Relief: Comfort Slings Help Relieve Abrasions and Dermatitis Beneath The Breast

by Margot Malin, CEO and Founder of Lots To Live For, Inc.

Patients who are undergoing radiation therapy on the underside of their breasts may develop radiation dermatitis, painful sores, and even weepy lesions in the skin folds beneath their breasts. The inflammation can be worsened by excessive perspiration and the chafing resulting from skin-to-skin contact. Once these side effects occur the patient experiences significant discomfort.

Relief: A new product called the ComfortSling(R) can help to improve comfort and prevent the continuing abrasion or fold over effect. The Breast Comfort Sling allows the breast to rest on a soft cushion giving freer air circulation while wicking away perspiration to keep the sore area dry. The straps are adjustable so there is no pressure on the neck or shoulder, or on the sore areas beneath the breast. The cushion provides a comfort barrier between the breast and the skin beneath it to prevent excessive chafing, and the antimicrobial material discourages bacteria growth.

The Slings are available in either a single sling, or a double sling.
The Single Sling: Women have found that wearing the Breast Comfort Single Sling from the onset of radiotherapy, even before any side effects have begun to appear, is the most effective way to minimize uncomfortable side effects to the skin. Wearing the sling as many hours as possible throughout the day, especially when sleeping, is most effective.
The Double Sling:  Women with large breasts often suffer yeast infections, skin rashes, fungus and other irritations due to excessive perspiration and poor circulation under their breasts. The moisture irritates the skin and the area becomes further inflamed as the breast tends to rub against the skin beneath it. The ComfortSling^® Double-Sling is an ideal solution.

The fabric for the Breast ComfortSlings and Pads was specially selected because it is very soft and has both wicking and antimicrobial qualities. The straps are soft enough to be comfortable yet firm enough to hold their shape when worn across the shoulders. The slings stay in place, yet they are loose enough to avoid pressure and constriction across the neck and under the breast.

Breast ComfortSlings and Pads were developed by Elizabeth Silver during her radiation oncology treatment and they proved so effective that her radiologist and oncologist were amazed at the excellent condition of her skin during her treatment. In fact, it was they who recommended that she begin to market the slings so that more women could benefit from the relief they provided.

Patients have found amazing relief from using the products, as described in these reviews: 

Life Saver!!

Posted on May 12th 2016

My cousin was in her 20th treatment of radiation and we started noticing that the crease under her left breast was raw and peeling to the point of extreme pain. I was desperately searching for some type of treatment that would help and I did. This breast sling is the best . It allowed her breast to heel so much faster. If anyone is going to be starting radiation, please, please get this before starting treatment! It will help sooooo much! 

Posted on May 31, 2016

Using the breast comfort sling and the pads, combined with clotrimazole (an antifungal cream found in lortimin AF athletes foot cream), I have managed to heal a 1/2 dollar sized very painful and itchy irritation under my breast. It has been there for months and within 5 days of using the pads and cream it has greatly reduced and virtually healed.

This post is a condensed version of  Comfort Slings Help Relieve Soreness and Abrasion Beneath the Breasts published on the Breast Cancer Yoga Blog in December 2015.

6 Tips to Help Cancer Patients Become More Organized and Comfortable During Treatment

by Margot Malin

This is a condensed version of a longer post that was published on the Breast Cancer Yoga Blog entitled:

Cancer Pre-Treatment Check List – 6 Tips To Make Your Life Easier Once You Begin Treatments

You can read the full post at: http://breastcanceryogablog.com/2014/01/22/cancer-pre-treatment-check-list/

Receiving a diagnosis of cancer can be overwhelming. There are so many questions swirling through your mind and so many things to put in order. Here is a short list of 6 tips suggested by other patients to help make your treatment both more comfortable and better organized.

1. Familiarize Yourself with Your Medications and their Side Effects
2. Schedule a Dental Appointment
3. Order some new products in advance to test them to see if you have any reactions to them, and to see if you like their feel and other characteristics.
4. Make a list of things that need to be done and circulate it to friends and family so that they can sign up to help you.
5. Create a treatment goody bag for yourself
6. Meet with a Naturopathic doctor

Each of these 6 tips should help to reduce the uncertainty and confusion that come with a cancer diagnosis and treatment plan. Try to organize and simplify your daily schedule whenever possible. Don’t forget to ask for help!

You can find products to add to your "Treatment Goody Bag" at www.LotsToLiveFor.com
Lots To Live For, Inc. sells products to reduce and relieve the unpleasant and uncomfortable side effects of cancer treatments including surgery, radiation and chemotherapy.

Radiant Wrap – Stylish and Comfortable Radiation Therapy Gowns - Inspiration During Treatment

We have transitioned to a new blog format. You can find the full copy of this post at our new Wordpress blog at:
http://blog.lotstolivefor.com/2013/07/09/radiant-wrap-stylish-radiation-therapy-gowns/

Thanks to Maria Lucas of Radiant Wrap a visit to a radiation oncology center doesn't have to mean wearing a frayed and faded gown. The inspiration for her idea came during her treatment and it is one of her ways to "pay it forward" and help other patients feel more comfortable during treatment.

Radiant Wrap founders - Maria Lucas and her son

Maria says "I knew I wanted something that was stylish and flattering, something that was closed and secure at the back and something that didn’t have ties, buttons, Velcro or snaps. I thought if I could cut up these gowns and design a one piece wrap around that tied at the waist, I would have a beautiful alternative gown. And that is exactly what I did. I had a prototype made of my design, and a first run of forty gowns made that June, six months after I was diagnosed and one month after I finished my radiation."

Read more in the blog post, where you can also read about how to order a Radiant Wrap for yourself or a loved one.

You can view and purchase Radiant Wrap gowns at: http://www.theradiantwrap.com/

CureLauncher Offers Personalized Clinical Trial Matching

Our blog has transitioned to a new format on Wordpress.
Please click on the link below to be taken to the full version of this blog post about CureLauncher.

If you are seeking new treatments and clinical trials  CureLauncher can help give you the power and the support to make a life changing decision. Warm, compassionate, and experienced relationship managers will guide you through the process of finding a new treatment.  Taking control and knowing your options opens up a whole new world of hope.  CureLauncher can help connect you with clinical trials in your area.


CureLauncher - Take Contol Know Your Options

 For more information and to read  a testimonial from Barb Hollingsworth click here: http://blog.lotstolivefor.com/2013/06/18/curelauncher-personalized-clinical-trial-matching/

Please subscribe to our new blog - you can sign up to receive new posts by email on the home page - on the right column.

The Lymphedema Breast Cancer App - A Comprehensive “On the Go” Guide to Lymphedema

The Lymphedema Breast Cancer App features information on what lymphedema is and how to reduce your risk. The App is a resource for all women who have had lymph node surgery or radiotherapy as part of their cancer treatment and who are at risk of developing Lymphedema. The App includes a “step by step” video teaching users how to measure their own arm. Users can save their arm measurements in the App’s measures diary, allowing them to track the size of their arm over time.

The Lymphoedema Breast Cancer App can be downloaded from the itunes and Google Play stores for $1.99. The App is compatible for both smartphone and tablet devices.

The Lymphoedema Breast Cancer App was developed by Kelly Foote, who is a cancer care physiotherapist and the app developer. She is a guest blogger for the article described herein and which you can access by clicking below.

Lymphodema Breast Cancer App

We are transitioning the Cancer Blog: Lots To Live For!  blog format over to our new Wordpress Blog.

You can click here to view the full post about The Lymphedema Breast Cancer App.

(http://blog.lotstolivefor.com/2013/05/07/tools-and-tips-for-managing-lymphodema/)

Please sign up to subscribe to our new blog format (you can do this on the new blog). 

If  you are a subscriber to this blog your subscription will not automatically carry over.

We appreciate your interest in our blog posts.  We have some awesome and informative posts scheduled in the near future so please be sure not to miss them!

Note: Kelly Foote is a Cancer Care Physiotherapist and the Lymphoedema Breast Cancer App Developer. Kelly resides in Brisbane, Australia.

Imerman Angels - Connecting Cancer Fighters, Survivors and Caregivers

By Jonny Imerman
Chief Mission Officer, Imerman Angels

Imerman Angels provides personalized connections that enable 1-on-1 support among cancer fighters, survivors and caregivers.      

On a Thursday morning in October 2001, my world came to a standstill. At 26 years old, I was diagnosed with testicular cancer. Although the surgery to remove my left testicle went well, it soon became clear that the cancer had spread, or “metastasized”. The disease was making its way up my body.

I knew what was nextchemotherapy -but I did not understand what that meant. What color is it? How will it make me feel? I called my brother. I started sobbing. I could barely talk. My world was shattered. But, I was not going to give up.

My oncologist told me that the treatments might make me sterile. So, I went to a cryogenics laboratory to bank sperm. After that, it was time to start intense cycles of chemotherapy.

The treatment weakened my body and wiped out most of my white blood cells. In fact, I was in such bad shape, the doctors were forced to delay my chemotherapy while my body recovered between cycles. In addition, the chemotherapy caused many side effects: throat sores, mouth sores, skin rashes, dry skin, cystic acne, extreme fatigue, hair loss, numbness in my fingers and toes, and partial hearing loss. But the most damaging side effect was a blood clot that developed in my left arm. The clot formed around my port, a medical implant that was an access point for my chemotherapy. The doctors had to remove my port, pull out most of the blood clot, and then pump me with blood thinners to break up the rest.

At last, after five months of brutal chemo treatment, I thought my fight was over. I slowly returned to the gym, started going out socially, and got back into life. Although I was happy to be alive, every day was a challenge. I did not have as much energy. I looked different. I struggled to find my post-cancer identity. Just as I was getting comfortable with myself, I learned the fight was not over.

Nearly one year after chemotherapy, a routine CT scan showed four tumors along my spine. Rather than risk cutting the spine, the surgeon went in through the stomach. He made an 11-inch incision, placed my organs to the side, and took out each tumor. The surgery lasted for four hours. It was successful, and finally I was freed from the disease and able to begin my road to recovery.

But my journey was certainly not over. I had made a vow to myself during the time that I was battling cancer. I had looked at others in the oncology clinic and realized that I was different. Each day, my room was filled with family members, close friends and my great doctors. With so much support, I did not have a chance to lose hope. However, in many of the other rooms, hope already seemed lost. As I walked down the hall with my chemotherapy IV-pole on the way to the bathroom, I saw other people fighting cancer alone. They were lying in bed, motionless, watching television or staring in space. Their only stimulation was a nurse checking in for a minute or two on the hour. I knew this was not right. It upset me.

So, my vow was to start helping my fellow fighters in the simplest way that I could. I walked into the other rooms, one at a time, and introduced myself. “Hey, what’s up, I’m Jonny. What’s your name?” Although they were exhausted just like me, everyone was friendly and welcomed my conversation. We shared stories, emotions, and different opinions about many things in life. Our common bond? We were all fighting for life.

Although I had my network of support in my family, friends and doctors, once I started introducing myself to these fellow fighters I realized that they were providing me something valuable that my caregivers could not. From deep discussions about the fears with fertility issues, to simply learning that sucking on Lemonheads candies alleviates the metallic taste from chemo, talking to others who also faced cancer was a powerful, insightful and uplifting tool.

I wondered: “What if every cancer fighter could talk to a cancer survivor who was uniquely familiar with their experience; who not only had beaten the same type and stage of cancer, but who also was the same age and gender as the fighter?” The cancer survivor would be an angelwalking, living proof that the fighter could win, too. What an amazing connection. This is why I created Imerman Angels.

What does Imerman Angels do?

Imerman Angels carefully matches and individually pairs a person touched by cancer (a cancer fighter or survivor) with someone who has fought and survived the same type of cancer (a Mentor Angel). Cancer caregivers (spouses, parents, children and other family and friends of fighters) also receive 1-on-1 connections with other caregivers and survivors. These 1-on-1 relationships inspire hope and offer the chance to ask personal questions and receive support from someone who is uniquely familiar with the experience.

The service is absolutely free and helps anyone touched by any type of cancer, at any cancer stage level, at any age, living anywhere in the world. Imerman Angels is a federally registered 501(c)(3) not-for-profit organization.

Visit www.ImermanAngels.org for information on how to support or join the network of cancer fighters, survivors and caregivers.

Today, we have the largest network of cancer survivors in the world; more than 4,000 cancer survivors and over 1,500 caregivers. They live in all 50 states, and over 60 countries.

We help thousands of families with cancer, across the world, every year.

1-on-1 cancer support works for one reason: we all BELIEVE.

Jonny Imerman, founder of Imerman Angels

No one should fight this disease alone. 

The author, Jonny Imerman is a young adult cancer survivor who strives to make sure no one fights cancer without the support of someone who has already triumphed over the disease.  After being diagnosed with testicular cancer at the age of 26, Jonny decided to found Imerman Angels, a non-profit organization, which carefully matches a person touched by cancer (a cancer fighter or survivor) with someone who has fought and survived the same type of cancer (a Mentor Angel). Imerman Angels now has more than 4,000 cancer survivors and more than 1,500 caregivers in its network, and has been featured by dozens of news organizations including The Wall Street Journal, Harpo Radio’s “Oprah and Friends” with Dr. Oz, Men’s Health, NBC5 Chicago, CBS2 Chicago, ABC7 Chicago, ESPN Radio Chicago, Chicago Tribune, Chicago Sun-Times, Detroit Free Press, LIVESTRONG Quarterly, and Clinical Journal of Oncology Nursing.  Jonny received a 2012 CNN Hero Award; 2012 Lincoln Park Young Professionals ‘Chicago Best of The Best’ Award; 2011 Twilight Foundation Detroit’s Civic Leadership Award; 2011 Chicago Social Magazine’s ‘Who is Chicago’ Award; 2010 Jefferson Award for Public Service; 2010 University of Michigan Humanitarian Service Award; 2009 Ulman Cancer Fund For Young Adults ‘Hope Award’; and 2007 Daily Candy ‘Sweetest Thing’ Award.  Jonny has been invited to speak at cancer centers such as MD Anderson, Memorial Sloan-Kettering, Mayo Clinic, Dana-Farber, City of Hope, Northwestern, Rush, and Children’s Hospital Los Angeles.  Jonny grew up in Bloomfield Hills, MI and lives in Chicago.
Visit Imerman Angels at: www.ImermanAngels.org
Follow Imerman Angels on twitter: @ImermanAngels

This blog post is part of the Resource Roundup series sponsored by Cancer Blog: Lots To Live For! in which the spotlight is shined on a resource that can help improve the journeys of cancer patients and caregivers. Past Resource Roundup stars have included Creating the 10 to Thrive eBook, Annie Appleseed Project and Caring Bridge, among others. To view products that can help alleviate the unpleasant and uncomfortable side effects of chemotherapy and radiation please visit www.LotsToLiveFor.com.
Lots To Live For, Inc. ~ Comfort, Hope, Inspiration

Help to spread the word about Imerman Angels by winning a free T shirt like Jonny is wearing above - visit www.facebook.com/LotsToLiveFor and "like" the both the page, and the link for this blog post to be entered in a raffle. The contest will end on 1/22/13 and the winner will be announced on 1/23.

Why is Our Breath so Important for Cancer Recovery?

Breathing for Cancer Recovery - Calm and Relaxation -  Managing Stress, Fear, Pain and Anxiety

By Diana Ross, Guest blogger

“Close your eyes and gradually bring your breath into your mind’s awareness. Experience each inhalation as it draws fresh energy in; feel the exhalation emptying you, carrying away fatigue, stress and unnecessary thoughts. Let your breaths flow softly and smoothly from one into the next without hurrying or pressing between breaths. Now breathe in, and breathe out.” Diana Ross

We hear from time to time the familiar saying “take a deep breath” when we become stressed, anxious or over excited. Ever wonder why? There are many reasons why but most notably taking a full, deep conscious breath has been known to settle us down when we are nervous or upset.

We create this internal calm by consciously tuning in to our breath. The immediate result of tuning into your breath is the ability to obtain control of your emotional state of mind. The positive potential which comes from controlling your breathing results in facilitating recovery from surgery and beyond. This healing ability of breathing consciously works by calming nerves and inviting relaxation. The immune system also benefits from proper breathing cycles. By conscious breathing we bring the mind/body/spirit state into balance and the nervous system runs with maximum efficiency.

Balancing the breath serves to maintain and equalize the complete breath cycle. The goal of conscious breathing is to have both inhalation and exhalation identical in volume and duration thus creating the natural flow of the breath. This natural flow brings the quiet mind with it. Concentration will be higher during this equalized state and invite a meditative mind. A meditative mind cannot happen until the breath is brought under control. You see now how vitally important the breath is in wellness and how it heals.

Habitually we resort to unconscious shallow breathing and therefore do not utilize our true lung capacity when we create uneven inhalations and exhalations. As you begin to focus on your breathing for the health benefits it may reap you may notice that your airflow might be unequal. Do not be concerned. It is a natural phenomenon, and you need not resort to any other method; just continue to practice breathing with awareness. Strive for an equalized airflow through both nostrils. Also in the effects of the new breathing practice may not be felt right away, but after a few sessions the results will become obvious. It is only through practice that we begin to master the conscious breathing practice, so don’t get discouraged. When practicing breathing techniques (pranayama) the mind will become still, and eventually the breath will become even. The energy we normally spend engaging and processing the world around us begins to bend inward and we begin to see with more clarity.

Breathe With Purpose CD

The importance of training the breath becomes a powerful tool in managing stress, fear, and anxiety as well as recovery. A focused breathing technique assists in restoring energy and calming the mind, so we need to breathe with greater awareness. The breath is an amazing vehicle in that it is always present. It is effective at every level of self inquiry and acts in both a preventative as well as a restorative manner. Once we bring an awareness of the breath into the moment, where it is most needed, we can then improve our quality of life. We can enjoy quiet moments of meditation: we can enjoy our be-ing.

We can begin or continue to heal. We can enjoy being present.

Diana Ross, E-RYT500, CYT, Certified KaliRay TriYoga

Founder, Breast Cancer Yoga

www.breastcanceryoga.com

Breast Cancer Yoga has a Two Breathing CD series “Breathe with Purpose, and Breathe for Health and Wellness.” It has a series of breaths that are easy to learn. You are guided the entire time, breath by breath. You can purchase them on the website.

5 Point Plan for Better Cancer Outcomes: Focus on a Natural Approach to Cancer

Complementary Medicine Options and Life Style Choices to Help Cancer Patients From a Patient/Advocate Perspective

By Ann Fonfa (founder Annie Appleseed Project), guest blogger

I was diagnosed with (breast) cancer in January 1993 at the age of 44. At the time I was suffering from extreme Multiple Chemical Sensitivity. I felt that the oncologist I consulted was incredibly dismissive of a health issue that caused me to take to my bed 3-4 days at a time. I was reacting with long-lasting headache, dizziness, nausea, rashes and more from exposure to fragrances, cleaning products, wet paint, formaldehyde (new furniture/carpeting), etc.

So I chose to explore what was then called Alternative medicine. My search brought me a lot more information than expected – specifically a wealth of information about nutrition - which is where I started. At this point most people have heard what is healthier to eat, but some have resisted actually doing it. If you want to reduce your risk of cancer occurrence, recurrence or to just be healthier, you MUST give up so much sugar, NO soda, and NO deep-fried foods. It’s that simple – these items (chips are deep-fried), are just not real food. We’ve let ourselves fall into these awful habits, so darn easy to eat chips at lunchtime instead of a salad or an apple.

Back to alternative cancer ideas: After some years, yoga became totally acceptable to the point that many cancer centers and most support groups offer it. Studies have shown that it really makes a difference to our health. The concept of complementary therapies was introduced and has gradually become accepted. There are simple and natural substances and protocols that could reduce toxicity and enhance the value of chemotherapy and/or radiation. (Here’s our Free Handout of Natural Strategies to Reduce Toxicities). Complementary therapies began to be called integrative because they COULD be used while undergoing conventional treatments. Let’s face it, the treatments offered by the mainstream cause harms – ranging from short-term to longer-lasting. Why is this allowed even now?

I have been gathering information about cancer prevention and treatment, and sharing it via the nonprofit I founded in June 1999: www.annieappleseedproject.org The Annie Appleseed Project provides information, education, advocacy and awareness for people with cancer and their family and friends. The Annie Appleseed Project offers information on natural therapies and substances, lifestyle issues, and complementary or alternative medicine, from a patient’s perspective. This is gathered in part from our network of volunteer advocates who attend educational cancer meetings around the globe, from medical, scientific/research journals, and emails from supporters.

It’s out there, it’s been studied. Sadly many researchers feel the need to look at natural substances the same way pharmaceuticals are examined, even though many natural items have been shown, during hundreds or thousands of years of human use, to be quite safe (except for personal allergy). Doctors have been taught to expect pharmaceutical-style clinical trials – but here’s the catch. The cost of a clinical trial, what is called Level 1, is in the hundreds of millions and natural protocols simply cannot be patented (nor should they), thus no pharmaceutical company is interested. This barrier is one I wrote about in a journal article many years ago and this still has not changed. Another major issue that blocks the full use of complementary therapies is the lack of insurance reimbursement.

The Annie Appleseed Project has a five point plan for better health in general and better outcomes if you have been diagnosed with cancer:

1. Eating Right If someone wishes to do a range of inexpensive, simple and protective things, start with healthier eating – adding more fruits and vegetables to the diet. Remove SODA and Deep-fried foods, eat less sugar and less salt; and add whole grains.

2. Physical Activity Take a walk, dance, shake, swim, bike, etc. on a daily basis. Good news from author Antronette (Toni) Yancey, MD, MPH, whose book Instant Recess explains her theories. Just 10 minutes a day of physical activity, full-out, is enough to keep our bodies healthy. Many studies have shown that physical activity is very beneficial to people going through treatment for cancer, or in recovery. Combining physical activity with healthier eating is EVEN better than either separately – studies show that too.

3. Dietary Supplements Fish oil, probiotics, vitamin D3 and curcumin are the basics because everything else depends on what you personally may need. You can visit a clinical nutritionist who does blood work, or you can get your own eating patterns assessed. Your doctors can test you for vitamin D3 but it seems from the recent work done in this area, that almost no one has enough vitamin D3. Make sure you supplement if you are low. The darker your skin, the more vitamin D you may need.

4. Detoxification We live in a world filled with chemical exposures, as a chemically-sensitive person (although I am so much better than I used to be); I KNOW when the air is bad. Plastic materials surround us, many being shown to be harmful. Pesticides in our food supply, and our water, formaldehyde and parabens in our clothing, furniture and hair/skincare products are all part of this problem. But some detoxification is possible – cilantro, dandelion leaves OR parsley can help the body remove heavy metals – one of these should be eaten every day. Making fresh (organic) raw juices can help a lot too. Using hot and cold showers, foot baths, far infrared saunas and more, can all help detox. Again our website can be a help in finding ideas. Always drink lots of water – do you have a simple filter? It’s better to filter your water than drinking it straight up these days. Try to drink from a BPA-free carry bottle.

Never use plastic in your microwave, better yet - DON’T use the microwave. It is really a time management issue. If you know you want to eat at 6:30, turn your oven (or toaster-oven) on ahead of time. Or eat a BIG salad for dinner. Some say eating less at night is healthier. I personally eat a big breakfast, a salad for lunch, and often fruit and nuts for dinner.

5. Relax and Enjoy Life Yoga and meditation are not the only ways to relaxation – that which gives you pleasure should be your focus too. Are you a gardener, a grandparent, a bowler – focus on your joy in action. I attended a meeting in Brussels, Belgium in 1999 – the second international conference ever held by the National Breast Cancer Coalition. My sister came with me as we planned, excitingly, to travel to Amsterdam together. She was astounded by the party held at the end of the conference. I asked her whether she thought we ought to be sitting around and crying instead of dancing? She realized then, as we all should, that life is RIGHT NOW. We are meant to enjoy this moment. If I had spent the last almost twenty years worrying about dying from cancer, that would have been an enormous waste of my life.

Happily I didn’t. I enjoy each day and live it fully. You should too.

For those seeking more information you can visit our Annie Appleseed Project Facebook page, follow us @annieappleseed on Twitter, visit our website www.annieappleseedproject.org (you can opt in for our monthly e-newsletter). We’ll host Evidence-based Complementary & Alternative Cancer Therapies conference February 28-March 2, 2013 in West Palm Beach, FL. Some scholarships are available for those in need. We offer CEs and CNEs for professionals. 5 organic meals, exhibits, networking, giveaways, much more. Ann Fonfa is the founder of the Annie Appleseed Project.

To learn about products that can help reduce and relieve the unpleasant and uncomfortable side effects of chemotherapy and radiation treatment please visit www.LotsToLiveFor.com

This blog post is part of the Resource Roundup series sponsored by Cancer Blog: Lots To Live For! in which the spotlight is shined on a resource that can help improve the journeys of cancer patients and caregivers. A Past Resource Roundup  was Caring Bridge.

Eight Awesome Tips To Help Cancer Patients

Acts of Kindness To Help Make Life Easier for A Patient Undergoing Cancer Treatment
By Margot Malin     

It may be an awkward moment when you learn that a friend, loved one, or coworker has been diagnosed with cancer. You may initially be at a loss for words and yet you want to offer empathy and comfort. Here are 8 Tips and Helpful Gifts of Kindness so you can create your own plan to help the cancer patient you know along his or her journey.

Food – Go grocery shopping – stock the refrigerator with fresh, healthy and easy to prepare items. Cook dinner for the family and deliver it.

Childcare – Cancer patients get tired, sometimes very tired. You can offer to baby sit for young children. Offer to arrange and take older children on play dates. If you know the children well, take them on a little outing – to the playground, to a movie, to a show or museum. During this stressful time, school work might suffer. Offer to tutor, or arrange for a tutor for those subjects that are particularly challenging right now.

Laundry and other daily chores – Laundry can be easily postponed when someone is not feeling well. Offer to do the laundry – at your home or theirs – or take it to a wash and fold service. Helping with other daily chores and activities can be a great way to relieve the patient of some activities which might be repetitive, tiring and stressful.

Chemotherapy and Radiation sessions – Offer to drive to radiation oncology sessions and chemo appointments. Sitting and receiving an infusion can be cold and lonely. Stay during chemo to help the time pass – you can write letters, read aloud, listen to music, or look at poetry during these sessions. Bring a warm and cozy blanket with you. Other things you can bring to pass the time: an ipad, a laptop, a Kindle, craft supplies.

Doctor appointments – Offer to drive to a doctor appointment or accompany the patient on public transportation – and if the patient is open to the idea – be present when the patient speaks with the doctor. A second set of ears is a welcome addition during this stressful time. Maybe you can think of questions that the patient might be too overwhelmed or nervous to consider. You can also take notes about the visit to be sure that the important takeaways are remembered.

Medical record keeping and medical research – You can help by doing medical research about the patient’s diagnosis as well as research into complimentary and alternative therapies. Personal health record keeping is especially important during treatment and beyond. Consider purchasing either a special loose leaf / workbook to keep track of paper records, or the Minerva Health Manager, electronic personal health record software.

Side effect solutions – There are many products to help unpleasant and uncomfortable physical side effects of chemotherapy and radiation. For example, you can find products to help radiation dermatitis, radiation burns, hair loss, dry mouth and mouth sores, nausea, and more. To learn about products that can help reduce and relieve cancer treatment side effects visit www.LotsToLiveFor.com.

Books, CD’s and Music – There are many inspirational books written by, and about cancer patients. Just two examples are: From Incurable to Incredible – Cancer Survivors Who Beat the Odds written by Tami Boehmer, a cancer survivor and When Cancer Hits – A Complete Guide to Taking Care of You Through Treatment authored by Britta Aragon, also a cancer survivor. There are rest and relaxation CD’s. Breast Cancer Yoga has created a CD for breathing and meditation and a DVD for gentle yoga. Recovery Fitness also has an Exercise for Cancer Patients DVD. There are also CD’s and DVD’s available to reduce stress and enhance relaxation.

A little thought and creativity can help you come up with many other helpful ideas. You can even ask the patient to give you a wish list of what kind of help they might appreciate for their situation. Some of the best expressions of support are inexpensive and some are free – but they are all priceless to the patient receiving your kindness.

Margot Malin is the CEO, President and Founder of Lots To Live For, Inc. which sells carefully selected products to reduce and relieve the uncomfortable and unpleasant side effects caused by chemotherapy and radiation. Lots To Live For, Inc. was founded after the passing of Margot’s mother and grandmother who both fought courageous battles against cancer.

To find products to help reduce and relieve the uncomfortable and unpleasant side effects of cancer treatment please visit: www.LotsToLiveFor.com
Visit our facebook page at: www.facebook.com/LotsToLiveFor for information and inspiration!

Cancer Survivors Who Beat the Odds – Attributes of Survivors Who Became Thrivers

by Tami Boehmer, Guest Blogger
Learn how to win a copy of Tami's book at the end of this blog post.

I was first diagnosed with breast cancer at age 39 in 2002 after finding a lump during a breast self-exam. There was no history of breast cancer in my family, so I was shocked, to say the least. Two weeks later my father died. My daughter was three, and my husband and I had been married less than five years. It was a devastating time, but I was heartened when my doctor told me I had no lymph node involvement and my prognosis was excellent.

After five years, chances are slim cancer will return. But again, I learned you can’t pay attention to statistics. In February 2008, I found a lump in my armpit, and after a series of scans, I learned it had returned as stage IV cancer. I went to a world-renowned cancer hospital only to be told I would certainly die from breast cancer. Luckily I turned it into a challenge to prove the doctor wrong.

I spent my career in healthcare public relations, and always loved writing patient success stories. I already knew my friend Buzz Sheffield, who was told five years earlier he had months to live. (Today, eight years later, he is alive and well.) I also read Bernie Siegel’s wonderful book, Love, Medicine and Miracles, which talked about Exceptional Cancer Patients and how the worst thing doctors can do is to give death sentences.

So I started my search for more incredible people who beat the odds of terminal cancer for my book, From Incurable to Incredible. I was searching for answers. It was an extremely personal journey. As someone facing a Stage IV breast cancer diagnosis, you could say my life depended on it.

My biggest question was: What sets people apart who beat the odds of a terminal or incurable prognosis? As I was putting the 27 stories together, I noticed many similarities among survivors nationwide who shared their stories. Rather than passively accepting their circumstances; they decided to transform them by:

• Refusing to buy into statistics and the death sentences many of them were given.

• Never giving up, no matter what. They may have had down times, but were able to pull themselves together and do what they needed to do.

• Relying on support from family, loved ones, or support groups. These connections gave them a reason to carry on.

• Choosing to look on the bright side and see the gifts cancer brings.

• Giving back and making a difference in other people’s lives, whether it was fundraising, lobbying, or supporting other survivors.

• Having a strong sense of faith. Even if they didn’t believe in God, they believed in something larger than themselves.

• Being proactive participants in their health care.

• Viewing their lives as transformed by their experience.

I continue to share stories of amazing cancer survivors on my blog, www.MiracleSurvivors.com, and continue to see these common threads. But I’ve found there are people in the cancer community who are offended by these observations. “Are you saying that people who didn’t make it weren’t positive enough?” Absolutely not! Cancer is complex, and I do know people who possess all of these qualities and still succumb to this awful disease … two of them whose stories are in my book. There are no absolutes or guarantees. In the midst of dismal statistics for people with late stage cancer, my purpose is to help show there are possibilities. There is always hope, and there are ways to live life to the fullest … with purpose and joy. As Deb Violette, a lung cancer survivor and advocate featured in my book shared, “This little voice in my head said, 'Why are you focusing on the 90 percent of people who didn’t make it; why don’t you focus on the 10 percent who do?'" She was diagnosed in 1998 and is very alive and well today.

No one should put a period where there should be a question mark.

Tami Boehmer is a speaker and an award-winning blogger and author. From Incurable to Incredible is available on Amazon.com and BarnesandNoble.com and via Tami’s blog, www.MiracleSurvivors.com.

If you are interested in reading the inspirational true health stories of cancer survivors who beat the odds, you can purchase the book from Amazon by clicking in the box below. Win a FREE copy of the book by visiting the Lots To Live For, Inc. facebook page by 10/7/12 by clicking here.


www.facebook.com/LotsToLiveFor  - To enter the raffle to win a free book "like" the page and "like" the blog post. Comment if you feel inspired.

To learn about and purchase products that can help reduce and relive the unpleasant and uncomfortable side effects of chemotherapy and radiation visit www.LotsToLiveFor.com. You will find solutions for: radiation burns, radiation dermatitis, dry mouth, mouth sores, nausea, sensitive and compromised skin, hair loss, and more.

The Genesis of Lots To Live For, Inc.- An Interview with IdeaMensch

IdeaMensch is a community of entrepreneurs who share how they bring their businesses to life. Margot Malin, the founder of Lots To Live For, Inc. was interviewed by IdeaMensch on September 4, 2012. IdeaMensch probes about the genesis of the business with insightful questions that let the founder's ideas, beliefs and experiences shine through.

Some excerpts of the interview:

"Where did the idea for Lots To Live For, Inc. come from?

The genesis and inspiration for the company came from watching both my mother and grandmother fight courageous battles against cancer while simultaneously trying to maintain normal lifestyles. Lots To Live For, Inc. offers one-stop shopping and solutions for cancer patients, by selling products and offering tips to alleviate, reduce and relieve unpleasant and uncomfortable side effects of chemotherapy and radiation.

Side effects from cancer treatments can be debilitating. During my mother’s and grandmother’s treatments, we found some really helpful products after exhaustive searching. It occurred to me that consolidating these items in a single place would be extremely helpful to others who are going through treatment. Our business slogan is: We recognize that you have lots to live for, and we offer solutions so that you can improve the quality of your life."

In the interview Margot also offers some advice to aspiring entrepreneurs - below is a quick quote:

"As an entrepreneur what is the one thing you do over and over and recommend everyone else do?
Keep your eyes and ears open. Treat customers and suppliers with respect. Read a lot. Try to think outside of the box. Look for disruptive technologies and try to jump on the wave. Never fall into the OPM (other people’s money) mentality. Treat equity investors’ money as if it were your own. Don’t spend frivolously."

In another section of the interview, Margot offers some personal inspiration to readers.

"Can you offer some words of advice for our readers’ personal lives?
1. Always act with integrity.
2. Accept personal responsibility.
3. Life is a marathon, not a sprint. Take time to have fun and reflect. Smell the roses.
4. Believe in yourself.
5. Dare to be different.
6. Be careful of the footprints you leave. Unfortunately, your indiscretions or social media gaffes can haunt you."

To read about some of the challenges in bringing Lots To Live For, Inc. to life, as well as thoughts about business opportunities, and general observations and advice about life you can read the complete interview with Margot Malin on the IdeaMensch website by clicking here.

Please visit www.LotsToLiveFor.com to learn about products to help relieve the unpleasant and uncomfortable side effects of chemotherapy and radiation. Lots To Live For, Inc. welcomes you as a facebook fan at www.facebook.com/LotsToLiveFor.

The Pink Vaccine - the Vaccine to Prevent Breast Cancer

By Elyn Jacobs, Guest Blogger, Founder of Elyn Jacobs Consulting and Certified Cancer Coach

What if? What if we had a vaccine that was safe and could eliminate 95% of all breast cancer? Would you take it? Would you hope that your daughters, sisters, lovers and wives would take it? For every man or woman who has battled this terrible disease, I’ll bet the answer is yes. I’ll bet it’s yes for all those who have not yet dealt with this beast. So when I heard that there was a vaccine that has been found to be 100% effective in preventing breast cancer in mice, yet is sitting on a shelf, I was horrified, angry and hell-bent on doing something about it, and I am not alone. Remember, that anything that works in humans worked first in mice. 

In June, I invited Dr Kathleen Ruddy (shown at right) to be a guest on my weekly radio show. Dr Ruddy spoke about a breast cancer virus that might be involved with 40-75% of breast cancer. She discussed a preventive vaccine developed at the Cleveland Clinic by Professor Vincent Tuohy that is ready for safety testing in women and may also be effective against the viral form of breast cancer. Cindy Sullivan, a breast cancer survivor living in Colorado, was listening in and made a comment in the chat room that she was really, really mad (ok, in her words, pissed off) that this vaccine was ready for clinical trials and still unfunded. Cindy contacted us, and Kathleen suggested that we band together with two other equally determined women; we set up a conference call and before you know it, we joined forces to get the word out and to get this vaccine funded. To read more about the champions for the Pink Vaccine, click here. To listen to my interview with Dr Ruddy, please click here.

The virus in itself was not news to me or others; Kathleen and I spoke about this a year ago, and it received national attention via a video Dr. Ruddy made that was nominated best short film of the Breast Fest Breast Cancer Film Festival 2010. However, what amazes me is that in addition to the paucity of attention about the virus, there is equal disregard for the first preventive breast cancer vaccine that Professor Tuohy developed, for he has yet to get the funding for clinical trials to test its efficacy in women. So why is it that there is not funding for trials? If not for lack of awareness, what is it?

In order to get the Pink Vaccine to clinical trial we need to raise approximately $6 Million. In the estimated $30 Billion spent on breast cancer every year in the U.S., $6 Million seems like the proverbial drop in the bucket. Breast cancer is a big territorial business steeped in politics and greed. Komen has turned Dr Tuohy down for funding several times and Avon has refused to even consider it. (Please watch this powerful video, Pink Ribbons). When you think about it, it’s not in the best interest of corporate America or Pink-America to prevent this costly disease. Still, I have a hard time accepting that there is not funding for such an important vaccine….not everyone profits from breast cancer, so why isn’t this vaccine funded? Breast cancer costs insurance companies billions; sisters, daughters, wives, mothers and lovers and men die every day. Isn’t this enough motivation? Something must be done. The US Government as well as those whose purported mission it is to find a cure or end breast cancer must step in. Yes, we absolutely need to find a cure for breast cancer; millions are dying of this terrible disease. Treatment is not enough, and it ruins lives with illness, toxicity and fear. Treatment is not a cure; this vaccine is not a cure. (However, it may help prevent recurrence and slow the growth: researchers found that mice already infected with breast cancer saw a marked reduction in tumors after being given this vaccine.)

And that word cure. That in itself is a quagmire. A cure to me is not just something that is a remedy or something that will bring back health; it is not something that indicates a remission of signs or symptoms of a disease. To me, a cure means that the cancer is gone and will not return. We ask if our cancer is curable, but due to the nature of cancer, it often revisits.

Komen did just issue a sizable research grant to a team with a potentially more effective treatment for triple negative breast cancer, one that will reduce the spread of cancer and prolong survival, and to me, that is exciting news; but again, if we can prevent this disease, let’s do that too. If I knew of a vaccine that could completely cure, I would push for that also. But for now, what we do have is The Pink Vaccine, developed by Dr. Vincent Tuohy of the Cleveland Clinic. It’s ready for clinical trials in humans. Remember polio? Polio is a crippling and potentially fatal disease. There is no cure, but there are safe and effective vaccines. If this vaccine works in humans the way it works in mice, we could eliminate breast cancer. The Pink Vaccine is not the only vaccine in the works; but it’s the only one to prevent breast cancer, and that is the best cure there is.

Elyn Jacobs
http://elynjacobs.wordpress.com
Twitter@elynjacobs
Facebook @Elyn Jacobs and @Elyn Jacobs Consulting
Linkedin @Elyn Jacobs
The opinions expressed in this blog post are those of Elyn Jacobs, the author. If you would like more information about this vaccine or would like to connect with others interested in finding money to fund additional research and clinical trials please feel free to contact Elyn Jacobs directly.

Elyn Jacobs is a breast cancer survivor, professional cancer coach, radio talk show host, speaker, and the Executive Director for the Emerald Heart Cancer Foundation. Elyn empowers women to choose the path for treatment that best fits their own individual needs. She is passionate about helping others move forward into a life of health and wellbeing. Elyn lives in New York with her husband and two young boys. To learn more about Elyn’s coaching services, please visit: http://elynjacobs.wordpress.com. To tune into the Survive and Live Well radio show, please visit www.W4CS.com, Tuesdays at 1pm (EST).

To learn about products that can help alleviate side effects caused by chemotherapy and radiation including radiation burns, mouth sores, compromised skin, and more,  please visit www.LotsToLiveFor.com

Yes, Ma'am! Mammograms Are a Must!

God turned my mess into a message
By Lee McCracken, Guest Blogger

Dressed like twins, even though we were 13 months apart, my older sister and I were a striking pair at ages 5 and 6. She had red hair and freckles, and Mom dressed her in blues and greens. I was blond, and I donned the reds and pinks. Perhaps it was foreshadowing, but probably not.

Fast-forward 45 years. Pink is a staple in my wardrobe. Having been diagnosed with Invasive Ductal Carcinoma (IDC) in 2009, I’m a member of the pink-ribbon club … whether I like it or not. I am lucky it was caught at Stage 1 (nothing had spread to the lymph nodes), and I now reflect on the nine months of surgery, reconstruction and recovery with a shrug as if it were no big deal. Truthfully, I’m a “glass half full” kinda gal and always tend to look on the bright side.

Before my diagnosis, I NEVER liked getting a mammogram — I was fibrocystic, and it always hurt and required an accompanying ultrasound. Today, I tell women breast cancer hurts even more!

In spring 2011, at the threshold of my 50th birthday, God laid a message on my heart … one that I thought just was going to be my team’s name for a breast cancer walk. Yet, the sassy, upbeat and inspiriting phrase has grown bigger than I could have imagined. At the urging of many marketing-savvy girlfriends, Yes, Maam! Mammograms Are A Must grew into a philanthropic social enterprise and a pink T-shirt I began merchandising on a local, and now a regional and national level.

It’s a simple, straight-forward message that doesn’t sexualize the female body. The feedback has been remarkable — women ages 25-85 and older say, “It’s really catchy!” And even though it’s for women about women, men are embracing the message in support of the ladies they love.

“Get Your Squeeze On!™” is my mantra, because early detection of breast cancer assures more options for treatment and higher survival rates. I envision women all over the country wearing their Yes, Maam! Mammograms Are A Must tee to the coffee house, grocery store and gym. It makes a sassy statement in southern style, and ladies take notice. I’ve seen them look at my tee and then shake their head, almost to say, “Oh yeah, I need to schedule that!” It’s even better when they give me a thumbs-up, indicating their annual appointment is behind them and the report was “all clear.”

Sadly, though, the fear factor is real … and women are BUSY. Research shows more than 50 percent of women ages 50+ either cancel their appointment or never get around to making it. Perhaps they don’t know this fact: When mammograms are scheduled every other year, some 30 percent of breast cancers can be missed.

To be totally honest, when a woman says, “Oh, I keep forgetting …” I want to smack her silly — especially if she has health insurance. Given the current economic climate, many women have to put the needs of their children first before tending to their own health. From the very beginning, T-shirt sales have helped to fund mammograms for women who don’t have health insurance. The cost of the tee is $20, and 25 percent ($5) is donated. Individuals, businesses/groups and stores that purchase or sell the tee are encouraged to designate a women’s healthcare charity in their community to receive the funds (hopefully earmarked for mammograms).

Having been a writer/editor - http://www.joyfulleewritten.com/ - for more than 28 years, I am energized by this second act of my life — an entrepreneur who’s engaging communities of women in the early detection of breast cancer. (Who knew a 50-year-old could master making memes and tweeting?) But beyond learning new skills, I’m living passionately with a new purpose. Building the Yes, Maam! Mammograms Are A Must  brand, connecting with awesome women and making new friends is a blessing I never could have imagined three years ago when I heard those fateful words: breast cancer. Yes, Ma'am, I'm a surTHRIVER!
                                                         
Lee McCracken
http://www.yesmaamtee.com/
www.Facebook.com/YesMaamMammograms
@YesMaamMammos (Twitter)



Lee McCracken lives with her husband, Stuart, in Denver, N.C., a suburb of Charlotte. She has a 20-year-old daughter, Megan, and an 11-year-old Bichon Frise, Benny. She enjoys traveling, photography, reading and gardening. Lee’s girlfriends keep her filled with inspiration and laughter!

For products to help alleviate side effects of cancer treatment please visit: http://www.lotstolivefor.com/
The skin care, hair care, oral care and anti-nausea products on this website can help you resume your normal lifestyle during treatment.

Not My Mother's Journey: Author Heather St. Aubin-Stout Shares Her Personal Story

Guest Blog by Heather St.Aubin-Stout; author: Not My Mother’s Journey

The Importance of Sharing Your Story - Catharsis and Inspiration

Heather shares her personal story about breast cancer and her passion about supporting those going through the journey.

From the time I could read and write I wanted to be an author.  Looking back on this now, I'm not sure this was really what I wanted to do or if this was something that was projected onto the oldest daughter by her mother who loved to write.

Although I went to college for architecture, and had a career in the field of architecture before my children were born, I continued to write for myself.  After staying at home, working part time substitute teaching and doing much volunteer work I was ready to go back into a career when I was diagnosed with breast cancer.

Then in 2009 at forty-six and in remission for a year after two bouts of breast cancaer within the last three years, I began to write again.  It was a release, it was cathartic, and although it was also painful to re-live everything, if was also exciting to do something I had thought about for years.

I felt the need to write about my experience and how it was different from my mother's, who at forty-five died from breast cancer just a year and a half after her diagnosis.  A life unfinished.

I was twenty-four at the time and two weeks away from getting married. Her doctor had told her not to plan on being at my wedding. Of couse the month before - when he told her that - we were outraged.  A few days before she died, the hospice nurse asked what I would do if my mother didn't live to see me get married.  I broke down in tears; it was unimaginable to me that she might die in the next week.  At this point during her illness my mother was not the mother she had been during the rest of my life.  I just refused to see it.

My mother was a stay at home mom, she was there for my two younger sisters and me while we were growing up.  She went back to school when I was in college, moving from ther Bachelors to a Masters in Clinical Psychology.  She was disgnosed during hter second year.  She plowed ahead with internships, classes, and her thesis anyway while she was going through treatments.  However, she never did get her thesis completed.  My father, sisters, and I accepted the first posthumous degree ever awarded from University of North Carolina at Charlotte the year after her death.

For years it seemsed cruel to me that death took her before she could finish her degree and experience the rewards of a career.  However, looking back on it now, she shaped all of our lives during those years she was at home with us.  This is a gift I've just now begun to realize and treasure.

So, here I am at forty-eight and trying something new. I've reinvented myself, yet again.  I've found, as I've matured, gathered those life experiences one can only gather from aging, that each of us has many facets to ones self.  These parts of ourselves can come out when we don't expect it.  Breast Cancer did this for me.  It taught me humility, patience and perseverance.

My book, released in January 2011, Not My Mother's Journey is my story, my mom's story and hopefully it will encourage anyone facing a diagnosis of cancer to be their own best advocate - our doctors have many patients, but we only have one.  Ask questions, interview your doctors, share your journey with others, because it may help someone else.

Ironically, despite the similarities of being diagnosed about the same age as my mom, I tested negative for the BRACA genes (a genetic predisposition).  So when my cancer recurred at the one year scans, the same time my mom's had metastasized, I had to battle psychological demons for the second year in a row.

As of this writing I'm in remission...with my friend NED- No Evidence of Disease!

So my journey continues to evolve and for this I am grateful.

I hope I've written a compelling story, that makes the reader think, one that you can relate to, and one that will validate your own feelings.  I hope it is a story that moves and inspires you in your life.  I have tried to do this.  You tell me!  You can visit my website at http://www.sharingmystory.com/ and connect with me. I welcome your feedback.

You may purchase my book via the website http://www.sharingmystory.com/, by clicking the Amazon link above, from http://www.barnesandnoble.com/, www.xlibris.com in print or ebook format.
 
For products that can be helpful in relieving uncomfortable and unpleasant side effects during treatment for cancer please visit http://www.lotstolivefor.com/. This is a useful and informative website for patients, caregivers, oncology nurses, cancer coaches and friends and relatives of cancer patients. On Facebook we post helpful information about new developments in cancer treatment, new products and resources. Please "like" us at www.facebook.com/LotsToLiveFor
 
To be your own best health advocate, consider purchasing the Minerva Health Manager personal health record software.  It might help to save your life. You are your own best advocate!

Are Metastatic Breast Cancer Patients Getting the Right Treatment?

According to a recent on line article by Melissa Weber published in www.curetoday.com as many as one in seven women with metastatic breast cancer could be receiving the wrong treatment because of a change in the cancer’s biology when it metastasizes.

“When breast cancer spreads to another part of the body, a HER2-positive cancer could become HER2-negative. Or estrogen receptor-negative cancer could switch to estrogen receptor-positive. Despite different treatment strategies for each, most oncologists rely on what they know about the primary breast tumor to fight the metastasis, says Giuseppe Curigliano, MD, PhD, co-director of the division of medical oncology at the European Institute of Oncology in Milan, Italy. But researchers now believe inhibiting one cancer growth pathway with treatment may activate signaling of a new pathway that allows it to survive and spread.”

A study presented over the summer at the annual ASCO meeting showed that in certain cases when the metastatic lesion was tested, it did not match the primary tumor. There are a few different hypotheses for why this might happen. “Experts suspect that because tumors are made up of different kinds of cancer cells, a small fraction of cells may have a different receptor status. If those cells are more resistant to cancer therapy, the resistant cells may outgrow the rest over time. At the time of recurrence or progression, the overall tumor will have subsequently appeared to have ‘switched.’”

Being aware of the potential that the biologic characteristics of the metastatic lesion might not match that of the primary lesion can have implications for treatment. The researchers quoted in the study suggest that rebiopsy should be performed after considering the safety of the procedure.

To read the full article on line on the curetoday.com website please click here.

For products that can ease side effects of radiation and chemotherapy for breast cancer patients, please click here.