On 7/16/2008
ANNOD44 wrote:
Hi I havent posted on here in a while so here it goes. My father in law was diagnosed with stage 4 lung cancer in September of 2007 and he has been doing chemo and radiation (cyberknife) . He always expressed he didnt want to do these treatments but, his kids wanted him to fight . Now in the last month his health has declined dramatically and he does not want to eat and feels sick to his stomach all the time. he is very weak in fact the only thing he did eat is one peice of chicken (leg) and a couple tablespoons of ensure in a week, so they took him to the doctors for his results from the pet scan. The doctor said he is full of more tumors (Im not there or I would of asked where the tumors are located) and chemo is not an option any more as radiation., In fact they said (I was told ) that the chemo made it worse? can that happen? and I thought they would of put him in the hospital for some fluids etc , but they told my brother in law to call hospice and they would take care of him. I was dumb founded because, he almost collasped going into the doctors office . Is this normal procedure for people who are dyeing of lung cancer? he is calling hospice today and I dont know how long it takes them to come out. Also when they put someone in hospice how long do they have to live ? sorry this is so long but Im feeling helpless at this point.. and I dont know what to do.. thanks
Hi,
Doctors need to feel that the person has six months or less to live to be able to have hospice care. Also, there can be no more treatment to save that person's life; hospice is about comfort care, only. But-- It is possible to start with hospice, and if there is a change, to go off hospice and again try to treat the patient. Sometimes hospice will go on for longer than six months. Nobody really knows how long someone will live.
My mother also had lung cancer. She was first diagnosed in January 2007 and had a lobectomy to remove a very small mass. No follow up treatment was reccommended at the time. Last August she started to run a fever and in September we learned it was caused by the return of her lung cancer which was now stage 4. Radiation made her so ill that she ended up in the hospital and we brought her home the last day of November with hospice care. This was arranged through the social worker at the hospital; a hospice nurse was waiting for us at my mother's house and a hospital bed, oxygen tank, etc. was set up immediately. My mother was quite ill and I think the common belief was that she would have days to a few weeks, but she lived until the end of February. I had a hard time choosing hospice at first, until I realized that it wasn't a commitment. My mother had just finished her radiation treatments and the radiologist told us that radiation would continue to work for up to three months after the last treatment. She seemed very surprised that my mother's main oncologist was reccommending no further treatment at that point. So hospice felt like I was giving up on my mom too early. But she was extremely ill when we brought her home and hospice was the highest level of care. (And we still needed to provide 24 hour care, mostly family and friends, as well.) Hospice was truly wonderful. The home aids were amazing and it was so helpful to know that there was someone to call with any questions or if there was an emergency. My mother's medications were delivered to the door whenever she needed them. I can't immagine what we would have done without hospice.
I hope this helps answer some of your questions. Feel free to ask me anything you like. Roz