2016 GWAPR Annual Fundraiser

I can’t believe that a week has already passed since our Gift With A Pink Ribbon Annual Fundraising event in Naples, FL on October 27th, 2016. Where does the time go?

It was such an exciting night! 😀

I had the opportunity to reunite with people that have been such a big part of my life growing up in Naples, and was also able to meet so many new faces. I can honestly say that I am still blown away by the turn out.

Gift With A Pink Ribbon was able to raise almost $2000 that evening, with the help of all of our Sponsors and Supporters. Wow! 😀

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I definitely had big dreams for GWAPR when I first started the organization, but I am truly humbled to see how many people have come together to support my mission.

The reality is that, GWAPR would not be what it is today without all of the help and support of family, friends, colleagues, our wonderful volunteers and generous sponsors.

I am eternally grateful to the time and dedication everyone has put into making this dream a reality, and I look forward to touching more lives as GWAPR continues to grow.

Stay tuned,

Elizabeth 😀 ❤

 

Are you interested in making a donation or learning more about our cause? Click Here! 🙂

 

 

The second addition to ” My Oncology Team”…

Today I was scheduled to meet with the radiation oncologist. This time, since it was so close to work, I booked the appointment late in the afternoon. When I walked in, the office was very quiet and there were two very cheerful young ladies sitting behind the front desk. After signing in, I was given a stack of forms to complete. “There goes another tree with my name on it”, I thought to myself. I quickly filled them out and returned them to one of the girls behind the desk.

I don’t recall waiting very long before the nurse called my name and lead me into an exam room. This office was very different from the last. There were no windows in the exam room I was in and it was lightly decorated. It didn’t feel as cozy or welcoming but, I later found out that it was due to them relocating to a much nicer facility. In any event, I wasn’t aware of that at the time so I became a little nervous, not knowing what to expect. Was the lack of decor suppose to resemble my new doctors personality? I knew she was a female based on the name but I hadn’t heard anything more about her. Was she going to be cold and dry? Well, I was about to find out.

As my brain was trying to connect the pieces of the puzzle, I heard a gentle knock on the door and in came the doctor with a huge smile on her face. She instantly lit up the room and gave it the makeover it needed. She introduced herself and with just a few words I felt an instant connection. I could sense that she was a very kind and compassionate person.

After a little game of “let’s get to know each other” she asked me to change into a gown so that she could take a look at my incision. I was still healing well which was great news because I was ready to start treatment as soon as I was cleared to do so. I wanted to make sure that there wasn’t even one cell that could do me harm left behind.

She explained I needed to give my wound a little more time to heal and since I was also going to Moffitt for a second opinion, she recommended I wait to see what form of treatment they suggested before going any further. If chemotherapy was needed, I would have to wait till I finished the chemo before I could move forward with radiation.

She also wanted me to schedule an appointment to see a genetics counselor so that they could test me for the BRCA 1 and BRCA 2 gene. The fact that I was so young and with no known family history of breast cancer was starting to raise suspicion. If indeed I was positive for either gene, I wanted to do anything I could to prevent someone else in my family from going through the same thing I was. I had a younger sister and two nieces to think about. With a positive gene, the recommendation is to have a double mastectomy and hysterectomy as your risk of breast and cervical cancer are much higher. This was important information to pass on and it would be selfish of me to keep it to myself.

My doctor asked me how I felt about the possibility of not having my own children, should that be the case in the future, and I remember thinking, “with all of the kids in the world that need a good home, why on earth would I want to risk passing on a faulty gene to my offspring”? I had always been happy with the idea of adoption. In fact on a more recent note, prior to my diagnoses, I had decided that it was the best option because I didn’t want to be pressed for time by my “biological clock”. It was hard enough with society wondering why at 31 I wasn’t already married with children.

The truth is, I wanted to experience life more without the responsibility of having a child. I didn’t want to conform to societies belief that at my age I should already have children when I knew I wasn’t ready to give up certain freedoms that came with not having them. Who made up that silly rule anyway and when did it become so taboo to decide not to have children? I don’t think my doctor was to convinced but, she listen to my reasoning, gave me a smile and reassured me I was going to get through this. I was very happy to have her on my team.

Once I left the office I immediately called the genetics counselor to schedule my appointment. I would soon be on my way to Moffitt and I wanted to get as much as I could done before arriving. Little by little I was checking off items on my to do list and slowly I was able to see the light at the end of the tunnel…

Stay tuned,
Elizabeth 🙂