Hanna was a happy, healthy 2 ½ year old girl until she complained of back
pain one day. Two days later she was diagnosed with Neuroblastoma, a cancer that develops in the nervous system in embryo.
After only seven short months, many surgeries, and 6 rounds of chemotherapy, Hanna lost her battle with this disease on Father’s
Day 2006. Although she is gone from this earth, her spirit lives on in all of us who choose to come together for the Butterfly
Walk. We can only hope that with further
research funding, children like Hanna will have a better chance for a cure in the future. Hanna showed us all how to fight
a battle, how to be courageous, and how to dream. Now it’s our turn.
Corey was a very happy-go-lucky little boy who loved everyone and loved to make people smile. In early 2007, at 2½
years old, he was fighting what everyone thought was a typical toddler cold/sinus infection with swollen glands. After about
a week of antibiotics with no improvement, and the "lymph glands" getting larger, he was sent to Cincinnati Children’s
Hospital for a biopsy of the lump behind his ear. On Feb. 2, 2007, the results of the biopsy found that it was not a swollen
lymph gland, but in fact was a cancerous tumor. Later that day, he was diagnosed with Stage 4 Neuroblastoma, an aggressive
and very deadly childhood cancer.He endured 7 rounds of chemotherapy,
multiple surgeries, a stem cell transplant that put him in the ICU and on dialysis for a period of time, several weeks of
radiation and another several rounds of chemotherapy. In April of 2008, he was NED (no evidence of disease).Then, in October 2008, he relapsed with a new tumor behind his ear. Once again, he went
through more chemotherapy and radiation. In January 2009, the tumor in his head was gone, but now there was a small tumor
on his right femur. More radiation and chemotherapy were given. On March 13, 2009, he was once again tumor free and NED.Corey continued with oral chemotherapy trying to prevent another relapse. Unfortunately
in mid-April of 2009, Corey relapsed again; this time with tumors throughout his entire skeletal system and on his liver.
Corey fought a courageous fight for more than 2 years – and rarely complained
about any of it. (We adults could learn a thing or two from Corey!!) Unfortunately, the cancer was too aggressive to fight
and on May 8, 2009, just a month before of his 5th birthday, Corey lost his battle and earned his angel wings. We miss him
dearly! We walk in memory of Corey to raise funding for further cancer
research so that no other children or their families have to go through this.
Shayna was a bundle of red velvet on her very first
Christmas Eve when we noticed that something didn’t look right in her eye. A week later she would have her eye removed
to prevent cancer from spreading to her brain and begin chemotherapy for the tumors in her remaining eye. Nothing prepares
you for that. After many months of treatment and a new prosthetic eye, she has now been cancer-free for 17 years. We say she
is one of the "lucky ones", but it has nothing to do with luck. Shayna’s treatment was successful because
of research. Determined that no child should have their childhood interrupted or cut short by cancer, our family started CancerFree
KIDS to fund the critical research that is necessary for every child to be guaranteed a cure. This research benefits not only
children, but all of us. Those participating in the walk understand how important it is. We thank you for your support!
To celebrate 10 years of being cancer-free, Shayna started her own fundraising
project to raise money for research. She created beaded bracelets that feature a pendant with the word "COURAGE"
that are various events and on the CancerFree KIDS website. Shayna funded a research grant entirely with these funds!
Charlie was diagnosed with AML,
Acute Myloid Leukemia, at age 16 months on January 30, 2006. This specific type of cancer is common in children with Down
syndrome. After Charlie's first round of chemotherapy, we were extremely blessed as he went into remission. Charlie underwent
a total of 8 rounds of chemotherapy accompanied by month-long hospital stays to be sure the cancer was gone for good. We are
happy to say that Charlie hit a very big milestone this past June and was moved into the Long Term Care Program at Cincinnati
Children's. (This means once a year visits; no more long clinic visits!) Charlie is thriving and healthy and enjoys playing
baseball, soccer, swimming, and playing with his friends at school and his very best friend, his sister, Madison. We met Hanna
and her family during Charlie's treatment and Hanna was such a great friend to Charlie. We couldn't be happier continuing
our participation in this walk to honor her memory and support such a wonderful organization. Like Hanna, Mary was just 2 ½ years old when she was diagnosed with a high grade, non-specified, infant brain tumor
on March 8, 2006. Four days later, surgeons at Cincinnati Children’s Hospital removed a baseball size tumor from her
right front lobe. Here began Mary’s journey. In the months that followed, Mary was given four rounds of chemotherapy,
aggressive radiation treatments, and an eight month regime of maintenance chemo. By the Grace of God, her last MRI on December
14, 2009, showed no changes and no return of cancer. Prayers from hundreds of friends and family had been answered. In 2016,
Mary's cancer returned and we traveled to Boston for surgery in the summer. She is now doing well overall, but it has been a long process with extra therapies, challenges, etc, but, Mary is resilient
and overcoming them. We have hope as each day passes
that Mary’s story will have a happy ending, that she will be a lifelong cancer survivor. The Butterfly Walk is an opportunity
for Mary’s family and friends to show their support for Mary, and the ongoing cancer research sponsored by Cancer Free
KIDS. Mary is a survivior because of outstanding care she has received and the research that continues at Cincinnati Children’s.
Please consider joining Mary for the walk this year; she was thrilled to have family and friends by her side last year. We
will continue to support Mary, research efforts, and the hospital with strength, hope, courage and faith in our hearts.
Parker was 10 weeks old when he was diagnosed with Neuroblastoma
on February 4th, 2005. He was a fussy baby that you just couldn’t seem to make comfortable. We found out later that
he had tumors in both adrenal glands, his liver; near his spinal cord and that it had spread to his bone and bone marrow.
6 days after being admitted to the hospital Parker started an intense research protocol at Cincinnati Children’s which
consisted of 8 rounds of chemotherapy. Six long months of injections, treatments and trips to Children’s and we are
happy to say Parker is a Cancerfree KID! Parker is now followed in the ATP long term survivor’s clinic at Cincinnati
Children’s. He is monitored now more for the effects of the chemotherapy he received and less for the disease itself.
We feel very blessed to have had the researchers at Cincinnati Children’s who worked so hard to save our child. We are
very grateful to them and their hard work. Without events like the Butterfly Walk, CancerFree KIDS would not be able to offer
grants to these outstanding individuals who work hard every day to save one more child.
On July 4, 2011, our sweet
6-year-old son/brother, Tony, left this earth and is now experiencing the joys of eternal life in Heaven. In October 2008,
at the age of 3, Tony was diagnosed with medulloblastoma, a pediatric brain cancer. He underwent surgery, 31 radiation treatments,
and intense high-dose chemotherapy (followed by stem cell rescue). Tony experienced about a year of clean scans, but relapsed
in June 2010. After another year of various chemotherapy treatments and two surgeries, Tony succumbed to the disease. We are
heartbroken, but are focusing upon treasuring every moment of this life just as Tony did. He had a zest and joy for life that
was infectious. Despite the hardships Tony faced, he rarely complained or cried. He attended school every day he was able.
He enjoyed playing t-ball and soccer. He loved spending time with his three big brothers. By his example, Tony showed many
what it means to be strong and faithful. "Pray~Hope~Believe" became the theme for Tony's journey and remains our
theme for healing and living life
Natalie's journey began on April 22, 2011 when she was three years old and was diagnosed
with Wilms Tumor on both kidneys. She endured chemo treatments, losing both kidneys, other miscellaneous surgeries and daily
dialysis treatments through her journey. On October 9, 2012 she received a kidney transplant from her Great Aunt and
has been doing amazing ever since. She is now enjoying life as a "normal" almost six year old and we couldn't
be more grateful. We're so proud to be a part of the Butterfly Walk!
Our journey began on April 6, 2011, after several months of nosebleeds, fatigue, paleness
and finally a blood test that revealed something was very, very wrong. We were sent to Children’s for more testing and
it was finally found that Maya had a more rare type of leukemia, called Acute Myeloid Leukemia (AML). AML is tougher to treat
than it’s more common counterpart, Acute Lymphoblastic Leukemia. In addition, Maya’s leukemia has a genetic anomaly
that makes it even more of a challenge to treat. Maya is a feisty ten year old
who fought HARD and beat leukemia twice over three gruling years of treatment and two bone marrow transplants. Maya
is now fighting for her life for a THIRD time. Maya is a tough, strong girl, but no child should EVER have to fight
as hard as she's had to and endured the nightmare that she is going through. Please help fund research so that NO more children
will be told that they have cancer... EVER AGAIN!
Becca has survived cancer twice! We are very thankful that she
is still here with use! We are also thankful for her bone marrow downer that saved her life and because of him we get to see
the smile on her face! Becca is strong,brave,and loud(in excitement or when she is angry)we all love Becca she
is a great girl she hopes sometime in her life time there will be a CURE!!
Timothy created Team A&W in memory of his two
cub scout friends, who died in 2011 as a result of cancer related complications. Arun and Wyatt were 11 years old. Let's
beat cancer one step at a time. Go Team A&W!!
October 25, 2008, Elizabeth Lothrop, 14 year old, was diagnosed with ALL, Acute Lymphoblastic Leukemia. Liz was currently
finishing out her volleyball season for Mason Middle School. Lizzy was very active and was never sick. She played Basketball
for Mason and played AAU ball, she played Volleyball for her school too as well as Junior Olympic Volleyball for Sports Express,
and ran track for Mason. Lizzy's back started hurting her the last two weeks of volleyball season;
we took her to see an Orthopedic specialist who confirmed she had a fracture in her lower spin. Liz had a pars injection four
days later in her lower spine and four days after that she spiked a fever of 103 and a massive nose bleed that took 28 min.
to stop. We took her to Children's at 10 pm and by 4:30 am we were told that she had cancer; all of this took place within
a five week period. It has been a battle since but cancer picked the wrong person this time. Liz is a true fighter and has
an infectious spirit. Lizzy has just started the Maintenance Phase of her treatment and
will continue on this course until her last chemo treatment on Feb. 17, 2011. She has endured weekly heavy chemos, blood transfusions,
platelet transfusions, very long hospital stays, severe side effects of chemo, and complete hair loss twice, but has remained
faithful to God, family, and friends. Lizzy was in remission until June 2015 when the doctors found she had a brain
tumor. After surgeries, radiation and chemo, Liz lost her battle in May, 2016. Because
of the prayers and financial support we know that one day there will be a cure. Lizzy's wish is that they find an easier treatment
protocol for people with cancer and of course, THE CURE!
In January 2009, just one month before Joel was due to be born, Susie and Adam found out on a routine ultrasound that their
baby Joel had a tumor above his left adrenal gland. Susie was put through a lot of testing to get a handle on what was going
on with Joel so the doctors would know what to do when he was born. He was born two weeks early on January 26th. Due to the
size of the tumor and it pressing on his lungs, he had breathing issues and was immediately taken to Cincinnati Children's
Hospital RCNIC where he then stayed for the next four months. At 8 days old he had his first surgery to biopsy the tumor and
remove a lymph node in question. He was later diagnosed with stage 4 neuroblastoma that had spread to that lymph node and
also to his liver. He required a central line to be placed and at just 10 days old, Joel began his first round of chemotherapy
and did a total of five rounds in the time he was in the hospital. Joel also had pyloric stenosis where the pyloris that drains
the stomach into the intestines thickens making it difficult for food to pass. Joel's was so thick that it was practically
closed, so he vomitted every time he fed. He required surgery on that too. Halfway through the five rounds of chemo, a PET
scan showed that the tumor had shrunk enough to now be removed, to then be followed up with additional chemo. So his next
surgery was for the tumor resection and to repair his pyloris. After four months in the RCNIC, 6 surgical procedures and 5
rounds of chemo, Joel came home on his four month birthday. Joel has now been cancer free since June 2009! He is a very busy
little boy who loves getting into everything he can, playing with his big brother, singing and dancing, doing puzzles, playing
outside and just being with his family. Joel is our miracle boy. We have seen what God can do, and the amazing results that
come from research to provide a way for our little boy to live a long, healthy life. Our prayer is that other children can
recover as well as Joel has and provide a way for other children to become cancer free.
In September of 2009, our 2 year old son, Aaron was diagnosed with High Risk Neuroblastoma. Since then he has
endured 18 months of grueling treatments including 6 rounds of high dose chemo, 2 bone marrow transplants, 2 tumor resections,
20 days of radiation, and 6 months of immunotherapy. Through all of this he has endured countless infections,
viruses, unbearable pain and even septic shock. And you know what? He's still so happy! Our
children deserve the best we can give them, we can do more about pediatric cancer than the world is doing.
|Gracie was just 7 months old when she was diagnosed with hepatoblastoma (liver cancer) in February of 2007. Doctors at Cincinnati
Children's Hospital found a tumor the size of a softball in her liver. She underwent four rounds of chemotherapy. In May of
2007 she had surgery to remove the tumor followed by two more rounds of chemotherapy. Gracie has been in remission since August
of 2007. Today Gracie is a happy, healthy and is enjoying every minute of life. We owe this outcome to the support, prayers,
and research of many people. Organizations like Cancerfree KIDS and Cincinnati Children's Hospital do amazing things for children
battling cancer. We are one of the lucky families who benefited from their research and hard work. We are honored to be a
part of the Butterfly Walk and look forward to helping fight pediatric cancer.
Jessica Michaela Elam was just a normal 7 year old girl when she was diagnosed with a brain tumor on October 29, 2001. This
rare cancerous tumor called EPENDYMOMA (type of cancer that only affects the Central Nervous System (brain or spine)) was
successfully removed 3 days later and was followed by radiation. Jessica survived and she was having the time of her life
when not 2 years later, on September 25, 2003, she was diagnosed with a recurrence, but this time we were dealing with a spinal
tumor. The doctors proceeded with radiation that shrunk the tumor about 25% and another successful surgery followed - the
whole tumor was removed and we didn’t have any complications. This was followed by chemotherapy and what we thought
was the worst 4 months of Jessica’s life. Jessica survived and we really thought that we had this cancer kicked when
another spot was detected on March 9th, 2006. We were very fortunate that we caught this early, but the location of this one
in the brain (near the main artery of the brain) was very critical. Radiation was really our only option to give us any hope.
This treatment had seemed to work except for the fact that her brain started to swell 5 months later. Steroids followed to
reduce the brain swelling along with some setbacks it caused but this strong willed girl just wasn’t about to give up.
Jessica survived and then for the fourth time in six years they found another spot on her spine on August 22, 2007. This tumor
again was irremovable (in a location housing all the leg, kidney and bowel functions) and the doctors’ only choice was
to proceed with yet another set of radiation. Jessica survived. In September 2008, just shortly after her 14th birthday, during
routine scans, they found another nodule in her brain. We opted for radiation--the radiostatic surgery for her treatment.
This went over a 5 day period in October. After that was over, she started the oral chemo. Her hair has started falling but
body tolerating it well and she was still going to school. When Christmas break was almost over, so was Jessica's blood counts.
As of January 2009, she has been off of chemo for about 2 weeks but her blood counts are still declining. Her faith and determination
to get her story out there is strong. Her faith in God has made her stronger
and even more eager to help find a cure for this awful disease. Jessica's fight continued for another 5 years. She was
in and out of the hospital, endured more chemo, radiation and surgeries than any human, let alone child, should ever endure.
Through it all, Jessica never lost her faith and never stopped fighting. She was able to go to her prom, graduate
highschool and see her 18th birthday all because of ongoing research that organizations like CancerFree KIDS provide funding
for. Jessica lost her battle in January of 2015 but her light continues to shine. Her hope was to help prevent anyone
else from having to encounter the lifestyle of a cancer patient at such a young age. Hi! My name is Hannah and on May 25, 2012 I will celebrate
my 5th year of being CANCER FREE! I was told I had a rare form of Acute Lymphocytic Leukemia (ALL) when I was 2 years old.
Due to research, the doctors knew right away that my only treatment option was to have a bone marrow transplant. I received
my new bone marrow cells on May 25, 2007! Treatment, transplant, and recovery was a very difficult journey, but this year,
I will be celebrating 10 years CancerFREE! My family and I are thankful to God for providing us with wonderful medical
care, and for the research and technology that enabled me to receive my transplant and help save my life. We are also thankful
for all the people who support pediatric cancer research. Without your donations, life saving research, which has helped me
and many other children, wouldn't happen. So I hope you will join me in walking and/or donating to this year's Butterfly Walk
and help more children be cancer free.
Hello Everyone! My name is Roman Michael
Fariello. I was diagnosed with Stage 4 Neuroblastoma, N-myc non-amplified, on April 25th 2007 at the age of 18 months. I had surgery
2 days after diagnosis for a tumor on my right adrenal gland. Luckily it was small enough to be completely removed.
The cancer had already spread above my right eye and also in my bone marrow. My eye was very swollen and looked like I
got punched. I had a central line put in and had six rounds of chemotherapy, a stem cell harvest, numerous scans and tests,
and blood and platelet transfusions. Far too many to count. I then had a seventh round of high dose chemo to knock
out my bone marrow for a transplant I had on Oct. 17th, 2007. Then, in Jan. 2008, I went thru 12 rounds of radiation
to the original tumor site in my tummy. I started oral chemo (accutane) in Feb.2008 I had alot of trouble with the
accutane because of my triglycerides being high. I only completed 5 rounds at half the dose. I also suffered eye pain and
pressure and severe headaches from it. It has been a very long journey for my family and I since I was diagnosed. I am seen
once a year now at the Survivor Clinic for a complete head to toe physical, bloodwork and a heart echocardiogram to check
for chemo damage. Everyday is a never-ending fear for my life as we hope and pray Neuroblastoma stays far away from me forever.
Thanks so much for your love and support for me and my family!
On January 14, 2009, we took Leah to the doctor due to paleness of the skin, multiple bruises and minor bloody noses. We honestly
thought we were going there only to be sent home. Leah was never sick. In fact, she hadn't been to the doctor's office in
over 3 years. From there we were sent to Cincinnati Children's Hospital where we waited for what seemed like an eternity to
be told that Leah had Acute Myelogenous Leukemia. After 6 months of living at the hospital, 4 intense rounds of chemotherapy,
2 trips to the ICU, 2 central lines, 3 picc lines, multiple blood and platelet transfusions, one lung biopsy, and one appendectomy,
we are proud to say that Leah has won her battle against cancer. Although Leah is not completely back to "normal",
she grows stronger by the day. She's back in school and has just been okayed to play softball. One of the biggest lessons
we learned from this experience is the importance of giving. We now realize that without the generous donations of others,
our daughter probably would not have survived this disease. We are so grateful for fundraisers such as The Butterfly Walk,
organizations such as CancerFree KIDS, and generous people who donate for giving our daughter, and many other children, a
second chance at life.
When Evan was just 15 months old he was diagnosed with bilateral
retinoblastoma, cancer in both eyes. He underwent surgery, six months of chemotherapy, and many hospital stays.
Evan went under anesthesia every couple months to ensure the tumors were gone. Because he was always so calm during these
scary times, at age four, he was one of the youngest patients to undergo MRIs and these eye procedures without anesthesia.
He is still continually checked and was deemed cancer-free on his fifth birthday! Much like Thomas, his favorite train,
Evan always believed that you could be scared and brave at the same time. He is the bravest kid we know!
In the fall of 2003 Madelyn was an active 2 year old girl that could not wait until her 3rd birthday was here. After 2 weeks
of being treated for an upper respiratory infection and not seeing any change, we were sent to Middletown Hospital for a routine
x-ray to rule out pneumonia. From the look on the nurses face I could tell that something was seriously wrong with our little
girl. We went immediately down to Cincinnati Children's Hospital to get a CAT scan to figure out what was wrong.
Monday, October 6, 2003 we were admitted to Children's Hospital and sent to the ICU floor. On Wednesday, October 8th Maddie
had her first of many surgeries and we were told the news that no parent should hear. Madelyn's chest was full of some sort
of cancer that had erupted and at that point could be anywhere in her little body. She had 1/3 of her right lung removed and
had a central line placed due to the apparent chemotherapy treatments which lay ahead. Maddie was finally diagnosed with Pleuropulmonary
Blastoma (PPB) which is a rare childhood cancer that attaches to the lung. With me having had a childhood cancer called Wilms
Tumor when I was 4 years old, we were fortunate enough to have the same wonderful doctor that I continued to see take Maddie's
case. From the start we knew that the road ahead was going to be difficult but once we got into the treatments no one could
prepare us for the ups and downs which you go through. The "PLAN" was to have 12 rounds of chemotherapy and 12 days
of radiation. It amazed me how nothing seemed to go by the "PLAN." In November, after Maddie's second round of chemo
we were admitted to the hospital for a high fever and extremely low blood counts. During this stay Maddie had a chemotherapy
induced seizure which only happens to a small percentage of children. Due to the intensity of the seizure we were taken to
the ICU to be monitored. A feeding tube was also placed in Maddie's nose that went directly into her stomach due to the weight
she continued to lose. In December after a routine ECHO/EKG test she was diagnosed with Coarctation of the Aorta. On December
8th Maddie had a heart procedure which helped open up her artery because of its limited size. After her December chemo treatment
we were admitted at 3am on Christmas morning due to another high fever. In January things continued not to follow the "PLAN."
After her January treatments and once again being admitted for a fever and low counts, we realized if we did not lower the
dosage of the chemotherapy treatments Maddie was not going to survive. We were hospitalized for 3 1/2 weeks and our doctor
decided to lower her dosage to 50% due to the damage it was doing to her little body. In March she had 12 rounds of radiation
that required her to be sedated for 12 straight days to receive her treatments. At the end of March, during a routine scan
we were told something was growing in the same location of the lung where the original cancer was thought to have developed.
After a failed attempt to get a sample from a biopsy the decision was made to go in and remove the growth through surgery.
One week after Madelyn's baby sister Emma was born she had surgery. Due to our prayers being answered, it was not a recurrence
of the cancer, just irritated scar tissue from the radiation treatments. Madelyn finished her last round of treatment in September
of 2004. We all learned early on that Madelyn was not going to follow anyone else's "PLAN" but her own. Courage,determination,
and a lot of prayers is what got Maddie through that year. In June of 2007 Madelyn had been blessed with having been off treatment
for over 2 1/2 years and was feeling great. She was enjoying her summer break and looking forward to starting her 1st grade
year of school. With scans now being scheduled every 4 months since we had hit what we thought was the magic number of 2 years
off of treatment, we received the news that we thought we would never have to hear. On June 19th, 2 days after our annual
"Relay for Life" event during her routine scans we were told that something was growing where the original tumor
had started. She once again had surgery which confirmed that the original cancer had reoccurred. Maddie's "PLAN"
is to have 4 rounds of chemotherapy, 23 days of radiation, and a stem cell transplant that will keep her in the hospital for
at least 4-6 weeks straight. We learned from the first treatment that Maddie only follows her own PLAN." What we do know
is that Maddie is a amazing little girl and with her strength and a lot of prayers she will make it through this and be CANCER
On June 30th, 2009, when Ava was just 3 years old, our lives changed forever. After a night of crying over a tummy ache, followed
by vomiting, Ava saw her pediatrician who sent her for an x-ray to see if she had severe constipation, to rule out appendicitis
or something more serious. We went straight to Cincinnati Children's. After the x-ray was read, calcifications were found
near her right adrenal gland. (A great catch based on comments from her oncologist and surgeons.) Ava then had an ultrasound
that confirmed Ava had a mass, thought to be Neuroblastoma...a malignant tumor. Cancer. Wow..a presumed virus, with symptoms
only lasting two days, brought us to discover this heartbreak. We can only think that this was a sign from God to catch this
before it had more time to spread. On July 10th, 2009 Ava had a very complicated abdominal surgery to remove the tumor that
was growing from her sympathetic chain (part of the sympathetic nervous system). About 99% of the tumor was removed, while the remaining sliver attached to her aorta had to be left behind. Two lymph nodes
that were near the original tumor were removed and one was confirmed to be diseased. Ava was staged 2B. Neuroblastoma is typically
discovered after it has progressed significantly. Confirming our belief in a Godly intervention. In October 2009, Ava suffered
from severe abdominal pain and vomiting for three weeks while under observation and going through many tests. On November
5th, 2009 she underwent another abdominal surgery and several adhesions were found that had formed after her first surgery,
one being the culprit of a bowel perforation, which eventually grew around the bowel twisting it, causing a bowel obstruction.
During this surgery she had a small section of her bowel removed. Ava has now recovered from this surgery and has started
to gain some of the weight back that she has lost. We are very fortunate that at this point Ava has not had to undergo any
chemotherapy or radiation therapy. She is under very close observation with labs monthly and scans every 2-3 months. We are
looking forward to the walk this year and thank everyone for their support of the event. We appreciate the continued prayers
for Ava and all of the kids who continue to battle this horrific disease and for the doctors and nurses who care for them.