September 29th, 2014 · Leave a Comment
Maryel Andison was a university communications and fundraising specialist living with her husband and children in Winnipeg when she suffered a stroke. It was a warm Sunday morning, she was watering flowers, and she was just 51 years old.
Maryel waited three days before deciding to see a doctor. By the time she was referred to a neurologist, she learned there would be more delays, including waiting for the imaging tests that would show exactly what had occurred in her brain. But instead of allowing more time to elapse, she decided to seek advice from Mayo Clinic.
Maryel's ties to Mayo go back decades. Impressed with the cancer care a friend received at Mayo Clinic in Rochester, Minnesota, her parents became patients there in the 1950s. As a child, Maryel remembers visiting her mother at the hospital, where a half century later her husband's daughter would be a neurosurgical resident. Now, needing care herself, she saw it as a logical choice.
Ultimately, it was also a life-saving one. [...]
September 24th, 2014 · Leave a Comment
Michael Tessmer got out of his parents' car and stared at the hospital building before him. His parents had brought him to a hospital in his home state of Iowa for the first of 14 surgeries to repair a cleft palate. Each time, young Michael would be dropped off on the front steps of the hospital, and he would not see his parents again until the hospital released him.
"I don't know if that was hospital policy or what," he says. "But I'd be down there anywhere from two weeks to a month each time, all alone."
That did little to instill trust and confidence in the medical world. In fact, it did just the opposite. "I was terrified of doctors and hospitals," Michael says. "I'm not ungrateful that they fixed me. I'm very happy they did.” But he admits it left him with questions about that approach.
So after the last of his surgeries, Michael stayed as far away from doctors, nurses and other health care providers as he could -- going in to be seen only when it was absolutely necessary. Thankfully, that changed after one of Michael's daughters decided to go to nursing school. [...]
September 11th, 2014 · Leave a Comment
By Paul Scotti
When 69-year-old allergist and rheumatologist Mike Mass. M.D., was diagnosed with multiple myeloma in August 2013, he quickly realized that being the patient and trusting the advice of a fellow physician with expertise in a disease outside of his realm of expertise would be a challenge.
“I’ve always advocated open communications with my patients about their treatment options, as it’s important for the physician and patient to be on the same page,” says Dr. Mass. “Although I’m not a cancer expert, I know enough about the disease to ask lots of questions of my own oncologist on the best treatment options available. It was hard balancing the need to express my opinions without impeding my physician’s own expert medical judgment.”
Dr. Mass was in private practice in the Jacksonville, Florida, area for more than 30 years before going part-time and joining an allergy group practice in 2008. That’s where he worked until his diagnosis in 2013, when he finally decided to retire from practicing medicine. He had known he was at a greater risk for contracting multiple myeloma for many years because of a condition called monoclonal gammopathy of undetermined significance , or MGUS, which he was diagnosed with decades ago. MGUS is a condition in which an abnormal protein (M protein) is found in the blood. That increases the risk of developing multiple myeloma at some point in the patient’s life. Dr. Mass had no symptoms but found out several years ago after some blood work that his M protein levels were at the point where he now had “smoldering myeloma,” an early phase of this cancer condition. [...]
September 2nd, 2014 · Leave a Comment
In 2011, Joan and David Hittner opened a letter from the Mayo Clinic Department of Development. Inside was a request: Would they consider donating $25 to support cancer research?
The Hittners quickly agreed that $25 wasn’t nearly enough.
“After what we’d just been through, that seemed a minuscule amount,” says David. “We started talking about what more we could do.”
The couple, from the Winona, Minnesota, area, had recently returned from Mayo Clinic in Rochester, where Joan had undergone surgery to remove tumors that had encompassed her pancreas and invaded her intestines.
Joan's battle with cancer had started six years earlier. She’d gone to her doctor with what she thought was a gallbladder problem. Instead, Joan found out she had carcinoid cancer, and she was told surgery was her only treatment option. “The cancer was incurable,” says David, and “chemo and radiation wouldn’t work.” [...]
August 25th, 2014 · Leave a Comment
By Paul Scotti
When a doctor suddenly becomes the patient with a life-threatening illness, Mayo Clinic’s commitment to high-quality medical care that puts the needs of the patient first takes on fresh perspective, especially as it relates to the principle of compassionate care, which is a hallmark of Mayo Clinic.
Such was the case when Joseph J. Tepas III, M.D., a 68-year-old pediatric surgeon in Jacksonville, Florida, learned that the wheezing and shortness of breath he was experiencing turned out to be idiopathic pulmonary fibrosis, a potentially life-threatening disease that occurs from unexplained scarring of the lung tissue.
In addition to doing pediatric surgery, Dr. Tepas is a practicing trauma surgeon and surgical intensivist. He is the medical director of the region’s only pediatric trauma unit, and, as a retired captain in the Navy Reserve, appreciates the critical importance of maintaining a personal commitment to health and fitness. Dr. Tepas had always lived a healthy lifestyle and, other than some occasional allergy symptoms, never had any significant health issues. But lying dormant in his otherwise healthy body was a disease that was quietly scarring and shutting his lungs down.
August 15th, 2014 · 12 Comments
I struggled for years with extreme fatigue, major skin problems, muscle weakness, escalating eye issues, and a host of other unexplained symptoms. I moved to Georgia with more and more symptoms. I developed relationships with new doctors and developed new symptoms – seizures and heart-related syncope. I went to see a neurologist, who began to run tests. In the meantime, I had regular quarterly blood panels by my regular physician, who upon reporting to me by phone noted no irregularities. I was told time and time again to stop chasing a diagnosis. My family continued to watch my decline.
After running numerous tests, my neurologist could only ascertain that I may have had some mini-strokes. My neurologist referred me to a major university hospital. After two visits, and being practically laughed out of the place, I began to have serious doubts about my symptoms and began to believe the many specialists and psychologists who told me it was emotional response. [...]
August 14th, 2014 · Leave a Comment
Todd Goldrick was living the dream. Good job. Loving wife. Two young, healthy kids. Weekends spent playing golf, softball, kayaking, hiking, running or just hanging around home with the family. But that changed suddenly in 2010, when he and his wife simply tried to buy some life insurance. He was just 28.
"Mine came back straight out denied," Todd says. "They told me the reasons. There was a whole long list -- high cholesterol, high blood pressure, and a few other things that I don't remember exactly."
Before that day, Todd says he'd been to see his doctor in the Minneapolis–Saint Paul area "maybe every two years," so the policy denial came of left field. In fact, he says it scared him into doing nothing about it, at least initially. "I was kind of naïve and a little scared to go back to the doctor," he says. "So I didn't do anything."
Six months later, he got a sinus infection that wouldn't go away, and eventually he went to urgent care, where some flags were raised unrelated to his sinuses. "They took my blood pressure, and it was 200 over 120," he says. "At that point, they told me I needed to go to the ER." [...]
August 13th, 2014 · Leave a Comment
By Paul Scotti
Some people who overcome a life-threatening illness feel motivated to give something back to those who helped make their recovery possible. Charlie Willwerth, a 61-year-old leukemia survivor and bone marrow transplant recipient from St. Augustine, Florida, is taking steps to help bring life-saving stems cells to others in need of a bone marrow transplant.
Two years out from his bone marrow transplant, and with his leukemia in remission, Charlie recently completed courier training with Be The Match, the world’s largest bone marrow registry, to become a volunteer stem cell courier. His new “job” -- transporting life-saving stem cells from a donor’s location to a matching recipient -- can take him anywhere in the world.
“This is the most direct way I can help others who have helped me get a second chance at life,” says Charlie. “If it wasn’t for my donor, I might not be here today to have the opportunity to help others with needs similar to mine.” [...]