A Life of Strength, Love, and Courage

Weighing in at 9 pounds, 10 ounces, Chrisean was big from the start. He had so many rolls that his family called him the “marshmallow baby.” As a child, he enjoyed dressing up in a suit and tie, especially to go to church. At the age of 13, he stood an imposing six feet tall and weighed 250 pounds. When he stopped eating, his mother, Machelle, knew something was wrong.

“He was complaining about body aches and pain everywhere,” Machelle said. “We went to the doctor several times and came home with different pain medicines. But no one could tell us what was wrong.”

One day, Chrisean called Machelle from school because his chest hurt badly. She took him to the children’s hospital, where the doctor pulled down his eyelid and noticed his skin was nearly white. When he ordered a blood test, the staff found a new problem – Chrisean was terrified of needles. He was so big that the nurses had to get two men and a security officer to hold him down to draw blood. The blood test revealed that Chrisean had acute lymphoblastic leukemia.

“When the doctor told us, I was confident that he would be alright,” Machelle said. “He had a game plan and said it was very treatable.”

During his hospital stays, Chrisean questioned everything. He researched every chemo he was to be given and asked questions of doctors, nurses, and anyone who provided care. A little more than a year into his three-year treatment, Chrisean developed a cough that turned into a fever. His breathing got progressively worse until his medical team decided he needed to be on a respirator. Things descended rapidly from that point. With his immune system depleted because of chemotherapy, Chrisean’s body was unable to fight off a virus.

“Chrisean called everyone in the family and asked them to come to the hospital,” Machelle said. “I think he understood that he was at the end. He got to say goodbye and tell us all he loved us before he passed.”

Chrisean passed on August 25, 2020.

“We met CURE in the hospital with meals, and CURE supported our family at Christmas,” Machelle shared. “But I didn’t know CURE would still be here for us after Chrisean died.”

Machelle has attended CURE’s Hope and Healing bereavement retreats and regularly enjoys gatherings with other bereaved mothers, as well as CURE’s Quiet Heroes luncheon.

“I just want to thank you. Hope and Healing has been a saving grace for me,” she said. “A lot of times, I didn’t want to exist in this world without my baby, and most people don’t know what it is like to lose a piece of your heart. It was a breath of fresh air being around other people who know this pain. I still need help and support, but I can help moms who are new to grief.”

It’s in the Genes

Ally has been through a lot in her eleven years. When she was two years old, she fell off a stool while playing with her brother. A large bruise appeared on her stomach almost immediately, and her parents took her to their local hospital. After blood work, they learned that Ally had B-cell acute lymphoblastic leukemia. “We were told that within days, she would have had uncontrollable bleeding without treatment,” said Ally’s mother, Amber. “Her body was working so hard to fight the cancer that her heart would have given out. It is hard to be glad for your child to fall, but that fall saved her life.”

Ally received her first dose of chemotherapy within 16 hours of diagnosis. Over the two years of treatment that followed, Ally struggled with almost every possible side effect. She suffered three life-threatening infections, temporarily lost the ability to walk, and struggled to rebuild her immune system after every round of chemo.

“We were given a bleak prospect of survival during her second fight with an infection,” shared Amber. “We prayed for a miracle and finally got one when her body started to respond to antibiotics.”

Her treatment finally ended on August 24, 2018, but her battle was far from over because her immune system did not recover as expected. Even years later, her doctors were concerned because she was still living with depleted immune function. In 2022, they decided to do genetic sequencing on Ally and her family to see if a disorder was causing her immune system deficiency. What the sequencing uncovered has lifelong implications for Ally and her family.

“My nephew was diagnosed with leukemia after Ally,” said Amber. “So I expected that if there was an inherited genetic trait linked to her cancer or her body’s response to treatment, it would be on my side. We found out that the opposite was true.”

Ally shares a genetic condition called Lynch syndrome with her father, Justin. This condition increases the risk of many kinds of cancer, including colon cancer, endometrial cancer, and other types. Knowing this will allow Justin and Ally to be monitored for early signs of cancer, giving treatment a greater chance of success. Ally sees a doctor with expertise in genetic conditions every year, and her parents are updated on new testing and protocols. Ally is doing great today. She is in her first year of middle school and enjoys competing in pageants. Her parents are grateful for her health and credit CURE’s investment in precision medicine as a big part of it.

“I have a friend who just went through breast cancer treatment, and her genetic testing cost $4,000 out of pocket,” Amber said. “The cost of repeated gene sequencing for us would have been staggering. But it didn’t cost us a dime because of CURE’s funding. We wouldn’t have known about the syndrome without it. With this knowledge, we can be prepared and should be able to detect any cancer in Ally or Justin early.”

Courage on Two Wheels

Finnley has been around motorcycles her whole life. Her uncle is a retired professional motocross racer, and her grandparents own a track called Georgia Practice Facility in Cairo, Georgia. Every year, they hold a competition called The Cla$h, which brings in riders from all over the country. When it was time for this year’s race, Finnley had an idea to raise money for children fighting cancer… because she knows how hard that is since she’s battling leukemia herself.

In early 2023, Finnley had ankle pain that went on for months, compounded with compression fractures. After many doctor appointments and tests, her mother, Stacy, knew something wasn’t right.

“We were told it might be growing pains,” recalled Stacy. “But I’m an emergency room nurse. So, as her pain increased, I just knew in my heart that it wasn’t right. I pushed for a blood test, and the doctor confirmed my suspicions immediately.”

Finnley was diagnosed with leukemia in April 2023. At just eight years old, she has proven how resilient she is time and time again. She has smiled and kept in good spirits even at the most difficult stages of treatment. Finnley is very social, so the most challenging thing for her has been missing so much school and being away from her friends.

“She didn’t suffer from too many side effects until she reached the long-term maintenance phase, which is supposed to be easier,” said Stacy. “She had more hospital stays and a lung infection that was difficult to treat. Going on our wish trip changed everything for her.”

When planning for The Cla$h began, the family looked to add a charity element to the weekend. Stacy and Finnley knew who they wanted to raise money for immediately.

“CURE was with us from day one,” shared Stacy. “When we were first diagnosed, we didn’t go home for eight days. We were in survival mode – only eating and leaving the room sporadically. One day, a lady from CURE peeked into the door with a bag of food. She said, ‘I know it’s hard right now, but you need to eat. So I’m going to leave this here for you.’ That was everything to me because I knew right then that I wasn’t alone. And CURE has been there the entire time.”

Finnley set up a table at the event to sell coffee and donuts and share CURE’s mission with all the riders and spectators. She set her own alarm and got up at 5:30 a.m. so she could get the donuts and be at the track when people began to show up. She stayed until 11:00 p.m. both nights and raised $1500 for CURE.

“We were so proud of her,” said Stacy. “She had a purpose, and it meant a lot for her to be able to give back.”

Finnley is doing great these days. She loves school and spending time with friends. Her treatment should end in June, but her mom believes that Finnley’s unselfish heart will always want to help children who have to fight cancer like she has.

A Community of Hope

Your Impact on Families During the Holidays

Last month, as decorations and lights adorned neighborhoods and holiday music filled the air, many families faced the sobering reality of childhood cancer. Between ongoing treatments, unexpected hospital stays, and mounting medical bills, creating holiday magic felt out of reach for many parents already stretched thin. But thanks to the extraordinary generosity of our donors, these families didn’t have to face the season alone. Your outpouring of support changed what could have been an overwhelmingly difficult month into one filled with moments of joy, hope, and community. We want to share with you the profound difference you made in the lives of families during the holiday season.

CURE’s Holiday Party

More than 500 family members were treated to an afternoon of fun at CURE’s Holiday Parties, where they enjoyed lots of special treats, dancing, face painting, crafts, and more. We heard so many parents share how nice it was to step away from treatment for an afternoon and just be a family.

“We had such a wonderful time at the CURE Holiday Party this year. Ever since our son was diagnosed with AML several years ago, our community has been so important to us, and CURE is at the heart of that community. Over the summer, when we were staying far away for months while our son received a bone marrow transplant, we encouraged ourselves by imagining what it would be like at the holidays when we were once again back at home and reunited with our friends and family. CURE made that vision a reality. At the CURE Holiday Party, watching the kids play and reconnecting with other families we’ve grown close to, we were so grateful for all we have to celebrate and this amazing community.”

-The Michael Family

Holiday Angels

Through our Holiday Angel program, donors fulfilled the wish lists of 150 families. These gifts were not only for the children fighting cancer but also for their siblings and parents. As you can see from the comments below, the families that received these gifts were more than grateful, they were deeply impacted by your generosity.

“Thank you for your kindness toward our family this Christmas! We were amazed at all the toys for our kids that you purchased along with the generous gift card. It is so touching to know there are people so kind and so thoughtful, and we have been blessed by that. Thank you for the abundance of gifts and support! We are so grateful!”

-The Croscutt Family

“The gifts we received have changed my whole mood and outlook towards my situation. The art supplies you sent have not gone to waste. They have awakened a creative spark in me like never before! I hope you all had the best holidays ever because you have made this mine. Thank you.”

The Haralson Family

Critical Financial Assistance

Your gifts also allowed us to provide more than $46,000 in financial assistance in December to families experiencing financial hardship as a result of their child’s cancer treatment. This crucial support played a vital role in helping these families maintain housing, utilities, and transportation.

When notified that their December mortgage payment had been paid, one mother said:

“Thank You! Wow! We are so very grateful! This will relieve a lot of pressure on our finances. Thank you all so much for all you do for us and all the families in the fight.”

Your generosity did more than just brighten the holidays – it strengthened an entire community of families facing childhood cancer. From the laughter at our holiday parties to crucial financial support and thoughtfully chosen gifts, each act of giving will help carry these families forward into the new year. Thank you for being part of our CURE community and for showing these brave families that they never have to face this challenge alone.

Jewelry with a Purpose

Stilla Vitae, Jewelry with a purpose.

How D. Geller & Son Turned Inspiration into Purpose

The Geller family has been in the jewelry business for 15 generations. In the late 1800’s, David Geller was a personal jeweler to Czar Nicholas II. After immigrating from Russia, the family swiftly integrated into the Atlanta community through active involvement in local charitable efforts. The support of nonprofit organizations is still an integral part of the business today.

Jonathan Geller is the current President and CEO of D. Geller & Son. After serving as an infantry officer in the U.S. Army, Jonathan returned to the family business in 2022 when his father was ready to retire. He learned about CURE Childhood Cancer soon after returning when the store donated a gift card to the silent auction for CURE’s Believe Ball. When a CURE board member came to the store to pick it up, Jonathan was moved as she shared CURE’s mission. She invited him to an upcoming event called Quiet Heroes. Quiet Heroes honors the mothers of children with cancer, and more than 250 were in the room during the event. The afternoon profoundly impacted Jonathan and his wife.

“We have three healthy children,” he said. “I looked around the room and knew we needed to do more to help those who aren’t as fortunate in that regard. Using the company’s skill at designing and marketing jewelry was the perfect way to support CURE, so I started planning a new line on the way home.”

While he has been around jewelry his whole life, he hasn’t done a significant amount of jewelry design. The drop of blood in CURE’s logo became his inspiration. The blood drop signifies life – every drop makes a difference. As he worked through the theme of the line, he landed on the name Stilla Vitae, which means “Drop of Life” in Latin.

“I was deeply moved by the remarkable courage and resilience of children battling cancer,” Jonathan shared. “The Stilla Vitae line recognizes the strength within us all and serves as a meaningful gift for anyone navigating life’s challenges – a beautiful daily reminder that we possess the inner strength to overcome any obstacle.”

The original Stilla Vitae pieces sold well, and the custom design group added new pieces. The website has a page dedicated to the line, and it is constantly in the marketing plan. Visit dgeller.com/pages/stilla-vitae to browse the very special pieces of jewelry with a purpose.

Building Hope: A Home That Helps

Alex and his daughter, Sydney

Alex is a home builder and a proud native of Effingham County, Georgia. As a husband and father of eight children, Alex has a vested interest in the future provided to our youth. He has always had a philanthropic spirit and recently started a new venture to support children with cancer.

In March, Alex and his daughter attended a local event by CURE Childhood Cancer called Catie’s Gathering. The event honors the life of a local child, Catie Wilkins, who passed away after a battle with a brain tumor. Attendees decorate their tables with a theme and dress up to match. While it offers a festive atmosphere, it raises money to fuel childhood cancer research and support local families fighting the disease. After the event, Alex approached Catie’s mother, Jenny, with a desire to help.

“As a parent, seeing the children at Catie’s Gathering really hit home,” Alex said. “I realize that people fighting cancer are going through the hardest time, and CURE provides a beacon of hope during that time. I want to be a part of that.”

Build for CURE was born out of that desire to make a difference. His goal was for his company, Lawrence Alexander Homes, to build a quality home and donate every dollar generated from its sale to CURE. With this in mind, he began securing suppliers and tradesmen to work with him by donating materials and labor.

On June 19, 2024, the company hosted a groundbreaking ceremony for the initial Build for CURE home in the Pinebrook subdivision of Rincon. More than seventy people attended, including many of the suppliers who will be involved in the home’s construction, most of whom have generously donated their services and supplies. Two special guests, leukemia fighter Myles and his brother Bryce, took turns with the shovels at the ceremony.

As construction began, many people visited houses in the subdivision, including a woman from Statesboro named Barbara Lynch. Barbara was planning a move to Rincon to be close to her daughter and grandchildren. She liked the subdivision and was prepared to offer a home under construction until she heard about the Build for CURE home.

“When I heard the story and purpose of the house, I felt like it was perfect for me,” Shared Barbara. “I lost my husband to cancer, and I’m absolutely tickled that money from the sale will go towards cancer research.”

Barbara will be moving into her special new home later this month, knowing she isn’t just buying a home. She’s a part of something much bigger – an idea brought to life through hard work, dedication, and a belief in building hope.

“None of this would have been possible without our trade partners,” Alex added. “They jumped on board right away and made it happen.”

Through Build for CURE, Lawrence Alexander Homes has transformed a personal moment of inspiration at Catie’s Gathering into a tangible way to support childhood cancer research. This proves that one person’s compassion can create meaningful change. As the first home nears completion, it is a testament to the power of community, generosity, and the enduring spirit of those who choose to make a difference.

Ring the Bell, Daniel

A few weeks ago, Daniel Morgan rang the bell to signify the end of his cancer treatment. He doesn’t like to be the center of attention and actually didn’t want to have the bell ringing. But his family knew this was a milestone to be remembered, so they convinced him to do it.

It’s been a long journey for Daniel – two years, four months, and two days to be exact. It started with a swollen lymph node on his neck and a fever. Because it was a weekend, his mother, Felicia, took him to an urgent care clinic, where the nurse thought it was a dental issue. He got steroids that suppressed his symptoms for a few weeks, but they came roaring back when the medicine wore off.

He finally went to the pediatrician, where bloodwork reviewed a high white blood cell count. Further testing on June 1, 2022, revealed that Daniel had leukemia. It was the first day of summer after his sophomore year of what turned out to be a very odd high school experience.

Daniel Morgan at graduation“Daniel’s freshman year and part of his sophomore year were from home because of COVID,” Felicia said. “He could only do partial days during his junior year because of treatment and finally got to go back to school full time for his senior year. He was very ready to get back to his friends and routine.”

“He didn’t really share what he was going through,” Felicia said. “He didn’t want to be treated differently or have people feel sorry for him. When he lost his hair, it was winter, so he was able to wear his beanie to school.”

Treatment was very hard on Daniel. He was often sick and had an allergic reaction to one of the chemotherapies. Because of this reaction, he was forced to have a very painful injection in his leg. He would have to psych himself up in the morning, knowing that he was going to get the shot that hurt badly.

Despite the interruptions and difficulty of treatment, Daniel graduated from John’s Creek High School with honors last spring. He is studying computer science at Kennesaw State University. He loves creating websites and programming.

“Our family feels compelled to give back to others fighting childhood cancer now that we’re done,” said Felicia. “Daniel has done surveys about the stress of treatment and described how he handled it. We’ve been proud of his responses. His thoughtful answers showed a great deal of maturity.”

CURE has been a support for the Morgans since day one. Felicia raves about the binder notebook that is in the Tote Bag we provided at diagnosis.

“I still have my binder and continue to keep records in it,” she said. “The Open Arms meals meant a lot. They allowed us to put all of our focus on getting Daniel well. It’s been a long road, but it is great to see Daniel happy, healthy, and loving life.”

Daniel Morgan standing near the bell

Milestones and Monsters: Navigating Life with Leukemia

When Levi was diagnosed with leukemia in 2022, his mother, Hannah, began to share the roller coaster ride that is a childhood cancer diagnosis. Her writing style is compelling because of its authenticity and truthfulness, and she finds it helpful to release some of the emotions through words.

Levi had a very rough first year of treatment. He was sick most of the time, suffered from neuropathy, and one of his medications gave him seizures. His treatment will last for three and a half years and should be complete in August 2025.

Here is a brief look into his journey through his mother’s heart. Hannah is mindful to celebrate milestones, including his kindergarten graduation:

I’m so proud of him.
All parents are proud of their kids.
But with him, there’s a deep, immeasurable amount of beaming pride.
He’s fought and is still fighting for his life.
He’s closed huge gaps in his “academics.”
He’s covered and conquered pre-k and kindergarten skills in a year.
He’s pushed himself even though not feeling good.
He’s never, ever once quit.
He’s so strong. And he’s one of the best people I know. Being his mama is my greatest pride.

A few weeks later she shared a glimpse into her own feelings that many parents can relate to:

I’m tired. Deep in my bones, deliriously tired from this journey. I’m tired of watching my child suffer with indescribable pain and nothing that helps him. I’m so tired of fighting to get him help. I’m tired of this being our life. I’m so tired of very, very few people understanding. I don’t know how I can do this for another year. But as he continues to fight, we will stand by him each step of the way.

Then she shared a glimpse of what is in Levi’s heart and mind on a visit to celebrate the end of treatment for a friend:

We walked into the hospital and Levi began having what I can only explain as a panic attack. He clung to me and wouldn’t let go. He was terrified to go back to the 5th floor where he was diagnosed. He kept saying, “Mama, don’t you remember how bad it is there? It’s my worst nightmare. Mama I already lived my worst nightmare.”

After leaving the hospital, he asked, “Mama, what if my cancer comes back?”

A day that was so exciting was also so heavy. I don’t have the answers to his question. I can’t tell him the cancer won’t come back. I can’t tell him everyone will be okay. It’s heartbreaking, and it’s not fair.

In dealing with all of the emotions inherent in this world of childhood cancer, Hannah found herself angry, which isn’t typical for her. CURE helped to connect her to a therapist who listened to her concerns and helped her understand that it is okay to feel angry, as long as she doesn’t park herself there.

“CURE’s Counseling Program has been a huge blessing for me,” Hannah said. “Because Levi became stoic and didn’t want to tell us when he was in pain, he began seeing a counselor also and learned that he doesn’t have to wait until the pain is at a high level before telling us.”

Levi is in the homestretch of his treatment now. He’s smiling more and loves to go swimming whenever he can. His strength and perseverance make an impression on anyone lucky enough to meet him or read his mother’s writing.

 

2024 Research Awards

We are excited to share a significant step forward in CURE’s 49-year effort to find cures for childhood cancers as we proudly announce a $5.6 million investment in innovative research studies – the largest amount we’ve ever committed in a single year.

This record-breaking investment represents an important advancement in our ongoing work. It reflects the growing support of our community, the persistent dedication of researchers, and our unwavering commitment to finding better treatments for children with cancer.

These studies are led by top scientists at leading pediatric cancer research institutions nationwide and focus on the most critical needs. Here’s what makes this investment so impactful:

  • Advancing Precision Medicine: We’re awarding $2 million to the Aflac Precision Medicine Program, reinforcing our leadership in this crucial field. This funding expands access to genetic sequencing for young patients. It accelerates research into targeted therapies, bringing us closer to truly personalized treatments and giving hope to many children with aggressive or recurring cancers.
  • Funding Diverse, Innovative Research: The remaining $3.6 million funds 11 promising projects carefully selected from over 90 applications. These studies address some of the most challenging childhood cancers with limited or outdated treatments, employing innovative approaches that could significantly improve treatment outcomes.
  • Bridging Research and Treatment: Time is precious in the fight against childhood cancer. That’s why we’ve prioritized studies with strong potential for rapid clinical translation, potentially bringing new treatments to children faster than ever before.
  • Harnessing Immune Power: Within every child’s body lies an army of potential cancer-fighting cells. Several projects focus on enhancing cutting-edge immunotherapy approaches, unlocking the full potential of the body’s own defense mechanisms, and offering new possibilities for children battling resistant forms of cancer.
  • Looking Beyond Remission: The fear of relapse looms heavy for patients and families. By investigating mechanisms of recurrence, these studies aim to improve long-term outcomes and quality of life for survivors – and offer children a chance at a cancer-free future.

As we make these awards, we’re filled with a sense of purpose and hope. While the road ahead may be challenging, each step forward brings us closer to our goal of conquering childhood cancer.

Thank you for being an essential part of this journey.

CURE’s 2024 RESEARCH AWARDS

Early Investigator Awards

Rula Green Gladden, MD, Fred Hutchinson Cancer Center
Redefining residual disease detection in pediatric AML

Elizabeth Young, MD, University of California, San Francisco
Defining determinants of a cGAS-STIGN-mediated anti-tumor inflammatory response in osteosarcoma

Translation to CURE Awards

Eric Sweet-Cordero, MD, University of California, San Francisco
Defining replication stress and DNA damage as a therapeutic vulnerability in osteosarcoma

Pavithra Viswanath, PhD, University of California, San Francisco
Targeting and imaging serine metabolism in the tumor microenvironment in pediatric brain tumors

Michael Andreeff, MD, PhD,  University of Texas, M.D. Anderson Cancer Center,
c-MYC protein degradation in therapy-resistant pediatric leukemias

Eugenie Kleinerman, MD, University of Texas, M.D, Anderson Cancer Center
Metabolic reprogramming of the Ewing Sarcoma tumor microenvironment using pramlintide to augment NK cell immunotherapy

Kristopher Bosse, MD, Children’s Hospital of Philadelphia
Development of a GPC2 CAR T cell amplifying RNA vaccine

Alex Huang, MD, PhD, Case Western Reserve University
Effective TGF-beta signaling blockade synergizes cryoablation-induced STING activation in treating refractory and metastatic sarcoma

Jason Yustein, MD, Emory University
Dissecting and targeting PAK4-mediated signaling in Ewing Sarcoma development and metastasis

David Robbins, PhD, Georgetown University
Defining the druggable GLI Interactome in medulloblastoma

Soheil Meshinchi, MD, PhD, Fred Hutchinson Cancer Center
Rapid Transition of B7-H3 Targeted Therapies to High-Risk Childhood AML

Precision Medicine Program, Children’s Healthcare of Atlanta
A program leveraging genomic sequencing for pediatric patients with high-risk tumors, with the goal of identifying alterations that can impact therapies and improve outcomes.

Cap, Gown, and Cancer

CURE Crew offers Savannah area high school juniors and seniors the opportunity to support CURE through fundraising, volunteering, advocacy, and awareness of pediatric cancer. Every year, it is difficult to say goodbye to the graduates. This year is especially hard because three of our graduates are childhood cancer survivors themselves.

In 2008, 2-year-old Cora Garola was diagnosed with acute lymphoblastic leukemia. After several weeks of persistent ear infections and low-grade fevers, Cora’s pediatrician did bloodwork that revealed an elevated white blood cell count that ultimately led to the leukemia diagnosis. Although Cora’s diagnosis carries the highest percentage for success, her treatment called for three years of chemotherapy, high-dose steroids, quarterly spinal chemotherapy injections, and multiple bone marrow biopsies.

Cora lived out her preschool years on chemotherapy. Thankfully, she successfully completed treatment and has gone on to experience minimal late effects of the harsh treatments she endured as a young child. She barely remembers her cancer experience now.

Cora has been on CURE Crew for two years, but since her mother is the Vice President of CURE, she’s been volunteering for a long time. Her favorite experience has been at the Holiday Party.

“I love helping with other events, but the Holiday Party is special to me because we get to interact so closely with the children and families,” Cora shared. “Last year, my friends and I dressed up, and the kids loved it.”

Cora is graduating from Savannah Country Day School. She is going to Georgia Southern and majoring in psychology. She doesn’t have a career in mind quite yet but knows she has plenty of time to figure it out.

Mason Riegner was diagnosed with a soft tissue cancer called rhabdomyosarcoma at the tender age of four. The tumor was on the right side of his face. During his treatment, he entered foster care. While he didn’t understand enough to be anxious about the treatment, going through it alone made it a challenging experience. Unfortunately, Mason relapsed when he was eight years old and had to have his jawbone removed. He has been cancer-free since.

He has also gained a large family. When he was ten years old, his pediatrician adopted him. He has four brothers, three sisters, and one half-sister. Since his mother is a doctor, she has been pivotal in helping with his post-cancer treatment and the reconstruction of his face.

“With no jawbone, my face is off-centered,” said Mason. “I’ve had three surgeries to try to fix it over the years, including adding an artificial jawbone taken from my fibula.”

Despite all of his setbacks, Mason radiates positivity. He has enjoyed working with the CURE Crew and is very diligent about helping wherever needed. He will graduate in May from Calvary Day School and plans to attend Georgia Southern University, where he will study to become either a child life specialist or a physical therapist specializing in children’s therapy.

At the end of 2017, Lily Stucky had been sick and had some visible knots on her neck. When a rare dusting of snow fell in Savannah, Lily didn’t have the energy to go outside to play. Her mother thought she was faking to stay home from school. But a fever took her to the local emergency room, where doctors discovered Lily had leukemia.

She started chemotherapy right away and was plagued by “rare” side effects.  She lost weight on steroids, suffered from neuropathy in her feet and hands, and spent a month in intensive care because of brain swelling. Fortunately, Lily went into remission very early and stayed there, although the harsh side effects of treatment continued.

Lily has served on CURE Crew for two years and volunteers an hour a week at the CURE office through one of her classes. She will graduate from St. Vincent Academy and attend Georgia Southern University in the fall. When she was in treatment, healthcare workers had a significant impact on her. So, she plans on becoming a physician’s assistant.

“I like volunteering for CURE and knowing that I’m helping an organization that helped me,” Lily said.

There are so many graduates who have been through more than twelve years of school. Let’s congratulate these three and many others who have been forced to beat cancer before grabbing their diploma.