Unless it’s Affordable, Curing Cancer is Just a Dream

August 30, 2011 – 12:43 pm | By Mari Serebrov | 5 comments

Although they’re the stuff of science, statistics too often lack the power to move us. After all, they’re just numbers. So when companies like Dendreon Corp. and Seattle Genetics Inc. price their cancer treatments at nearly $100,000 or more, we may arch our eyebrows, but we don’t really think about the impact those prices will have on the individual faces and names behind the numbers. Instead, we wonder, as reported in BioWorld Today, why more patients don’t take advantage of promising drugs like Dendreon’s Provenge.

Unlike statistics, faces and names have stories that can bring us to tears, that make us want to shout at the unfairness of life, that inspire us to reach beyond ourselves to make the world a little bit better for someone else. My niece Jaymi is one of those names.

She was diagnosed with Hodgkin’s when she was 15. After a cocktail of chemo and radiation, full-body radiation and an unsuccessful bone marrow transplant, her doctors basically told her to enjoy what little life she had left. She took them at their word. She went to college. She married her high school sweetheart. And, against all odds, she gave birth to a beautiful, healthy baby girl (pictured here with Jaymi).

At 23, Jaymi is a senior in college, majoring in technical writing and communications. Next year, she plans to start her MBA. Outside of school, she enjoys every minute she has with her 2-year-old daughter and her husband, who also is a college student. But her life is shadowed by the cancer that continues to spread throughout her body.

Jaymi doesn’t need hope. She sees that every time she looks in her daughter’s eyes. What Jaymi needs is a cure. But she needs one that is affordable.

Because she’s a married college student with cancer, Jaymi doesn’t have private insurance. And although she’s eligible for disability and Medicaid, she’s still waiting for the forms to enroll in the government programs. She’s also been warned by Medicare staff that pursuing full-on cancer treatment may not be feasible in light of budget cuts.

Years before Jaymi was born, scientists dreamed of finding a cure for cancer. Those dreams are coming true. But for people like Jaymi, the cure is still just a dream they can’t afford.

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4 Comments

  1. Posted September 3, 2011 at 1:08 pm | Permalink

    Powerful! I know it’s expensive to create new medications, but it seems when a company discovers a cure, or even a helpful medicine, it’s their moral responsibility to share it with someone like Jaymi, a vibrant, productive member of society who has so much to offer. When the bottom line is more important than offering a chance for healing, where have our values gone???

  2. Posted September 7, 2011 at 10:46 am | Permalink

    Please help this young woman find a clinical trial. She will not need health insurance to participate

  3. RRRRR
    Posted September 15, 2011 at 8:05 am | Permalink

    Inspiring story, indeed. However, medicine is expensive, you can’t blame these companies, especially emerging medicine like these cancer treatments. Companies need an incentive to spend millions to research these treatments and then additionally large amounts to get them to market and to manufacture them. It’s not about moral values, it’s about maintaining a business. And, if everyone gave into some emotional story every time, they won’t be able to maintain their business, thus everyone loses out on treatments. Actually, Dendreon is struggling right now, so reducing the cost of Provenge seems out of the question.

    We only hear these stories when they can’t afford them. However, I know someone who works at Dendreon and they’re moving treatments on a 24-hours-a-day operation (which is also costly).

    This is life. We live and learn, fall down and get up. And Jaymi’s story isn’t about trying to fight the medical companies, but it’s about our internal struggles, to take what we have and live beyond our expectations, not letting physical ailments define our lives.

  4. Mari Serebrov
    Posted September 15, 2011 at 9:18 am | Permalink

    Clinical trials aren’t always the answer. Few trials are available anywhere near Jaymi’s area, and she doesn’t meet the inclusion criteria for the two or three that are recruiting.

One Trackback

  1. By What Would Albus Do? And What Should We? | BioWorld on February 13, 2012 at 11:27 am

    [...] to defend sky-high drug prices. As my colleague Mari Serebrov has movingly written about on this blog post, a cure that no one can afford is no cure at all. And I rather suspect that even after you take the [...]

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