Archive for the ‘Articles’ Category

What’s Life Like After Lung Transplantation?

Aleem Siddique, MD

Aleem Siddique, MD

Lung transplantation is a life-changing event. Before transplantation, the lung transplant recipient will have been very limited in his/her day-to-day activities because of severe lung disease. They might have required assistance for even the simplest of tasks, such as having a shower or changing clothes. That degree of limitation leads to significant de-conditioning, hence, after recovering from the transplant surgery, the recipient will begin a process of rehabilitation.

Over time, most lung transplant recipients will experience significant improvements in their functionality and correspondingly will describe significantly better quality of life. They will find it easier to breathe and most patients will no longer require oxygen therapy. The impact of this is difficult to describe or quantify, simply put, breathing itself had become an enormous burden and that strain is lifted.

Lung transplantation is not without it’s own burdens. Principal amongst these is the constant need for immuno-suppression medication to prevent rejection of the transplanted lung(s) by the recipient’s immune system. Conversely, the possibility of acquiring an infection goes hand-in-hand with use of immuno-suppression medications. Therefore close monitoring is required to prevent and treat both rejection and infection, this means that the transplant team is always close at hand. For many patients, the transplant team becomes like family.

Despite some difficulties, most lung transplant recipients report being highly satisfied with the transplant outcome, and that, if they had to make the decision again, they would still choose to have a lung transplant.

Hope for Stroke Patients: Recent Treatment Advances Offer Better Chances for Recovery

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Stroke is a severely debilitating disease that can permanently change the lives of patients and their families. Everyone knows a family member or a friend whose life has been permanently changed by stroke. Stroke is a very common disease around the world. Every year more than 795,000 people in the United States will suffer a stroke and more than 130,000 will die as a consequence of stroke. In Nebraska, stroke is the fourth leading cause of death and more than 36,000 people live with stroke. Despite these frightening numbers there is hope for stroke patients.

Stroke prevention

The best way to prevent a stroke is to take care of  you health. More than 90% of strokes are the result of poorly controlled medical conditions. Avoid tobacco, control your weight, watch your diet, exercise and follow up regularly with your primary care physician. Work closely with your doctor to control your high blood pressure, diabetes, high cholesterol or heart disease. Just by reducing your blood pressure by 10 points you can decrease your chance of having a stroke by one-third. Controlling the other risk factors will decrease your chances even further.

Sudden signs of stroke: remember them easily with “FAST”

Stroke can present in many different ways: confusion, severe headache, dizziness, double vision, facial droop, difficulty swallowing, arm or leg numbness or weakness, sudden loss of balance, inability to speak and slurred speech all are symptoms of stroke. One easy way to remember the sudden signs of stroke is by using the F.A.S.T. acronym. F is for facial droop, A is for arm weakness, S is for speech difficulties and T is for time to call 9-1-1. If you think you or a loved one is having a stroke, the best course of action is to call 9-1-1. Patients who call 9-1-1 arrive faster to the nearest hospital capable of treating stroke and have better chances of receiving treatment.

FAST

Stroke types and treatments

There are two major types of strokes: ischemic and hemorrhagic. Ischemic strokes are by far the most common type in the United States and in Nebraska. An ischemic stroke is usually the result of a blockage in a blood vessel, whereas a hemorrhagic stroke is due to a blood vessel rupture. Treatment is different for each type; however rapid treatment is essential in both.

Since 1996, the only FDA approved treatment for acute ischemic stroke has been to administer alteplase. This is a medication that is given to patients with an ischemic stroke who arrive to the Hospital within 4 ½ hours from the onset of symptoms. Patients who receive this drug have a 33% increased chance of being independent or less disabled at three months after their stroke, when compared with people who did not receive the drug. In the last year there have been significant advances in the treatment of acute ischemic stroke. Five new studies show that patients who suffered a large stroke and were treated with new devices called stent retrievers – within 6 hours of onset, in an experienced stroke center – have a 33% to 71% percent chance of regaining independence or experiencing less disability at three months.

New, advanced treatment options available at Nebraska Medicine

Nebraska Medicine has the capacity to offer these novel treatments to stroke patients who qualify. To make these crucial advancements in stroke treatment available to more people in Nebraska and neighboring states we launched the Nebraska Medicine Tele Stroke Network. Tele Stroke brings stroke neurology expertise to the bedside of community hospitals. Working together, the neurologist and emergency department physician collaborate on the most appropriate treatment for the stroke patient. This program provides local and rural emergency rooms with 24- hour access to stroke neurology expertise and the advanced treatment options available at Nebraska Medicine.

Dr. Kalil is lead author on new pneumonia guidelines

By Stephanie Goldina, Infectious Diseases Society of America

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Andre Kalil, M.D.

ARLINGTON, Va. — Hospital-acquired pneumonia (HAP) and ventilator-associated pneumonia (VAP) — which account for 20 to 25 percent of hospital-acquired infections — should be treated with shorter courses of antibiotics than they typically are, according to new guidelines released by the Infectious Diseases Society of America (IDSA) and the American Thoracic Society (ATS) and published in the journal Clinical Infectious Diseases. In addition, the Society of Critical Care Medicine (SCCM), the American College of Chest Physicians (CHEST), and the Society for Healthcare Epidemiology of America (SHEA) endorsed these guidelines.

At a glance

•Seven days of antibiotics are effective for most hospital-acquired pneumonia (HAP) and ventilator-associated pneumonia (VAP) infections, according to the new guidelines published by the Infectious Diseases Society of America and American Thoracic Society.
•The new guidelines also recommend that each hospital develop an antibiogram to determine which strains are causing infection and ensure the right antibiotics are used for treatment.
•HAP and VAP cause 20 to 25 percent of hospital-acquired infections, and these may be fatal 10 to 15 percent of the time.

The recommendation of seven or fewer days of antibiotics for most of these infections reflects a change from previous guidelines to ensure safe and effective treatment while limiting the development of antibiotic resistance.
Created by a multidisciplinary panel led by infectious diseases, pulmonary and critical care specialists, the new guidelines also recommend that each hospital develop an antibiogram, a regular analysis of the strains of bacteria causing pneumonia infections locally as well as which antibiotics effectively treat them.

When possible, the antibiogram should be specific to the hospital’s intensive care unit patients, according to the guidelines. Antibiograms should be updated regularly, and the most appropriate frequency should be determined by the institution, the guidelines note.

“Once clinicians are updated regularly on what bugs are causing VAP and HAP in their hospitals as well as their sensitivities to specific antibiotics, they can choose the most effective treatment,” said Andre Kalil, M.D., lead author of the guidelines, professor of medicine in the Division of Infectious Diseases and director of the Transplant Infectious Diseases Program at UNMC. “This helps individualize care, ensuring patients will be treated with the correct antibiotic as soon as possible.”

Published in 2005, the previous guidelines recommended different lengths of treatment time for antibiotic therapy based on the bacterium causing the infection.

The 2016 guidelines recommend seven days or fewer for all bacteria. Newer evidence suggests that the shorter course of treatment does not reduce the benefits of therapy, Dr. Kalil said. In addition, he said this can reduce antibiotic-related side effects, the risk of Clostridium difficile, a serious diarrheal infection, antibiotic resistance and costs. In some cases, such as when a patient doesn’t improve or worsens, longer treatment may be necessary.

Mechanical ventilators help patients breathe. They are used when a patient is having surgery with general anesthesia or for those who suffer from impaired lung function. One of every 10 patients on a ventilator gets VAP, which is fatal about 10 to 15 percent of the time.

VAP also increases: the amount of time patients remain on a ventilator — from 7.6 to 11.5 days on average — and length of hospital stay — from 11.5 to 13.1 days on average.

While HAP typically is a less severe infection than VAP, half of patients have serious complications, including respiratory failure, fluid in the lungs, septic shock and kidney failure.

Life After A Double Lung Transplant

Andrea Mayberry

Andrea Mayberry

I was diagnosed with cystic fibrosis (CF) at birth. I was in and out of hospitals my entire life.

As my disease progressed, doctors said I would not live to be 16-years-old. I was put on the double lung transplant list at Nebraska Medicine – Nebraska Medical Center at the age of 12. I was on the waiting list for over two years.

I received “the call” in July of 1996 — I was almost 15. My mom got the call at 3:00 p.m. on a Friday and I was in surgery by 3:00 a.m. The surgery lasted 12 hours and all went smoothly. I was in the hospital for three weeks after surgery, which was half the time my previous stays were becoming. I was lucky to have lived so close to the med center, as I know many have to travel far for treatment.

Nebraska Medicine became my second home. All the staff including doctors, nurses, respiratory therapists, x-ray technologists and lab techs all knew me by name and were all part of my support system. Many continue to be part of my “family.” After my transplant, I still had appointments with my doctors. Luckily, my transplant coordinator was amazing at keeping things going and keeping everyone on the same page.

Before my transplant, I was on oxygen 24/7 and had multiple breathing and physical therapy treatments throughout the day — just to maintain my rapidly declining health. The way it was going, I would have been lucky to graduate high school, let alone attend college or get married. I am blessed to say that I did graduate high school, I graduated college with a bachelor’s degree in Medical Imaging and am engaged to my fiancé, Merl!

I have worked at Nebraska Medicine as a mammographer for over 11 years now. Life is amazing. I have the med center and its staff to thank, but most importantly, I have my donor and their family. I will forever be grateful to Nebraska Medicine for the care I received then — and continue to receive. They will always be family to me and I’m thankful to live so close to such an extraordinary medical center.

Surgeon’s Legacy Continues, 45 Years after First Kidney Transplant in Nebraska

Richard Steenburg, MD was destined to be a physician from the time he was a child, following in the footsteps of both his father and his grandfather. “My grandfather was a horse and buggy doctor who provided health care for a 60-mile radius covering most of the middle of the state of Nebraska. My father was a Harvard-trained general surgeon,” he recalls.  “From an early age, all I ever thought about doing was becoming a surgeon. In fact, by 10 years of age, I would go after school and observe my father in surgery.”steenburg2

Richard Steenburg, MD (left) performed the first kidney transplant in the state of Nebraska. In his 17-year career at Clarkson Hospital, he performed more than 500 transplants.

 

A graduate of Aurora Public Schools, Dr. Steenburg attended Stanford University, Harvard Medical School and completed his surgical training at the Peter Bent Brigham Hospital. Early in his career, he served on the faculty at Johns Hopkins and became chief of surgery at Baltimore City Hospital, as the first transplant program in Maryland was developed. In 1970, he moved back home to Nebraska, where he built a transplant program from the ground up, and where his education, training and passion continue to have an impact on patients and families today.

“He trained with the best of the best. It was amazing he was willing to come back to the Midwest and get the program started,” says Tavi Baker, who worked for Dr. Steenburg in the 70s and 80s and continues to serve as a nephrology coordinator at Nebraska Medicine.

“He taught us everything. You watched and listened; he talked and explained,” remembers Mary Ellen Krobot, a kidney/pancreas transplant coordinator, who also worked with Dr. Steenburg throughout his 17-year career at Clarkson Hospital. “It’s how I learned the basics. He was a great teacher and wanted people to understand what’s going on.”

Much has changed since 1970, when Dr. Steenburg performed the first kidney transplant in Nebraska. “At the time local surgeons weren’t trained in the proper technique of recovering organs,” he says. “On many of the first transplants, I would fly or drive to hospitals in outlying areas and recover the organs.” Once the kidneys were tissue typed, the team would identify the most appropriate recipients and have them come to the hospital. Then, the patients would receive dialysis, a blood transfusion and be prepared for surgery. “The typical transplant usually took about three hours. Between recovering the organs, preparing the patients and then transplanting the kidneys into the recipients, it wasn’t uncommon to work 24-30 hours straight,” Dr. Steenburg says.

All the work was completed without modern electronic health records – or even computers. Baker and Krobot remember sorting through handwritten lab results and communicating with typed letters. Paper flow sheets were hanging on the walls outside patients’ rooms and Dr. Steenburg memorized many of each patient’s details. “All of the patient information, drug therapies and lab work was kept in paper copy in the patient’s chart,” he says. “But many subtleties of managing a patient were done using one’s head.”steenburg1

Richard Steenburg, MD with transplant coordinators Mary Ellen Krobot and Tavi Baker in 1989. Krobot and Baker continue to work at Nebraska Medicine, and describe Dr. Steenburg as a dedicated surgeon and teacher.

 

Before Dr. Steenburg retired in 1987, he performed 501 kidney transplants. Many of the transplant patients are still living, including some of the first patients from 1970 and his final transplant patient, who received a kidney in April 1987. “Historically, patients with renal failure requiring dialysis were kept on dialysis until their insurance ran out. We were able to provide these very needy patients a chance to live,” he says.  Because of Dr. Steenburg, teens were able to go to college, women were able to raise their families and older people were able to meet their grandchildren.

Dr. Steenburg’s impact continues to be strong today, as Nebraska Medicine treats more than 1,500 functioning kidney/pancreas patients following their transplants. Hundreds more are impacted by the Nebraska Organ Recovery System, which serves all of Nebraska and Pottawattamie County, Iowa. The basis of the nonprofit organization started in a closet of Dr. Steenburg’s operating room. Now, it handles the recovery, transportation and distribution of all organs and tissue for transplantation in the area.

Nearly 30 years have passed since Dr. Steenburg’s retirement, one thing that hasn’t changed – his patients adore him. “They looked at him as their lifeline,” says Baker. Children drew pictures of him, patients continue to ask about him and many participated in a card shower in honor of his 75th birthday fifteen years ago. “Patient satisfaction is probably the best indicator of performance. Hearing from so many patients so many years later led me to believe that we provided a high standard of patient care,” says Dr. Steenburg. That standard of care continues to be Dr. Steenburg’s legacy, more than four decades after his first, ground-breaking kidney transplant in Nebraska.

How Breast Cancer Research Saved My Life

In September 2015, Janet Tinney was diagnosed with breast cancer.

In September 2015, Janet Tinney was diagnosed with breast cancer.

As you listen to the news, read the paper, check Facebook or talk to others, you’re frequently made aware of someone that’s been diagnosed with cancer. You think about them often, pray for them and their family, but then go on with your day-to-day life. Until that one day, when you’re the one receiving the devastating phone call. Where they ask you to come back in – because something doesn’t look right.

Janet at her chemotherapy treatment.

Janet at her chemotherapy treatment.

Over the years, due to very dense breast tissue, I’ve had many calls asking me to return for further testing following a mammogram. I’ve even had a couple biopsies and other procedures. Fortunately, each time the extra tests were performed, I received a phone call with good news that everything was benign – until September of 2015. That’s the year I received a phone call, informing me I had breast cancer.

For the first few minutes, I was stunned and speechless. Then the tears came. My emotions got the best of me. Until you’re the one getting that phone call, you never truly know what it’s like. My father passed away due to cancer. I spent nearly two years going to appointments and treatments, waiting through every surgery. Even though the experience with my dad was unpleasant in the end, I knew I had been given the knowledge and strength to deal with my own cancer battle.

As a caregiver, my first thoughts were about my husband and children. I knew this situation would be tremendously stressful for them. At the time, I felt helpless, but knew my family and friends would be my rock.

The day I was diagnosed with cancer, I was sent to a local surgeon in North Platte, Nebraska. He was incredible, but knew I needed to see the very best.

I was referred to Nebraska Medicine surgical oncologist Edibaldo Silva-Lopez, MD, PhD. During the first visit with Dr. Silva in Omaha, I barely let him speak before peppering him with questions about my future. Did I need to get my things in order? If so, how long did I have? He looked me straight in the face and said, “that is not even a concern for you.” He was certain I would survive. My heart danced!

Edibaldo Silva-Lopez, MD

Edibaldo Silva-Lopez, MD

Dr. Silva’s recommended treatment plan for me was newly approved, but research showed the results were very positive. Within the next couple weeks, we began treatment at the cancer center in North Platte. Everything started to happen just like Dr. Silva said it would. He anticipated my cancer journey would be about a year long, barring any complications.

But, after two rounds of chemotherapy, we were in for quite a surprise. During an ultrasound of my breast, the tumor was nowhere to be found. My radiologist was completely shocked. What a happy day!

I completed two more rounds of chemo, followed by a regimen of drugs. In January, Dr. Silva performed surgery, removing a margin of tissue where the tumor once was, along with 17 lymph nodes. About a week later, I received a phone call from Dr. Silva’s nurse, Carol, telling me all the tests performed on the removed tissue and lymph nodes were negative for the cancer! The treatment plan Dr. Silva gave me worked.

When this journey began, my husband and I both prayed for a miracle. That miracle was not for the cancer to just go away, but for me to be directed to the right physicians with the knowledge to cure my disease. In my opinion, my prayers were answered and my miracle was granted. Without cancer research and the dedication of physicians who put it to use, who knows where my journey would have led. But, because we are fortunate enough to have these services in Nebraska, I am able to look forward to a bright future.

I now pray for a financial miracle so that breast cancer research can continue to evolve at the Fred & Pamela Buffett Cancer Center for many, many years to come. I am living proof that this research does make a difference.

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Computer Aided Detection: New tools to help your doctor find cancer

Neil Hansen, MD

Neil Hansen, MD

Prostate and breast cancer are two of the most common cancers around. Unfortunately, most people know someone who has one of these. Many doctors have spent their careers trying to design screening tests to find these tumors at an early stage when they are still curable. This usually means finding them when they are really small. That sometimes means smaller than a pea.

So, how do we find these cancers? For breast cancer, the standard screening exam for years has been mammography – taking an x-ray of the breast and looking for cancer. Recently, Nebraska Medicine Radiology has adopted a fancier version of this – tomography—which is a 3D x-ray. On mammography, finding cancer can be tough. It can be seen as only a few tiny dot sized areas of calcium—little blips of white on the screen. To help find these doctors use computer aided detection (CAD). This is a computer program that takes the mammogram and identifies these calcifications. Studies have shown that these programs allow doctors to find earlier cancers better, especially younger and less experienced doctors.

While CAD has been used in mammography for years, it is relatively new for looking at prostate cancer. Screening for prostate cancer has been controversial, but traditionally has relied on physical exam (the finger / glove test frequently dreaded by men) and a lab test called Prostate Specific Antigen (PSA). If one of these is abnormal, that leads to a biopsy. In the prostate, biopsies are often randomly aimed because we don’t know where the cancer is. If one of the biopsies is positive then you know there is prostate cancer, but not necessarily its stage. If the biopsy is negative, then the tumor might have just been missed. This is where prostate magnetic resonance imaging (MRI) comes into use.

Prostate MRI uses a powerful magnet to take pictures of the prostate. It is sometimes hard to differentiate cancer from an old infection on MRI. This is where CAD is used. We recently acquired DynaCAD at Nebraska Medicine Radiology. It is a new tool where a computer program helps us identify cancer based off of blood flow in the prostate and other imaging parameters. A similar program has been in use for breast MRI, and we just acquired the latest software package for this as well. Our use of these doesn’t cost patients anything extra. The goal in the future is to use this program to do targeted prostate biopsies of suspicious areas and avoid randomly missing tumors.

These exciting new products will help us find early stage curable cancers. They aren’t perfect though and still require an expert radiologist to interpret their findings. At Nebraska Medicine Radiology, our specialty trained radiologists are committed to apply our expertise and all tools available to provide extraordinary care to our patients.

Look How Far We’ve Come!

Cancer-Center-Nov.-20[1]Our skyline is changing! The photo to the left was taken Nov. 20, 2015 of the Fred & Pamela Buffett Cancer Center. It’s a dramatic comparison to the next photo, which was taken on July 15.

The new cancer facility, which is expected to open May 2017, will ensure Nebraskans and patients throughout the region will have convenient and quick access to the latest breakthroughs in cancer therapy. A joint project of Nebraska Medicine and UNMC, the Fred & Pamela Buffett Cancer Center will include three areas dedicated to cancer: a 10-story, 98-laboratory research tower named the Suzanne and Walter Scott Cancer Research Tower; an eight-story, 108-bed inpatient treatment center named the C.L. Werner Cancer Hospital; and a multidisciplinary outpatient center.7-19-Cancer-Center-picture-from-July-151-300x225

After Losing My Husband to Cancer, Nursing Saved My Life

Sara-nurse-OHSCUSara Weging is a nurse on the Oncology Hematology Special Care Unit at Nebraska Medicine.

I always knew I was meant to help people, but it wasn’t until I met a very special person that I was able to recognize how I was supposed to achieve that goal.

As a new undergrad, fresh out of high school, I felt that the world was completely open to me. I could do anything I set my mind to – what I wanted to do was nursing.

Luckily, my university had a week immersion program for perspective nursing students to make sure that nursing was the correct fit. By the end of the week, all twenty students were sitting around a large oak table going on and on about how nursing was the career for them. When it got to be my turn to speak, all I could muster was an emphatic, “No way!” I could not fathom the thought that I would be responsible for another human life. I had just graduated high school, moved out on my own and was expected to take care of myself for the first time. I was in NO WAY ready for the huge responsibility that is nursing.

So, I pushed nursing to the back of my mind and moved on to other pursuits. Fast forward fours years later, I was a new graduate moving to Chicago and ready to take on the world. Life in Chicago was not easy, but it was new and exciting. I craved adventure. Adventure found me in many ways, but the best way by far was in the form of my amazing husband, James. It didn’t take long for James and I to find adventures of our own and for both of us to enjoy the city in new and exciting ways. Whether it was touring the different neighborhood festivals, taking in a White Sox game or simply sitting on the great lawn in Millennium Park, life was great and neither one of us wanted it to change.

Right before Thanksgiving 2011, we received a phone call that forever changed our lives. James, when he was sixteen, was diagnosed with Acute Lymphoblastic Leukemia (ALL). He underwent treatment with chemotherapy and by the time we met, he was five years into remission. Unfortunately for us, that Thanksgiving would not be a day of thanks, but a day of worry and dread.

After a routine clinic visit, James received the call that his cancer had returned. Together, we returned to the life that he thought he was done with. This new world of clinics and hospitals was completely foreign to me. To turn and run would have been all too easy and honestly, expected. But, James handled everything with such courage. Every time he would look at me with his big blue eyes, all I could feel was the enormous amount of love I had for him. He was my sun in a sky full of dark clouds.

So, I charged forward and did everything in my power to help James. I didn’t want him to feel like he was “the man with cancer,” yet again. At first, it was the small things – taking him to clinic visits, making sure we had food in the apartment that he had an appetite for, keeping the apartment clean and just trying to keep our lives as normal as possible. Making cancer something that was a part of our lives – but not the thing that defined it.

Sara-and-James

Sara’s husband, James, lost his battle with leukemia in 2012.

As time when on and treatment continued, James grew increasing sick. I decided to take time away from my day job and become his full time caregiver. This was not an easy decision to make, but it was killing me to be away from him. James would have to stay in the hospital for multiple days and he would never say it, but I could always see it in his eyes – he hated to see me leave.

Soon, I was learning how to clean and dress any wounds that he may acquire, how to hook him up to hydration when he was getting to dehydrated, mix medications together, keeping track of more pills than I had ever seen and how to give shots. This was a world that I had once envisioned for myself, but in a very different setting. It alarmed me at how comfortable I had become in such a short amount of time. I felt myself watching the nurses to see how they interacted with patients and how they performed certain tasks. The nursing staff quickly became more like friends than anything else. They were people that I could openly share my fears, share plans for our future and truly anything that was on my mind. They were the ones that were there during the hard nights, holding my hand and giving me words of encouragement.

The nursing staff was with James and me until the every end. At 8:52 a.m. on August 12, 2012, James took his final breath. After only two and a half years together, I had to tell the love of my life goodbye.

After James died, I was a wreck. I couldn’t eat or sleep. All I could do was sit and cry. Cry over not only losing the love of my life, but also losing my future – a future I desperately wanted. I felt like I was drowning and everyone around me was just watching me struggle as they continued on with their lives. Life for me continued in this fashion for about two years. Once I started to come out of the fog that was now my life, I couldn’t figure out what to do. What next? Surely, I couldn’t live in my mother’s basement for the rest of my life, curled up in blankets that were saturated with tissues and stained from tears.

It was at this time that I remembered nursing. I remembered taking care of James for all those months and not only loving the fact that I got to take care of him, but knowing that I wanted to do that for others as well. I vowed that I would give anything I had left to other families going through exactly what I had gone through – hopefully making James proud along the way.

I applied for the accelerated nursing program at Creighton University and within a year’s time, I was Sara Weging, BSN, RN. I started working in the Oncology Hematology Special Care Unit (OHSCU) at Nebraska Medicine – Nebraska Medical Center. I could not ask for a more perfect job.

Being in the OHSCU is oddly comforting and feels a little like home. Not only being able to take care patients at the most vulnerable points in their lives, but being able to bond with the families. I love it when my experiences are able to be shared and help others that are in similar situations as I was. I truly believe the patients and families on OHSCU are a very special group of people. It’s a gift when I can tell them I know exactly how you feel. They are not alone.

There are still days when I feel very lost. When something funny is on TV, or a special song plays on the radio, I find myself turning to talk to James about it. Then there are days that I wake up and pray it was all a bad dream. When I realize it’s not, I feel like I have lost him all over again.

It has been really hard to live each day like I know James would want me to. He wouldn’t want me to cry over him. He would want me to go on living and he most definitely wouldn’t want me to give up on my dreams. Nursing is slowly bringing me back to life and helping me realize that it is okay to move forward. Life doesn’t stop moving just because I fell off the ride

Mother Hears Son’s Heart Beating for First Time in Three Years


April is National Donate Life Month, a time to raise awareness about organ donation and celebrate those who have given the ultimate gift of life. On April 1, a unique event took place at Nebraska Medicine – Nebraska Medical Center involving heart transplant patient Terry Hooper and his donor’s family.

In June 2003, Hooper was diagnosed with cardiomyopathy, a disease of the heart muscle in which the heart loses its ability to pump blood effectively. In April 2005, doctors at Nebraska Medicine discovered Hooper’s aortic valve was leaking – something that had probably gone undetected since birth. He underwent an aortic valve replacement, but his heart was still only functioning at 30 percent. By August 2012, his heart function had declined to 5 percent and he was placed on the transplant waiting list in October of that year. After being on the list for 52 days, Hooper received a heart transplant on Dec. 10, 2012.

Lisa and Terry Meet
On April 1, Lisa Swanson met Terry Hooper, the Nebraska Medicine patient who received her son’s heart.

At the time, Hooper had no idea his donor was 18-year-old Levi Schulz of Horace, N.D. Levi was killed in an automobile accident Dec. 7, 2012. His body was kept on life support so that his organs could save others.

In the spring of 2013, Hooper wrote a letter to his donor family. That May, he received a letter from Levi’s mom, Lisa Swanson. Over the years, they continued to correspond, but never spoke on the phone or met face to face.

Lisa-and-Terry-meet

On Friday, April 1, Hooper met Levi’s mom and twin brother, Shelby Schulz, for the first time.

The family got to see and hear Hooper’s heart beating through an echocardiogram. At the end of the meeting, Hooper surprised Swanson with a HeartBeat Bear that had a recording of his heartbeat.

Nebraska Medicine is home to one of the most reputable and well-known organ transplant programs in the country. It’s one of a few institutions nationwide to offer all solid organ transplants under one roof.

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