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We provide real support for people facing glioblastoma.
KBStrong helps people diagnosed with glioblastoma and the family and friends walking alongside them.
We connect people with financial assistance, community, and support through two programs: The Warrior Fund and HEROES.
TWO WAYS kbstrong can help
Start with the support you need.
WARRIOR Fund
Direct financial support for people facing glioblastoma.
KBStrong provides $2,500 unrestricted grants to eligible people diagnosed with glioblastoma across 10 counties in Central Illinois.
Warriors and their families decide how the money can help them most.
Grants have helped with practical needs at home, special experiences, and other expenses that can make life a little easier during treatment.
WARRIOR Fund
Eligibility at a glance:
- Diagnosed with Glioblastoma (physician verification required)
- Lives in one of the following 10 Central Illinois counties: Tazewell, Peoria, Woodford, McLean, Fulton, Marshall, Mason, McDonough, Knox, and Logan
Thanks to our generous donors, every applicant who meets the requirements has been approved.
Our Warriors
Every Warrior Has a Story
Ben Jeffreys
Ben Jeffreys
October 2025 | Warrior Story:
Greg Leeper Jr.
Greg Leeper Jr.
September 2026 | Warrior Update:
One of my favorite pieces of advice actually came from my buddy Derek when I was having a rough time during chemo and radiation. He told me, “Just exist out of spite. You’re not allowed to go anywhere. Just exist out of spite.” It made me laugh, but there were days when that was actually pretty good advice. I also have an aunt who has been fighting cancer for around ten years. Seeing her continue fighting gave me something to look at and say, if she can keep going, then I can keep going too.
I really do think you guys at KBStrong do amazing work. Please keep doing what you’re doing and getting the message out there.
August 2025 | Original Warrior Story:
Mary Iliff-Engelbrecht
Mary Iliff-Engelbrecht
September 2026 | Warrior Update:
July 2025 | Original Warrior Story:
Randy McGuire
Randy McGuire
June 2026 | Warrior Story:
Gary Reneau
Gary Reneau
June 2026 | Warrior Story:
Johnathan Rose
Johnathan Rose
June 2026 | Warrior Story:
Debbie Lonsdale
Debbie Lonsdale
May 2026 | Warrior Update:
April 2025 | Original Warrior Story:
Jody Gama
Jody Gama
April 2026 | Warrior Update:
One year ago, we had the privilege of meeting KBSTRONG Warrior, Jody Gama. Below is an update from Jody:
In December, I had what they believed to be a reoccurrence and decided to go on a trial with immunotherapy. On April 12th, I went to the emergency room for a severe headache. The MRI observed inflammation and a possible change in the area of the tumor. The neurology team has decided that surgery is the best option. I will be undergoing my 2nd craniotomy on April 24th, approximately 14 months after diagnosis.
I want to thank the KBStrong Foundation for all they do for those affected by this terrible disease. I would like to encourage the community to continue to donate to this terrific foundation in the fight to find a cure.
Please join KBSTRONG in praying for Jody, her family and friends as she fights the fight!
April 2025 | Original Warrior Story:
KBStrong is honored to recognize Jody Gama, 49 years-old, as our next Warrior Fund recipient. Jody grew up in Peoria and now lives in Washington, IL. She married her high school sweetheart, Matt, and they have 3 amazing children: Matthew, Zachary and Lainey. Jody and Matt also have a beautiful granddaughter, Milena.
Jody worked at OSF for 14 years, until recently taking a position with Easter Seals.She loves spending time with her family, taking vacations...especially the beach and the ocean.
Prior to her diagnosis on February 22, 2025, Jody was experiencing mild vision disturbance, nausea and balance issues. The following week, she explained that when she would look at people, their appearance would be slightly altered. Something Jody describes as "deja vu moments." These symptoms led to an MRI and ultimately a successful surgery on February 26th. Since surgery, Jody has begun the standard of care, which includes 6 weeks of radiation along with Temodar, a chemo pill. She has completed her 2nd week of treatment.
When asked about her "call to action," and what she would want others to know, Jody said she would like to encourage others to pay attention to their body. If something seems off, get it checked out. In addition, she asks for individuals to donate in order to fund research for this extremely rare disease.
Nic Harness
Nic Harness
March 2026 | Warrior Update:
November 2024 | Original Warrior Story:
Patrick Davidson
Patrick Davidson
January 2026 | Warrior Story:
The KBStrong Foundation is honored to introduce KBStrong Warrior Patrick Davidson. Patrick was born and raised in Peoria, Illinois. He and his wife, Elisa, are parents of two sons, Kyle and Sutton. The family also has a dog, Dash, and a cat, Pumpkin.
Patrick is an accomplished woodworker and has made several pieces of wood furniture for his family’s home. In addition, Patrick is a lifelong fan of the St. Louis Cardinals (his favorite) and Notre Dame football, though he enjoys all sports.
Patrick’s first experience with glioblastoma was when his father, Jerry Davidson, was diagnosed with glioblastoma and passed away at age 48 in 1990.
Patrick’s own glioblastoma journey began on Monday April 22, 2024, at age 50. Patrick had a seizure at work. While in the emergency department, a tumor was found on his left occipital lobe and was removed four days later. Patrick was diagnosed with GBM in May of 2024. He completed the standard treatments of radiation and chemotherapy. In August 2024, Patrick began wearing an Optune device. His family states, “The adjustment was challenging, but after a few weeks, we were able to establish a new normal.”
Patrick was fortunate to maintain clear scans until September 2025, when three tumors were found in his left temporal lobe. Early in October, a majority of the largest tumor was removed. He is currently continuing chemotherapy.
Patrick’s wife, Elisa, reminds us that the best way to support a family impacted by glioblastoma is to “be present for those impacted. Text them. Call them. Send them memes. Check in on them. Spend whatever time you can with them. Help them feel as normal as possible.”
Please join us in lifting Patrick and his family up to support them through this difficult time.
Wil Buse 🪽
Wil Buse 🪽
In loving memory
January 2026 | Warrior Story:
We are honored to introduce KBStrong Warrior Wil Buse. Wil was born and raised in Beason, Illinois, to Bob and Kathy Buse. Wil has four siblings: Ben, Max, Sam, and Molly, and two sisters-in-law, Amanda and Randi. Wil is a proud uncle to Ellie, Vera, and Eliza. Wil also enjoys his many close friends and extended family members. Prior to his diagnosis, he worked at Roland Machinery, in charge of rentals and construction equipment.
Wil’s glioblastoma journey began on September 16, 2024, with a “terrible headache not even touched by morphine.” A CT scan revealed a peach-sized tumor, and Wil continued to experience headaches in addition to numbness at times in his foot, arm, and hand. After his first surgery on September 18, 2024, in which the tumor was partially removed, the pathology report indicated cancer. Wil and his family sought second opinions after the initial diagnosis.
A second surgery in October of 2024 was followed by proton radiation at OSF in Peoria, and in February 2025, Wil began chemotherapy treatments. Wil’s surgical team placed radiation gamma tiles in a third surgery in July, but he experienced seizures due to brain swelling. Further treatments included gleostine and reduced steroids, which have come with hand, arm, and leg weakness, and blood clots that are treated with blood thinners. As Wil continues treatments, he also goes to physical and occupational therapy in Lincoln.
Wil continues to battle glioblastoma and its effects with courage and determination. Please join us in lifting Wil and his family up to support them in this extraordinary and difficult journey.
Chris Renken
Chris Renken
November 2025 | Warrior Update:
Honored to bless Chris Renken with his third Warrior Fund! Keep Fighting the Fight!
November 2023 | Original Warrior Story:
Carol Taylor
Carol Taylor
November 2025 | Warrior Update:
October 2024 | Original Warrior Story:
Russ Garey
Russ Garey
November 2025 | Warrior Story:
Connie Shepherd 🪽
Connie Shepherd 🪽
June 2025 | Warrior Story:
David Anderson 🪽
David Anderson 🪽
In loving memory
February 2025 | Warrior Update:
February 2024 | Original Warrior Story:
Thank you to David and his family for letting us join their fight against glioblastoma.
Terry “Rose” Rose 🪽
Terry “Rose” Rose 🪽
January 2025 | Warrior Story:
Audrey Reed 🪽
Audrey Reed 🪽
November 2024 | Warrior Story:
Audrey was diagnosed with glioblastoma in October 2024 and unfortunately passed away on November 25th, 2024, at the age of 70.
Audrey was born and raised in East Peoria. She turned 70 years old on September 29th and retired the following day from Morton Community Bank, after 19 years. Audrey also served as a bookkeeper for various small businesses over the years and impacted countless lives while teaching dance for over 50 years at Debby's School of Dance.
Audrey is survived by her husband, Gerald "Jerry" Reed and their two children, Skyler (and Myra) Reed of Peoria and Mesia Reed (and Michael Nelson) of Richardson, TX. She had two sisters, four grandchildren, a niece, a nephew and three great-nieces who love and miss her dearly!
When Audrey celebrated her 70th birthday and retirement, her journey with glioblastoma had not begun. Unfortunately, within a month, she began experiencing memory loss, difficulty making decisions and trouble forming sentences. Audrey was diagnosed with three brain tumors. The first tumor was removed 5 days later. After having an emergency procedure to have a shunt placed on November 9th, the plan was for another surgery on November 13th to place a permanent shunt that would help with draining fluid from her brain. Unfortunately, Audrey and her family learned the tumor that had been removed was back, and bigger than the original size.
Like so many of our Warriors, Audrey's family had never heard of glioblastoma prior to her diagnosis. They are overwhelmed with the number of individuals that have been affected in our area, as they hear from other families and friends who have also been touched by this terrible disease.
When asked what "call to action" they have for those not impacted by glioblastoma, they stated that this disease needs more attention, similar to what they have seen with diseases such as breast cancer. We agree with the Reed family! Without awareness, there is no funding. Without funding, there is no research. And without research, there is no cure.
James Smith 🪽
James Smith 🪽
October 2023 | Warrior Story:
Bethany Canopy 🪽
Bethany Canopy 🪽
In loving memory
September 2024 | Warrior Update:
Bethany was a true Warrior and fought such a brave battle against glioblastoma. Unfortunately, Bethany passed away in September 2024. Please keep Nick and their children in your prayers!
August 2024 | Original Warrior Story:
Collins Bruer 🪽
Collins Bruer 🪽
In loving memory
August 2023 | Warrior Story:
Derek Roberts 🪽
Derek Roberts 🪽
May 2024 | Warrior Story:
Matt Jones 🪽
Matt Jones 🪽
May 2024 | Warrior Update:
Matt and family, thank you for continuing to share your journey with the entire KBStrong family so we can continue to build awareness and Fight the Fight. WE ARE WITH YOU!
May 2023 | Warrior Update:
April 2021 | Original Warrior Story:
Rob Schmidt 🪽
Rob Schmidt 🪽
August 2024 | Warrior Update:
We are saddened to hear of the passing of KBSTRONG Warrior, Dr. Rob Schmidt! Please keep Megan, their boys and all family and friends in your prayers!
October 2023 | Original Warrior Story:
Brandi Mooberry 🪽
Brandi Mooberry 🪽
October 2023 | Warrior Story:
Mary Sherwood 🪽
Mary Sherwood 🪽
September 2023 | Warrior Story:
Steve Kallay 🪽
Steve Kallay 🪽
May 2023 | Warrior Story:
Arlene Smith 🪽
Arlene Smith 🪽
April 2023 | Warrior Story:
William “Bill” Bridges 🪽
William “Bill” Bridges 🪽
December 2022 | Warrior Story:
Victoria “Vickie” Riddle 🪽
Victoria “Vickie” Riddle 🪽
December 2022 | Warrior Story:
Geri Heisler 🪽
Geri Heisler 🪽
November 2022 | Warrior Update:
In Geri's honor, please join the fight against glioblastoma!
September 2022 | Warrior Update:
September 2021 | Original Warrior Story:
Angela Bossard 🪽
Angela Bossard 🪽
January 2022 | Warrior Story:
Doug Schoenman 🪽
Doug Schoenman 🪽
July 2021 | Warrior Story:
Karen Brashers 🪽
Karen Brashers 🪽
June 2021 | Warrior Story:
Polly Fuller 🪽
Polly Fuller 🪽
January 2023 | Warrior Update:
February 2022 | Warrior Update:
February 2021 | Warrior Update
January 2020 | Original Warrior Story:
Robin Closen 🪽
Robin Closen 🪽
December 2020 | Warrior Story:
Landon Meece 🪽
Landon Meece 🪽
In loving memory
July 2020 | Warrior Story:
KBStrong is honored to recognize Landon Meece, from Bloomington, IL, as our third recipient of the KB’s GBM Warrior Fund.
Please keep Landon's family in your prayers!
Earl Boitnott 🪽
Earl Boitnott 🪽
March 2020 | Warrior Story:
Coach Kevin Brown 🪽
Coach Kevin Brown 🪽
In loving memory
Some say Kevin overachieved in every aspect of his life. That wasn’t because he was lucky… he had an amazing work ethic, he was determined, passionate and confident. He expected a great deal from his players, his coaching staff and everyone in his life, including himself. This is why Team Brown always felt he could do anything that he set his mind to.
In the winter of 2017, Kevin decided that he wanted to develop a five-year plan for retiring from education. He set age 55 as his potential retirement date. In January 2018, he decided to purchase a small campground in Carlock, Illinois. He loved Kamp Komfort and looked forward to this being his retirement job someday. This was where he would someday transition from Coaching Kevin to Camping Kevin… and these were sometimes distinctively different people.
Life was great. We decided to downsize and move into a newly remodeled home at the campground. When not teaching and coaching basketball, Kevin would sit in our cabin-like master suite and overlook Kamp Komfort. He was so proud of his new venture and he was great at it! In June 2018, five months after starting this new adventure, he began to experience what he would call minor issues. It began with slurred speech, as if he was numb from going to the dentist and a strange taste in his mouth. It would come and go and he could never really explain it. He decided that he thought it may be an issue with a root canal that got infected several years before, so he decided to see his dentist. There was nothing there to explain his symptoms, so he agreed to see a nurse practitioner that ordered him an immediate MRI to rule out a small stroke. I will always remember the call... "there is no way I can lay there with my head strapped to a table for 30-45 minutes." I asked what they said when he explained… his response, "I just left without telling them anything." Yep, that was Kevin.
A month later we were on our annual trip to Colorado. Kevin loved the mountains and spending time with our family and friends on this trip every year. We all noticed that he didn’t seem himself, but he went along with all of our plans and seemed to enjoy himself. The morning before we left, he was walking the dog and experienced a brief spasm in his jaw. He didn’t act like it was a huge deal, but I know he was starting to get a little concerned. Up to this point, he had decided that his previous symptoms were related to sinuses or maybe even stress as he was working a ton of hours with summer basketball and the campground. As we were driving home to Illinois, Kevin behind the wheel of our 45-foot motorhome, he began to have the strange taste in his mouth immediately followed by the spasm in his jaw. He turned to me and the left side of his mouth was completely drawn downward like a stroke. As scary as it was, all symptoms were gone within minutes and he finished the drive back home. Yes, not a wise choice to drive another ten hours back home… yep, that was Kevin.
The next morning, we contacted my mom’s doctor and he agreed to see Kevin as a new patient later that week. Long story short, we met with him on a Wednesday, had a sedated MRI the following Thursday and two days later (Saturday, August 4, 2018) our lives were forever changed. We were told Kevin had a brain tumor on the right side of his brain, and they believed it to be aggressive.
Before we left the office, we already had a plan to meet with a neurosurgeon that week. The next couple days were horrible. We were scared to death. Kevin said he just wanted to walk in there and find what he would consider his kind of doctor… someone who was confident and would say we are going to get this taken care of, and that is what he found. He immediately knew this was his guy and there was a plan to get the tumor removed that same week. We were so relieved and almost celebrating when he left. Then, the words that meant nothing to us at the time. The nurse came in to discuss the plans. She also informed us of the type of brain cancer he thought Kevin had… Glioblastoma (GBM). I have often said they could have called it anything. We hadn’t done any research, so we didn’t even know there were different types of brain cancers. The nurse gave us the news that if Glioblastoma, it isn’t a matter of if it comes back, but it is when. It is impossible to cure. Not the best news, but we had a plan. And everyone who knows Kevin, he always had a game plan.
From what I can remember of the days leading up to surgery, I am sure that we thought he would beat it. He would be the exception. Kevin would tell me that you could see it in some people’s faces that they were what he called "non-believers," but he always said that he was okay with it… he loved to prove people wrong. I often said it was like being down big with a minute to go and both he and I were the only ones in the gym that thought we could still win. Again… yep, that was Kevin.
Kevin had his tumor removed on August 10, 2018. It was a successful surgery and he set a goal to return to coaching that season. He learned several weeks later that it was indeed Glioblastoma, but he was going to once again overachieve and be the exception… he was scared, but never allowed for failure to be an option. He returned to teaching and coaching basketball on October 31, 2018, after six weeks of chemo and radiation. It was amazing, he was back to working out and looked and felt great.
After suffering a partial seizure on January 31, 2019, Kevin coached his last basketball game on February 1, 2019. Some may think that is crazy, but that was Kevin Brown. He showed amazing work ethic, determination, confidence and commitment to his team. Kevin was in so much pain, but he showed that night that he loved his boys. He never wanted to quit on them. The next day, as we sat in the emergency room, he cried so many tears saying, "what lesson am I teaching my boys??... I am not a quitter." The truth is he taught them so much about life as they watched him battle this horrible disease. They knew he was not a quitter, but instead a warrior. Yep, that is Coach Kevin Brown.
After having surgery in February, March and April, Kevin lost his battle on June 11, 2019. But, as his wife for almost 27 years, I have never been prouder. He gave it everything he had and he again overachieved. Kevin was there for his players, his coaching staff, his family and his friends until the day he passed. Kevin was my best friend and my hero. He will forever be loved and missed. We are continuing his battle against Glioblastoma, and my goal is to bring HOPE to patients and families affected by this terrible disease!
I am committed to making him proud. We are taking on his battle against Glioblastoma. We donated Kevin’s brain to Northwestern, where his April 13, 2019 surgery was performed, to help with research of this dreadful disease. An NFP foundation, KBSTRONG – Fighting the Fight, has been formed and the efforts are in full force. The board, made up of Kevin’s father, brother and some of his very best friends have established a plan to raise awareness for brain cancer. Much of the money raised will be donated to the University of Illinois School of Medicine to fund Glioblastoma research in Peoria, Illinois. Their events can be followed on the Facebook page, KBstrong – Fighting the Fight.
In honor of Kevin, the national basketball tournament that takes place in Washington, Illinois has been renamed the Kevin Brown Memorial Tournament of Champions. The tournament will partner with the KBSTRONG Foundation to raise awareness and help with funding research for Glioblastoma.
We are thankful for those who want to join our fight. If you are interested in learning more, please contact us through social media or our email address.
- Jodi Brown -
HEROES FAMILY SUPPORT
Connecting the friends and family of GBM Warriors
HEROES stands for Honoring Each, Remembering Ours and Expanding Support. It connects friends and family members affected by glioblastoma with people who understand what they’re going through.
HEROES can find support, build connections and turn their experience into action. Many go on to volunteer, attend events, raise funds, and help carry KBStrong into their own communities.
Each July, HEROES comes together for an annual event tied to Glioblastoma Awareness Day, giving the community another opportunity to connect, remember, and stand together.
Your community is waiting.
Get connected.
Stay in the loop about HEROES events, volunteer opportunities, fundraisers, and KBStrong news.
Have a question before you apply or join?
Reach out, and we’ll be happy to help.
Email your question