My younger sister was diagnosed with Stage IV NSCLC Adenocarcinoma in April of 2001 at age 47. She was not a smoker - not that it matters.
She is in her fourth chemo series, she always has some positive response to chemo but doesn't stabilize long. She's had:
1 - taxol & carboplatin
2 - taxotere & gemzar
3 - navelbine
4 - navelbine & carboplatin (currently)
She also had mets to the brain, treated with gamma knife surgery (a true miracle of modern medicine) followed by one month of whole brain radiation. No recurrence going on 18 months.
Expanded access program for Iressa was a disaster.
She's been told more than once to get her affairs in order. Last November she was told the spread was so extensive she should immediately make arrangements for her children.
She has had more medical & physical complications than I care to remember. Her current chemo significantly reduced tumor # & size. She is a single mom with 2 little girls & currently working FULL TIME as a middle school teacher!
I am always searching for new, non-toxic, targeted therapies, which is where I think our advocacy should focus. I don't believe that poison is the long term solution for lung cancer. There are just so few options available now, it is very frustrating. I feel that effective treatment for LC as a chronic disease is just around the corner, just down the road . . .
I get my best information from stock market sites, especially those that report on biotechnology companies. They seem to be the first with news of new drugs & clinical trials. Much, much, better & more current information than NCI site or other "official" cancer sites. Here's my favorite: http://www.biospace.com/ just go there and do a search for "lung cancer." You have to wade through the information on CEOs & quarterly reports, but the drug information is fabulous. Plus, you get links directly to drug companies. I've frequently called drug companies directly to ask about new drugs & clincial trials. They are usually very responsive.
This is a wonderful site. My sister has actively resisted any support group-type association, but I'm going to see if I can get her here. I so want her to know that 1. There is hope, and 2. She is not the only one. Thanks.[/i]