March 24th, 2017
Just four months after being in a coma, Mike Short was crawling through tunnels, jumping over fiery logs, and scaling walls as part of a 5K race known as a "rugged maniac." The Georgia native owes his ability to participate in the race to the neurocritical care team at Mayo Clinic that helped him recover from a brain injury he suffered shortly after his 50th birthday.
Diagnosed with a seizure disorder in childhood, Mike had had only a handful of grand mal seizures in his life. But on April 9, 2016, while visiting a friend in Black Sheer, Georgia, he had another. It was his first in 10 years. The seizure caused Mike to fall and hit his head. He was transported to a local hospital where he had another seizure.
“I aspirated everything into my lungs and passed out due to lack of oxygen,” Mike recalls being told.
March 7th, 2017
Barry Connell couldn’t be happier to have his wife of 53 years, Maureen, back.
Though the couple spent 16 years traveling cross-country after Barry retired as president of a manufacturing company in Connecticut, nothing prepared them for the difficult journey they would embark on when Maureen’s health began to decline rapidly in 2015.
For the first five months of that year, The Villages, Florida, resident noticed his normally lively wife wasn’t as alert as she used to be. She was also much slower to respond to situations. Then, on Mother’s Day, Maureen collapsed in the bathroom of the restaurant where their family was celebrating.
That incident led to months of debilitating symptoms for Maureen, along with a series of ineffective treatments. No one could explain what was happening to her. In desperation, the Connells turned to Mayo Clinic, where they were able to finally find the source of Maureen’s problem — hydrocephalus, a buildup of fluid in the brain.
“After struggling with this for three months, we got a preliminary diagnosis less than 24 hours after arriving at Mayo,” Barry says. Read the rest of this entry »
February 13th, 2017
For more than a year, Mike LaBorde thought he had carpal tunnel syndrome. His left hand and arm often tingled and felt numb. He wore a brace for a while, but it didn’t help. Then he had carpal tunnel surgery, not once, but twice. The surgeries made no difference.
“I was quite aggravated that the surgery was not successful,” Mike says. “But I was told that nothing is 100 percent guaranteed. I just kept working and doing the best I could. And it kept getting worse and worse.”
When the symptoms didn’t fade, Mike’s primary care doctor suspected a herniated disc, so Mike had an MRI. What that test revealed changed everything. Read the rest of this entry »
February 10th, 2017
In October 2016, Judith Johnson, Ph.D. — who is retired from the library at Florida State College at Jacksonville — was at home recovering from back surgery. While she was sitting in bed talking on the phone with a friend, something suddenly went wrong. Judith felt herself sliding in between the bed and the nightstand. Though Judith doesn’t recall what she said, her friend realized something was happening, hung up, and immediately called 911 and called Judith’s son.
February 1st, 2017
Nathaniel Kirera wasn’t expected to survive birth. When he did, then he wasn’t expected to live to see his first birthday, much less his 14th. He also wasn’t supposed to be able learn, let alone write a book. But he’s done all that, and today his medical odyssey is behind him.
That Nate has achieved so much despite having multicystic hydrocephalus, a condition in which half of his brain and its fluid drainage system formed abnormally, is no surprise to his mother Ann Makena, who, while she was pregnant, dreamed of a son walking and talking.
“The doctor said. ‘I’ve seen very bad conditions, but I’ve never seen anything this bad,’” Ann says. “I said, ‘It’s not that I don’t trust you … but I really felt very confident about this child. I said, ‘No I’m just going to leave it up to God.’”
January 19th, 2017
Five weeks before she was born, Marissa B. had a stroke in utero. When her mother went into labor, Marissa had another stroke. Diagnosed with epilepsy at birth, Marissa spent her first month of life in the neonatal intensive care unit.
“When she was six months old, they did a brain MRI,” Marissa’s mom, Lisa, says. “They said she would never walk or go to a regular school.”
The strokes took a significant toll on the left side of Marissa’s body. She doesn’t have fine motor skills in her left hand. She has a blind spot in her lower left eye and hearing loss in her left ear. Sensation on her entire left side was also affected.
“I’ve been on seizure meds since birth,” says Marissa, who is now 24 years old.
January 13th, 2017
After a 37-year career at a petroleum company, Dan Hofferber was looking forward to retirement. But in 2014, Dan started having trouble with one of his legs. The muscle in his left thigh would tighten up, causing unbearable pain that made it hard to walk.
“I was used to walking a mile or two, and I couldn’t do that anymore,” says Dan, who travels to Florida for spring training every year with his wife, Carol.” I couldn’t even walk from the parking lot to the baseball stadium.”
The pain prompted Dan to seek care in his hometown of Billings, Montana. After several months without relief, a family member urged him to go to Mayo Clinic. Dan took that advice, traveling to Mayo Clinic's Rochester campus. There, he met neurologic surgeon Mohamad Bydon, M.D. Dan was immediately impressed.
December 22nd, 2016
For much of her adolescent and adult life, Erica Laney, 31, had frequent petit mal seizures. Less often, she had grand mal seizures that led to loss of consciousness and violent muscle contractions. The cause of the seizures was abnormal electrical activity throughout her brain.
“The seizures started when I was 11 years old. I would experience three to four a month,” Erica says. “I was unable to talk during these auras and couldn’t remember anything afterwards. I felt like I was on a rollercoaster, and I was heading for the big drop. Then darkness came from behind me, enveloping me in a haze that would lead to a seizure.”
The Mims, Florida, native was diagnosed with seizure disorder and had a series of tests, including MRIs, CT scans, and electroencephalograms, or EEGs. Erica also went through intracarotid sodium amobarbital, or Wada, testing, which looks at language and memory on one side of the brain at a time. While under the care of an Orlando neurologist, Erica took several medications to control her seizures. But she was never fully seizure-free.
December 15th, 2016
It’s a condition with no outward symptoms. But for the hundreds of thousands of teens and adults in the U.S. living with postural orthostatic tachycardia syndrome, or POTS, the medical disorder has a significant impact on their lives. Christine Esposito is one of those people.
POTS is a disorder that affects a person’s autonomic nerves — the nerves that control involuntary body functions, such as heart rate, blood pressure, body temperature, perspiration, and bowel and bladder functions. Not everyone has the same symptoms, but the condition universally causes rapid heart rates and dizziness when moving from a resting to standing position.