Dedicated To Helping Financially Needy Patients With Free Medical Air Transportation
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Airlift Hope is a non-profit organization serving patients in need and their families. We provide air transport to specialized medical facilities for evaluation, diagnosis, treatment and rehabilitation.

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Bonds Formed at Gathering of Eagles

Pilots in the Mid-Atlantic region had a chance to slip the surly bonds of the work week and come together for an eventful trip to Virginia Beach on Saturday, April 19. Seventeen volunteer pilots drove or flew to A Gathering of Eagles, the first of an annual event that featured a pilot briefing, a question and answer session, training for individuals wanting to become Community Representatives, and a banquet that recognized award-winning pilots from the region.

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Oceanfront 5K Race Raises Friends and Funds
Sunshine, blue skies and surf made the perfect backdrop for the blur of shoes crossing the finish line of the Ninth Annual Airlift Hope Run/Walk held March 10 at the Virginia Beach oceanfront.
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Proud member of:

Angel Flight Americ Combined Federal Campaign Independent Charities of America

Other Key Links:

Health Links National Patient Travel Center Office of Rare Diseases American Legion Child Welfare Foundation American Legion
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Mission – To provide free medical air transportation to those in need.

To ensure that no patient in need is denied access to distant specialized medical evaluation, diagnosis, treatment, or rehabilitation for lack of a means of long-distance medical air transportation.

 

Airlift Hope provides medical air transport for patients departing from: North Carolina and Tennessee.

Airlift Hope Story
Before the mid-1980’s, little was known about mitochondrial disease. Patients were likely to be misdiagnosed as having cerebral palsy, Parkinson’s or other disorders.

Such was the case with Emily, a 14-year-old girl from Ellicott City, Md., whose parents were told she had cerebral palsy. Emily, who exhibited symptoms at birth, is fully dependent and unable to walk, eat, or talk.

“Her disorder is in the muscular dystrophy family,” says her mother, Kathy.

Kathy is a former pediatrician who stays home to care for Emily and two other children who also have the illness but with milder symptoms. Kathy herself has mitochondrial disease and says her symptoms include muscle twitches, GI problems, a weakened immune system and allergies.

John, 7, has autism and Crohn’s disease. Kelly, 17, has severe ADHD. Both suffer from muscular problems due to low muscle tone and weakness.

Through advanced research, scientists have learned more about abnormalities in the molecular powerhouse known as the mitochondria, which converts glucose and oxygen into energy.

But due to an inherited condition, the mitochondria can fail, causing cells to lose energy and become damaged and even die.

Last summer Emily was able to take two flights provided by Airlift Hope —first to be evaluated and diagnosed, and then to undergo surgery.

“She seemed to enjoy the flight,” Kathy notes. “The pilots couldn’t have been more wonderful. There was no other way we could have gotten down there.”

Emily suffers from severe scoliosis and, following diagnostic tests, was deemed to be a good candidate for the spinal fusion surgery.

The complex seven-hour surgery required inserting rods and screws in her back.

“She was in the hospital for a week,” her mom says. “She is still on bed rest. It’s a long recovery.”

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