Yeah, it varies a bit with the type of pancreatic cancer that you have. The range I've seen is 3 to 8%.All the Cancer data shows the 5 year survival rate as 12% that seems high to me.
Yeah, it varies a bit with the type of pancreatic cancer that you have. The range I've seen is 3 to 8%.
When I was first diagnosed, the M.D. Anderson oncologist told me that there were two primary versions of PC. One is the kind Patrick Swayze had and the other is the type Steve Jobs had. I quickly pointed out that both of them are DEAD, so either he was telling me to give up or he needed A LOT better examples. Jobs apparently had one with a higher survival rate than Swayze, but Jobs insisted on trying alternative treatments - shark cartilage and such - and that didn't work. I turned out to have a more rare kind, which in cancer treatment is a bad thing. Treatments are based on statistics, so you want something that lots of people have had (and a significant number have survived). Major surgery - losing a few organs - months of chemo, and years of follow up. The last time I saw the doc he said that I no longer needed annual testing. He said that they usually recommended testing in 10 years, "..but you'll probably be dead by then anyway, so I wouldn't worry about it." True story.
I had a friend that was diagnosed in her mid-40s after several ER trips due to painful stomach aches. She finally saw somebody that realized she wasn't trying to con them out of drugs and took the time to run some tests, which resulted in a referral to an oncologist.Yeah, it varies a bit with the type of pancreatic cancer that you have. The range I've seen is 3 to 8%.
When I was first diagnosed, the M.D. Anderson oncologist told me that there were two primary versions of PC. One is the kind Patrick Swayze had and the other is the type Steve Jobs had. I quickly pointed out that both of them are DEAD, so either he was telling me to give up or he needed A LOT better examples. Jobs apparently had one with a higher survival rate than Swayze, but Jobs insisted on trying alternative treatments - shark cartilage and such - and that didn't work. I turned out to have a more rare kind, which in cancer treatment is a bad thing. Treatments are based on statistics, so you want something that lots of people have had (and a significant number have survived). Major surgery - losing a few organs - months of chemo, and years of follow up. The last time I saw the doc he said that I no longer needed annual testing. He said that they usually recommended testing in 10 years, "..but you'll probably be dead by then anyway, so I wouldn't worry about it." True story.
There is also supposed to be a link between Januvia and PC, and I was on Januvia for several years before diagnosis. There have been announcements from attorneys trying to put together a class action lawsuit, but I refuse to join. I have no interest in making attorneys rich.I had a friend that was diagnosed in her mid-40s after several ER trips due to painful stomach aches. She finally saw somebody that realized she wasn't trying to con them out of drugs and took the time to run some tests, which resulted in a referral to an oncologist.
Stage II Pancreatic Cancer.
Unfortunately, she was pressured into 'alternative treatment' by a quack 'doctor' (that held a doctorate in an unrelated field, not medicine), which actually caused the cancer to become more aggressive, I don't think she lasted 2 years, despite being in pretty good health prior to diagnoses.
I have since lost another friend to pancreatic cancer, although he hid that he was sick and had a history of major health problems.
Both of my friends were chronic diet soda drinkers, she because 'sugar is bad' (it isn't, sodas are) and he because of Type 1 diabetes. A conversation with an oncologist confirmed what I thought, there is a strong correlation between use of sugar substitutes and pancreatic cancer - there just isn't a definitive link, so it's still allowed.
'Diet' is banned in my house, and my children know it isn't allowed.
Eli
Pain! Extreme pain! The emergency room originally identified it as gall bladder and told me to see a specialist to get it removed, even though no stones showed up when they did an ultrasound. My wife was sick (hospitalized), so I didn't see a doc for a couple months. One day it was so bad I was in agony. I had to go to work that day because the plant was doing one of those "management by panic" things and I had to be the one to bring sanity to the situation. As soon as that meeting was over, I told my boss I was going to the hospital. At the ER, the triage nurse asked what my pain level was on a scale of 1 to 10. I said, "What level makes you cry?" She said, "We'll call it an 8." They gave me morphine and it did absolutely nothing. Then they gave me Dilaudid, which is strong enough that you could do your own surgery, and it helped some. They sent me for another ultrasound and this time the young technician who was doing the scan was on her first day solo. She couldn't find the gall bladder, but noticed the other mass. (It was about the size of a tennis ball.) She called in a supervisor, they looked and whispered a bit, then sent me back to the tiny ER room. Then they did a CT scan and came in and told me I had PC.I'm glad you lived. There are some things I'm terrified of. ALS, Alzheimers, and pancreatic cancer. What symptom finally made you go to a doctor?
It's known that oftentimes blood sugar becomes uncontrollable early in the course of pancreatic cancer, as to why the doctors didn't check my diabetic friend...There is also supposed to be a link between Januvia and PC, and I was on Januvia for several years before diagnosis. There have been announcements from attorneys trying to put together a class action lawsuit, but I refuse to join. I have no interest in making attorneys rich.
The last time I saw the doc he said that I no longer needed annual testing. He said that they usually recommended testing in 10 years, "..but you'll probably be dead by then anyway, so I wouldn't worry about it." True story.
I told the oncologist, "There are people who would be happy to see me dead, so I plan to live just to piss them off." He replied, "Well, whatever motivation works is ok."
God bless that man. I was an Oregonian most of my life until it went to progressive hell. I lived in Eastern Oregon for a time, and always wondered if Paul was filming south of Bend, possibly near LaPine. I wish pancreatic cancer on no one (well, maybe Kim, Xi and Putin ...).
Oddly enough, he decided cancer was too depressing and quit. Last I heard he was going to move to some middle state (Kentucky?) and become a small town general practitioner. I was billed over $1000 every time I saw the primary doctor and sometimes that was for 5 minutes.Your oncologist is a jackass and I hope you've fired him and moved on to someone with an ounce of bedside manner.
Your earlier post about cancer being evil is spot on. My wife has survived, just barely, throat cancer, is now an invalid and will be until she dies.Oddly enough, he decided cancer was too depressing and quit. Last I heard he was going to move to some middle state (Kentucky?) and become a small town general practitioner. I was billed over $1000 every time I saw the primary doctor and sometimes that was for 5 minutes.
For the most part, EVERYBODY at M.D. Anderson sees every patient as someone who is about to die. My mother was a nurse at a nursing home and she had to be careful not to like any patients because, like it or not, they are in Heaven's waiting room. So I get why they act the way they do. As a patient, you are nothing but a "medical record number" for most of your time there. (You have to memorize the number and be prepared to recite it before anyone will test your blood pressure, operate on you, feed you, mop the floor, etc.) Now, after you've survived a few years, they suddenly know your name and they'll ask about your family or your pet dog or whatever, like as if you suddenly became human. And the funding people will always tell you how much you are loved and how much more they will love you if you donate lots of money.
So, in a nutshell, who is Paul Harrell?
So, in a nutshell, who is Paul Harrell?
ThanksHe is the YouTube gun daddy - either on the very early edge of Gen X, or the tail of the Boomer generation - but that doesn't matter....