do. Just get some rest and you’ll be okay. Why are you selling cookies? Did you join the Girl Scouts?”

“It’s for people who want to sponsor my team for the MS Walk in May. You get three for a dollar,” said Jennifer.

“MS… that’s what Michael J. Fox has, right?” asked the neighbor. “He looks fine to me. Saw him on the Olympics a few weeks ago. Once an actor, always an actor.”

“I believe he has Parkinson’s,” said Jennifer. “I raise money for Multiple Sclerosis.”

“I’ll tell you what,” said the neighbor. “I just gave money to those people in Haiti, and I’m sure you’ll make someone else happy with these cookies for Multiple… whatever it is. Right now, my pizzas have arrived.”

As Jennifer walked back to her house, the guy from Domino’s made his delivery.

“Sir, that’ll be $18.98”.

“Here’s twenty five,” said the neighbor. “Keep the change.”

Paul Strikwerda © 2010
www.nethervoice.com

FACTS*
MS is a chronic, unpredictable neurological disease that affects the central nervous system.

Approximately 400,000 Americans have MS, and every hour someone is newly diagnosed. Worldwide, MS affects about 2.1 million people. Even though there is no cure, there are now FDA-approved medications that have been shown to “modify” or slow down the underlying course of MS. In addition, many therapeutic and technological advances are helping people manage symptoms.

MS SOCIETY
The National MS Society is the largest nonprofit organization in the United States supporting research for the treatment, prevention and cure of multiple sclerosis. Approximately 83% of Society income is devoted to research and service programs that enhance the lives of people with MS and their families.

WALK MS
Every spring nearly 300,000 people unite across the country to participate in Walk MS. All walks have an accessible route so people of all abilities can participate. Funds raised support the Society’s research and services programs. For more information click on the MS banner on the right, and visit walkMS.org.

TO GIVE AND TO GET
And finally… If you’re enjoying my articles and found them to be of value, I am thrilled. But what would make me even happier, is if you were to make a donation as a sign of your appreciation. To add your contribution, click on the MS banner to go to my Walk MS site. Your support means the world to me! Thank you.

*Source: National MS Society

PS Are you ready for my most popular article ever?

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A Cure for Christmas

Easton peace candleHow much money would you pay to flip a switch? How about $770! That’s Superior Court Judge Jack Panella’s winning bid to turn on the Easton Peace candle. At 106 feet high (32 meters), Easton’s Peace Candle is the worlds largest non-wax candle.

Easton Pennsylvania is my home town, and if you look at a map, you’ll see that it’s right next to towns like Bethlehem and Nazareth. I always joke that I live in the unholy part of the county. Unholy maybe, but not unimportant. George Taylor, a signer of the Declaration of Independence, had a tavern in Easton where customers like George Washington and Ben Franklin used to enjoy their pint. The building dates back to 1753 and was recently sold for one dollar.

Kids might know Easton because it’s home to the Crayola Factory. And if you’re a boxing fan, you have heard of the “The Easton Assassin”, former heavyweight boxing champion Larry Holmes. On November 27th, Holmes helped his friend Panella to light the Peace Candle. How many men does it take to flip a switch these days?

O TANNENBAUM
Easton has a strong German heritage. Rumor has it that the Germans put up one of the continent’s earliest Christmas trees in Easton in 1816. There’s a plaque suggesting that the very first Christmas tree in America was erected here, but several other towns are making that claim as well. Do we really care? Then why am I telling you this?

Even though the Dutch are celebrating St. Nicholas Eve (known as “Sinterklaas”), I have my eyes and ears set on December 25th. In fact, I just narrated two versions of the Nativity story, one taken from the New King James Bible and the other one from the Good News Testament. These recordings are my thank you gift to those who are willing to sponsor me for taking part in the yearly Walk MS Event in the spring of 2010.

As a voice-over actor I do a lot of talking but not enough walking. Here are two of my reasons to start ‘walking the talk’ for MS:

  1. raise awareness
  2. raise money

MS buttonTHE BIG UNKNOWN
One of the unfortunate things about Multiple Sclerosis is, that it’s hard to pin down. Like Christmas, MS is a bit of a mystery. We’re still pretty much in the dark about a cause as well as a cure. MS symptoms are unpredictable; they differ from person to person and can vary from day to day. One day, you might see my wife Pam walking with a cane, struggling to get to the car. The next day, you might spot her on a morning walk in the park. That’s something people don’t always understand.

How can someone appear to be doing fine one day, and almost ready for a wheelchair the next? Well, luckily you don’t have to be an expert to be informed. But some people don’t get it, until they get it. Believe me, you don’t want to be that person.

Then there’s a group that seems to think that MS is “all in the mind”, and that MS patients are “faking it”. Thank goodness it’s a minority, but to address these kind of misconceptions, there are stickers and shirts that say things like:

“My disabling chronic illness is more real than your imaginary medical experience.”

or

“You can have my handicap parking spot, if you take my MS too!”

FAMOUS FACES
Raising money to fight MS is not always easy, in part because MS doesn’t really have a familiar face. President Josiah Bartlet in the West Wing (played by Martin Sheen) had MS; actress Teri Garr and television personality Montel Williams have MS , but other than that, there aren’t too many “celebrity sufferers” to champion the cause. I’m not saying that it’s a must, but it doesn’t hurt to have famous spokespeople with whom the public can identify.

Phil KeoghanThis year, “The Amazing Race” host Phil Keoghan took the MS Movement on a Ride Across America. Keoghan and others biked 3,500 miles from Los Angeles to New York City and raised half a million dollars.

GIVING A VOICE TO MS
My goal is not as ambitious, although I’d love to give Keoghan a run (or a bike ride) for his money! Phil had hundreds, sometimes thousands of people join him at every stage of his Amazing Ride. Corporate sponsors, local businesses and other teams injected his journey with cash. For now, I am just a one-man band, kicking off my “Giving a Voice to MS” campaign. That’s why I am asking you to join me, and please, let your friends, family and colleagues know about it too. The more the merrier, especially around Christmas!

LIVING AND GIVING
Meanwhile, snow has started to fall in Easton. The Peace Candle lights up the historic town square. I wish I could flip a switch and MS (and any other disease) would be gone forever. But it’s going to take a whole lot more than 770 dollars. We do need the wisdom of a Judge and the fighting spirit of a boxing champion to shine the light on Multiple Sclerosis, and find that cure. But in the meantime, there’s a lot that can be done to make the lives of people with MS so much brighter.

MS CureCome walk with me; join my campaign and become a sponsor, wherever you are! My Walk Website has all the details, including how you can get the 9-minute mp3 Nativity story read by yours truly.

Christmas-sample, NKJV

Christmas-sample, GNT

Thank you!

Paul Strikwerda © 2009

PS you’ll find more information about MS on the website of the National MS Society.

PPS Christmas 2009 is history, but we’re just warming up for the MS walk in May. On my personal MS-site, you’ll find a new voice-over thank you gift for your donation.

PPPS If you’re an independent contractor like me, you probably wear many hats. Can you afford not to? Either you run your business, or your business runs you. But is it possible to be everything to everyone? My next article is about a unique man of many talents, and his journey from Broadway to the center of America’s military power.

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