When Caroline Floyd and Natali Pulver met for the first time recently, they had plenty to talk about.

The women – Floyd lives in Rock Hill, Pulver in SouthPark – are two of several people in the Charlotte area who have fibromuscular dysplasia, or FMD, a rare disease that affects fewer than 500 people, according to a national registry.

Floyd and Pulver originally met on FMD Chat, a website that connects those with FMD from all over the world. Its private Facebook page has become a place where they can connect with others who share their experience.

Pulver said the first thing she did after her diagnosis was conduct an online search for support groups. She now goes to FMD Chat regularly with questions about her health.

“The anxiety of (the symptoms) was the worst part,” Pulver said. “I had a support system (of family and friends), but no one could say, ‘I know how you feel.’ ”

FMD is characterized by abnormal cell growth in the walls of medium and major arteries. It often goes undetected and can cause heart attacks, strokes and other serious symptoms. FMD is most often diagnosed in women between age 30 and 50.

Because so little is known about some rare diseases, doctors often can’t provide patients much information.

“Using social media gives us this community of fellow patients, so that whether it’s a good day or a bad day, we have a group of people who understand what it’s like to be a patient with FMD,” said Sarah Kucharski, founder of FMD Chat, who lives in the N.C. mountains.

“As much as our friends and loved ones want to understand, they simply can’t.”

Floyd, 36, and Pulver, 32, share remarkably similar stories.

Both are slim, healthy and athletic mothers of young children who, seemingly out of nowhere, developed high blood pressure. Both then survived life-threatening medical events caused by dissected arteries leading to the brain. Floyd had an undiagnosed mini stroke, and Pulver had dissected arteries that required a stent.

Two weeks after having a baby in 2006, Floyd fell at home after feeling as if someone had hit her in the back of the head with a baseball bat. She couldn’t walk or speak.

Her husband was in the driveway, washing their car. Floyd crawled to the door and pushed it open, lying in the doorway until he saw her.

Floyd was rushed to the emergency room, where she was given an MRI, which showed no cause. A neurologist told her at a checkup three days later that she must have fainted.

“They look at you like, ‘You’re just dramatic and crazy,’ ” Floyd said. “But I always knew in the back of my head that something was really wrong.”

By 2010, Floyd still suffered mysterious episodes and Googled her condition. She took her BlackBerry to her physician to show the doctor her online research. A scan of her arteries led to an FMD diagnosis three weeks later.

Pulver, a stay-at-home mother of children ages two and four, felt a painful “pop” in her neck while out to dinner with girlfriends in early 2012. She went to an urgent-care center several days later and was sent home with muscle relaxers.

She was back in the ER a few days later with chest pains.

Her FMD might have gone undiagnosed but for a medical student who listened to an artery in her neck just before a doctor was about to discharge her. The student heard a sound that indicated a blockage in her arteries. A scan revealed that she had dissections – or separations of the artery walls – in her vertebral arteries. An FMD diagnosis followed.

The benefits of connecting patients with rare diseases go beyond providing much-needed support. Patients’ conversations can lead to helpful information about the disease as they compare symptoms and medical histories.

Floyd, who also has two other rare diseases, said she’s found other FMD patients who also have another disease.

FMD Chat continues to serve as a growing international support group for people who may not know anyone in person who has the disease.

“There’s no point in having an FMD support group (in person) because if you’re lucky, you might have one person show up,” Kucharski said. “This provides a place for patients, whether it’s a good day or a bad day, to celebrate it, vent about it, and rely on each other for support and information.”

Read more here.  Written by Marty Minchin.

 

1 thought on “Two Women Linked by Rare Disease, Fibromuscular Dysplasia (FMD)”

  1. Traci Eno says:

    Hi,
    I came across this website and was wondering if anyone has had any success with fixing their carotid arteries? I was diagnosed with FMD after suffering a series of strokes on March 27, 2015. I’m a healthy, active 41 year-old female and was working out at the YCMA and tore my right carotid artery pretty bad which created a clot. The clot broke down into smaller clots and traveled to my brain which caused the series of strokes. The MRI showed years of damage to both carotid arteries, lots of tearing and scar tissue appeared on the x-rays. It looked like a pearl necklace instead of arteries. I would like to know if a vascular surgeon can clean this mess up? Seems like no doctor in Neuro or general practice knows anything about FMD. Please help. Thanks!!!

Comments are closed.