My Worldcon Schedule

Over Labor Day weekend, I’ll be a program participant at LoneStarCon 3, the 71st Annual World Science Fiction Convention in San Antonio, Texas. I usually sit on hard science panels at conventions. Here’s my schedule for this Worldcon. Hope to see some of you there!

The Practice of Space Medicine
8/29 Thursday 15:00 – 16:00
Whether you’re suffering from a case of Andorian shingles or just a mild version of numb tongue, you can be sure that our panelists have a higher patient survival rate than Dr. McCoy. What really happens when you have the flu in space?

Scientific Literacy vs Human Knowledge
8/30 Friday 13:00 – 14:00
The entirety of human knowledge is growing constantly. How can we even decide what the baseline of scientific literacy should be? What’s the process by which the baseline changes?

The Future of Medicine
8/30 Friday 18:00 – 19:00
What ever happened to farmacology? Is the futue of medicine all about genetics? Our panelists will predict the future for you.

Can Machines be Conscious?
8/31 Saturday 13:00 – 14:00
Inventing a better Türing test: neuroscientists are coming up with new definitions of consciousness. They also seek to determine how to measure consciousness.

Using Philosophy to Analyse a National Health Service
8/31 Saturday 15:00 – 16:00
Health is important, but health systems are often criticized, sometimes with good reason. Perhaps philosophy is needed to make premises clearer? Who should be treated, how, and where? Is “more health for the money” valid, or should we consider quality? What are the technology challenges, like ICT? Can we treat more old people at home? Should the patient just be patient, or become a stakeholder?

Stroll with the Stars Sunday – Alamo edition
9/1 Sunday 09:00 – 10:00
The Sunday Stroll with the Stars will head towards the Alamo, a few short blocks away. It will be led by Alamo aficionado and LoneStarCon 3 Chair Randall Shepherd. Meet Randy in the lobby of the Marriott Rivercenter for his personal tour of this famous Texas garrison. Visiting the Alamo is free; note that you will not be able to take photos inside parts of the Alamo.

Cutting Edge Cancer Research
9/1 Sunday 13:00 – 14:00
A look at what is currently possible in the field in combating cancer.

Moves in the Cancer Endgame

My dad taught me to play chess when I was small. I learned the game fast, and could soon beat other kids older than me. However, when I faced an opponent who was much more skilled than I, my attention eventually wandered. I lost the endgame because I’d lost patience.

A chess game transitions to the endgame when few pieces are left on the board. Whatever strategy positioned pieces prior to the endgame becomes irrelevant. The pawns, which initially were the least powerful pieces, become important.

Recently I was playing a much more highly-rated player online (thank you, Nancy Kress) and realized something in my attitude had changed: I had developed patience for the endgame. Even though I had been outmaneuvered and did not possess enough pieces to win, I kept looking for my next move. I wanted to keep the game going as long as possible.

Metastatic lung cancer is a tough opponent, and the odds favor it winning. Several powerful treatments didn’t finish it off. I haven’t many therapy pieces left. But I keep searching for my next move, even if it can’t give me victory. Clinical trials are now my best pieces in the cancer endgame. I want to keep playing — and living — as long as I can.

Cancer taught me patience for the endgame. Maybe someone else will learn from how I played.

Insurance Considerations for Travelling Cancer Patients

Over the past 40 years, I’ve travelled to all seven continents and most of the US states. I didn’t feel much like travelling most of the time I was on cancer treatment, but now that I’m feeling fairly normal on Xalkori, I’ve begun to venture out again.

When I buy expensive tickets on common carriers (airlines, cruise ships, train), I buy travel insurance. Before I was diagnosed with lung cancer, I bought it primarily to cover non-refundable payments in case I had to cancel due to illness or family emergency, or to cover lost luggage and medical expenses abroad. Now that I’ve got metastatic cancer, and I’ve learned how much quality of cancer care varies, I’m more concerned with covering expenses if I have cancer-related problems while on a trip.

The CDC has a good page that summarizes the three types of insurance for travelers: travel insurance, travel health insurance, and medical evacuation insurance. Here’s what I’ve learned from the travels of myself and others.

Travel Insurance and Travel Health Insurance

These policies are usually purchased for a specific trip, and cover the following travel medical problems, along with baggage insurance and other things.

Trip cancellation provides reimbursement for non-refundable trip payments and deposits if I must cancel the trip before it starts. If the trip is expensive — say, a two-week cruise — and purchased many months in advance, I want my deposit and payments to be reimbursed if changes in my treatment plan (say, radiation for a new met) force me to cancel my trip.

Trip interruption provides reimbursement for non-refundable trip payments and out of pocket expenses if the trip is interrupted after it starts. If I have a health problem on the cruise, and the ship departs without me while I’m waiting on a doctor or hospital, I will get reimbursed for the extra airfare to catch up with the ship after treatment, and meal expenses I had to pay out of pocket while I’m off the ship.

Emergency medical and dental pays medical or dental expenses incurred on the trip. Cruise ship doctors are pricey, and expect payment at time of service. Medicare and Medicare supplements usually do not cover medical expenses incurred outside the USA.

Emergency medical transportation arranges and pays to medically transport me to an appropriate medical facility when I need care, and get me home after I’ve received care. More on this under Medical Evacuation Insurance.

Frommer’s has compiled a list of companies that offer travel insurance and travel health insurance. The US State Department has another list of companies that provide coverage for overseas travelers. AAA-hosted trip usually book me through Allianz, and I’ve booked through Allianz myself online.

Medical Evacuation (Medevac) Insurance

If I become severely injured or ill while away from home, I might need an air ambulance to transfer me to a major medical center, or even my home hospital. Such transfers are EXPENSIVE. A friend with cancer paid $20,000 to be flown by air ambulance from Seattle to Kentucky. If you’re overseas, the cost could be $100,000 or more if you’re in a remote area with little medical care available. Travel insurance policies often don’t provide sufficient coverage for this.

Medevac policies can be purchased separately or in combination with travel insurance. Some Medevac insurance providers have their own network of specially-equipped airplanes whose flights are not restricted to airline timetables and routes; other providers are simply brokers that make arrangements for evacuation with contractors. Most medical evacuation insurance companies offer policies that cover the insured on all trips during a set period, be it short- or long-term. Annual policies are typically around $200. Terms and availability vary from carrier to carrier.

Some carriers that offer Medevac insurance are listed below. I don’t have personal experience with any of them; this list is just offered as a starting point for readers.

Allianz
Global Rescue
IMG
MedjetAssist
TravelAssist Network
Travel Guard MedEvac Plan
WorldMed

Buyer Beware

Here are a few lessons learned from my own experience:

1. Read the insurance policy to be sure my specific travel situation is covered. Some policies will allow me to cancel within a short period after purchase if I discover my situation isn’t covered.
For my first trip to Denver for a clinical trial, I bought Alaska Airlines travel insurance through what was then AccessAmerica (now Allianz). The full policy was emailed to me after I bought it. Good thing I read it immediately: it didn’t cover travel for medical treatment! Fortunately I was able to cancel and get a full refund within 10 days, if I hadn’t already left on the trip. Without travel insurance, however, I would have to forfeit my cheap non-refundable ticket if the clinic changed my appointment day. I was able to reschedule a non-refundable flight for free once by playing the cancer card, but I wouldn’t want to rely on that approach.

2. Disclose pre-existing conditions (lung cancer!) and check for pre-existing conditions waivers that might disqualify me for coverage.
Because I have lung cancer, AAA travel agency told me I had to buy non-refundable travel insurance at the time I made my initial deposit on a cruise, months in advance of the trip. If I had waited to buy the insurance, any claims related to my lung cancer would not be covered. My healthy son was able to wait to buy his insurance until he made his final payment for the cruise.

3. Check for dollar limits, deductibles, and terms regarding medical evacuation.
Be sure the coverage limit is high enough to pay for evacuation from wherever I plan to travel. Ask what air carrier the insurance company would use for evacuation from the travel location—they may not have contractors in all countries. Check the policy to see who decides whether I’m sick enough to qualify for air ambulance, and whether I would be transferred to “the nearest appropriate hospital” or a hospital of my choosing.

Celebrating World Lung Cancer Day

Today I celebrate World Lung Cancer Day.

Lung cancer claims more lives than any other cancer. According to the American Cancer Society, each year, more people die of lung cancer than of colon, breast, and prostate cancers combined. Yet the survival rate and funding dollars per death are lower for lung cancer than for those cancers (and almost all other cancers). The CDC lists lung cancer (not breast cancer) as the leading cause of cancer death among women.

Lung cancer deserves more research funding. Anyone who has lungs can get lung cancer. About 60% of newly-diagnosed lung cancer patients are non-smokers or never smokers, and lung cancer in never-smokers ranks among the top 10 fatal cancers in the USA. And, regardless of one’s habits or behaviors, NO ONE deserves to die of lung cancer.

Already more metastatic lung cancer patients like me are living longer thanks to targeted therapies, maintenance chemo, and changes in standard of care. Lung cancer statistics will continue to improve as more patients start to benefit from upcoming early detection methods (like CT screenings and biomarker testing), improvements in treatment options, and an increased national focus on lung cancer research.

Here’s hoping for more successful treatment options for all lung cancer patients, and a cure in my lifetime — which means SOON.

LUNGevity announces its 2013 Research Awards

I received the information below in a news release email from LUNGevity today. It’s encouraging to see the research undertaken for lung cancer patients, especially research related to the KRAS mutation (for which few therapies currently exist), lung cancer resistant to radiation therapy, and acquired resistance to targeted therapies (like Tarceva).

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LUNGevity is proud to announce our 2013 Research Awards!

New LUNGevity awards are enabling promising research into managing lung cancer treatment more effectively, as well as preventing the disease in high-risk populations.

Six exceptional researchers have received 2013 LUNGevity Lung Cancer Research Awards. They join a community of brilliant LUNGevity-funded scientists across the country who are working to help people with lung cancer live longer and better.

 

2013 Career Development Awards for Translational Research were made to the following researchers.

Timothy Burns, MD, PhD, University of Pittsburgh Cancer Institute, is working on targeted therapy for non-small cell lung cancer (NSCLC) patients with mutations in a gene called KRAS, using a new class of drugs.

David Kozono, MD, PhD, Dana-Farber Cancer Institute, will identify which genetic types of lung cancer are the most resistant to radiation, and which of these may be best treated with a combination of radiation and bortezomib, a drug already FDA-approved for another type of cancer.

Meredith Tennis, PhD, University of Colorado Denver, will identify biomarkers that signal whether a patient is likely to benefit from iloprost and pioglitazone, two drugs that have demonstrated promise in reducing NSCLC risk, and whether they work in a clinical trial setting.

 

2013 Targeted Therapeutics Awards for Translational Research were made to the following researchers.

Balazs Halmos, MD, Columbia University Medical Center, is working on a way to increase the effectiveness of radiation and chemotherapy that could also lead to personalized NSCLC treatments, especially for the third of all lung cancer patients with locally advanced lung cancer.

Lecia V. Sequist, MD, Massachusetts General Hospital, will develop models that explain how NSCLC patients can acquire drug resistance to targeted therapies after a period of initial successful treatment, leading to the development of new treatments to help patient overcome the drug resistance.

Frank J. Slack, PhD, Yale University, is studying the KRAS-variant, a recently discovered KRAS mutation found in over 20% of NSCLC patients, which has been shown to predict a patient’s response to cancer treatment. His research aims to confirm the role of the KRAS-variant to direct cancer therapy for lung cancer patients and as a potential future target for therapy.

 

The work of these talented researchers will help ensure continued progress in fighting lung cancer. Special thanks to Genentech and our other donors for their support of the LUNGevity Scientific Research Awards Program. Read more about these exciting projects. In addition to these awards, LUNGevity will announce funding for awards through its Early Detection Awards Program later this year. Please stay tuned!

Death and the Cost of Immortality

Western culture is obsessed with avoiding death. For many, it is a terrifying concept.

Yet death is a natural part of the cycle of life throughout the universe. When plants, animals, mountains, planets, solar systems, and galaxies die, their components are released and transition to become essential components of other lives. If stars had not completed their cycle and died violent deaths, the elements necessary for life elsewhere would not have been created.

Some today seek immortality through plastic surgery, elixirs, and cloning. Others imagine a future with cryogenic preservation, or uploads to new organic or inorganic bodies. All of these options consume significant resources. In most cases, the technology is (or would be) affordable only by the upper levels of society.

Speaking as one who is consuming more than my fair share of resources to survive cancer, I wonder whether I’m giving back more than I’m taking from Earth’s resource pool. I’m not afraid to transition to the next stage of existence, whatever it may be, but my autistic son isn’t ready for me to leave him yet.

If people wish to love well and experience life to the fullest by means of a healthy lifestyle, more power to them. However, when we start seeking to extend life with artificial means, I wonder if perhaps we’re being selfish. Might those resources be better applied towards ensuring good water, food, and health are available for present and future generations?

How Much Do CT Scans Increase the Risk of Cancer?

This is the title of a great article published today by Scientific American about risks of developing future cancers from CT scans. Since cancer patients get frequent CT scans, this subject comes up frequently among lung cancer survivors. I learned some key facts:

(1) Estimates of cancer risk have until recently been based on “cancer rates among the long-term survivors of the atomic bomb blasts in World War II,” a data set that doesn’t really mesh with the radiation exposure generated by CT scans. About a dozen studies worldwide are now looking at cancer rates in patients who’ve had CT scans.

(2) The amount of radiation exposure generated by a CT scan is not regulated by the FDA in the US. Some centers use higher levels of radiation than others. Last year the American Association of Physicists in Medicine published standards for CT procedures and doses. Also, as of 2012, facilities that accept Medicare Part B must be accredited by the American College of Radiology and follow their dosage guidelines if they want to get reimbursed.

(3) Radiologists Sarabjeet Singh and Mannudeep Kalra “discovered that they can diagnose certain abnormal growths in the lungs and perform routine chest exams with about 75 percent less radiation than usual.” Massachusetts General Hospital has adopted this approach, and the researchers are sharing their methods around the globe.

From now on, I’m going to be sure any facility that scans me has American College of Radiology accreditation, and I’ll ask if they’re aware of Singh and Kalra’s work.

Insuring the Terminal Patient

When I returned home from my recent road trip, a letter from Blue Cross Blue Shield of Illinois (my health insurance company, also known as BCBSIL) was waiting for me. Even though I already knew they denied my appeal for last September’s biopsy, I was amazed at how quickly I transitioned from tired but happy traveler to enraged cancer patient.

The upshot of their message was this:

“You already have metastatic lung cancer. A biopsy won’t change the fact that you’re going to die from cancer.”

The statement probably came from the independent “physician who specializes in Internal Medicine/Pulmonary Disease” who reviewed my appeal. You can judge for yourself whether I’m overreacting from this excerpt. I bolded some words for emphasis.

” … in this case the member is already known to have progressive Stage IV Bronchogenic carcinoma even after therapy. Specifically identifying the histopathology of this right upper lobe lesion is not going to affect long-term health outcomes.”

Boy, do I feel special.

A Bit of Background

Up till now, I really couldn’t complain about my insurance coverage. I’m fortunate enough to have Boeing Traditional Retiree medical insurance through my husband, and it’s paid for almost everything related to my cancer diagnosis and treatment (except for 10 cents of each carbo-taxol chemotherapy — go figure). I thought I had the gold standard of enlightened coverage.

After my first recurrence of cancer, which gave me my stage IV determination in October 2011, a large ugly tumor grew fast above my right collarbone. It was 3 inches long after about 2 months. In January 2012 I started second line chemo — 6 rounds of Alimta-Avastin which shrunk the tumor almost 90% — followed by radiation.

Six weeks after this second line treatment, a PET-CT scan showed the little sucker was dead. However, two new nodules had formed in my formerly-clear right lung. The nodules glowed hot enough on the PET scan to make them highly suspicious for cancer, but only a biopsy could determine whether the nodules were cancer, radiation pneumonitis (lung inflammation) or BOOP. BOOP stands for Bronchiolitis Obliterans with Organizing Pneumonia, a pneumonia-like condition that sometimes occurs in lung tissue after radiation in nearby tissue. If one or both nodules were cancer, I needed to go back on chemo — probably Alimta, which was effective against my cancer but eventually made me feel like I had the flu for three weeks out of every month. If one or both were pneumonitis or BOOP, I needed to go back on prednisone, an oral steroid with unpleasant side effects. We weren’t looking for lung cancer histology, although that would have been interesting info to have. Histology can determine whether a new cancer tumor is the same type of cancer as the patient’s previous tumor. A different tumor type might indicate a different type of treatment would be useful.

One of my nodules was too small to biopsy. The larger nodule was not accessible by more common biopsy methods of needle biopsy through the chest wall or endobronchial ultrasound. My pulmonologist recommended using the newer electromagnetic navigation bronchoscopy (EMN) to determine if the nodule were cancer or something else. We knew BCBSIL would probably not pay for the procedure because they have a policy stating EMN is “experimental” for all situations (despite the fact that Medicare pays for EMN and 2013 treatment guidelines list EMN as an acceptable diagnostic). BCBSIL had denied all EMN claims made to date by my hospital.

When BCBSIL denied the claim, I appealed. I explained my treatment history, including that my cancer is aggressive, and we needed to know if the nodule were BOOP or cancer to give me appropriate treatment. My doctor reviewed my letter and wrote a letter of his own to stick in the packet. I included scan CDs and appropriate medical reports.

Evidently that wasn’t enough. Because, well, I’m gonna die anyway.

FYI, the biopsy showed inflammation, but no cancer cells. The tumor board thought it was radiation pneumonitis; my pulmonologist wasn’t so sure. We tried prednisone for a month, but it had no effect. A follow-up CT one month after the biopsy showed the biopsied nodule was unchanged, while the other nodule had grown by 50%. My pulmonologist and oncologist agreed I needed to restart chemotherapy.

Misinterpreting Long-Term Health Outcomes

What frosts me about this letter is that a “specialist” decided there was no urgency to get a biopsy because it wouldn’t change my “long-term health outcome.” Did he expect me to go on steroids AND chemo (both of which have a significant impact on quality of life) in case one of them MIGHT work? Or do nothing, since I’m going to die anyway? Well, here’s a news flash: we’re ALL going to die! The purpose of medicine is to keep us as healthy as possible while delaying that inevitable long-term outcome as long as possible.

Unfortunately, such statements from doctors are not an uncommon occurrence for lung cancer patients. Many members of Inspire’s Lung Cancer Support Forum who’ve been diagnosed with metastatic lung cancer have been told, “There’s nothing more I can do.”

My biggest frustration is that in my case – and for an increasing number of lung cancer patients — the doomsday doctor is WRONG. I’m a perfect example of a stage IV patient who has a good prospect for years of a reasonably active life despite my disease.

I was lucky to have enough slides from a 2011 biopsy to have the University of Colorado test my tumor for the relatively new ROS1 genetic mutation in my tumor tissue. Because I tested positive for ROS1, I was able to enter a clinical trial for the targeted therapy crizotinib, a drug which inhibits my ROS1-driven cancer. The trial treatment eliminated both nodules and has given me No Evidence of Disease Status for five months. I am once again able to enjoy traveling, writing, and doing things with my family. If I had not had leftover biopsy slides, an EMN biopsy would have been my only opportunity to obtain enough tissue to test for ROS1. Without that ROS1 trial and crizotinib, I might be dead by now.

Doctors who don’t keep current on new treatment options and then decide a biopsy “is not going to affect long-term health outcomes” for metastatic lung cancer patients are insuring those patients will die sooner rather than later.

That’s not the kind of health insurance I want. Do you?

The Places I’ve Been … June 2013 Edition

I’ve been neglecting this blog for over a month for two reasons:

1. I helped my Aspie son with a 70-page college geology term paper (serving as typist, scribe, interpreter, cheerleader, and organizational consultant), and

2. Hubby and I took a two-week road trip through six states (Washington, Idaho, Montana, Wyoming, Colorado, and Oregon), three national parks (Yellowstone in WY, Grand Tetons in WY, and Craters of the Moon in ID), two national monuments (Fossil Butte in WY and Hagerman Fossil Beds in ID), and my monthly clinical trial visit in Denver.

The summary: we had a great trip, I had another clean PET-CT scan, AND the kid earned a 3.7 out of 4.0! I intend to write some entries about traveling with lung cancer, geology, and the sites I was privileged to see … as soon as I recover from vacation.

In the meantime, here are some previews of coming attractions:

 


Old Faithful in Yellowstone National Park

 


Grand Tetons National Park

 


Craters of the Moon National Park

It’s My Cancerversary — And I’m Choosing to Live

Today is my cancerversary. Two years ago on this date, I was diagnosed with advanced lung cancer.

While my current status is No Evidence of Disease, I know the cancer is still lurking in my body; it’s only being suppressed (not cured) by the targeted drug crizotinib.

I’ve felt myself sliding towards depression this week. I know from past experience what depression feels like, and I do not want to go there again. I suspect subconcious awareness of my cancerversary is part of the reason. Physical discomfort due to treatment side effects (especially hand pain), steroid-induced excess weight and a newly-diagnosed partial hamstring tear aren’t helping matters. It also bugs me that fatigue has kept me from being as supportive as I’d like when my husband recently had cataract surgery.

When I woke up this morning, I realized that somehow, sometime, I had adopted a victim mentality. I have been passively accepting the crap that my body was handing me. That is simply not acceptable.

True, the cancer ain’t gone, but neither am I! Through no small effort of many people, including myself, I am alive. I am not going to waste the gift.

I can’t choose not to have cancer, but I CAN choose how I want to feel about it. Today, I choose to feel empowered and hopeful.

I can’t choose not to have side effects, but I CAN choose not to let the discomforts of my body keep me from exercising. Exercise makes a huge difference in my mood. Today, I choose to go swimming for the first time in years.

I can’t choose not to be fatigued, but I CAN choose how I react when the irritability rises unbidden. Today, I choose to hold my tongue and listen for understanding.

Today, my cancerversary commemorates not just the start of my cancer battle, but my renewed efforts to LIVE.

To celebrate, I bought new underwear. Take THAT, cancer! 😛