Nine Years in Remission!

In December, I celebrated nine years in remission from large B cell non-Hodgkin’s lymphoma. Thanks to my generous donors, my Light The Night team and I have raised over $25,000 to help the Leukemia and Lymphoma Society help fight blood cancer and save the lives of people like me. For more, visit https://pages.lls.org/ltn/nyc/manhattn22/JCaserto.

Seven Years Later

Obligatory milestone selfie, 2020 edition

I’VE COMPLETED ANOTHER TRIP AROUND THE SUN since my diagnosis in 2013 of large B-cell non-Hodgkin lymphoma. And what a trip it has been. 

Along with everyone in NYC, I scrambled in early March as the Corona Virus started to spread exponentially. I kept remembering the saying, “This, too, shall pass.” Early in my treatment, I walked by a local restaurant and saw it written on the sidewalk chalkboard. It was an affirmation of hope and boosted my resilience.

I used the phrase and shared that I was a cancer survivor during my first Zoom session of the course I teach at Pace University to reassure my students. The class transitioned to remote learning in days, and many of my understandably anxious pupils had to pack up and leave campus. It must have felt like they were living in a sci-fi thriller. One had to find a flight home to Europe where the virus had already hit, and Italy was in lockdown. Another, from India, had no choice but to stay in the city. Others went to their homes within New York City and the metropolitan area where transmission rates were alarming.

I often reflected on counting off each of the 18 weeks of chemo and beyond. July became August, summer became autumn, and the holiday season approached. After chemo, the time between follow up scans and visits increased, and at my annual checkup last December, Dr. Raphael, my oncologist, told me that I didn’t need to come back anymore. 

I wondered, too, what it must be like for all the cancer patients during the pandemic. I had to go to NYU Langone daily for five straight days of infusions, and, again, the day after finishing for an injection of Neulasta, a drug to boost my blood cell production because the chemo wiped out my immune system. That was challenging enough in normal times, much less during the chaos of a highly contagious virus, with patients lining the hospital’s hallways, where many would take their last breaths. 

When I learned that the Leukemia and Lymphoma Society developed a fund to help blood cancer patients impacted by COVID, and I kicked off my Light The Night fundraising early. Thanks to the generosity of so many, I have already raised over $2600. Please visit my page to learn more and donate online.

Yes, cancer did indeed pass, and COVID will, too. Meanwhile, we have the opportunity to learn what is important to us, how the human spirit can get us through challenging times, and how to savor life. Most importantly, it’s also ok and necessary to feel joy, despite it all, which is what surviving cancer has taught me.

Hear Me Tell My Story

The question I’ve been asked and answered most is, “how did you find out you had lymphoma?”  The Leukemia and Lymphoma Society invited me to share my story with a group, as a prepared speech, this summer. I was honored to be the keynote speaker at their Light The Night Manhattan 2016 kickoff event, held for the Barclays team in New York City, on July 14, 2016. It was an emotional and cathartic experience, which I hope helped to inspire the team. While it isn’t the live version, you can hear my lymphoma adventure by clicking here

If you can, please donate to my Light The Night fundraising efforts and help me fight blood cancer.  

Please Help Me Light The Night, Again!

Me, with my teammates Margaret and Sue, at the Light The Night Manhattan kickoff party in July, 2015.

Me, with my teammates Margaret and Sue, at the Light The Night Manhattan kickoff party in July, 2015.

Thanks to everyone who supported me and helped me raise money through The Leukemia & Lymphoma Society’s Light The Night Walk in 2013 and 2014, and to those who have already given to my 2015 efforts. This November will mark two years of remission for me, which is a very important milestone. If my lymphoma hasn’t come back—and it’s very unlikely that it will—my chances of being cured jump from 80-81% to 98-99%! (More of my story is at my fundraising page.) Your generous donations to Light The Night will help to find better treatments and cures for blood cancers, so patients like me can live better, longer lives. In fact, I personally received one of these treatments, the chemo drug Rituxan (Rituximab)I’m walking again this year, on October 1 in Manhattan, and if you’re able to help, please make a tax-deductible contribution!

You can give in two easy ways:

  1. Online: Please go to http://pages.lightthenight.org/nyc/Manhattn15/JCaserto to donate online quickly & securely. You will receive an email confirmation of your donation as soon as it is made.
  2. By Check:
    1. Please make payable to The Leukemia and Lymphoma Society.
    2. Put Joseph Caserto: Light The Night 2015 in the memo.
    3. Mail to:
      The Leukemia & Lymphoma Society
      Attn: Light The Night
      61 Broadway, Suite 400
      New York, NY 10006

Whether you give $5 or $50, your generosity is greatly appreciated and any amount will make a difference in the lives of thousands of patients like me, who are battling blood cancers. 

Thanks,

Joe

P.S. Please share this with as many people as you can to encourage them to donate as well!

The People We Meet

This French short beautifully captures how we can affect each other’s life, and the music is as charming as the illustration and animation. I love that it uses balloons as a symbol of friendship, love, and caring, which I realized is a nice connection to the Light The Night Walk, which also uses them. Just a reminder, I’m walking on Wednesday, September 25th, and you can help or join me.

If you can’t see the video here, just refresh your browser.

FLOATING IN MY MIND from GOBELINS pro on Vimeo.