Wednesday, August 19, 2009

Final story


Friday, August 14, 2009
Childhood center gets loan in time

"Drink your milk," said the teacher in Spanish. The 2-year-old reached again for the glass before her, and after several gulps earned a milk moustache. Meanwhile, outside on the playground, teachers blew soap bubbles toward little hands eager to pop them. "Bubbles!" the children cried in English.

The large house where these toddlers play and are taught in two languages is home to a nonprofit that came under threat in November during the housing and economic crises. The House of Mercy's Rosemount Center, an early childhood development center in Mount Pleasant, found itself scrambling for funds to pay the bills for a previous, much-needed $6 million renovation. Its endowment had sunk in the crisis, its previous loan had fallen through, and it was looking for a new one.

"And in November that was not easy to do," said Barbara Jones, president of the House of Mercy's Board of Trustees.

Cardinal Bank stepped up to the plate and extended a loan to the nonprofit, allowing the House of Mercy and the Rosemount Center to stay afloat.

"We find it important to be supporting the community," said Kathleen Carr, president of Cardinal Bank Washington.

House of Mercy, the oldest Episcopalian charity in Washington, has been serving the District since 1884. Its origins began with a meeting in St. John's Church - the so-called Church of the Presidents, across from the White House.

The Rosemount Center, formerly a home for troubled girls and unwed mothers, changed its focus to young children more than 30 years ago, but still operates in the old home that was built in 1911. After almost a hundred years of use, the house desperately needed an update. Cardinal Bank is now supporting the Rosemount Center as it pays for its renovation.

And the center is supporting 323 families in the Washington area, many of them low-income. It offers Early Head Start and Head Start curriculums for children ages 6 months to 5 years, as well as home-based programs to help meet the needs of struggling families. Rosemount currently enrolls 147 children, and hundreds more remain on the waiting list, said Ms. Jones.

"There is a crying need for [the center]," said Jacques Rondeau, president of the Rosemount Center.

Marsha Riggio, interim program director, agreed, saying Washington lacks free early childhood development programs.

"D.C.-wide this is an issue, especially for those under the age of 3," she said.

It costs about $20,000 a year per child for the Early Head Start program, which serves infants and toddlers, and $9,000 a year per child for Head Start, aimed at preschool-age children, Mr. Rondeau said.

The Rosemount Center stands alone in the District in offering these programs for free in a bilingual setting. Seventy percent of children enrolled come from Spanish-speaking families, and children in every class have two teachers, one English-speaking and one Spanish-speaking. Many of them stay in the programs for all five years, and then enter kindergarten with bilingual abilities.

"The House of Mercy is critical to the well-being of low-income families," Ms. Carr of Cardinal Bank said.

Sunday, August 9, 2009

Cathedral


Friday, August 7, 2009

U.S. military is Cathedral tour's focus

Shrapnel, swords and bayonets crown Christ's head in the small side chapel, tucked between the expansive Gothic nave and another small room, the Children's Chapel. Stained-glass figures of war heroes - from Richard the Lion-Hearted to Nathan Hale - look down on Linda Strating as she addresses her tour group on its last stop, the War Memorial Chapel of Washington National Cathedral.

"I think it's so appropriate that the soldiers are protecting the children. Even the way [the builders] juxtaposed everything. ... Everything has a meaning," she says.

It was this meaning that inspired Ms. Strating, a volunteer docent at the cathedral, to craft the military-themed tour called Service and Sacrifice.

The Cathedral of St. Peter and St. Paul in Northwest functions as a church and place of prayer for the nation. It is the site for presidential funerals and memorial services for famous Americans - including Presidents Reagan and Ford and in May, former Rep. Jack Kemp. Also, every president since Mr. Reagan - with the exception of Bill Clinton - has attended Inauguration Day services there.

Ms. Strating started giving the Service and Sacrifice tours in May and has trained about seven other docents to give them as well. They are available upon request.

"The people that built this place had that [military theme] in their minds. I'm really just picking it up and showing it to people," she says.

Ms. Strating, whose father was an Air Force colonel and Korean War veteran, found her first inspiration for the tour in the cathedral's large stained-glass window honoring the Air Force. Building on her docent training and some of her own research, she created the hourlong tour that seeks to honor soldiers and the military.

The Washington National Cathedral is the sixth-largest cathedral in the world. Its first stone was laid in 1907, with President Theodore Roosevelt presiding. Two world wars and the Great Depression halted construction temporarily. The last stone was laid with in 1990 with President George H.W. Bush in attendance. It was built stone upon stone, with no structural steel, using the same methods medieval workers used. The only difference was help from cranes and trucks. Some plaques remain blank for future generations to commemorate future leaders and heroes.

The Service and Sacrifice tour highlights the cathedral's military connections in its history, sculptures, carvings and needlepoint kneelers. Ms. Strating starts at the oldest part of the cathedral, Bethlehem Chapel, where Adm. George Dewey is buried. Dewey served on the original planning committee for the cathedral and was first to suggest that the building be constructed in the Gothic style. Ms. Strating also points out that the chapel, completed in 1912, served as a place of prayer for many soldiers heading to the battlefields of World War I.

Ms. Strating also thoughtfully dwells on another member of the military who heartily supported the effort to build the cathedral: Gen. John J. Pershing. He helped raise $16 million for the cathedral in the first half of the 20th century - a key contribution, as the building was completely funded by private donations, not the Episcopal Church or the government.

"It's simply one huge present," Ms. Strating says.

In the Chapel of St. Joseph of Arimathea, Ms. Strating points out a mural's depiction of St. John. The saint's face was modeled after that of a young, thin student who worked to gain enough weight to join the Marines and died on the last day of the 1945 Battle of Iwo Jima.

The tour traces these threads - touching everything from the Civil War to Sept. 11, 2001, to the enormous cost of war itself - throughout the cathedral.

Military chaplains, veterans and families of soldiers soon to be deployed have all requested the tour. Ms. Strating remembers taking one man - a Walter Reed patient wounded in the head by a roadside bomb in Iraq - through the tour. They ended at the War Memorial Chapel, where the young war veteran was struck by the image of Christ as the ultimate heroic sacrifice, crowned with symbols of the devastation of war.

"His eyes opened up, and he was blinking, nodding his head. His mother started crying and said, 'He understands. ... This is the most peace I have felt since this happened.' "


http://www.washingtontimes.com/news/2009/aug/07/us-military-tours-focus/

Thursday, August 6, 2009

Tech story

Thursday, August 6, 2009

Real-time text capability on horizon

The next big advance in telecommunications may be a silent one. Widespread access to technology known as real-time text is likely on the way, largely as a result of the deaf community's petitions for increased accessibility.

Real-time text allows users at each end of a conversation to see each character as it is typed, even before they hit the "send" button. It would allow users to integrate text into their voice conversations, allowing them to type out addresses and names that are otherwise tricky to communicate.

"I think that we'll actually see situations where people are talking and typing at the same time," said Gregg Vanderheiden, director of the Trace Research and Development Center at the University of Wisconsin at Madison.

Every new phone will support real-time text if the federal agency that oversees accessibility for the disabled - the U.S. Access Board - adopts new regulations. And that is a move it is likely to make within the next few years, according to Mr. Vanderheiden.

The implications of real-time text on every phone are numerous, Mr. Vanderheiden said. Deaf people could use any phone to instantaneously communicate with any other phone, an ability that is especially important during emergency and catastrophic situations.

Though some 911 call centers are experimenting with emergency instant messages, they do not transmit until the user presses "send." With real-time text, a deaf person could type "I am having a heart attac," and even if the message remains incomplete, 911 would receive the characters.

Mr. Vanderheiden also predicted the hearing world would enthusiastically adopt real-time text, as it did captions for television, another initiative first championed by the deaf. Hearing users could use real-time text to supplement voice conversations or to completely replace voice in noisy environments.

Mr. Vanderheiden spoke last week before an audience of deaf, hard-of-hearing, deaf-blind and hearing individuals at the biennial Telecommunications for the Deaf and Hard of Hearing (TDI) conference in Washington.

Steve Brenner, a 72-year-old deaf Maryland resident, attended the conference presentation on real-time text.

"I think it's fantastic. It's really a revolution," he said. "We'll never be falling behind the hearing world. ... It blew my mind when they gave the presentation."

AOL Instant Messenger already incorporates real-time text, as do a handful of products geared specifically to the deaf. Google Wave, set to debut this year, has real-time text on steroids, Mr. Vanderheiden said. The e-mail, instant messaging and wiki hybrid lets people create a document together through instantaneous, simultaneous editing.

Claude Stout, executive director of TDI, said telecoms generally support new standards for accessibility and have a real desire to meet the needs of the deaf, though they seek out the most inexpensive way to do that.

Mr. Stout also praised real-time text for more closely resembling actual conversation than instant messaging. He also said it would serve as a bridge between the deaf and hearing communities.

"It will place us more on a level playing field," he said.

Mr. Vanderheiden agreed.

"The nice thing about text is the universal nature of it," he said.

http://www.washingtontimes.com/news/2009/aug/06/silent-revolution/

Monday, August 3, 2009

Full page color clip, with four photos


Sunday, August 2, 2009

Home sweet McDonald House

Paper signs guard the two doors. "ISOLATION," they warn in bright yellow. "Do not enter this area." Inside, a boy calls himself "the prisoner" and his mother "the warden."

The boy must limit his contact with the outside world. In May, doctors eradicated his bone marrow with radiation and chemotherapy before transplanting new marrow into his diseased body. He is on the mend, but his white blood cells have not yet rebuilt their former defense system. A common cold could put him back in the hospital.

This is the story of Alex Ramsey, 16, and the house where he has lived for the past 60 days of isolation.

Alex has severe aplastic anemia - his body started killing its own blood cells. It is a terminal illness. In January, he and his parents found themselves choosing between life spans: Should Alex continually receive blood transfusions and live perhaps another 20 years? Or should he undergo chemotherapy and bone-marrow transplant - fraught with risks - and perhaps live to a ripe old age?

They chose the transplant. However, finding a place to live during the chemotherapy, transplant and subsequent 100 days of isolation proved difficult. It was too long to drive every day to Washington, where their hospital is located, from their home in Hampton, Va. Hotels were expensive, and carpets there could hold thousands of germs lethal to the boy. Then a hospital social worker told them about the Ronald McDonald House, which offers housing at a nominal cost to families in situations similar to Alex's.

"The Ronald McDonald House has been the healthiest and safest bet. And the cheapest. The only thing that would have been better is staying in our own house," says Alex's mother, Missy Leonard.

So for Alex and his mother, the Ronald McDonald House jokingly became their "prison" but in reality became their sanctuary.

ALEX

In October, Alex scratched his leg on the way home from a Boy Scout meeting - just a small cut that should have scabbed quickly. It didn't. It kept bleeding and wouldn't stop. So his parents took him to the emergency room, where they discovered his blood platelets had essentially vanished. The count was 2 - a low normal is 141. After numerous tests, transfusions and a week in the hospital, Alex was diagnosed with severe aplastic anemia.

"I was scared because I had no idea what it meant, no idea what was going to happen. And of course, the typical mom thing: 'Why? Why my child? Why me?' " Ms. Leonard says.

Alex's disease is what doctors call idiopathic, meaning they do not know how or why he got it. It is not hereditary. It is not necessarily a childhood disease.

Unlike anemia, aplastic anemia causes the body to kill off all blood cells - including white blood cells and platelets - not just red blood cells. This wipes out the immune system.

"In other words, I'm my own worst enemy," Alex says.

However, rather than continue to live in fear after his diagnosis, Alex's family chose to remain positive. His father refused to believe his son's disease would be terminal. His mother remains upbeat and cheerful. Together she and Alex make an effort to have fun and laugh often, nicknaming nurses and bantering with them during hospital visits.

"Vomiting?" asked nurse Bonnie Yates, running through a list of symptoms during a recent checkup at Children's National Medical Center in Northwest Washington.

Alex pretended not to hear correctly: "Comedy?"

"Vomiting. Comedy I'm well aware of," she replied with matter-of-fact affection.

Alex's mother says they try to go through their days tongue in cheek.

"We've had a lot of scary moments. But we don't live on them. We live on the fun times," Ms. Leonard says.

They also have poured their time into fundraisers for organizations that help children with terminal illnesses.

"Our way of coping with this was raising money and helping somebody else so that they could get healed more quickly," Ms. Leonard says.

Over the past year, they helped sell aplastic anemia wristbands to raise money for foundations that fight the disease, shaved Alex's head to raise $1,100 for cancer research and helped recruit more than 200 people to donate platelets to their local hospital during a recent shortage.

Now they want to help the Ronald McDonald House Charities (http://rmhc.org).

THE HOUSE

The little boxes by the cash registers at local McDonald's restaurants are easy to overlook. However, they help fund housing for the hospital stays of children across the nation, including Alex. The Ronald McDonald House on Quincy Street Northeast has 16 bedrooms, including one bone-marrow transplant isolation suite, where Alex and his mother stay.

The house, just a few minutes' drive from Children's National Medical Center, charges a nominal donation - $10 a night - for its services but sometimes waives even that. Brightly colored decor, a game room, toy room, computer room, patio and playground make the time pass faster for families.

But the Quincy Street house was built in 1912, and the cost of maintenance continues to increase. In addition, the house usually operates at full occupancy, with no room left for families, especially long-staying bone-marrow transplant patients - some of whom may be turned away and forced to find more expensive housing.

So the charity plans to build a new house with 26 bedrooms and four isolation suites. Donors already have given $4 million, but about $1.3 million remains to be raised, says Cortney Kelly, manager of the D.C. house.

Lynn Hardesty, a social worker at Children's National Medical Center, says the need for the new housing is acute.

"We have a growing number in our transplant population. People are coming from all over the area, from farther and farther away," she says, adding that if families cannot get into the Ronald McDonald House, they have to choose between hotels or apartments.

"There is no other low-cost option," she says.

Alex and his mother hope to help with fundraising for the new house. In addition, to celebrate the halfway mark of Alex's isolation period this month, they started gathering friends' donations of items on the Quincy Street house's "Big Ticket Wish List," including a crib, a highchair and a DVD/VCR player.

"Laughter was the best medicine for us. And helping others," Alex's mother says.

Friday, July 24, 2009

Holocaust memories. "We suffered terribly."


Friday, July 24, 2009

Holocaust experience

The 88-year-old woman still remembers the day of the week that Germany invaded Poland. Friday. She remembers the time on Sunday when German soldiers came to her town. Eleven a.m.

And she remembers the words of the Germans as they entered the city. "All the Jews out!"

As Helen Breitowitz, at age 18, stepped out into the courtyard to face the Nazis, she stepped into a world in which she can no longer imagine how she survived.

The clock ticks loudly as Mrs. Breitowitz sits in her Rockville apartment, slowly and patiently recounting her life and Holocaust survival. Though she became an American citizen in 1955, a thick accent still steeps her words. Photos of family - some killed in the Holocaust, some kept alive, some born after it - line her walls.

She recounts the time before the war, when she dreamed to have a dozen nylon stockings. And she recounts the time during the war when all she wished for was a piece of buttered bread with cheese.

On Aug. 9, Mrs. Breitowitz and other Holocaust survivors will share their experiences at a luncheon sponsored by the Progress Club at Ring House in Rockville. About 20 survivors live in the retirement community. The club will invite young volunteers, club members and survivors' guests to gather and learn from the Holocaust experiences.

Mrs. Breitowitz says she and her family want the next generation to remember those years.

"In the beginning, we never talked about it. And in the later years, we never stopped talking about it," she says. "I don't know [why]. Maybe we wanted to forget. And now we think it's very important to talk about."

'Very much in love'

In 1935, Mrs. Breitowitz's best friend introduced the 15-year-old to David Breitowitz, who was then 18. He had come to Sosnowiec, Poland, to work and live with his brother.

They became neighbors. She lived in house No. 9, and he lived in No. 11. As she walked home every day from work, he came outside to talk to her.

Soon she called him "boyfriend."

As the Germans entered Sosnowiec in September 1939, Helen, her family and David hid in their cellar. They came out at the sounds of Nazi screams, and the soldiers arrested the men. The Nazis eventually released Helen's father and brother, but David remained in prison.

Meanwhile, the Nazis gradually were emptying the city of Jews, especially young women. Helen's parents sent her to Russian-controlled eastern Poland to live with an aunt and uncle and their two daughters. She thought she would never see David again.

"I was really, really, very much in love with him," Mrs. Breitowitz recalls. "It was a terrible time. We didn't know what to do. It's just impossible to imagine what was going on. People were running this way and that way."

Then one day, the doorbell rang. She opened the door. It was David.

"I was standing with my mouth open," she says. "I couldn't believe it. And he said, 'Helen, aren't you going to invite me [in]?' "

Mr. Breitowitz had escaped prison by making friends with one of the German guards. He was renting an apartment with his brother in another city. After showing up on Helen's doorstep, he traveled four hours by train to see her, every day, for two months. He wrote to her parents for permission to marry her. They agreed, but she couldn't leave her young cousins, for whom she helped care.

Then one day, the children were out.

"So he gave me an ultimatum. ... 'You have to go with me, and we'll elope.' "

So she did.

"Life is so strange," she says. "He really saved my life, my husband. Because I would have gone back with my aunt. And they didn't survive."

Her aunt, uncle and two cousins perished during the war. Her parents died at Auschwitz.

Darkness and cold

Five months after they married, Russian soldiers came in the night and arrested the young Jewish couple. It was May 1940.

The Soviets gathered the Breitowitzes and 1,000 other Jews who refused to become Soviet citizens or Communists or fight in the Soviet army. The soldiers loaded them onto cattle trains.

"We didn't have anything, just the clothes on our back," Mrs. Breitowitz remembers.

They traveled for six months by cattle train, trucks, large boats, small boats. The train rolled to a stop every night, and their captors gave them hot water, maybe soup, maybe bread. The soldiers forced them to walk for about a day to their final destination, a wood deep in Siberia.

"It was nothing. It was just a jungle with trees. No houses. Nothing, nothing. They gave us an ax and they said, you build your own houses."

The Jews had no knowledge of house-building, but it was November and bitterly cold. They eventually managed to build log cabins. Thirty people slept in a single cabin, kept warm by a large makeshift stove in the center of the room. The Russians gave them rations of wheat and barley. Some prisoners died from lack of nutrition.

"We suffered terribly," Mrs. Breitowitz remembers.

They washed themselves with snow. They cut ice with an ax and melted it for drinking water. There was no work for them to do other than daily to survive each day.

"All day long the women were talking about food, what we used to have, what we used to eat," she says.

The men played cards and dominoes.

Nine months of the year in Siberia were winter and constant darkness; three were summer and constant daylight. The prisoners fought bedbugs in summer.

The local Russians were kind to them, teaching them how to pick summer berries to supplement their diet. Occasionally the Russians would give them candy. Mrs. Breitowitz would eat hers right away, but Mr. Breitowitz would save his and give it to her later.

"We had such a good marriage. He loved me so much, and I loved him, too," she says.

The first winter, Mr. Breitowitz took his gloves off in the cold. His hands turned black with frostbite - "Just like coal," she says. She walked about 10 kilometers every day for several months to a nearby Russian clinic to bring him medicine. Yet he stayed sick, unable to move, until a Russian paramedic came and peeled away the blackened skin with tweezers.

"When he started to take off the skin ... I fainted in the room," she says.

Three years passed in the Siberian prison camp. The Jews were then moved to the Siberian city of Yakutz and then to central Russia. In 1946 - a year after the war ended - the Soviets finally freed them, gave them Polish passports and put them on a train back to their homeland.

"I cannot believe it, that we lived through, we made it," Mrs. Breitowitz says. She can now see the benefit of the suffering in cold Siberia - they were saved from German concentration camps.

"That was our salvation, that they sent us so far away," she says.

They returned to Poland to learn that her brother had survived Auschwitz but most of the rest of her family had been killed. Seven of her husband's siblings had died and also his mother.

"I came back to the city where I came from, and nobody was left," Mrs. Breitowitz says.

A life continued

In 1949, the Breitowitzes came to New York City

"I kissed the ground," Mrs. Breitowitz recalls, beaming while she speaks about America. "I am very grateful to America. I'm a big patriot."

She found work as a seamstress, and her husband, despite not knowing any English at first, became a salesman. He once sold two lamps to a woman who had no table.

"He literally could sell you the London Bridge," Mrs. Breitowitz remembers, smiling.

She says she thought her husband more handsome than Clark Gable. They stayed in love - she remembers how he even would clip her toenails and care for her calluses.

"I never went to a podiatrist, because no one could do it like him," she says.

He died in 2003.

The couple had two sons, both of whom are rabbis, nine grandchildren and one great-grandchild.

As the World War II generation ages, Mrs. Breitowitz wants her grandchildren to remember what happened during those years as the voices of Holocaust deniers speak louder.

"It's very important to me that the grandchildren should know how we survived. Because if it had not been for the survival, there would be no grandchildren," she says. "The Holocaust didn't start with the killing. It started with just words."

Monday, July 20, 2009

A favorite...

Sunday, July 19, 2009

Therapy in a saddle

When Joseph Grist was 6 years old, his doctors recommended equine therapy for his cerebral palsy. His torso and arms were very weak, his leg muscles contracted.Riding a horse, experts said, could strengthen his core and leg muscles. But when Joseph's parents looked for equine therapy centers, they found only astronomical costs and long drives.

So they thought of another solution.

"We looked at each other and said, 'Why not do it ourselves?' " Joseph's mother, Dawn Grist, said.

Thus the Grists began a journey that uprooted them from their six-figure jobs and their Gainesville, Va., home and planted them on a 35-acre farm. Three years, nine horses and more than 50 students later, they are convinced they are doing something good in the world.

Anthony and Dawn Grist run Misty Valley Therapeutic Riding Center, which provides riding lessons to disabled, handicapped and at-risk children. There are dozens of therapeutic riding centers across Virginia, and hundreds across the nation, but one thing about the Grists' stands out: It's free.

Mrs. Grist said therapeutic riding lessons usually cost about $45 per hour. Some centers charge up to $150 per hour.

At Misty Valley, riders only have to pay for their safety equipment: boots, helmet, kneepads.

Mrs. Grist said this usually surprises parents; some react negatively.

"They're usually looking for the hidden agenda," she said. "I've actually had people ask, 'Well, why don't you charge anything?' I say, 'Well, because it's a service that's needed, and some people can't afford it.' I guess it's just hard to believe that there are good people in the world who are trying to do the right thing."

LOOKING FOR A DIFFERENT LIFE

The Grists started by trying to do the right thing for their family. In 2005, they lived in an 8,000-square-foot house with nine bedrooms, six bathrooms and a nanny for their six children. Mrs. Grist was working 12-hour days, Mr. Grist 16-hour days. Together they made $550,000 a year. But something was wrong.

"Our family life was nonexistent. Our nanny was raising our kids," Mrs. Grist said.

They also needed therapeutic riding lessons for Joseph.

So Mrs. Grist quit her job, and the family moved to their investment property in Culpeper. Mrs. Grist, who had taught horseback riding in the past, became a certified therapeutic riding instructor and completed a yearlong internship to learn how to work with various disabilities.

They started Misty Valley in 2006. This year, they have 41 students, whose disabilities range from Down syndrome to autism to muscular dystrophy.

"It's so rewarding, just to see the kids smile, when you see a kid change over time," Mrs Grist said. "I get a lot of satisfaction helping and giving back to the community. I've been given so much in my life and can now give back to people."

The couple also have accomplished their original goal: helping Joseph. Mrs. Grist said riding has strengthened his muscles and also his confidence.

"It's amazing the difference it's made in his balance and coordination and just his self-esteem," she said. "He's never going to run track or play football. ... He's just not physically capable of those things. But when he's riding horses, he's on the level playing field with everyone else."

STRENGTH IN RIDING

Dee Brown's 5-year-old daughter, Cheyanne, takes lessons at the Grists' farm. A therapist at her school recommended riding at Misty Valley to help Cheyanne's autism and attention-deficit/hyperactivity disorder.

"We couldn't keep her focused very long on one thing, which causes educational problems in school," Ms. Brown said.

Since Cheyanne started riding in March, her attention span has increased from eight minutes to 40 minutes, Ms. Brown added.

Therapeutic riding works because it treats the whole person, said Sandy Artichoke, program and projects manager for the North American Riding for the Handicapped Association (NARHA).

"The horse has a three-dimensional motion that is closely related to a human walk," she said. "So when a disabled person is riding, they get the kind of motion they wouldn't get on an exercise machine."

Riding can build muscle strength and tone and also help riders emotionally.

"They'll bond with an animal much more quickly than they will a human. They might open up and let some things go," Ms. Artichoke said.

Ms. Brown said riding is teaching Cheyanne, who struggles with change, how to adapt. The young rider has a favorite horse, Trigger, and having to ride different horses helps her understand "you don't always get what you want," her mom said.

In the past, doctors recommended after-school activities such as dance or gymnastics for Cheyanne.

"And all of these things are expensive, not just the course itself, but the fuel to get there," Ms. Brown said. "I couldn't afford it. There was just no way."

She said she could not afford riding lessons if not for Misty Valley.

AN UNCERTAIN FUTURE

Mrs. Grist said she doesn't know if her riding center can stay open next year. Despite some fundraisers and donors, about 90 percent of the center's funding still comes from the Grists' own pockets, and Mr. Grist had to take a lower-paying job. At minimum, it costs $1,200 per month to keep Misty Valley open. Unexpected costs, such as a recent $700 veterinarian bill for a horse's sliced foot, make it even more expensive.

Mrs. Grist said they don't want fundraising to cover their mortgage or personal expenses, but just basic costs for the center, such as horse feed.

They also would like to buy an adaptive saddle - a $6,000 device that would enable amputees and those with certain muscle disorders to ride. A recent yard sale supported by riders' parents raised $200 for the saddle. If they can raise the additional funds, Misty Valley could start helping more local students and also veterans from Fort Myer.

The Grists are applying for various grants, including one from the Christopher and Dana Reeve Foundation, but so far, the future remains unclear. If they don't find outside funding, Mrs. Grist said, Misty Valley may have to start charging riders a nominal fee or close its doors.

"That's really what I'm trying to avoid," Mrs. Grist said. "I don't want to give up helping these kids. I really don't."

Tuesday, July 14, 2009

Culinary classes under pressure

Tuesday, July 14, 2009

Culinary arts classes pare down

In 1995, 20 D.C. high schools worked with a successful nonprofit for culinary education. This fall, the vocational training program is scheduled to work with two.

The Careers through Culinary Arts Program (C-CAP), a curriculum-enrichment program that gives teacher training, equipment and scholarships and hosts student cooking competitions, is being slowly cut from D.C. schools, even as a film touting the success of the program in Philadelphia opens this week in the District.

The independent film "Pressure Cooker" features educator Wilma Stephenson's culinary "boot camp" and three of her students' journeys to college and scholarships through the C-CAP program. It will run at the E Street Theatre for one week, starting Friday.

Meanwhile, the District's C-CAP program has been steadily dwindling. In the 2006-07 school year, eight schools participated. In 2007-08, six. And in 2008-09, three. This fall, Ballou High School in Southeast will have a nighttime culinary class, and Roosevelt High School in Northwest will be the only remaining daytime culinary arts program in the District.

Iris Wilson coordinates D.C. Public Schools' Academy of Hospitality and Tourism, a career-training program that operates within schools, including Roosevelt. She said the C-CAP decline results from budget cuts, funding, teacher availability and the city's emphasis on reading and math.

"A lot of it is funding. Culinary arts is what we call a big-ticket item," she said. "If you're not going to have the latest technology involved in working with these industries, you're really doing these students a disservice."

But as other D.C. schools cut their C-CAP classes, the nonprofit will move into 11 Prince George's County schools, starting this fall. C-CAP founder and President Richard Grausman said the county's programs will help C-CAP stay in the area until the District is able to participate again.

Troy Williams is the C-CAP program coordinator for D.C. and Prince George's County. He said D.C. schools' career preparation now operates on a different vision.

"I just feel D.C. has a lot of other focuses right now, other than culinary," he said.

The D.C. culinary classes will now be more narrowly focused and rigorous. Mr. Grausman sees that as a problem.

"[D.C. schools] took on curriculum from different organizations that was beyond what their teachers could teach and their students could learn. We have been saying for years, that for inner-city schools, where their budget is nonexistent or very small, that teachers should focus on giving their students the ability to get entry-level jobs."

He said high school culinary classes need to focus on "soft skills" -- initiative, punctuality, teachability -- and basic industry knowledge, such as sanitation, knife skills and identification of products and equipment.

"They need to be a realistically achievable package," Mr. Grausman said, adding that the pressure to have larger curriculums and larger recipe lists pushes up the costs of programs.

Ms. Wilson doesn't deny that a more rigorous curriculum is also more expensive, but she said, "Our students can and have stepped up to the challenge."

To make sure D.C. students have the latest technology at Roosevelt, the school district installed a $1.5 million facility that included a full-scale commercial kitchen, a bakery, a 100-seat cafe and a mock hotel lobby complete with front desk and an industry-standard guest-registration system.

The D.C. program now pushes students to graduate with both a high school diploma and professional certification, which Ms. Wilson says chefs increasingly need to enter the industry. Thus, the tougher curriculum.

"If you're a slacker here, you're not going to make it, because it's too competitive," she said.

Basia Davis,18, made it. She graduated from Roosevelt this year with an $80,000 scholarship to Johnson and Wales University's culinary program in Charlotte, N.C. She won the money through a cooking competition hosted by C-CAP, and that made college an attainable goal.

"It took a big burden off of my family's shoulders," she said.

Miss Davis competed in several culinary contests across the nation this year. She said the lack of competitors in the District made it harder to hone her skills. She and her classmates had to practice against one another.

"It's hard to master your field against somebody when you're going against your friend," she said.

She said she hopes the District doesn't continue to cut culinary education "because that's a great opportunity for us."