#29361 09-19-2007 08:18 AM | Joined: Feb 2007 Posts: 1,940 "OCF across the pond" Patient Advocate (1000+ posts) | "OCF across the pond" Patient Advocate (1000+ posts) Joined: Feb 2007 Posts: 1,940 | Robs biggest anger was that he went through all the agony of surgery and radiotherapy and still wasnt cured.He said many many times that he would never had had any treatment at all and enjoyed being able to eat and have some sort of quality to his life.The only thing that stops most people making such a choice is the survival instinct which is so strong in all of us julie.
liz
Liz in the UK
Husband Robin aged 44 years Dx 8th Dec 2006 poorly differentiated SCC tongue with met to neck T1N2cM0 Surgery and Radiation.Finished TX April 2007 Recurrence June/07 died July 29th/07.
Never take your eye off the ball, it may just smack you in the mouth.
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#29362 09-19-2007 11:56 AM | Joined: Apr 2005 Posts: 2,219 Patient Advocate (old timer, 2000 posts) | Patient Advocate (old timer, 2000 posts) Joined: Apr 2005 Posts: 2,219 | I think there is a big difference between:
1. Choosing not to have treatment when it is offered and there is a chance that it could work.
and
2. Choosing not to have treatment when you are told that the chances of a successful outcome are nil to none.
Liz, I can certainly understand how Rob felt after finding out that his treatment was not successful. I assume that he was given some hope that it could work or he would not have decided to go through with it.
We really don't know enough about the poster's father here to really be helpful in any way. We need to know what he was told about staging, treatment options etc.
Jerry
Jerry
Retired Dentist, 59 years old at diagnosis. SCC of the left lateral border of the tongue (Stage I). Partial glossectomy and 30 nodes removed, 4/6/05. Nodes all clear. No chemo no radiation 18 year survivor.
"Whatever doesn't kill me, makes me stronger"
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#29363 09-19-2007 12:04 PM | Joined: Aug 2007 Posts: 580 "Above & Beyond" Member (500+ posts) | "Above & Beyond" Member (500+ posts) Joined: Aug 2007 Posts: 580 | Well quite a quandry.
I agree with Jerry, we don't have enough detail to be at all reliable in our advice and opinion is only that.
As for the money, what is he going to do with it if he has no treatment? This route will most certainly lead to a possibly lengthey time in palliative care which, often times, exceeds the treatment cost by quite a large margin. Spend it now or spend it later.
Selfishness, should not be misinterpreted for concern, love and caring. Get the facts and pass them along to your father don't be pushy be the loving son that brought you here to look for help. You would make any father proud!
Just my 2 cents.
Cheers,
Mike
Dentist since 1995, 12 year Cancer Survivor, Father, Husband, Thankful to so many who supported me on my journey so far, and more than happy to comfort a friend. Live, Laugh, Love & Learn.
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#29364 09-19-2007 04:20 PM | Joined: Aug 2003 Posts: 1,627 Patient Advocate (1000+ posts) | Patient Advocate (1000+ posts) Joined: Aug 2003 Posts: 1,627 | Julie, what do his doctors say? Give us that information so we can help you further. I don't want this thread to get off track and I DO NOT want us to point you in the wrong direction without the facts. Hope to hear from you soon. Minnie
SCC Left Mandible. Jaw replaced with bone from leg. Neck disection, 37 radiation treatments. Recurrence 8-28-07, stage 2, tongue. One third of tongue removed 10-4-07. 5-23-08 chemo started for tumor behind swallowing passage, Our good friend and much loved OCF member Minnie has been lost to the disease (RIP 10-29-08). We will all miss her greatly.
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#29365 09-19-2007 05:50 PM | Joined: Sep 2007 Posts: 9 Member | OP Member Joined: Sep 2007 Posts: 9 | Thank you everyone for your opinions
I guess i was so upset with my dad cuz he refuses to even go see if he can recieve treatments. It just makes me so upset that he doesnt even wanna see if there is a chance of survival. | | |
#29366 09-19-2007 06:56 PM | Joined: Feb 2007 Posts: 1,940 "OCF across the pond" Patient Advocate (1000+ posts) | "OCF across the pond" Patient Advocate (1000+ posts) Joined: Feb 2007 Posts: 1,940 | I wish paul was about on the boards as his journey through his mums choice to have no treatment was very moving and i am sure he could help.
Liz in the UK
Husband Robin aged 44 years Dx 8th Dec 2006 poorly differentiated SCC tongue with met to neck T1N2cM0 Surgery and Radiation.Finished TX April 2007 Recurrence June/07 died July 29th/07.
Never take your eye off the ball, it may just smack you in the mouth.
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#29367 09-19-2007 11:28 PM | Joined: Jun 2007 Posts: 35 Contributing Member (25+ posts) | Contributing Member (25+ posts) Joined: Jun 2007 Posts: 35 | We have all watched either our loved one or ones self go through the treatment and all the horrid effects. But throught this board we see much more success than failure. Hope is the word to focus on.
David finished treatmetn on 6/22 and the last 3 months have been long and everyday a step forward but the side effects linger. He still has such dryness and sore throat and most of all cannot eat but he is improving. Energy is better. Skin is beatiful. We like to say he got great chemical peel and microabrasion through all this. We try everyday to find the humor and positives.
The cancer is gone according to his RO in his mouth/throat...But the tumor on the right is still large...possibly dead cells but still will probably be removed. He had his first followup pet/CT in August. The left side may still have active node. WE had another CT/Pet the 17th this past monday and will get results on this Monday. The RO told us IF we lose the battle it will be in his neck. He has stated no more radiation. But we have talked that we wait and face the choice once we know exactly again what we are delaing with adn that will be this Monday the 24th. We started this adventue friday April 13th. and we are not doe yet. What we have is the hope and each day. Each day even though everything is not perfect and we do not get the I am survivor shirt yet we keep Hoping we are in the right line.
Caregiver in Florida DX tonsil cancer 4/13/07 both tonsils removed both positive.,. Stage 4 with 3 nodes on Right and 2 nodes on left. Just finishd 2 chemo - cisplatn and 35 Radiation 6/22/07
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#29368 09-20-2007 01:40 AM | Joined: May 2007 Posts: 44 Contributing Member (25+ posts) | Contributing Member (25+ posts) Joined: May 2007 Posts: 44 | I'm sorry if anyone misundersttod my post. I was trying to tell the OP to get all the facts from his father as there maybe things he isn't being told. We are talking about a man here.( no offense men) In my experience, its a lot more macho to tell someone its too much money than to tell them its hopeless. Not that that has to be the case but he needs to talk to his dad and find out before trying to pressure him. My comment about radiation and chemo for terminal cases was also based on my experience. Rich was told there was no hope witout extensive surgury. Then when it was found his heart wouldn't tolerate that he was told he should have radiation and chemo because he would die a very horrible death if he did nothing. When I asked what the radiation and chemo would do to ease it I was told it would just slow the progress of the cancer. I still can't understand that reasoning. Not only would he still have the cancer but the effects of radiation and chemo. How does that make it easier? I never got a reply to that question. | | |
#29369 09-20-2007 02:46 AM | Joined: May 2007 Posts: 632 "Above & Beyond" Member (300+ posts) | "Above & Beyond" Member (300+ posts) Joined: May 2007 Posts: 632 | Julie, I think docs give us the worst scenarios to prepare us, but also don't rule out the fact that miracles DO happen--back to the 'everyone is different, ignore the statistics' bit. In my case, I was offered the 'palliative' chemo route and given 3 'scenarios'
1.--Good result is it halts the growth/spread. 2.--Best--it shrinks the tumours 3.--Miracle--it makes em go away!
In my case, it has halted the growth, for now, the treatment itself wasn't too horrendous, and it's made me focus on the 'enjoy one day at a time' bit, for which I've been very grateful.
I may be offered radiation to the jaw in the future, if the pain becomes too bad, but that will also be in small doses and palliative.
Please let us know alwyz if/when you have any more information
Brenda
Brenda in UK--Diagnosis 30/5/07--undifferentiated carcinoma in right jawbone and muscles. Stage 4 6/7/07--new diagnosis primary is in lung. Finished 4cycles of palliative carboplatin/gemcitabine therapy September 07 Now dying to live!
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#29370 09-20-2007 03:20 PM | Joined: Sep 2007 Posts: 9 Member | OP Member Joined: Sep 2007 Posts: 9 | Cookey-I have read the posts that Paul had up about his mom. Thanks tho.
TonsillessinFL-Good luck with everything.
JulieKay- I understand what you mean about finding everything out Before i pressure him. But thats the problem..Once he found out he had it and that it was in stage three, he never went back and wants to act like he doesnt have it. he tries to use the excuse of money for doctors visits..But seems like he doesnt want to face reality. P.S. Im his daughter..not his son haha
brenfran-Thank you for your input and good luck.
So i think i started this post with the wrong words. I was just really upset about my dad. I guess the real question i wanted to know was that how long do i have left to get to know him. I know nothin about the stages and all that...But without treatment, Whats the estimation of time i have left? Anyone know? Thanks everyone... | | |
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