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<div>If you’ve spent any time in Eagle River, there’s a good chance you’ve crossed paths with the Kirby family. Through sports, church, and community involvement, they’ve always been the kind of family that shows up for others.
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<div>Now, we’re asking our community to help show up for Rylan.
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<div>Rylan Kirby has officially qualified for the 2026 CrossFit Games in San Jose, California—an accomplishment achieved by only 20 teenage boys in the world.
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<div>The CrossFit Games are the highest level of competition in the sport of CrossFit. Athletes from around the globe spend months competing through multiple stages in pursuit of an invitation. This season began with the CrossFit Open, a worldwide competition involving more than 200,000 athletes.
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<div>Rylan finished 1st in the world in the 16-17 Boys division during the Open and continued his incredible performance through Quarterfinals and Semifinals!
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<div>What makes this accomplishment even more remarkable is that Rylan only began seriously training CrossFit a year ago.
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<div>When he started, the goal was simple but ambitious: qualify for the CrossFit Games.
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<div>Rylan is much more than a CrossFit athlete. He is a follower of Christ, a loving son and brother, a hardworking student, and a talented hockey player. Earlier this year, he helped Team Alaska 18U capture the Pacific District Championship, proving his dedication extends far beyond one sport.
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<div>Throughout this journey, Rylan has been supported by his family, coaches, training partners, and the incredible community at CrossFit Iron Refined, where he trains under Coach Shelby Fields, owner of CrossFit Iron Refined.
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<div>Over the past year, Rylan and Coach Shelby have spent countless hours training, traveling, competing, and preparing for this opportunity. We are proud to see him represent not only our gym, but the entire Alaska CrossFit community on the world stage.
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<div>Your donation will help offset the costs associated with competing at the 2026 CrossFit Games, including:
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<div>• CrossFit Games registration fees
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<div>• Airfare to and from San Jose, California
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<div>• Hotel accommodations
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<div>• Transportation and meals during the event
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<div>• Travel expenses for both Rylan and Coach Shelby throughout competition week
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<div>Every contribution, no matter the size, helps make this opportunity possible.
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<div>If you’re unable to donate, we would be incredibly grateful if you would share this fundraiser and help spread the word.
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<div>Thank you for supporting Rylan as he represents Eagle River, CrossFit Iron Refined, and the State of Alaska at the 2026 CrossFit Games.
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<div>See you in San Jose.
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Help Send Rylan Kirby to the 2026 CrossFit Games!!

<div><em>Update: Giving can continue even as goal is reached (thank you all! -read below) - </em>Jamie suffered a tragic accident the morning after Christmas when his vehicle slipped on glare ice and rolled several times down a steep 50' drop. His neck was broken (C6), his spinal cord injury resulted in his paralysis from the chest down as the truck was totaled. Jamie used Siri to call 911; first responders arrived quickly, and a neurosurgeon (Dr. Fix) performed three surgical procedures in the first 30 hours after the injury. He is awake and lucid (no brain injury) he has begun to recover some limited sensation and movement in one foot and his arms after the surgeries and much prayer. The surgeon is pleased with his progress, and we continue to pray for a miraculous recovery. During his recovery period, his family will have a loss of income as Jamie is self-employed. <strong>He will have a lengthy rehabilitation process in Chicago, which will involve his wife Erica and three kids flying from Alaska to support him.</strong> <strong>All funds will go directly to the Rose family to assist with their expenses related to his injury: loss of income, recovery, and rehabilitation which may be up to two years. Even with his initial goal met, please feel free to give as you feel led as the expenses for this journey will far surpass the fundraising goal and will be long and significant.</strong>
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<div>Jamie has always been physically and mentally strong, capable, optimistic, and a problem solver. He is a man of faith, a good friend to many, and has a heart for helping others - now is an opportunity to lend him and his family support so they can focus on healing and recovery.
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<div>They have a bank account set up for the Roses for direct deposits/wire transfers and if you want to mail them a check, please message me if you need their address or have questions.
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<div>Thank you for your support for his family during this difficult time.
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Help Jamie Rose's Family After Tragic Accident

<div>Friends and Family of Tom and Jessica Mute: The Mute family could really use our help right now. He is unfortunately battling stomach cancer and has been admitted to ANMC. Although Tom is in good spirits and surrounded by his family, he has quite a battle ahead of him. The Mute's are so very grateful for all of the well wishes, prayers and support they have been receiving. Please continue praying. Tom will not be going back to work for the unforeseeable future. Alaskans are known for taking care of each other. Please donate if you can. Tom and Jessica are the most generous, kind and caring people amongst us.
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<div>All funds will be deposited into the Mute's account. 
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Tom Mute and Family

<div>  Our kind, loving, most beloved dad, grandfather, son, brother, uncle, and nephew has passed away. Edgar Mark Anagick will always be known for putting a smile and laugh on others faces and always able to lift those up when they are down.  He was always willing to help others without expecting anything in return. 
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<div>   Please donate to his family during this time to help with the unexpected expenses of death and all the grief that comes with it. Your donation and love will make a huge difference during this most difficult time for his children Danielle, Michael, and Bruce as they have to pave the way to honor their father the way he would have wanted to be honored.
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Edgar Mark Anagick

<div>I’m Lucas’s Dad, Eric. We’re raising funds to help Lucas (6) and our Family while he conquers Acute Lymphoblastic Leukemia (A.L.L.) at Providence Medical Center in Anchorage, AK.
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<div>Lucas's leukemia story so far........
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<div>In early February Lucas randomly complained of his feet/ankles being sore. Being an active and growing 6yr old, we chalked it up to growing pains. He had been eating more than usual,and seemed due for a growth spurt....so it made sense.
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<div>Feb 15th we headed to Hawaii for some sunshine. Lucas continued to complain of sore ankles and feet, and sometimes his left shin while we were on vacation. We'd rub his feet and legs and he'd put on a tough face and move on.....
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<div>We noticed he seemed kind of lazy, didn't want to swim in the pool the entire time (which is COMPLETELY out of character for Lucas), and that he was laying around a lot more, and sleeping more as well.....again, we figured he was a growing boy, and maybe just needed more rest. Nobody was going to give him a hard time about being lazy on vacation...
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<div>Feb 28th we got home to Eagle River, and resumed "normal life" on Wednesday March 1st. Both Lucas and his brother, Nathan, went to school Wednesday through Friday and all was good. After school on Friday, both boys took the dogs on a walk around the block. When they returned, Lucas complained his feet, ankles and left leg (below the knee) were all hurting. He got on the couch and stayed there until he cried himself to sleep around 7pm.....at that point, it was decided something was wrong.
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<div>Saturday he woke up, crawled from his room to the couch, and immediately fell back to sleep. Kim (Mom) took Lucas to ER where she explained that this is completely out of character, and described the pain he had complained of. Lucas fell asleep more than once while at ER....
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<div>Blood work was performed at Kim's insistence (and unbeknownst to us...labs were confirmed a second time before delivering the news), and then they told Kim......
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<div>...."preliminary bloodwork indicates leukemia"
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<div>I received a call from Kim's phone at 5:46pm, but Kim wasn't on the other end of the call. It was a PA named Alana, and she asked me to come in as soon as I could, I said I could, "but why."....she said "it looks like Lucas has Leukemia". It was a blur. Lucas hasn't been home since that morning of March 4th.
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<div>Kim immediately left her work at Ravenwood Elementary School so she could be with Lucas full-time, and Kim's parents flew into ANC on the earliest flight they could book on March 5th. Nana and Papa have been HUGE in making sure "life at home" keeps moving forward while Lucas beats leukemia.
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<div>The following Monday the Pediatric Oncology Team at Providence obtained a bone marrow sample from Lucas's hip. Sample was sent to Seattle Children's Hospital for a full pathology report. The results we received on Tuesday confirmed that Lucas had acute lymphoblastic leukemia (A.L.L.). As terrifying as this sounds, it was a win..... A.L.L. can be treated in Anchorage, which meant no private med-flight to Seattle Children's Hospital (Thank goodness). It was also positive news because this type of leukemia is extremely treatable, has a very high success rate, and most pediatric patients respond amazingly to treatment. Essentially, his oncology team knew exactly what to do.
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<div>Meeting with our oncologist that Tuesday was one of the hardest meetings I've ever had, but Kim and I left the room feeling optimistic....scared, but optimistic. We were told 97% of Lucas's blood cells were currently infected with Leukemia....but, we get to stay in Alaska, and we now have a plan...time to get to work.
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<div>Lucas required blood and platelet transfusions before he could start his chemo. Unfortunately, he also developed a blood infection, which meant he was placed on a heavy-duty antibiotic for 7 days (started on March 7th). Even worse, this meant he couldn't get his port installed prior to beginning his treatment. His Oncologist opted to place a PICC line so we could still begin his treatment ASAP. Lucas will eventually get his port at a later date, but starting chemo is priority #1.
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<div>That Thursday March 9th, Lucas received his first chemotherapy, three doses in total. He received one chemo directly into his spine via Lumbar Puncture...(oof), and two other chemo's through his PICC line. During that first lumbar puncture, they also took a sample of spinal fluid to test for leukemia.
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<div>We heard the next day that Lucas's spinal fluid <strong>DID</strong> in fact contain leukemia. This means the leukemia was present in his Central Nervous System (CNS)....spinal fluid and the fluid around his brain. It was terrifying. This change resulted in Lucas's diagnosis status being changed to "high-risk". It really didn't change a lot for the first month of treatment (known as the Induction Phase). Only now he'd receive weekly lumbar pokes (instead of two, total) and he'd get a different dose of steroids for two weeks instead of all 29 days.
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<div>It didn't change what was immediately in front of us, so we pressed on....one task, one procedure, one blood draw, one antibiotic, one blood or platelet transfusion at a time. However, it DID mean we were going to be staying at Providence for longer.
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<div>Week one after his first chemo was rough. That's about it......leukemia sucks
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<div>Lucas got to see his brother for a few hours, and that was the highlight of the week, by far. It was the best medicine that could've been prescribed.
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<div>Telling Nathan that his little brother had leukemia is something I can't describe, but I told him that I'd tell him the truth the entire time, and that we may as well be scared together. Nathan has done SO well through all of this. He's mature beyond his age.
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<div>On Induction Day #8 (Thursday, March 16th) he got his second round of chemo. A lumbar poke was performed, and they took another sample of the fluid. Only this time, his spinal fluid contained "No Detectable Leukemia"......in seven days after his first treatment.....SEVEN DAYS...incredible.
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<div>He's been collecting his "Beads of Courage" throughout this fight. Each bead represents a different task, procedure, milestone, etc. It's a wonderful program, and we've been told his string of beads will probably be 10-15ft long when he's done! It's almost as tall as he is already, and we're just over three weeks in.
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<div>Last week he did his third Thursday with all three chemos.....he knows the drill and does absolutely amazing...they collected the same spinal fluid sample, and again, "No detectable leukemia" in his CNS. He's beating it.
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<div>It's now March 28th @ 1045pm and I am writing this all down as if it's new information, but we've been going for 24 days now....it feels like a year, and it also feels like an instant.
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<div>Lucas is doing really well. He has started acting like himself and making the same goofy jokes and comments that we've been missing for a couple months now. He seems to have more energy, and he is always doing his best to be in a good mood. The other day he proudly stated..."well, I haven't worn underwear in like three weeks...."...he must be feeling better.
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<div>Lucas has also been on a steady regimen of zofran, so he hasn't really been sick at all, it's a blessing. Each week he does better and better until we get to Thursday/Friday, then he starts over again. He was also placed on gabapentin for help with nerve pain, which is a side effect of one of his chemo's. Since being put on gabapentin last Wednesday, he hasn't had a single pain med, not even chewable tylenol. Plus, he's been out of bed and walking at least three times each day. It's very encouraging to see how well he is doing.
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<div>He is so tough, and he has no idea. I don't think Kim and I have been able to take many pictures of him without a smile on his face. Despite everything his little body has been through, he's a trooper. He enjoys playing games on his switch, playing (he'd say BEATING) his Nana in Uno, facetiming with his brother and grandparents in Colorado, watching youtube videos, and I think he's trying to watch every disney movie he can find. His appetite is impressive, to say the least. He's actually gained weight since his admission to the hospital.
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<div>If all goes well, on April 7th we'll receive the full pathology report from his bone marrow sample, and it will be nothing but good news.
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<div>April 18th is the day we'll begin phase 2 (known as Consolidation). We've been told it's difficult.....but that's OK, it's all difficult. His Oncology Team will be putting together a plan based on the results we receive on April 7th, and we'll press on. "Consolidation" phase should last somewhere in the 6-8 month range.
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<div>Lucas, Kim, Nathan and I want to thank our Family (near and far), Friends, FRamily, Doctors, Nurses, PA's, Bosses, Coworkers, Teachers, Neighbors, everyone at The Crossing &amp; Birchwood Christian School......absolutely EVERYONE for all of your help &amp; support. It means more than we can say.
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<div>I'll post updates so we can all fight together with Lucas through every step of this journey. He has a long road ahead, but he's a tough little boy that will beat Leukemia....no doubt in my mind, 100%
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<div>We appreciate every single Prayer, gift card, note, puzzle, game, meal, doordash, handshake, hug and all of the kind words we received from everyone.
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<div>Thank you to everyone from the entire Kozlowski Family -
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<div><strong>Be #LucasStrong</strong>
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Be #LucasStrong - Help Lucas Beat Leukemia

Nick Bruckner

Faith

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Medical

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Nick Bruckner

Nick Bruckner

What they care about

Featured causes

Help Send Rylan Kirby to the 2026 CrossFit Games!!

Help Jamie Rose's Family After Tragic Accident

Tom Mute and Family

Edgar Mark Anagick

Be #LucasStrong - Help Lucas Beat Leukemia

About me