Cure Childhood Cancer

CURE Blog


December 29th, 2011

Sarah Barr’s Caps for CURE

In August 2009, at age 12, Sarah Barr was diagnosed with Ewing’s Sarcoma, a type of bone cancer, in her right femur. From August 2009 to April 2010, Sarah had 14 rounds of inpatient chemotherapy. Extra hospital time came when she was so sick from treatment or when she ran unexpected fevers. The tumor was surgically removed in December 2009, and a portion of Sarah’s femur was removed as a result. To replace the missing bone, a segment of a femur from a cadaver was put in.

When Sarah was on treatment, an elementary school in Locust Grove held a “caps” day for the Barr family, raising more than $350. A school employee, the sister of a close friend of the Barrs, shared Sarah’s story with others at the school which led to the idea to hold the “caps” fundraiser.

Sarah and her family were moved by the generosity. “This touched us for many reasons,” says Heather Barr, Sarah’s mom. “Obviously because it is so kind and such a show of support for Sarah, but even more than that – it was a school full of people that didn’t even know Sarah, yet they wanted to get involved. With Sarah being home schooled and this school not even being where our neighborhood would be zoned to go, I was floored by this act!”

Heather was really inspired by the school’s fundraising efforts. She explains, “I thought if they can raise $350 for a family when there is a specific need, just think what could be raised by schools for childhood cancer in general if we shared the need and they caught the excitement about this. When you are only asking for $1 per child, almost everyone can join the fight, at no great sacrifice, and the combined total can still be amazing.”

Heather and Sarah contacted area schools and encouraged them to hold “Caps for CURE” days. Students would be allowed to wear their favorite cap for the day, with a donation of $1.00 to CURE Childhood Cancer. Not only do students love the novelty of wearing a cap to school, but the event is also symbolic of the hats, caps, and bandannas cancer patients wear during their treatment. Many of the schools Heather and Sarah approached jumped on board. In September alone, fourteen schools raised more than $3300 for CURE.

“To me,” says Heather, “these schools that have joined together are living out the Helen Keller quote, ‘Alone we can do so little. Together we can do so much.’”

“We are so inspired by Caps for CURE,” says CURE Executive Director Kristin Connor. “The money raised through this initiative will go to fund life-saving research into cancers affecting children, giving hope to kids like Sarah,” continued Connor. “Most importantly, the ‘kids helping kids’ aspect of this initiative is so special. This is really about school children helping their peers — their friends. We think this plants the seeds for selflessness and thoughtfulness, and we are so proud of Sarah for fostering these traits.”


December 27th, 2011

CURE’s Holiday Luncheon

As part of CURE Childhood Cancer‘s Open Arms program, restaurants, families, and individuals donate meals to be served by CURE volunteers to children and their families who are in the hospital. These meals are something families look forward to throughout their weeks, or months, living in the hospital.

During the holidays most of us spend time with all of our families, sitting around the dinner table enjoying homecooked meals and treats. However, for the families of children battling cancer, their time is spent in the hospital. To ensure that these children, their families, and the hospital staff are not left out from the holiday traditions, Greg and Ginger Kindred – parents of one of CURE’s Kids, Trenton Kindred – organize and host a Holiday Feast at Children’s Healthcare of Atlanta.

This year marked the 5th Annual Christmas Eve Luncheon hosted by the Kindreds. The Kindreds began planning for the luncheon back in October, organizing 50+ cooks, 60+ filled stockings, 60+ pet pals, and gathering more than $3,000 in gift cards for the families. The Kindreds couldn’t do it all alone, with their family volunteering to serve the lunch on Christmas Eve and members of their community donating dishes of food. Ginger said she loves seeing all of her neighbors and friends show up at her doorstep Christmas Eve morning, still dressed in their robes and slippers, to drop off cooked turkeys, hams and casseroles.

This year’s luncheon was just as successful as ever! Greg filmed a few short videos from the celebration, which we are sharing with you below. We hope each of you had a wonderful holiday season with your friends and family.







December 21st, 2011

Incredible Southern Poundcakes – Incredible Southern People!

If there is one singular thing that could be said about Kathy Shepherd it is that she does NOT take “no” for an answer.

Tim and Kathy Shepherd, owners of Incredible Southern Poundcakes in Stockbridge, Georgia, became acquainted with CURE Childhood Cancer more than six years ago. Since then, they have become tireless supporters. It is said there is nothing they will not do for CURE.

They came to CURE through the “A Tribute to Our Quiet Heroes” luncheon. Kathy, working her fledgling poundcake business out of her home, was approached while peddling her cakes by a Quiet Heroes volunteer who thought the little baby cakes would make perfect table gifts for attendees of the luncheon. When asked about baking five hundred cakes, Kathy didn’t hesitate. Opening her first store just days in advance of the second annual luncheon, Kathy and husband Tim became fast and furious supporters of CURE.

Kathy’s cakes are now famous at the luncheon – as large a part to the attendees as the swag bags and fabulous speakers. In addition to now providing 600 cakes per luncheon and securing countless auction items, Kathy a true Southern Belle, also donates 200 cakes to CURE to give as gifts to nurses for nurses’ appreciation week each year.

But Kathy and Tim do much more than bake. They put their hearts into helping. A few years ago, they got word of a family with a child with cancer facing staggering struggles. Without hesitation, they “adopted” this family, getting them into safe housing and truly meeting every need – from stocking their pantries to providing a washer and dryer to buying toys for the kids. They continued to support this family through the years to come, helping as needs arose. When the child relapsed, Kathy and Tim were there, and when he passed away, they fed guests at his celebration service and continue to provide emotional support.

In September, having endeared themselves to Tom and Chris Glavine, Kathy and Tim held a huge fundraiser at their bakery. Tom signed autographs for donations and Kathy donated the proceeds of sales of her amazing baked goods. True to style, they convinced many of the surrounding businesses to participate, donating proceeds, setting up booths to sell ice cream and other goods. At the end of the day, Kathy and Tim raised more than $2,500 for CURE and provided an opportunity for several Henry County children battling cancer to meet Future Hall of Famer Tom Glavine.

There is nothing they won’t do when asked and are constantly looking for ways to do more. Tim and Kathy personify volunteerism in its purest form and we love them.


December 20th, 2011

CresaPartners Raises Funds for CURE

CresaPartners LLC, North America’s largest tenant representation company, raised more than $76,000 for five charities including CURE Childhood Cancer. The funds were raised by CresaPartners employees during the second annual Silent Auction held at its recent Spring Meeting in San Diego, CA.

CURE was nominated by Atlanta’s Paula Fowler, Senior Vice President of Operations. “I nominated CURE because it is close to my heart,” explains Paula. In 2000, dear friends of the Fowlers lost a son to neuroblastoma. That experience really impacted the Fowlers. In addition, Paula thought childhood cancer would have “universal” appeal to all CresaPartners’ offices across the U.S. “Everyone knows someone whose lives have been impacted by cancer,” says Paula.

CresaPartners has 55 offices across North America. A committee of management members from several of the offices selected the five charities which received the proceeds from the fundraiser held at the firm’s national meeting.

“CURE is proud to have been selected as a recipient,” says Kristin Connor, Executive Director. “We are very grateful for the generous support of this highly respected and regarded company.”


December 19th, 2011

Primary Care Providers After Treatment

During cancer treatment families become used to seeing their oncologist for most of their healthcare needs. Usually the oncologist will send updates to their patients’ pediatrician or primary care provider (PCP) about their progress in treatment. After finishing treatment, however, it is important for families to reconnect with a PCP. Some families will see a pediatrician for primary care, others may see a family medicine doctor. It is important as you choose a PCP that you find someone you trust.

Why is having a PCP important?

A PCP will serve as your medical home, the head of your healthcare team. Seeing your PCP regularly will help him stay up to date about the needs of your child and be able to provide the best care possible. It is also important that your PCP has a complete list of any medical problems your child has or has had in the past. This will help him when coordinating your child’s healthcare needs.

Transitioning back to your PCP after cancer treatment

Many times transitioning care back to a PCP can be scary for families. After all, you’re used to calling your oncology team whenever your child has a problem. After treatment is finished many of your child’s health needs should be met by your PCP. Your oncologist will tell you when it’s time to transition back to your PCP for most of your child’s healthcare.

Communicating with your PCP: Cancer SurvivorLink can help!

After treatment you want to make sure your PCP is up to date on your child’s cancer history and any health problems that could develop after treatment (called late effects). When patients are two years off treatment they can be seen in the Aflac Cancer Survivor Clinic. During this visit survivors will receive a Survivor Healthcare Plan (SHP) which consists of three parts:

  • Treatment summary including information about cancer diagnosis and all cancer treatments.
  • Individualized risk profile for late effects of cancer treatment based on the cancer therapies received.
  • Individualized surveillance plan to screen for late effects.

Your PCP should have a copy of your child’s SHP as should any of the  other healthcare  providers you see, for example a cardiologist or orthopedist. You can electronically store your SHP in a protected website, Cancer SurvivorLink, created by doctors and researchers at Emory University and Children’s Healthcare of Atlanta. You can also store other important health documents, for example a letter from your oncologist or a report from cardiology. Using Cancer SurvivorLink, you can share a copy of your SHP and any other health documents you have stored with your PCP, and any other doctors your see. You can also use Cancer SurvivorLink to quickly pull up your stored health documents if needed in an emergency or when you see a new healthcare provider. If you haven’t been to a survivor clinic yet, you can use Cancer SurvivorLink to find a clinic in your area.

To learn more about childhood cancer survivorship visit www.cancersurvivorlink.org or www.choa.org/cancersurvivorship.


December 15th, 2011

CURE Funds New Clinical Trial for Pediatric Leukemia Patients

As a new fiscal year began in July 2011, CURE Childhood Cancer announced more than $1.5 million in research grants, including a $100,000 award to Dr. Kuang-Yueh Chiang and Dr. John Horan at the Aflac Cancer Center at Children’s Healthcare of Atlanta. The doctors are working on an exciting proposal for a Phase I clinical trial using a drug called Plerixafor, formerly known as AMD3100. Plerixafor improves the efficacy of the depletion of leukemia cells from bone marrow prior to transplantation—potentially a huge breakthrough for childhood leukemia patients who previously have been resistant to chemotherapy or radiation treatment.

Originally developed for the treatment of HIV to block viral entry into white blood cells, Plerixafor proved expensive to produce and sat unused for a long time until doctors discovered its use in stem cell transplants for patients with leukemia and lymphoma. The drug helps extract the stem cells living in bone marrow and transfers them into the circulatory system, making it easier to destroy cancerous cells with chemotherapy. “Leukemia cells often hide in bone marrow, making them much more difficult to destroy with traditional chemotherapy methods,” explained Dr. Horan, who attended New Jersey Medical School and did his residency and fellowship at the University of Rochester Medical Center. During his fellowship, he began his study of adult and pediatric hematology stem cell transplantation.

“We believe this might be one of the reasons leukemia recurs, so we’re hoping if we use this drug with childhood leukemia patients, we’ll be able to extract the cancerous cells from the bone marrow so they’ll go into circulation and be easier to destroy.”

Plerixafor could prove a huge breakthrough in treating patients who are chemo-resistant and otherwise would have very little chance of survival.

Because of CURE’s grant, Drs. Chiang and Horan will be putting together a road map for running a clinical trial, which they anticipate will be approved by the FDA by the end of the year. “Developing a clinical trial protocol and applying for FDA approval is extremely expensive,” said Dr. Chiang, who has a medical degree from Taiwan and studied pediatric hematology and oncology at the University of Minnesota before coming to the Aflac Cancer Center in 2001. “The chances of us bringing this drug to trial without CURE’s funding would be very, very slim.”

Once approved, the trial will take place in two phases. Those patients selected for the trial will be patients who have previously shown resistance to chemotherapy and radiation.

During the first phase, six leukemia patients will receive a prescribed dosage of the drug for three days while simultaneously receiving chemotherapy or radiation. If there are no complications, the trial will move to its second phase, during which those same six patients will receive five days of the Plerixafor regimen.

If successful, the trial could lead the way for a larger trial and eventually FDA approval for Plerixafor to be used in childhood leukemia patients, providing a critical lifeline for that small percentage of children who haven’t responded well to other cancer treatments. “We cannot thank CURE enough for their support of our research,” said Dr. Horan. “This drug could be a gamechanger in treating childhood leukemia patients and significantly increase survival rates. We simply couldn’t afford to do this important work without CURE’s support and funding.”


December 14th, 2011

Spotlight on Andrew Appert

We were a happy family of four with many reasons to be grateful. My husband and I often commented on how lucky and blessed we were to have two beautiful, healthy boys and very few worries. Life was good. But all that suddenly changed. Our descent into the nightmarish world of pediatric cancer officially began on August 21, 2001 when our then five-year-old son, Andrew, was diagnosed with acute lymphoblastic leukemia. From the moment our lives were drastically and irrevocably altered with the terrifying reality that our child had a life-threatening illness.

Several weeks before the diagnosis I knew something was wrong. Our once “healthy as a horse” little boy who never even seemed to catch a cold just wasn’t himself; he ran fevers, had severe stomach aches, was lethargic, and frequently complained of bone pain. I was in the pediatrician’s office often, desperate for answers but fearful of what we were going to find. I was repeatedly told Andrew had a virus which would run its course or growing pains which would subside. Then one night I was awakened by Andrew screaming from leg pain. My husband and I rushed him to the ER where blood tests showed severe anemia. We were sent home and told to follow up with the pediatrician in the morning. When we got home, Andrew took a turn for the worse. he spiked a fever, was nauseous, suffered from all-over body pain, and was unable to walk. As soon as the pediatrician’s office opened, I was there, delicately cradling Andrew in my arms because the slightest movement caused him pain. Again, we were sent home with instructions to return the next day.

During the night, Andrew continued to deteriorate. I remember lying in bed next to him and every time I moved to shift my body on the mattress, he would cry out in pain. The next morning back at the pediatrician’s office, a group of doctors gathered to discuss Andrew’s symptoms. I finally got up the nerve to insist that they tell me what they suspected was wrong with my son. I’m not sure why, but I specifically asked if he could have cancer. I supposed I asked about cancer because that was the worst case scenario I could think of, never really imagining I would be right. however, the doctors believed Andrew either had a bone infection or juvenile arthritis and wanted to order x-rays. At that point, Andrew was in severe pain, still unable to stand or walk, let alone lift his head. In addition, his heart rate and blood pressure were causing some concern. While holding his limp little body on my lap, I tried to gently adjust the blanket I had wrapped around him without causing him pain when I noticed little bruises on his arm and back. Instantly, I knew we needed to head to Scottish Rite Hospital.

Upon entering Scottish Rite’s ER, we were immediately escorted to an exam room. Andrew was so weak he didn’t even make a sound the entire time they poked, prodded, and stuck him with needles. Then a new doctor entered the room and began asking questions about Andrew’s health history. I immediately noticed the doctor’s name tag – not his name, but the title under his name: “Pediatric Oncologist.” All I could do was stare at those two words on his name tag like a neon sign was flashing in my face. Eventually the doctor, Dr. Bergsagel, broke the horrifying and shocking news that Andrew had leukemia – and in that instant our world came crashing in on us.

“Dr. B became Andrew’s oncologist and a God-send along with “Nurse Mary” and all the amazing and compassionate people at the Aflac Cancer Center at Scottish Rite. Andrew underwent three years and two months of chemotherapy and never once complained or felt sorry for himself. (I wish I could say the same about myself.) Just a couple of weeks after his diagnosis, Andrew began kindergarten; Dr. B urged us to send him to school to help maintain some sense of normalcy in his life. Once, a few months into his treatment, he had a seizure, a rare side effect from the high dose of intrathecal chemo. When I got to his school, Andrew was on the floor, still having a seizure, with a group of teachers and staff gathered around him in prayer, waiting for the paramedics to arrive. Overcome with feelings of helplessness and fear at the sight of my sick little boy, all I could do was fall to my knees and pray… and, of course, sob uncontrollably. During the ambulance ride, Andrew was not lucid. When he finally woke up in the hospital and we told him what had happened, he was disappointed that he didn’t remember the ambulance ride. After all, what little boy isn’t fascinated by ambulances?

As his parents, we struggled emotionally through three terrifying  years of clinic visits for chemo, spinal taps, and various medical procedures in addition to the difficulty of managing side effects. Sometimes the overwhelming worry and fear, combined with the never-ending roller-coaster of mixed emotions, seemed debilitating, but Andrew always handled everything with astonishing courage and grace and an uncanny steadfast faith that inspired all of us. He actually looked forward to going to his chemo appointments because he loved the people at the clinic and understood everyone was working to make him well. He pushed through the treatments and side effects with a positive attitude and focused on just being a happy kid who loved soccer, video games, Legos, and books. Less than a year into his treatment, Andrew came up with the idea to help brighten the day of other clinic patients by collecting donated toys from our community. To this day, Andrew maintains his charity, called “Friends of Andrew”, to help bring new toys to the kids at the Aflac Cancer Center.

Andrew is now a healthy 15-year-old excited about starting high school and learning to drive. I often look at him and think about what he has been through and what he has taught our family. While I wouldn’t wish our experience on my worst enemy, I am grateful for the many blessings and positive experiences that came out of it. We have adjusted our lives to make family our number one priority; we have grown tremendously in our faith and continue our life-long faith journey with a sense of gratitude to God; we have gained an appreciation for the power of prayer; and we have experienced first-hand the positive impact of a loving and supportive community where even the smallest act of kindness can make a difference. We will never forget the support of the doctors, nurses, and staff at Scottish Rite, The Lighthouse Retreat, Camp Sunshine, Make-A-Wish Foundation, CURE Childhood Cancer, and the many people (friends, family, and strangers alike) who helped us over the years. But we realize that the fight is not over. We continue to pray for every child and family impacted by cancer, and we hope to bring awareness to pediatric cancer causes until a cure is found and this devastating disease is a thing of the past.


December 13th, 2011

The 5th Annual Sam Robb Memorial Holiday Classic

CURE Childhood Cancer is excited to announce The 5th Annual Sam Robb Memorial Holiday Classic, a basketball tournament in memory of one of CURE’s Kids, Sam Robb.

December 27, 2011 – December 29, 2011
Locations: Blessed Trinity Catholic High School, Queen of Angles, St. Jude, and Holy Redeemer Catholic Schools
Click here to register.

Sam Robb lost his battle with cancer in 2007, at the age of 20. Sam was always focused on sports, primarily basketball and football. At 6′5″ and 230 lbs. in the 10th grade, Sam was a “Can’t Miss” college prospect starting in the first varsity football game at Blessed Trinity High School in Roswell, GA. As a sophomore, he led the team to the first varsity victory in school history.

In 2002, X-rays of a nagging stress fracture in Sam’s left knee led to the diagnosis of osteosarcoma, bone cancer. After chemotherapy and limb salvage surgery, essentially a knee replacement, Sam knew his promising football career was over. Instead of dwelling on what he couldn’t do, he focused on a new goal: to become a baseball pitcher. Although it did not come easy, particularly with a prosthetic knee, he managed to play for a highly competitive East Cobb team. He even pitched and won the final game of a world series in Tampa. Sam went on to play baseball at Young Harris College and was enrolled at Clemson University for the Fall of 2007.

However, in the Spring of 2007, Sam began feeling discomfort in his lungs. X-rays revealed that a grapefruit sized mass had taken over his lungs and chest cavity. Sam never made it out of surgery.

In honor of Sam’s courageous spirit, The Sam Robb Fund was founded. The Fund supports the Sam Robb Fellow at the Aflac Cancer Center and Blood Disorders Services of Children’s Healthcare of Atlanta and Emory University School of Medicine. In addition, The Sam Robb Fund helps defray the costs of prosthetic devices for children with a cancer diagnosis who cannot afford to purchase and/or maintain them.

To honor Sam and raise money for CURE, The Sam Robb Fund hosts numerous sporting events throughout the year. The Sam Robb Memorial Holiday Classic is one of those events. The basketball tournament is open to teams of boys or girls, grades 4-8. The invitation is specifically extended to CMLA Teams, Catholic, and Christian organizations in the Atlanta Metro area.

This event is always very exciting and is something we look forward to each holiday season.

If your basketball team would like to participate, there is still time to register! Registration deadline is this Thursday, December 15th. Click here to register online.

Thank you for your support of CURE and Sam Robb.


December 12th, 2011

CURE’s Annual Campaign

Children with cancer are racing against time. They need all of us.

Imagine this. Today a doctor stares you in the eye and tells you, “Your child has cancer.” The most terrifying race you can imagine – to save a child’s life – is upon you.

It’s an unfair race. A young, defenseless child up against an insidious, growing army of merciless cancer cells. Doctors, hospitals, and scientists constantly at the mercy of treatment and research breakthroughs, which are only made possible by the hard reality of financial funding.

CURE Childhood Cancer exists to give children better odds in their race against time. The children are betting that you’ll help. And now is the moment.

It’s your opportunity of a lifetime. Our Annual Campaign gives you the chance to be all the human being you can be. To genuinely make a difference in the ambushed lives of children affected by cancer.

Through your unrestricted gift to our Annual Campaign, you help us uphold our undying mission – discovering cures for childhood cancer through targeted research. And providing support so essential for devastated patients and their families.

Our goal is to raise $525,000 by June 30, 2012. You can pledge now and pay over time. All pledges should be paid by June 30, 2012. We accept pledges, cash, credit cards, checks, recurring gifts, and stock. Gifts of any amount matter!

A gift of $60 will feed 10 hospitalized children or give their caregivers a deserved dinner.

A gift of $500 will help one family with out-of-pocket medical costs – copays and prescriptions for their child with cancer.

A gift of $800 will send four families to CURE’s Bereavement Weekend, with professionals to help them in their journey with their loss.

A gift of $25,000 will fully fund one promising research project selected by our Scientific Advisory Council.

Whatever you give, CURE’s children and families thank you for believing with us. That we we will cure childhood cancer in our lifetime.


December 9th, 2011

CURE’s Named Funds

Named Funds offer a way for friends, family members, neighbors, colleagues and others to commemorate special individuals, such as a child who has bravely battled cancer or an individual who has demonstrated a particular dedication to the field of pediatric cancer. In CURE Childhood Cancer‘s 2010-2011 Fiscal Year, we launched one new Named Fund, the Carlos S. Alvarado, M.D. Pediatric Cancer Research Fund, and continued five others.

The Carlos S. Alvarado, M.D. Pediatric Cancer Research Fund

The 2010-2011 CURE Challenge resulted in a new research fund named in honor of Dr. Carlos Alvarado, a dedicated pediatric oncologist who retired in 2009 after nearly three decades of service at Children’s Healthcare of Atlanta. Dr. Alvarado skillfully and compassionately cared for children with cancer while also contributing mightily to the search for a Cure through his research. The Carlos S. Alvarado Fund will continue his work into the future by funding lifesaving research at the Aflac Cancer Center at Children’s Healthcare of Atlanta.

The Trenton W. Kindred Research Fund

Proceeds from this fund were used to support research into cures and better treatments for children with neuroblastoma. The Kindreds and their supporters are committed to advancing better treatment for neuroblastoma. The fund contributed more than $29,000 to neuroblastoma research spearheaded by Dr. Kelly Goldsmith at the Aflac Cancer Center at Children’s Healthcare of Atlanta.

Press On to CURE Childhood Cancer

Press On provides desperately needed funding for basic, translational and clinical research relating to pediatric cancers, specifically neuroblastoma and acute myeloid leukemia (AML ). Press On provides grants to scientists conducting research aimed at developing novel, targeted therapies for neuroblastoma and AML . Through generous individual gifts and events such as concerts by 12 Bands and Play for Patrick, Press On raised an astounding $354,000 for lifesaving research.

The Sam Robb Fund

Proceeds from the Sam Robb Fund were used to pay for the second year of fellowship training for Dr. Nicole Schlesinger, the second Sam Robb Fellow. The Sam Robb Fund and its dedicated supporters worked tirelessly, hosting golf tournaments, fun runs, basketball tournaments and other events to raise more than $64,000.

The Catie Wilkins Memorial Fund

The primary purpose of the Catie Wilkins Memorial Fund is to fund clinical research which evaluates and treats the side effects, both acute and late effects, of treatment for childhood cancers, and other research that CURE is supporting for more effective and less toxic treatments for childhood cancers. The Catie Wilkins Fund benefited from proceeds from “Elves from Catie,” which, in addition to raising money for research, provided holiday joy to hundreds of hospitalized children. The Fund also raised money through the “Sisters on a Journey” dinner, held in remembrance of Catie’s loving spirit and determination.

The Hayley Hunter Research Fund

The Hayley Hunter Research Fund provided funding for basic and clinical research relating to neuroblastoma, a pediatric cancer for the central nervous system. With funds raised primarily through the Second Annual Hayley Hunter Golf Tournament, the Fund raised $25,000 for neuroblastoma research at the Aflac Cancer Center at Children’s Healthcare of Atlanta.

It is with the help of these named funds, and your support, that each of CURE’s research initiatives are funded. We thank you all!


  • SOMETIMES YOU GOTTA FIGHT

    Musicians VANN and Ryan Burton's song "Sometimes You Gotta Fight" is available now! Click here to watch the video and click here to download. All proceeds are donated to CURE.

  • YOUTH COUNCIL

    Rising High School Sophomores are invited to apply for CURE's Youth Council. Applications are due June 30, 2012.  Click here for more information.