Cure Childhood Cancer

CURE Blog


July 31st, 2009

Spotlight: Eli Polk

Unknown-3He is a Fireman, a Soldier, a Pilot, a Dinosaur, a Knight, a Pirate, a Big Game Hunter and would only answer to “Oinky” for quite some time. He is a 3 1⁄2 foot, forty pound five year old perpetual motion machine. He is without a doubt the toughest person I know, and he’s our son Eli. He has Acute Lymphocytic Leukemia, but it certainly does not have him.

On January 9, 2007 Eli woke with small petechiae on his face, and a few hours later we were sitting in the Emergency Room at Scottish Rite. There we met Dr. Lew and Dr. Watt; further testing was ordered, and soon Dr. Watt was explaining our son had leukemia. A little while later, Dr. Lew explained where we were and what would need to happen over the next few days. Over the next several days, time simultaneously stood still and moved at the speed of light. Peggy and Eli settled into a room at the Aflac Cancer Center and his long journey began. We tried our best to explain the unexplainable to our daughters, Emily and Hailey. Meanwhile, Eli underwent more testing, exams and evaluations in the first three days than most of us will experience in a lifetime. Peggy never left his side; she has been his Mom, Nurse and Bodyguard. Almost overnight she became an expert on the medications, treatments and protocols our son would face.

During his month long stay on the Aflac Cancer Center ward we met many families. Some were like us, new to the community and still trying to figure out how to get through the day. Others were the veterans who appeared to have a firm grip on the situation. Volunteers from CURE Childhood Cancer were some of the first “non- medical” people to meet with us. I came in one day and there was a big blue sack, a white Teddy Bear, a sweat shirt and a small library of reading material. CURE volunteers had spent time with Peggy explaining the different programs and support CURE could provide. They answered our questions, but the greatest thing was, at a time when it seemed everyone had something to say, they simply listened. They brought food for the staff and families and let us know we were not alone and that there was a light at the end of the tunnel.

Throughout all of this, our daughters, Emily and Hailey, have been remarkable. Peggy and I have tried to ensure they lead a normal life and not become “the other kids.” There have been times when their plans were changed or canceled in order to meet the needs of their brother. They have been there at every turn in the road, rarely complained and have shown a level of maturity far beyond their years. It’s my hope that one day they will understand the positive impact they have had on Eli. There is no way I can express in words how proud I am of them. They have been the quiet heroes of our family. From his initial hospital stay through our now monthly clinic visits, I’ve watched in amazement as the physicians, nurses and staff work tirelessly to care for Eli and the other children entrusted to their care. Eli’s leukemia is now in remission, and he is well into the maintenance phase of his treatment.

Since leaving the hospital in January 2007, he has only spent one other night in the hospital. Most days a stranger would have no idea he has leukemia. Almost anywhere you look in and around the Aflac Cancer Center, you will see CURE at work. It can be seen in the form of the training our physicians and nurses receive, in support of various support programs, or sometimes, best of all, you see their sticker on the snacks in the infusion room. Faith, family, friends, events and occurrences all have and will continue to “shape” Eli’s character throughout life. At five years of age, he is already very strong in his sense of faith and family.

As of this writing we are 802 days into Eli’s journey and have about 365 days until the first steps of his journey are over. In the beginning, I would not have even considered looking so far into the future. However, now it is a foreseeable reality, there is LIGHT and LIFE at the end of the tunnel. I look forward to seeing the man our son will become.

Thanks,

The proud father of Emily, Hailey and Eli

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July 30th, 2009

Board of Directors Spotlight: Alan Thomson

alanthompsonCURE Childhood Cancer is honored to have a diverse and well-connected Board of Directors and we would like our community to get to know them.  In this spotlight series we will highlight a board member and share why they are dedicated to CURE.

Alan Thomson is currently our Treasurer. Alan is married and has 3 children, and he has been on the board for 2.5 years. Alan is also a Wealth Advisor at The Daniel Financial Group, LLC.

Below Alan shares a personal experience that lead him to get involved with CURE Childhood Cancer.

“Dayna and I lost our daughter, Hayley, to AML – an aggressive form of leukemia – in December 2004, two months shy of her 2nd birthday. Hayley’s struggle was a nine month battle that included over 200 days in the hospital, several intense chemotherapy regimens, total body irradiation, and a bone marrow transplant. Through it all, Hayley learned to walk, talk, and be a fun loving little girl with whom many a nurse and doctor fell in love. She inspired Dayna and me to continue to fight the good fight so that one day non-toxic treatments will CURE Childhood Cancer.”


July 29th, 2009

Childhood Cancer Survivors Face New Threats as Adults

This article provides great background on why CURE Childhood Cancer is investing in a crucial new initiative to ensure pediatric cancer survivors in Georgia and beyond receive recommended survivor care.

By DAWN FALLIK

Jamie Deibel was 12 years old when she was diagnosed with leukemia. During her two years of treatment, she took seven pills a day, except on Thursdays. That was her 21-pill night, each swallowed while watching the television show “Survivor.”

Five years after being cured of cancer, the junior nursing major at Eastern Kentucky University, is undergoing a new round of tests—this time for heart disease. The worry is that the chemotherapy that fended off her leukemia may have taken a hidden toll on her heart.

Ms. Deibel is one of an growing number of pediatric-cancer survivors who won their battles thanks to treatment advances. Now, some of these survivors are finding that the same treatments that saved their lives could come back to haunt them in new ways in their 20s and 30s. Because the onset of heart problems can come a decade or more after the last round of chemotherapy, patients and doctors alike are often caught by surprise.

“Many [cancer] survivors don’t have a clue” about the long-term effects of cancer treatments, says Paul Nathan, an oncologist at the Hospital for Sick Children in Toronto. “Many of them were treated as young children and have no recollection of what drugs they had or what they should be watching for.”

The biggest risk is believed to come from a class of drugs called anthracyclines, one of oncology’s workhorse chemotherapies that is effective against leukemia and a wide range of other cancers. The drugs’ toxic effect on the heart is well-established in adults. That they have similar effects in children is now becoming increasingly understood as these patients reach adulthood. Radiation treatments also come with risk of long-term side effects, especially when given in combination with anthracyclines.

According to the National Cancer Institute, some 10,400 U.S. children under the age of 15 are diagnosed with cancer each year. About 80% of them survive beyond five years and are considered cured. Twenty years ago, by contrast, about 58% of children survived cancer.

Researchers estimate that 10% of patients treated with anthracyclines eventually develop cardiomyopathy, a progressive weakening of the heart muscle that can lead to congestive heart failure. Most of these patients exhibit treatable symptoms, including exhaustion and shortness of breath. But in rare cases, the first manifestation of cardiomyopathy is an arrhythmia causing sudden death.

Among female survivors, cardiac dysfunction can first become apparent during pregnancy. Medical experts say women who received radiation or anthracyclines should be evaluated by a cardiologist before or during early pregnancy.

Doctors say anyone treated with an anthracycline as a child should get regular diagnostic tests for heart problems every one to five years, depending on the dose they received. But many patients don’t recall what drugs they were on, never mind how much they got or for how long.

Even though she received treatment only five years ago, Ms. Deibel says she couldn’t list her medications off the top of her head. During a recent checkup, however, her oncologist recommended that she go for an echocardiogram—an ultrasound of the heart—because one of the drugs she had taken was the anthracycline doxorubicin.

“When the [cancer] diagnosis happens, they’re talking to you about so many things, it’s a blur,” says her mother, Taylor Deibel. “I don’t remember a conversation where we sat down and said, ‘This is what could happen down the road.’ You’re just trying to get through the day.”

Joseph Carver, a cardiologist who is also chief of staff at the Abramson Cancer Center of the University of Pennsylvania in Philadelphia, says he’s seen a significant increase in the past five years in the number of pediatric cancer survivors who are turning up with heart disease in early adulthood. He attributes that to improved childhood cancer survival rates. Often, signs of trouble are subtle.

“Maybe they used to be able to jog four miles. But now they can only do two and they chalk it up to getting older or they’re just tired,” Dr. Carver says.

Ashley King, 28, was 8 when she was diagnosed with Wilms’ tumor, a kidney cancer. It spread to her spine and lungs. But after three years of radiation and chemotherapy treatments that included the anthracyline idarubicin, she was “clean.”

Then, three years after finishing treatment, Ms. King was diagnosed with cardiomyopathy. Initially doctors thought her condition was serious enough that she would need a heart transplant. But now she’s on two heart medications and says she feels fine, other than tiring more easily than she used to. “I go see Dr. Carver every year and I get an EKG and an echocardiogram,” says Ms. King, who owns a clothing store in Lewes, Del.

Patients with cardiomyopathy are treated with beta blockers and ACE-inhibitors. But there are only general guidelines for treating childhood cancer survivors who have developed heart problems. Dr. Carver says more research is needed to determine everything from an optimal schedule of preventive checkups to whether giving medicine before symptoms arise would prevent or delay harm to the heart.

Another issue is that when patients become adults they begin seeing new doctors who aren’t familiar with the problems they face. “With a 90-percent cure rate, now you’re having a lot of survivors hitting primary-care offices and family practices that may not have a great awareness of the issues that come with long-term pediatric-cancer survivors,” Dr. Carver says.

CureSearch National Childhood Cancer Foundation (CureSearch.org), a private fund-raising and patient support group, recommends that anyone treated with anthracyclines get a heart checkup every year and an initial electrocardiogram two years after completion of therapy. Among other known risks, pediatric-cancer survivors have a greater-than-average chance of developing skin and other cancers.

When Ms. Deibel, the Kentucky college student, passed the five-year mark as a cancer survivor in January, she celebrated with friends at school. “We had a piñata shaped like a star,” she says. “We put the word ‘cancer’ in the middle and I smacked it.”

Now, as she prepares to undergo the echocardiogram and various post-cancer tests, she and her family aim to strike a balance between vigilance and victory over her illness.

“You have to approach it as it comes along,” her mother says. “Because you can freak yourself out, and I don’t want to live with that constant fear.”

Write to Dawn Fallik at Dawn.Fallik@wsj.com

Source : Wall Street Journal, 7-28-09


July 28th, 2009

Why Should You Give Money to CURE?

CURE is funding critical research at the AFLAC Cancer Center and Blood Disorders Services of Children’s Healthcare of Atlanta and Emory University School of Medicine. We support local research that positively affects research on a global scale. We also offer innovative programs that address the critical and urgent needs of pediatric cancer patients and their families. In addition, we provide continuing education and training opportunities to nurses and other caregivers who care for children with cancer.

Still not sure about donating to CURE? Visit our website and learn about the families’ lives that CURE has touched.


July 27th, 2009

Here to Serve Restaurants Team Up with CURE

Join us this Thursday, July 30th as Lola Bellini Bar and Restaurant and parent-company  Here to Serve Restaurants team up with CURE Childhood Cancer for a fun event!

Lola has become a great new hot-spot in Buckhead and will provide the perfect atmosphere for a great cause. Tickets are only $25 and include all-you-can eat and drink. A mix of great food stations will be set up and drink specials include Lola’s house bellini, Peroni, and well vodka. A percentage of all of the proceeds made Thursday, July 30, will be donated to CURE on behalf of Here to Serve.

Lola is located in the heart of Buckhead in the Terminus Building on the corner of Piedmont Road and Peachtree Street. Reservations are required to ensure you get a table, call Lola at 404.892.9292 to make your reservation today!

For more information on CURE visit us at www.curechildhoodcancer.com


July 24th, 2009

Optimism is…

Unknown-2By Blake Sorrell

What is optimism? For the past year and a half, my sister has been dealing with something that no human being should have to go through. This thing is leukemia or what we call cancer of the blood. Leukemia is when you don’t have enough red blood cells because there are too many white blood cells. Optimism helps us get through this tragedy. Don’t be gloomy and disappointed, look at the positive. Just look at where we are today. She is alive.

My sister’s amazing story has also inspired so many people to be optimistic. My family has spoken at many events that have helped to raise money to fi nd more cures for childhood cancer. Many optimistic people have helped to support families that have to go through chemotherapy. Real optimism is facing a disease with faith and hope. Watching her have her port (which is like an IV in her chest) accessed, taking shots in her legs, and swallowing pills every single day has made me optimistic.

She was only three years old when this long journey began. She has continued to have chemo every month since March 2007. She will finish all of the treatments in June 2009. Without optimism, this entire process would have been unbearable. She is one of the bravest people you will ever meet. She is in kindergarten. She was so optimistic that last year I remember her literally crying during home school saying, “Mommy I’m going to go to school next year,” and now she is. Isn’t optimism great? She even tried out for the talent show and made it.

I am so proud to be related to this little angel. Some kids basically call their brother or sister names just to offend them. It is a different story in my house. She is a great person and did not deserve to have cancer. But it made us (as in my family) better people and more optimistic.Unknown-1

 

 Find out how you can help families like the Sorrells at www.curechildhoodcancer.org


July 23rd, 2009

CURE is Worthy of Your Investment: Here’s Why

Like no other organization, CURE Childhood Cancer is focused on supporting childhood cancer experts, locally and nationally, who are working daily to discover the ultimate solution. While most organizations are focused on treatment, facilities, education or a program related to what today’s knowledge and medicine can offer, CURE is focused on expanding the platform of research to uncover new treatments. Specifically, these are the treatments that speed healing, are less invasive and less damaging—and can actually eradicate the cancer itself.

We are 100% focused on children’s cancer efforts and committed to educating the public about childhood cancer. We fund the work of some of the most talented scientists in the field of pediatric oncology, and we’re involved in the training of future doctors and researchers who will continue on with our passion to find a cure for childhood cancer.

For more information on what we do visit us at www.curechildhoodcancer.org


July 22nd, 2009

Reflections on CURE’s Annual Bereavement Weekend

UnknownHaving joined CURE’s staff in September 2008, this year’s Annual Bereavement Weekend was my first, and what a powerful, moving experience it was for me. When I told friends and family I was working the weekend of January 24th and 25th, they asked what I was doing. I explained I was helping to put on a weekend for parents who had

lost children to cancer. Understandably, everyone had similar responses: “Wow that’s awful,” and, “That must be so depressing.” Not having been to a Bereavement Weekend before, I didn’t know what to expect. What I found was that there was more love and hope in the room with the parents in attendance than I had ever witnessed. These parents were truly grateful to have a setting in which to share memories of their precious children with other people who understood their grief. Sherry and Dirk Tucker, a remarkable couple from Orlando, Florida who lost their son Zach in 2007, shared their story and experiences with the group on Saturday. They were able to truly connect with the other parents and shared ways in which they have been able to move through their grief journey. The Tuckers inspired me with their belief that their purpose in life now is to help others work through their grief and find meaning in life after the loss of a child.

On Sunday, the second day of the workshop, Brenda Tuminello spoke candidly about her life in the decade after losing her only daughter, Stacey. She shared her story of going down a treacherous path and ultimately finding spirituality as her redemption. These stories and many others were shared among the attendees in small group discussions and throughout the weekend.

One of the most special aspects of the weekend was the candlelight ceremony, which included a slideshow of the children we remembered and honored. As a child’s name was called, his or her parent(s) lit a candle that had been specially decorated in remembrance of the child, while pictures of the child were projected on a large screen for all to see. The ceremony was moving and awe- inspiring, much like the rest of the weekend. The strength and resilience of the parents I met made a deep and lasting impression on me. They truly are heroes. The fact that they persevere and find meaning, hope and joy in life is inspirational. Many parents find joy and purpose in helping other families who have lost children to cancer. Others work passionately on the efforts to find a cure for childhood cancer so that other parents will not have to endure what they do. They all seem to find comfort and solace in their immediate family and friends and in honoring and remembering their child. It was a privilege to be able to share in that remembrance with them.

In the evaluations of the weekend, many expressed their heartfelt gratitude for being able to share memories of their child in such an accepting and compassionate environment. Parents also shared that Bereavement Weekend is a time that they look forward to each year. We hope to provide the support for these courageous parents for many years to come and to broaden our support in any way we can.

 By Meri Long, Interim Director, Patient & Family Services 

To receive information about Bereavement Weekend 2010, please contact Meri Long at meri@curechildhoodcancer.org or 770.986.0035 ext. 22

 For more info on CURE events visit our website


July 21st, 2009

Caitlin Dopheide: Sacrifing her 13th Birthday

Unknown-1Caitlin Dopheide decided when she was 10 years old that she wanted to do a Charity Birthday party for her 13th party. CURE has a named fund in honor of Sam Robb and his family. Last year Sam Robb’s dad was Caitlin’s basketball coach, and she also goes to school with Sam Robb’s sister. When she heard the story of Sam and his life, she knew she wanted to raise money to support the Sam Robb Fund.

Caitlin’s birthday was on May 13th, and she had her party on May 16th. So instead of asking for gifts for herself, Caitlin asked that her friends and family donate to the Sam Robb Fund. Caitlin raised $1820.00. What an inspired young lady.Unknown

For information on how you can donate to the Sam Robb Fund or one of our other Named Funds check out the Named Funds page of our website.


July 20th, 2009

Thursday Thunder: Fundraising Event

AtlantaMotorSpeedwayThursday Thunder, a 10-week series that hosts Bandolero, Legends and Thunder Roadster racing, is one of the most affordable, exciting family activities in Atlanta. Legend’s racing is teaming up with Speedway Children’s Charities to help raise money for different children’s charities, including CURE. Every Thursday night from June 4 to August 6 they’ll have a smorgasbord of games, contests, giveaways and hot on-track racing excitement.

This is also a fun evening with lots of activities for kids so please feel free to bring the whole family. Tickets are just $5 for adults and $1 for children 6-11 (children under 6 are free) for each evening of fun and grass-roots racing on the paved quarter-mile track at AMS, the Thunder Ring. Drivers as young as 8-years-old come from all over the nation to battle each night in eight different classes for the right to be called champions at Atlanta Motor Speedway.

But the racing is only part of the fun and excitement at Atlanta Motor Speedway. On the concourse, there will be weekly themes and contests, exciting intermission activities merchandise and ticket giveaways. Group parties and children’s birthday parties are also available during Thursday Thunder. Gates open at 6 p.m., heat races start at 6:15 p.m. and feature races start at 7:30 p.m. Don’t miss this summer’s most fun and affordable activity. Come see the region’s up and coming drivers each Thursday night at Atlanta Motor Speedway.

And on July 23rd, Legends’ racing and Speedway Children’s Charities are teaming up with CURE Childhood Cancer. CURE will be selling $1 raffle tickets next Thursday July 23rd from 6:00-8:00 pm to raise money for CURE. So come out, enjoy the fun, and help support CURE Childhood Cancer.

All Donations will go to CURE: Childhood Cancer

For more information on Thursday Thunder contact Jann Jones


Concert for Callie

Join us for Concert for Callie, featuring No Parachute and Sailing to Denver, on February 4 at 9pm at Tavern 99. To learn more, Click Here.

Sam Robb Memorial 5K and 1 Mile Run

Join us for the Sam Robb Memorial 5k on February 4 at Newtown Park, Johns Creek, GA. To learn more, Click Here.