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Finding My Way w/ Danielle Maz's avatar

I, too, live with cancer. I was diagnosed with stage four adrenocortical carcinoma. It is an ultra rare cancer. 1 in 1 million people will be diagnosed. I am able to reply to your note eight years into this diagnosis.

I could feel the air stop moving in and out of my lungs when I read about the results of your bone marrow biopsy. It stung.

As some who has been fighting tooth and nail to have cancer excised from my body completely, I know how important it is to have your TRIBE near you.

Reading about your small joys with photos made me think deeply about the joys I have experienced these past few months. Thank you for the spark to reflect beyond the treatments. Here are a few of my joys.

I love that my spouse and I fall asleep next to each other holding hands. It makes me feel like we are growing old together. He is my favorite person and loving him in a simple manner fills my heart.

I had Pulmonary rehab this past week and I walked just over half a mile. It was the farthest I have been able to walk without stopping to sit after having open heart surgery in June. Sitting down when the timer went off felt like such relief, but hearing what I accomplished invigorated me to keep pushing my body forward.

My last joy is a two-parter. I only know the joy of the first half right now. Last evening, my spouse and I were gifted tickets to watch the evening session of the US Open tennis quarterfinals. We have wanted to go to the US Open for many years. Cancer treatment or cancer recovery always seemed to get in the way of us making time to complete a bucket list item. This year, I will be in Flushing Meadows to celebrate my 13th week post-op.

I could write so much more about the joy of watching beautiful sunrises and sunsets as well as some CRAZY rain or thunderstorms roll through our corner of VA, just miles outside of DC.

It may have been a hard few months. Ok, harder than I ever could have imagined, but allowing myself to enjoy these moments have carried me to this very moment.

Thank you for sharing yours and taking a moment to read mine.

Best,

Danielle

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judy fine-edelstein's avatar

As usual, reading your letters brings me joy, and teaches me about living. I also have AML, 34 months post transplant, and am also unfortunately too familiar with MRD results. I'm also a physician, and this journey since I was diagnosed in May, 2020, has taken a bit bite out of my joy. But I read what you just wrote about the small joys, and I realize, I have been living in what I call "small chunks" of time. I enjoy seeing the zucchini growing in my garden, I look forward to a eating a delicious chocolate cookie, seeing my children and hugging my dog. Thank you for putting into words, those experiences that have meaning, evening the tiny ones. BTW, I do a lot of volunteering for the Leukemia and Lymphoma society, and am the co-chair for the patient advocacy at Dana Farber, where I am treated, trying to continue to give back, even though I can no longer practice clinical neurology. Sending lots of love.

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