Cheers to Seven Years of Remission

Joseph indoors, holding a cocktail, and with a lit Christmas tree behind him.
This year, the COVID-19 pandemic makes it especially important to celebrate good health.

MY REMISSION ANNIVERSARY IS A WEEK BEFORE CHRISTMAS. On December 20, 2013, I received my first PET scan after finishing six rounds of R-EPOCH chemotherapy, and the results were normal. It was the gift I was hoping for and was ecstatic to receive. The chemo worked, and my large B cell non-Hodgkin lymphoma was in remission, where it has remained ever since.

During this crisis, people battling cancer face the terrifying reality of getting treatment at hospitals filled with COVID patients. Paradoxically, to get better, they need to be where the risk of getting the virus is very high, while their immunity is deficient.

2020 is also the seventh year that I’m raising money for the Leukemia and Lymphoma Society (LLS) through their Light The Night event. LLS has resources for patients, families, and caregivers during this unprecedented challenge.

Thank you to everyone who has given this year and in the past. If you haven’t donated and want to, time is running out! There are only two days left to help before the cutoff on December 31! Please visit my fundraising page to make your gift

I wish you and yours a happy and healthy 2021 and thank you as always for your support. 

Five Years Later

5-Year Selfie in Times Square on the Q Train

My lymphoma adventure began five years ago, on July 10, 2013, when what I thought would be a routine doctor appointment lead to a chest x-ray, CT scan, and a diagnosis of large B cell non-Hodgkin lymphoma. Since I don’t have much news, I’ll share a few random thoughts.

A year ago, today, I posted my progress, and officially came out publicly. I had pretty much been living as out, and wanted to put any question on that front behind me, so I could live the life I want. The support from my family and friends has been wonderful and means a lot.

I started this blog with the goal of helping others by sharing my story. As I continue on my road to recovery, several friends have reached out with news of their own diagnoses, and questions about my experience with treatment. I’m glad that I was able to support them in some small way by sharing my story, and send love and healing to them and their loved ones.

I continue to do well, and will celebrate five years of remission in January. Meanwhile, I’m looking forward to a summer of traveling, friends, and working on my house.

Thank you all for your continued support. ❤️

Two Years Ago, Today

From my Instagram feed on my birthday in April: “Thanks for all the birthday wishes! Celebrated with ice cream sundae this afternoon. (For the record, only the front one was mine.)”

Selfie, taken after my last oncologist visit in June.

July 10, is a kind of second birthday for me. My first one is in April, when I turned 46, and I celebrated it in San Francisco with old friends who I hadn’t seen in a long time. But, this afternoon two years ago, I would visit my primary care doctor with a swollen face, and she would say to me, “This may sound strange, but I’m going to send you for a chest x-ray, because there are nerves that go from the chest to the face, and I want to rule out that there’s nothing there causing the swelling.” About an hour later, I would know that there was most definitely something there: a mass behind my heart, and after a surgical biopsy a week later, I would learn that it was the size of a grapefruit. The next day I would have a CAT scan, and a day after that I would get the news that I had lymphoma.

Two years later, I’m starting to feel that the journey I’m on is taking a new turn. With the diagnosis from a followup visit to my oncologist a few weeks ago that I am, “boring,” because I am continuing in remission with an excellent prognosis, and my chances of being cured improve each day. I’ll have a scan at the end of the year, which will mark two years in remission. If the scan comes back clean—which is extremely likely—it will be my last unless I exhibit any symptoms that warrant another one. At the two year point, Dr. R. said the chance of a recurrence is about one or two percent, and the risk of exposing me to radiation to get scanned becomes greater than the risk of not getting it done. In two more years, at four years with no recurrence, my lymphoma will be cured.

I still continue to experience fatigue and a range of emotions, which is normal, and as he said, “time is the ultimate healer.” My return to work part-time is proof of that in a way, because it has made me realize that I’m not yet ready for full time. Thankfully, I have long term disability insurance, which I get through Freelancers Union, so I can focus on my health, without worrying about paying my rent.

I can’t say I’d sign up for another go around, but my diagnosis of Large B Cell Lymphoma has taught me so much, and given me a different set of priorities. I find it easier to say, “no,” to things and people that don’t fulfill me, and I see the importance of rest and downtime, which before cancer, would usually be the first two things to be sacrificed. My second birthday wish for all of us, today, is to enjoy good health, and experience all the joys that life has to offer.

Status: Clean Scan, All Normal, Remission Continues!

Hello!

I wanted to share a quick update with everyone.

My most recent 2-month checkup with my oncologist, Dr. Raphael, was at the end of June. I got good results of my 6-month CT scan, assurance that everything is progressing normally, and confirmation that remission continues.

Going forward, I’ll see Dr. R. every 3 months, and my next scan will be in the fall. My plan is to continue focusing on my recovery through the end of the summer, and officially return to working part time after Labor Day.

Look for more posts in the next few weeks, and enjoy the summer!

Lotsa love,

Joe/Joseph