“Genetic Testing in Oncology To Improve Clinical Outcomes”

myoncopath white paper

I’m super excited to share a white paper with you today from MyOncoPath, an innovative company helping cancer patients and their healthcare providers identify genetic testing that could play a role in personalizing cancer treatment plans.  They also provide a hereditary risk assessment for patients and family members with preventative care.  They are a telemedicine clinic working to support patients and healthcare providers!

Genetic testing is one of those things that we keep hearing more and more about but it’s great when a company actually explains a topic’s importance and breaks down all of those clinical-sounding terms!  MyOncoPath has written a white paper doing just those things, entitled, “Use of Genetic Testing in Oncology to Improve Clinical Outcomes in Preventative Care and Personalized Medicine.”

“Hereditary tests are important for patients already diagnosed with cancer, as the results can expose crucial information about the specific, most effective treatments available, the patient’s risk of cancer recurrence, and the risk of the patient’s blood relatives developing cancer.”

Check out the rest of the report!

Genetic Counseling Before And After Testing

When I think back to the last 8 years, I cannot believe how far I have come. It has been quite a ride and I would not change a thing. My BRCA2 mutation has given me so many things, some good, some bad — none of which I would change.

My mutation gave me an 87% chance of developing breast cancer and a 40% chance of developing ovarian cancer. These risks provided me with immeasurable fear, uncertainty, and vulnerability. As a result, I underwent surgeries to reduce my cancer risks, which were then followed by complications and many recoveries. Most importantly, my mutation gave me a wake up call.

Life is short and I always knew that I wanted to live it to the fullest so when I got the news that I was positive for a hereditary mutation, I knew that I was going to do everything in my power to keep myself healthy. I never once second guessed my decision to have risk reducing surgeries. I feel fortunate that I had many tools, as well as professionals, at my disposal.

One of the most important people I dealt with from the moment I found out about the BRCA mutation was my certified genetic counselor. Genetic counselors are health professionals with specialized training and experience in the areas of medical genetics and counseling. Genetic counselors work as members of a healthcare team, providing individuals and families with information on the nature, inheritance, and implications of genetic disorders to help them make informed medical and personal decisions.  For more info about genetic counselors, go here!

Genetic counselors wear many hats — all of which are essential. They can be the bearer of good or bad news, and play important roles in decisions you make. First and foremost, they are able to assess your genetic risk to see which genetic tests are appropriate for you. When dealing with general practitioners, many will often order a genetic test for BRCA mutations if they feel it is needed; however, the BRCA mutations are not the only mutations that can put you at a higher risk for cancer. Various organs can be involved for hereditary cancer syndromes. Other cancer concerns aside from breast and ovarian cancer include: colon, pancreatic, prostate, skin, peritoneal, and uterine cancer.

Genetic counselors can provide you with the proper paperwork so that you will have minimal insurance issues. They can also provide you with connections to a social workers and psychologists. Genetic testing can often be a very emotional experience and there is nothing wrong with speaking with someone — in fact I encourage it.

When seeing a genetic counselor, it is a good idea to take family members with you who you think might also be affected by a mutation. They can help map out your family tree and provide documentation that you can share. If you are not able to take a family member with you, a counselor can provide resources and tools to help share the information with family as it is often very difficult to start that type of a conversation.

A family medical history is health information about you and your family. A family medical history includes information about the health and illnesses of your mother, father, siblings, your children, aunts, uncles, cousins, and grandparents. The more information you can provide, the better. If cancer has been in the family, please try and find out the age of onset, along with cause of death. If you notice patterns of medical issues, mention that as well. It can help determine whether there is an increased risk of developing certain conditions.

Aside from a family medical history, here are some other tips that will help. If you can, it’s a great idea to ask relatives if they have ever gone for genetic testing. If you do have the ability to ask, it would be great if they are able to provide a copy of those reports. It is extremely helpful and might even reduce the cost of testing. If a relative cannot join you for the appointment, I would also advise you to bring someone with you to your appointment. That way you have someone who is able to be a second set of ears. If not, you can always record the meeting. It can be overwhelming and sometimes things are forgotten.

Genetic testing is not for everyone however I truly believe that knowledge can be power. Many who undergo genetic testing feel a sense of relief. Knowing whether you are negative or positive can allow you determine a course of action. It can help with a surveillance plan or a prophylactic surgery path. It will also help with screening measures for your family. If you have tested positive for a genetic mutation, there is a 50% chance that each one of your family members may also be at risk.

It is important to remember that genetic testing can save your life if you use the information to be vigilant and take action. I truly believe this with all of my heart. Hearing that something is beyond your control is scary but there are steps that can be taken to decrease your chances of developing cancer. It can give you treatment options that weren’t available to you prior to a positive result. It allows more aggressive surveillance measures such as mammograms, ultrasounds, and colonoscopies to name a few. A positive genetic test is not a death sentence and I am proof of that. Without the knowledge, my story may of have had another ending.

Everyone does what is best for them and there is no right or wrong way to deal with genetic testing but having information at your fingertips is priceless — I am living proof of that.

If you are considering genetic testing or are waiting for results, reach out, talk with someone, find a support group as no one should ever feel alone. There will always be a soft place to fall, regardless of the results if you are positive for a hereditary cancer mutation.

If you have questions about genetic testing and counselling, please check the National Society of Genetic Counselors.


If you have tested positive for a BRCA mutation or any other hereditary cancer syndromes including Lynch syndrome, please come join the BRCA Sisterhood. They are over 6600 women worldwide and all of us are dealing with similar issues. https://www.facebook.com/groups/brcasisterhood/   Everything is private. Talking with others who “get it” is priceless.

Much love,

How I Turned My Mastesctomy Into Art

mastectomy tattoo

I have always loved tattoos. Shortly after my 18th birthday, I walked into a tattoo shop filled with courage and a bit of cockiness. After studying the wall of images, I confidently pointed to a small cartoon devil named “hot stuff” and said, “Perfect!”

Many people ask whether or I not have any regrets about my first tattoo, but, honesty, I don’t. 23 years later, I look at it and smile. It’s a part of my history, a personalized scar of sorts.

Over the years, I have added other tattoos, so it’s no surprise to anyone that knows me that I decided to add one more. This one however, is the most meaningful piece of art I have ever added to my skin. It is a beautiful ending to a very difficult 6 years. Choosing to remove my healthy breasts because of my 87% chance of developing breast cancer is a decision I don’t regret for one minute. My BRCA gene mutation has forced me to make decisions that no woman should ever have to make. By choosing this tattoo, it was an opportunity to turn my mastectomy into a work of art!

After my mastectomy, I suffered complications with my reconstruction and endured an additional 4 surgeries. I was not interested in another operation to recreate nipples that would never look, feel or work like my real ones. That is when I knew that I was going to do things differently.

My search for a tattoo artist was a personal one. There are many talented artists in Montreal but I needed an emotional connection as well. After meeting with a few I met Meaghan Goeb. Her “realism tattoos” were spectacular and we bonded right away. I knew in that moment that she was the one! She was just as excited about this project as I was and I soon learned that breast cancer had affected her family as well. She understood that I was looking for a piece of art that would become an extension of my body, a new beginning. We both couldn’t wait to get started!

I decided on Magnolias and Cherry blossoms. Magnolias are very tough flowers that represent endurance, eternity and long life. Cherry Blossoms represent fragility and are a reminder that life is beautiful yet short. I gave Meaghan complete creative freedom with the design and colors. We spoke often throughout the month and when I went into the shop to see the final design and layout on my chest, it was above and beyond what I could have imagined.

The day of my first session I was up early, too excited to sleep. I had booked 4 hours. For those who have never had a tattoo that is a LONG time. I was prepared for the worst but hoping for the best. I no longer have feeling in my chest so I was hoping that maybe it would not be so painful. Well I was wrong! It was the most painful tattoo I have done to date. Thankfully, Meaghan and I got along great so the 4 hours were enjoyable.


After the second 2 hours session was complete and I walked to the mirror to see it fully finished, I could not believe my eyes. It surpassed all of my wildest expectations. The softness and realism of it looks like a painting. It feels like an extension of my body and I am ecstatic with the results. My scar has been transformed and I cannot stop staring!


With an interest in documenting this life altering journey I have been working closely with a videographer named Chris Alsop. Chris is producing a 10 minute documentary in an effort to raise awareness to hereditary breast cancer, mastectomy tattooing and accepting beauty on your own terms.

Although it was not an easy decision, I decided to share my journey because so many women that I have spoken with post mastectomy feel ugly and scarred. Many do not feel sexy anymore and I hope that my story can help change that. Society shows an unrealistic version of what beauty is. I chose to keep one breast scarred because I like the story it tells. I like seeing where my story began.

Remember beauty comes in all forms and I am embracing mine on my terms, scars and all.

You can read more about my mastectomy tattoo in the NY Daily News and in the Global News.

mastctomytatDo you have a mastectomy tattoo or know someone who does?

Genetics’ Effect On Cancer – And My Future

Not every cancer is random, or because of life choices. Some cancers, an estimated 5-10%, are due to genetics. This is generally referred to as inherited cancer, which means an inherited abnormal gene led to cancer. Unfortunately, it’s not always easy to tell without genetic testing whether or not you carry an abnormal gene, and genetic testing isn’t usually easily available unless you know your family has a history of some sort of cancer.

My mother’s side of the family apparently carries the abnormal gene that causes colon and rectal cancers, especially cancer that occurs at a younger age than most cases. We had no clue though, thanks to faulty information about how several relatives had died. After my mother’s diagnosis, we finally got the correct information, and discovered that her family has a history of early colon and rectal cancers. Hers was caught soon enough that it will not be fatal, but her tumor had been in the works for a very long time – since long before the age when doctors usually recommend getting colonoscopies. If we had known our family history, the doctors would have suggested she start them earlier than normal and perhaps this tumor would not have grown as it did. Odds are it still would have already been in the works, though, since it began so early.

This doesn’t have much of an impact on her, except for some understanding of how and why this happened. It does have an impact on my brother and I, however, especially since we now know some relatives had their first polyps removed as early as 35. That’s only 10 years away for me, less for my brother, and we’re starting to realize that in order to prevent this in ourselves, we may need to start colonoscopies as soon as now.

That thought is a little scary, and yet oddly liberating. There’s something in my genetics that could kill me, but there’s ways that I can prevent it from doing so. I feel equipped with the knowledge I’ve gained to be able to stop what’s happening to my mother from happening to me – I’ll possibly be able to avoid this happening at all. That likely means getting early and frequent colonoscopies, but doing so could mean living until I have great-grandchildren. That sort of knowledge is amazingly empowering; thanks to modern medicine, I can put that knowledge to use in order to have a long and healthy life.

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