Carol Lin Reporting

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The Real Enemy—by Steve Kirsch

November 4th, 2007 · 3 Comments

Before running Daryn Kagan and my cancer series, I had written a post about rare cancers. I shared the story about Silicon Valley billionaire Steve Kirsch’s battle with a rare blood cancer, Waldenstrom Macroglobulinemia.I am so glad that Steve saw the post and reached out.   He said I could share his email:

“i see my story is on the front page your website. thanks for
the press. it is so sad when you look at the numbers. 224 people die from
terrorism each year. government spents $100B per year on that.
500,000 people die from cancer. Government spends $5B per year.
go figure.and then they pass a bill to authorize $250 million for blood cancers
like mine. But then they don’t appropriate the funds!!!!!!!!!

I want Steve to tell you more directly about his fight for more funding and the absolute, mind-boggling rationale by the government to fund or not fund when it comes to saving…or in our case…ignoring lives at stake: I asked Steve if he would share directly with you some of those thoughts. The real enemy is not the terrorist abroad. According to Steve, it’s the terror not dealt with right here at home:

Terrorists are just a distraction. The real enemy is government stupidity. Here’s how I know that. Last week, I was diagnosed with a rare incurable blood cancer called Waldenstrom’s Macroglobulinemia (WM).  Because it kills, on average, only about 1,200 people per year, it’s considered an orphan disease so it gets very little money and attention from the government and drug companies. It’s basically a death sentence. I have a little more than 5 years to live.

As I learned more about my disease, some of the most significant things I learned were:

  • the lifetime risk of developing cancer is 1 in 2 for men and 1 in 3 for women
  • there is a 25% chance that you will die from cancer
  • 500,000 people die from cancer each year
  • the government spends about $5 billion a year on research; $114M of which is spent on non-Hodgkin’s lymphomas collectively, but zero dollars are spent on WM specifically.
  • Only 8% of the research proposals to the NIH get funding. Researchers spend about 30% of their time writing grant proposals. Since 92% are turned down, this is an enormous waste of our most precious medical talent. Even prominent, highly decorated researchers such as Ken Anderson at Harvard, only have 8% of their research proposals granted.
  • our society spends $200 billion a year on medical care for cancer victims (40 times the amount we spend on prevention)
  • Gleevec is proof that we now have the technology to create real “wonder drugs” that cure cancers that were previously untreatable
  • the researchers on my particular cancer said that they could efficiently deploy more funds to accelerate their research. They are confident that they can create a “wonder drug” for my disease. They just lack the funds. They get zero dollars from the government now.
  • the research dollars for cancer have been going down every year in real dollars for several years now
  • cancer research has never been a national priority

To put the cancer numbers in perspective, a disease called “terrorism” in the US kills, on average, about 224 people per year. Approximately 0 people per year are killed by terrorists from Iraq. At that size, it should be categorized like my disease as an orphan disease and it should get no government funding at all. Yet, we spend over $100 billion a year fighting it in Iraq alone. Not only that, but every year, four times as many lives are lost fighting it, than are directly killed by the disease itself! In short, we’ve save more lives by not fighting it at all. Even worse is that the more money we spend fighting this disease, the more prevalent it becomes and the more people unnecessarily lose their lives!

(more from Steve tomorrow) Thank you, bloggers, for staying with me. Thank you for posting, responding, being angry and by doing so, making a difference. Now go to The Poll and Vote!

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Vicki Tashman joined every support group possible while going through breast cancer treatment four years ago. But she didn’t find what she wanted — another woman who had the same type of breast cancer and same type of treatment that she had. Now three years into recovery, Tashman created the very thing she was looking for. Pink-Link.org is an online matching service for breast cancer survivors and patients. This 47-year-old mother of two just jumped in knowing nothing about creating a non-profit or online community.
She self-educated, now helping thousands of women around the world. Learn more at Pink-Link.org.

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