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.
December 10th, 2016
When Tyson Cluever, a 32-year-old mother of two from Benson, Minnesota, learned that she had an aggressive brain cancer, her first thought was of her children. At just nine months and five years old, her sons stood to lose one of the most important people in their lives if she were to share the fate of many individuals diagnosed with grade IV glioblastomas.
“It’s brain cancer, and you have between 12 and 18 months to live,” says Tyson’s husband, Jon. “It just totally messes you up inside when something like this happens.”
The couple’s next thought was to fight the cancer with everything they had. Read the rest of this entry »
November 21st, 2016
When Reilly Steidle came to Mayo Clinic in the summer of 2013 at the age of 20, she brought with her two rolling suitcases full of medical paperwork and a hope that the physicians could make sense of the recurring headaches, chronic fatigue and widespread pain she’d been dealing with for two years.
Reilly had been a healthy college student majoring in business at Northern Illinois University in the fall of 2011. But by the end of the school year, the Plainfield, Illinois, resident had dropped out, debilitated by her mysterious symptoms. Reilly spent the summer of 2012 visiting doctors.
When no one could decipher her symptoms, she decided to try another approach. Reilly went to a chiropractor, who asked to see her MRI images. After looking at them, the chiropractor urged Reilly to get an enzyme-linked immunosorbent assay test, confirmed by a Western blot test, to check for Lyme disease. Reilly did so, and on her 19th birthday, she received the news that the test results were positive.