Categories
Amanda McGovern cancer cancer management cancer recovery cancer treatment recreation Seas IT Todd McGovern

Todd McGovern’s Legacy — Seas IT

Todd McGovern died at home on January 29, 2013. I read the obituary in the New York Times and found the story very inspirational. I want to share it with you because I think it will encourage you and your loved one to be as involved in life as he was as he battled cancer. He outlasted his diagnosis by several years. He fought the good fight, as so many cancer patients do. But what he left behind, what goes on in his absence, is his legacy.

Todd was just thirty, married for all of two months, when he received his terminal cancer diagnosis. Imagine that blow. Here you are, starting out your new life with your new wife. The world is your oyster. You have just about all of your adult life ahead of you. You imagine growing old with the woman you love. You’re planning your future together. And then this has to happen.

Todd didn’t take it lying down. He fought back. He made decisions about what he, not the cancer, was going to do for him. I have little doubt that it was not an easy struggle. Anyone who’s been around a cancer treatment center knows what a tough foe cancer can be.

But this young man, still so full of promise, was determined to impact the trajectory of his life. He was not willing to surrender himself to the despair of the disease. Todd wanted to live life to the fullest.

Sometimes ordinary people become extraordinary through circumstances not of their own making. They reach deep inside and they pull out that rabbit from life’s hat. Todd was such a young man.

But Todd had a partner, a supporter like no other. Amanda was surely a big part of that whole enterprise. She started Seas IT, a cancer recreation program to help them stay focused and positive throughout Todd’s cancer treatment and management. She understood the beauty of the great outdoors, with all of its restorative energy. She understood that being involved and passionate about your life was a key to living, not just existing.

I get that. When I was pushed to the edge as a caregiver, especially during my mother’s declining days, hiking was my one real pleasure. Every time I discovered a new trail, I was reconnecting to life. Every time I took a break from my mother’s cancer, I was renewing my spirit in the sights, the sounds, and the pleasures of nature. I would come home and face my caregiver duties with a determination to start fresh. I left the house weighed down by my responsibilities and I returned refreshed. That’s what recreation is all about, whether it’s running a marathon, enjoying a play, or visiting a museum.

I recall lugging my mother’s medical equipment through more than one art exhibit, pushing her wheelchair. Nothing made her feel more human again that visiting an art museum. We made our way through the centuries in three very different bastions of art history. And every time we returned home, my mother was satisfied that her disease had not gotten the better of her. It had not kept her from the things she loved most.

Recreation is that respite time we save for ourselves, for our wounded spirits and our challenged bodies. It’s that time we throw ourselves into what makes us most happy because it helps us to be true to our souls. For some, it’s running. For others, it’s fishing, knitting, or maybe even finally getting around to taking those piano lessons you always wanted to have, but never got around to doing. Recreation is all about you, not your disease. It’s about working on your putt instead of fretting how long your bone cancer will take to kill you. It’s about throwing that clay onto your potter’s wheel and creating a masterpiece.

It’s about doing, not just dreaming. It’s about getting off that recliner and getting back out into the world, where you belong. It’s about shutting off that little voice in your head that says you should just raise the white flag and be done with it. It’s about shaking off the terror of having cancer and living your best life inspite of it. Todd had cancer, but Todd also had life and a woman who loved him. That’s a very powerful force that creates positive energy, that extends life even against the odds.

So often cancer patients find their lives limited by the rigors of treatment. They spend their lives going back and forth to the hospital, getting scanned, getting chemo and/or radiation. That’s really when a lot of people begin to give up. If all you see is your bed and your doctor, the message you receive is that life as you knew it is over.

Todd and Amanda McGovern saw past that limitation. They knew they needed more. They knew other cancer patients needed more. Seas IT is all about staying as active as is possible during cancer management. It’s about using recreation to keep spirits up, to keep hearts open, to keep hope alive.

Todd lived long enough to see his twin sons born last June. He lived long enough to pass along his passion for recreation to those cancer patients who walk in his footsteps, who come up behind him. He lived long enough to share with us a very important secret for cancer patients. The more normal your life is with cancer, the better you will survive it.

Why is this important? Any cancer patient can tell you that in each new day that dawns, the promise of a cure hides within the heart. That promise wasn’t there unendingly for Todd. His life ended too soon when his time ran out. But because he and Amanda shared their secret about the pleasures and the power of recreation, they may have saved countless other lives, not by Todd’s dying, but by his way of living. In surviving so long with his terminal cancer, Todd showed us that the individual has some personal power to overcome even the toughest of foes. Couple that with new cancer research and new medicines, and that is how a cure is discovered. One small step at a time will lead us to the end of this insidious disease.

Even as his small sons begin to find their way in this world, their father’s legacy will live on. As they grow, as they thrive, let them be inspired by a man who wasn’t willing or able to surrender to his cancer. He rose above it and was made better by it. He became an inspiration and a teacher, whose lessons live on now in Seas IT.

If you would like to know more about the organization Amanda and Todd McGovern created, follow this link:

Seas IT
 
 
Categories
cancer caregiver cancer treatment holiday celebrations for cancer patients

Holiday Tips for Cancer Caregivers

If you’re a cancer caregiver, you know that cancer treatment sometimes knocks the stuffing out of your loved one. That doesn’t mean you can’t both enjoy the holidays. Plan ahead.

1. Know when your loved one is likely to be full of energy and when your loved one is likely to be dragging his or her wagon. Chemotherapy, radiation, and other treatments sometimes leave patients feeling exhausted, in pain, or otherwise debilitated. Don’t let this deter you!

SOLUTION: Plan for fun — If you’re loved one is lively in the morning, why not start a new tradition? Brunch can be a tasty alternative to a big, heavy meal at the end of the day, when your loved one is ready for bed. Brunch often includes foods that are appealing to cancer patients and have a lot of calories to keep the weight on. You can even slip in foods that are easy to eat — shakes, eggs, pancakes, waffles….

2. Know when your loved one is more vulnerable to germs, bacteria, and other things that can cause serious health threats — the immune system is already working hard, so take precautions!

SOLUTION: Plan for a safe holiday — Make hand sanitizer available for visitors, limit contact with crowds, and request people with the sniffles stay away (they can still offer video chats, phone calls, emails, and other greetings.)

If you go out and about, choose quieter, less-crowded restaurants, movie theaters, and other public spaces — take in a matinee, instead of an evening movie; have dinner in a less hectic restaurant, where you and your loved one won’t feel rushed; go for a scenic drive and take in the sights.

3. Know your own limits on how much energy you have to put into the holiday!

SOLUTION: Take as many shortcuts as you can to make it easier to entertain. Focus on having fun. Break the guilt cycle by reminding yourself that these shortcuts are because of your loved one’s needs and your own limited energy. Next year, you can go back to the traditions.

4. Know what you will do if your loved one becomes too exhausted to enjoy the activity!

SOLUTION: Talk ahead of time and know how your loved one wants to handle any emergency. If you’re at home, he or she may just want to go lie down for a bit, or may want to call it a day. If you’re out somewhere, you may want to leave. If you’re at another home and your loved one feels comfortable, you might suggest a short lie-down on a sofa or bed.

Be encouraging in presenting options. Choose the activities wisely. Surround your loved one with people who are supportive, patient, and understanding in how cancer and treatment affect your loved one. Always respect your loved one’s decision on what to do. It’s important that cancer patients feel empowered.

In the meantime, don’t feel shortchanged — be creative!

If you’re having pizza on paper plates, choose a festive design. Easy clean-up. Add napkins and colorful cups, throw up some decorations and streamers, and it’s all about the party, not the cancer.

Ask family and friends to help decorate the house, inside or out — put on a pot of coffee, sit back, and watch the lights go up.

Let others pitch in — make the meal pot luck and they can bring food and drink to share.

Focus on the conversations, the connections. That’s what really matters.

Don’t sweat the small stuff. Celebrate the good things you have in your life at this moment in time.

Categories
cancer treatment GE Healthcare Is My Cancer Diffferent molecular-level testing

Has Molecular-Level Cancer Testing Made a Difference for You?

Some time ago, I was approached by a GE Healthcare representative doing an outreach program on new molecular-level cancer testing. This approach tailors cancer treatment to the specific needs of each patient. The question is has this type of cancer treatment made a difference in the lives of patients?

Every cancer patient will have a unique experience, based on the type of cancer, its progression, other non-related health issues, and factors such as stress level. No two cancer patients will ever have identical experiences. I learned long ago that cancer patients can have similar experiences, and by identifying not just differences, but also similarities, cancer treatments can be improved.

Let’s be honest. In this day and age of expensive health care treatments, there is little point in using technology that costs a fortune, but has no positive gain. That’s wasteful spending. Kind of like throwing gold-flecked snake oil at a rattlesnake bite. If it doesn’t fix things or improve things, there is no point in wasting time or money to continue.

I would love to hear from cancer patients and/or their caregivers. You’re the folks on the front line in the fight against this disease. The question is this. Has molecular-level testing for your cancer or your loved one’s cancer made a difference?

Some people new to cancer may read this and think the question is silly. Anyone who has managed cancer over the years, or cared for a loved one who has, will understand the difference. Right now, every single day, the battle against cancer advances. From doctors and researchers who have the disease, we have volunteers willing to use themselves as guinea pigs for new treatments and trials. Who better to understand how to fight the war than someone who understands what it feels like and why it feels that way? When we shift from a one-size-fits-all style to an understanding that there are differences and nuances inside each cancer, we begin to match patients with treatments that are far more effective and do far less harm. Instead of just forcing a patient to undergo a treatment doctors guess might work, research begins to show improvements.

As a blogger who follows cancer research and treatment trends, I have been optimistic in the last several months that there is some serious progress in the war on cancer. Why? Because I am beginning to see reports of untreatable cancers being treated successfully. Cancers that were diagnosed as Stage 4 are suddenly succumbing to new treatment options still in the testing stages.

Anyone who has ever had cancer or a loved one with cancer knows that very often it’s the treatment that does more damage to the body than the actual cancer. Heart damage, tissue damage, and a myriad of other health issues can result. That’s why I think molecular-level cancer testing is going to make a difference in the lives of people with the disease.

I know that researchers can test blood and tissue samples. I know they can examine patients, measure results, and even chart their progress. But what does it look like from a patient’s point of view? What does it look like from a cancer caregiver’s point of view?

I remember when my mother was being treated for lung cancer. She got frustrated at times with the physical limitations imposed upon her by the disease. But I also remember the hope that trickled forth when she began to regain some of her mobility, when she could once again go out and live her life. In her case, she gained some extra months, and she put a lot of effort into making them count. She wanted to live as long and as fully as she could. I often think that’s something that cancer patients and their families share.

If you have a comment you would like to share with readers of my blog on molecular-level cancer testing, I encourage you to make it. Don’t make it just for me. Don’t make it just for GE Healthcare, one of the makers of the testing equipment. Make it for the cancer patients now in treatment and for those to come. Make it because you have a voice that wants to speak and you have insight into the situation. You and your love one may not realize it, but you have much to say to researchers about how cancer affects your life. Let them know what does and doesn’t work for you. The more that is known about how cancer treatment affects your life, the better treatments can be better tailored to help, not hurt, patients.

If you would like more help with your cancer caregiving, please visit The Practical Caregiver Guides

Categories
cancer treatment caregiver caregiver education Dr. Robert D.Siegel Dr. Robert J. Dowsett Helen and Harry Gray Cancer Center

Where You’re Treated Matters — Helen and Harry Gray Cancer Center

I’ve heard horror stories from cancer patients and their caregivers about their experiences with cancer treatment in various hospitals and medical centers. From people being shuffled off into solitary confinement for the lonely hours of intravenous drips to a serious lack of communication on the part of medical staff with such relevant information as a loved one’s terminal condition, the list of complaints is often long and scary.

That was not my mother’s case when she was treated by the Helen and Harry Gray Cancer Center and I can prove it. After more than two years, I can still tell you a little something about the people who cared for her. That’s because they were memorable for the compassion and kindness they showed my mother throughout her treatment.

What can I tell you about Dr. Dowsett? Behind his serious demeanor lurked a good sense of humor, and sometimes he would make a wry, unexpected comment that had us laughing. He always sported a really spiffy tie, thanks to his bargain-hunting wife, also a physician. My mother loved that he appreciated his wife’s efforts to make him a “GQ” guy. If I asked about a new kind of treatment in the news, he would explain what was and wasn’t appropriate in my mother’s case. That may not sound like a big deal, but it demonstrated to me that he was up-to-date in his knowledge of advances in radiation practices for cancer treatment. That instills confidence in the patient and family.

My mother adored Shelley, the radiation nurse who checked her in on each visit to radiology. “You remind me of Meryl Streep!” she would say as Shelley took her vital signs. With a calm, patient manner, Shelley would smile sweetly, never mentioning that she was much, much younger than the Oscar-winning actress. Never rushing my mother, always supportive, Shelley was a reassuring presence during exams.

Diane was the nurse who would always stop by to say hi while we were waiting in the radiology lounge. Cheerful, approachable, she always wanted feedback on what was working and what wasn’t working. This genuine interest in helping us get my mother through cancer treatment counted for a lot. Diane, like my mother, loved good movies, and she introduced us to the joys (and convenience)of Netflix. When my mother was too ill to go out, we signed up for Netflix and she had the chance to see some really good movies.

Carl and the other “kids” in the radiology meant a lot to my mother. That’s because they always treated her with affectionate respect. Carl used to surprise my mother when he spotted her waiting for her chemotherapy. He would sneak up, appearing at my mother’s side to offer a big, friendly greeting. She was thrilled for him when Carl graduated from school and was hired as a full-time radiation tech.

Anne, the nutrition expert, was literally a life-saver. As a lot of cancer patients do, my mother lost too much weight before we were able to reverse the trend. Anne sat with us in her office, explaining how to feed a cancer patient who also happened to have diabetes. With a hearty laugh and a quick wit, she offered encouragement and sage advice, and she helped us understand my mother’s frustration with the need to eat and lack of appetite, offering positive solutions to get her back on track.

With a radiant smile and twinkling eyes, Denise was one of the kindest, gentlest people in the oncology department, which was good, because she was the one taking blood samples. I remember her as “the hugger”, who would wrap her arms around my mother and tell her how happy she was to see her again. My mother looked forward to seeing her on visits to the hospital and to receiving that hug.

Karen was my mother’s oncology nurse, always sashaying in and out of the treatment room with the patience of a saint, no feathers ruffled even on the most hectic of days. What I liked about Karen was that I could call her with a question and she would get back to me with the answer. She was always good at sharing tips about managing the side effects of the cancer drugs my mother was receiving, clearing up any confusion and helping us to know what to expect.

When Karen had a day off, Donna would often fill in, dispensing my mother’s chemotherapy drugs. A very experienced nurse, she was always available if there was a problem. I ran into her at the grocery store after my mother passed away and I felt compelled to thank her for all of the wonderful treatment she and the others provided. They made chemotherapy bearable for her.

Marcia? Oh, full of life and passionate! On her stark white lab coat, she used to add her own whimsical touches, like big, colorful buttons. Marcia, as a nurse practitioner, was the one who explained things about over-the-counter medications interfering with the chemotherapy. If one pain reliever didn’t work well enough or was dangerous on certain treatment days, she had no qualms about prescribing another. Comfort was paramount. Marcia was a problem-solver who liked things to go right for patients, so she often went out of her way to make good things happen.

Dr. Bob’s office was like a whimsical version of what a doctor’s office would look like on the Cartoon Network, and I think it defined him not only as a doctor, but also as a human being. There were illustrations done by his young patients taped up to the walls, along with a Sponge Bob Square Pants figure. The jungle-print drapes, solar-powered pith helmet, and photograph of him jogging in Africa amongst a herd of elephants were all part of a decorating blitz by Marcia and a few others in the department to celebrate Dr. Bob’s vacation in Africa. You’ve got to love a guy who does such serious work and surrounds himself with very “unserious” stuff. Dr. Bob was a straight-shooter as an oncologist. He was big on quality of life, something my mother really appreciated. Dr. Bob always treated her with respect, making it clear that it was her decision on when to say enough was enough. It made it easier for me, when her health had seriously deteriorated, to ask her if she felt she was ready to go into hospice care. As a result, we got a lot done in her final weeks, tackling the things that mattered most to her and fulfilling her wishes.

I could go on and talk about the valet parking attendants, who always hustled to get the car back as quickly as possible. My mother loved the greeter at the front desk and even the “gift shop lady”. I appreciated Dr. Dowsett’s and Dr. Bob’s schedulers. They offered appointments that fit my mother’s physical limitations and need to rest.

Does the Helen and Harry Gray Cancer Center sound to you like a scary, cold, or unfeeling place to go if you have cancer or like a patient-focused medical facility where the staff is welcoming and warm? A cancer treatment center is always more than just a single doctor or nurse. It takes many people to get the job done. With a disease like this, especially if the cancer is manageable, you and your loved one are likely to spend a great deal of time there. All the more reason to make quality of life and treatment a priority by picking a good cancer center.

For more help as a caregiver, visit:
The Practical Caregiver Guides

For a free copy of my ebook in popular formats, visit:
The Practical Caregiver’s Guide to Cancer Care: How to Help Someone You Love

You can also find my free caregiver guides at Barnes and Noble, Sony, Kobo, Diesel, Baker and Taylor, as well as Smashwords.

Categories
cancer cancer management cancer treatment caregiver caregiver education Caris Life Sciences early diagnosis mycancer.com oncologist oncology radiology

CARIS’S CANCER TECHNOLOGIES PERSONALIZE TREATMENT

One of the most impressive women I ever met when my mother was undergoing cancer treatment was a lady who had survived two decades with the disease. How did she do it? She paid attention to her body. She got to the point where she could tell when the cancer was spreading or returning. She went in search of cancer treatment. She was not content to just accept it as her fate in life. Her husband was a supportive partner as she endured, managed, and directed her own cancer care. Why does this matter? I learned a lot from her that day as we talked in the chemotherapy room. She knew life is precious, that we are here to live life and to love. One moment in time can change a life for the better or for the worse. When we hesitate, when we accept the status quo without question, we are victims of our fate. When we accept the opportunity to learn what we can about cancer, when we begin to embrace the opportunities provided by emerging technologies, we help our loved ones to manage the disease better. Don’t close your eyes and look away because your loved one has cancer. Be proactive. Become aware of what’s available and what it can do for you and your loved one.

I’m a big believer in using technology to attack cancer and knock it out of the loop. Caris Life Sciences has a new program for cancer patients that enables better, smarter treatment:

http://www.mycancer.com/biopsy

Caris even has a checklist of questions to ask the oncologist, so that you and your love one better understand the type of cancer and the options for treatments. The idea is to individualize the cancer in order to provide the best treatment for the specific situation.

Anyone who has ever had cancer or cared for someone with cancer knows that it can be tough to withstand the rigors of treatment. Sometimes that’s harder than the cancer itself. With a more personalized treatment plan, unnecessary guesswork goes out the window. Cancer treatment is no longer “one-size-fits-all”. When oncologists and hematologists can see markers in blood that indicate cancer long before it shows up on a scan, that’s a head start on cutting cancer off at the pass. The sooner you know, the sooner you or your loved one can be treated. That means less treatment because it’s more effective at catching the cancer earlier.

One of the hardest things for cancer patients is to hope when things look bad. If your loved one has late stage cancer, you might be tempted to give up and give in. Would it help you to know that a new study showed that even late-stage cancer patients increased their survival rate by almost 30% using molecular profiling? That means that 3 out of 10 late-stage cancer patients thrived by using this technology. Three more people now live who would have died without the technology.

Any good cancer caregiver knows that working with a loved one’s radiology, oncology, and surgical team is imperative in keeping him or her healthier. It’s always important to be able to discuss the cancer and the options, because the better you and your loved one understand cancer, the better you and your loved one can manage the disease. And the better the cancer is managed, the better life will be for the whole family.

For more help with cancer caregiving, visit The Practical Caregiver Guides:
www.practicalcaregiverguides.com

For a free copy of “The Practical Caregiver’s Guide to Cancer Care: How to Help Someone You Love” in popular ebook formats, visit my Smashwords page:
http://www.smashwords.com/books/view/110999

Categories
cancer cancer advice cancer treatment caregiver caregiver education Kathy McGonigal oncology

INTERVIEW: KATHY MCGONIGAL, ONCOLOGY NURSE

In honor of National Family Caregiver Month, I’ve invited Kathy McGonigal, an oncology-certified nurse with almost 20 years of experience to answer some questions. My goal is to help cancer caregivers do a better job of helping their loved ones manage the disease as much as is possible.

 Sara:
 Hi, Kathy. I’m so glad you could join us. I really value your experience as an oncology nurse.  Let me ask you this. If you could give one piece of advice to caregivers at the start of treatment for their loved ones, what would that be?

 Kathy:
 It’s hard to give just one but I would say take care of “you”. This is the most difficult for the caregiver to understand. They feel like they have to be everything to their loved one all the time. Let others help you. Admit when you are overwhelmed. Taking a break is important. Eat healthy and get a lot of rest.

Sara:
So, so true. It really is critical that we take care of ourselves, so we can be there for the people we love. What the most common mistake you’ve seen caregivers make in taking care of loved ones with cancer? Is there more than one way to overcome this?

Kathy:
When patients hear the word cancer, everything changes. Most patients want to talk about their fears. Listen. Really listen. Instead of the usual “Don’t talk like that” or “Everything will be fine”, it is important to acknowledge their fears. It is also okay for you to tell them you are afraid too. Once words are spoken out loud, some of the fear disappears.

Sara:
I think listening is probably the best tool a caregiver can have in the caregiver tool box. It helps you to recognize when there’s a serious problem and to get the right help from your cancer treatment team. And a caregiver who is a good listener makes a cancer patient feel much more connected. It’s scary enough to hear the word, “cancer”, so knowing you have good support can make it all a little less lonely. How important is it for cancer families to understand the type of cancer their loved ones have and to understand the treatment that’s being given? Does it make a difference?

Kathy:
Families who understand the disease their loved one is suffering from is very important. You will be getting a lot of advice from other cancer survivors and caregivers. Not all cancer is created equal. Knowing what you are dealing with allows you to help make educated decisions and make reachable goals. The more educated you are, the less afraid you are.

Sara:
I think that’s really true about getting advice from other cancer survivors and caregivers. I met some amazing people during my mom’s treatments, and having the chance to talk to them about their experiences really helped me to do a better job in caring for my mom. One issue that seems to come up a lot with cancer patients is eating. Nutrition is often an important element in helping cancer patients get through the rigors of treatment. Do you have a good tip for feeding a reluctant patient?

Kathy:
Eating is important but it can also be a source of frustration between caregivers and patients. Feeding an illness is something we have all learned from our mothers. The patient knows how important it is to eat but it is not always possible. Think about how you feel when you are ill before you try and “force” your loved one to eat. Let the patient go. Make sure there are a lot of simple nutrient rich foods on hand. Cook simple so the smells are not overwhelming.  Don’t make the patient feel like you are monitoring everything they eat or not eat. It will cause too much anxiety. The patient will eat when they can. Leave it up to the doctors and nurses to address nutrition.

Sara:
Ah, what could be more annoying than the Food Police? How true. That’s a good point, too, about the cooking smells, especially if your loved one doesn’t already feel well. Reaching out to the medical team for help is good, solid advice, Kathy. As an experienced oncology nurse, you’re working on the front lines and I’m sure you’ve seen a lot over the years. Dealing with cancer can be stressful on a daily basis. A lot of cancer caregivers become overwhelmed. Do you have your own favorite ways of dealing with stress when you’ve had a tough week at work?

Kathy:
Wow, that’s a hard one and it is sometimes very difficult. I try to apply everything I learn from my patients into my personal life. I try to take nothing for granted. No matter how long you live, it is always not long enough. As stressful as my job can be, I have been privileged and honored to be invited into the lives of my patients at what might be the most vulnerable time of life. They have all enriched my life in ways most people do not get to experience. It is amazing to watch the human spirit take over. If you are a caregiver, you too will learn that while the patient says they couldn’t get through it without you, you will be the one who gets the biggest gift of all. You make it possible for your loved one to fight.

Sara:
What a great point to make to caregivers. I’ve seen that time and time again. Caregivers are the wind beneath a loved one’s wings and yet we’re the ones who benefit when we really make an effort to give the right kind of support for those we love. It changes lives, especially our own. Thank you so much, Kathy, for sharing your insight and wisdom. I know caregivers will be inspired by your words.

Contact:
Kathy McGonigal
kathymcgonigal@gmail.com

Categories
British Columbia Cancer Agency cancer research cancer treatment colon cancer Dana Farber Cancer Institute Dr. Matthew Meyerson Dr. Robert A. Holt Fusobacterium Gina Kolata New York Times

CAN NEW RESEARCH IN COLON CANCER BE A REASON TO HOPE FOR A CURE?

If you’re caring for a loved one with colon cancer, you may take heart from new research. Two cancer studies have identified unusually high levels of a specific bacterium not usually found in the colon, Fusobacterium, in colon cancer tumors.

The study at the British Columbia Cancer Agency, headed by Dr. Robert A. Holt and his team, used genetic analysis to identify the unexpected connection in Canadian patients, according to a report in the NY Times by Gina Kolata:
http://www.nytimes.com/2011/10/18/health/18cancer.html

Another study at the Dana Farber Cancer Institute, led by Dr. Matthew Meyerson and his associates, found similar results in patients from the US, Vietnam, and Spain.

All patients studied had higher levels of the Fusobacterium in their tumors than found in normal colon cells. Dr. Holt found that some of his patients had an average of 415 times as many Fusobacteria as normal cells. Dr. Meyerson’s research focused on the DNA aspect. He was unable to determine if the Fusobacteria is the trigger of the colon cancer or the cause of it, but the findings are considered provocative. Why? Because this may allow researchers to develop a vaccine to prevent colon cancer.

One question that cancer researchers will have to answer is whether inflammation, caused by the bacteria, is the start of colon cancer or if it speeds the development of cancer. Both Dr. Holt and Dr. Meyerson admit uncertainty in the cause and effect of Fusobacterium in colon cancer. But at least scientists have a potential culprit to investigate, examine, and follow.

For families with a loved one who has this disease, it can offer hope that somewhere, somehow, at some point in time, there may be answers about colon cancer, and with answers, there can be better disease management, treatment, and hopefully even a cure. Never give up hope!

Categories
cancer cancer management cancer treatment caregiver caregiver education GE Healthcare Is My Cancer Different

LAUNCHING “IS MY CANCER DIFFERENT” — CAN IT HELP YOU?

I’m a big believer in managing cancer by proactive effort. The more caregivers and cancer patients ask for information, the more they learn about it, the better the result. I’ve talked to a lot of people over the years and I am always surprised when I find out how many missed opportunities there are. Whether I am talking to a cancer widow who had no inkling that her husband’s cancer situation was so dire, or a new caregiver who doesn’t realize how important nutrition is for cancer survival, it strikes me that cancer education is critical to cancer management.

Sometimes the biggest obstacle for cancer patients and their families is that they are afraid to learn the truth. They hold back and hold it in, terrified to ask. Don’t be afraid to dip your big toe into the water. Don’t be afraid to get wet. Get yourself into the ocean of information about cancer. Learn to swim. The more you know about cancer, the better the outcome. Every cancer is different, just as every patient is different. It’s not a one-size-fits-all situation, so being able to target the kind of cancer, the stage it’s at, and the overall health of the individual patient means a better chance to manage the cancer. Generic cancer treatment often means the side effects overwhelm the patient, creating more problems than are solved. An individualized treatment plan takes into account the actual needs of the patient and works to insure that his or her health is better preserved. When an oncologist really seeks to understand a patient’s specific cancer situation, the outcome will be improved.

GE Healthcare just launched a new health initiative designed to help cancer patients ask, “Is my cancer different?” Why is this question so critical? Not every cancer responds to normal cancer protocols of treatment. Not every cancer patient does well with every cancer drug. Molecular level diagnostics can make a difference in outcome. This allows the oncologist to individualize the cancer treatment. The goal is to utilize molecular level diagnostics to better fit individual needs.

As a cancer caregiver, one of the most important jobs you have is to understand that the right treatment can make all the difference in the world. You want your loved one to have a fighting chance. The smarter the fight, the better the outcome. Sometimes surviving that extra day in better shape allows a cancer patient a window of opportunity to move forward towards a cure. With cancer, there are never any guarantees, but you can and you should always advocate for the best treatment available for your loved one’s cancer.

What does “Is My Cancer Different?” offer? This is a cancer education website. You can see patient-friendly informational videos. You can learn about new developments in cancer treatments. You can begin to understand that the better managed cancer is, the longer your loved one can not only live with cancer, but thrive. More birthdays, more joy, more laughter, more adventures, more life.

If you would like more information on “Is My Cancer Different?”, check out their link:
http://www.IsMyCancerDifferent.com/