One Man’s Experience with CAR-T Cell Therapy

By George Bailey & Jennifer Gillette LMSW
George Bailey reflects on his CAR-T cell Therapy experience for his Stage IV Follicular Non-Hodgkin’s Lymphoma.
My Blood Brother

By Nick Hudson
Nick was a perfect match for a four-year-old “toe-head” boy named Cameron who had leukemia, and needed a bone marrow transplant. I was “the match.” Cam’s transplant was successful and his parents told him he had a “blood brother.” You will enjoy learning how these “strangers” became friends.
The hope and magic of words…

By Jennifer Barish
The power of hope and stress reduction literally helped save this young mom and wife.
Karen’s CLL Journey- Wisdom, Inspiration, Resilience and Much More…

By: Karen Raman
Follow Karen’s cancer treatment journey and the multiple changes that occurred along her route. Lessons learned: you are your own best advocate; stay on top of your meds; and most important of all, keeping a positive outlook is at least fifty percent of the battle.
Transplant (An Unexpected Journey)

By: Jean C. Carroll
Discover how the support of community and extended family and a strong faith carries this young family on a seventeen-year journey into the unknown world of bone marrow transplant. There is a happy ending to their story.
Zen and the Art of Surviving a Bone Marrow Transplant

By: Peter Thomason
Peter shares how he found his way to handling the different issues that accompanied his post-BMT challenges. His discovery of Zen, a Japanese word for “meditation,” brought a sense of peace to his living each day as a cancer survivor.
One Woman’s Experience with Photopheresis

By: Jennifer Gillette and Lola Reich
Photopheresis is a wonderful option for transplant patients. Lola Reich answers Jen Gillette’s questions.
A Donor’s Story

By: Maureen Sonntag
A beloved fourth grade substitute teacher and a mother’s struggle with cancer opens the door to Maureen’s commitment to one day donating bone marrow for a stranger’s transplant … right place, right time, strong faith and a fond memory of Mrs. O’Reilly.
He Said: She Said: All Said with Love!
Lewis & Merle Christie
Lewis and his wife, Merle tackled his AML diagnosis together. Read their story of being “recalled to life” more than once by transplants, the support of family, friends, and medical personnel; and their sheer determination that Lewis would survive … period!
Embracing the Suck of Cancer

By: Michael Ansley
Read Mike’s story about how the term he learned in his Navy career, “embracing the suck,” became the mantra that guided his approach to handling GvHD and ultimately defeating leukemia. In the process, he gained perspective on what is truly important: God, Family & Friends … everything else is “just stuff!”
On the Psychological Preparation for Bone Marrow Transplant

By: Roy Proctor
“Deliberately” developing a positive, even “joyful” frame of mind can make all the difference in one’s approach to the experience of cancer. Read about how Roy used these mind-sets to deal with the effects of BMT and how it altered his life.
Cancer Sucks, Death Sucks, and Yet Life Can Still Be OK.

By: Stacey Town
On September 6, 1996, Stacey was “born again” … it was her second birthday. After a year and a half, her AML had returned. Discover how she courageously tackled multiple set-backs on her way to a bone marrow transplant that saved her life.
Moving Cancer to the Back Burner

By: Laura Weinger Housley
“I can’t wait to be on your side of the fence.” Laura was speaking with an AAL survivor. A relapse a year after her initial diagnosis and treatment, a bone marrow transplant was recommended. Today, she is a committed volunteer, helping other cancer survivors. Learn how giving back is its own reward.
The Strength of Our Anchors

By: Rob Minton
No one makes the transplant journey alone. Rob’s experience began with his closest companion, his wife Sharon. Other “anchors” who accompanied him on his multi-year trip that began in 2012 included doctors, nurses, medical technicians, friends and family members who kept home fires burning during his and Sharon’s long absences. Read their story and about Rob’s “blood brother” donor, Clint.
Meet Greg Rose: an awe inspiring umbilical cord blood transplant survivor

By: Greg Rose
Check out Greg’s BMT Cancer Survival Guide after his diagnosis of Acute Myeloid Leukemia (AML). Excellent advice when traveling a ten-year, very bumpy road to “a normal life.”
Finding Hope

By: Barry Stebbing
An extraordinary caregiver, Barry Stebbing wasn’t afraid to ask for help and it sure paid off.
James Bond Cycles On!

By: James Bond
James Bond keeps moving and grooving, showing cancer who’s boss. You won’t soon forget this fella.
Jennifer Nsenkyire

For this new U. S. resident who emigrated from South Africa, a bone marrow transplant unexpectedly cured two non-cancer diseases – Sickle Cell Disease and Multiple Sclerosis – and freed her from a lifetime of pain.
Jordan Segal

The unexpected gratification for a young stem cell donor leaves a lasting impression on this young man.
Peg McIvor – Second Opinion? You bet! Hear why here.

Pursuing a second opinion saved this woman’s life and gave the LINK one of its most valuable and loyal volunteers.
A nbmtLINK Salute to Caregivers

Caregiving is not a “sprint” … more often than not, it becomes a “marathon.” The “runner” or caregiver needs support too. Read about the LINK’s salute and its resource publication that provides that support to these unsung heroes.
Taking Time to Smell the Flowers

By: Rhonda Jokot
The positive connotation of the expression, “take time to smell the flowers” takes on special meaning for Rhonda: for her it means a “new normal,” her “second birthday,” a major fund raiser for Gateway for Cancer Research, and valued relationships with the LINK. You’ll feel good when you read her story.
Recalled to Life

By: Lewis J. Christie
Discover how the main character in Charles Dickens’ “Tale of Two Cities” describes Lewis’s “recall to life,” which can apply to most who experience a blood marrow transplant and its multiple challenges at every interval of its process. Lewis learned he has plenty of company.
Survivor Pat Sears on Paying It Forward Through the nbmtLINK Peer Support Program

By: Pat Sears
Learn how Pat’s introspection during her healing process from a BMT and GvHD led to her connecting with the nbmtLINK and discovering the personal benefits of “paying it forward.” “There is nothing like that feeling!”
Meet Jackie: We All Need Someone on This Cancer Journey and We Are Not Meant to Go It Alone

By: Jackie Pryor
A Diagnosis of stage IV Anaplastic Large Cell Lymphoma at age 29, was only the beginning of Jackie’s challenge. Cancer returned three more times, requiring multiple stem cell transplants. Discover how her courage and faith supported her on the journey to overcome the ravages of her disease.
Thankful and Thriving — Yes, you can do it!

By: Cathy Morris
Cathy doesn’t mean to spoil the ending of her story, but take time to learn how she and her husband, Glen knew “everything will be OK.” Bumps, challenges, fear were there to be sure; but one year post-transplant she is “thankful and thriving.” Her story has a happy ending.
Meet Faith: Making a Donor Difference in All That She Does!

By: Faith Metzinger
Faith’s personal experience as a donor “match” for a three-year-old boy with leukemia has, in her words, “changed me in so many ways.” It also was the impetus for her to lead a bone marrow drive in her town in the child’s honor. That was nine bone marrow drives ago.
Meet Janine: Surviving and Sharing Her Strength and Best Tips

By: Janine Hewitt
Learn about Janine’s initial diagnosis and treatment, and her ultimate struggle with GvHD. She explains helpful tips and insights she shares with others who are just beginning a similar journey.
Mary Clare: Parenting through cancer with grace and strength

The effects of a cancer diagnosis on family, especially a young child, and trying to get back to “normal.” For Mary Claire, it was a challenging journey; for her young daughter, mysteries for work through.
Meet Alana Werth, a Peer Support Volunteer for nbmtLINK

Alana Werth
Read about the great value Alana discovered in being a peer support person—how she was able to help patients who are facing what she had personally experienced.