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OMRF Stories

Higher Powers:
How 1,100 nuns, priests and brothers are helping OMRF researchers unlock the secrets of Alzheimer's.

Cooties in the Lab:
Whither the White Lab Coat?

Going With the Flow:
Dr. Margaret Clarke, OMRF Microbiologist.

Research Tower:
OMRF unveils the greenprint for a historic campus expansion.

Meagan's Miracle:
An OMRF discovery saves a dying college student.

Lessons In Philanthropy:
Putnam City School students learn early that giving to OMRF’s cancer research efforts is a good thing.

Prayers Answered:
Two Oklahomans suffering from a rare, life-threatening disease.

The Giver:
Jim Chapman’s generosity helped make OMRF what it is today.

Cancer From Every Angle:
OMRF researchers seeking clues to a variety of cancers.

Next of Kin:
It doesn't matter if you're a banana, fruit fly or writer; DNA is inside all your cells. Join OMRF's Greg
Elwell as he peels back his own genetic skin

The Strange Case of Tom Little
The Strange Case of Tom Little

The Comeback Kid:
An OMRF Discovery helped bring Rayna Dubose back from death, then Rayna had to learn to live again

Mighty Mice
Mighty Mice

Predicting Disease:
Live, Long and Prosper

This Is My Brain on 3-Tesla MRI

Autism: A Personal Story
Bringing up Jeremy

OMRF People
Bon Appetit

A New Birthday

Hitting the Right Note: Bob Floyd

Running Man: Gary Gorbsky

Family Matters: Kathy Moser

The Gospel According to Luke (Szweda)

Autism, Our Story

The Survivor

It's In The Genes

 

 

As her car pulled to a stop at the grocery store, Sandy Roark felt a rush of shame, but no blush came to her cheeks. She didn’t have enough blood to show color.

Parking in the handicapped spot, even with her tag, she still drew looks. At age 60, she looked as healthy as anybody else. She wasn’t in a wheelchair or using a walker. Yet each step from her car to the sliding glass doors was a battle.

“I would look at people walking, and I would get mad,” she says. “They take for granted how easy it is to just get up and go without a second thought. I had nothing but second thoughts.”

As she struggled through the supermarket aisles, other shoppers couldn’t see the bruises her clothes disguised, the plum-colored blotches that mysteriously appeared on her body in places she didn’t remember being hurt. And in the churches where her husband has preached, sitting in the pews, the other members of the congregation didn’t understand the effort it took to get up in the morning just to be there. She looked just like the Sandy of old, the one with the energy to garden and travel and cook and visit after the final hymn. But she wasn’t the old Sandy. No, right around her 60th birthday in 2000, that person had disappeared.

When she went to the doctor, blood tests at first revealed that her platelet levels had dropped to less than 10 percent of normal levels. After months of additional testing and countless consultations, physicians finally gave her a name for the pain: paroxysmal nocturnal hemoglobinuria, or PNH, a rare, incurable blood disorder.

“After I found out I had PNH and read about the disease, I was in a panic,” she says. The threat of a developing a blood clot, she learned, was constant. The clots could form anywhere: deep veins, the abdomen, the kidneys, the liver. And the strong chance that one of those clots would break off and cause a fatal event—like an embolism or stroke—explained the most sobering statistic she encountered: Once diagnosed with PNH, a person could expect to live only another eight years.

Not even a decade. Not long enough to see her first grandchild graduate from college. Or to celebrate her 70th birthday. “Generally, I try to look at the glass half full,” says Roark. But now when she peered into the future, she saw only darkness. “I thought my life was over.”

She felt what anyone in her situation would feel: anger, frustration, despair. “I was searching for answers. Not just, Why did this happen to me? But why does this happen to anybody?” And the permanence of her situation only underscored its bleakness. “This wasn’t a passing thing. It’s not like I could get an operation and it would be gone. This was for the rest of my life”—however long that might be.

So she did the only thing she could: She asked the congregation, her family and everyone she knew to pray for her.
The prayers she requested did not seek a cure. Or even to bring an end to her pain. “I just asked them to pray for me to have the strength to face each day. To have the strength to fight the disease.”

Go to interactive.omrf.org to hear Sandy in her own words.

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