International Waldenstrom’s Macroglobulinemia Foundation
Sharing your story with us is a fantastic way for you to help others who are traveling down the same path that you are — whether you are a patient, caregiver, or family member— we would love to hear from you.
Patients and others who visit our website often tell us that one of their favorite features of our communications are the stories of the lives of people who are affected by WM. We would very much enjoy learning about you, your story, and how your experiences can motivate, help and inspire others we serve.
We invite you to read, enjoy, and learn from the following first-person stories by patients and caregivers, worldwide, affected by WM.
If you are interested in sharing your story with us so that we may share it with others on our website, please submit your contact details.
Lisa Weldy: Resilient and Grateful It’s been five years since I wrote my story for IWMF. A lot has happened since then, but most importantly, my WM has remained stable, and I remain in a deep response, meaning that I have responded well to...
Tom White: Coming Full Circle Rituximab: How My Work Got Personal It all began in 1971 when, armed with a BS in Chemistry and an MBA, I began my career at Cutter Laboratories (soon to be acquired by the Bayer pharmaceutical company). At...
From Australia- David Rabie: My Story of Hope Hope is an optimistic expectation of a positive outcome for future events. Hope is more than a mere wish as hope implies a belief and confidence that positive outcomes will be attained. “Hope is a...
Introduction: A Life Full of Family and a Sudden Health Challenge I am Barbara Richter, an 86-year-old former registered nurse, and a proud mother of five children, ten grandchildren, six great-grandchildren, with an ever-growing extended family....
From Canada—Paul Kitchen's Familial WM Story Paul's mother, Mary Kitchen My story of hope began in the late 1970s when my mother, Mary Kitchen, was diagnosed with WM. Without any treatment available, her disease steadily progressed - terrible nose...
From Iceland - Gunnar Ármannsson: And the Adventure Continues The Big Repair Year 2019. I anticipated receiving chemotherapy later in the year, but that didn’t stop me from setting an ambitious running schedule–highlighted by a marathon in...
Ryan Scofield's Update: Young WMers Shared Challenges Life continues for me, with WM being low on my list of daily concerns. I have continued Ibrutinib with great success. No side effects and a disease that cowers in shame. Low IgM and normal...
At the time of my husband Mark’s diagnosis almost 14 years ago, I can easily transport back to the minute we were given the diagnosis. It felt like lead weights had been tied to my ankles and I was dropped in the middle of a dark ocean. It was all...
Chris Moakley: The Story Continues On First of all, let me say it’s a thrill to still be here and able to write and share this update. I last wrote an update five years ago, finishing with “I hope to write again soon.” My Waldenstrom’s lives up to...
Part 1: My journey The word cancer is scary enough, and adding incurable in front of it only intensified the fear. In August 2020, at the age of 34 I was diagnosed with WM. The diagnosis came out of the blue as I was a young, fit and healthy mother...
Julianne & John Flora-Tostado: Our 49th Anniversary Making the best while facing the unknown together. Seven years ago, after John completed his initial and only treatment for WM (five rounds with Cytoxin, Rituxan and Prednisone in 2016), he...
From Canada: Lucie Martineau's Six-Year Sequel When I last wrote my Story of Hope, I had so many items on my bucket list that I vowed to keep healthy in order to live a long life and accomplish as many of them as I could. In 2021, my IgM...
Laurence Elliott: “Nautical Distancing” and Other Great Stuff, the New Normal My life was always fast-paced—working and playing hard with family and friends. But life has a way of letting you know who is boss and, boy, did it ever! My energy had...
Martin Vanderlaan: Celebrating 5-Years Post Stem Cell Transplant with a Wedding! With a small group of friends on March 20, 2022, we celebrated the 5-year anniversary of my autologous stem cell transplant (ASCT). I say “we” since the last 5...
“The secret to health, both mind and body is not to mourn the past, not to worry about the future, but to live the present moment wisely and earnestly.” ~Gautama Buddha We’ve all learned to live with the following words: “Not curable but...
Bob Lynch: Still Rowing On with WM! The rowing goes on, and the singing is still strong here on the ROW BOB ROW TEAM in Sebastian, Florida. In August of this year, I will be celebrating my 75th birthday with a row to a local pub. Upon diagnosis of...
Julie Davidson: My Journey With WM and Bing-Neel Syndrome Published in the Torch 23.2 (April 2022), page 5 On February 14, 2011, I was diagnosed with both WM and Stage IIIA breast cancer followed by ten months of chemotherapy, a double...
Margit Novack: Who gets to Live Like This? I saw my internist’s number appear on my cell phone. “There is an unusual result in your routine bloodwork. I think you should see a hematologist.” “Why? What do the results suggest?” I asked. “You might...
From Canada - Ron Ternoway: The Trials Continue! It's been more than 14 years since my Waldenstrom diagnosis, and I've spent half of that time on clinical trials. Over the last year, I have been enrolled in a U.S.-based clinical trial of...
Where Hope Is Found by Julie Richardson, diagnosed with WM at age 44 www.someonestolemycoffee.com March 13, 2020. A Friday the 13th I will never forget. On the one hand, it would turn out to be my then twelve year-old daughter’s last day of...