Living with Victory Ministries' Mission for 36 years is to give hurting people, worldwide, Hope and Encouragement through faith in God, while going through life's storms; bringing them from darkness to Light through Online Radio Podcasts and Community Outreach programs.  

We want to Introduce you to Jesus.  He is a wonderful Friend.  You will enjoy getting to know   Who He is, His personality and attributes, so you can fully know Who you are trusting; and that you can trust Him. 

He is not a distant God, He wants to walk and talk with you and, most importantly, He is FOR YOU, NOT AGAINST YOU!  HE LOVES YOU!


There is a Friend that sticks closer

than a brother

Proverbs 18:24

We invite you to receive Jesus into your heart and your life.  Receive the free gift He died to give you by repenting of your sins, turning from your old life and living for Him from this day forward.

I thank you that you died on the cross and shed your blood for my sins that I may live.  I choose, this day, to turn from my sins, totally repent and, give my life to you.

In Jesus name I pray, Amen.

If you have prayed this prayer, and truly repented of your sins and invited Jesus into your heart, your adventure of walking with Jesus has just begun.

The following verse explains how to walk with Him daily.

Hebrews 11:6 Amplified Bible

6 But without faith it is impossible to please and be satisfactory to Him. For whoever would come near to God must [necessarily] believe that God exists and that He is the rewarder of those who earnestly and diligently seek Him [out].

We must read His Word and pray daily.  Apply His Word and commandments to our lives.  Salvation is based on a relationship with Jesus.  The only way to have a healthy relationship is to talk with him daily.  Get to know your Friend; His personality and character.  Find a full gospel church and attend diligently.

We would be happy to send you material to help you with your walk with Jesus.



P. O. Box 1982

Maggie Valley, N.C. 28751


Call us 828 926-4600

For 35 years Tony and Laureen have served their communities by giving their time, energy and resources, as well as prayer to those they have served and are still serving.

Since 1984, when they helped a 2-year-old with AML, a serious form of cancer who was sent home to die because he only had a 10% chance to live and parents were already indebted to the hospital for treatments.  

They jumped in to help and Compassion Children's Foundation was born. By the way, that little boy is 35 years old now.  

Compassion now has become Living with Victory Ministries.  LWVM includes the Radio Ministry "Living with Victory" and our Community Outreaches; 

Fuel for Life Program-a program sending gas cards to various hospitals so that outpatient seriously ill children would not miss their treatments due to working parents having difficulty with gas prices.

Hospitals receiving gas cards: Arnold Palmer Children's, Fl, Nemours Hospital Children's, Fl, Pittsburgh Children's Hospital, PA, East Tennessee Children's Hospital, TN, and Mission Children's Hospital, NC 

CD Program-Free CDs to cancer patients of Laureen went through her time with breast cancer.  These are in the waiting room of Hope Cancer Center in Asheville NC and sent to anyone who requests them.

Hope & Encouragement Program-Free books and CDs to help hurting people through their storms, upon request.

We share our life stories of hope and encouragement through our faith in Jesus Christ.

After 51 years of marriage and all of the twists and turns through those years; bankruptcy, loss, breast cancer, just to mention some of the storms we have been through, we have learned Who our Rock is, Jesus.  We have, also, learned that He can be trusted.  

Helping families with seriously ill children, who were facing death, taught us the true values of life.

We share how God brought about miracles with these families and how He guided us every step of the way to be able to help them.  Without Him we can do nothing.  


We are very transparent when telling our experiences because we want you to know that, we know, and have been there.  We want to give you the Foundation that will never crumble under your feet when the storms are raging and the waves seem like they are about to over take you.  Jesus is walking on the water towards you. Stop Him and have a little talk!  

You too can have Peace, Joy and Victory in the midst of your storms.  We know, we have been there! 






                          ARMED WITH COMPASSION




            The Guy Who Started A  




   By Mike Thomas


Condensed from Florida Magazine

April 1990


The tumor was as big as a thumb. In Heather Allen's backbone, it pushed against the delicate nerves in her spinal column, causing her head to tilt downward.


The three-year-old with curly brown hair and a sweet smile could not look up or straight ahead. Her chin seemed glued to her left shoulder.


Only one surgeon possessed the skill to remove the tumor, Heather's physicians said. That doctor was Fred Epstine in New York City.  Without surgery, Heather faced paralysis and possible death.




     "If it was my daughter," one of her doctors said, "I'd be on that plane now."


When contacted, Epstine agreed to do the operation. But there was no time to waste. It was a Wednesday, and he told the family to get to New York the next day.  Surgery was scheduled for Friday.


There was a hitch, though. Heather's dad, Dan, was told his insurance company would pay only $300 a day for Heather's New York hospital stay. Yet the hospital room would cost $I,600 a day, and a $16,000 deposit was required.


A real-estate agent, Allen could get the money.  He could raise it.  But this would take a couple of days, time that Heather did not have.


If it was my daughter, I'd be on that plane now.


Check my credit, a desperate Allen told the hospital.  I am good for the money.  You are talking about a three-year-old. Why be concerned about money?




A neighbor told Allen to call the March of Dimes.  But the March of Dimes could not help. The organization, did, though, tell Dan Allen about a group called the Compassion Children's Foundation.

     As it turned out, the foundation - Allen's last hope was located in a cluttered garage in a nondescript subdivision outside Orlando, Fla. Outside the garage was a rusty Volkswagen Rabbit with a busted muffler and 170,000 miles on it.


The car belongs to a man named Tony Giorgio, who works at Walt Disney World and makes far less money than Dan Allen.  He can't, in fact, even afford to get his Rabbit fixed.


Tony Giorgio is Compassion Children's Foundation.


He listened to Dan Allen's story over the phone and said he would call him back.  A half-hour later, he did.  Pack your bags, Giorgio said.


Everything had been taken care of.


The hospital was waiting. Heather got her operation.  Less than three weeks later, she was up and about.


A recent test showed the tumor has not come back.  And each day Heather regains more head and neck movement.


How did Giorgio do it?


"They wanted a guarantee on the payment. So I faxed them an IOU."  At the time, Giorgio's foundation had $200 in the bank.


It is unfortunate that children sometimes die because their families don't have enough money for treatment.  "I don't want to suggest it is a major problem," says Dr. John Graham Pole, a pediatrics professor at the University of Florida. "But it has happened.  It is a terrible problem, a national problem.


"It is so expensive and so many children have catastrophic illnesses.  There is no way the families can foot the bill. Tony is trying to do something.  He can only touch the surface of the iceberg, but he tries. My gosh, he tries."


Tony Giorgio, 46, steps in when children are snubbed by insurance agencies, state welfare bureaucrats, and a medical establishment that wants its money guaranteed.


He looks, acts, and even talks a little like a young Rodney Dangerfield. He tugs constantly at the collar of his shirt, as if he is fighting off his tie’s attempt to strangle him.  A large man at 6 feet 4 inches and 240 pounds, his posture is slightly stooped.  He never seems to be still, even when sitting.


He charges into battle in his trusty, rusty, Rabbit, the one with the loud sputtering engine and interior that looks like it has been home to a pack of Great Danes.

Tony Giorgio looks very much like someone who has come to sell you aluminum siding.


        "I don't have any affiliation," he explains, "so I can rattle anybody's chain I want."


Giorgio helps kids by getting doctors and hospitals to reduce or drop their charges.  He goes over the heads of state bureaucrats by appealing directly to governors and representatives.


Giorgio also raises money.  He washes cars and cooks spaghetti.  He goes door-to-door.  He calls corporations.


Giorgio works at the grass-roots level.  He says laws need to be changed to help families with sick kids.


      Truth be told, though, Giorgio doesn't even know the law well enough to recommend how it should be changed.  He is not a big-picture man.  If you assigned Giorgio the task of ending hunger in Florida, he would grab some bread and bologna and head for the street. No study groups. No task forces.


Giorgio gets a lot of help from Laureen, his wife, who also works at Disney.  She keeps the foundation's books straight.


   They do their work in their spare time.  They don't get paid for it.  In fact, they lose quite a bit.  Giorgio is paid by the hour at Disney and frequently dips into company time for his foundation work.


"He's a charity, we aren't," says Elliott Winit, general manager of central reservations operations for Disney.  "We dock his time. We can't do any different for him than anyone else.  We are flexible, but he takes it in the shorts, no doubt about it."


Out of his reduced pay, Giorgio often covers a lot of foundation expenses.


The story began six years ago near Kissimmee Fl., where the Giorgios lived.  A neighborhood boy had leukemia.


The family did not have insurance. It could not get State assistance because one parent owned a small business.


The medical bills piled up. The family eventually lost the business, the house, and the car, and they were facing $27,000 in medical bills.


Giorgio held a fund-raiser. "I didn't know anything about fundraising," he says.  "I'd just call all these companies and ask for money. Everywhere I called they asked if I was a tax-exempt organization. I said, 'No.' They said, 'No.' "


So Giorgio took his American Express card to an attorney's office and charged the $300 it cost to set up the Compassion Children's Foundation.


American Express canceled his card shortly thereafter because he exceeded his spending limit.  "Yeah, well," he says, "I couldn't afford the card anyway. "


Giorgio did, however, raise $11,000 for the family and got Florida's Department of Health and Rehabilitative Services to pay the rest.  And the experience exposed Giorgio to other families in similar predicaments.


"I had been brainwashed into thinking kids always got help," he says.  "Then I talked to people and I realized this was not the case."


There was a child from Virginia who needed a bone-marrow transplant.  Virginia did not have the facilities for the procedure, yet state officials would not pay to have it done out of state.  This is a common problem: states are reluctant to pay for medical treatment in other states, even if the treatment is not available in their own.  Giorgio contacted Virginia Governor Charles Robb's office, and in a few days, Robb approved the transplant funds.



Not all stories have such happy endings.  When three-year-old Ross Farmer had cancer and needed a bone-marrow transplant, Shands Teaching Hospital in Gainesville, Fla., required a $40,000 deposit before they would treat him.  The boy's family did not have insurance at the time and could not receive assistance because one parent made too much money to qualify.



Giorgio heard of the family's plight and helped them with fundraisers.  After six weeks, he raised enough money for treatment.  The delay in the bonemarrow transplant, though, had hurt the boy's chances of survival.  "When something like that is needed," says his doctor, John Graham Pole, "it's needed tomorrow."


Ross died in early I 986, about seven months after the transplant.


The delay infuriated Giorgio.  After the boy died, Ross's parents gave Giorgio the boy's Raggedy Ann doll.  He keeps it in his garage office.



Since Ross's death, Girogio has spent practically all his free time working with families, generally handling one or two cases at a time.  He helped a Texas family who had a child in Gainesville's Shands Hospital but couldn't get back home because the car was broken.  Giorgio called a gas station near the hospital and arranged to get the car fixed.



A couple from Lee County, Fl., faced more than $70,000 in hospital bills after their child died from a birth defect. Giorgio clipped a copy of the news article that detailed how much profit the hospital made that year and sent it to then-U.S. Representative Connie Mack.  His office contacted the hospital, which soon wrote off the child's bill.


Then, there was Steven and Ann Ewing of Kissimmee.  They faced eviction from their home because they could not afford the rent.  Their son, Clay, was diagnosed with neuroblastoma, cancer of the nervous system.  Ann Ewing quit her job to care for him, and the combination of expenses, insurance deductibles, and lost income caused them to fall behind in their bills.


Giorgio set up a fund for the family, keeping them in their home and helping with expenses.


Chuck and Debbie Hilton, also of Kissimmee, found themselves in a similar predicament when their son Rusty was born premature.  He weighed little more than a pound.


Then the family’s insurance ran out.  Bill collectors demanded money while the Hiltons struggled through losing their two businesses, a restaurant and a video store, which they couldn’t keep up while caring for Rusty.  At one point, Debbie Hilton says, a state social worker actually told her she would be better off divorcing her husband so she would be eligible for Medicaid.


Giorgio recently helped the family get back on its feet by giving the Hiltons $1,000 to set up a small sandwich shop. And when Rusty Hilton turned one year old early in 1990, Giorgio went by the shop unannounced for his birthday party.


"He shows up in the beat-up old Rabbit and gives Rusty a $50 savings bond," says Chuck Hilton. "Geez, the guy's car is falling apart and he gives Rusty $50."


Tony Giorgio, the man who adopts Florida's sick kids, has no kids of his own.  That's because he's had some bad luck of his own.



Raised in New York, he started working early, digging ditches at age 14 as a plumber's helper.  He was a scrappy kid who hung out with the neighborhood gang.



"I was the typical teenager in New York - black leather jacket, the whole bit," he says.  "If they could see me now, my friends wouldn't believe it."



He joined the Marines at 17, after graduating from high school.  But he didn't last long because of medical problems with his feet.  He was discharged early and took a job at a factory.  He made extra money playing drums in a band.



Then he met Laureen on a blind date, and they married.  He was 24; she was 21. They put everything they had into a hamburger stand on Long Island, working 19 hours a day.  At the time, Tony weighed 300 pounds, and the stress on his legs caused him to develop phlebitis. When a clot from his leg dislodged and went into an artery, it caused a heart attack.



Giorgio spent five weeks in the hospital.  He had no insurance



"I was laying there and this hospital administrator comes by and throws the bill on my food tray," he says.  "I couldn't believe it."


Giorgio lost the hamburger stand and applied for government assistance.


"Trying to get help when you're down is very, very difficult," he says.  "They would lose paper work.  Checks were late.  That was my first experience with agencies that are supposed to help you."


Giorgio then suffered another setback, this time surgery to remove polyps from his voice box.


   "Two guys from Social Security came by the house to hold a hearing on my eligibility. They sat at my bedside and told me I was not eligible, and I couldn't say anything.  They got up and walked out and that was that."


Giorgio moved to Fort Lauderdale, Fla., in the 1970s and got a good job driving a linen truck and took a weekend job there playing drums in a band.  He eventually was promoted.  Laureen became an office supervisor at the company



       When the business went bust six years ago, the Giorgios moved to Central Florida where they took jobs at Disney World.  When their income dropped by two-thirds, they couldn't afford the payments on their Fort Lauderdale house and so the Mortgage company foreclosed.

 "We have had so many ups and downs in our married life - lost a business, lost a house, always struggling."  He says. "Time caught up with us. We are thinking of adopting now.  We've always wanted kids. We love kids."


Giorgio is most animated when talking about kids.


"They say kids are the future of America, and then they turn around and treat them like garbage.  To see someone pull the plug on a kid for the almighty dollar drives me crazy."





May 18, 2001, Governor Bush signed a Bill into law preventing Florida's electric utilities from turning lights off on seriously ill children and adults. Tony and Laureen Giorgio put the Bill together, and worked three years to get it passed unanimously in the Florida State Legislature.




Award Recipient


Winn-Dixie Good Citizenship Award

WESH-2 TV Jefferson Award

Walt Disney World Special Judges Award

Service to the Families Award

Florida State Jaycees

General Chappie James Memorial Award

SCACD Louis Galpin Humanitarian Award

Star 94.5 FM & Holler

Hometown Hero Award, 1995/96



Major Benefactors


Orlando Magic Youth Foundation


Robert Vincent Sims “The Garden Rebel”

Ryan Foundation

Chatlos Foundation

Maitland Rotary

Walt Disney World

Downtown Orlando Rotary


United Trophy

Star 94.5 FM

Dr. Phillips Foundation

Winn Dixie

Publix Charities

Greater Orlando Board of Realtors

Sanford Flea World

Ford Dealership Association


Delta Airlines Fare Share Program

Weggive Foundation