January 16th, 2015 · Leave a Comment
Bill Steele, a patient at Mayo Clinic's Arizona campus, shares his story about hisÂ battle against Stage 4A cancer in the throat area without undergoing radiation or chemotherapy. In the video he produced, he explains how his surgical care team, led by Michael Hinni, M.D., a Mayo head and neck cancer surgeon, used transoral laser microsurgery to treat his cancer and help maintain hisÂ quality of his life.
January 2nd, 2015 · Leave a Comment
Kristine Long, a patient at Mayo Clinic'sÂ Arizona campus, has had anÂ incredible journey as a three-time Hodgkin's lymphoma survivor. In the course of her struggle, she has also overcome congestive heart failure and subsequent voice impairment.
In the video below, she explains how the care provided by her Mayo Clinic physicians, James Slack, M.D., a hematologist;Â D. Eric Steidley, M.D., a cardiologist; andÂ David Lott, M.D., an otorhinolaryngologist, along withÂ their care teams, hasÂ made her a whole person again. She also talks before and after repair to her vocal chords about what that procedure has meant to her personally and how it's given her renewed confidence as well as giving her voice back.
October 15th, 2014 · Leave a Comment
There are certain sounds that Scott Malmstrom had never known. He was born with hearing impairment, and it gradually got worse throughout his life. By fourth grade, he began experimenting with hearing aids. Over time, he became what he calls a â€śprofessional lip reader.â€ť
Hearing aids didnâ€™t help much with the type of hearing loss Scott had. â€śWhere he struggled was speech discrimination â€“ being able to recognize and understand what's being said,â€ť he says. â€śThat's where they eyes take over. That's what I've done over many years and became very good at it.â€ť
But his diminished hearing did keep him from experiencing certain things, and he says it affected his communication with those he loved. Today, through the magic of cochlear implants, Scott is hearing new things and experiencing life in a way he hadnâ€™t quite imagined.Â Read the rest of this entry »
October 6th, 2014 · Leave a Comment
In January 2013, Carly Edgar, an otherwise healthy 20-something, found herself in the hospital and in severe pain. The pain seemed to originate from near one of her ribs, but her local doctors couldnâ€™t identify the source. She spent a week in the hospital without any answer. She was released, but it wasnâ€™t long until she was back again.
Carly rated her pain at 10 on a 10-point scale, but doctors started to doubt her symptoms. They gave her pain medicine, but they also recommended antidepressants. When her boyfriend noticed a bump forming on her nose, she was told it was likely just a pimple. After a second week in the hospital, with things only looking worse, Carly asked to be discharged, and she and her boyfriend traveled to Mayo Clinic in Rochester, Minnesota, in search of answers.
Within a few days, Carly had her surprising answer â€“ a rare autoimmune disease called relapsing polychondritis. The disease attacks cartilage, and it was affecting not only her ribs and her nose, but also her heart, where doctors at Mayo found inflammation. She admits that it was a difficult diagnosis, but it also gave her hope that treatment could control her symptoms.Â Read the rest of this entry »
February 19th, 2014 · Leave a Comment
For her first 38 years, Jayne Bushman was a picture of health. But then one morning she woke up with an earache, something she says she'd never before experienced. Her first stop was to see her Family Medicine doctor at Mayo Clinic in Rochester who, unable to pinpoint the exact cause of her pain, sent her to Mayo's Department of Otorhinolaryngology. It was there that after a series of additional tests and examinations, Bushman learned she had much more than and ear infection. The diagnosis was Wegener's granulomatosis, a rare disorder that inflames the blood vessels and restricts blood flow to various internal organs.
The ear issues were simply one manifestation of the disease, which often affects the kidneys, lungs and upper respiratory tract. The restricted blood flow caused by the disease can damage these organs.
As Bushman listened to doctors explain her diagnosis, she says she felt "shocked." That only got worse after she went home and began using the Internet to research her disease. "The very first thing I did after my diagnosis is what a lot of people do, which is the very wrong thing," she says. "And I now tell any person I meet or talk to online who gets diagnosed with Wegener's disease to stay off the Internet. It'll do nothing but scare you. That's exactly what it did to me."
Still, Bushman says she only allowed herself to feel that way for a moment or two. "Initially, it was a huge shock," she says. "But I had three kids at home, I have a career â€¦ and I sure as heck wasn't going to let this get in the way of that. I've always tried to not live in my disease and to instead live with my disease.â€ť Read the rest of this entry »
February 5th, 2014 · Leave a Comment
By Seth Locketz
I was diagnosed with eosinophillic esophagitis (EE) by another provider, who said I needed to have my esophagus stretched every six months with a balloon. I decided to get a second opinion at the Esophagus Clinic at the Mayo Clinic. Wow, am I glad I did! At first, I was given a soft steroid, which may the EE go away! Which was great news! However, then Dr. Alexander and his team did some additional testing of my esophagus, and they were able to figure out that my EE (for which I had 10 times the normal amount of eosinophils) was actually caused from eating eggs, peanuts and dairy! Through the great care of Dr. Alexander and his team, not only did I not have to have my esophagus stretched, I did not even need to take medicine!!!! Read the rest of this entry »
May 31st, 2013 · Leave a Comment
I was born profoundly deaf due to auditory neuropathy and did not hear a single sound until I received a cochlear implant when I was 4 Â˝ years old. My parents said that I was always a happy, sweet child and I was born with a smile on my face and a twinkle in my eye. Throughout my life, Iâ€™ve had to deal with many obstacles due to my deafness that most people donâ€™t have to deal with. However, my cochlear implant, this miracle of sound, gives me an appreciation of sound and richness to life that others may take for granted. Through it all, Iâ€™ve held onto my belief that you shouldnâ€™t just live life, but love it! Read the rest of this entry »
January 15th, 2013 · 19 Comments
Imagine listening in real time to the thump, thump of your own heartbeat, the rush of your blood pulsing through your veins, and even the slightest twitch of your eyes - all in surround sound.Â Those are but a few of the symptoms that Wendy Tapper was experiencing when she arrived at the Mayo Clinic in May of 2012.
The Journey to Mayo
Outgoing and energetic Wendy, of Kansas City, Mo., enjoyed a career as a producer and publicist.Â Bringing people and ideas together was second nature to Wendy and aided in her determination to find the answers in her own health care.
For three years prior to coming to Mayo Clinic in spring 2012, Wendy went from doctor to doctor and endured batteries of tests, scans, appointments and misdiagnoses.Â Her rare condition ultimately revealed by Mayo physicians was masked in part by two distinct illnesses - breast cancer and a stroke.Â
While those illnesses and the treatments Wendy was receiving are life-altering, they were compounded with the escalation of an underlying third and separate issue.Â It was the escalation of her symptoms of dizziness, hearing loss and a drastically diminishing quality of life that brought Wendy to Mayo Clinic. Read the rest of this entry »