The Mark White Show

On this Make a Difference Minute, I have Wes Madrigal as he shares about the effort he and his family have started to help people in Manizales, Colombia, following a devastating 7.4 magnitude earthquake. Wes lives in Colombia with his wife, who is from the area, and their recently born daughter. Although the epicenter of the earthquake was roughly 100 miles away, Wes says the shaking was strongly felt in Manizales. When he went into the city afterward, he quickly realized the extent of the damage. Buildings had collapsed, the city's iconic cathedral suffered significant structural damage, and members of his wife's extended family and several of her friends experienced damage to their homes. While Wes says no one his family personally knows had been physically injured at the time of our conversation, lives have been lost and families are facing the reality of rebuilding. That challenge is made even greater because, according to what Wes has learned locally, many people do not have the type of homeowners insurance that could help them recover from a disaster like this. Wes and his family are now doing what they can to help their neighbors through the difficult days ahead. If you would like to support their effort, go to GiveSendGo.com and search Manizales Colombia Earthquake. This Make a Difference Minute is brought to you by Athens Bible School, proudly supporting stories and the people who make our communities strong. Real stories. Real people. Real impact. News That Unites!™️

Tonight on The Mark White Show! On the first two segments, I'll be talking with Maximo “Max” Villagomez at Gabriela's Latin Fusion in Athens, Alabama. Born and raised in the South American country of Ecuador, Max has brought the flavors of Latin America to North Alabama in a big way! We'll talk about his journey from Ecuador, the story behind Gabriela's Latin Fusion, and what it means to build a business and become part of the community here in North Alabama. After that, in the Mary Faye Headrick Good Deed Segment, we'll travel to Colombia, Ecuador's neighbor, where I'll be talking with Wes Madrigal following the powerful 7.4 magnitude earthquake that struck the region yesterday. Wes, his wife, and their baby daughter are in Manizales, Colombia, where they have a coffee farm. Thankfully, his family is safe and their home is intact, but others in the community have not been as fortunate. Friends and family have lost their homes, and Wes is organizing an effort to help provide food, temporary shelter, rebuilding assistance, and support for a local animal shelter. Real stories. Real people. Real impact. News That Unites!™️

On this Make a Difference Minute, I have Holly Parrish as she shares about her four-year-old daughter, Ruthee, who lives with Kabuki syndrome and needs specialized care that has been difficult to access. For Holly, one of the biggest needs right now is finding people who have already walked a similar road and can help point her toward the next step. She has closely followed Jessica Davenport and the Kruzn for a Kure Foundation, watching how Jessica Davenport has advocated for Kruz and Paizlee, pursued specialized care, raised money for research, and kept pushing when the answers were far from home. Holly says she found herself taking notes and treating Jessica's efforts almost like a roadmap for what she may eventually have to do for Ruthee. That's why hearing from another parent who has successfully navigated Medicaid denials, waivers, exceptions, or other barriers for a medically complex child could be so valuable right now. If you believe you may be able to help Holly and Ruthee, you can email Holly at HollyGraceParrish@gmail.com. This Make a Difference Minute is brought to you by Green's Dependable Hardware, proudly supporting stories and the people who make our communities strong. Real stories. Real people. Real impact. News That Unites!™️

Tonight, you're going to meet a little girl who has been fighting since the day she entered this world. Ruthee was born weighing just 1 pound, 6 ounces. She spent 284 days in the NICU, and there were times her mom, Holly, didn't know if her little girl was going to survive. Today, Ruthee, who is a twin, is four years old and living with Kabuki syndrome, a rare genetic condition that has affected multiple areas of her life. Ruthee is nonverbal, has faced liver issues, is legally blind and continues working incredibly hard toward walking independently. Beside her is her twin sister, doing many of the things Ruthee is fighting every day to be able to do. Right now, Holly is fighting for specialized care for her daughter. Ruthee was referred to Kabuki specialists in Philadelphia and Cincinnati. After months of Holly, doctors and social workers working to get everything Medicaid required for the Philadelphia visit, the appointment was supposed to happen this Thursday, August 13th. Holly had to cancel it. As of today, she says the request had still not been approved or denied. Holly believes specialized care could provide something she desperately needs, care plan specifically designed around Ruthee, where she falls on the Kabuki spectrum and the challenges she faces. During our conversation, Holly said, “I refuse to tell her there's nothing else we can do. I refuse.” Tonight, you'll hear this mother tell her daughter's story herself. This family isn't asking for money. They're looking for connections, information & someone who may know how to help them navigate the system. Maybe you know a rare-disease advocate or you understand Medicaid appeals, waivers or exceptions. Maybe you work with medically complex children, know a Kabuki specialist, or you're another parent who has traveled a similar road. If you don't fit in any of those categories, what you can do is listen and share Ruthee's story until it reaches the person who can help. As we have seen so many times before, one connection can change everything. Let's help Holly find the right door for Ruthee! Real stories. Real people. Real impact. News That Unites!™️

On this Make A Difference Minute, I have Ashley Russell of Athens, Alabama, sharing how small acts of kindness have helped carry her through cancer treatments and chemotherapy. When people hear about a cancer diagnosis, they often wonder what they can do to help. Ashley's answer is that it's the little things matter. A surprise package in the mail filled with items to help during chemotherapy. A bag prepared by friends with snacks, blankets, fuzzy socks, and comfort items. Head wraps given with love after losing her hair. Help with her child when she needed support. None of these acts could take away the diagnosis, but each one reminded Ashley that she wasn't facing the journey alone. Sometimes encouragement doesn't have to be grand or expensive. A thoughtful gesture, a helping hand, or simply showing up can make a difficult day a little easier. This MADM is brought to you by Bama Estate Planning by Attorney Harlan D. Mitchell, proudly supporting stories and the people who make our communities strong. Real stories. Real people. Real impact. News That Unites!™️

On this MADM, Julie Garner is sharing about Project Yellow Light as they seek to educate everyone on distracted driving. This Make a Difference Minute is brought to you by Bankston Motor Homes, proudly supporting stories and the people who make our communities strong. Real stories. Real people. Real impact. News That Unites!™️

On this Make a Difference Minute, I have Mrs. Alabama 2025 Brianna Sistrunk as she shares about Chasing the Rainbows, an organization supporting families experiencing infertility, miscarriage, pregnancy loss, and infant loss. For Brianna, the mission is deeply personal. After losing her daughter Madison, she eventually began sharing her experience through a series of videos on YouTube. Her goal was simply to help other women who had experienced a similar loss. After that, women she had never met began reaching out. Some found her through YouTube and then searched for her on social media. Others were friends who knew her story and felt comfortable turning to her after experiencing a miscarriage of their own. Brianna began that series in 2016. Ten years later, women are still finding those videos and reaching out to tell her, “I've been through this too.” It's a powerful reminder of what can happen when we're willing to share the difficult parts of our stories. Something you experienced years ago may become exactly what another person needs to hear today. To learn more about Chasing the Rainbows and its work supporting families through infertility and pregnancy and infant loss, visit ChasingTheRainbows.org. This Make a Difference Minute is brought to you by Hydration Lounge, proudly supporting stories and the people who make our communities strong. Real stories. Real people. Real impact. News That Unites!™️

Tonight, I'm joined by Brianna Sistrunk, Alabama State Ambassador for Chasing the Rainbows. For Brianna, this work is personal. In 2015, Brianna was 19 weeks pregnant when she lost her daughter, Madison. A year later, she experienced an ectopic pregnancy. Those losses became part of her story and, over time, part of her desire to help other families walking through infertility, miscarriage, pregnancy loss, & infant loss. Tonight, Brianna will share Madison's story, her own journey through grief, and why she has chosen to use her voice to help others know they're not alone. We'll also talk about her new role as Alabama State Ambassador for Chasing the Rainbows and the effort to connect families across our state with support, resources, and others who understand. Real stories. Real people. Real impact. News That Unites!™️

On this Make a Difference Minute, I have Johnny Owens, son of country music legend Buck Owens, as he reflects on his father's life, music, and the legacy he left behind. For Johnny, one word captures much of what mattered to his father: true. Buck Owens helped define the Bakersfield Sound, bringing a distinctive California edge to country music while remaining committed to what he believed country music should be. Johnny says his father appreciated many different kinds of music, but staying true to country remained at the heart of his work. That influence stretched far beyond Bakersfield. Buck's recording of “Act Naturally” became a country classic, and The Beatles later recorded the song with Ringo Starr singing lead, introducing it to another enormous audience. Decades later, Johnny still sees his father's influence in the music people are discovering, streaming, and making today. Songs like “Made in Japan” continue to connect with listeners and inspire artists who came long after Buck first recorded them. For Johnny, that's an important part of his father's legacy. Buck Owens knew his sound, believed in it, & stayed true to it. This MADM is brought to you by Singing River Dentistry, proudly supporting stories and the people who make our communities strong. Real stories. Real people. Real impact. News That Unites!™️

Tonight, I have the privilege of talking with Johnny Owens, son of country music legend Buck Owens, for an in-depth conversation about one of the most influential figures in country music history. We'll take a deep dive into Buck Owens' remarkable career, the Bakersfield Sound that changed country music forever, the story behind the timeless classic “Act Naturally,” and Johnny's decision to record a brand-new version of the song, releasing tomorrow, August 7th! This year marks the 60th anniversary of The Buck Owens Show: Live at Carnegie Hall and the 20th anniversary of Buck Owens' passing, making this a special tribute to a man whose music continues to inspire generations. Whether you've been a Buck Owens fan for decades or you're discovering his music for the first time, I think you'll enjoy this conversation. Real stories. Real people. Real impact. News That Unites!™

On this edition of The Mark White Show, I'm talking with Jewell Brown, a mother and grandmother who is courageously living with end stage kidney failure and searching for a living kidney donor. Twenty years ago, Jewell received a kidney transplant from her mother, a gift that allowed her to raise her sons, build a life, and become the proud Mimi of three grandchildren. That transplant gave her years she is deeply grateful for. Now, as that kidney begins to fail, Jewell faces the difficult reality of daily dialysis while hoping someone will step forward to give her another chance at life. In this conversation, Jewell shares what life is really like while waiting for a transplant, the physical and emotional challenges of kidney failure, and the hope she holds onto as she continues her search for a living donor. This episode is a reminder that sometimes the simplest act, sharing a story, can help connect someone in need with the person who can change their life. Real stories. Real people. Real impact. News That Unites!™️

On this Make A Difference Minute, I'm sharing Jewell Brown's journey and her need for a kidney donor. After facing kidney challenges since childhood and receiving a transplant from her mom that has lasted 20 years, Jewel is now in renal failure and searching for a living donor. This segment highlights both the reality that transplants are not always permanent and the opportunity for someone to make a life-changing difference. To learn more about becoming a living donor for Jewel, you can follow Be Jewell's Lifeline and/or contact Lara Reed with the transplant team at the University of Cincinnati Health at 513-584-8313. This MADM is brought to you by Green's Dependable Hardware, proudly supporting stories and the people who make our communities strong. Real stories. Real people. Real impact. News That Unites!™️

On this edition of The Mark White Show, I'm sharing the story of Rory Amos, a husband, father, and hardworking provider who continues to push forward in the face of serious health challenges. Rory has been on peritoneal dialysis for the past three years and is currently on the transplant list for a kidney at UAB and St. Thomas in Nashville. His journey has included life-changing complications from diabetes, including the loss of a leg, yet he continues to work, provide for his family, and press on with determination. Alongside his wife Jessica, Rory is raising five children and has opened his home and heart to a foster child they are working to adopt, showing what it means to care for others even while facing his own fight. This is a story of resilience, family, and a real need for a kidney donor. If you feel led to learn more about becoming a living donor or to share Rory's story, this is an opportunity to make a difference. Register: NKR.org/TFG957 Real stories. Real people. Real impact. News That Unites!™️

On this Make a Difference Minute, I'm sharing a portion of a conversation I had with my Uncle Sewell Hall, who passed away last Sunday at the age of 96. This interview was recorded in the spring of 2019. As Uncle Sewell reflected on his childhood, he remembered a family that moved often because his father was a preacher. Though money was tight, he never spoke of hardship with bitterness. Instead, he remembered a home where they always had what they needed, were surrounded by faithful friends, and spent countless hours together in worship. He recalled attending church meetings almost every night, watching his father quietly serve the family by washing dishes before dawn after long evenings of ministry, and growing up in a house where singing was simply a way of life. If one person started a song, it wasn't long before the rest of the family joined in with four-part harmony echoing through the house. He also remembered the importance of hospitality. Their home was always open, welcoming friends and visitors, reflecting values that would shape the rest of his life. Listening to Uncle Sewell's memories reminds us that some of life's richest blessings aren't measured by what we own, but by the love, faith, service, and togetherness we experience along the way. This MADM is brought to you by Athens Bible School, proudly supporting stories and the people who make our communities strong. Real stories. Real people. Real impact. News That Unites!™️

Some of you have asked if I would re-air my conversation with my Uncle Sewell Hall. Tonight, I'm honored to do just that. Originally recorded in the spring of 2019 for the Athens Bible School graduating class & beyond, this conversation has taken on a much deeper meaning following Uncle Sewell's passing. You'll hear him reflect on the family that shaped him, the lessons he learned through decades of preaching and missionary work, and the wisdom he wanted to pass on to the next generation. More than anything, you'll hear the voice of a man whose life consistently pointed beyond himself. Real stories. Real people. Real impact. News That Unites!™️

On this Make A Difference Minute, I'm sharing the story of Rory Amos, a husband, a father, and a hardworking man who is in need of a kidney donor. Rory addresses one of the biggest concerns people have about donation, the cost, and explains how his insurance covers it. He also shares how even if you're not a direct match, you can still help through paired donation programs that connect donors and recipients. This is an opportunity to make a real difference, not only for Rory, but for many others in need. To learn more or consider becoming a donor, visit nkr.org/TFG957. This MADM is brought to you by Bama Estate Planning by Attorney Harlan D. Mitchell, proudly supporting stories and the people who make our communities strong. Real stories. Real people. Real impact. News That Unites!™️

On this Make a Difference Minute, I have Jamie Gatlin as she shares about her husband, Jeff Gatlin, and his search for a living kidney donor as he lives with polycystic kidney disease (PKD). Jeff has known since his teenage years that he had PKD, a hereditary disease that also claimed his father's life and affects one of his sisters. For years, he was able to live a relatively normal life, but now his kidney function has declined to about nine percent, and he is preparing to begin dialysis while waiting for a transplant. Jamie shares that Jeff is currently listed for a kidney transplant at Vanderbilt and is also working toward being listed in Birmingham. Like so many families facing chronic illness, they're navigating the uncertainty of waiting while hoping that someone will choose to become a living donor. A living kidney donation has the potential to change not only Jeff's life, but the lives of his wife, Jamie, and their 23-year-old twins. This MADM is brought to you by Premier Structures, Inc., proudly supporting stories and the people who make our communities strong. Real stories. Real people. Real impact. News That Unites!™️

Jeff Gatlin has lived with Polycystic Kidney Disease (PKD) since he was a teenager. Now, his kidney function has declined to just 9%. He's now preparing for dialysis while hoping and praying for a living kidney donor. Tonight, Jeff's wife, Jamie Gatlin, shares their family's journey with honesty, courage, and hope. You'll hear what PKD has meant for their family, why a living donor offers the best chance for a transplant, and how one person's decision could completely change Jeff's future. You may not be able to donate a kidney, but you can listen, learn, and share Jeff's story. Real stories. Real people. Real impact. News That Unites!™️

On this Make a Difference Minute, I have part two with Andrea Barnes, store manager of the new Food City in Athens,AL as she shares how a part-time cashier position became a career she never imagined. Ten years ago, after moving to Chattanooga, Andrea was looking for a fresh start. A stay-at-home mom for 15 years, she applied to Food City after her daughter encouraged her to do the same. What began as a part-time cashier position soon became an opportunity to grow. Andrea embraced every challenge that came her way, serving as a floral manager, receiver, assistant manager, and ultimately earning the role of store manager. She credits the leaders who believed in her, invested in her development, and opened doors as she proved herself ready for each new opportunity. Her story is a reminder that where you begin doesn't determine where you can go. With hard work, a willingness to learn, and a company that invests in its people, remarkable opportunities can become reality. To learn more about Food City and career opportunities, visit FoodCity.com. This MADM is brought to you by Singing River Dentistry, proudly supporting stories and the people who make our communities strong. Real stories. Real people. Real impact. News That Unites!™️

Yesterday, I had the opportunity to interview Food City Athens,AL, Store Manager Andrea Barnes, and I believe you're going to enjoy her story. Andrea's journey began as a part-time cashier in Chattanooga. Through years of hard work, dedication, and leadership, she worked her way up to become the store manager of the new Food City in Athens. She's also right at home in North Alabama. A graduate of Rogers High in Green Hill, Andrea has a daughter who teaches kindergarten in Limestone County, and she's enjoying one of life's greatest blessings, being a grandmother. During our conversation, we talk about the remarkable history of Food City, from Navy veteran Jack Smith purchasing a Piggly Wiggly in Grundy, Virginia, to opening the very first Food City in 1955. We also discuss the incredible response to the Athens grand opening, support from local officials, what customers can expect, the new stores coming to Oneonta and the County Line Road area, Food City's commitment to giving back to the communities they serve, and the incredible team members who have worked tirelessly over the past several days to prepare for and serve our community. Most of all, this is a story about opportunity. It's a reminder that where you begin doesn't have to determine where you finish. If you enjoy stories about hard work, perseverance, and people making a difference, I think you'll enjoy this one! Real stories. Real people. Real impact. News That Unites!™

On this Make a Difference Minute, I have Andrea Barnes, manager of the new Food City in Athens, AL, as she shares how the company's Friends in Need program helps fight food insecurity right here in our community. Each holiday season, Food City invites customers to purchase a bag of groceries at a reduced price. Once the campaign ends, those grocery bags are ordered by the pallet and donated to local organizations that help families facing food insecurity. Andrea says it's one of the many ways Food City gives back to the communities it serves, ensuring that neighbors helping neighbors becomes more than just a slogan. As we talked, I shared that my own family once stood in line for commodity food assistance. Those experiences stay with you. They teach empathy and remind you that many hardworking families still struggle to put food on the table. That's why programs like Friends in Need matter. They give all of us an opportunity to help someone who may be going through a difficult season. To learn more about Food City and its community initiatives, visit FoodCity.com. This MADM is brought to you by Athens Bible School, proudly supporting stories and the people who make our communities strong. Real stories. Real people. Real impact. News That Unites!™️

Tonight on The Mark White Show, I'm honored to welcome Ron Adams and Tabitha Ridlehoover of the Rising Courage Foundation. After surviving cancer himself, Ron turned one of the hardest chapters of his life into a mission to encourage others who are walking the same road. Along with Tabitha, he is helping provide Courage Kits to chemotherapy patients, offering practical items, comfort, and a reminder that no one has to face cancer alone. I also want to thank James Spann for using his platform to shine a light on this incredible effort. When we see people making a difference, we have an opportunity to take the next step by sharing their story and helping their mission reach even more people. Join us as we talk about the inspiration behind the Rising Courage Foundation, the impact these Courage Kits are making, and how you can become part of this growing effort. Real stories. Real people. Real impact. News That Unites!™

On this Make a Difference Minute, I have Ron Adams, founder and president of the Rising Courage Foundation, as he shares how his own cancer journey inspired a mission to encourage others facing one of life's toughest battles. Ron was diagnosed with testicular cancer in 2014 and underwent surgery before entering active surveillance. Eight years later, he heard those life-changing words once again: “You have cancer.” As he sat through chemotherapy treatments during the COVID-19 pandemic, visitors weren't allowed. Day after day, he spent hours in the treatment chair with only nurses, doctors, and other patients who were facing similar fears and uncertainties. It was during those quiet moments that Ron realized how desperately people battling cancer need hope and encouragement. He made a promise that if he made it through, he would use his own pain to help others. That promise became the Rising Courage Foundation, whose Courage Kits are designed to bring comfort, encouragement, and practical support to individuals undergoing cancer treatment, reminding them they are not alone in the fight. To learn more or support this mission, visit RisingCourageFoundation.org. The full interview will air at 9p CST/10p EST tonight. This MADM is brought to you by Bama Estate Planning by Attorney Harlan D. Mitchell, proudly supporting stories and the people who make our communities strong. Real stories. Real people. Real impact. News That Unites!™️

On this Make a Difference Minute, we continue our three-part series highlighting the family behind Aubrey's Love Foundation. After hearing from Aubrey's dad, Allen, and her mom, Amy, today we hear from Aubrey's sister, Abby. Abby shares what it was like in the days and months following the accident that claimed Aubrey's life. She remembers wanting to be alone, but says her parents refused to let her face her grief in isolation. Looking back, she's grateful they stayed by her side through one of the darkest seasons of her life. Abby says Aubrey's Love Foundation gave her family something they desperately needed: purpose. By carrying on Aubrey's legacy of kindness and service, they found a way to give Aubrey a voice while bringing hope to others. Today, Aubrey's Love Foundation continues to award scholarships, support schools, invest in teachers, and meet needs throughout the community, ensuring Aubrey's love continues to make a difference. Learn more at AubreysLove.com. This MADM is brought to you by Bankston Motor Homes, proudly supporting stories and the people who make our communities strong. Real stories. Real people. Real impact. News That Unites!™️

On this Make a Difference Minute, I have Stokes Kasmeier from Killen, Alabama, as he shares his lifelong journey with hydrocephalus and why raising awareness is so important. Born prematurely after complications during his mother's pregnancy, Stokes spent months in the neonatal intensive care unit at Huntsville Hospital as doctors worked to save his life. Along the way, he was diagnosed with hydrocephalus, a condition many people have never heard of until it affects someone they love. Stokes explains that while hydrocephalus affects thousands of children and adults across the United States, there is still no cure. Many people living with the condition endure repeated brain surgeries and ongoing medical challenges throughout their lives. Today, Stokes is determined to use his story to educate others, increase awareness, and help fund research that could one day change the future for those living with hydrocephalus. If you'd like to support Stokes' efforts in the Walk to End Hydrocephalus, visit walk.stokeskasmeier.com. This MADM is brought to you by Hydration Lounge, proudly supporting stories and the people who make our communities strong. Real stories. Real people. Real impact. News That Unites!

Imagine being born 11 weeks premature, diagnosed with hydrocephalus as an infant, and undergoing approximately 30 brain surgeries before adulthood. For Stokes Kasmeier of Killen, Alabama, that's his story. A Brooks High School graduate, Stokes has faced challenges that most of us can hardly imagine. Most recently, a shunt failure and infection led to a month-long stay in the Neuro ICU. Instead of allowing those experiences to define him, he's chosen to turn his journey into a mission of hope. Listen in as Stokes shares what it's like to live with hydrocephalus, the battles he's fought, the people who've stood beside him, and why he's leading Team Stokes in this year's Walk to End Hydrocephalus to raise awareness and support research for the more than one million Americans living with this condition. Real Stories. Real People. Real Impact. News That Unites!™

On this Make a Difference Minute, I have Katie Humphres-Cagle with Barking Cow Farms as she shares the heart behind a special community event honoring Maddie Bishop while supporting Cooper Terry and his mother as they continue their battles with cancer. Katie encourages people to visit Fight with Maddie and learn about a young girl whose smile never seemed to fade, even through the hardest days. She says Maddie's story isn't defined by sadness, but by courage, joy, and the example she left behind. Those who knew her remember a warrior whose positive spirit inspired everyone around her. The event will also benefit Cooper Terry, who was diagnosed with cancer as a teenager. During his treatment journey at MD Anderson Cancer Center, his mother received devastating news of her own—she, too, had cancer. Today, the fundraiser is helping ease the financial burdens both families continue to face through medical treatments, travel, and everyday expenses. The Back to School Jeep Jam will be held Saturday, August 8th, from noon until 8p at Barking Cow Farms, located at 17446 Highway 278 in Brilliant, Alabama. The day will feature family activities, entertainment, and an opportunity for the community to come together in support of two remarkable families. This MADM is brought to you by J. Calvert Farms, proudly supporting stories and the people who make our communities strong. Real stories. Real people. Real impact. News That Unites!™️

Over the years, The Mark White Show has walked alongside families facing some of life's toughest battles. Tonight's show is about two of those journeys and a community determined to make a difference. I'll be joined by Katie Humphres-Cagle, Marketing & Business Strategist for Barking Cow Farms (owned by Maegan Adrian), to talk about the upcoming Back-to-School Bash and Benefit in Brilliant, Alabama. What started as a community event has become something much bigger. The benefit will honor the life and legacy of Maddie Bishop, whose courageous battle with Ewing's sarcoma inspired so many, while also supporting Cooper Terry and his family as they continue their own fight against cancer. We'll talk about the heart behind the event, why it was important to honor Maddie's legacy, how the community has rallied around both families, and how you can be part of making a difference. I hope you'll join us tonight as we share another story of compassion, resilience, and a community coming together when it's needed most. Real stories. Real people. Real impact. News That Unites!™

On this Make a Difference Minute, I have Paul Bruyneel, better known to many as Santa Paul, as he shares about his recovery following his third shoulder replacement surgery. After decades of physically demanding work, degenerative arthritis took a devastating toll on Paul's shoulder. Finding a surgeon willing to perform such a complex revision surgery wasn't easy, and by the time the procedure could be done, additional damage had occurred, making the operation even more challenging. Now facing more than two months away from work, Paul is focused on healing while relying on the unwavering support of his wife, Sandy. He says she's been his rock through every surgery, helping with even the simplest daily tasks during recovery. For someone who has spent years bringing joy to children and giving back to others as Santa Paul, this season has required him to accept the kindness of the community he's worked so hard to serve. If you'd like to support Paul and his family during his recovery, you can give through GoFundMe by searching “Taking the Weight Off His Shoulders.” This MADM is brought to you by Premier Structures, Inc., proudly supporting stories and the people who make our communities strong. Real stories. Real people. Real impact. News That Unites!™️

Tonight, I'm coming to you from J. Calvert Farms! Most people know him as Santa Paul. Tonight, you'll meet the man behind the beard. Paul Bruyneel has spent years bringing joy to others. Now, after a third shoulder replacement surgery, he's facing financial hardship while he and his wife, Syndee, continue caring for their three grandchildren. Join me for “The Heart Behind the Beard” as Paul shares his story, his heart for serving others, and why it's sometimes the people who give the most who need our support the most. Real stories. Real people. Real impact. News That Unites!™

On this Make a Difference Minute, I have Shannon and Sherry Ball, founders of Waiting to Hear, as they share how their daughter's hearing loss became the inspiration for a mission that is now changing the lives of children and families across the country. When their daughter, Sarah, was slow to develop speech, they assumed she simply needed a little extra help. But one day, Shannon called her name several times with no response. It wasn't until he closed a door and she felt the vibration that she turned around. Soon after, a hearing test confirmed the life-changing news that their daughter was deaf. Rather than allowing that diagnosis to define their family, they turned it into a purpose. Today, Waiting to Hear provides hearing aids to children who are deaf or hard of hearing when insurance falls short. Through Camp Hear, families also find something just as valuable, a community. While children connect with others who share similar experiences, parents receive practical training and resources, including guidance on navigating IEPs and advocating for their children in school. Waiting to Hear is helping families realize they don't have to face the journey alone. To learn more or support their mission, visit WaitingToHear.org. This MADM is brought to you by Athens Bible School, proudly supporting stories and the people who make our communities strong. Real stories. Real people. Real impact. News That Unites!™️

On tonight's edition of The Mark White Show! In our first segment, I'll be joined by Breanne Crowden and Arah Crowden Harkins at Donna & Friends as they share about 16-year-old Kade Worley and his courageous journey living with seizures. They'll talk about the challenges Kade has faced, the road ahead, and how the support of family, friends, and the community has made a difference during this difficult time. In our second segment, thanks to my friend, Brenda Lynn Allen, I'll welcome Shannon and Sherry Ball, founders of Waiting to Hear. After their daughter, Sarah, suddenly lost her hearing at just two years old, they turned one family's heartbreaking experience into a nonprofit that is changing the lives of children with hearing loss and their families. We'll also talk about the upcoming Key West concerts benefiting their incredible mission. Real stories. Real people. Real impact. News That Unites!

On this Make a Difference Minute, I have Breanne Crowden as she shares about her 16-year-old son, Kade Worley, and the incredible support their family is receiving as they prepare for the next stage of his medical journey. Breanne talks about the generosity of Donna & Friends, who organized a benefit bean dinner to help the family as Kade faces additional testing and surgery. With Breanne expecting to be away from work while caring for her son, the outpouring of support from their church family, friends, and community has been a tremendous blessing. Kade's journey continues with an ophthalmology appointment in Birmingham tomorrow, followed by specialized brain imaging to map the blood vessels before a stereo EEG (SEEG) procedure. During that hospital stay, doctors will monitor and induce seizures to accurately identify where they originate, helping determine the best surgical treatment moving forward. As Kade and his family face the days ahead, they continue to lean on the support of those around them and the hope that comes with each step toward answers. If you would like to support Breanne and Kade, you can send a Venmo donation to @BreanneCrowden. This MADM is brought to you by Bama Estate Planning by Attorney Harlan D. Mitchell, proudly supporting stories and the people who make our communities strong. Real stories. Real people. Real impact. News That Unites!™️

On this Make a Difference Minute, I have Dr. Larry Charleston IV, a board-certified neurologist and headache medicine specialist, as he discusses the challenges of treating migraine disease and cluster headaches. Migraine disease affects an estimated 43 million Americans, while cluster headaches, though much rarer, are considered among the most painful neurological conditions. Dr. Charleston explains that one of the biggest challenges is making sure patients receive the correct diagnosis. Without it, finding an effective treatment becomes much more difficult. He also points out that many people with migraine experience severe nausea and vomiting, making it hard for oral medications to stay down long enough to provide relief. That's why having treatment options tailored to a patient's specific needs is so important. Dr. Charleston's goal is simple: to help people move beyond simply managing their symptoms and instead achieve the best possible quality of life. To learn more about migraine disease, cluster headaches, and available treatment options, visit Brekiya.com. This MADM is brought to you by Bankston Motor Homes, proudly supporting stories and the people who make our communities strong. Real stories. Real people. Real impact. News That Unites!™️

On this Make a Difference Minute, I have Jamie Schanbaum, a survivor of meningococcal disease whose life changed forever while she was attending college in Texas. Like many college students, Jamie was simply enjoying campus life when what seemed like flu-like symptoms quickly turned into a medical emergency. Within hours, she was fighting for her life. She spent seven months in the hospital, and to save her life, doctors amputated both legs below the knee and all of her fingers. Today, Jamie has found a new purpose. She shares her story so other families will understand just how serious meningococcal disease can be and why informed conversations matter. Jamie says that if she had known more about the disease and the steps that could be taken to help prevent it, she would have been proactive. Her hope is that no one else has to endure what she experienced. Parents are encouraged to talk with their child's healthcare provider about meningococcal disease and learn more about the available prevention options. For more information, personal stories, and conversation starters, visit Ask2BSure.com. This MADM is brought to you by Hydration Lounge, proudly supporting stories and the people who make our communities strong. Real stories. Real people. Real impact. News That Unites!™️

On this Make a Difference Minute, I have Dr. Michael Milobsky, a practicing pediatrician and founder of Pediatrics at the Meadows in Castle Rock, Colorado, as we discuss meningococcal disease and why parents should have an informed conversation with their child's healthcare provider before the new school year begins. Although meningococcal disease is uncommon, it can become life-threatening in as little as 24 hours. Dr. Milobsky explains that one in ten people who contract bacterial meningitis will die, and one in five survivors may face lifelong complications, including brain damage or limb loss. Teens and young adults, particularly those between the ages of 16 and 23, are among those at increased risk because of common activities such as sharing drinks, food, utensils, toothpaste, kissing, coughing, and living in close quarters like college dorms, military housing, or shared apartments. Dr. Milobsky encourages parents not to wait until there's a problem. Instead, talk with your child's healthcare provider about meningococcal disease, understand the risks, and ask whether vaccination is appropriate for your teen or young adult. To learn more and prepare for that conversation, visit Ask2BSure.com. This MADM is brought to you by Bama Estate Planning by Attorney Harlan D. Mitchell, proudly supporting stories and the people who make our communities strong. Real stories. Real people. Real impact. News That Unites!™️

Tonight, we're sharing a conversation that every parent, grandparent, and caregiver should hear. Meningococcal disease, often called meningitis, is uncommon, but when it strikes, it can change a life in a matter of hours. Joining me tonight are Dr. Michael Milobsky, practicing pediatrician, Jamie Schanbaum, a meningococcal disease survivor, and Patsy Schanbaum, Jamie's mother. Together, they share a powerful story of survival, resilience, and why it's so important for families to have informed conversations with their healthcare providers. As teens prepare to head back to school and college campuses, we'll discuss who is most at risk, how quickly this disease can progress, Jamie's remarkable journey from surviving a life-threatening illness to becoming a gold medal cyclist and advocate, and what parents should know about meningococcal disease prevention and vaccination. Real stories. Real people. Real impact. News That Unites!™️

On this Make a Difference Minute, I have Lennon and Camryn Curtis, along with Irie Blade, as they share how a simple lemonade stand became an opportunity to help seniors in their community. Through Cousins for a Cause, the cousins came together to raise money for Meals on Wheels. Everyone had a role, from making lemonade and creating signs to pouring drinks, greeting customers, and explaining where every dollar would go. While they were a little nervous when the first customers arrived, that quickly turned into excitement as the very first donation was $20. Throughout the day, they were surprised not only by how many people stopped by, but by the generosity of those who gave more than the cost of a cup of lemonade. Now, these young difference-makers hope their effort inspires other families, neighborhoods, schools, churches, businesses, and community groups to pass the pitcher by creating their own lemonade stands to support causes that matter. Sometimes making a difference begins with something as simple as a pitcher of lemonade, willing hearts, & a community that cares. This MADM is brought to you by Premier Structures, Inc., proudly supporting stories and the people who make our communities strong. Real stories. Real people. Real impact. News That Unites!™️

Tonight, I'm excited to introduce you to some young difference makers who prove you're never too young to change someone's life. Joining me are Lennon Curtis, Irie Blade, and Camryn Curtis as they share the story behind Cousins for a Cause, a special effort that also included Miles Curtis, Mia, Lily, and Holly. Together, these cousins hosted a lemonade stand to benefit Meals on Wheels and the seniors it serves throughout the Shoals community. What started as a simple idea became an opportunity to teach children about compassion, generosity, and serving others. Even more inspiring, they're hoping the effort doesn't stop with them. Through their “Pass the Pitcher” challenge, they're encouraging other families, neighborhoods, teams, and organizations to host their own fundraisers and continue spreading kindness. I hope you'll join us for this encouraging conversation about small hands, big hearts, and the difference one family can make when they decide to serve others. Real stories. Real people. Real impact. News That Unites!™️

On this Make a Difference Minute, I have Misty George with Jagger's Journey as she shares why supporting families facing rare diseases goes far beyond medical care. When Jagger was first diagnosed, Misty and her family entered a world they knew very little about. At first, they feared leukemia. When doctors explained it was a rare disease instead, there was a brief sense of relief. That relief quickly gave way to the reality of navigating insurance denials, unanswered questions, and the uncertainty that often comes with rare diagnoses. Misty says one of the greatest needs families face is support. Financial burdens quickly add up as parents miss work, travel for treatment, and spend weeks or months away from home. Her own family benefited from generous supporters and A-Team Ministries in Birmingham, which provided housing during one of the most difficult seasons of their lives. Those experiences now fuel Jagger's Journey and Misty's vision for the future. She hopes to build a stronger support network so that families facing similar battles know they are not alone. To learn more about Jagger's Journey and how you can help, visit JaggersJourney.net. This MADM is brought to you by Green's Dependable Hardware, proudly supporting stories and the people who make our communities strong. Real stories. Real people. Real impact. News That Unites!™️

Yesterday, I had author Anna Grace Miller and her 97-year-old grandfather, Edgar Michael, at CoraNation for a TMWS interview! Born in 1929, Mr. Michael is one year younger than my grandfather who raised me. Anna has written Where Bluewater Runs: A Southern Boyhood in the Great Depression, a book inspired by her granddad's childhood and the real people, places, and events of 1938 Lexington, Alabama. I had such a good time visiting with Anna and Mr. Michael about the stories behind the book, the memories of growing up in Lexington, and what it means for a granddaughter to preserve her grandfather's experiences for future generations. You can meet Anna and Mr. Michael at the special book release on Saturday, August 1st, from 10a until noon at Miller's Feed & Seed in Green Hill! Real stories. Real people. Real impact. News That Unites!™️

On this Make A Difference Minute, Hope Snoddy Hagan shares what the outpouring of love, prayers, and support from the community has meant to her family as her 19-year-old son, Adyn, battles severe aplastic anemia. Hope also shares an important message for others facing difficult circumstances: let people help, accept the support, and allow your community to surround you with love during the times you need it most. This MADM is brought to you by Athens Bible School, proudly supporting stories and the people who make our communities strong. Real stories. Real people. Real impact. News That Unites!™️

On this edition of The Mark White Show, I'm coming to you from LifeSouth Blood Centers in Florence, Alabama, where I'm joined by Hope Snoddy Hagan and Misty George with Jagger's Journey. In 2018, I first connected with Misty as her son, Jagger, battled severe aplastic anemia. Although Jagger passed away in 2020, his legacy continues through Jagger's Journey and Misty's efforts to support other families facing the same rare and serious disease. Today, that journey has connected Misty with the family of 19-year-old Adyn Hagan, the son of my Lauderdale County High School classmate, Hope Snoddy Hagan. Adyn was diagnosed with severe aplastic anemia in April and has become dependent on blood and platelet transfusions as he prepares for a bone marrow transplant. During our conversation, Hope shares her experience as both a nurse practitioner and the mother of a son facing a life-threatening illness. She discusses how quickly their lives changed following Adyn's diagnosis, the importance of blood and platelet donations, and what the support of the community has meant to their family. Misty shares Jagger's story and how the support her family received during his battle inspired her to continue helping others through Jagger's Journey. She also discusses the emotional and financial challenges families can face during extended medical treatments and why it is so important for families to know they do not have to face those challenges alone. We also discuss the importance of accepting help during difficult times and the many ways each of us can support families facing circumstances they never expected. I hope you'll listen and share as we highlight Adyn's battle, Jagger's continuing legacy, and the difference we can make when we come together to support others. Real stories. Real people. Real impact. News That Unites!™️

On this Make a Difference Minute, I have 11-year-old Alabama actress Gabby Davis as she shares about landing the lead role of Izzy in Houdini the Magical Dog, currently being filmed in Athens, Alabama. After auditioning for the movie and receiving a callback, Gabby continued through the process until she received the call every young actor hopes for. She had been chosen to play Izzy. Her response was immediate. She screamed with excitement! Gabby's journey into acting began unexpectedly after years of participating in beauty pageants. One opportunity led to another, eventually opening the door to the entertainment industry and now a leading role in a feature film. For Gabby, however, some of the best parts of acting are the people and relationships she discovers along the way. She loves meeting the cast and crew, working with the animals, and especially spending time with Kilo, the “magical” dog on set. At just 11 years old, Gabby is discovering where hard work, opportunity, and a willingness to try something new can lead. To find out more about Gabby Davis and Houdini the Magical Dog, follow Alabama FilmWorks on Facebook and Instagram. This MADM is brought to you by Bama Estate Planning by Attorney Harlan D. Mitchell, proudly supporting stories and the people who make our communities strong. Real stories. Real people. Real impact. News That Unites!™️

On this Make a Difference Minute, I have Bro Richmond, son of actor and stuntman Branscombe Richmond, as he shares about his experience working on Disney's live-action Moana. Bro was selected from a large casting search that brought together Polynesians from across the United States with a wide variety of skills and experiences. With his background in stunt work, Bro was chosen to portray one of Moana's ancestors in scenes filmed aboard a boat placed on a massive gimbal designed to recreate the movement and conditions of the high seas. Following in his father's footsteps, Bro says he feels fortunate to have been handpicked for the role and to be part of a film that gives him the opportunity to represent his Hawaiian culture on the big screen. For Bro, the experience is about more than being part of a major film production. It's an opportunity to honor where he comes from while continuing to build his own path in the entertainment industry. This MADM is brought to you by Bankston Motor Homes, proudly supporting stories and the people who make our communities strong. Real stories. Real people. Real impact. News That Unites!™️

On this Make a Difference Minute, I have actor and stuntman Branscombe Richmond as he shares how a simple drive through Athens, Alabama, helped bring the production of Houdini the Magical Dog to the community. While visiting North Alabama, Branscombe asked Ashley Chewning to show him a small town. She brought him to her hometown of Athens, and when he saw the downtown square, something clicked. A conversation with the mayor followed, along with a vision of what bringing film productions to Athens could mean for the city, its businesses, and its people. Now, that vision is becoming reality as Houdini the Magical Dog is filmed in Athens. During our conversation, I also had the opportunity to share my own connection to the city. After moving away when I was nine years old, I always hoped I would someday find my way back home. Years later, I did. For Branscombe, Ashley, and the team behind the film, Athens represents opportunity and possibility. Sometimes all it takes is someone seeing the potential in a community and being willing to dream about what could happen next. Follow Alabama FilmWorks on Facebook and Instagram to learn more about Houdini the Magical Dog and other film projects happening in Alabama. This MADM is brought to you by Hydration Lounge, proudly supporting stories and the people who make our communities strong. Real stories. Real people. Real impact. News That Unites!™️

Tonight, I'm joined by Dr. Antoinette “Toni” Farmer-Thompson, president of Strayer University, for an important conversation about the changing face of higher education and the rapidly growing impact of artificial intelligence on the workforce. Today's college student may be a working adult, a parent, a career changer, or someone trying to gain new skills while balancing the responsibilities of everyday life. At the same time, AI is changing the workplace at an incredible pace, leaving many people wondering how they can prepare and avoid being left behind. Dr. Farmer-Thompson shares why AI fluency is quickly becoming a new form of literacy, how higher education must better connect learning to real-world careers, and what working adults should consider when choosing a college or university. I hope you'll join us for this timely conversation and share the show with others who may be considering the next step in their education or career. Real stories. Real people. Real impact. News That Unites!™️

On this Make a Difference Minute, I have Dr. Antoinette “Toni” Farmer-Thompson, president of Strayer University, as she discusses the rapidly changing role of artificial intelligence in education and the workforce. Dr. Farmer-Thompson says the question is no longer whether AI will transform the way we work. That transformation is already happening. The challenge now is making sure students, especially working adults who cannot afford to be left behind, have the skills, tools, and credentials necessary to remain competitive. She believes higher education must help people become more than observers of emerging technology. Students need the opportunity to develop AI fluency and become practitioners who can use these tools to transform themselves and the organizations where they work. At Strayer University, that means incorporating AI throughout the educational journey, redesigning programs to meet changing workforce demands, and staying connected with hundreds of employer partners to better understand the skills businesses need. As technology continues to change the workforce, the purpose of higher education must also evolve to prepare people not only for the jobs of today, but for the opportunities of tomorrow. This MADM is brought to you by Premier Structures, Inc., proudly supporting stories and the people who make our communities strong. Real stories. Real people. Real impact. News That Unites!™️

Tonight, we're celebrating a group of young athletes who have given Athens, Alabama, plenty to be proud of! The Athens 6U Girls All-Stars won the pre-area tournament, the area tournament, and then went undefeated to capture the Alabama state championship in the gold bracket! Now, these state champions are headed to the World Series, and they won't have to travel far. They'll have the opportunity to represent Athens and compete right here at the Athens SportsPlex! Tonight, I'm joined by Coach David Gough and the entire team: Treasure Allen, Paisley Adams, Emma Pope, Noey Miller, Kinsley Moore, Jade Grimme, Jincee Faulkner, Ella Lott, Emerson Duncan, Willa Claire Zirbel, Betsey Gough, & Gracelyn Kelley. You'll hear from Coach Gough and each of these young athletes as we talk about their championship season, their favorite moments, what it means to be part of this team, and their excitement about playing in the World Series! A special thanks to team parent Christen Lott for reaching out and helping make tonight's show possible. Real stories. Real people. Real impact. News That Unites!™️

On this Make a Difference Minute, I have children's book author Ashley Nicole Seals as she shares the inspiration behind A Friend Like Kip, a story inspired by her youngest son, Kohen. The idea began when Kohen was in preschool. Ashley watched as he faced challenges in social situations, not because he wasn't friendly, but because other children sometimes misunderstood the way he communicated and interacted with the world around him. At first, Ashley simply wanted to write a book Kohen could take to school each year to help his classmates better understand him. Through her work in special education, however, she realized there were many other children facing similar challenges. Too often, she says, children are noticed for their differences before others take the time to see their hearts. A Friend Like Kip introduces readers to a little boy who loves music, dancing, fall, and, most of all, his friends. Through his story, Ashley hopes to encourage greater kindness, empathy, understanding, and inclusion in classrooms and communities. You can find A Friend Like Kip on Amazon. This MADM is brought to you by Athens Bible School, proudly supporting stories and the people who make our communities strong. Real stories. Real people. Real impact. News That Unites!™️

On this edition of The Mark White Show, I'm joined by Ashley Nicole Seals, gifted specialist and special education director with Winfield City Schools and author of the new children's book, A Friend Like Kip. Inspired by her youngest son, Kohen, Ashley wrote A Friend Like Kip to encourage kindness, inclusion, empathy, friendship, and a better understanding of children who may communicate, interact, or experience the world differently. During our conversation, Ashley shares her journey in education, how being both an educator and the mother of a child with autism has shaped her perspective, and why behaviors are often a form of communication that others may misunderstand. She also discusses the emotional journey of writing and publishing her first book, Kohen's reaction to seeing himself represented in the character of Kip, and the overwhelming response the book has received from families and educators. Ashley also shares her hope that A Friend Like Kip will become a resource in homes, classrooms, libraries, and schools, helping start meaningful conversations about differences, understanding, acceptance, and friendship. Real stories. Real people. Real impact. News That Unites!™️