October- Think Before you PINK

October is Breast Cancer Awareness month.

Breast Cancer has become synonymous with pink ribbons and the color pink in general. Companies have made millions of dollars off of these pink items claiming that these funds go towards breast cancer research. Did you know that last year the largest breast cancer fundraising organization contributed approximately 19% of their proceeds to breast cancer research. Metastatic Breast Cancer research received only 2% of total contributions to breast cancer as a whole. Metastatic Breast Cancer WILL kill me. Hopefully not for a long time but someday it will take over my life unless……..a CURE is found. The only way that this is going to happen is if more research is done. While I completely support that early detection is important, a CURE is really the only way to eradicate breast cancer and it taking the lives of people like me.

So before you pink this month and donate, please make sure that you are giving to an organization that gives all of their proceeds to cancer research and not to boost the salaries of their already overpaid board of directors.

National Metastatic Breast Cancer day is October 13th this year. There are currently over 155,000 people in the US living with Metastatic Breast Cancer. This special group of people and I like to call ourselves Metavivors! Please  visit metavivor.org is you would like more information on this disease.

** I also realize that we recently did the Jimmy Fund walk clad in PINK t-shirts, with PINK bracelets so we are guilty of the PINK movement as well. The difference is 100% of the funds that we raised were donated to the Jimmy Fund and Dana Farber for Research and pink just happens to be one of my favorite colors!

FIGHT LIKE HELL IT IS

“We have two options, medically and emotionally: GIVE UP OR FIGHT LIKE HELL”-Lance Armstrong

FIGHT LIKE HELL IT IS!! I cannot and will not give up this fight.

I walked this past weekend in the 2016 Jimmy Fund walk to benefit cancer research with an amazing team of over 60 people. Together we raised over $27,000 and donations are continuing to roll in. We had a great day and I am so proud of our accomplishments in our first year participating and look forward to making this bigger and better for many years to come. Trevor and I are so blessed to have looked out on Sunday at the sea of people in pink Cabral Crusader’s shirts and then to have photos sent to us of people who couldn’t make the walk but wore the shirts to show that they were with us in spirit! WE thank each and everyone of you. This situation that we have found ourselves in with this diagnosis is awful but each and everyone of you have brought a smile to our faces and have helped us through this in some way whether you realize it or not.

A couple of weeks ago, my friend Eileen passed away from cancer. When I was first diagnosed Eileen told me that having cancer is a marathon not a sprint and she helped me with some positive words that got me through the initial shock of my situation. This year I walked in Eileen’s memory.

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Here is a video of our walk that was put together by the amazing Melissa Scungio!!

 

 

Stability

pic-2I had my first set of scans since my diagnosis on Monday. What a long day! We got into Boston around 7:45 and did not leave until 6:40 at night! I was poked, prodded, and scanned all day long. It was all worth it though! My oncologist said that all of my scans look great! There are no new spots in my bones and it actually looks like my bones are starting to heal. During the physical exam, my oncologist stated that she could not feel the tumors in my breast and that my lymph node, which was originally how we found this, had returned to its normal size and consistency! All great news. While I will never be cancer free or in remission, the goal for me is to be stable and have control of the cancer and these test results confirm that I AM stable and the cancer is under control!! Now we will stay on this regimen of medicines until they no longer work…….hopefully in many, many years.

This photo here is of my “Dana Farber Support team”!! Trevor as previously noted has been a rock for me through this whole ordeal. Sarah is my close friend who not only pulled some major strings to get me in with the best of the best at Dana Farber but managed to get me an appointment faster than some would dream possible! She has not missed one of my appointments and has provided Trevor and I great support while we are at these appointments. Keeping Trevor company while I am in my scans, hanging out with us in waiting rooms, showing us where to go b/c DFCI is not an easy place to get around and just basically being there! For this, she will never understand how much we adore and love her and how appreciative we are for all that she does for us! ( I know this is an awful photo but I think at this point we were on hour # 6 at the hospital!)

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Cabral’s Crusaders

When I started this team for the upcoming Jimmy Fund walk last month, I did not expect much to come of it. I thought this was going to be our trial run as it was our first year participating. Maybe I could get 10 people to join me, raise a couple thousand dollars and sell some shirts! Boy was I wrong! As of this morning OUR team has 30 members, has raised over $20,000 towards a cure for all cancers and has sold 95 t-shirts!!! I am amazed by this! We have started off at an amazing place and I cannot wait to see how this will grow over the years! This is going to be my way of giving back to me new cancer community and when I am gone (hopefully in a really long time) this will be a way for my kids to keep my memory going!! So thank you all for the support. You will never know how much this truly means to me.

Someone in one of my support groups recently described my diagnosis as having the sand timer flipped over! I am essentially watching the sand and waiting for it to run out. While I am waiting for the sand to run out (I am confident that my sand timer is HUGE and that sand is flowing really slowly!), life in general is short! No one’s tomorrow is guaranteed! So live life to the fullest every day! Surround yourself with people who bring the best to your life and get rid of all of the negatives! I have always tried to live this way but now more than ever see how important it is!

Cycle#4

IMG_0275This past Tuesday was my 5th appointment at Dana Farber and my 4th treatment cycle. No news is good news I guess!! Everything still looks good, the NP who did my exam said she could not feel the tumor in my breast anymore!! Huge news!! Next month I will have my first set of scans since beginning treatment. This will be when the doctors can confirm that the meds are working and that I am on the right path!!!

Our Jimmy Fund walk team, Cabral’s Crusaders, has raised $16,074 as of this morning which will all be donated to finding a cure!! I am so humbled by all of the support from so many and am honored that we are all walking together against this awful disease. Since my diagnosis, the more people I talk too about my situation, the more I realize that there are so many people affected by this. In my direct circle of friends, I have two friends that have recently fought and BEAT breast cancer!! I recently learned of a girl from my hometown whose young son is battling cancer as well. I am glad that we are giving back, not only to find a cure for me but also for all the others that are battling this!!!

I wanted to give a shout out to my hubby, Trevor. He has been my rock through this whole ordeal. We all know that I am a control freak and that I am usually the one in the drivers seat of our life (figuratively and in real life, since I get car sick when he drives!) so it is hard for me to let him take charge but he is wonderful! He has not missed an appointment, takes notes and asks questions when needed, reminds me to take my meds and hydrate and is there constantly to remind me of how many positive things are on our side with this! I know my constant eye rolls and short fuse with him is not easy to deal with but I am so grateful to have him by my side with this diagnosis and in life!!! XOXO

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Something good?

One week ago, I decided to join the Jimmy Fund walk to benefit cancer research and Dana Farber. I went back and forth on whether I wanted to announce that I was walking and why and at the same time announce my blog. Doing so would leave me exposed and vulnerable. Ultimately, I decided to post it and I could not be happier, as I know I made the right choice.

In the past week, I have heard from people I have not heard from in years, had people say wonderful things and show so much love and support, had some bring back great memories, opened up my prayer network, had someone share a story of someone living well with this disease, had over 300 hits on my blog, and raised almost $10,000 for cancer research through my team Cabral’s Crusaders!!!! All in a WEEK! To say I am amazed by all of the wonderful people in my life is an understatement.

When I first received this diagnosis, I naturally questioned “Why is this happening to me?” “What did I do to deserve this?” While is still ask these questions daily, this IS happening and I have to make something good come from it. Something that one day my kids can look back on and be proud of. Maybe I can raise awareness of this awful disease.

SO. Here are some facts on Metastatic Breast Cancer: (from MBCN.org)

1. No one dies from breast cancer that remains in the breast. Metastasis occurs when cancerous cells travel to a vital organ and that is what threatens life.

2. Metastasis refers to the spread of cancer to different parts of the body, typically the bones, liver, lungs and brain. ( in my case, it is the Bones)

3. An estimated 155,000 Americans are currently living with metastatic breast cancer. Metastatic breast cancer accounts for approximately 40,000 deaths annually in the U.S.

4. Treatment for metastatic breast cancer is lifelong and focuses on control of the disease and quality of life.

5. About 6% to 10% of people are Stage IV from their initial diagnosis. ( i am in this group)

6. Early detection does not guarantee a cure. Metastatic breast cancer can occur 5, 10 or 15 years after a person’s original diagnosis and successful treatment checkups and annual mammograms.

7. 20% to 30% of people initially diagnosed with early stage disease will develop metastatic breast cancer.

8. Young people, as well as men, can be diagnosed with metastatic breast cancer.

9. Like early stage breast cancer, there are different types of metastatic breast cancer.

10. Treatment choices are guided by breast cancer type, location and extent of metastasis in the body, previous treatments and other factors.

11. Metastatic breast cancer is not an automatic death sentence. Although most people will ultimately die of their disease, some will live for many years. (Hopefully MANY, MANY years)

12. There are no definitive prognostic statistics for metastatic breast cancer. Every patient and their disease is unique.

13. To learn more about National Metastatic Breast Cancer Awareness Day on October 13 and to access resources specifically for people living with metastatic breast cancer and their caregivers, visit www.mbcn.org.

Treatment Cycle #3

I had my fourth appointment and third treatment at Dana Farber a couple of days ago. My oncologist was unavailable so I saw her RN so there was really not much news. Things seem to remain steady and the medicine seems to be working still. My next set of scans will be in September so that will be when will be able to confirm if things are headed in the right direction! I am still feeling great for the most part. I am having some small side effects from the meds (tired and dizzy mostly, but wasn’t I always!). My current drug regimen is the following:

Lupron- a big shot in the butt once a month that shuts down ovaries. So currently I am going through menopause! Hot flashes are no joke!!

Zometa: a monthly infusion which I am receiving in the attached photo. This strengthens my bones since the oral chemo I am on is breaking down the cancer in my bones and essentially weakening my bones at the same time.

Letrozole- this daily pill shuts down all of the hormone production in the rest of my body.

Ibrance: This is the oral chemo I take daily to attack the cancer in my bones.

Since my cancer is so hormone receptive, the hormone therapy is basically taking the fuel out of the disease while attacking the cancer in the bones all while strengthening my bones. As my doctor said the 1,2,3 punch of medicines!!!

April

Ugh

I am doing a good job at putting on a brave face most of the time. Many days I am able to push this awful new reality of mine to the back of my mind and move on. Go to work, take care of my family and home, and just be. But every so often this harsh reality pushes itself to the front of my mind and consumes me…..that is what has been happening the past few days. I can’t get it out of my head that I have an incurable cancer. That my future is now so unknown. That the plans I had for myself and my family may never come true. Everyone keeps telling me, “You’ll be fine” “Stay positive” “Keep that Faith”. All of that is really hard to do given the circumstances. I get it that my doctor’s say I have the best circumstances in a really bad situation and that they are optimistic and hopeful but all of the stats are not in my favor. I know that my mind is going to be the most powerful source in this fight and that I have to try to remain positive and hopeful but quite frankly this all sucks. For whatever reason I am having a hard time getting out of my own head this week and I thought that writing it down may be therapeutic. I was wrong……..

Life goes on

april-familyBig week in my house this week!

I am now the proud mama of a Pre-K graduate!! I’ve always celebrated everything so the mini graduation party we had after her ceremony was nothing out of character! But the tears that I shed at the graduation and for days after may have some people questioning my mental stability!? Truth is I am not sure if it is the hormones, or lack thereof, or the fact that the whole time i questioned if this would be the only graduation ceremony of hers that I will see. While my doctors are confident and optimistic that i can and will live with this disease for a “good long time” i can’t help but wonder if this disease will get the best of me before i’m good and ready. At this point i feel entitled to the good cries and the bad days but I’m trying my best to stay positive, optimistic and hopeful that in 13 years i will be writing another post about her high school graduation.

I also had my monthly appointment with my oncologist. It is funny how easy they are becoming….we are learning our way to the hospital and timing our trek through the city of Boston during rush hour perfectly. I have found my favorite nurse, Roxanne, who can get my IV and take my 9 tubes of blood in one stick!! I learned that i can get acupuncture and a hand massage while getting my infusion making it all a little bit better. Luckily this infusion of Zometa produced no side effects which was a huge relief b/c my first infusion had me in bed for 3 days with terrible pain and flu-like symptoms. So thankful for this b/c we are also in the middle of dance recital week which is no easy feat in itself (#dancemoms)! We also found out that my tumor markers have continued to go down meaning that the hormone therapy is working! So now we continue to ride this wave of “good progress” until next month!! It is funny b/c we are starting to make goals based on Dr’s appt (i.e Let’s get Colin potty trained b/f our next appt) HA!!

My Story

On April 11, 2016 I celebrated my 35th birthday. On that day I was a wife of eight years to Trevor and a mother to 5 year old Quinn and 2 year old Colin. I was a daughter, a sister, a friend, a co-worker, and the life of the party. While I’m still all of those things, I’m now also someone living with Stage 4 Metastatic Breast Cancer, which there is currently no cure for.

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