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Monday, January 12, 2009
Janice Shaw Crouse :: Townhall.com Columnist
Learning About Leukemia
by Janice Shaw Crouse
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During the past six weeks, our extended family has been learning things that nobody ever wants to learn.  On December 1, 2008, my niece’s 7-year-old daughter, Lily, was diagnosed with Acute Lymphocytic Leukemia (ALL).  Today’s adults remember when such a diagnosis was a death sentence; 40 years ago patients with ALL had a four percent survival rate.  Now children with Lily’s type of leukemia have a 90 percent survival rate, because St. Jude’s hospital in Memphis made it their main mission in the 60s to discover treatments that work against childhood leukemia.  Researchers at St. Jude’s were criticized by those who believed that children with cancer should be allowed to die in peace rather than go through the horrible treatment that they had to endure.  Our family and thousands of others are so grateful that the researches prevailed and persevered.

My niece has spent hours researching the medical aspects of leukemia, including several medical textbooks. She discovered that a couple of well-funded research studies in the 60s and 70s produced huge advances in treating ALL.  In fact, a treatment developed in 1961 is still the protocol widely used today.

Sadly, over 3,000 children die each year from childhood cancer, yet only three percent of national funding goes to childhood cancer research.  We see ribbons for all sorts of diseases, like AIDS and breast cancer.  But there is little awareness of the paucity of funds for childhood cancer.  Studies that provide life-saving treatment protocols take years and years to complete, and they are appallingly underfunded. 

Let’s look for comparison at the bailout money for Chrysler (with 20,000 employees).  Chrysler’s share of the bailout money is 100 times the amount designated for childhood cancer research.  So do the math: During the time that it would take to raise an amount for childhood cancer research equal to Chrysler’s bailout dollars, over 300,000 children would die.  In addition, hundreds of thousands more would be diagnosed, suffer through harsh treatments and/or suffer life-long disabilities from the treatments.

We know that increased awareness means increased funding to eradicate a disease.  Over a decade ago, an effort was launched to raise awareness of autism.  As a result, federal funding for autism has tripled over the past decade. 

We must now do more to raise awareness of the need for research about childhood cancer and massively increase the amount of federal funding.

The wonderful doctors at Vanderbilt Children’s Hospital in Nashville described leukemia for Lily as a weed that was taking over a garden.  They challenged her to help them get rid of the weeds in her blood.  As a result, Lily named her website Lily’s Garden, www.lilysgarden.org. She wants to replace the weeds in her garden with beautiful lilies!

Lily’s family is challenging people to sign up for Nashville’s Country Music Marathon (CMM) on April 25, 2009, with the Leukemia/Lymphoma society as the main charity for the event. Anyone can register by going to www.cmmarathon.com.  Those who register for the CMM, can join Lily’s team by registering at her website, www.lilysgarden.org.  Lily’s team will have T-shirts and arm bands emblazoned with the slogan, “Walking to Weed Out Leukemia.”  The shirts are a shade of purple that suits both men and women.  More than 50 people have already signed up with Lily’s team; we’d love to have a sea of purple.

There will be plenty of actual runners for the full marathon and the half-marathon, but there will be even more walkers (CMM gives up to seven hours to complete the half-marathon — around 13 miles!).  The kid’s marathon is the night before, and the children prepare by doing 25.2 miles at home during the month before the race and then run the last mile in Nashville.  Lily will be in her most intensive treatment in April, but she is hoping to be able to watch the end of the race.

All the proceeds raised by Lily’s Garden are going to the Leukemia and Lymphoma Society and CureSearch, a national research group that conducts studies for childhood cancer.  The website, www.lilysgarden.org, provides further information.  Participants are asked to raise $250 by asking family and others to sponsor their walk in the race.  This works out to about $10 per mile if you are doing the marathon or about $20 per mile if you are doing the half-marathon.

Lily’s family is covering the administrative and overhead costs, including the T-shirts and arm bands.  So all the money for purchases and the money raised will go to the organizations that are working to find a cure for leukemia.

Lily’s family is also working on a benefit concert with the help of some that are committed to finding a cure and raising money.  In a recent concert, Wynona Judd dedicated a song to Lily and Hannah Montana (Miley Cyrus) came to see her in the hospital; both raised awareness, but it is only a beginning.  Lily faces up to three years of treatment.  During that time, she cannot go to school and her interactions with others, as well as her activities, will be restricted to protect her health.  She is beginning a long, hard road, but her prognosis is very hopeful — all because 40 years ago research studies were funded that provided the treatment protocols that are saving her life.

What are we doing today to provide research for cures for those hundreds of thousands of children over the next 40 years who will be diagnosed with childhood cancer?

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About The Author
Janice Shaw Crouse is a former speechwriter for George H. W. Bush and now political commentator for the Concerned Women for America Legislative Action Committee.
 
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Country Music Marathon conscious raiser
Janice, my dear mother died in 2000 from a quick-growing peritoneal cancer. I pray every night for Lily and her entire family. I pray that a cure will be found soon. If not for the fact that I'm soon to be 67 years old, and will also have knee surgery on Friday for a torn medial meniscus, I'd join the Country Music Marathon - at least as a "walker". I'll have TWO bum knees without the medial meniscus (cartilages), and that does cause a lot of wear and tear on the ball/socket of the knees. One is already somewhat worn from the operation on it in 1974 and 35 years of wear and tear afterward.

Maybe I can find someone to sponsor who will enter the race. I'll seek someone to do so.

Keep the faith everyone and keep praying.

cancer survivors
I am a 14 plus year breast cancer survivor and I have a teenaage nephew who is a 5 year leukemia survivor. Janice, my heart goes out to you and your family. It won't be easy, but don't give up. God Speed.

You think donating bone marrow is hard?
Children with leukemia (well - anyone with leukemia) go through lumbar punctures and bone marrow aspirations on a regular basis. If these little children can get through those procedures so often, the least I can do is be willing to do it ONCE in order to provide one of them with a chance at living.

It only takes a cheek swab to get typed - then you only have to get your bone marrow aspirated IF you are matched with someone needing a bone marrow donor. Small, insignificant price to pay for the enormous, life-saving benefits.

K-9 and Writ'r-MOM
K-9 - God bless you for what you have done. I myself am an organ donor, plenty healthy and in shape. To help someones life like that is not only unselfish but even with a little extra life the recipient received was something that sounded like it made a world of difference to the family.

Writ'r-MOM- Even though you've been in remission for 10 years I'll pray for you. With your family I still think the big man upstairs has something for you.

Janice- great article by the way.

out of the woods

Sadly, ALL patients are not "out of the woods" even though their prognosis is good. With their immune systems weakened by the harsh treatments, they are very susceptible to infections, viruses and colds that can turn into dangerous pneumonia. They require almost around the clock care for nearly 3 years; the slightest rise in temperature can be very dangerous and must be monitored constantly. Fighting leukemia involves the whole family, lots of friends and extended family. Lives are put on hold throughout the treatment -- but the hope of ultimate victory over this awful cancer provides renewed strength to carry on the fight when fatigue brings on discouragement and fear.

I am a survivor
God bless Lily that she has a complete recovery.

I am a leukemia survivor. Mine was a rare form that usually hits elderly men. I was a 40 year-old mother of 4 at the time.

I have been in remission for going on 10 years now.

Let's hope that Cancer research is not left on the back burner, especially children's cancer. They deserve to live long and ultimately healthy lives.

Praying for Lily's Recovery
I just lost my mother, far too early, to this type of leukemia. Sadly, she was past that cut off age where stem cell or bone marrow transplants are an option. I pray that Lily will recover and I hope that my donation, which I'll make in my mother's name, can help her and others suffering from this cancer.

Team In Training
As a long time participant of the Leukemia and Lymphoma Society's Team In Training (TNT)Program, I would like to let everyone know that massive amounts of research funds are raised every year by ordinary people through this program. The TNT program trains individuals for endurance events (marathons, century bike rides, triathalons) in return for raising funds for leukemia research. I have seen what this program can do (15 century rides and countless hours training and assisting in fundraising). If you ever wanted to do something and get in shape at the same time, I can not recommend this program enough. Call your local LLS chapter and inquire about their program.

A Triumph of Federal Funding
Since the survival rate for children with leukemia has gone from 4% to 90%, it is worth mentioning that most of the research that made this survival possible was done with federal money. The National Institutes of Health in the Washington DC suburb Bethesda, Maryland has, for decades, been the mother lode of medical research in the United States, while other research centers work very much on federal grant money. Please note that it wasn't Corporate America that figured out how to keep those children alive. Government sometimes does very good things.

Bone Marrow Donors (part 2)

About a year later, I got a letter from the woman's daughter. She had just had a baby of her own. While the would-be grandma did not win her bout with leukemia, my donation bought her a little more time. The daughter said in her letter that the six extra months her mother was alive gave them time to shop for baby clothes, reconcile past differences, and show each other how much they loved one another. When I read the letter, I wept like a baby. I was so frustrated that she did not survive, but just knowing that she and her family had that little bit of extra time (and hope) was indescribably... well, awesome.

Shortly afterward, I got a call from the cancer center again, saying that I may be a match for another patient. They said it is rare that anyone would put themselves through that experience more than once, and they'd understand if I declined. Without hesitation, I said I would continue to donate until I had no more red blood cells or marrow left in my body. For some reason or another, I did not have to go in the second time, but I stand ready to do it all again if I get the call. For anyone even remotely interested in registering to be a donor, please take the time to visit the page listed above. There is a much less invasive procedure called apheresis that extracts stem cells from platelets without having to have 30 holes drilled into your pelvic bone (it's sort of like giving blood multiple times under the influence of a steroid that helps stem cells replicate more productively in your blood). It's such a small commitment to make, and can help save someone's life.

We have the ability to treat a lot of these ailments with the use of cord blood and ADULT human stem cells. If just 10% of the people reading this decide to become donors or help spread the word, a lot of families will get that precious extra time they want and need to live, laugh, and love.

Bone Marrow Donors (part 1)
If anyone out there really wants to help, visit this site and register to be a bone marrow donor: http://www.marrow.org/.

Shameless plug over. In 2000, I registered at my local red cross to see if I was a compatible donor for a 14 year-old girl in the community where I lived at the time. I wasn't a match, and after a couple of years had passed, completely forgot that I was in the registry. In 2003, I got a call from the NMDP saying that I was a match for an anonymous patient with acute myelogenous leukemia. All they would tell me was that she was in her early 50's, and had been undergoing treatment for about three years, waiting for a suitable bone marrow donor. I went to the James Graham Brown Cancer Center Center in Louisville, KY after all the tests were completed, and underwent surgery to extract the marrow from my pelvis. It was one of the most painful things I have ever experienced (the recovery, that is), but I never let the pain get in the way of the purpose... whatever I was experiencing could not possibly be as bad as what this woman and her family must have had to endure the past three years.

very important article

Not only is it a shame that this form of leukemia often affects children, but it is also a horrible disease in itself. Please provide as much support as possible. It will benefit not only the children, but also the many adults suffering from other types of leukemias and lymphomas.

Take a field trip
Visit the pediatric oncology floor of a children's hospital. You will never be the same. It will instantly set your priorities straight.
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