Condition Update: Nicole had scans in October. Thankfully, she remains in remission. Special thanks to Dr. Kaplan for filling in so well for Dr. Trippett. Dr. Kaplan, is held in special regard as she has cared for Nicole throughout the transplant process.
Nicole was recently recognized for her work in raising awareness about the Catastrophic Illness in Children Relief Fund For Children. We thank all the committed members of that fantastic organization. We applaud their dedication and hard work in aiding families so devastated by childhood disease with the resources to deal with the financial burdens of childhood illness.
Upcoming Events: Wayne Valley High School Blood Drive - Tuesday November 18, 2008
In Her Own Words
Below is the text of a speech Nicole wrote herself. She volunteered to speak to the youth in our church as they approached Confirmation.
Growing up my family and I were pretty much like any other
family in Wayne. We rarely missed church and always tried to do the right
thing, whatever that may have been at the time. I was so active and wanted
to do everything and anything. I played softball, basketball, tae kwon do,
dance and more. I felt as though nothing could get in my way in life and nothing
could go wrong.
But, on a day that would shake the faith of many Americans, mine was shaken
too, but for another reason. I felt like my life had ended On September 11,
2001. On that fateful day I tried to go to my teacher because I felt that
something was wrong with me but I didn’t know what. I had a lump. She
sent me back to my seat saying it was probably just a mosquito bite. I went
home told my mom and then she told my dad and they took me to the hospital.
I was sent home with what was thought to be a broken collar bone, and we thanked
god that nothing was seriously wrong. Unfortunately the doctors were wrong.
I went back to the hospital that next day and I was admitted to see what exactly
was wrong with me. I stayed there for a little over 2 weeks. All I could say
is why me, why is this happening. A couple days after I was there I had surgery
and my life had really ended. The doctors said I had cancer, but I didn’t
really understand what that meant or what was going to happen to me. The doctors
threw all these terms at me but the only thing that I could understand was
that I had to cut my hair really short because I was going to lose it. When
I finally went home I cried for a long time, hated God and stopped believing
in one, because what God would do this to a 10 year old child.
I went through 6 Months of intense Chemotherapy, which was the treatment for
my type of cancer, known as Hodgkin’s Lymphoma, and felt every side
effect from treatment. Leg pain, nausea, and eventually all my hair was gone.
I got a wig and wore it every day and let no one see me without it, not even
my family. But those six month were finally over and my family and friends
were still there and I started to let God back into my life. I started to
get back to all the sports I had played and couldn’t wait to go to middle
school. I felt it was all a nightmare and my life was going to get back go
the way it should have been.
All of this didn’t last long. I relapsed and had to go through all of
this treatment once again, and lose my hair for the seconded time. Only this
time I went to a different hospital that was filled with kids with cancer
and all you saw when u walked in there was bald heads. I couldn’t handle
that, so I was off in the corner by myself with my mom and dad, screaming
inside. All I wanted to do it is go home and be with all of my friends. But
I did what I had to do to live. The doctors told me his time around was going
to be even harder for me.
While I was there I met a couple of my best friends and the best people that
I would ever meet. One of the first people I met at the hospital was Sean
Hanna. He took me under his wing, so to speak. Sean got me out of my room
and made me feel a little more comfortable in a terrible situation. I also
met Jessica Foti, Mike Romano, Jesse Disanto, Jesse Spina and Lauren Payton.
Jessica was a girly girl and I really connected with her. We talked about
nails, fashions and just girl talk. Mike was a little younger than me and
I think he had a crush on me at one point. He was full of life. We used to
play cards together all of the time. Jesse Disanto. Was the “bad boy”.
He was older and always made fun of me and do things that I only thought people
did in the movies, although I shouldn’t have been surprised because
he had this “get in your face” personality. Jesse Spina was more
quiet and really never talked in the hospital for reasons known only to him.
I use to get him out of bed and get him to talk to me. We even hung out outside
the hospital and went to the mall. Our family’s even got together for
bbq’s. And last but not least, there was Lauren. She is so funny and
doesn’t care what people think about her. She calls me her "mini
me" because we like all of the same things and always made fun of the
doctors and nurses. She is one person that I will always keep in my life.
Even with all my new friends at my side I was going to have to got through
the hardest experience ever, alone. I was going to have a transplant, which
means I was going to be put into isolation for over a month in 12X12 room.
Not even my parents could touch me without gloves on. This was because I was
given mega high doses of chemo and my immune system was completely gone. It
was awful, I couldn’t do anything but watch t.v and play board games,
oh and sleep. At one point I was out of it the doctors were really starting
to be scared of my mental state of mind, but they knew I had some pep because
I was still really nasty to them, so I guess that counted for something. When
I finally came home I couldn’t be in large crowds and couldn’t
really be with my friends for 100 days. While all this was happening my mom
got very religious and I just couldn’t handle it because I felt that
I had finally let God back into my life and he let this happen to me again.
I stopped believing. I stopped everything, praying, going to church, everything.
After almost losing my life twice during transplant I began to think again
that this event in my life was over. I started to go back to school and find
my old group of friends. While I started to live life again, the life of one
of my really good friends had ended. Jessica Foti was dead. I couldn’t
believe it and just stood there and stared, I didn’t have one thought
enter my mind other than Jessica’s face. One month after I found out
about Jessica, I found out that I relapsed for the second time.
I went back to the hospital and told them that I wasn’t going to do
it anymore and my parents, doctors, and nurses were leaving it up to me whether
I was going to do the torturous treatment again. For a while I didn’t
know what to do but then I realized what I had to do to live. I knew exactly
what was going to happen to me and I hoped for it to be easier than the last
2 times. I felt the pressure to live.
I ended up doing 21 more months for chemo. During the beginning I lost 2 more
of my best friends, get in your face Jesse, and Mike. Jesse’s parents
promised if he made it to his 18th birthday that they would get him a BMW.
He did make it but it wasn’t long after that he passed away. Innocent
Michael passed away, I don’t remember anything of him at the end because
I think I blocked it out and try to remember him a wake and jumping around.
The first month I lost my hair again and all remember doing was coming out
of the shower screaming for my mom and fell to the ground because I was told
that I might not lose my hair and I did. I think I was kind of ok with doing
the treatment. I just didn’t want others to see what was happening to
me, because then everyone would know. This time I was much easier with it,
I wore bandanas instead of my wigs and let my close family see me without
it on, I guess I started to feel more comfortable.
After, a couple months one of my closest friends Jesse Spina had died. I couldn’t
believe that it was true until I went to his funeral and actually saw him.
I couldn’t even go near him and felt like I was going to throw up because
I had just seen him alive and moving around. All I could do it go to his mom's
arms and cry. All I kept thinking was what God would do this to children.
I started thinking what if I was next, what if the doctors where going to
say to me that there was nothing more that they can do?
Thankfully, by the end of my treatment the doctors were now getting more comfortable
with taking me off treatment, and they did. The nightmare was finally over.
I have been in remission for over 3 years and still can’t believe it.
Although going back to school was so hard for me because a lot of my friends
moved on without me. I guess they thought I was old news. It was so confusing.
It hurt so much. Even school itself was not as easy as I thought it would
be. I had a lot a catching up to do because I had missed so much. But I figured
I had been through cancer I would make it through this, and I have. I have
a close group of friends and my family is stronger than ever. It is still
very hard for me but I have slowly started to let God back into my life a
little more each day.
I believe that God has a plan for everyone and I think my ordeal happen for
a reason. I came to the realization last year that I want to be a doctor.
I don’t think I ever would have known that nor had the strength to pursue
if I didn’t gain the strength from my ordeal. Hopefully I can influence
someone in the future just like the doctors have helped me.
Click on picture to read about the impact Nicole has had on others she has met and to hear our dedication |
"I Hope You Dance" |
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Nicole ready for Junior Formal
Life Goes On
It may shock some of you to read this, but but it's also hard to be a survivor. Nicole has had to overcome a great deal of adversity since treatment ended. She has had to learn with tutoring the school she missed during nearly four years of treatement. She has had to make new friends when old friends seemed to fade away, one at a time, during those four long years. Nicole has had to play "catch-up" when once again playing the sports she loves so much; forced to give up Tae Kwon Do, and to play behind players she once dominated on the softball field. Yet, Nicole continues to persevere, gaining more and more confidence with every new day; one long day at a time. Nicole now earns straight A's in School, confident enough to proclaim recently that something in the medical field would be a goal she has set for herself. She has made new friends and has a special someone who makes her very happy. Surviving is hard, but with every new day comes a new opportunity to overcome the adversity that is her life.
Nicole
makes a catch for her high school varsity softball team



The people above are the wonderful teachers of the Huntington Learning Center. They have helped Nicole tremendously in her effort to "catch up" after missing so much school.
With Nicole (right) are: Christine, Liz, Randy, Sharon & Lauren
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Pay it Forward, Acts of Kindness A Wise man once said, "We have become not a meltin pot but a beautiful mosaic. different people, different beliefs, different yearnings, different hopes, different dreams." Individuals contribuite to the community in order to make the communtiy thrive. at the same time, we are molded and shaped from our interactions with one another. If the contributions came from all the same type of individuals, man would not have achieved but a fractionof his accomplishments. Nicole has been in remission for almost 2 years. We feel blessed to have come this far without the bone marrow transplant we thought she would need. While we are humbled by the community's remarkable response to our cry out for help in finding her a donor, we only truly understood the depths of our achievment when we learned of the 9 matches (with more coming in every day) to other cancer patients from Nicole's drives. It is this accomplishment and our gratitude to the community that we now set out to "pay it forward" by holding more Bone Marrow Drives!!!
I Wrote the following poem in an attempt to describe what the family undergoes while we await the results of scans taken every three - four and now six months. Crossroads My daughter felt a lump on September eleventh, two thousand and one; A cancer that would eventually spread to her lung. This Lymphoma, we were told, would be easier to cure, Only six months of treatment, one Dr. would assure; Not the four years of anguish she would ultimately endure. My little girl was only ten, full of innocence and grace. Her parents forced to witness the pain upon her face. Now the Doctor has told us, this is the case; The cancer is gone, not even a trace. Yet, we still worry, loving parents to the core, For we have been told all of this before; Prior to her becoming sick, two times more. Never really knowing what is truly in store, We often ask God why this road we must travel; But, the answer we can never unravel. After three months she undergoes more tests; More Scans, more pain. She never rests. They have to make sure the cancer has not returned. The Drs will call us to tell us what they have learned. As the phone rings, the sound cuts like a knife. We are at the crossroads of her life, And that of my son, myself and my wife. If the Dr says everything is alright, Then, her future must be bright. Life will be as it was before. Only, this fact we cannot ignore: We will be doing all of this in three months more. If the Dr. says the cancer is back, We will know we will have to travel that dreaded track. We would be so scared, knowing what is in store, Having been down that track before. This is why we are so afraid; Such a dear price, she has already paid. We thank the Dr. for her compassion. Ending Cancer’s devastation is her passion. While my wife may have given her birth, My angel’s future is now only on God’s turf. |
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