The top 5 in-your-face moments of Matt Barnes’ 14-year career The explosive forward’s retirement brings the role of NBA ‘bad boy’ close to extinction

The days of the NBA “bad boy” are coming to an end. If you think otherwise, your take on the concept is all wrong. We’re talking about the trash-talking, brawl-beginning, fine-and-suspension-inducing, me-against-the-world mold of player that has flourished in the league for decades. With Matt Barnes’ Instagram-announced retirement (as a player) Monday, only a few are left in the league.

There’s DeMarcus “Boogie” Cousins, Draymond Green and perhaps even LeBron James. But even within this diminishing cohort, physical altercations have been replaced with petty wars of attrition. Instead of meeting toe-to-toe on the hardwood, players throw shade at each other via pregame outfits and custom T-shirts and hats. Players defending themselves via photos or in 280 characters or less — sometimes even under the alias of a dummy account (sorry, Kevin Durant). But don’t get it twisted: This new version of warfare is still entertaining. It’s just different.

On Nov. 28, James did earn his first career ejection since joining the league in 2003, but the outburst only cost him a $4,000 fine — chump change compared with what the league has levied on a player like Matt Barnes. In 14 seasons with nine different teams, Barnes accrued a whopping $414,276 in fines and six games of suspension, according to spotrac.com, which compares with James’ career total of $51,000 in fines and zero games of suspensions over 15 seasons and counting.

With Barnes saying farewell to the game, the NBA has lost a bad boy from a long lineage of audacious NBA players, often traced back to the “Bad Boys” era of the late 1980s/early 1990s, Detroit Pistons teams, featuring Isiah Thomas, Bill Laimbeer, Dennis Rodman, John Salley and Rick Mahorn. The fraternity of infamous hoopers also includes Larry Bird, Charles Barkley, Charles Oakley, Reggie Miller, Vernon Maxwell, Latrell Sprewell, Isaiah Rider, Kevin Garnett, Rasheed Wallace, Kobe Bryant and Metta World Peace, aka the man formerly known as Ron Artest.

Like many of these players, maybe Barnes crossed the line one too many times throughout his career. Or, maybe, he’s just fearless. Here are the top five moments from the now-retired forward’s playing days that embody his bad boy nature while blurring that fine line between craziness and passion for the game.


March 7, 2010 — MATT BARNES vs. KOBE BRYANT

Fine: None

It takes a certain type of man to go at Bryant — and that man has to have a backbone like Barnes. In a March 2010 game between the Orlando Magic and Los Angeles Lakers, less than a year removed from the teams’ matchup in the 2009 NBA Finals, Bryant and Barnes went back and forth all afternoon until their chippy confrontations climaxed in the third quarter, when they came chest-to-chest and the resulting jawing led both players to be whistled for technical fouls. “He’s the man, but s—,” Barnes said of Bryant after the game. “You gotta clean it up or something is gonna happen.” On an inbounds play after the verbal altercation, Barnes faked as if he would throw the ball in Bryant’s face, but the reigning Finals MVP didn’t budge. “I knew he wasn’t going to do s—,” Bryant told reporters after the Lakers’ 96-94 loss. “What would I flinch for?” Barnes came at the Black Mamba, and, technically, he missed. But he came correct, which you gotta respect. (In July 2010, Barnes became a teammate with Bryant after signing as a free agent with the Lakers.)

Dec. 12, 2014 — Matt Barnes vs. the water bottle

Fine: $25,000

In three seasons playing with the Los Angeles Clippers from 2012 to 2015, Barnes received a total of 32 fines, including one for $25,000 after a road matchup with the Washington Wizards in December 2014. After Clippers head coach Doc Rivers pulled his starters with about two minutes remaining in the fourth quarter, essentially conceding the game, Barnes returned the sideline, where he kicked a water bottle into the stands before cursing at the home team’s fans. This is one of four $25,000 fines that the NBA issued to Barnes during his tenure as a Clipper, but spoiler alert: It’s far from the highest fine of his career.

May 6, 2015 — Matt Barnes vs. Monja Willis, aka James Harden’s mom

Fine: $52,000 ($50,000 for remark to Monja Willis, $2,000 for technical foul)

OK, sometimes Matt Barnes’ went wayyyyy too far with the trash talk. In the first quarter of Game 2 of the 2015 Western Conference semifinals between the Houston Rockets and Los Angeles Clippers, James Harden received a hard foul from Barnes, his primary defender. As Harden walked to the free throw line, Barnes intentionally bumped into him, which led a referee to whistle him for a technical foul. The play resulted in a rain of negative chants from Houston fans directed toward Barnes, who responded by reportedly yelling, “Suck my d—, b—-!” to the crowd. On the receiving end of the profane remark was Monja Willis, Harden’s mother, who would later tell TMZ that the Clippers player immediately apologized for the comment. “My older son walked over to him and told him to apologize … and he did,” Willis said. “What he told me was that he would never want to disrespect anyone’s mother because his mother passed from cancer … and that he was sorry. I accept his apology.” Barnes denied making the reported remark, calling it “untrue” and “crazy.” Regardless of what exactly was said, c’mon, Matt. You gotta leave mothers out of it.

March 17, 2016 — Matt barnes vs. John Henson … and the Bucks Locker room

Fine: $32,205 (one-game suspension without pay)

What happens when a referee ejects a player before Barnes has a chance to speak his mind to him? Well, Barnes runs off the court, through the arena’s tunnel and to the opposing team’s locker room, of course. That’s exactly what happened during a March 2016 game between the Memphis Grizzlies and Milwaukee Bucks, when John Henson received his second technical foul of the night and an immediate ejection after the big man’s vicious block on Barnes, who also received a technical foul for his part in the ensuing verbal altercation. Technically, Barnes wasn’t ejected from the game. However, he checked himself out of the contest, left the court to find Henson and reportedly made it all the way to Milwaukee’s locker room before two security guards had to escort him from the arena. The dedication is oddly commendable, but … For his antics, the league slapped Barnes with a huge fine and made him sit out for a game.

Jan. 17, 2016 — Matt Barnes vs. Derek Fisher

Fine: $35,000 (two-game suspension without pay)

“Knicks coach Derek Fisher was attacked in Los Angeles by NBA bad boy Matt Barnes, who drove 95 miles to ‘beat the s–t out of him’ when he found out Fisher was romancing his estranged wife,” reads the opening line of an October 2015 story from the New York Post. The NBA didn’t take action on the matter involving Barnes, Fisher and Gloria Govan until December, when the league suspended the then-Memphis Grizzlies forward for two games without pay. Yet, leading up to a January matchup between Memphis and New York — the first encounter between the player and coach, who were former teammates with the Lakers — Barnes spoke negatively about Fisher, including calling him a “snitch” and saying he doesn’t “talk to snakes.” The negative comments resulted in a $35,000 fine from the league for “condoning violence.” A month later, Barnes’ reputation made it all the way to hip-hop: I just be like, it was my idea to have an open relationship / Now a n—a mad / Now I’m ’bout to drive 90 miles like Matt Barnes to kill … / 30 hours, Kanye West raps on his track “30 hours” from The Life of Pablo. A shout-out like that certainly meant his legacy as an NBA bad boy had been cemented.

Robin Roberts reports on importance of early detection for black women with breast cancer The ‘Good Morning America’ anchor and cancer survivor teamed up with WebMD to tell stories of survival

In 2007, Good Morning America anchor Robin Roberts conducted a self-exam of her breast after reporting on a friend who had died of cancer.

“It all started a few weeks ago,” she wrote in an email that was shared with the world. “We had gotten the news that our dear colleague and friend Joel Siegel had passed away and we began preparing for our special tribute show for him. I did a piece about Joel’s courageous battle with cancer, reporting on the way my friend had lived his life and been such a successful advocate for the importance of early cancer screenings.”

She found a lump.

Roberts had a biopsy, then surgery, and by January 2008 she’d gone through eight chemotherapy treatments and six weeks of radiation. She later learned she had myelodysplastic syndrome, which is “a disease of the blood and bone marrow and was once known as preleukemia,” Roberts said in a new message posted on the ABC News website.

In 2012, she received a bone marrow transplant from her sister.

Now she has teamed up with the online human health and wellness publication WebMD to help tell stories of early detection, support and bravery. Advanced Breast Cancer: Courage, Comfort and Care with Robin Roberts, a five-part video series, was released in August. The series tells the stories of women with advanced breast cancer, “plus the families and friends who provide encouragement and support, and includes insights from medical experts leading the charge to combat the disease,” WebMD announced.

In one episode, Roberts looks at the effects of breast cancer in the African-American community and promotes the benefits of early detection.

She introduces Felicia Johnson, a Philadelphia woman and two-time cancer survivor who said the disease also attacked her maternal grandmother, her sister and her first cousin. Including Johnson, 11 women over three generations in her family have been diagnosed with cancer.

“It seems like our list just goes on and on,” Johnson says in the episode.

“Felicia’s connection to breast cancer is not unusual,” Roberts reports. “Death rates from breast cancer are higher in the African-American community, and research shows that African-American women are now being diagnosed with breast cancer more frequently.”

Roberts also introduces Lisa Newman, a surgical oncologist and director of the Breast Oncology Program for the Henry Ford Health System in Detroit. Newman says many black women are not getting preventive treatment, so she spends a lot of her time advocating for early detection.

“Every opportunity to get the message out to African-American women regarding breast cancer screening and early detection is critical,” Newman says.

“We completed several series for WebMD on a variety of health subjects, but this series represented a chance for us to take a deep look at the many facets of breast cancer treatment and survivorship,” Roberts told Essence in August.

“From personal experience with the disease, I know there’s a lot of fear associated with breast cancer, especially when a patient is first diagnosed and when the disease has already reached an advanced stage — I also felt the series could help people learn how to better cope with the fear and anxiety, and offer them hope for their future.”

Many minorities still don’t participate in clinical trials, but changing the narrative can save lives Researchers and patients can join forces to change the perception and the numbers

ESPN’s 2017 V Week runs through Dec. 8. During the fundraiser for cancer research, The Undefeated is telling stories about early detection, clinical trial studies and research in minority communities. ESPN hopes to raise funds and awareness about the important cause championed by our friend, coach Jim Valvano. One hundred percent of all cash donations go directly to cancer research. Donate here today.


Fact: According to the U.S. Food and Drug Administration, African-Americans make up about 5 percent of clinical trial participants and Latino Americans constitute 1 percent. As a result, treatments become biased toward whites’ reaction to drugs.

African-Americans are diagnosed with more advanced cancer, and death rates are higher. One way to help combat the issue is to have more people of color participate in clinical trials. But overcoming historical stigma is a big deal for minority populations and is likely one of the most common factors driving the low participation numbers.

For the black community, the clinical trials are reminders of the often negative intersection of ethics, race and medicine that has led to distrust. It is rooted in a history of exploitation of, and experimentation on, African-Americans that ranges from the Tuskegee Syphilis Study to a 19th-century doctor experimenting with gynecological treatments on enslaved women without anesthetics.

No one wants to feel like a big experiment, especially when they’re already sick and trying to fight a disease such as cancer, even if the medical research can lead to better outcomes.

Now more than ever, with the high death rates among black men and women, it’s time to change the narrative. Here are some ways to get the ball rolling:

First, clinicians can go into minority communities and contact community leaders, especially those who may have knowledge of clinical trials. They do exist. Many are even cancer survivors. They can also partner with churches and other agencies in the community, whose opinions are valued.

Next, clinicians can work on a plan to help minority communities gain trust in the health care system. Meanwhile, patients can search for a physician who can be trusted, one who is willing to explain the health care system to them. Another way is to garner the expertise of a health coach, an occupation that’s on the rise in many communities. Health coaches are trained to act as hands-on liaisons between patients and their plan of care. They are found to be more engaged with patients and can often build the trust and compassion between patients and doctors.

Finally, clinicians can lean on public relations professionals to increase communications between them and the community. Clinical trial enrollment barriers include the lack of proper access to health information services, socioeconomic patterns, social perceptions, time spent on travel to office visits and clinics, health literacy and drug side effects (there are many clinical trials that do not involve drug treatments at all). Clinicians and researchers could use help from trained professionals with disseminating studies into cancer communities, especially in communities of color. Cancer research terminology is often not translated for the lay public’s consumption, which is an immediate turnoff for even the most educated. Communication efforts to the public seem distant. Many patients have even expressed that researchers and clinicians should consider eliminating the term “clinical trials” altogether and use wording that is more patient-friendly and not pegged to a history of traumatic events.

In a 2014 article, Janet Stemwedel, associate professor of philosophy at San Jose State University, who studies ethics and scientific processes, was asked what steps have been taken by clinicians to dispel concerns of minority populations and she replied, “I can’t think of any positive trust-earning step that was taken, off the top of my head.”

Despite the low efforts, or those that haven’t properly traveled from the peer base to the community base, dollars from places such as the Stuart Scott Memorial Cancer Research Fund, formed by The V Foundation and family members representing Stuart Scott, have pitched in to help. This fund is dedicated to help minority researchers fight cancer in minority communities. It continues to advance Scott’s fight against cancer and assist some of the most vulnerable and disproportionately affected communities battling the disease.

Scott himself participated in a clinical trial study. He believed attitudes, beliefs and perceptions can change the thought pattern.

“Our father got seven years after he was diagnosed with cancer, and that is seven years we may not have had,” his oldest daughter, Taelor Scott, told The Undefeated.

Dr. Edward Kim, a lung cancer expert clinician, chairman of Solid Tumor Oncology and Investigational Therapeutics at Levine Cancer Institute in Charlotte, North Carolina, and a recipient of the Stuart Scott Memorial Cancer Research Fund, conducts a clinical trial on blood markers dealing with lung cancer.

“I think it’s still something that health care professionals, different support groups and education need to occur so that folks can understand what the opportunities are, and what’s the benefit for them,” he said. “I’m not saying that everybody should be on clinical trials, and every clinical trial can be a little different, but it is a way where we make progress. We can’t get a new drug unless we have a clinical trial. That’s what leads us to the next study, and the next study. I’m a strong advocate for people to be on clinical trials. I feel like we need more clinical trials out there. You find the right biomarker and identify the patient that’s going to benefit, that drug works really well.”

There are organizations that host clinical trial outreach campaigns and programs such as the federal Department of Health and Human Services’ Office of Minority Health, which can be a great resource for patients.

It’s Cancer Screen Week, and getting tested could help save your life Five reasons early detection is important

ESPN’s 2017 V Week runs through Dec. 8. During the fundraiser for cancer research, The Undefeated is telling stories about early detection, clinical trial studies and research in minority communities. ESPN hopes to raise funds and awareness about the important cause championed by our friend, coach Jim Valvano. One hundred percent of all cash donations go directly to cancer research. Donate here today.


Besides V Week, it’s also Cancer Screen Week. According to the World Health Organization, 8.8 million people die from cancer worldwide and African-Americans have a higher death rate than other groups.

Over the past three years there have been more and more studies questioning whether early detection and cancer screenings actually save lives. But don’t tell that to the millions of survivors who got their cancer diagnosis early and are sharing their stories.

For instance, NFL wife and Greenville, South Carolina, native Niya Brown Matthews is a two-time cancer survivor who received her first diagnosis of stage 2 cancer in her left breast when she was just 27.

Matthews said she had no symptoms. She completed a breast self-examination in the shower and felt a knot under her arm. She underwent a lumpectomy and endured several rounds of radiation.

“When it came back in the second breast, I opted to get that one cut off and just rebuild,” Matthews said.

Now cancer-free, she is a cheerleader for early detection.

According to the National Cancer Institute, in 2016 an estimated 1,685,210 new cases of cancer were expected to be diagnosed in the United States and 595,690 people would die from the disease.

Despite the debate over cancer screenings, here are five reasons that they are important, especially in communities of color.

Early detection can help get an early start on fighting cancer.

Screening tests can help determine whether and when a treatment works best. It also determines specific precursors of genes or family history and in its early stages can reduce death rates.

Early detection may extend your life expectancy.

Early detection may mean remission for many, but it can also mean more years with your loved ones. Screenings can place you on a path to a proper treatment plan, which can extend longevity.

You can beat cancer.

Screening tests can find precancerous cells that can be removed before they turn into cancer. Cancers of the colon, rectum and cervix can be prevented through screening and can oftentimes detect cancer before symptoms appear.

Screening can prompt patients to lead a healthy lifestyle.

Some early detection includes conversations regarding family history, which can lead to testing for genes that may determine whether you are at risk for specific cancers. Knowing your risk factors can spark a healthy lifestyle that may help combat certain precursors.

Screening can cut down on health care costs.

Early detection can also cut the cost of treatment. In 2010, the total annual economic cost of cancer through health care expenditure and loss of productivity was $1.16 trillion. According to WHO, studies have shown that treatment for early diagnoses are less expensive than treating patients at advanced stages.

This couple shares 47 years, beat cancer twice and are now stealing hearts in these photos Meet the Brewingtons. Their photographer daughter posted their anniversary pics and they’ve gone viral.

When photographer Amber Robinson posted photos of her parents on her company Facebook page and on Instagram last week commemorating their 47th wedding anniversary, she didn’t think it would become a poster moment for the hashtag #relationship goals, but that’s what happened.

Those six photos unfolded a love story that proves the traditional wedding ceremony vows for “in sickness and in health” are real.

“In this wonderful creative industry that I worked in, I focus so much on providing couple hours with a day of beautiful photography,” Robinson posted. “To be honest, rarely do I stop to think about the day, weeks, months or years that follow a wedding day.

“So today I share with you what those years after can look like when true love exists. These are my parents: married for 47 years, they have triumphed over cancer … twice. Have raised two successful daughters. They have been poor together and rich together. They have fed, sheltered, and advised countless lost souls. They love with out expectation and give freely, whatever it is they have to offer.

“I am SO proud to call them Mom and Dad. They are the epitome of where I strive to be in my own marriage and a constant reminder that a wedding is only a day, but a marriage is forever.”

Robinson’s mother, Wanda Brewington, is 67. Her dad, Marvin, is 70. The couple recently shared their secrets of love with Essence, and they include “honesty and communication, never going to bed upset, and finding a way to compliment your partner.”

The two met at Livingston College in Salisbury, North Carolina, and were married in 1970 in Wanda Brewington’s hometown of Wilkesboro. Marvin Brewington was diagnosed with multiple sclerosis in 1973 and with colon cancer in 1987. In 2013, he’d learn he was living with prostate cancer, and that same year Wanda Brewington was diagnosed with Parkinson’s disease.

The two told Essence that their “love for each other and faith in God” was the bond that helped them through their health problems. “We made a vow on our wedding day, through sickness and health, and have always been determined that we can and will overcome anything. On the days that one of us is down, the other one picks us up.”

Robinson, a mother of four, lives in Raleigh, North Carolina. She recently told Yahoo! Lifestyle that growing up, she thought “it was disgusting to see our parents hug and kiss so much. But now, as a married woman, I understand.

“But we also grew up with a realistic version of love — my dad has multiple sclerosis and survived prostate cancer twice, and he leaned on my mom for support.”

Instagram Photo

 

These two athletes are thankful to be cancer-free after treatment at St. Jude’s Meet Nicholas London and Kane Hogan as they share their journeys

During the holidays, St. Jude Children’s Research Hospital makes an even stronger effort to make sure that “kids still get to be kids, even while undergoing treatment. The mission and history of St. Jude is to advance cures, and means of prevention, for pediatric catastrophic diseases through research and treatment. Treatments invented at St. Jude have helped push the overall childhood cancer survival rate from 20% to more than 80% since it opened more than 50 years ago.”

Families who travel there from near and far for treatment still celebrate the holidays, maintaining some of their old traditions as best as they can in a new environment.

Two teens are familiar with the atmosphere at St. Jude, and this holiday season they are thankful for the loving “familylike” atmosphere they received and the gift of life they now have. St. Jude stands on the proclamation that they are “leading the way the world understands, treats and defeats childhood cancer and other life-threatening diseases,” according to its website.

Nicholas London is thankful for life. It’s the holiday season. Most teenagers are shopping, gifting or making their lists. But the 18-year-old high school shooting guard is getting his body stronger. He’s beaten cancer. And he’s ready to get back on the court.

London was diagnosed with acute lymphoblastic leukemia (ALL), a type of blood cancer, in 2014. It is the most common form of childhood cancer. He was in treatment at St. Jude Children’s, where the world-renowned treatment center has increased the survival rates for acute lymphoblastic leukemia from 4 percent in 1962 to 94 percent today.

The 6-foot-6 standout basketball star was just 14 when he started treatment at St. Jude. His father, Paris London, was a powerful basketball player at the University of Memphis. He noticed Nicholas, known by his friends and family as Nick, was struggling to catch up during Rockets point guard Chris Paul’s basketball camp they’d attended at Wake Forest University in 2014. Nicholas, the second-oldest child of Paris and Tangela London, was also complaining of a stomachache and grew tired fairly quickly when on the basketball court or just doing household chores. The Londons have five sons and two daughters.

The couple took their son to see his pediatrician on Aug. 4 of that year, and he was immediately sent to St. Jude for treatment, which he underwent until March. Now cancer-free, London reflects on his time in treatment.

“You would think it would be kind of rough, being away from home at Christmas,” London said. “I was at St. Jude for my birthday and Thanksgiving. The crew made me feel really at home. They gave me whatever I wanted. They were always there for my needs and really had conversations with me as if they were my family.”

London has also turned to music as a new way coping with overcoming cancer. He has performed his song about being a patient at St. Jude in front of more than 1,200 St. Jude employees and at a Miami gala, and he is working on his album release.

“I actually got started with music by going through treatment,” London said. “I was going through a rough patch, and I went to one of these events with one of my friends that used to go to St. Jude. They put on a beat and I actually started freestyling to it, and the teacher decided I could do a song for the upcoming St. Jude talent show. I did it and the people really enjoyed it. I came to find out that it really helped me get a lot of stuff off my chest that I was feeling. That’s kind of how I got into music, and now I’m getting ready to get an album together that details my journey through St. Jude and how they helped me.”

London said his first love is basketball. He picked up a ball when he was just 7 years old and remembers practicing with his father, who, with his mom and siblings, has been very active in his progress as an athlete and on his road to healing.

“I really enjoyed playing basketball, and the cancer came and really took that away from me. I want people to know how hard I had to work to get back and how St. Jude really gave me that opportunity. Without them being there, I wouldn’t have made it. I wouldn’t have been able to get back to what I love, but also finding another love, and that was my music.”

His album is titled United 14.

“The reason we came up with 14 is because I was diagnosed in 2014, I was 14 years old and I wore the same jersey No. 14 as my pops.”

For other children going through treatment, London wants them to keep the faith.

“Keep your trust in God, because it’s a hard journey. It is. But going through St. Jude and through my experience, I can say that they really made me feel like it was something that we all went through together. It made it feel like they were my family and they were fighting for me no matter what. Just keep faith in God, because it’s going to be hard days, but it’s going to be better days ahead.”


Courtesy St. Jude Children’s Research Hospital

Consistent with the vision of St. Jude’s founder Danny Thomas, no child is denied treatment based on race, religion or a family’s ability to pay.

Families never receive a bill from St. Jude for treatment, travel, housing or food — because all a family should worry about is helping their child live. The facility has treated children from all 50 states and from around the world.

Fifteen-year-old Kane Hogan was traveling back and forth between Memphis, Tennessee, and Huntsville, Alabama, to get treatment once a week. His travel decreased as time went on. Kane, whose very first word was “ball,” loves sports. He’s played basketball, baseball and football, which all came to a halt in January 2015 when he found himself tired and lacking energy. He slept all the time, and he couldn’t keep up in practice.

After he was initially being treated for a sinus infection, a blood test revealed Kane suffered from acute lymphoblastic leukemia, the same diagnosis as London. Kane, who lived in Alabama, was transported by ambulance to St. Jude for treatment.

“It was very tiring going back and forth, but St. Jude’s an amazing place, and they make it as easy as they can on us and without them it’d been a whole lot worse than it was,” Kane said.

Kane’s treatment included 2½ years of chemotherapy, which he recently finished. The end of his treatment coincided with the beginning of Kane’s senior year in high school, and three days before his first football game of this season. This holiday season he will be spending time with his family and his girlfriend’s family. Family, he said, is what he’s most thankful for.

“After I was diagnosed, it changed the whole meaning of it [the holiday season],” Hogan said. “It gave me a whole new perspective and just being thankful for St. Jude, and for my community, and just being thankful to be alive. It’s just amazing.”

Hogan’s advice to other children spending time at St. Jude during the holiday season is to “keep their heads up, because it’s just hard, but having that positive attitude about everything helps a lot. You wouldn’t think it would, but it helps you. St. Jude is a wonderful place. They understand that you not getting to go home is not very happy, but they make it as good as they can there.”

‘My Cause My Cleats’: The top 24 Week 13 customs — and why players wore them Reppin’ everything from the American Cancer Society to the Trayvon Martin Foundation to Kaepernick

Week 13 in the National Football League, at least since last season, is all about creativity, customization and cause. Through the “My Cause My Cleats” campaign, which the league started in 2016, players can bend uniform guidelines and wear cleats designed to represent a cause of their choice.

Typically, players are only allowed to wear custom-painted kicks during pregame warm-ups. Then switch to uniform footwear while the game clock is rolling. But in Week 13, flashy cleats in vibrant colors, featuring unique illustrations and messages, are the norm. Athletes all across the NFL, from every position group, commission the hottest designers in the sneaker game to create the perfect pair of cleats for their cause. This year, around 1,000 players reportedly took part in the initiative, and after games ended, select cleats were sold at auction, with 100 percent of the proceeds benefiting causes such as the #BringBackOurGirls campaign, Colin Kaepernick’s #KnowYourRightsCamp, Habitat for Humanity, autism, POW and MIA families, anti-bullying, social justice and criminal justice reform, the Trayvon Martin Foundation and more.

“This weekend, you’ll really see the impact art has had on the NFL,” Los Angeles artist Troy Cole, aka Kickasso, tweeted before Sunday’s games. Last season, he designed every pair of New York Giants wide receiver Odell Beckham Jr.’s anticipated pregame cleats. “Art is a powerful way to tell a story #MyCauseMyCleats.”

Here are The Undefeated’s top 24 “My Cause My Cleats” customs, along with the players who wore them, the causes they supported and the artistic geniuses who brought charitable creativity to life.


Chidobe Awuzie, Cornerback, Dallas Cowboys

Cause: #BringBackOurGirls campaign

Joe Barksdale, Offensive Tackle, Los Angeles Chargers

Instagram Photo

Cause: Fender Music Foundation

Designer: DeJesus Custom Footwear Inc.

Michael Bennett, Defensive End, Seattle Seahawks

Cause: National League of POW/MIA Families

A.J. Bouye, Cornerback, Jacksonville Jaguars

Cause: American Cancer Society

Designer: Kickasso

Antonio Brown, Wide Receiver, Pittsburgh Steelers

Instagram Photo

Cause: RAINN (Rape, Abuse & Incest National Network)

Designer: Corey Pane

Kurt Coleman, Safety, Carolina Panthers

Cause: Levine Children’s Hospital

Designer: Ryan Bare, SR Customs

Mike Daniels, defensive end, Green Bay Packers

Cause: Anti-bullying

Designer: SolesBySir

Stefon Diggs, Wide Receiver, Minnesota Vikings

Cause: American Heart Association

Designer: Mache Customs

DeSean Jackson, Wide Receiver, Tampa Bay Buccaneers

Instagram Photo

Cause: Brotherhood Crusade

Designer: SolesBySir

Malcolm Jenkins, Safety, Philadelphia Eagles

Cause: Social Justice and Criminal Justice Reform, Players Coalition

Designer: Sixth-grade class at Jubilee School, Illustrative Cre8ions

Eddie Lacy, Running Back, Seattle Seahawks

Cause: International Relief Teams, Hurricane Katrina

Designer: Bizon Customs

Jarvis Landry, Wide Receiver, Miami Dolphins

Instagram Photo

Cause: Cystic Fibrosis Foundation

Marshon Lattimore, Cornerback, New Orleans Saints

Cause: Social injustices and honoring close friend Dayton Williams, who was shot and killed in 2010 in Euclid, Ohio.

Rishard Matthews, Wide Receiver, Tennessee Titans

Instagram Photo

Cause: Colin Kaepernick, Know Your Rights Camp

Designer: SolesBySir

Gerald McCoy, Defensive Tackle, Tampa Bay buccaneers

Instagram Photo

Cause: “The Life of a Single Mom”

Designer: The Hulfish Project

Eric Reid, Safety, San Francisco 49ers

Cause: Colin Kaepernick, Know Your Rights Camp

Designer: Tragik MCMXCIII

A’shawn Robinson, Defensive Tackle, Detroit Lions

Cause: Leukemia patients

Jaylon Smith, Linebacker, Dallas Cowboys

Cause: Autism

Designer: The Hulfish Project

Torrey Smith, Wide Receiver, Philadelphia Eagles

Instagram Photo

Cause: Torrey Smith Family Fund, Show Your Soft Side, Players Coalition, NO More Campaign

Designer: Kreative Custom Kicks, Dez Customz

Shane Vereen, Running Back, New York Giants

Cause: Children’s Hospital of Los Angeles

Designer: Kickasso

Anthony Walker, Linebacker, Indianapolis Colts

Cause: Trayvon Martin Foundation

Designer: Desmond J. Jones, Art is Dope

Deshaun Watson, Quarterback, Houston Texans

Cause: Habitat for Humanity

Designer: 5-year-old twins Kayla and Jakwan; Evan Melnyk, Nike

Russell Wilson, Quarterback, Seattle Seahawks

Cause: Why Not You Foundation

Designer: Kate Neckel and Dash Tsai

 

Daryl Worley, Cornerback, Carolina Panthers

Instagram Photo

Cause: CeaseFirePA

Designer: SR Customs

Dr. Edward Kim is helping lung cancer patients with a Stuart Scott grant North Carolina researcher knows early detection and clinical trials can save lives

Tuesday marked the start of ESPN’s 2017 V Week. During the fundraiser for cancer research, The Undefeated will tell stories about early detection, clinical trials and research in minority communities. ESPN hopes to raise funds and awareness about the important cause championed by our friend, coach Jim Valvano. One hundred percent of all cash donations go directly to cancer research. Donate here today.


No one in Edward Kim’s family was in the medical field. His father was a finance professor and his mother was an artist, but he knew he always wanted to be a doctor. After finishing a seven-year medical program at Northwestern University, he thought he wanted to become a cardiologist, or maybe a surgeon. But he ended up in internal medicine.

“Internal medicine is one of those fields where you go there because you need to buy more time,” Kim said. “I knew I liked medicine, and I thought I would be in a teaching institution down the road. That’s what I really liked. My father was a teacher, and I really enjoy that education part.”

He started his residency in Houston at Baylor College of Medicine. In the fourth month, he was in an oncology rotation.

“After that month, it changed everything inside of me,” Kim said. “I really appreciated the patients and how their perspective was fighting this type of disease. Cancer is still one of the diagnoses that resonates very differently than most other diagnoses. It just brings a whole different connotation to it than just spending an extra couple minutes with a patient with cancer. They get it. That’s what really turned inside of me.”

Now Kim is chairman of Solid Tumor Oncology and Investigational Therapeutics at Levine Cancer Institute in Charlotte, North Carolina. And he has received grant money from the V Foundation’s Stuart Scott Memorial Cancer Research Fund, which allocates dollars to minority researchers to fight cancer in minority communities. The fund helps to continue Scott’s fight against cancer and assist some of the most vulnerable and disproportionately affected communities battling the disease.

“We’re very excited about being part of the V Foundation,” Kim said. “We’re very excited to bring this type of research to our patients.”

Kim’s research under the grant involves collecting information to try to develop a blood-based test that will help determine which patients being treated with an immunotherapy drug will receive the best benefit.

“That will hopefully help us refine treatment for those patients, not overtreat patients, or perhaps treat them adequately so they don’t need to continue treatment if their blood marker status looks good,” Kim said. “It’s still in the very early stages. We have a scientist here who has developed a blood marker, and that’s what we’re going to try. I think the scientific community sees the need of trying to identify those patients at highest risk, or who may benefit the most, or those who may not benefit so much.”

The V Foundation has awarded more than $7 million from the Stuart Scott Memorial Cancer Research Fund. The groundbreaking minority cancer research initiative funds outstanding minority researchers and research that explores the biology behind why some cancers are more likely to occur, are more aggressive or are harder to treat in some minority populations. Nineteen grants have been awarded since the fund was started in 2015.

Before joining the Levine Cancer Institute, Kim landed a fellowship across the street from Baylor at the MD Anderson Cancer Center, where he gravitated toward lung cancer and head/neck cancer patients. This opportunity led to his current research.

“Tobacco-related cancers, and how to prevent them, was a lot of my research there,” Kim said. “They asked me to stay on staff and faculty there. I stayed there, and I was there for 12 years, tenured and doing very well.”

Five years ago, he took the position at Levine because he was captivated by its vision to deliver regionally based health care. He began as a cancer care expert treating patients with lung cancer.

“Over the years, I’ve done a lot of research with treatments, prevention, cancer markers in lung cancer,” he said. “It’s naturally evolved to what we’re doing here in Charlotte, and really in the Carolinas, because we are so regionally spread that we had an opportunity to compete for V Foundation grants.”

Kim was part of a V Foundation grant in Houston.

“You have to have a strong team, a strong bench, to succeed or even really battle,” Kim said. “That’s what we’ve put together here.”

Kim said the unique aspect of their patient population in the Carolinas is that they’re on the front lines.

“Part of the attraction of leaving a great center like MD Anderson is that the patients you see there are all usually very well-educated, they have the means to travel or the savvy to travel to a top-notch cancer center, whether that be New York, Boston, Houston,” he said. “But the majority of patients treated out there, 85 percent of them, are seen in the community. That is what our system is structured around. We see patients who don’t know about clinical trials, who don’t know about the cutting-edge therapies. This is an opportunity to try and test, not only have them participate in this type of study, but also keep them informed of these types of things that are going on.”

It has been well-documented, especially in recent research, that minorities respond differently to medical and pharmaceutical treatment. So it’s important to Kim that he has a diverse population of patients.

“We know that there are characteristics that are different in each individual patient,” Kim said. “I’m Asian. We know that some drugs work better in patients who are Asian than others. We know that this is different among Hispanics, Caucasians and African-Americans. That is one of our primary objectives, to make sure we have cohorts of different ethnic subgroups to look at those differences. There’s also a big cultural aspect. Each culture is very different. I’m not even talking about whether you grew up in the North, or the South, or the East, or the West, or Indiana versus Tennessee. The cultural aspect of perception of clinical trials, experimental therapy, has a very checkered history among different groups.”

Near the end of his life, Scott participated in a clinical trial study. Socially disadvantaged and racial/ethnic minority groups have been historically underrepresented in clinical research. Lack of African-American participation in clinical trials stems from distrust historically, most notably with the Tuskegee Syphilis Study (1932-72). Earlier this year, the story of Henrietta Lacks and her stolen cells was made into a movie. The convoluted history of medical experimentation on African-Americans in the United States, along with many other structural factors, plays a huge part in the lack of participation by the black community.

“Part of what we are trying to overcome is that participation in these trials really doesn’t do any harm because we’re not giving experimental drugs or anything,” Kim said. “We’re collecting extra blood, blood that normally would be tested for standard lab values, to try and learn from them, learn from their experience, and hopefully can benefit someone down the road. That’s how research is. It really is an altruism where you’re trying to get some benefits now, but you’re hopefully benefiting those down the road.”

Like Scott, Kim has a vision that includes increasing early detection and participation from minority groups in clinical trials.

“I think it’s still something that health care professionals, different support groups and education need to occur so that folks can understand what the opportunities are, and what’s the benefit for them,” he said. “I’m not saying that everybody should be on clinical trials, and every clinical trial can be a little different, but it is a way where we make progress. We can’t get a new drug unless we have a clinical trial. That’s what leads us to the next study, and the next study. I’m a strong advocate for people to be on clinical trials. I feel like we need more clinical trials out there. You find the right biomarker and identify the patient that’s going to benefit, that drug works really well.”

For early detection, Kim is an advocate for identifying at-risk populations to try to intervene and prevent cancers.

“It’s great that there is a CT screening exam now for people who are heavy smokers, that are at high risk for developing lung cancer,” Kim explained. “That study finally was positive, and now Medicare reimburses.”

Besides his study with the V Foundation grant, Kim and his team have built a mobile lung cancer screening unit that’s called the lung bus, a project at the Levine Cancer Institute spearheaded by his boss.

“Just like you see these mammograms on these buses driving around and stuff? Well, we did it with a CT screener. Since April this past year, we go to underserved communities in North Carolina and offer free CT screening to them. These are people who would not have sought out this treatment.”

More funding means more research. More research means more lives saved. Join our campaign to raise $200 million by 2020. You can contribute by visiting this link: www.jimmyv.org/stuartscott.

‘Don’t Ever Give Up’: ESPN takes the fight against cancer to the gaming world Marc Spears, Domonique Foxworth join gamers around the world in the fight against cancer

Can gamers help cure cancer?

On Giving Tuesday, The Undefeated and ESPN are teaming up with Twitch to use esports and gaming to drive awareness of cancer research. For ESPN’s Don’t Ever Give Up Day, Marc Spears and Domonique Foxworth join Jared Jeffries, David Jacoby, Rachel Nichols, Marcellus Wiley and LZ Granderson for a 24-hour gaming stream charity benefit for the V Foundation.

Cancer affects all communities, but African-American outcomes tell a grim story about racial divides. According to the American Cancer Society, “in 2012, the death rate for all cancers combined was 24 percent higher in black men and 14 percent higher in black women than in white men and women, respectively.” With 1 in 2 African-American men and 1 in 3 African-American women expected to be diagnosed with cancer in their lifetime, the lack of consistent funds for research is fueling a health crisis in the African-American community.

Watch live video from ESPN Esports on www.twitch.tv

Cancer has claimed the lives of millions of people around the world, including beloved ESPN anchors Jimmy Valvano and Stuart Scott. While their lives were cut tragically short, their legacies live on. Since 1993, the V Foundation has funded more than $200 million in cancer research grants nationwide. It awards 100 percent of all direct cash donations to cancer research and related programs.

Join Spears and Foxworth on Twitch from 6-10 p.m. PST: https://www.twitch.tv/espnesports

And check back here for the best clips and takes from an unforgettable evening.

Want to help? You can donate directly to the Jimmy V Foundation here or through our Twitch Channel here.

The V Foundation is helping fund cancer research in the black community Fund in memory of Stuart Scott focuses on poor survival rates among African-Americans

Tuesday marks the start of ESPN’s 2017 V Week. During the fundraiser for cancer research, The Undefeated will tell stories about early detection, clinical trial studies and research in minority communities. ESPN hopes to raise funds and awareness about the important cause championed by our friend, coach Jim Valvano. One hundred percent of all cash donations go directly to cancer research. Donate here today.


“Don’t give up … don’t ever give up.” These words were a staple for North Carolina State’s legendary basketball coach and ESPN commentator Jimmy Valvano. The V Foundation, formed in 1993 by ESPN and Valvano, raises money for cancer research. A huge part of the foundation’s mission is to build more opportunities for cancer research in minority communities.

There are more than 15.5 million cancer survivors today. Survival rates for many cancers continue to increase. New technology and a better understanding of genetics have allowed doctors to create individualized therapies, leading to more success. But according to the American Cancer Society, African-Americans have the highest death rate and shortest survival of any racial/ethnic group in the U.S. for most cancers.

According to the U.S. Centers for Disease Control and Prevention’s most recent data, black men have the highest cancer incidence rates, and black men and women both have a higher cancer death rate than their white counterparts. Cancer is the leading cause of death among Hispanics, accounting for 21 percent of deaths overall and 15 percent of deaths in children.

To combat the problem, the V Foundation, through the Stuart Scott Memorial Cancer Research Fund, is allocating dollars to minority researchers to fight cancer in minority communities. The funds will help continue Scott’s fight against cancer and assist some of the most vulnerable and disproportionately affected communities battling the disease.

The Stuart Scott Memorial Cancer Research Fund was formed by the V Foundation and Scott’s family. Near the end of his life, Scott participated in a clinical trial. He was a passionate voice for improving outcomes for African-Americans and other minorities with cancer. The Scott Fund supports research designed to discover why some cancers are more aggressive and more fatal in African-Americans.

“It was not lost on Stuart that his diligence and education about cancer research helped extend his life,” said Susan Scott, Stuart Scott’s sister. “Stuart’s passion for education was unmatched. He researched every aspect of his treatment to live with and beat cancer. His research revealed cancer’s disparities and the inequities faced in the African-American and Hispanic cancer-fighting communities. I know that he would be proud that the V Foundation is setting up this fund in his name to accelerate research for all communities.”

Since its start, the V Foundation has granted more than $200 million nationwide and has become one of the premier supporters of cutting-edge research. Because of generous donors, the foundation has an endowment that covers administrative expenses so it can award 100 percent of all direct cash donations.

The V Foundation is committed to raising another $200 million between 2013 and 2020.

“Cancer is more than 100 individual diseases,” said Susan Braun, CEO of the V Foundation. “As research accelerates our knowledge, we recognize how varied each individual cancer is and how the same type of cancer can vary among different people. Many cancers pose more of a problem in different ethnic groups, and cancer overall affects diverse populations in complex ways.

“We also know that innovation happens with diversity of thought. Funding V Scholars, the brightest minds in cancer research, through supporting people who are part of disproportionately affected communities can make research stronger.”

A dedicated friend of the V Foundation and a committed participant in the Jimmy V Celebrity Golf Classic and other foundation events, Scott helped raise funds and awareness for the V Foundation for more than 20 years. Scott was first diagnosed with cancer in 2007. From that moment, sports fans, his peers and athletes from around the world supported him in his battle.

The V Foundation has a page on its website, www.jimmyv.org/stuartscott, for donations to the Stuart Scott Memorial Cancer Research Fund. ESPN made an initial $100,000 donation in his memory.

“Stuart inspired others by how courageously he battled cancer,” said ESPN president John Skipper. “He and I talked about this horrible disease and opportunities he saw to expand the scope of research being done. He was taken from us way too young, and given what he stood for and what he clearly meant to so many, this fund is a fitting way to honor his legacy and significantly add to what he did so valiantly — fight cancer.”

More funding means more research. More research means more lives saved. Join us in our campaign to raise $200 million by 2020 and donate today. You can contribute by visiting this link: www.jimmyv.org/stuartscott.