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Meet the Barnhart Family

I had never heard of a Legacy Retreat® or Inheritance of Hope (IoH) until my daughter, Emma Barnhart, told me about it – how her family had been nominated to be a part of one of those retreats and how excited she was about Inheritance of Hope’s purpose and mission statement. They exist solely to honor families where one parent has a life-threatening illness. And in that honoring, they also offer fun, support, a listening ear, a shoulder to cry on, and assistance in leaving a legacy.
 
“Every person deserves a legacy,” Emma said, “even if it’s a story of an excitedly terrifying ride on a roller coaster! How cool is that?”
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Meet the Reese Family

Paul Reese and his family live in Mississippi, but lately he hasn't been home very often.
 
Paul makes regular visits to his oncologist in Little Rock, Arkansas. His wife, Cheryl, started training with a ministry in Missouri. And in May the Reeses attended an Inheritance of Hope (IoH) Legacy Retreat® in Orlando.
 
“This has been one of the most unusual summers of my life,” Paul said. “I have probably spent more time away from home than at home.”
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Meet the Allen Family

Rawd Allen was first diagnosed with brain cancer in 1994, but February 2014 happened to be the opportune time to attend an Inheritance of Hope (IoH) Legacy Retreat®.

 
Rawd's last tumor surgery was 10 years ago, when his children, Nathan and Jordan, were very young.  Besides a seizure, Rawd’s wife, Jan, said her kids saw very little of Rawd’s illness.  However, doctors noticed spots during a routine check-up late last year.  The Allens were preparing for Rawd to resume treatment when they received an opportunity to go to Disney World with Inheritance of Hope.
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Meet the Rye Family

The wintry weather in New York City was a bit of a challenge for the Rye family from Florida, but Joel Rye said it didn't stop his family from making memories at the Inheritance of Hope Legacy Retreat® in November 2013.
 
“We'll always remember all the people of IoH being so loving and giving,” he said. “It was just stress free.”
   
The past two years have been particularly challenging for Joel's family. Almost a decade after doctors first discovered melanoma on his ear, Joel learned his cancer had spread. Doctors said he had mere months to live.
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Meet the Johnson Family

At first Paul and Alexis Johnson from Fresno, Calif., weren’t sure if the Inheritance of Hope (IoH) Legacy Retreat® was right for them. Paul was feeling better and their children were both less than three years old. But much in their past five years has been unexpected.

“When you’re living your life MRI to MRI, it’s hard to plan ahead,” Alexis said.

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Meet the Maier Family

“We knew about Inheritance of Hope (IoH) for a while but never realized how incredible it was until we were a part of it,” said Jay Maier.  Jay, his wife Tara, and their five children lived near IoH Legacy Retreat® Director Jill Thompson in Rochester, Minn. Tara said her family prayed for the families that went on Legacy Retreats® but didn’t expect to attend one themselves.

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Meet the Young Family

Phyllis Young learned about Inheritance of Hope when a local North Carolina television station featured the organization. She immediately knew her family would enjoy going to an IOH Legacy Retreat®.

“I knew we took things for granted and we needed to take some time to step back and enjoy being a family,” she said.

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Meet the Martin Family

When Amy Martin from North Carolina was diagnosed with ovarian cancer in 2007, her two oldest children, John and Jennifer, were respectively off at college and working in California. But her youngest, Lyndi, was 7 years old and still lived at home.  “She has grown up with the ups and downs of the cancer world,” Amy said. “You worry about

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Meet the Hichkad Family

Amanda Hichkad has stage IV cancer that started as cervical cancer in 2008 but spread to her spine, lungs, and liver. She’s been through surgeries, radiation, and 13 rounds of chemotherapy, and she visits doctors several times a week to keep the illness under control.

That’s all in addition to being the mother of three boys

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Meet the Coleman Family

Mike Coleman wears a patch to treat tumors in his brain that his 5-year-old daughter, Leah, calls his “snow cap.”

Leah has started kindergarten, joined the Girl Scouts, and loves dancing and Disney princesses. Although she may not know the technical term for her dad’s Novocure device, the Colemans from Lock Haven, Penn., started making efforts to

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