Stories

What you need to do when you are diagnosed with an MPN. 🔟. Have a good support system - When you are first diagnosed, it feels like you are on...

I was definitively diagnosed with WM in December 2020. I was having progressively worse bloodwork with my GP. It took approximately two years and bone marrow biopsy to conclude that...

In October 2019 I started writing down symptoms that I had been feeling off and on for a few years. All of a sudden it seemed like they were happening...

My name is Tony. I was diagnosed with ET..essential Thrombocythemia in the fall of 2019. I’m now 57. I had a BMB in February of 2020 to check for myelofibrosis...

I never thought of myself as an over-achiever, but as a cancer patient, I guess I am. I am fighting Multiple Myeloma and Therapy-Related Acute Myeloid Leukemia. My diagnosis of...

A little intro to my story… I have been a very active 73-year-old, walking, biking, hiking, etc. I do not like to go to doctors and was always healthy, so...

Diagnosed in 2019. Yet work as hard..as if I’m a teen....and they said you’re strong. For that keeps me going....and helps my knowing....and they said I’m strong. Out of sight...

"Hey! You look great!" I give a half-smile and nod and think of the reflection in the rearview mirror I'd seen a few minutes ago. I'd seen dark circles around...

In 2020 I started losing weight, looking pale, feeling exhausted, and very stressed. Was working from home. Had agonizing pain in my ribcage. No cracked ribs per x-rays. My sis...

Recently, I posted an update on Facebook. I wrote about how I was competing in a tennis tournament. I included two pictures- one of myself in the hospital after my...

I had polycythemia vera for about 15 years. I have been giving blood twice a month to keep h&h (hematocrit and hemoglobin) in normal lab values. Last year I have...

Hi to my understanding new friends, I am not great on the computer but I do my best. I was diagnosed with thyroid cancer in 2014. The whole thyroid had...

I am making a new life. Because of childhood cancer I am making a new life after spending my entire youth fighting for the life that I was promised. Because...

I was diagnosed with Multiple Myeloma in 2017, it has been quite the journey dealing with changing of meds to side effects. I am learning to surrender to the unknown...

I am 46 years old, a mother of 3 and I also have 3 stepchildren. I was diagnosed with Multiple Myeloma on February 25th of 2021. I had had serious...

I was 14 when I was diagnosed with leukemia. I relapsed twice. When I relapsed for the first time we found that I had blast cells growing on my brain...

It was 2 weeks before Christmas when the headaches started and as my work week continued, my headaches seemed to get worse rather than better. My primary doc suggested it...

I am a Multiple Myeloma survivor of 5 years living daily pushing through this disease. I have my challenges but life is good! I went a year undiagnosed with several...

Where do I begin? Almost a year ago, my mom was diagnosed with MDS. After a few months, she was re-diagnosed with AML. I’ll be honest, I had no idea...

I had no symptoms with Lymphoma NH when I was diagnosed at 55 except for a swollen abdomen which I put down to menopause. Fortunately, my GP sent me for...