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Showing posts with label events. Show all posts
Showing posts with label events. Show all posts

Monday, June 3, 2013

Mission Monday: Mission Day



This year's Federal Mission Day is here, with advocates scheduled to arrive in Washington, D.C. today for training and to take the Capitol by storm on June 4th. This dynamic meeting partners Executive Directors, Patient Services staff, and engaged volunteers with The Leukemia & Lymphoma Society's (LLS) Office of Public Policy, working together to help accelerate new cures and treatments for our patients and ensure they have access to quality, coordinated cancer care. This meeting will bring together the three pillars of the LLS mission: research, patient services, and advocacy, to drive better public policies that will help our patients live better, longer lives.

If you didn't make the trip to Washington, DC this year, you can still help participate in our efforts to educate Congress about the need to find a cure for blood cancers.    Add your name to the Mission Day petition today to let your members of Congress know that blood cancer patients are counting on them to support research and treatment options to help patients live longer, better lives - not someday, but today.

SIGN the Mission Day petition now and send out to your network of family and friends to do the same.

Wednesday, April 24, 2013

National Volunteer Week: Big D Climb

Here's to all volunteers, those dedicated people who believe in all work and no pay. 
~Robert Orben

Kim Carter, center, with two trainers from 24 Hour Fitness
at the 2013 Big D Climb

This week is National Volunteer Week and while The Leukemia & Lymphoma Society is thankful for its volunteers year round, we are taking this opportunity to highlight seven outstanding volunteers that help make the North Texas chapter run so efficiently.

Kim Carter, the Regional Manager of Corporate Sales for Texas for 24 Hour Fitness, first became involved with the Big D Climb shortly after she became a club manager at the Downtown Dallas 24 Hour Fitness location.  24 Hour Fitness had become a sponsor with the event a year earlier but it is Kim who is credited with expanding the sponsorship and getting 24 Hour Fitness more involved with the Big D Climb and The Leukemia & Lymphoma Society (LLS).

Kim's connection to LLS and its mission is very personal.  Her mother, Johanna Carter, was diagnosed with MDS in her early 60s and it quickly turned into leukemia.  Johanna's age at the time of diagnosis kept her from being eligible to receive a bone marrow transplant and after three weeks of chemotherapy, she lost her battle.  During her treatment in Annapolis, Kim flew in every week and stayed at the Hope House when not with her mother in the hospital.  It was during those trips that Kim pledged to get move involved in the effort to find a cure for blood cancers.

Several years after first getting 24 Hour Fitness involved with the Big D Climb, Kim continues to ask "what more can we do?"  She has expanded the involvement of 24 Hour Fitness as a sponsor, created teams of trainers and members to participate, and is now working to expand 24 Hour Fitness' involvement with LLS' stair climbing events to other cities.

We are so thankful for Kim!

Friday, March 29, 2013

Freebie Friday: Meet Greg Clarkson, President of the North Texas Board of Trustees

Greg and his son, Ryan, volunteering the
morning of the 2013 Big D Climb
Greg Clarkson, President of the North Texas Board of Trustees, shares in his own words why he is involved with The Leukemia & Lymphoma Society.

We are all called to volunteer at some time during our lives. I urge you to answer the calling. It is an opportunity to use your talents and resources in a way that helps your neighbor, your community, or a stranger in need. My calling was to the North Texas Chapter of The Leukemia and Lymphoma Society (LLS). I am finishing my sixth year as a member of the Board of Trustees and serving my final year as President of the Board. As I make the transition from an active Board member to the Advisory Board, I have taken a moment to reflect on how I became involved with the Society and it's mission to cure blood cancer.

I have not personally had the pain of losing a family member to blood cancer or any cancer for that matter. Prior to becoming a Board member, I did not know anyone that had leukemia or lymphoma nor did I even know that these were afflictions of the blood. I didn't spend much time in hospitals or around doctors or sick people. I am in the banking industry and manage a nationwide small business lending unit for BBVA Compass in Dallas Texas. Our bank used LLS' Light the Night function as our annual employee participation event. This gave our employees a chance to raise money for a charitable cause while remembering friends and family members that had been impacted by the disease. We would all gather with other fundraisers during an October evening and literally Light the Night with glowing balloons honoring those who have fought the cancer fight. This is how it started for me.

After meeting the LLS staff at the North Texas Chapter I knew that these were the people that had the energy and the desire to tirelessly fundraise, educate, and work for the cause. After meeting the scientists and doctors, I knew that this was the cutting edge research at the headwaters of all cancer breakthroughs. This is a disease that can attack anybody at anytime. There is no early warning, no lifestyle change, no preventive maintenance. There is only the need for a cure. So, we volunteers reach out to our friends, family, co-workers, customers, and communities, to help us raise funds for research and a cure. We ask for time, we ask for money, we ask for donation items, or we ask for a moment to tell you about someone that has touched our lives. If not by their name, at least by the way we remember the expression on their face as they traveled on their cancer journey.

During my tenure, I have seen things that would make your hair stand up on end and I have seen things that would make your hair fall out. I have seen the hair grow back and the smiles return. I have seen life renewed and living regained. I have seen the dedication and selflessness of healthcare workers, volunteers, fundraisers, researchers, and legislative advocates. I have seen family and friends, young and old, search for the words to answer the question "why me?".  I volunteered to fill a need and that need remains great.

If you feel it is time to volunteer, don't wait any longer. Even if you have not been personally impacted by blood cancer or fear you cannot make a difference, I can assure you that your efforts will be honored. It is the most rewarding thing you will experience. So take the first step and give T

This month The Dallas Morning News ran an article about a breakthrough treatment that cured a particularly nasty form of leukemia in a few patients. The article was a reminder that everyday somebody is being cured of blood cancer. Someday, everybody will be cured of blood cancer. Let's make that someday, today.

Monday, March 25, 2013

Mission Monday: Celebrating Team In Training's Rich History



Commemorating a 25th anniversary is a timeless tradition.  And the North Texas Chapter of Team In Training invites you to celebrate this extraordinary milestone at the Team In Training 25th Anniversary Gala on Sunday, June 30, 2013 at the Westin Galleria.

Over the last quarter century Team In Training and its thousands of athletes have raised more than $1.3 billon, funded countless new programs and lifesaving drugs, touched the lives of thousands of families, while creating an organization of lifelong friendships. Now that is something to celebrate!

So leave your workout shoes at home, put on your finest clothes and join us for a beautiful evening that includes a delicious three-course dinner and a silent auction benefiting TNT.

Tickets are $85 per person are available now from your local Team In Training Staff.

Get a group together, buy a table of eight, and make it a memorable evening with teammates. 

We look forward to seeing you soon!

Thursday, March 21, 2013

Thankful Thursday: An Inspirational Letter


The Williams family at the LLS Volunteer
Appreciation Night at the Texas Legends.
Below is an inspirational letter Kirsa Williams wrote to inspire a Team In Training team as they work to raise money and train for an upcoming event.

Dear Team,

I want to tell you about our amazing three year old little boy, Bennett. Our lives were forever changed on April 9th of 2011. We were sitting in an exam room in the ER at Children’s Hospital waiting on blood test results, when a team of doctors entered the room and gave us the news that our 13 months old son had leukemia. From that moment on, our entire family started the fight against cancer. In support of our baby boy who was even too young to speak, we educated ourselves on blood cancer, and learned what we needed to do, and where we needed to go to give him the best chance at survival. His chemotherapy treatment would last a little longer than 3 years, with the first 9 months being the toughest. Since his diagnosis, he has endured several rounds of chemotherapy, bone marrow tests, lumbar punctures, blood transfusions, and many days and nights at the hospital. Watching Bennett receive treatment for leukemia is the hardest thing my husband and I have ever had to do. We would trade places with him in a heartbeat.

These past couple of years have taught us the meaning of community, friendship, faith, and grace. It showed us the faces of true courage and strength in the children and the families that we have met along this journey. Some who are no longer with us, some who fight on in vein, and some who are winning the battle; all of whom share the same indomitable spirit. Whether you joined TNT to run in honor of someone, in memory of someone, or because you are a survivor yourself, my family thanks you so much for taking on this challenge. It is because of people like you that my sweet boy can run and jump and play like a normal three year old should! Thank you for a being a part of finding a cure!

Blessing to you all, and good luck training for your race!

Kirsa Williams

Monday, March 18, 2013

Mission Monday: First Connection Program

Would you like to reach out to others
diagnosed with Leukemia, Hodgkin Lymphoma,
Non-Hodgkin Lymphoma, Myeloma or MDS?
The Leukemia & Lymphoma Society’s
First Connection Program
connects patients and their families with individuals who have personally experienced the challenges of dealing with a diagnosis of a blood cancer.
We are currently looking for patients, parents and caregivers who
are at least one year post treatment/acute phase who want to listen
and help newly diagnosed patients understand the road ahead.
If you are interested – our next training session is
Saturday, April 6, 2013
9:30 a.m. to 3:30 p.m.
(lunch will be provided)
All interested persons must complete an application
and a short phone interview.
Space is limited – please call or email to reserve your spot.
We need patients with all blood cancer diagnosis who have been
treated within the past three to five years. We have a particular need for
parents of children with a blood cancer, patients with CLL, MDS and
multiple myeloma and caregivers of all blood cancers.

Contact:
Kim Brown - Patient Services Manager
(972) 996-5905

Monday, February 18, 2013

Mission Monday: Ray Johnston


When the North Texas chapter of The Leukemia & Lymphoma Society (LLS) hosted a volunteer appreciation event at the Texas Legends in early February, Ray Johnston volunteered to sing Gold Bless America.  He has a strong connection to LLS, being the 2012 Linda Adleta Heart of Gold Award winner at the Saint Valentine's Day Luncheon and Fashion Show, but also as a blood cancer survivor.
Ray was born and raised in Montgomery, Alabama. He played basketball for The University of Alabama and for the Dallas Mavericks until he was diagnosed with leukemia in August 2004 marking the end of his professional basketball career. Ray’s leukemia has relapsed 4 times but as of June 2011, he is beating the disease.

Ray taught himself to play guitar and thanks to basketball, he understands the importance of having top-notch teammates. Ray secured some of the best talent in the industry; hip-hop, jazz and soul heavy-weights Keith Anderson and Bobby Sparks to form the Ray Johnston Band.

Ray’s supporters; family, friends and strangers alike continue to help his dream grow into reality.

Friday, February 15, 2013

Freebie Friday: Meet Stacey Russell

Deputy Executive Director Stacey Russell
with Executive Director Patricia Thomson.

Just yesterday at the Saint Valentine’s Day Luncheon and Fashion Show, I was again amazed by the number of people that are touched by blood cancers. The event honored a young boy who generously and without question, donated his bone marrow to his younger brother, now a survivor of leukemia. A committee member spoke about her battle with lymphoma; another was there in honor of her brother who is battling leukemia as we speak. It is stories like those that I hear at the various events and programs that The Leukemia & Lymphoma Society (LLS) hosts each year to help raise funds and awareness that keeps me motivated to do what I get the privilege of doing every day.

I was lucky enough ten years ago to stumble upon a job opening at LLS and it has definitely changed my life, for the better. Some things have changed ten years later, like the amazing advancements that have been made in treatments, some of the events that take place and some of the people that are no longer here as they lost their battle. Some things have stayed the same… like the generosity of people. Each day, there is a scientist hard at work trying to find the link to a cure due to the generosity of people in the community giving of their time, donating to someone doing a marathon through Team in Training or climbing stairs at the Big D Climb, becoming a corporate sponsor for the Links Fore Leukemia Golf Tournament or coming to the Lone Star Blood Cancer Conference as a caregiver wanting to learn more about how they can help their loved one through their cancer journey.

We all have days where we think what else could go wrong? Its raining and I have a flat tire or whatever the case may be. It seems disastrous then, but in the grand scheme of things, I am healthy, my husband, my kids, my family and friends are healthy, and that is what is important. However, there are so many people here in North Texas, across the US and the world that are not as fortunate. Instead, they are fighting for their lives or their loved one is. This is why getting involved with LLS in whatever way you can is so important, especially now. We are in the business of saving lives, literally, and invite you to be a part of that too. Someday Is Today!

Thursday, February 7, 2013

Thankful Thursday: Blood Brothers


A little boy battles leukemia with the help of his older brother

Sharply dressed in slacks and a tie, Jude Cobler came home from his fourth day of kindergarten at All Saints Catholic School, on Aug. 19, 2010, with a 105-degree fever.

His mom, Boots, and dad, Keith, had previously noticed lumpy bruises on Jude’s legs and talked to their doctor, who said not to worry unless the bruises popped up above his knees.

Keith called his insurance company’s nurse line. They instructed him to call 911. After the paramedics arrived and examined Jude, they told Boots and Keith to take their 6-year-old to Children’s Medical Center at Legacy in Plano. Soon after their arrival, they found out Jude had leukemia. An ambulance transported him to Children’s Medical Center of Dallas where he spent three days in intensive care and another three on the Center for Cancer and Blood Disorders floor.

“After ICU, Jude went through a lot of blood draws and procedures,” his mom says. “They started chemo right away.”

With an 85 percent survival rate for acute lymphoblastic leukemia, his parents felt optimistic, but were concerned about the lack of cancer medications on the market for children. After a month of chemotherapy, Jude’s leukemia decreased by 75 percent and doctors said he was in partial remission, but wasn’t in the consolidation phase where there is no measurable leukemia in the blood. Boots and Keith continued to spend their nights with Jude in the hospital while their parents took care of his 12-year-old brother, Joshua, at home.

During Jude’s second month of treatment, something drastic happened — his cancer increased tenfold.
“That’s when we started talking about a bone marrow transplant,” Boots says.

Keith worried about his son because Jude is half white, half Filipino. His donor would need to have a similar genetic makeup. So the day the Coblers found out Jude needed a marrow transplant, they picked up Joshua from All Saints to have his blood drawn — and hoped the 25 percent chance he had of being a match would pan out.

“There was definitely a lot of fear of not being a match,” Joshua says. “There was still a lot of grief about Jude being diagnosed and anger about why this was happening.”

Two days later, to everyone’s relief, Joshua turned out to be a positive match for his younger brother.
“Most people you talk to on the street have no idea what a bone marrow transplant is like,” Keith says. “It can be as simple as giving blood, or with younger kids, they put them to sleep and extract the marrow from a larger bone.”

Before Jude could undergo the transplant, which would strip his whole body of his type A blood and replace it with Joshua’s type O blood, he had to undergo a process where all of his live bone marrow was killed off to prepare for the new marrow. It took 10 days of aggressive chemotherapy and five days of total body radiation twice daily to prepare him for the transplant.

“It was very difficult because we had to trust people to take our son away and we couldn’t see him for hours,” Boots says.

That December the two brothers underwent the bone marrow transfer, a life-saving technique that Jude will never forget.

“[Joshua] gave me a second chance at life,” says Jude, now 8. “He’s one of the best family members I can have in my whole life.”

Once Jude received the transplant, Keith says, it was a waiting game for the new bone marrow to take over and his immune system to rejuvenate, a process that took about another month. Around that time, Jude contracted veno-occlusive disease, causing blood to pool in his abdomen, which swelled and became “taut as a drum,” Keith says.

Boots says during those agonizing days, Jude was in his hospital bed screaming the entire night and there wasn’t a thing anyone could do. They couldn’t give the child any more morphine.

Finally the disease corrected itself. Doctors were able to remove drains pumped into his body to remove excess fluid from his body cavity. In early February, Jude was finally stable enough to go home, though his plight was far from over. Jude had to take 20 pills a day while he and family members wore medical masks and obsessively cleaned the house because of his still-susceptible immune system. When Jude started to feel better, he was able to attend school on and off beginning in the fall. And finally, he was able to play outside.
“I always thought there was going to be an end to this,” the now-healthy Jude says. “Even through tough times I thought, ‘I’m going to get through it.’ ”

Joshua, now a Jesuit College Prepatory School of Dallas student, was nominated for The Leukemia & Lymphoma Society’s Spirit of Tom Landry Award for his articles, advocacy and the newspaper he launched while Jude was hospitalized called The Sibling Times. He’ll receive the award at the society’s Saint Valentine’s Day luncheon Feb. 12 at the Meyerson Symphony Center.

As for Joshua’s younger brother and transplant recipient, after two years of medicine, painfully sleepless nights, a family hidden behind medical masks and $2 million of medical bills, Jude is leukemia free. The experience gave him an idea about what he wants to be when he grows up.

“I want to be a pediatric oncologist so I can save lives,” Jude proudly says.

Read original article from Advocate here

Monday, February 4, 2013

Mission Monday: The Inspiration Behind Bennett's Buddies

Bennett Williams looks like a normal, healthy and cute little boy, with two loving parents and two older sisters. When his parents, Kirsa and Keith, took him to his one-year doctor’s appointment, he passed with flying colors. But, one month later, Kirsa noticed red spots on his body. They took him to the doctor the next day, and their pediatrician told them to get him to Children's Medical Center of Dallas right away. There, the doctors confirmed their pediatrician’s concern: Bennett had leukemia.

Now two, Bennett has faced intense treatment, including a regular routine of chemotherapy, 16 blood transfusions, as well as numerous spinal taps and bone marrow tests.

Since his diagnosis, the Williams family has made a big difference for other children with leukemia through their dedication to raising money for non-profits such as The Leukemia & Lymphoma Society —and they have improved their health in the process.

One day Kirsa got a flyer in the mail with a purple jersey on it. It was from the Leukemia & Lymphoma Society, for a marathon called Team in Training (TNT). She decided to go to an organizing meeting at Luke’s Locker, and she asked her friend Amanda to go with her.

Williams said, “I went because I wanted to educate myself with anything to do with leukemia or childhood cancer. I then made the decision to run the marathon, and Amanda agreed to do the fundraising. Even if you never run a mile in your life, they train you on how to do it. Somehow we would find the time to do it.”
Kirsa and Keith ran the marathon in Dallas, and with Amanda’s help, they raised over $60,000.
The trio continued their fundraising as they signed on for the TNT San Diego marathon in June. They recruited three more friends from the Park Cities and raised $30,000. Keith then signed up for a triathlon with TNT and raised another $60,000. In total, they raised $150,000 in one year between the three races.
Williams said, “Keith contacted everyone he knew in his industry across the country. You never know who has been touched by leukemia and what their story is. We would get letters saying things like, ‘my brother died of leukemia, so enclosed is money to support your efforts.’”

When Keith and his friends participated in the triathlon in Washington, D.C., The Leukemia & Lymphoma Society called the family up to the stage, and the Williams' were informed that they had raised enough money to be awarded a research grant in Bennett’s name.

After the ceremony, a woman from the crowd sought them out. Williams said, “The woman asked if Bennett had a port. When I told her yes, her eyes teared up. The woman then said, "‘Ten years ago I did my first team in training, and all the money we raised went to develop an infant port. And here he is in front of me, and he has the port from the money that we raised.’” The Williams then realized what a huge impact their grant could make, and they decided the money should go to research childhood leukemia. “We raise this money, and it makes a difference if even one child survives,” Williams said.

Read the original Bubble Life article here

Friday, January 18, 2013

Friday Freebie: Meet Michelle Northcutt


I have been with the North Texas chapter of The Leukemia & Lymphoma Society for almost seven years now and have been in charge of several events in that time span.  But none of them compare to the Saint Valentine’s Day Luncheon and Fashion Show (website) that is going on 30 years.  Having an Apparel Merchandising degree makes this type of event right up my alley but it’s not all about the clothes.  The Spirit of Tom Landry winners each year are my favorite part of the show.  The Spirit of Tom Landry award honors a youth (through age 20) with courage, integrity, dignity and dauntless spirit who has battled blood cancer through personal experience OR who has volunteered extensively on behalf of others who suffer from blood cancers.  This year’s recipient, Joshua Cobler, is a wonderful advocate on behalf of his brother Jude.  I encourage you to visit this website and read more about Joshua and Jude’s journey.  Both will be honored at the upcoming Saint Valentine's Day Luncheon and Fashion show on Tuesday, February 12, 2013 at the Meyerson Symphony Center.  Visit the event’s website at www.saintvalentinesdayluncheon.org to learn more.  I hope to be out of this job one day as we have found the cure for blood cancer’s and my role here is no longer needed.

Friday, January 4, 2013

Freebie Friday: Meet Ashley Desper


Until two months ago, I was one of those fortunate people in the world with no personal connection to cancer. You read the heartbreaking stories and see the horrifying effects it has on others and their families, but it’s hard to comprehend until it’s staring you in the face.

I was working late on a Thursday evening and my mom had text me that she needed to speak with me. The day before I had called her and my dad to tell them some exciting news, but she had seemed unusually down even though I knew she was happy for me. I repeatedly asked her what was wrong. She insisted everything was fine. I called her immediately, as I was having a bad evening at work and needed to vent a little bit. Even though she gave me her usual perfect words of encouragement, I could tell something was wrong. A few moments later, she told me was diagnosed with breast cancer. There’s nothing in life that can ever prepare you for that moment. Suddenly, nothing else mattered….work, stress, social life. It all seems so insignificant when someone that close to you tells you they have cancer. My father, being a physician, got on the phone and insisted she was going to be fine. I trusted my dad, and I knew he would make sure she was ok. She is our family rock.

I remember driving home and being an emotional wreck. I left everything on my desk with a strict deadline and just walked away. At that moment, it just didn’t matter. I booked my flight home the next day. My mom was having surgery that Wednesday which would determine if/where the cancer had spread. That was 5 days away, and she needed me. I’ve never seen her so excited to see me when she picked me up from the airport! It was a long few days leading up to that Wednesday morning. The family was there in the waiting room. Although it was a short procedure, it felt like the longest hour of my life. The doctor came out and told us all the cancerous cells had been removed and that the cancer had not spread to her lymph nodes. They caught it very early, and her prognosis couldn’t be better. It was the most unbelievable moment of my life.

My mom is half way through her radiation treatments now and has to take a pill every day. In the world of cancer, this is a blessing. She is doing so well, and I could not be more thankful for how lucky and blessed we are. It puts life into perspective and makes you appreciate every moment of quality time you have with your loved ones.

Ironically, the day before my mom announced her diagnosis, that exciting news I called to tell her about was that I was offered the position as Campaign Manager for the Leukemia & Lymphoma Society. Joining this organization came at such a critical moment in my life, and I knew it happened for a reason. It means so much to me to work for such as amazing cause that will find a cure for blood cancers. I want to be a part of that and help others so that they never have to hear those tragic words from a loved one again. I truly do believe that someday could be today!

Ashley is the lead contact for both the Big D Climb (www.bigdclimb.org) and the Links Fore Leukemia Golf Tournament (www.linksforeleukemiadallas.org)

Thursday, January 3, 2013

Thankful Thursday: Advocacy

Take action now.
Make your voice count.
You are cordially invited to join The Leukemia & Lymphoma Society (LLS) for a discussion about the role that grassroots advocates play in finding a cure for blood cancers.  Together, our voices have a powerful impact on legislators that will result in much needed support for blood cancer research and patient care.

SAVE THE DATE:Tuesday, January 15, 2013

2:30-4:30p
Presentations & Town Hall Discussion
Baylor University Medical Center
Charles A. Sammons Cancer Center
10th Floor Conference Center
3410 Worth St.  Dallas, TX 75246
Parking in Garage 4 (off Worth St.)
Vouchers are available for attendees

Feating presentations by:
Scott Riccio, Vice President, LLS Advocacy and External Affairs
Brian Rosen, Vice President, LLS Government Affairs
Jon Hoffman, Manager, LLS Advoacy and Volunteer Engagement

Please RSVP by Tuesday, January 8, 2013 to Kim.Brown@lls.org or (972) 996-5905

What does it mean to be an advocate?
  • Make your voice heard
  • Communicate with legislators about issues that affect blood cancer patients, family members or caregivers
  • Represent blood cancer patients among local healthcare coalitions

Thursday, December 20, 2012

Thankful Thursday: Winning Awards

Stanford University Awards The Leukemia &
Lymphoma Society the "Sprit of Hope" Award


Stanford University School of Medicine has presented John Walter, CEO of The Leukemia & Lymphoma Society (LLS), with the 2012 Spirit of Hope Award for Outstanding Health Care Organization in recognition of LLS’s 35 years of funding support to Stanford’s researchers.

In the last 15 years alone, LLS has awarded more than $27 million in research grants to Stanford University investigators, who are at the forefront of discovering innovative diagnostics and treatments.

The event was hosted by one of Stanford’s esteemed researchers, Beverly Mitchell, MD, director of Stanford Cancer Institute, who has made many significant contributions to LLS over the years. Dr. Mitchell currently leads an LLS Specialized Center of Research (SCOR), a program that funds teams of researchers representing different disciplines who are engaged in collaborative efforts to discover new approaches to treat patients with hematological malignancies.

Among their many cutting-edge projects, the team is testing a new targeted drug for patients with myelodysplastic syndromes (MDS), with a long-term goal of preventing the disease from advancing to acute myelogenous leukemia (AML). This same drug is being advanced in clinical trials by Onconova Therapeutics Inc., a partner in LLS’s Therapy Acceleration Program, a strategic initiative to form corporate partnerships to advance sponsored research in the clinic.

Dr. Mitchell also served as a as a past chair of LLS’s Medical and Scientific Advisory Committee and was a member of its national Board of Directors.

“It is truly a great honor for LLS to be recognized by a world-class research institution such as Stanford,” Walter said. “For more than 35 years we have shared a commitment to advancing outstanding cancer research and transforming the most promising discoveries into treatments to help patients live better, longer lives.”

Photo: LLS CEO John Walter Addresses the Audience at Stanford Before Accepting Award as Beverly Mitchell, MD, Stanford, looks on.

Friday, December 7, 2012

Freebie Friday: Light The Night




The 2012 Light The Night Walks raised more than $1 million in North Texas for The Leukemia & Lymphoma Society.  Did we pique your interest?  Want to learn more about this three night event?  Check out this video Aksala Productions made at the Fort Worth Walk location.  

Friday, November 30, 2012

America’s Most Beautiful Bike Ride


Train for the 100-mile event in Lake Tahoe, NV., while fundraising for lifesaving cancer research
By Liz W. Robbins
Is completing a century in 2013 one of your New Year’s resolutions? Want to do so while giving back to a worthy cause? If yes, look no farther than Team In Training (TNT), an endurance fundraising program supporting the Leukemia & Lymphoma Society (LLS). TNT is currently recruiting cyclists for its summer season, which includes 18 weeks of preparation for “America’s Most Beautiful Bike Ride (AMBBR),” to be held June 2 in Lake Tahoe, NV.  
Considered a favorite of alumni, the event has been on the roster since 1997 and averages 1,300 TNT cyclists per year from chapters across the nation (registration is capped at 3,000). A staggering $80,232,400 has been raised for blood cancer research over 16 years of participation.
What makes it so special?
For starters, “it’s more than a bike ride,” explains TNT alum Becky Kaye, who has completed the event 11 times both as a coach and participant. She notes that when cyclists train together while supporting the larger cause they develop a special bond. “People take care of each other and cheer you on. They genuinely want you to succeed.”
TNT alum Bruce Levy, who completed the event in 2010, agrees, adding that his experience was especially meaningful because his mother was also battling cancer at the time. “I’ll always associate Tahoe with memories of my mother and the way she encouraged me and insisted that I do the ride.”
“Someday there will be a cure for blood cancers,” adds Dana Howe, a survivor of non-Hodgkin’s lymphoma who has completed the event twice. “Being part of the legacy of supporting the research and patient advocacy through training and fundraising for an event is a worthy achievement.”
When event day comes, cyclists are rewarded for their hard efforts, on and off the bike, with an amazing location.  “Breathtaking scenery is all along the course,” explains Will Wardy one of two team coaches for the summer season.  Adds Coach Albert Chavira, who has completed the event nine times: “Lake Tahoe is always at your right side, so it’s a great visible deterrent to keep you from thinking of the hills!”
Speaking of hills, Tahoe offers a challenging 800-foot climb to a rest stop overlooking scenic Emerald Bay, as well as a 1000-foot climb to Spooner Junction. Although challenging, both are very doable, even for beginners. “If participants follow the guidance of their coaches, on event day they can expect an amazing ride they’ll never forget,” says Wardy.
 TNT alum Tom Eschenbrenner, who completed the ride this year, agrees, noting that “the cycling program lived up to my expectations, building endurance, improving my cycling skills and providing the structure necessary to train for a century.” Lynn West, who completed the event in 2011 when weather conditions were cold and wet, says the training and support also helped her build mental endurance. “I was prepared physically, but my success against the conditions came through the encouragement of my coaches and my husband who supported me to the end.”
For more information contact TNT Cycle Coordinator Kelly Donovan at (972) 996-5921, Kelly.donovan@lls.org or go to: http://www.teamintraining.org/ntx/cycle.