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    Keeley Noworyta

    Keeley Noworyta

    Eight-year-old Keeley is a lover of arts and crafts, dolls and on a normal year, she would be spending her spring and summer months on the soccer field. Unfortunately that is not her current reality. Earlier this year, she was diagnosed with a form of Hodgkin’s lymphoma – a cancer that has targeted her lymph nodes and lungs.

    “Now that she has a routine down, she’s rolling with it,” says her mom, Laura. “She is just amazingly strong.”

    From losing parts of her hair and having to shave her head, to having to have a mediport inserted to receive chemotherapy, Keeley has kept that strong spirit, making comments like, “This is cool…I am bald!” Her mom says that she has encouraged not just her as a mother, but also the many people they have met in this cancer journey.

    After her fifth round of chemo, Laura says that Keeley should be done with treatment, as there are no signs of cancer cells detected. Through it all, she says community kindness has kept them all going as a family.

     "It all started in early January when we discovered that something was wrong and fast forward to now, we are doing remarkably okay and people, like the doctors and childlife specialists at Roswell and Del from 26 Shirts, have helped us more than they realize.”

     Laura says that she has always followed the stories of those who benefit from the 26 Shirt campaigns, and now that her daughter is one, she is extremely thankful for the outpouring of compassion.

    “Everything is still surreal. We feel grateful for the position that we are in that we have good health insurance, but it doesn’t cover gas, parking, extras – everything really adds up. We are so grateful that there are so many people who are willing to help.”

    So, what is next for Keeley? She turns nine in a few weeks and at the same time, she should be able to ring the victory bell, signifying no more cancer! She also looks forward to lacing up her cleats and getting back on the soccer field very soon.

    Keeley’s 26 Shirt campaign launched 6/14 and runs through 6/27. This story provided in partnership with Kate Glaser of Hope Rises. Learn more at www.hoperisesnews.com

    Adrian Gomez

    Adrian Gomez

    Like every energetic young boy, Adrian Gomez likes to climb and jump around. Though it always made his mother, Diane nervous, she says his playful spirit likely saved his life.

    “When he was jumping around and fell from a chair, a hardened dot formed on his foot, and we thought it was just a result of him falling,” she says. “But the tiny bump continued to grow, and we couldn’t ignore it.”

    At first doctors told her it was a cyst and there was nothing to worry about. However, it didn’t go away and after a few months, Diane requested more action to be taken. An MRI and biopsy revealed that Adrian had a very rare form of soft tissue sarcoma. Just six years old, Adrian was now in the fight of his life against childhood cancer.

    “It came as a shock – how could this be? It was so hard because everything moved so quickly. He had two surgeries in one week and then started chemotherapy immediately. My husband and I went through the motions of feeling sad, angry, scared and it really was all overwhelming.”

    Adrian’s left pinky toe was removed to try to stop the spread of the cancer, and a port was inserted to receive chemo. Unfortunately, the cancer spread quickly from Adrian’s foot into his lymph nodes and bone marrow. For months, the chemotherapy he was receiving was not responding, and cancer cells were found in his spine. Adrian is now on a higher dose of chemotherapy three days in a row, which is very hard on his tiny, fragile body.

    His mom says that although the cancer is strong, he’s stronger. “He is resilient, and so brave.”

    When Adrian’s teacher referred him as a recipient for 26 Shirts, Diane says both her and her husband felt instantly supported and like they weren’t in this fight alone.

    “Especially in Buffalo, you don’t have to know people and they still send their love, positivity and strength. Every person in Buffalo always goes above and beyond. The community is there to support you – you feel the love and support from afar.”

    Adrian Gomez’s 26 Shirt campaign launched 5/17 and runs through 5/30. This story provided in partnership with Hope Rises at www.hoperisesnews.com

    Kevin Newton

    Kevin Newton

    Kevin Newton was a healthy 45-year-old, who loved to travel with his family and enjoy outdoor life, like fishing, golfing and boating. But one day, in the fall of 2020, a scan on his bladder revealed the devastating news – stage 4 cancer.

    “They said, ‘there is a tumor the size of your kidney on your kidney’ and they also told us that the cancer spread to his lungs,” says Tammy, Kevin’s wife. “Never in a million years did we imagine this nightmare.”

    Just weeks later, his diseased kidney was removed and a biopsy on his lung gave them more insight as to what was going on with Kevin internally. Tammy says that the kidney cancer he had spread to his lungs and the oncologist recommended the strongest and most aggressive medicine to treat it.

    “He did it for three months and it just didn’t work, and the cancer continued to spread throughout his chest.”

    With the even further devastating news, Kevin took a trip to Myrtle Beach to make memories with those he loves most. The heaviness of his diagnosis weighed on them all, including the couple’s son, Tyler.

    “The one thing the doctors kept telling us is that they are not giving up on him.”

    Kevin is now on a chemo regimen and it’s been really challenging for him, making him so sick that he has a hard time functioning.

    “Kevin thinks about the slideshow of his life, knowing how fragile it is, and we’ve all had such a good life together, but he is too young and this is not the outcome we want,” Tammy exclaims.

    She adds that Del from 26 Shirts called her to offer financial support and it couldn’t have been at a better time – especially after having to leave his job because of the debilitating impact of the cancer.

    “I cannot even put it into words what this means for us and for families that are going through cancer or other terminal illness. We are blessed, beyond grateful and fighting hard.”

    This blog provided in partnership with Hope Rises. Find their stories of hope and kindness at hoperisesnews.com 

    "Let's Be Good Neighbors" provided by Jake Watkins of Trainwreck Sports

    "Let's Be Good Neighbors" provided by Jake Watkins of Trainwreck Sports

    "God doesn’t give you more than you can handle.”

    Now I’m not a particularly religious man, but for the past week that phrase has been on repeat in my head. It’s not because of anything that’s happened to me. I’m a fortunate man by all accounts. But last week Thursday, I got a phone call at 1:44 p.m. It was a 716 area code, but not a number I had saved (or blocked). I was fairly certain that someone was about to check on my car warranty or my student loan payments.


    To preface this, recently, Trainwreck Sports and 26 Shirts entered into a media partnership, the terms of which I can’t disclose. The cliff notes of it: Trainwreck Sports is going to be spreading the word about all of the difficult, inspirational and necessary work that 26 Shirts does.

    When the partnership began I tried to think about how I could best use my skills and knowledge to hold up our end of the bargain. I began thinking back to my video production days, at St. Francis High School and beyond. I remembered an Alumni Spotlight I produced with the help of our mentor Mr. Messore (I say mentor because he was genuinely much more than a high school teacher moderating a club). That Alumni Spotlight was about Dan Gigante, a member of the class of 1991, who started his own “Buy One Give One” t-shirt company called You and Who. 

    Fast-forward to 2021 and I have another opportunity to promote Dan’s work. I pondered, conceptualized, and came up with Good Neighbors, an interview series with the beneficiaries of 26 Shirts individual campaigns. The beneficiaries are often people and families who have fallen on hard times. I knew the conversations would be difficult, but they’d be worth it. I figured I knew what I was getting myself into.


    That phone call that I received on Thursday, April 8 at 1:44 p.m. was from Phil VanKoughnet, the father of Sophie VanKoughnet, 26 Shirts’ latest beneficiary. I answered the call, but the audio kept cutting out.

    “I can’t hear you,” Phil said.

    “How about now?”

    “Oh, that’s better.”

    “Okay great! So I’m looking to inter…”

    “I’m sorry I can’t hear you anymore.”

    “Oh really? Maybe I’m connected to Bluetooth by mistake?” (I was in fact connected to bluetooth but the problem persisted even after I figured that out)

    This happened for two out of the three minutes we were on the phone. I’m not kidding. But Phil wasn’t frustrated at all. He was just as confused as I was. Somehow we decided that I’d interview them at noon the very next day, even though I’m pretty sure he just guessed at that being what I said. I texted him the next morning to make sure we were on for noon and thankfully he said yes. He said yes even though I forgot to send him a Zoom invitation, but I did email his wife, Stephanie, to ignore the invitation’s 1:00 p.m. end time.

    No, I never claimed to be a perfect person. Nobody is.

    But Stephanie and Phil… they’re perfect for each other, and despite the hand they’ve been dealt, they’re doing an amazing job raising their children, which brings me to the reason I was interviewing them in the first place. Sophie was born with Pallister-Hall Syndrome, an extremely rare genetic condition that has less than 100 confirmed cases in the world. 

    Stephanie described the diagnosis as numbing. Phil likened it to being struck by lightning, but they had an inkling that something was wrong before finding out the exact details of Sophie’s condition. Imagine knowing that you were going to be struck by lightning, knowing that a phenomenon with a 1 in 500,000 chance of occurring was going to happen. I’ll be honest. I can’t. I’m shaking typing this, just imagining that, especially because being born with Pallister-Hall is even less likely than coming into contact with a lightning strike. But those two, reliving the moments as they dictated what is likely one of the worst moments of their lives… they were strong. No tears. No wiping their eyes. Phil’s hands were folded and Stephanie fiddled with her gold bracelet, while my eyes were filling up. 

    They described Sophie as headstrong, brave and happy, three traits that she absolutely inherited from her parents. They said that she inspires them to be strong every day, and I don’t doubt that whatsoever. But from an outside perspective, I truly believe that strength runs in that family.

    When they said that they took the kids to the Rochester Museum of Play, it was the first mention of her brother. I asked how he handled the situation. This didn’t make it into the video. A lot of great stuff didn’t make it into the video.

    They said that he’s been great, but, as any six and half-year-old might react to having a little sibling with a serious genetic condition, he at first didn’t understand why she was getting so much more attention than him. That’s something that I never thought of. How do you tell your son that his little sibling is going to take up most of mommy and daddy’s time? Being a perfect parent is an impossible task, especially under circumstances like the VanKoughnets’. But these photos are of a brother who loves his sister. I imagine them growing up, him being overprotective when she brings home her first boyfriend.  His face just says how much he cares for her. 

    Stephanie, Phil, you two have done an amazing job raising your children and it shows.

    This photo came while they were telling me how they met. How’s this for a love story: they met in grade school when they were six. They went to high school together but rarely talked. They went to college together, took the same Psychology class, and didn’t even know until they reconnected on Facebook nine years ago.

    I met my girlfriend in UB’s dining hall and one of the first things she learned about me is that I wanted to steal glassware from the dining hall for my apartment in Elmwood Village.

    These two were always in each other’s lives and barely knew it. They were actually made for each other. And through everything they’ve been through together, they still get this happy telling the story of how they met. 

    These complete strangers that I’ve talked to for a cumulative 21 minutes and some change… I have so much respect for them. These are GOOD people. Before I mentioned that old mantra “God doesn’t give you more than you can handle.” I’m convinced Stephanie and Phil can handle anything that gets put in their way. They’re an inspiration for me as someone who looks forward to becoming a parent someday (very well after I finally move out of my girlfriends’ parents’ basement). These are people who don’t deserve gargantuan medical debt due to a genetic condition they have no control over, and they don’t deserve to have to ask for anyone’s help. 

    So allow me. 

    Buffalo, Bills Mafia, and anyone anywhere else reading this, go to the 26 Shirts website and get yourself one of these incredible shirts, or a hoodie if that’s more your style. And in so doing, support my new friends, the VanKoughnets. 

    Buffalo is The City of Good Neighbors, so let’s live up to the name.

    Sophie VanKoughnet

    Sophie VanKoughnet

    3-year-old Sophie VanKoughnet is described by her mom, Stephanie as vivacious and full of life with strength well beyond her years. That strength is coupled with fierce determination to fight more than any toddler should have to.

    “It all started even before she was born,” says Stephanie. “I had a lot of problems prenatal, but doctors weren’t quite sure what was wrong and even after she was born, she passed all health checks.”

    However, Sophie was not gaining weight and her tiny body struggled with nursing. Every time she tried to eat, Sophie could not swallow properly and would aspirate. Stephanie says at just five-weeks-old, she had immediate surgery to have a gastrostomy tube or feeding tube inserted. Through 11-months, Sophie only took in liquids through her g tube.

    “Sophie was eventually diagnosed with Pallister-Hall Syndrome, an extremely rare condition with less than 100 diagnosed cases in history. There is a man diagnosed with Pallister-Hall in Australia that we have reached out to, but there really isn’t much information out there.”

    Since the diagnosis, the family has asked many questions regarding Sophie’s health, but there have not been many answers. In her short and fragile life, Sophie has undergone ten surgeries and also deals with hypoglycemia, causing complications with her blood sugar, as well as a hematoma in her brain, which could eventually lead to blindness.

    “My husband and I were in zombie mode when she was a baby and even now it’s extremely difficult, but we are all adapting,” Stephanie says. “One thing I can say loud and proud is that Sophie faces so many obstacles, but she adapts to them all. Her complex condition is a tough pill to swallow, but she has changed me as a person for the better.”

    The family is tight knit, with Sophie having a six-year-old brother, who is also impacted by the struggles of her critical condition. The family are die-hard Buffalo sports fans and think so highly of the impact the community has in helping those in need. That’s why when they heard about a shirt drop for Sophie, they were “over the moon” thrilled to have awareness around Sophie’s journey.

    “26 Shirts…Buffalo…WNY and this campaign give me hope. Sometimes it all seems like too much, but then things like this come up and I feel hopeful,” Stephanie explains.

    She adds, “Sophie has taught me and others to live in the moment and never give up. I hope out of anything that comes from Sophie’s story that people feel inspired to keep going, no matter the challenge ahead.”
    This story is provided in partnership with Hope Rises. Learn more at www.hoperisesnews.com.