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Eli Sykes: MS Athlete Extraordinaire

Meet Eli Sykes, an athlete with multiple sclerosis from Wenatchee, WA and a Choose Your Own Adventure rider for Bike the US for MS. This year, he’s already raised over $2000 and is tearing it up in multiple races while repping our signature jersey!

Eli doesn’t let MS stop him — he leans into the challenge and learns from living with it.

Eli in the Gran Fondo race in Ephrata, WA

Why Eli Rides for Bike the US for MS

It’s been a longtime dream of Eli’s to bike across the country after hearing stories from people who have ridden across the US. He loves listening to a close friend who reminisces about the kindness of strangers and memories of incredible scenery. 

Eli remembers a transformative documentary that set his adventure in motion: “Truly, it was when I watched a series on PBS called Shadow of a Wheel that I realized how transformative a journey can be supporting people with MS. I wanted to support an organization out there that supported this fantastic journey. That’s how I landed on supporting this cause.” 

Finishing the Gran Fondo

Mechanical Failure and a Life-Changing Phone Call 

Last May, Eli knew there was something wrong: “my body had a mechanical failure…I woke up with clouded vision in my right eye.”

After what felt like a million tests, a doctor called Eli and diagnosed him with Multiple Sclerosis. Eli was on a bike ride with his friend Bart in Winthrop, WA. The realization shocked him and he got off his bike to listen to his doctor.

What happened next changed how thinks about life: “Bart, knowing we had many miles to go, yelled out to me, ‘we have to keep going’. He was right, I needed to keep going. I need to keep fighting. I got off the phone and kept riding. And from that day, I’ve adopted what he yelled at me as a motto: do the right thing, do the next thing and keep going.

“New Eyes”: advice for those recently diagnosed with MS

Eli explains, “Your signs and symptoms mostly don’t make sense at first, and you are allowed to have questions.

Find yourself a journal to write down anything new that you have started to notice, but don’t get lost in them. You should bring up new things to your doctor and send a message. I felt peace even in the uncertainty of knowing what was happening to me and you can too. 

You’d be amazed at the support of my wife and friends. I’ve received so much when I have opened up about my journey. I can’t control the MS, but I want to end it for others. I’m now fighting my MS and you join the fight by helping out organizations like this one.

If MS has given me anything it has given me new eyes and I see things differently now and I want to help.”

Eli began bikepacking in 2020

Who inspires Eli?

Eli is following in the footsteps of his grandfather Jack Rogers and his uncle Lee, who used to do long bike trips. His grandfather encouraged him to ride without training wheels and taught him the value of always wearing a helmet – something that we at Bike the US for MS can absolutely agree with!

His uncle passed away from Parkinson’s disease and Eli remembers that “watching him degrade from the neurological disease was hard for all of us. He was so funny and athletic.” 

Eli credits his father as well: “My dad gave me the boldness and knowledge to not be afraid to fix anything, an essential skill when on a bicycle journey.” 

After years of hand-me-downs, Eli purchased his first brand-new bike in 2020 and started bikepacking.

Eli and his wife, Jacqueline Sykes

Eli’s Bucket-List Rides

Eli shares that he would love to participate in a Tour Divide, a self-supported race from Banff, Alberta to Southern New Mexico: “The challenge and scenery are a definite draw to me.” 

Eli also wants to explore his home state and ride across the country from West to East. We think he’s more than capable! Comment below if you’d also like us to introduce a West to East ride…

Eli’s positive attitude, grit, and commitment to himself and others inspires us immensely. We’re so glad to have Eli wearing our jersey this year and raising money for people with multiple sclerosis.

Support Eli and people living with MS by donating to his fundraising page. Follow Eli on Instagram to keep up with his adventures.

logo bruce randall

Rolling with Randall: An MS Warrior’s Journey through Virginia to the Pentagon

Some people let life’s challenges slow them down. Randall Pope? He hits the gas.


On May 28th, Randall—an Army veteran, wheelchair bowler, and all-around force of nature—will set off on a 250-mile journey from Christopher Newport University, through Virginia to the Pentagon. But unlike most endurance riders, he won’t be on a bike—he’ll be rolling the entire way in his power wheelchair, accompanied by longtime friend and Bike the US for MS alumni, Bruce White.

This ride, planned to coincide with Memorial Day, isn’t just about personal achievement. It’s about raising awareness for multiple sclerosis (MS), the disease Randall has been battling for 30 years. It’s about proving that physical limitations don’t define a person. And it’s about giving back—Randall is partnering with the Mid-Atlantic Chapter of the Paralyzed Veterans of America, of which he is a dedicated member, to support his fellow veterans living with spinal cord injuries, MS and ALS.

“Bruce, You In?” – The Birth of an Idea


The seed for this journey was planted on a quiet Sunday last September. Randall was at his desk when it hit him—this marked his 30th year living with MS. He’d never seen someone in a power chair take on a ride like this, but if anyone could do it, it was him.

So, he called Bruce.

The two met through bowling and bonded over their shared connection to MS—Bruce’s brother also has the disease. Years ago, Bruce cycled from Seattle to San Diego in honor of Randall. Now, Randall was asking him for a different kind of ride.

The request was simple: “Would you like to ride across Virginia with me while I go in my wheelchair?”

Bruce didn’t even hesitate. “I’m in.”

Life Before MS: Military, Discipline, and an Unexpected Diagnosis

Randall’s life before MS was fast-paced, disciplined, and structured—qualities shaped by his time in the U.S. Army.

But that changed on June 27, 1994.

That morning, he had gone for a three-mile run on a golf course in Texas after his usual calisthenics. By the time he returned to formation, his vision in one eye was gone—a cloudy blur where clarity used to be.

Doctors initially shrugged it off—blaming the Texas heat. But when his symptoms persisted, the truth became clear: it was optic neuritis, a condition often linked to multiple sclerosis.

It took nine long months before he received an official MS diagnosis. In the meantime, he was removed from active duty, unable to work on aircrafts—a career he had dedicated himself to. He was working on Apache helicopters—intricate machines that required precision, patience, and skill. But MS stripped him of that career. His discharge came on April 8, 1995, and with it, his entire life changed.

But Randall wasn’t done fighting.

In 2016, another blow came—throat cancer. He drove to the University of Virginia every day for 40 days straight to get radiation treatment, enduring the brutal regimen with the same resilience that got him through the Army. He beat cancer, just like he refuses to let MS define him.

Living with MS: The Hardest Part Isn’t the Disease

MS has taken its toll—since 2016, Randall has used a wheelchair full-time. But when asked what the hardest part of the disease is, he doesn’t hesitate.

“It’s not dealing with MS myself—it’s watching my wife, my kids, Bruce, and my friends have to deal with it.”

Randall met his wife, Joann, after leaving the Army—she was his landlord at the time. She jokes that he only started dating her to get out of rent payments, but the truth is, she’s been his rock ever since.

They built a life together, raising kids and running a farm with cattle and goats. Randall stays as active as possible—moving hay with his tractor, rearranging furniture while Joann’s at work (even if it takes him ten times longer than it would someone else).

Randall is both stubbornly strong and realistic: “I’m going to do what I can do until I can’t do it anymore.”

The Ride Setup: Testing the Limits

A challenge like this isn’t just about distance—it’s about endurance, preparation, and overcoming the unknown. Randall and Bruce have been doing test rides to work out the kinks, pushing the limits of Randall’s wheelchair, his body, and the team’s strategy.

With hazard lights flashing behind them, a support van trailing, and another car snapping photos ahead, the duo rolled through town, getting a taste of what May 28th will bring. They covered 7-8 miles, and even at that distance, Randall could feel every crack in the road. The vibrations wore on his body, the chair shifted in ways they hadn’t anticipated, and he realized just how punishing the ride might be over 250 miles. They’ll need more test rides, more fine-tuning, and plenty of grit to pull this off. But one thing is certain—Randall isn’t backing down.

There are still tweaks to be made to ensure his comfort, but the core of the plan is solid.

Mapping the Miles

At first, the plan was to go straight across Virginia, but after looking at the roads, they decided on a safer route that would take them through some of Virginia’s scenic college campuses. Their final path includes stops at:

  • Christopher Newport University
  • The College of William & Mary
  • Virginia Commonwealth University (via the Virginia State Capitol)
  • University of Richmond
  • Randolph-Macon College
  • Mary Washington University
  • George Mason University
  • The Pentagon

It’s a route designed for safety, visibility, and impact—passing through communities where their message will resonate the most.

The Cadillac of Wheelchairs

Randall won’t be rolling in just any wheelchair. His Permobil F5 Corpus Power Wheelchair is top-of-the-line—think of it as the Cadillac of mobility. With three gears, cruise control, and the ability to maintain speed even on hills, it’s built for endurance.

At first, Randall worried that Bruce would have to hold back while riding next to him. But after some test runs, it looks like they’ll be a good match.

“I’ll be rolling at 7 mph. Bruce can keep up,” Randall jokes.

Building the Dream Team

Randall compares this team to his Army days—a tight-knit unit where trust and teamwork matter more than anything. Randall and Bruce have assembled a team of support crew, including:

  • Kevin Goldrick
  • Jerry “JT” Thompson
  • Emily Michaels
  • Isabelle Pryor and Victoria White
  • Randall’s wife Joann Pope and daughter Amy Ridge

Keeping the team tight makes logistics easier. But more than that, it strengthens the bond.

Randall looks forward to ending each day looking his team in the eyes, sharing a meal (maybe a beer), and reflecting on what they’ve accomplished.

“That’s what it’s about,” he says.

What’s Next? Rolling with Randall Part II

Even before this journey begins, Randall and Bruce are already dreaming bigger.

The next goal? A multi-week ride with other wheelchair users living with MS—to show the world what’s possible when people refuse to let their diagnosis define them.

But first, there’s the May 28th ride.

Before they even hit the road, they’ll be in the spotlight—Randall is throwing the first pitch at the Fredericksburg Nationals Game on May 20th—a moment that will shine a national spotlight on his mission.

Randall and his team are working on one more goal: To have Washington Nationals legend Ryan Zimmerman and his mother join him on the mound as he throws out the ceremonial first pitch. Mrs Cheryl Zimmerman was also diagnosed with MS 30 years ago, and is a member of the Board of Directors of Ryan’s project, The ziMS Foundation.

Join the Journey

Randall’s story is one of resilience, grit, and heart. He’s proving that MS doesn’t get to write his story—he does.

Want to support Randall and the team? Share this story. Donate to the cause. Follow their journey. Let’s make sure the world knows what’s possible when you refuse to back down.

Donate directly to Randall’s Page:  https://www.paypal.com/donate?campaign_id=LUFLEYQ6VGN4A

Check out Rolling with Randall’s Facebook Page: https://www.facebook.com/people/Rolling-With-Randall/61571752194366/ 

See the PVA page for Rolling with Randall to watch a video featuring Randall and Bruce: https://www.pvamidatlantic.org/rollingwithrandall/

Show your support with Rolling with Randall merchandise: https://wheelersdepot.com/rolling-with-randall/