Sunday, June 16, 2013

Relay for Life! Celebrate. Remember. Fight Back.

Tara and I walking the survivor lap at relay for life in Medway, Ma

I have gone to many relay for life events in my lifetime, starting when I was young. Usually we would go in my father’s hometown of Medway to meet up with my aunts, uncles, cousins and my Grammy. My memories of it are always a night of fun, packed with a lot of people and tents set up for the 24 hour relay. The night was brightly lit by the candles in the luminaries bags. We would always buy one for my grandfather with his picture on it. To me relay for life was always an inspiring day that I never thought would impact me more directly later on in life….okay well maybe not too much later, but at just 18 years old. Being diagnosed changed my world. I never thought at 20 I would be a part of relay, or better yet be walking in it as a survivor! Never ever did I think I would have to add another family member to my luminary bag or add names of my jimmy fund clinic friends, all who are under the age of 20 who have passed away from this disgusting disease. I use to hear the honorary speaker when I was younger and sure, I felt inspired by their stories, but this relay I listened to my close friend Tara Daniels speak about her journey and felt many more emotions along with being inspired. As I sat and listened to her talk about her journey, all I could think about was how much I could relate, how we’ve lost so many friends, been through so much hell yet still somehow wouldn’t change our cancer because it made us who we are TODAY. I couldn’t be more proud of her. Since being diagnosed I went to a relay last year but felt weird walking the survivor lap and didn’t want to alone. This year I proudly walked with Tara and even Jerry Remy was by our side with so many other survivors that I felt an immediate bond with. It was my first relay for life survivor lap. As we started walking, everyone was cheering for us along the track; so many emotions got to me. I was proud but also shocked still that I have been battling cancer for almost three years and what made me more overwhelmed with tears is the fact that some of my clinic friends couldn’t walk the survivor lap with me. Instead cancer took them away at such a young age; it is not fair at all. I missed them immensely while walking that survivor lap and they were all I could think about. They inspired me to keep walking that track. 


If anyone is reading my blogs I want them to know one thing: events such as relay for life do SAVE lives, the money raised is going to where it needs to be and every year it is helping for there to be more survivors like me. I know we all see fundraisers or donation boxes at restaurants/banks/stores and you might not know what it is going towards but I DO. It is the reason I’m here; it is the reason for more research leading to new medications and options for patients. Please next time you pass one just put a simple couple of quarters maybe even a dollar or two each time because it does add up and it can make a difference in someone’s life. I don’t want another person in this world to suffer from cancer, either being diagnosed themselves or someone they love being diagnosed. Relay for life is an amazing event that gives you an instant new outlook on life. In honor of Kaylee, Nahge, Leah, all the rest of my Jimmy Fund family, and my grandparents Frank and Barbara, I will continue to live for them and continue to walk in events like these for the rest of my life. And you can assume that these wonderful people I have lost through Cancer will live on in my memory, evoking my emotions every time I walk that survivor lap.

My cousins & I at the relay for life

I only have 11 more days of chemotherapy! June 27th is my last day followed by a bone marrow biopsy on the 28th!!! :)

Wednesday, June 5, 2013


My new Youtube channel documenting my 100 days left of chemotherapy treatments! Feel free to watch & follow :)

Saturday, January 26, 2013

Tackling Chemo




Sunday January 13th my friend Jen and I went to the Patriot’s playoff game against the Houston Texans! We met through clinic and past jimmy fund trips. She invited me to go with her and even though I just had a procedure and was starting a new chemo cycle, I said yes. I know how awful I feel during my two-week cycles but nothing was stopping me from first row in the end zone of a playoff game! In the past I’ve gone to many bruins and red sox games on chemo so I knew to pack my puke bucket and a ton of meds to get me through! Regardless of how bad chemo side effects are I try not to miss opportunities like this and I’m so glad I didn’t miss this game! When we arrived to Gillette stadium we were lucky the weather was nice, for January at least. When we got to our seats we couldn’t believe our view, every player was right there it was incredible! We took plenty of pictures that I’ll share throughout this post. Jen and I didn’t feel too sick during the game, which was a miracle.



              During the last quarter of the game a man came down to our seats then started talking to us. The Jimmy fund gave Jen the tickets so he asked which one was Jen and he introduced himself. We then find out it was former Patriots player Joe Andruzzi! Jen immediately also introduced me and told him how I’m also a cancer patient at Dana Farber with her. I think he wouldn’t have guessed because how much my hair has grown during my maintenance chemotherapy! He thought it was cool how we met through clinic and became friends because of our cancer diagnosis. In 2007, Joe himself was diagnosed and treated at Dana Farber and now has a foundation helping other cancer patients. He signed picture for us and even let us wear his super bowl ring, and those things are heavy! Since my phone died I asked if he would send me the pictures we took that day. Later on that night I texted him letting him know that not only was it awesome for us to meet a Patriot’s player but also, more importantly, another cancer survivor. Being a part of the Jimmy Fund provides me with opportunities to meet so many different well-known people but nothing compares to just meeting other cancer patients/survivors. The instant bond is unforgettable. Joe Andruzzi texted me back saying, “I’m glad I had time to get down and meet you both. Remember to take it 1 day at a time and stay positive. Keep smiling. Laughter is the best medicine. Stay Strong. God bless you both.”  He was extremely nice to us and made our day! He’s dedicated to his foundation that provides financial assistance for patients and their families, as well as funding pediatric brain cancer research. I hope everyone can look online and check it out! Donate if you can :)

joeandruzzifoundation.org/






Monday, December 24, 2012

My last Christmas on Chemo!



Quick Update: 

    I know I haven’t written much on here lately, sometimes It’s overwhelming to write and explain all my thoughts. On Friday it marked two years since I’ve been diagnosed. That day I can’t get out of my mind because that day two years ago I remember it clearly up until hearing the most devastating words “you have cancer”. It makes me think a lot about all the pain I experienced but mostly all the great things that came out from this. One being now I have a full head of hair that I love. It’s more than just hair to me, it’s a symbol of what I’ve overcome, every inch of it was earned. I can’t wait to someday have it grow long enough to donate for another young girl battling cancer.

    Also on Friday I went into clinic for Acupuncture. It helps with most of my side effects on my maintenance chemotherapy. Nausea, headaches, anxiety and my sleep problems are slowly getting better from this. And no the needles don’t hurt at all I suggest it for anyone who is battling cancer or anyone with migraines. After my appointment I went up to 6thNorth the floor I was inpatient during most of my treatment. One of my nurses Linda remembered that today was the date I got diagnosed two years ago. I didn’t expect her to even remember that date but now thinking about it I don’t doubt that any of the nurses forget. They truly love their jobs and have spent so much time with each family that they became apart of ours. I love visiting 6th north and the doctors and nurses love it that much more seeing their patients conquer cancer and back to a normal life.

    And today being Christmas Eve I can’t believe how blessed I am. Christmas two years ago was not how I ever want to spend a Christmas like ever again. Instead of opening presents I received my first chemo ever on Christmas morning.  I didn’t understand or appreciate how the only important thing is spending the holiday with all of my family healthy. It’s so amazing I can’t even explain.
  


    I’d like to lastly mention the New Year, 2013, is going to bring big changes to my life. Starting January 11 I will be starting my 2nd to last chemo cycle, EVER! I can’t believe I’m so close to the finish line. Each cycle is 84 days just knowing I’m two cycles away from beating this motivates to just push through as much as I can. So far Fourth of July is my last day of chemo, best believe I’m counting down the days!

I truly wish everyone a Merry Christmas and a happy HEALTHY New Year<3

Wednesday, October 10, 2012

Footprints...When you saw only one set of footprints, it was then that i carried you.


Today marks the third anniversary of my Grammie (Barbara Boczanowski) who passed away.  It made me think about a ton of different things today. First was how lucky I feel to have such an amazing angel watching over me. During my chemotherapy treatment everyday’s a long struggle, physically and mentally draining. With all of this the only thing I believe that gets me through this isn’t just my support by friends and family but also those watching over me. My grandmother was an amazing woman always helping others and involved in everything. One thing she loved being a part of was The Catholic Daughters church group. I’m not heavily into my religion but because of her I do believe she’s in heaven with God watching over me. I feel so blessed to have such an angel. Another thing that crossed my mind was what she thought of all of this. She didn’t live to see me diagnosed and battling cancer but she’s in heaven watching down on me, what could she possibly think of all of this? I thought of how much it saddens her to know her 20-year-old granddaughter is battling leukemia. On the other hand I reflected on how proud she would be of me. She must be so amazed by me going through what I go through everyday. She would love how involved I am with spreading cancer awareness and inspiring others. Mostly she would be so proud of me for being a survivor. As much as I miss her I can’t help but to think she’s there in heaven for a reason, to guide me through all of this. I can fight as hard as I can but cancer is a disease that’s out of my control and it’s a relief to know my grandmother is watching over me. I feel like anytime my treatment has a difficult part I somehow amazingly always make it through and I owe that all to my beautiful Grammie, my angel in heaven.
*My grandmothers from both sides of my family* to the right is Grammie, RIP<3


My Grammie isn’t the only angel I have though I have five others; Kristie, Kaylee, Nahge, Seshu and Avalanna. In the past two years I’ve met so many friends from The Jimmy Fund and the harsh reality is being a survivor you watch a lot of your friends sadly pass away from cancer. It gets really frustrating to see them fight so hard but lose their battle because of this terrible disease. The Jimmy Fund is an amazing group we support each other like no other and the bond is instant no matter gender, age, or type of cancer. It’s the closest bond I’ve actually had with anyone. I’ve gained a lot from all of this heartache however. I’ve been given a bigger reason to fight and a greater reason to spread awareness. I miss all of my friends dearly and going into clinic isn’t the same without their smiling faces. I like to believe I’m living my life for them and they are all in return watching over me.

*picture of Nahge, Rachel & I*

Saturday, February 11, 2012

What doesn't kill you TRULY makes you stronger...


Yesterday marks my one-year of being cancer free! Looking back to last year I honestly couldn’t think of how I was going to make it through all of this. I wish I could say giving up never crossed my mind but anyone fighting cancer, my family and friends know there were a few times it did. Beating cancer seemed unthinkable. Everyday the mental and physical pain of my illness increased.  Seeing my loved ones watch me go through this gave them the pain too as if they were also fighting. I would try so hard to only show my positive side because I didn’t want anyone seeing me so scared too. Everyday I somehow got through it mostly for them. On February 10 2011 is the day my oncologist told me I reached remission. I was so happy I couldn’t even believe it. Although it meant I still had to finish my 2 years of treatment, it gave me a huge push to keep going. I had beaten cancer, now all I had to do was endure the side effects and keep up with my chemotherapy. Now one year later it AMAZES me how everyday dragged on and seemed never ending. How you can’t even begin to think of how you’ll make it through these curves life throws at you. Also its crazy to think a year has past just like that. I’m so thankful for my family and friends who pushed me everyday. Beating this has been more positive than negative. So what that cancer temporarily took my hair and life. Hair grows back and my life has only now changed for the better. I’ve truly never felt so happy in my life. Cancer made me appreciate everything and everyone. It also helped me with my future. I know I want to work with children and be a child life specialist. It’s an emotional job but no one can relate to them as much as I can. I want to help them overcome this and give them hope! Being diagnosed with Leukemia was a day I’ll never forget, but how it’s impacted my life, family’s life and friends it’s been a blessing. Cancer has definitely given me way more than it has taken and for that I’m so thankful!



Sunday, December 25, 2011

It's The Most Wonderful Time Of The Year!



This past week has brought up so many memories. It has now been 1 year since I was diagnosed. Its emotional to think about the awful experience I encountered and at the same time how blessed I am that I survived. The beginning of 2011 was pure hell I never thought I’d make it past each day but they all seemed to somehow add up to weeks, months and now a year. Last Christmas instead of opening presents, I was preparing for chemo. Christmas day 2010 I received my first chemo ever. I couldn’t stop throwing up and felt so helpless attempting to get my chemo down. If someone told me I’d be here today surviving this I would of thought they were INSANE. My body couldn’t handle the chemo and I didn’t know how I was going to get around this. Also on Christmas the tests confirmed that I had M3 AML leukemia, which is so important to treatment. There are all sorts of leukemia and subtypes which tailor what treatment you receive and survival rate. My oncologist came in with our treatment plans, which seemed unachievable. They used so many terms I’ve never heard of explaining what the cancer has done to me and what I will be doing to fight this. There are three phases the Induction, Consolidation, and Maintenance phase. If I even made it to the last phase I would have to be in the hospital for at least 6 months. Reading this on the plan was unbelievable; I wanted to just give up right there. I’m so glad I didn’t. Although this was literally going to hell and back it’s been the most positive/crazy/amazing things I have ever experienced. Its changed my mind set towards everything and I know my family and friends feel this way as well. It makes you appreciate everything so much more. Opening up presents gave us a smile but they didn’t seem to matter as much. This Christmas the greatest present was just being with my entire family from both sides, healthy & happy. I truly feel blessed that it all has changed this past year in my favor. To have a second chance at life is an amazing gift that I will never take for granted! I hope everyone somewhere in his or her life experiences this feeling of realization, just not in the way I had to.

^ My cousins and I this past Christmas Eve! Thankful.

Ps. My next post might be incredibly long. I want to explain the three phases of treatment in depth and also what leukemia is! AWARENESS will bring a cure.