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Welcome to The Lymphomaniac's Homepage
Oct 11, 2011
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Life changes in an instant, and when it does, you find yourself asking yourself, and anyone who cares about you, anyone who will listen- what can you do to fight this?
I started sending out emails like this one about 3 years ago, when I was first diagnosed with Non-Hodgkins Lymphoma, a cancer for which there is treatment to slow it down, but no known cure. (Not yet, anyway.)
Back then I learned I have a ticking time bomb inside my lymphatic system. Drugs make it quiet, but no one can tell me when, or exactly how, it's coming back. There are thousands of adults and little kids just like me. I've met a lot of them- in chemo suites, hospital waiting rooms and fundraising events. We are all haunted by the same ugly monster. And we all ask…what can we do?
So we start out doing the same thing...we seek out a team of doctors who will create a plan to fight our disease. But as you may know, we all have our own stories of ups and downs from there...
Last winter, I'd been in remission from NHL for almost 2 years, when I felt enlarged nodes in my neck. I got a sinking feeling in my stomach. A huge node in my pelvis is what started this thing...I cringed at the thought of telling my wife. We came to learn that I now had a different type of blood cancer, Hodgkin's lymphoma, with the largest node, the size of a lemon, growing between my heart and my lung. Bad news- I had cancer again. Good news- the old one we believe is still in remission.
Almost six months later, I've had surgery and 11 of 12 chemo treatments. My wife has had months of taking care of me and our 3 children. I’m happy to report that my test results have been good, the tumors have shrunk, and I am starting to feel healthy again.
But if or when my first lymphoma (NHL) or, although less likely, this latest one (HL) comes back, I have one less drug in my arsenal...The most powerful drug known to fight lymphoma is also the most toxic. I've already used up the maximum allowed dose due to its potential for permanent damage to my heart if I were to use any more.
So now what?
I need your help...All those thousands of kids and other adults with leukemia and lymphoma need it, too. I fight for myself, for my wife and children, and for the faces of all those other cancer victims in my mind- some of whom, sadly, have lost their battle.
Federal funding does not come close to the amount of money needed to develop targeted therapies or to fund the clinical trials to test them. Yet, these are the efforts vitally needed to save lives. There are many studies going on right now that could provide significant breakthroughs. However, without crucial, private funding to keep them going, many of these studies will never benefit anyone.
My family and I have been walking in the LLS's annual Light the Night Walk for 10 years. The first 7 of those were in support of my wife's brother, Bobby, who is also a young dad, in remission from NHL.
It's even more personal now! I now walk in hopes that each dollar of each year will help me and him and so many others stay alive.
Last year many of you generously helped our team raise over $243,000. That was an awesome achievement that you were a crucial part of. I was touched and humbled by your generosity and for the number of people that were there in person to walk by my side, again braving the wind and rain as we crossed the Brooklyn Bridge. I am so thankful to you.
In total, The Lymphomaniacs have raised $507,000. Now, that is money with real potential for an impact. We are truly making a difference.
Today, my team and I ask for your support again. We are aggressively setting our goal this year at $300,000.
Let's beat this thing and our annual fundraising goal! With your support, we can do it.
Please join Julie, Lexi, Corie, Jake and me along with the entire Lymphomaniac team on Wednesday, October 5th for a short, yet memorable walk across the Brooklyn Bridge. Your friends and families are welcome to join or donate too! Please feel free to forward this email on. Together with perseverance and determination, we will fund a cure.
Thank you for your continued support. It means the world to me, and it will make a real difference to thousands of people with cancer.
Let's Go Lymphomaniacs!!
You can join our team or make a donation by clicking on the following link:
Please don’t forget corporate matching!
If you would like to send a check, please send to:
Michele Zellers
Senior Campaign Director, Light The Night
The Leukemia & Lymphoma Society, NYC Chapter
475 Park Avenue South, 8th Floor
New York, NY 10016
make check payable to The Leukemia & Lymphoma Society, NYC Chapter
In memo field: Lance Meyerowich LTN
Lance's Speech at the 2011 LTN Walk:
http://www.youtube.com/user/TheLymphomaniac?blend=2&ob=5#p/a/u/0/PHi7_H8hOsA
Please look for the Lymphomaniacs on Facebook:
http://www.facebook.com/pages/The-Lymphomaniacs/145388275474028
Please watch the following video of last year’s walk.
http://www.youtube.com/watch?v=_O2_QtJJCDg
The Lymphomaniacs ring the Opening Bell at the NYSE after the 2009 LTN Walk
http://www.nyse.com/events/1255602498965.html
Nancy Zuckerbrod
Mon Sep 12 11:02:08 EDT 2011
William & Juanita Levant Jr
Fri Sep 16 12:42:34 EDT 2011
Craig & Monette Leva
Fri Sep 30 05:02:33 EDT 2011
Mario Colella
Mon Oct 03 09:14:09 EDT 2011
Melissa Jones
Wed Oct 05 06:43:18 EDT 2011