patient stories

Amy’s Story of Resilience, Recovery, and Second Chances

At first glance, Amy’s bright smile and determined spirit don’t reveal the extraordinary journey she has traveled to get here.

Amy is a proud mother of two boys, a dialysis patient, a college student, a recovery advocate, and a woman rebuilding her life one step at a time, quite literally.

Years ago, after receiving a kidney transplant, Amy experienced a series of personal struggles that eventually led to addiction, declining health, and the heartbreaking loss of her transplanted kidney. Ashamed and overwhelmed, she stopped attending medical appointments and drifted further from the support she needed.

“I had given up on myself,” Amy shared honestly.

Her health deteriorated rapidly. Eventually, severe infection and sepsis led to the amputation of both of her legs above the knee. Doctors told her she might not survive.

But Amy did survive.

What followed was not an overnight transformation, but a journey of recovery. Supported by her family, healthcare providers, her dialysis team at Puget Sound Kidney Centers, and her own fierce determination, Amy committed herself to rebuilding her life.

She returned to dialysis consistently. She learned how to navigate life with prosthetic legs. She taught herself to walk again in just six months, far sooner than expected. She learned to drive independently and began setting goals for her future.

Today, Amy is thriving in ways she once had not thought possible.

She is pursuing college courses in addiction studies and human services, making the honor roll along the way. She has completed recovery coach training and now leads a women’s support group for individuals navigating recovery, homelessness, domestic violence, and other life challenges.

“I want people to know recovery is possible,” Amy said. “You can lose everything and still rebuild your life.”

Throughout her journey, Amy says dialysis care and the encouragement of those around her helped restore not only her health, but her confidence and sense of purpose.

Her story is a powerful reminder that healing is about more than medical treatment. It is about compassion, dignity, support, and believing in people even when they struggle to believe in themselves.

Today, Amy continues working toward another kidney transplant while raising her sons and helping others find hope in their own journeys.

And perhaps most importantly, she no longer defines herself by what she lost but by everything she fought to regain.

Wrapped in Hope: Quilts that Bring Comfort and Connection to Whidbey Island Patients

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At Puget Sound Kidney Centers, care goes far beyond treatment. Sometimes, it begins with something as simple as a forgotten blanket and grows into something extraordinary.

When Lisa T, Administrative Assistant at our Whidbey Island clinic, first joined PSKC, she was tasked with cleaning out patient lockers. Inside, she found a beautiful pineapple quilt, along with several fleece blankets. She took them home, washed them, and gave most away but something told her to hold onto the quilt.

A few weeks later, a nurse asked if there was an extra blanket for a patient who had forgotten theirs. Lisa knew immediately she had saved that quilt for a reason.

The pineapple quilt became a shared comfort, washed and available for any patient who needed warmth during treatment. And stitched onto that quilt was a small tag: Quilters on the Rock Whidbey Island.

For months, Lisa thought about reaching out. One day, she mentioned the idea to Pauline, a PSKC patient, who smiled and encouraged her: “They love doing it, and need something to do.” They both laughed.  Lisa sent an email. The response was immediate and enthusiastic. “This sounds like something we can make happen.”

What happened next was more than anyone expected.

After meeting with members of the quilting group, one comment changed everything: “Well, they all deserve a quilt.”  With that, Quilters on the Rock committed not only to providing quilts for new patients but also for every current patient at the PSKC Whidbey Island clinic, which is about 44 patients.

Soon after, the first round of more than 20 handmade quilts arrived at the clinic.

Each one is unique, created with care, creativity, and collaboration. Some are made start to finish by one quilter, while others are assembled in group “play days,” where members come together to piece, quilt, and bind them. Every quilt represents hours of work and a deep desire to give back.

When the quilts were ready to be shared, Pauline, the patient who first encouraged the connection, was invited to choose the very first one.

As she entered the room, her face lit up. Surrounded by color, texture, and craftsmanship, she took it all in with wonder. And then, in a moment that felt meant to be, she began talking about her dear friend Leon, a quilter.

As the conversation unfolded, it became clear: Leon was connected to the very same quilting community standing in the room.

A full-circle moment. One of those quiet, powerful reminders that kindness has a way of finding its way exactly where it’s needed.

“It warms my heart to see all this,” Pauline shared, holding the quilt she had chosen.

For patients receiving dialysis, often spending 3-4 hours in treatment 3 times each week, these quilts offer more than warmth. They offer dignity, comfort, and connection.

Lisa now carefully washes each quilt before it is given, just as she did with that very first one. And with every new patient who receives a quilt, the impact continues to grow.

“It’s such a great feeling,” Lisa shared. “Patients are truly humbled by the gesture.”

Because of the generosity of Quilters on the Rock and supporters like you, our patients are not only cared for, they are wrapped in compassion, community, and hope.

Sometimes, the smallest moments, like saving a quilt, turn into something much bigger than we ever imagined.

Quilters on the Rock

Mr. & Mrs. Hollywood: Finding Freedom, Faith, and Family Through Home Dialysis

At Puget Sound Kidney Centers’ Port Townsend clinic, Jerry and CeCe are known affectionately as “Mr. and Mrs. Hollywood.” They arrive at each monthly appointment with a spread of food for the staff, warm smiles, and a deep sense of gratitude despite a journey with kidney disease that began in fear and uncertainty.

“We went in pretty scared,” Jerry recalls. “But from the very beginning, we had the absolute best care. They made me feel comfortable and treated me with such kindness all the way through.”  Jerry and CeCe give high praise to all of the PSKC staff they have worked with, from Port Townsend clinic’s medical director Dr. Gill, to their “beautiful angel Joel, and the wonderful Nurse Vickie with her beautiful smile that greets us every time.”

The happily retired couple, former Seattleites who spent 30 years in Los Angeles where Jerry was chef/owner of a restaurant that CeCe calls “the best on the planet”, returned to Washington to be closer to family. Not long after, Jerry’s learned he needed to begin dialysis. What followed was a life-changing transition to peritoneal dialysis (PD) at home, with CeCe as his dedicated care partner.

“CeCe really takes care of me,” Jerry says. “She handles so much of what I need to do to be on this system.”

With her background as a nurse’s aide in the Air Force and a lifelong exposure to healthcare through her mother who was a newborn ICU nurse, CeCe embraced the complex training. “When we got the nighttime PD machine, it was God’s gift,” she says. “It gave him his strength back.”

After a difficult period on in-center hemodialysis during a surgical recovery, the difference was unmistakable. “With home PD, I really have no bad effects,” Jerry shares. “It gave me my life back.”

Their journey has not been without challenges including supply disruptions, power outages, and the long, uncertain wait for a transplant. In every moment, the PSKC team has been there. They still talk about the night a staff member, Joel, drove through a blizzard to deliver warm dialysis solution so Jerry could safely complete his treatment.

“I will never forget that,” CeCe says. “I can call anytime, and they are there for us.”

For staff, the impact is mutual. “They are supportive and so thankful for their care,” says nurse Vickie. “They both encouraged me to finish school, and it gave me the strength to finish.

Today, Jerry is active on the transplant list and looking toward the future with hope. “On a good day, I feel it’s coming my way,” he says.

To PSKC donors, CeCe offers a simple message: “Your money is well spent. This is the best organization on the planet.”

And Jerry adds, “It’s the best family you could ask for at a time like this.”

Where there’s a will, there’s a way: Walt’s story

Meet Walt, who has been on dialysis at our Everett dialysis center since October 2013. Believe it or not, he has never missed a single treatment—and that’s something to be proud of!

From 1983 to 1989, while serving as a U.S. marine, Walt travelled around the world in service to his country. His service to others continues today as a member of The Road Back to Life, a mentor program that helps fellow patients cope with the effects of end stage kidney disease (ESKD). In these efforts, Walt has helped recruit new patients to serve as mentors and regularly participates in the mentor group meetings which, now offered online, support kidney patients locally and nationally.

Hoping to qualify for a transplant, Walt is working hard to lose weight. As many of you know, this can be especially challenging when you’re following the renal diet. To support this effort, he has reached out to many popular weight loss programs but has been turned down once he tells them he is a dialysis patient. So, for now, it’s his treadmill and his self-determination that keep him going. Walt believes his commitment to dialysis comes from his upbringing, being raised by his grandparents who survived the great depression. He says he learned a strong work ethic from them which was, “Do it, or don’t do it; pick ONE!” This, and other life lessons he learned as a marine, continue to drive Walt today as he navigates dialysis and the pursuit of a kidney transplant.

Walt also stays busy as the patient representative for his center’s monthly quality improvement meetings. He was recently recognized as a subject matter expert for the Patient Advisory Council and the National Patient and Family Engagement and Action Network. In his spare time Walt loves to cook, for himself and others, and he has put together a cookbook of his many favorite recipes along with a few kidney friendly diet suggestions.

“The world isn’t all sunshine and rainbows,” says Walt, reciting one of his favorite quotes. “No one is going to hit you as hard as life. But it isn’t about how hard you get hit, it’s about how hard you get hit and keep moving forward!”

Definite words to live by! Thanks, Walt, for being an inspiration to us all and for all you do to help others with kidney disease.

Kidney care comes full circle

Jacee Numbrado, dialysis tech at the Cogen Center in Bremerton.

At the young age of 18, while living in the Philippines, Jacee Numbrado was diagnosed with glomerular nephritis, resulting in end-stage kidney disease. He had been experiencing gouty arthritis symptoms for a week when he awoke one night with such intense pain, he was taken to the hospital where lab studies revealed a high creatinine level. He was given the choice of treating his condition with medication or starting dialysis. Jacee opted for medication which sadly did not help— he ended up going on dialysis two times a week while living in the Philippines.

Jacee and his family moved to the United States in 2019; he started dialysis at Olympic Peninsula Kidney Center (now Puget Sound Kidney Centers-Cogen Bremerton) that June. Soon after, with the support of clinic staff—who Jacee says “were always positive, made him feel comfortable and hopeful”—Jacee decided to pursue a kidney transplant.

In August 2021, Jacee received a kidney transplant at Virginia Mason. He did well during his weeklong stay in the hospital and was then released for observation at home for a month.

In July 2022, Jacee was hired as a dialysis technician at Puget Sound Kidney Centers-Cogen Bremerton. He is now helping provide care where he himself received care—a true full circle. Jacee wants to bring back what he received as a patient—hope and positivity.

“Every day is a new day and the staff at PSKC made this possible for me,” he says, “so I hope to do the same for patients I care for.”

Helping fellow patients live their best lives

On any given day, you might see Bob Crabtree teaching a class on how to make low-sodium sourdough bread as part of our CKD education program, leading an online support group for kidney patients, or presiding over a PSKC Foundation Board meeting to discuss ways to raise funds for PSKC and our patients. Recently retired from a 38- year career as a mechanic, Bob works tirelessly for people with kidney disease.

“Having a deadly chronic disease is terrifying to think about, let alone live,” he says. “If I had to deal with this alone, I’m not sure my outcome would have been as positive as it has.”

Diagnosed with polycystic kidneys as a child, Bob learned early on that his kidneys would likely fail in the future.“When you’re told at age 12 that you won’t live to see 50, you don’t take anything for granted.”

For Bob, education, preparation and the support of his family and friends were key in helping him manage his kidney disease, dialysis and eventual transplant. “My wife, Robin, along with my father and mother were very supportive. I was lucky to have a support system in place.”

Bob fondly remembers the support he received from a fellow patient during his first dialysis treatment—a simple act of kindness when he needed it most that ignited his lifelong desire to help other kidney patients. When asked why he works so hard, Bob says, “I’m happy to pay forward the gifts of kindness that have been given to me.”

How one patient’s love of sports impacts the health of his community

Top to bottom: Jon today, Jon circa 1983, and Jon with his family.

Meet Jon. M—Jon dialyzes at our Smokey Point Kidney Center and has been coaching basketball, football and baseball since he was 16 years old. At age 4, Jon was diagnosed with Type 1 diabetes. He credits his love of sports and his participation in sports for making such a difference in his health.

“I know I am still alive because I ran so much playing basketball,” he says.

Jon has lived his entire life in the Tulalip area and still has a hand in coaching the Tulalip Men’s baseball team, even travelling with them recently for a tournament. Players on the team range in age from 17 to 55 and while his son is “officially” their coach, Jon provides input whenever and wherever needed.

He also stays active by attending local games whenever he gets a chance—he recently went to see the Seattle Storm and the Seattle Mariners, and has also gone to see the Everett Silvertips and Aquasox, despite his busy dialysis schedule.

Jon’s coaching experience started when he was the assistant to the Parks and Recreation Department of the Tulalip Tribes—he had a knack for getting kids into sports, even if they were hesitant at first.

“At one point I had 50 kids show up, and I got every one of them involved in some way.”

Jon stopped actively playing when he was in his late thirties and made coaching his focus—he’s since coached basketball, football and baseball teams, proud that they’ve played some of the best teams in the area and even if they did not win, they always kept it close and competitive.

Jon’s impressed with the Tulalip Tribe’s focus in recent years on building new venues for sports, like baseball and football fields with Astroturf, a step up from the muddy fields where Jon played growing up. Jon also has another interest; his 10-year-old grandson has just started playing basketball. The legacy continues!

A dedication to helping others

Kidney failure did not come as a surprise for Richard Beach; almost 25 years ago, he was told that his kidneys had begun deteriorating and that one day, he might need treatment. He closely monitored his creatinine levels and was able to put that off for many years.

About two years ago, to learn more about kidney disease and how to live well with it, Richard and his wife attended Puget Sound Kidney Centers’ chronic kidney disease education program, Survive and Thrive. He describes this six-week program as “very concise” and a great way to reteach them how to menu plan, shop, and prepare foods that were tailored to their health needs and, helpfully, how to “cut corners with salt.” Richard really appreciated the PSKC program, taught by various medical professionals, especially the level of detail provided and the amount of time allotted for discussion each week—talking through examples and experiences other patients have had really helped reinforce the impact changing behaviors can have.

Richard is currently retired from the Air Force and a phone company but continues to volunteer his time as a critical member of the Snohomish County Emergency Management team, developing and implementing radio communication for natural disasters, including earthquakes, fires, floods. The team prepares for any situation that communication may be compromised (i.e. loss of internet) so that emergency services can continue to operate and provide help to those who need it. They also look at ways of linking with other networks on the state and federal level, so that key information regarding events can be handled appropriately. He is part of a core group of volunteers who, up until the coronavirus pandemic, were meeting twice a week at Paine Field in Everett. They now still meet once a week but hope to ramp back up in the near future.

These days, Richard dialyzes at Puget Sound Kidney Centers’ Mountlake Terrace facility, having started a couple of months ago, and is feeling better already. Richard, we certainly hope we won’t need your radio skills, though we’re sure glad that you and your team are there in an emergency!

Living Life to the Fullest

Musician, actress, singer, poet, activist, student and social worker are all titles held by Andrea Skywalker over the course of her extraordinary life. Born in Germany to a German mother and a Black American/Cherokee father, she credits her father’s military background and her mother’s meticulous nature with instilling in her a discipline and drive that would help her pursue her many interests. She has traveled extensively, and, with a degree in Human Services, she has enjoyed a long career as a social worker for the State of Washington. During her tenure as a social worker, she worked with victims of domestic violence, seniors and other people in need. “I like helping people who can’t help themselves.” She adds, “I want to leave something positive and beautiful in this world to promote unity.” Andrea enjoys the performing arts and has appeared on the stage and screen as a singer, musician and actress. She continues to perform at local venues.

In 1999 she suffered a major stroke which left her in the hospital for 2 months. She had to re-learn how to walk, talk and function, and her determination would be essential in her rehabilitation efforts, “As soon as I could walk, I went back to work. Never give up” she advises based on her own experience. When her doctor told her six years ago that her kidney function was declining and she should prepare for dialysis, Andrea was adamant that dialysis was not for her and she managed to keep her kidneys functioning for six more years. Eventually her kidneys would fail and she was faced with the ultimate choice. At this point, she did choose to continue living with the aid of dialysis treatments; “I decided I’m too busy to die.” Just a few months after beginning dialysis Andrea celebrated the debut of her first book, entitled “The World As I See It.” Now Andrea has just completed a second book and will soon be recording a music CD. She shares, “Even though dialysis is time consuming and takes up three days of each week, I often think about where I’d be without the dialysis. I choose to be grateful and to be happy that I’m still alive.

Enjoy a poem from Andrea’s new book, “The World As I See It”:

I’M SUPPOSED TO LIVE
I GOT THINGS TO GIVE
I GOT PLACES TO SEE
DON’T YA KNOW
I GOT PLACES TO GO
IN WIND – RAIN – AND SNOW
AND THE CLOCK KEEPS TICKING
REAL SLOW

WHEN I WAS 63
I WAS TIRED AND CRANKY
AND MY PRESSURE
WAS WAY TOO HIGH
AS MY KIDNEYS WERE FAILING
AND I LAY AILING
I WOKE UP AND SAID
NO – I’M NOT GOING TO DIE

I’M SO LUCKY I GET A SECOND CHANCE
TO WALK AND TALK
AND LEARN HOW TO DANCE
MAYBE FIND A LITTLE ROMANCE
TO APPRECIATE EACH MOMENT AND SAY
HOW ARE YOU TODAY

LET’S TAKE A CHANCE
AND DANCE THE NIGHT AWAY
CAUSE I’M SUPPOSED TO LIVE

By Andrea Skywalker @2017