Cure Childhood Cancer

CURE Blog


August 31st, 2009

True Friends: An Essay by Marc Nolan

Unknown-2Marc Nolan and Sean Michael Dever have been friends since they were toddlers. The boys are now 13 and their friendship remains stronger than ever. When Marc received a school assignment to write an oratorical about “A Person Who Has Touched Many Lives,” the choice was obvious. He wrote about his friend, Sean:

When you ask people to name someone who has touched many lives, their first responses would usually be of religious figures, athletes, entertainers and so on. The person whom I believe has touched many lives is a friend. He is 13 years old like me and I’ve known him since before kindergarten. He used to attend St. Joseph School and was on my soccer team that our dads coached. His name is Sean Dever. Almost two years ago, he was diagnosed with cancer on his left knee. I for one spazzed out. Wouldn’t you be spazzing out if you found out one of your best friends had cancer?

But it wasn’t only me. Everyone was upset. Everyone was sad. Everyone was afraid. It was a shock to many of us how this could happen not only to someone we cared about, but to someone who is so young like we are. This is because so many people cared for Sean and his family. We couldn’t imagine what he and his family were going through. This news triggered an outpouring of support and prayers for Sean’s healing. I’ve always know Sean to be a tough person. Through his illness and pain, Sean remained strong, brave and most of all, faithful.

Through word of mouth, emails and a Caring Bridge website, more and more people learned about Sean, and they were touched with how he was coping with his day-to-day battle with cancer. People from all over the world were leaving Sean messages of support. It was amazing!

Those people who have been touched by Sean say that they appreciate life more and don’t let the small things bother them. Many people became aware of childhood cancer and are volunteering their time or donating money to help find a cure. We have had rallies and races to raise money and awareness because of what Sean has experienced and how it has affected his life and his future. A lot of us have stronger faith in God because through Sean, we were reminded of God’s love.

Eventually, Sean had to go through chemotherapy and had to have his left leg amputated. So many thoughts and prayers came pouring in and the miracle today is that Sean can walk and play sports with a prosthesis and is cancer free. I’ve played basketball against Sean recently and it is awesome how he doesn’t let anything stop him. He now also plays lacrosse and gets better everyday with his prosthesis.

Many people become famous and touch people’s lives once they are grown ups. To me, it is a bigger achievement to be able to touch people’s lives while you are young. I am glad Sean is my friend and has touched so many lives – especially mine.

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For more information on CURE, visit us at www.curechildhoodcancer.org


August 28th, 2009

The 1st Annual Hayley Hunter Research Fund Golf Tournament

Hayley Hunter is the 9 year old daughter of Eddie and Tammy Hunter of Ball Ground, Georgia.  In April 2008, she was diagnosed with stage IV neuroblastoma, a rare and aggressive childhood cancer.  It has taken surgery, six cycles of toxic chemotherapy, twelve rounds of radiation and an autologous stem cell transplant to rid Hayley of this disease.

In honor of Hayley and her fight against childhood cancer, The 1st Annual Hayley Hunter Research Fund Golf Tournament will be held on September 17, 2009 at the Bradshaw Farms Golf Course in Woodstock, Ga. Registration is at 8:00 am followed by a 9:00 am Shotgun Start. It’s a Four Player “Best Ball” Scramble Mulligans Tournament, $100 per player.

There will also be silent auction items available for bidding before and after the tournament.

Click here for more information on this event.

Questions about donations? Contact Eddie Hunter at ewinghunterjr@comcast.net or 404.663.9440

For more information on other CURE events, visit us at www.curechildhoodcaner.org


August 27th, 2009

Experimental Immunotherapy Markedly Improves Cure Rate for Children With Neuroblastoma

Researchers from the Children’s Oncology Group (“COG”) have demonstrated that a new experimental immunotherapy treatment using the chimeric monoclonal antibody ch14.18, that targets a specific carbohydrate/lipid molecule ganglioside, GD2 which is present on the surface of neuroblastoma tumor cells and cytokines IL-2 and GM-CSF resulted in a 20% improvement in cure rates compared to the standard treatment used in the past.

The findings of the COG Phase III study were published in May 2009 online on the American Society of Clinical Oncology ASCO website www.abstract.asco.org.

Neuroblastoma is a cancer of early childhood in which the cancer cells arise from cells of the sympathetic nervous system in the neck, chest, or abdomen. Annually, there are approximately 650 new cases of neuroblastoma diagnosed in the U.S. Neuroblastoma is the most common cancer diagnosed in the first year of life and is responsible for 15% of cancer-related deaths in children. Most patients are diagnosed as toddlers, but neuroblastoma can present in infants and older teenagers as well.

“This is the first clinical trial to document that [the] combination of anti-cancer monoclonal antibodies mAbs with cytokines natural hormones that help the immune system is an effective anti-cancer therapy,” said COG lead study investigator, Alice Yu M.D., Ph.D., Professor of Pediatrics at UCSD. She goes on further to say that: “So far, all FDA approved therapeutic anti-cancer mAbs or vaccines are directed against protein or glycoprotein antigens. More importantly, this is the first study that proves that immunotherapy is effective in improving cure rates for this childhood cancer, and we are now focusing on making sure immunotherapy can be available to all children with this disease, and that we can improve on these results in the future.”

The researchers analyzed data from 226 eligible patients with high-risk neuroblastoma with a high likelihood of treatment failure and relapse. The patients were randomized to standard therapy, which consist of intensive chemotherapy followed by autologous hematipoietic stem cell transplantation and post-transplant isoretinoin, or the experimental immunotherapy moAb ch14.18 plus cytokines IL-2 plus GM-CSF and isoretinoin post transplant. Standard therapy was well tolerated, and as anticipated, the aggressive immunotherapy had significant side effects but these were manageable. The study showed that children receiving the experimental immunotherapy had a 20% better chance of remaining disease-free, and this resulted in a significantly improved cure rates. The study was stopped early due to the benefit seen in early analyses of the trial results.

John Maris, M.D., COG Neuroblastoma Disease Committee Chair, responds, “This is the first clinical trial to show a substantive increase in cure rate in well over a decade for this highly malignant childhood cancer.” Moreover, he states, “The 20% improvement in prevention of relapse for children with neuroblastoma receiving the experimental immunotherapy makes this therapy the new standard of care.”

According to COG Group Chair, Gregory Reaman, M.D., “The clinical benefit of this approach in a notoriously recalcitrant cancer of childhood is extraordinary and COG is anxious to continue its investigation of this approach to better define the toxicities and confirm its satisfactory risk: benefit ratio.” Dr. Reaman continues, “In addition, we are hopeful that this further study will result in commercialization and FDA approval and licensing of this experimental immunotherapeutic agent so that it can be made readily available as standard therapy to all children with this dreaded disease”.

For more information about new research, visit us at www.curechildhoodcancer.org


August 26th, 2009

Cherokee County Issues Proclamation Declaring September Childhood Cancer Awareness Month

Cherokee County is issuing a proclamation declaring September Childhood Cancer Awareness Month. They will be presenting this proclamation to CURE Childhood Cancer at the September meeting of the Board of Commissioners.

We would love to have as many kids and their families from Cherokee County, who have been touched by cancer, come to this event. CURE hopes to get some of the commissioners behind our cause so we can move forward in a great way.

So, that’s where we need your help! The meeting is on Tuesday September 1, and the more support we have there, the better. There are two things you can do to help. Firstly, come out and support us. And secondly, contact everyone you know that has also been touched by childhood cancer to come support us as well. The meeting will be held at the new admin building located at 1130 Bluffs Parkway in Canton, GA 30114. The meeting starts at 6:00pm, so please meet us at 5:45pm to get organized.

Please come out and show your support for CURE. This is another time when we need to ban together for the cause that we all believe so deeply in and that we all hold so dearly to our hearts.

For more information on this event contact Jann at CURE 

For more information on other upcoming events at CURE, visit us at www.curechildhoodcancer.org


August 25th, 2009

From the Desk of Don Campbell: President, Board of Directors

UnknownThe last two years have represented significant growth in many ways for CURE Childhood Cancer. Under Ken Biggerstaff’s leadership as President of the Board of Directors for the past two years, CURE has achieved many accomplishments. Here is a sampling:

• Achieving 12% growth in fundraising from $1.7 million to $1.95 million, allowing CURE to increase funding of critical research.

• Funding of six specific research projects covering neuroblastoma, leukemia and brain tumors.

• Reaching 75% of newly diagnosed patients and their families in Georgia through our Early Outreach Program.

• Assisting 224 families with emergency financial assistance through our Family Emergency Fund.

• Adding eight new members to the Board of Directors.

• Strengthening our CURE staff to add important expertise to accomplish our mission.

Please join me in saluting the contributions that Ken has made during the past two years and throughout his 11-year relationship with CURE. We look forward to his continuing support and guidance in the fight to cure childhood cancer.

On behalf of all CURE Board members, I would also like to congratulate our Executive Director, Kristin Connor, who serves as our day-to-day leader. Her personal commitment, unending energy and leadership have built the foundation for CURE’s ongoing and future success toward curing childhood cancer. She has earned the respect and admiration of the Board, her team and the greater CURE community. Her contributions are a key reason that CURE has been and will continue to be successful.

Each of you reading our newsletter has a vested interest in finding a cure for a disease that devastates our children and their families. Your trust and confidence in CURE’s mission also cannot go unrecognized. Thank you all for your support – through your donations, your time, and your guidance. And thank you for spreading the word about CURE’s vision and mission.

NEW FISCAL YEAR

Our fiscal year ended in June and as noted above, we had an excellent year – especially considering the recessionary economy. Regardless of what’s happening in the economy, though, childhood cancer never abates. CURE’s effort to fund a cure, therefore, cannot abate.

This past spring, the Board of Directors developed and approved a strategic plan to guide CURE over the next three-to-five years. CURE’s strategic plan builds on the key strengths of the organization and sets new goals to take CURE ever closer to our vision and ultimate mission.

We believe strongly that our mission must balance two critical objectives: 1) funding significant and impactful research on one side; and 2) helping patients and their families throughout their journey with childhood cancer on the other.

On the research side, we invest in the stellar childhood cancer research programs at the Aflac Cancer Center of Children’s Healthcare of Atlanta and Emory University. As noted earlier, we funded six research programs last year and will continue to support like programs in the coming year. Our patient and family support programs will also continue in earnest

You will receive shortly the CURE Annual Report where we will outline last year’s accomplishments and our plans for the coming year. Thank you for investing in CURE.

For the children with cancer,

Don Campbell, President; CURE Childhood Cancer Board of Directors

For more information on CURE, visit us at www.curechildhoodcancer.org


August 24th, 2009

Announcing CURE'S Kids Conquer Cancer One Day at a Time

September is recognized as National Childhood Cancer Awareness Month. This September, CURE Childhood Cancer has committed to raising awareness and raising money to help find a cure for childhood cancer in our lifetime and put an end to this terrible disease through a special program CURE’s Kids Conquer Cancer One Day at a Time!

We will honor a different CURE child each day during the month of September. Each child’s goal is to raise $1000 for CURE.  These young heroes hope to help others who may be going through the same journey with childhood cancer.   

Please help us in our goal of raising $30,000 in the month of September while honoring special CURE kids each day of the month who have been effected by childhood cancer.

Click here for a full list of families participating in CURE’S Kids Conquer Cancer One Day At A Time.

For more information on CURE, please click here.


August 21st, 2009

CURE Golf Classic

Join us for this year’s CURE Golf Classic to be held on Friday, September 25th, 2009. The Oaks Golf Course in Covington will host the tournament again this year and support CURE Childhood Cancer as its designated charity. All of the proceeds from the tournament will benefit CURE Childhood Cancer.

It is $125 to play. Help us reach our tournament goal of $100,000, keeping CURE assisting families and funding critical research. Your $125 fee includes golf, cart, breakfast, lunch, awards, snacks and beverages. There will be two shot-gun starts, 8:30 am and 1:30 pm on a “first-to-register” basis. All golfers will be served lunch from 12:30 – 2:00 p.m.

This year we are also having a raffle. The winner of the raffle will win 4 days and 4 nights in Costa Rica at the Las Ventanas Resort. This is a once in a lifetime raffle. Each ticket is 20 dollars and if you sell or buy 50 you golf for free.

September is Childhood Cancer Awareness Month, which means its even more important for you to do all you can to sponsor, donate, play, and buy and sell raffle tickets for the 20th Annual CURE Golf Classic.

Click here to play

Click here to learn more about sponsorship

Click here for directions to the golf course 


August 20th, 2009

Tommy’s Treasure Sale

Tommy Peterson Photo 1One of CURE Childhood Cancers amazing families has found yet another creative way to help raise money for CURE.

We know everyone has all kinds of stuff around the house that they’d love to get rid of. Well how about cleaning your house and supporting CURE at the same time? We would like you to consider gathering up some of that stuff and donating it to Tommy’s Treasure Sale. All proceeds from this event will benefit Tommy Peterson’s Heroes Like Me Foundation, CURE Childhood Cancer, the Aflac Cancer Center and Camp Sunshine.

Tommy’s Treasure Sale is on September 26, 2009 from 8 am until 4 pm, however treasures are being gathered now. The treasures that will be featured include: gently used household items, furniture, clothing, sporting goods, crafts, baked goods, BBQ, Chili, and a raffle featuring great prizes. Volunteers and cash donations are also welcomed. Tommy’s Treasure Sale will be held at Lilburn Marketplace at 4805 Lawrenceville Hwy in Lilburn, GA.

Tommy Peterson was only 7 years old when he passed away as a result of cancer. Tommy’s Treasure Sale is in memory of Tommy and his courageous fight with childhood cancer. Please help us support Tommy’s memory by donating.

To read more about Tommy, visit www.tommypeterson.com.

For more information on this event contact Robin Peterson at rpeterson_rdld@att.net

For more information on CURE, visit us at www.curechildhoodcancer.org


August 19th, 2009

Leslie Zacks: An Inspiration to Us All

Leslie Zacks is on the General Counsel at Sciele Pharma, Inc., and he’s on CURE’s Board of Directors.  Below is a comment from Leslie on why he got involved with CURE Childhood Cancer.3230d791-6615-4453-ba34-49c73144d304

“Children should play. They should not be forced to lie in bed worrying about white blood cell counts, tumor sizes or whether they will see their next birthday. CURE understands the personal and emotional impact cancer has on children and their families. CURE understands that tackling this disease requires significant resources. CURE understands…that is why it invests in the training and education of pediatric oncologists and in much needed clinical research. There are a lot of non-profits out there, but only one that focuses on pediatric cancer clinical research and understands what it will take to discover the ultimate solution. My heart breaks with each diagnosis and I am committed to ensuring that my time, money, sweat and energy will make a difference in this important fight.”

In addition to being on CURE’s board, Leslie has decided to take fundraising into his own hands.  Leslie has a goal to raise $9,000 for CURE and so far he has raised $7,627.50.  Check out his story:

“Say hello to my friend Patrick. Patrick likes baseball, fishing, superheroes and swimming. Unfortunately Patrick does not get to do those fun things as much as he likes. That’s because Patrick has cancer. Specifically, he has neuroblastoma, a rare and aggressive pediatric cancer that affects his central nervous system.

On September 27, 2009, I will attempt to complete a half-Ironman triathlon in Augusta, Georgia. The event consists of a 1.2 mile swim, a 56-mile bike and then a 13.1 mile run. It won’t be easy.

The pain and sacrifice I am experiencing during my training and that I will certainly feel on race day are nothing compared to the pain endured by Patrick, his family and far too many kids and families with cancer.

Please help me help them by donating to CURE Childhood Cancer. The race is 70.3 miles long and I am hoping that you will donate at least $70.30.

CURE is a fantastic organization that provides financial assistance to families and also funds much needed clinical research that will hopefully lead to a cure within our lifetime.

Donating through this website is simple, fast and totally secure. It is also the most efficient way to support my fundraising efforts. Many thanks for your support — and please forward this to anyone who you think might want to donate too!”

All the best,

Leslie

Donate  and help Leslie’s reach his goal for CURE Childhood Cancer. 

To learn more about CURE, visit us at www.curechildhoodcancer.org


August 18th, 2009

When A Friend's Child Is Diagnosed With Cancer

Ellianne Rivers has been my friend for more than fifteen years. We met when we were about to become wives, and motherhood was a very distant thought. When she found out she was pregnant with Jake, I was thrilled. I was secretly trying to be pregnant myself and was successful just a few months later. Because she was ahead of me in the pregnancy I looked to her for advice, for the “what happens now?” questions… we were both having boys- it was fun to share yet another aspect of a long-lasting friendship.

Childhood cancer was not something I knew anything about- was not even on my radar. And then Ellianne’s precious two year old, Jake, got leukemia. I received the news via email and sitting at my computer that day, looking at my own two-year old, I felt something change inside of me. I was angry, indignant. I knew a child having cancer was not right.

What came next, as I watched my sweet friend almost lose her child, was a desperate need to do something, anything to help her. I could do meals and I could pray. I could listen and if she stopped long enough, I could hold her…but I needed more- I needed to really make a difference for Ellianne and for other mothers like her. The more I learned about Jake’s disease and the more families I “met” through Ellianne, the more desperate my need became. And then, there was a way.

Through the Rivers’ Caringbridge site, I met Kristin Connor. Jake’s site linked to the Caringbridge site of Kristin’s son, Brandon, and I had been following their journey, too. Kristin wrote that she and Chris Glavine were trying to put together a “small little luncheon” to honor the mothers of children with cancer and the terrible burden they carry as caregivers. There was an “all call” for volunteers and I responded.

During our first meeting on that June day in 2005, my life changed. I was drawn into a new sisterhood of women just like me who desperately wanted to honor a friend’s struggle and journey into the world of childhood cancer. As we shared our stories and some tears that day, I knew I was where I needed to be.

We worked together closely for three months to put on the first annual “A Tribute to Our Quiet Heroes” luncheon. That September day, watching those mothers… watching my friend, who still unbelievably was “one of those mothers,” I was filled with so many emotions, but the prevailing one was one of gratitude- gratitude that I could do something to honor Ellianne and know I was also working to raise money to cure Jake and other kids like him. There were five-hundred people in attendance at that “small little luncheon” in 2005 and over $100,000 was raised. To date, we sit at almost a million dollars raised and are preparing for our 5th annual “A Tribute to Our Quiet Heroes” luncheon.

For my family, one Quiet Hero and the Quiet Heroes luncheon was a pathway to a mission. My husband and I have actively volunteered for almost five years now, and I am honored to sit on the Board of Directors of CURE Childhood Cancer. I support our mission wholly, and I see every day how we are making a difference in the world of childhood cancer and in the lives of these precious families.

The Quiet Heroes committee, at its core, is made up of women just like me… women who were desperate to do something to help. And we have, and we are.

Immediately after Jake was diagnosed he had some life-threatening complications and there was the very real chance that he might die. Incredulous, I thought, “Two year-olds don’t die”… they don’t, do they?

Unfortunately, they do. And one-year olds and ten year olds and babies. Jake was one of the ‘lucky’ ones. I use the word lucky and I shudder because really, not one child with cancer is lucky. It is better to say that Jake has survived. I am the lucky one in this story because I get to live my life with more purpose and I truly believe that in my lifetime, we will cure childhood cancer.

We are blessed as women to have friends who enrich our lives in so many ways daily. I am blessed to have one who changed mine. And I will honor her and so many others like her who I have grown to love by never giving up this fight for their children, for my children, for the future.

If you find yourself “desperate,” I encourage you to jump in. Join the Quiet Heroes committee, become a volunteer with CURE Childhood Cancer, work an Open Arms dinner, donate. You’ll get more than you give… I promise.

By Elesha Bateman, CURE Board of Directors


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    Nacho Average Taco

    For May and June, order the CURE taco at Red Pepper Taqueria and $1 will be donated to CURE. The taco features chargrilled calamari, crispy eggplant, tomato, onion, sorrel, and ginger pico.


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    Purchase Admission & Raffle Tickets

    Sample international red, white, and sparkling wine, as well as craft beer at Cheers to CURE, held at City Club of Buckhead on Friday, July 19th from 6pm to 9pm. Click here to purchase an admission ticket or raffle tickets.