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I’m the kind of person who follows my gut. So, when I looked up my symptoms online and thought I had , I kept pushing to get tested, even when my doctor told me no. When I went to get fitted for bras in 2016, the woman who measured me pointed out that my left breast was “huge” compared to my right one. I figured everyone has a little asymmetry and brushed off her comment. Several weeks later, I got an infection after my cat scratched my chest. My doctors diagnosed me with cat scratch fever, but it didn’t get better with antibiotics. My left breast was still swollen with lots of pain for weeks. I did my own research, and the symptoms pointed me to inflammatory breast cancer. I told my doctor in my hometown of Columbus, Nebraska. He suggested.
When most people hear the word “cancer,” they usually react with fear or distress. That’s why I’m so glad to work as a nurse navigator at : because I get to empower patients with knowledge to hopefully reduce those feelings. My job is to be the first point of contact between. MD Anderson. and patients who’ve just been with . That can be a very scary time. So, I do my best to put people at ease — both by meeting them wherever they are emotionally and by giving them solid, accurate information to use. That way, they can make the best possible decisions about with their families and care teams. Planning ahead for consultations. My job requires me to be a good investigator. That means finding out patients’ hopes and expectations, and identifying a.
The way I practice medicine is heavily influenced by the fact that I’m a mother. Many of the same qualities that are useful in parenting my four children — such as flexibility and perseverance — also come in handy while treating my patients. But of all the traits that serve me well in both areas, compassion is probably the most important. Compassion is. MD Anderson’s. secret ingredient. It’s not just our expertise, but the way we interact with our patients and their families. Obviously, our goal is to leave people cancer-free. But we treat people the way we would want to be treated. And that makes all the difference. The. MD Anderson. difference. Working at the is amazing. You can see that compassion and feel it in action the minute you walk thr.
In late 2016, I was eating , and had never missed a . Yet, I still ended up with a at age 50. I felt a lump in my right breast one day and knew it wasn’t normal. So, I went to my primary care physician. She ordered a diagnostic mammogram, and a to . Then she referred me to a local oncologist. Originally, I’m from Chicago, but I’ve lived in eight different cities since then. So, while I’d probably heard. MD Anderson’s. name in passing, I was completely unaware that it was the nation’s top-ranked hospital for cancer care. That’s why I didn’t even think of it when I was diagnosed on Dec. 27, even though I live just down the street. Today, I am so glad that I landed there. Because I am fairly picky, and everyone on my team at. MD Anderson. was amaz.
Natural killer cells – or NK cells – are part of our immune system. They patrol our bodies for abnormal cells like cancer and destroy them. But cancer cells can make themselves invisible, making it much more difficult for NK cells to find them and do their job. Through clinical research,. MD Anderson. is developing a new type of called CAR NK therapy. This type of treatment enhances the cancer-fighting power of NK cells. “We’re trying to build on the natural ability of NK cells by giving them the skills to recognize and destroy cancer cells that have made themselves invisible,” says co-leader of MD Anderson’s . Enhancing cancer-fighting ability of NK cells. Through the , Rezvani and her team gather NK cells from donated umbilical cord blood an.
Until November 2018, I’d never been hospitalized before. So, the suddenness of my at age 65 that year caught me completely off-guard. I’d had a persistent cough for several months. But I felt it was allergy- or acid reflux-related, so I wasn’t overly concerned. Then I started having trouble climbing the stairs in my Dallas home. I didn’t have much energy, and I was losing weight. The rapid decline in my health was unnerving. Finally, I went to a doctor. My physician ordered a chest X-ray, which showed a collapsed left lung and a growth in my chest. I knew it was serious, so I made the decision to get checked out at MD Anderson immediately. My wife, Leslie, had already been in there for for about 18 months, so I knew I’d be in the best hands.
Facing a or caring for someone during can be extremely . And, when you’re dealing with stress, your emotions, memory and relationships can all be affected. But journaling can help, says counselor Tiffany Meyer. “Journaling is an intentional act of honest reflection about yourself and the things going on in your life,” says Meyer. “It can help cancer patients and caregivers navigate one of the most mentally challenging times in their lives.”Here’s how journaling can make a difference -- and Meyer’s advice on how to get started. Journaling can improve your memory. Cancer and its treatment can sometimes cause problems with short-term memory, also known as . A daily journal practice can help you keep track of appointments, conversations or impo.
Losing bone density is common as you age, when cells that help rebuild bones aren’t replaced as quickly. Because of this, your bones may become thin and full of tiny holes, making fractures more common. While is a part of aging for many people, certain of cancer and cancer may lead to bone loss – no matter your age. To better understand bone loss in cancer patients and options for keeping bones healthy, we spoke with Here’s what she had to say. Are certain cancer patients more likely to have bone health issues? In general, women are at the highest risk, regardless of whether they’ve had cancer. That’s because bone loss usually happens after menopause. Patients with or also are at risk for bone loss because they’re often treated with drugs t.
If you, or someone you know, has ever had a cold or the sniffles, you may have already come into contact with a coronavirus. There are several different types of coronavirus circulating in the world, and the majority of them do not cause severe illness. Here are seven things cancer patients should know about coronaviruses, including the 2019 novel coronavirus (2019-nCoV) that was first detected in Hubei province, China. What is a coronavirus? Human coronaviruses are a family of viruses that are found throughout the world. There are . Four of those types (229E, NL63, OC43 and HKU1) cause only mild or moderate upper-respiratory illness, such as the common cold. According to the Centers for Disease Control and Prevention (CDC), most people wil.
It’s unlikely you’re ever going to meet anyone quite like my wife. For one thing, Susie is a two-time survivor. That alone makes her amazing. But she’s also still alive — more than 20 years after her initial . That makes her unique. We were so worried when Susie’s tumor was first discovered. Our kids were both really little back then: just 3 years and 2 months old. Susie feared, if she died, they wouldn’t know or remember her. Now, our youngest is 21 and studying biochemistry in college. Our eldest recently earned a master’s degree in biomedical engineering and is working in a neuroscience lab in Boston. Susie and I have traveled around the world and back. It’s all been possible because of the folks at. MD Anderson. . A brain cancer diagnosis.
I’d always heard that people should wait a year before at. MD Anderson. , so they could make sure they were “over it” after finishing their . But even when treatment is over, it’s not completely over — at least, not in your head. So, I don’t know who is ever “over it,” because I don’t think you ever really “get over” having cancer. I just knew when I was capable of being helpful again after a . So, I started volunteering in March 2018, about four months after I returned to work. And I’ve done a lot of volunteer service gigs in my life. But I never enjoyed any of them as much as I do this one. What spurred me to give back after my breast cancer treatment. I received a lot of support from people at. MD Anderson. , particularly when I first learned.
People never want to be just a number, a chart or a . They want their doctors to know them — to see them as real people and not just as patients. That’s why the first thing I do when I meet a new patient is listen. I want to hear people’s stories, so I can find out what they’ve been through that has gotten them to this point. Whether it’s an abnormal lab result, a suspicion of cancer, or a late-stage diagnosis that requires urgent , my priority is opening up a line of communication. That way, not only can I figure out what’s going on; I can also start building trust by answering any questions patients might have and explaining the steps necessary to move forward. Listening well is a critical part of caring for cancer patients. Doctors alread.
Before my in 2007, I didn’t know anything about . But then I came to. MD Anderson. for a second opinion after surgery, and scans done there revealed an enlarged lymph node in my chest that nobody else had noticed. Living in Houston, I was well aware of. MD Anderson’s. reputation. So when , and Dr. Ritsuko Komaki (now retired) said they thought I’d be a good candidate for proton therapy, I said OK. I trusted them completely. One reason my doctors recommended proton therapy was because the cancerous lymph node was so close to my heart, and this would limit its exposure to radiation. I had about seven weeks of proton therapy daily under their supervision, along with a reduced dose of weekly to make it more effective. And I’ve been cancer-free ever.
is a rare cancer that’s most commonly found in the lining of the lungs or abdomen, but it can also start in the lining of the heart or testicles in rare cases. Mesothelioma is most common in men ages 45 to 85. Typically, it occurs in those who’ve been exposed to asbestos, a fibrous mineral used in construction and manufacturing until it was banned by the in 1989. But not everyone who’s been exposed to asbestos will get mesothelioma. In rare cases, mesothelioma can be passed down in families through the BAP1 gene, or BRCA1-associated protein 1. Not everyone who’s been exposed to asbestos will get mesothelioma, but if you’ve been exposed, you could be at risk. To learn about mesothelioma , and options, we spoke with Here’s what she shared. Wh.
Since becoming a doctor, one of the most important things I’ve learned is that the more we can lower patients’ , the better off they are. Educating patients about what to expect improves both how they do during and how they feel about it. It’s like giving people a passport to their own healing. That’s why I’m so pleased to be involved in. MD Anderson. initiatives that ensure our patients receive the best possible care. My role lets me keep enjoying the remarkable relationships I’ve developed by treating individuals, while also putting entire systems in place that help all of our patients. Enhanced Recovery Program gets cancer patients feeling better faster. As a physician, my goal is to do the right thing for the right patient at the right tim.
When I first due to , I often heard people say, “Don’t worry. It’s only hair.” The implication was that it would grow back — eventually. But after a while, I began to notice that it was always the people with a full head of hair who said it. And I am one of the very small percentage of women whose hair didn’t grow back after . So, I am still bald to this day. It doesn’t feel like “just hair” when you’re the only one who doesn’t have any — especially when you’re a woman, and you realize that yours is probably never going to grow back. But I’m OK with being bald now, three years after my . Because I am cancer-free, too, and that matters far more to me than having hair. Most unexpected treatment side effect: permanent hair loss. At first, I cou.
My doctor didn’t notice anything unusual during my well-woman exam in February 2018. When I felt a lump in my breast two months later, I wasn’t overly concerned. I was only 38 years old. My husband said I should get checked again, but I didn’t think it would turn out to be . When I went to see my gynecologist a couple months later, my husband insisted that she re-examine me. My doctor ordered an ultrasound, a biopsy and a . They showed I had breast cancer. The weeks after my diagnosis were a blur of appointments and tests. The worst part was the uncertainty. I felt weak and completely vulnerable. My breast cancer treatment at MD Anderson League City. I've lived in Houston for 15 years. Even before coming to MD Anderson, I knew about its repu.
Genetic disorders can be really scary, but learning that I have one probably saved my life. It also led me to my current career. As a fundraiser for a children’s cancer hospital, my work supports research on , a rare genetic condition that I actually have. Originally, I was planning to become a pediatric oncology nurse. But my own and Li-Fraumeni syndrome took me down a different path. I dropped out of nursing school two weeks before classes began, because I’d just started for . But being in a hospital as a cancer patient ultimately showed me that nursing was not for me. I’ve still made supporting people with cancer my life’s work — just in a different way than I originally envisioned. Early detection is critical with Li-Fraumeni syndrome. I.
I’ve always wanted to be a mom. I became an aunt at a very young age, and I loved taking care of my nieces and nephews. I worked at a child welfare organization throughout high school, too, so kids have always been a part of my life. That’s why finding out I had stage II in August 2016 was a pretty bitter blow. By the time I was diagnosed at age 31, it had already spread to my cervix and both ovaries. My best chance at a cure was a total hysterectomy followed by . The alone would send me into immediate menopause — and end my dreams of having biological children. Choosing to have the surgery anyway was not an easy decision, but it was one my husband and I agreed upon. I’m still making my peace with it. Some days, I am perfectly content. Othe.

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