Editor's Note: A new report today from the Institute of Medicine of the National Academies addresses improving the health of people with chronic illnesses. Karen Basen-Engquist, Ph.D., professor in MD Anderson's Department of Behavioral Science, is one of 17 experts nationally who co-authored the report.
By Karen Basen-Engquist
In
fighting the war on cancer, emphasis has been placed on detecting
disease early and, hopefully, curing it. Many battles have been won, and
because of this we have more than 12 million Americans living today who
have had a previous diagnosis of cancer.
While those gains are to be celebrated, many cancer survivors suffer from after effects of treatment, or undergo extended treatment over a period of years to keep their disease in check.
In
essence, cancer is becoming a more chronic condition, a fact
acknowledged by the ground-breaking 2005 Institute of Medicine report
From Cancer Patient to Cancer Survivor: Lost in Transition, which
documented the experiences of cancer survivors after treatment, and the
gaps in the health care system which often resulted in a failure to
properly address survivors' problems and concerns.
Since then, MD Anderson and other centers have worked to address the needs of cancer survivors in health care settings.
A new IOM report released today, Living Well with Chronic Illness: A Call for Public Health Action,
draws attention to the need to help cancer survivors and others with
chronic illnesses manage their disease effectively, reduce
complications, prevent additional health problems, and optimize their
health.
Continue reading A Call for Change To Help Cancer Survivors, Others With Chronic Disease.
By John Chattaway, MD Anderson Staff Writer
Part II of Monday's post- Short Circuit: MD Anderson Robots Provide Safety in the 21st Century
"Autobots, roll out!"... and into the next lab
"I am a robot."
If you've traveled Floor 4 of the Main Building, you may have heard those words spoken by "Tess," the Swisslog SpeciMinder used by Laboratory Medicine to transport specimen batches between labs.
The robot is on loan from Swisslog while Pathology and Laboratory Medicine determines if it's a technology we want to invest in.
Laboratory Medicine technicians have a button or "bell" they push to call Tess. The robot has a pre-programmed map of our facility that it uses, along with external sensors, to find its way to the technician. Once Tess arrives, the technician loads specimen batches into it and tells it where to go.
Once Tess delivers the specimens to the required destination, if that destination has nothing to send, Tess returns to a docking station in the central specimen processing area.
"Tess minimizes the need for manual transport of specimen batches between labs. This enables our lab employees to stay focused on high value and patient-oriented work," says Lila Pulido, director, Pathology/Laboratory Medicine Operations. "It's also fun because you can program what Tess can say. I once heard it say, 'Sorry, I haven't had my morning coffee,' when it bumped into a wall."
Don't be fooled by Tess's simple, R2-D2-like appearance. The robot can hold up to 150 tubes of blood and a bag of microbiology specimens, or up to 50 pounds of cargo.
Continue reading Short Circuit: MD Anderson Robots Provide Safety in the 21st Century Part II.
By John Chattaway, MD Anderson Staff Writer
Robots. The word conjures images of science fiction characters from movies such as The Terminator, Star Wars or Transformers.
But those characters actually are androids, forms of human-like artificial intelligence. Robots are machines that, when programmed or operated by a person, can perform specific tasks.
At MD Anderson, we're using them to improve the safety and efficiency of our care.
"I'll be back"... with your medication
Pharmacy has been taking advantage of robot technology since 1998.
The first outpatient robot was installed in the outpatient pharmacy on Floor 2 of the Main Building. Now, all three outpatient pharmacies use the ScriptPro SP 200 prescription dispensing system.
Our outpatient pharmacies dispense approximately 1,300 prescriptions a day. According to Lori Bertrand, manager, Pharmacy Operations, the robots account for almost 55% of our prescription volume. The SP 200 robot can fill and label 150 prescriptions an hour. "It would be closer to 95% except that chemotherapy, narcotics and investigational drugs can't go into the ScriptPro robot," Bertrand says.
Continue reading Short Circuit: MD Anderson Robots Provide Safety in the 21st Century.
By Andrew Griffith
Andrew Griffith has mantle cell lymphoma and has had an auto (November 2009) and an allo (August 2011) stem cell transplant. He lives in Canada and is married with two young adult children. He blogs at www.lymphomajourney.wordpress.com and can be followed on Twitter @lymphomajourney.
Most
of us find it challenging to make sense of the wave of information when
we enter our cancer journey. This is foreign territory, with its own
language, culture and routines. It takes time to absorb and understand.
We're not oncologists or hematologists. However, we can learn to improve our discussion with our medical team.
Tips to help
Build your knowledge:
By the time you start your treatment, you'll likely have searched the
web and read brochures on your cancer. Ask your medical team which sites
have reliable and up-to-date information to avoid old and possibly
discouraging information on treatment outcomes.
While blogs and
support forums help give a real-world view of the range of experiences,
you're an individual, and too much thinking about what happens to
others, good or bad, increases worry further. Moderation!
To save time, set up Google Reader for news sites, blogs and forums, and use the search function (general terms like cancer or lymphoma) to narrow down articles of interest.
Continue reading Organizing your medical file.
By Isaac Van Sligtenhorst
Isaac
van Sligtenhorst is a physician-in-training in the Texas Medical
Center. He blogs about his training, as well as battling cancer from the
perspective of a caregiver. Read more about his approach to grief, hope and life in general at heartofalonelyhunter.blogspot.com.
Fifteenth floor, leukemia and lymphoma ward. My dad was admitted here twice, the second time the same day my brother died.
I knew the floor well.
I
had just finished with my patient and was waiting for the elevator. A
phenomenal case. History of four different cancers, pulmonary embolism,
triple coronary bypass, a stroke 80 years young, still alive and
kicking.
Truly a touching experience.
Connecting with compassion
While
waiting for the elevator, a young guy walks up slowly with his IV pole.
He's big and broad shouldered. I'm not exactly slight of frame, but he
towers over me. Probably in his early 20s, he sports a baldness that
could easily be fashionable. But his absence of eyebrows says the lack
of hair is due to far more grim reasons.
Below his eyebrows, his eyes catch me. There is a yearning in them. Something so elementally human, which desired contact.
Continue reading Strength in Weakness .
By Holly Easley
I began my journey about five years ago when I had some temporary blindness. I went to the doctor and my blood counts were low, so I was sent to a hematologist oncologist.
After a bone marrow biopsy, I was diagnosed with myelodysplastic syndrome (MDS). Once I got my diagnosis, I went straight to MD Anderson.
My doctor at MD Anderson was Guillermo Garcia-Manero, M.D., in the Department of Leukemia. I can't say enough good things about this man. From my first appointment with him, I knew he was the best doctor in the world. It turns out he's considered the leading authority in the world on my disease.
I never doubted him, did everything he told me to do and constantly sought his advice.
When my MDS became more vicious and progressive last spring, I became transfusion dependent and my quality of life was deteriorating, he decided it was transplant time. It was now riskier not to have the transplant than to wait. He also told me that after the transplant and when I no longer had MDS, he would no longer be my doctor.
I cried.
I had a stem cell transplant on May 24, 2011. Chitra Hosing, M.D., is my stem cell transplant doctor and I love her. She has a great team. She has helped bring me out of some tough times. Just as I had with Dr. Garcia-Manero, I have extreme confidence in her.
Continue reading Tips for Newcomers at MD Anderson .
By Val Marshall
Val Marshall's cancer journey began in May 2009, when her son Addison was diagnosed with acute lymphocytic leukemia. A visit to the family doctor for what they thought was a simple high school football injury turned out to be much more.
Inspired
by her son's strength and hope, Val strives to be a voice that connects
other parents on this journey. Her series shares insight into her life
as a mom of a typical teenager who just happens to be fighting leukemia.
Addison Marshall Crush Cancer
I
have to say that I was happy to ring in the New Year and say "hasta la
vista, baby" to 2011. Last year was a huge mountain for Addison to
climb. But he scaled it with a heavy load, while refusing to yield to
leukemia's wrath.
I remember when I saw the protocol with 104 weeks of chemotherapy
at the time of his relapse. I never thought the end of treatment would
occur. He's now looking down at 81 weeks -- "run Forrest, run!" We're
crossing our fingers and hearts that he will finish chemo in June, in
time to ship off to Texas A&M this fall.
Addie started the
year like he lives each day. He fell on jump boxes while working out and
split open his shin. I didn't flinch but realized that his platelets
must have been decent, even though it took a while to stop the bleeding.
Boy, I am getting lax.
Continue reading Happy to Say Ta-Ta to 2011.
By Sarah Cook, Department of Social Work
An acute leukemia diagnosis can make you feel as if the world has stopped -- for you, the patient, and for your loved ones.
Before
diagnosis there was grocery shopping, work, coffee dates and laundry.
Now, suddenly, life is lab work, test results and an endless stream of
medical professionals --many of whom you can't identify by name.
The
information comes fast and furious: "you have leukemia," "we're running
tests," "you're being admitted" and "we're placing a PICC line."
A
PICC line? What's a PICC line? Will my insurance pay for this? Will I
lose my job? What the heck is a stem cell transplant? Is that the same
as a bone marrow transplant?
To say that a new leukemia diagnosis can be overwhelming would be putting it mildly.
If
this has been your experience, please know that you're not alone. Also,
know that there's support to help you and your loved ones cope with
your diagnosis and treatment. MD Anderson social work counselors are available to offer emotional support and to help link you with helpful resources.
If
you or your loved one has recently been diagnosed with leukemia, there
are a few things you need to remember as you begin to cope with this new
situation.
Three things to remember:
Continue reading Learning to Cope With Leukemia.
By Sapna Patel, M.D., assistant professor, Department of Melanoma Medical Oncology
When a patient is diagnosed with uveal melanoma, he or she should be evaluated by an ocular oncologist, an ophthalmologist who specializes in treating cancer of the eye.
The
objective of this examination is to find out whether the uveal (or
intraocular) cancer has spread to the optic nerve or nearby tissues of
the eye socket, or has moved through the blood to other parts of the
body.
Depends on diagnosis
When uveal melanoma is
diagnosed, the treatment depends on whether the disease has metastasized
to other organs. Most patients whose disease has not metastasized are
treated with surgery known as enucleation or some form of radiation therapy.
A
commonly used radiation treatment for uveal melanoma is plaque
brachytherapy, in which a tiny radioactive disk is placed on the
affected part of the eye for a few days, minimizing exposure to
surrounding tissue.
Dan Gombos, M.D., associate professor and chief of the Section of Ophthalmology,
is an ocular oncologist who specializes in the treatment of
uveal melanoma, in addition to other intraocular malignancies. He works
in coordination with Beth Beadle, M.D., and William Morrison, M.D., in the Department of Radiation Oncology, to manage these patients.
The latest diagnostic techniques
and treatments for eye cancer are available at MD Anderson, where cutting-edge translational research is conducted,
continually driving laboratory discoveries forward to application in the
clinical realm.
Continue reading Treating Uveal Melanoma.
By Andrew Griffith
Andrew Griffith has mantle cell lymphoma and has had an auto (November 2009) and an allo (August 2011) stem cell transplant. He lives in Canada and is married with two young adult children. He blogs at www.lymphomajourney.wordpress.com and can be followed on Twitter @lymphomajourney.
One of the hardest things after a cancer diagnosis is telling others: family, friends and colleagues. I preferred a more open approach for a number of reasons:
- Keeping everything inside was harder; talking and writing was a form of release.
- People close to you need to know to support you.
- Letting people know avoids awkward questions and provides an invitation for support.
- Experience with others who didn't share made it harder on others and me.
Looking back over the past three years, a number of steps helped me talk to people:
Identify your circles: Who needs to know, after the obvious close family and friends? Do you have natural support groups (religious or other organizations)? What about colleagues at work -- how wide should the net be?
Write out your script and be direct: I think better by writing out things. Particularly at work, a script allowed me to get out what I wanted to say and ensure that I didn't forget anything important.
Continue reading Letting People Know.
With so many transformations in health care, it sometimes seems that the world is spinning faster. To organize each hectic day, I think about it like it's a string.
My strategy for dividing the string into various fragments is important. You need string of a certain quality and length to do things that require deep thought, like writing a paper or making major strategic or personal decisions.
Other things, like signing routine documents or filing things, can be accomplished using the lower quality portion of the string (i.e., the fragmented string toward the end of a long day).
This idea of strings -- what one faculty colleague called my "string theory" -- triggered a memory of a patient who told me an inspiring story. Inspirations are a gift shared by so many patients and part of the huge privilege of being a physician.
Here is the story that I recalled: "Look at the Strings."
Mr. Z. was a liberal arts professor with widespread cancer, in the midst of chemotherapy. A subspecialist colleague called to ask if I'd see this patient who seemed to have a distinctly profound problem with fatigue.
Continue reading Look at the Strings .
By Laura Nathan-Garner, MD Anderson Staff Writer
Your pap test isn't the only reason to see your gynecologist.
Your
doctor also can address unusual symptoms that could be cancer. And, he
or she can help you decide what do about body changes that may affect
your cancer risk at different stages of life.
Here are some topics you may need to discuss with your gynecologist at your next appointment.
1. Gynecologic Cancer: Symptoms Besides Pelvic Pain
Unfortunately,
gynecologic cancers -- including cervical, ovarian and endometrial
cancers -- have vague symptoms. And, many women often overlook or
mistake them for less serious conditions.
Talk to your doctor if you have any of these symptoms for more than two weeks:
Continue reading Conversation Starters for Your Next Trip to the Gynecologist .
Exercise Benefits Lung Cancer Patients, Study Shows
A typical patient of Vickie Shannon, M.D., is on oxygen and confined to a wheelchair. Often a family member is there, too, to offer information.
"'Mom can't walk from here to the bathroom. She struggles to get out of bed,'" is a common theme of these family members, according to Shannon.
"'She doesn't go to the store anymore. She's not cooking. She's not doing any kind of cleaning,' they say."
Shannon, a professor in the Department of Pulmonary Medicine,
listens carefully and takes notes. When she suggests putting the
patient in rehab -- which includes some exercise -- she gets startled
looks.
"You want her to do what? Have you listened to a word I've said?"
According to Shannon, much is now known about the pulmonary rehabilitation of patients with chronic obstructive pulmonary disease (COPD).
Still
in question is whether patients with COPD and cancer, or cancer
patients who may have lung disease due to other causes, benefit from
pulmonary rehabilitation during their treatments.
Continue reading You Want Me to Do What?.
By Stephen Collazo, Department of Social Work
Whether
you're the doctor or the patient, having conversations about future
care should be an integral part of the overall treatment planning
process at every stage -- beginning at the time of diagnosis. It's a
team effort and a partnership that ensures patient choices are given the
utmost respect.
Steps for planning
The following steps
are by no means an exhaustive list for fully implementing the advance
care planning process in one's specific medical situation, but it serves
as a good starting point for the patient and health care provider.
1. Evaluate quality of life
For
the patient -- Begin to think about what living with quality of life
means to you. Discuss your thoughts with the people who would be
involved in making decisions for you if you aren't able to make them
yourself. This will ensure that care choices are made to support your
quality of life in the way you'd like.
For the provider -- Ask patients what quality of life means to them. Explain their current treatment plan and the side effects
involved in terms of these ideas. Also, talk about how possible
life-prolonging treatments relate to the patient's concept of quality of
life. Remember, often the patient is waiting for you as the
professional to broach the subject of what they should do in end-of-life situations.
Continue reading Advance Care Planning: A Patient and Provider Partnership.
By June Stokes
June Stokes was diagnosed with stage IV ovarian cancer
in April 2000. She was told she had 12-18 months to live. June has been
cancer free for 11 years, and hopes her experience will offer comfort
and peace to those who are beginning their journey with (or after) a
diagnosis of cancer.
In June 2001, 14 months after my ovarian
diagnosis, my daughter, Lisa, told me that she found a lump in her
right breast. She called the same day and got an appointment with Dr.
David McCoy, an oncology surgeon.
Dr. McCoy did a needle
biopsy. The following day, I anxiously awaited Lisa's pathology report.
She called around mid-morning and said it was benign. Dr. McCoy would do
a lumpectomy the following week.
The lumpectomy was performed and the report would be back the following day.
As
I drove into my driveway the next evening, I noticed that Lisa's car
was parked in front of my home. I walked in and asked, "How bad is it?"
She started crying and I grabbed the paper and started reading
the pathology report, which stated, "duct carcinoma" and "differentiated
carcinoma." Unable to control my emotions I ran through the house, room
to room, crying hysterically while clutching the report.
Continue reading The Importance of Genetic Testing.
By Jennifer Texada, MD Anderson Staff Writer
About a month before my baby was due, my obstetrician asked me, "So, have you thought about what you want to do with the cord blood?"
Without hesitation, I said I wanted to donate it to the Cord Blood Bank at MD Anderson. She scribbled a note on my chart and we went on with the appointment.
Because I work at MD Anderson, I'm aware of the cord blood donation program. But if you've never heard about it, it's easy to miss.
Cord blood remains in the placenta and umbilical cord after a baby
is born. It's a source of stem cells that can be used as an alternative
to bone marrow to treat patients with many diseases, including cancer.
Continue reading Grace Saves a Life.
By Judy Overton, MD Anderson Staff Writer
Felipe Corrales has blown out the candles on 103 birthday cakes so far. He's also survived a prostate cancer diagnosis. However, the greatest challenge for the 17-year cancer survivor has been recurrent bouts of urinary tract infections.
The infections have been managed by Issam Raad, M.D., professor and chair of Infectious Diseases, Infection Control and Employee Health, through various antibiotics. Yet, Raad states, "The best care to prevent these infections is to place one of the antimicrobial urinary catheters being developed by our team."
The antibiotic coated central venous catheter (CVC), invented by Raad and his team of researchers in 1994, was first introduced through a randomized, double-blinded study in 1997 (published in Annals of Internal Medicine).
Now 14 years later, the Center for Disease Control is recommending it for all high-risk patients who continue to have infections after all the best practices fail.
According to Raad, "The CDC Guidelines that came out in May 2011 highlight our invention and placed it in the highest category, Category IA. The antimicrobial catheters are in practice now in Europe, as well as in the United States."
Continue reading Novel technology undermines infection.
Mesothelioma
is a rare cancer that starts in the cells lining certain parts of the
body, especially the chest and abdomen. Primary risk factors include
workplace exposure to asbestos.
Anne Tsao, M.D.,
associate professor in MD Anderson's Department of Thoracic/Head and
Neck Medical Oncology and director of its Mesothelioma Program, answers
questions about mesothelioma. (See related story on mesothelioma patient
Sherry Moore.)
What is mesothelioma?
Mesothelioma
is a cancer that arises from mesothelial cells, which normally make up
the lining around our organs. Mesothelioma can originate from the:
- Pleura (lining around the lungs)
- Peritoneum (lining around the abdominal cavity)
- Pericardium (lining around the heart)
- Testes
Is mesothelioma rare? In
the United States about 3,000 cases of mesothelioma are diagnosed each
year, and in Western Europe approximately 5,000. There is some
speculation that the 9/11 event that destroyed the Twin Towers in New
York City may lead to increased incidence of mesothelioma and other
cancers in the first responders who worked in the affected site.
Continue reading Q&A: Focus on Mesothelioma.
By Lauren Schoenemann, MD Anderson Staff Writer
Before mesothelioma,
Sherrie Moore dreaded the idea of getting older. Now, three years after
being diagnosed with the challenging illness, she celebrates each
birthday with joy.
"I used to not want to grow old, but now I
want to have a major celebration each year," says Moore, who celebrated
turning 55 at her home in Carl Junction, Mo., on Nov. 30.
In early 2008, Moore was supporting her husband, Ed, in his battle with prostate cancer.
When she began to feel fatigued and noted an elevated heart rate, she
called her general physician. He referred her to a cardiologist, whom
she had seen in the past for high cholesterol.
When her blood
work revealed a low hemoglobin count, Moore received a blood
transfusion. She also was instructed to visit a gastrointestinal doctor
for an endoscopy and colonoscopy. Those yielded normal results.
Results inconclusive
She
followed up with her cardiologist three months later and learned that
her hemoglobin levels had returned to almost normal. By that time, she
was feeling better.
In July 2008, Moore returned to her physician
with a pain in her right side that extended into her back. She
associated the aches with the stress and physical exertion of taking
care of her husband.
The doctor ordered a CT scan of her liver
and pancreas. While he found no abnormalities in these organs, he
recommended she find a pulmonary specialist. Something didn't look right
with her lungs.
Continue reading Mesothelioma Survivor Finds Hope, Appreciation for Aging.
By Lauren Schoenemann
A growing body of research has revealed that diet is thought to account for about 30% of cancers in Western countries.
Clare McKindley, clinical dietician in MD Anderson's Department of Clinical Nutrition, says choosing the right foods comes down to knowing one's physiological needs and practicing self-respect.
"Knowing what your food behaviors are is the first step in determining the most healthful feeding frequency for a person's nutritional and health goals."
Balancing your plate
The American Institute for Cancer Research (AICR) recommends that two-thirds of one's plate include vegetables, fruits, whole grains and beans. Foods and beverages that may support a reduced risk for cancer include:
- Beans
- Berries
- Cruciferous vegetables
- Dark green leafy vegetables
- Flaxseed
- Garlic
- Grapes and grape juice
- Green tea
- Soy
- Tomatoes
- Whole grains
Continue reading Diet and Cancer .