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Hennessy
For Hennessy, her Disney dream was more than a wish in the making.
It turned out to be an amazing succession of firsts for the outgoing
7-year-old! It was her first plane ride, her first cruise, and her
first time at the Disney theme park. Although confined to a wheelchair,
Hennessy found enough accessible rides to add to the thrills of
seeing Dora the Explorer and the Disney characters on board ship.
There was even a pool in the shape of Mickey's head! The vacation
fun was shared with her 3-year-old sister Alannah, her parents and
her grandfather.
Hennessey has been in a wheelchair since she was two years old.
That was when the cancer in her chest cavity, diagnosed when she
was just 1½ , was surgically removed. After surgery, a substance
was used to stop the bleeding, which reacted internally, compressing
her spinal cord and causing paralysis.
Her sunny outlook is remarkable. When asked by her classmates, "Why
are you in that chair?" Her matter-of-fact answer was, "I
have a spinal cord injury and my legs don't work."
One of the dream highlights for Hennessy was meeting the Disney
princesses at the magical castle. She was so excited-but her wonderful
attitude towards life puts Hennessy head and shoulders above any
fairy tale princess!
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Caitlin
A week on a dude ranch! It was a dream
come true for Caitlin, a lithe 7-year-old who loves horses! It didn't
take Caitlin long to pick her favorite horse at the Rocking Horse
Ranch in Highland, NY. "Brady had the best trot," explained
Caitlin. She not only rode him on the trails every day but learned
how to brush him down, feed him and take good care of him. At least
part of Caitlin's love of horses was inspired by Laura Ingalls Wilder's
Little House on the Prairie books and by Elizabeth and Felicity,
her two American Girl dolls whose characters and stories are based
in America's Revolutionary times. In spite of her Type I diabetes
which requires Caitlin to check her blood six times a day, she kept
on the go sun up to well after sun down.
Caitlin's parent's Laura and Don as well as her 10-year-old brother
Ryan accompanied her for the activity-filled week. "There was
something to do every minute," said Caitlin's mother. "They
had paddle boats, miniature golf, a climbing wall, haunted hay rides,
and a fun barn that was always open. It was a great week for all
of us."
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Jacob
Imagine being 11 years old, tackling
the grown-up sixth grade when the really serious learning
subjects start challenging students and already having faced
four surgeries with more expected. Welcome to Jacob's world. Jacob
was diagnosed with V.A.T.E.R Syndrome before he was even born. He
has only one kidney and his esophagus had grown through his lung
in vitro, a condition that had to be corrected immediately after
birth. Currently he deals with recurring reflux due to the flap
at the end of his esophagus not sealing correctly. His esophagus
is also narrower than normal, causing food to lodge there instead
of easily being swallowed.
Intelligent and quiet, Jacob is also an avid Yankee baseball fan.
When the weather is good, he'll likely be out hiking or riding his
bike. If it's not, Jacob will probably be found playing video games
with his brother Daniel or his friends. Jacob's dream was to have
his own unlimited video gaming system in his room. His dream became
a reality in November when several boxes filled with his X-Box,
Play Station, Wii and lots of games for each platform arrived at
his home. To say his smile was radiant doesn't even begin to tell
the story!
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Daniel
Daniel, age six, is a Red Sox fan who likes baseball, riding his
bike and playing video games with his brother.
Daniel was diagnosed at birth with Cystic Fibrosis and spends every
morning of his life doing breathing treatments to keep his lungs
clear. He has many medications that he needs to take everyday and
must watch his diet closely but always has a smile on his face.
Daniel's dream is to get slimed at Nickelodeon studios, which he
visited with his family in February 2008.
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Ariel Meets Cinderella at the Royal Lunch at the
Castle.
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Ariel
Thirteen-year-old Ariel of West Haven has Cerebral
Palsy and cannot walk.
Her dream was to go to Disney World and meet the princesses. Ariel
and her mother went to Disney in August and had a trip to remember.
Ariel got to eat lunch at the Royal Table in the Castle with Cinderella
and Prince Charming and many other princesses.
Ariel said this was definitely the highlight of the trip and that
she will never forget it.
Her mother confirms this: her daughter has not stopped talking about
the trip since they got home.
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Ryan
Ryan is a young man affected by severe Stevens
Johnson Syndrome.
A disease that affects the skin, this disorder causes a widespread
rash that can develop into blisters and mucous membrane inflammation.
Sometimes skin, nails and hair can peel away.
Ryan wanted a room makeover with a sports theme, and we wanted to
deck his environment out in style.
His space is now complete with a ping pong table, pool table, dart
board and a case to display his trophies.
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Mary
Mary, who suffers from Alagille's Syndrome,
a genetic liver disorder, dreamed of seeing Zebras and to swimming
in the ocean.
The Dream Team found a way to combine the two in San Diego.
Mary caught a flight with her parents and younger brother to a resort
destination on the Pacific.
They spent two days this April at the San Diego Zoo, where the zoo
staff worked with us to arrange behind-the-scenes time and tours
of the Zebra and Elephant facilities.
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In Memory of . . .
Sydney, Bryanna DeSouza, Zachary Zowine,
Samantha Potter, who have recently passed away. The volunteers of
Dream Come True would like to express our deep regrets to the families
of these dream children.
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