24-year-old's fainting was a clue to her fatal heart condition

By American Heart Association News

Melissa Russom and her husband, Braden, enjoy a beach vacation with their daughters in Cape Cod. The sisters, Kate (left) and Cora inherited a genetic heart condition called long QT syndrome. (Photo by Sarah Murray)
After her sister Christie died, Melissa Russom (top left) was diagnosed with a genetic heart condition. Her two daughters with husband Braden also inherited the condition. (Photo courtesy of Sarah Murray Photography)

Christie Tolosky went to her family doctor's office to get a prescription for a toothache. She collapsed and was dead within an hour, leaving doctors looking for clues about what happened to the otherwise healthy 24-year-old.

An autopsy revealed the answer. While planning the funeral, Barbara Tolosky, Christie's mother and a registered nurse, saw the cause of death listed as arrhythmia, an irregular heart rhythm. That started a chain of events that led to three generations of the family being diagnosed with long QT syndrome, a disorder of the heart's electrical system that can cause irregular and potentially fatal heartbeats.

Christie had experienced fainting spells – the first in her high school cafeteria in upstate New York. She was taken to a hospital. Her blood sugar was low, and a follow-up visit confirmed hypoglycemia, a condition caused by low blood sugar. She was told to follow a certain diet. There was no reason to check an otherwise healthy teen's heart.

Christie's second episode was in college. She told her mom she woke up with her alarm going off, and the next thing she knew, she was on the floor.

The final time was in the doctor's office.

Within days of Christie's death in June 2005, the family's physician wanted the Toloskys to be checked to see if there was something genetic going on.

Christie Tolosky lost her life at age 24 to her fatal heart condition, long QT syndrome. (Photo courtesy of the Tolosky family)
Christie Tolosky died at age 24 from an undiagnosed heart condition. (Photo courtesy of the Tolosky family)

Long QT syndrome is a rare condition. It's marked by the lower chambers of the heart taking too long to contract and release. The name comes from letters associated with the waves on an electrocardiogram: the problem is found when there's too much time between the letters Q and T.

Long QT can be hereditary, usually affecting otherwise healthy children or young adults. Others can get it as a side effect of medication.

Christie's older brother, Nick, was fine. But mom Barbara and younger sister, Melissa, were both diagnosed with the condition.

At the time, Melissa was 22 and about to spend a year in Belgium for graduate school. After multiple consultations, she opted to get an implantable cardioverter defibrillator, or ICD, a device that tracks heart rate and can deliver an electric shock if needed to restore a normal heart rhythm.

Four months later, another death rocked the family: Barbara's mother died. Two days later, Barbara felt her heart flutter and went to the hospital. While there, she had a cardiac arrest. She also now has an ICD.

By 2014, Melissa had moved back to the Albany area to be near her close-knit family and was working as a communications consultant. She and her husband, Braden Russom, were expecting their first child.

She found out about a fetal arrhythmia study that was recruiting pregnant women with long QT syndrome and enrolled. The couple flew to Wisconsin and met with the specialist overseeing the research. Melissa was hooked up to a machine that could separate the fetal heart rhythm from her own. Right away, they detected the 24-week-old fetus had long QT.

From that point, the doctor became part of the care team, and a crowd of medical staff was in the delivery room, providing extra peace of mind.

They named the girl Cora. Her middle name is Christie.

Two years later, the couple was pregnant again. Their second child, Kate, had the same test and she too was diagnosed with long QT. She and her big sister take medicine called beta blockers to help regulate their hearts' workload.

"The way that we tell them about it is that they have a special heart, and that's why they have to take their medicine," Melissa said.

In the years since Christie died, several of her aunts, cousins and their children – all on her mom's side – also have been tested and diagnosed with long QT.

Christie Tolosky (right) with her mom, Barbara. In the years since Christie's death, Barbara and many of her relatives have been diagnosed with long QT syndrome. (Photo courtesy of the Tolosky family)
Christie Tolosky (right) with her mom, Barbara. In the years since Christie's death, Barbara and numerous relatives have been diagnosed with long QT syndrome. (Photo courtesy of the Tolosky family)

This extended family has learned that people can have it without showing any symptoms. Others may faint. Sometimes, an everyday circumstance can trigger an arrhythmia, such as being startled, experiencing intense emotion or working out. In fact, Barbara believes a lunch bell ringing at school may have triggered Christie's first fainting episode, and her alarm clock may have caused the second.

"For us, when we hear anyone has fainted, we always say, 'Ask, ask, ask if it could be cardiac-related,'" Melissa said.

She volunteers for the American Heart Association, sharing with others what happened to her sister. The family also participates in their local AHA Heart Walk wearing T-shirts in Christie's favorite color, purple.

"To me, it's getting anyone who potentially has a warning sign to get them to check it out," Melissa said. "If they had found Christie had long QT, they could have treated her. It's not like it's a death sentence. It's just that she didn't know."

Stories From the Heart chronicles the inspiring journeys of heart disease and stroke survivors, caregivers and advocates.

If you have questions or comments about this story, please email [email protected]

American Heart Association News Stories

American Heart Association News covers heart disease, stroke and related health issues. Not all views expressed in American Heart Association News stories reflect the official position of the American Heart Association. Statements, conclusions, accuracy and reliability of studies published in American Heart Association scientific journals or presented at American Heart Association scientific meetings are solely those of the study authors and do not necessarily reflect the American Heart Association’s official guidance, policies or positions.

Copyright is owned or held by the American Heart Association, Inc., and all rights are reserved. Permission is granted, at no cost and without need for further request, for individuals, media outlets, and non-commercial education and awareness efforts to link to, quote, excerpt from or reprint these stories in any medium as long as no text is altered and proper attribution is made to American Heart Association News.

Other uses, including educational products or services sold for profit, must comply with the American Heart Association’s Copyright Permission Guidelines. See full terms of use. These stories may not be used to promote or endorse a commercial product or service.

HEALTH CARE DISCLAIMER: This site and its services do not constitute the practice of medical advice, diagnosis or treatment. Always talk to your health care provider for diagnosis and treatment, including your specific medical needs. If you have or suspect that you have a medical problem or condition, please contact a qualified health care professional immediately. If you are in the United States and experiencing a medical emergency, call 911 or call for emergency medical help immediately.