stage 4 nsc lung cancer

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RE: stage 4 nsc lung cancer

by sloughj on Thu Sep 25, 2008 12:00 AM

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On 8/26/2008 sergeantmajorette wrote:

Mostly they give Tarceva after you finish chemo (and radiation, if you need that too); like a maintenance drug.

Most important, though, is a positive attitude. You really, really, really have to fire that doctor!! That is going to be a pivotal factor in your mom's survival!

As I read, it seems to me that there is one statistical marker for long term survivors - they fired their first doctor! It can be unpleasant to fight with a doctor, but it has to be done. If a doctor won't talk to relatives and caregivers, gives you attitude about a second opinion, and won't answer questions (my brother's first doctor refused to spell the names of drugs or medical terms; he told me not to look things up on the internet!), that doctor is not a competent clinical oncologist.

The current wisdom is that you must treat for the psychological aspects of the disease: the doctor is the coordinator of the "treatment team" which includes relatives, friends, and any support the patient can marshall! When I had my breast cancer scare, the nurses told me to round up a posse, and never go to an appointment alone!


 

HI thanks for your message. I have tried to change Onocologist's. Guess what Mum has finished her radiotherapy with no follow up. I now have to try to speak to the medical secretary to see when we can see someone , (or what is going on with her case if anything)hard nor what. Meanwhile my mum is in severe constant pain, (her doctor has been brilliant).

I wish our NHS system was a bit better.

i am her main carer there is no one else

I am sorry that i sound so negative feeling a bit worn out with home life work and mum.

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