If nothing changes, nothing changes! Every year in April the National Cancer Institute updates their survival data for all cancers, and every year I have high expectations the numbers for the average life expectancy for multiple myeloma will show significant improvement. And also in some small way I and my fellow advocates might have had a limited but important part to play in this success, and that our efforts would have some value to the myeloma patient community for this improvement in survival.
But as is the case again this year, the average life expectancy remains at just 4 years. It has not improved at all for the last four years. I had seen some progress in the 1st year survival and hoped this would translate into improvements in the two and three year survival the following year and it has, but only marginally. The two and three year life expectancy improved by 6%. The one year survival went down from 81.4% to 80.7%. To view the NCI myeloma survival table CLICK HERE.
So is this another example of insanity as defined by Albert Einstein? Do we continue to do the same things year in and year out, and expect the different results? On the surface I think not. We do see a number of new drugs coming to market, myeloma specialists have survival rates 2 to 3 times the 4 year average, Clinical Trials continue to identify new promising drugs like the monoclonal antibodies, and the continued and expanded efforts by patient advocates, doctors, IMF, MMRF, and LLS to improve awareness. Or is what we are doing the definition of "FUTILITY"? Futility is doing the wrong things over and over again and expecting different results. - Anonymous
Everything which has been accomplished seems to be the right things, however if the results do not improve, I can only think we are not pushing the right buttons to improve results in a Revolutionary not Evolutionary manner. Might we be missing the things which when accomplished would improve results in a Revolutionary way?
Let us look at the history of other cancers to see what in fact has caused their Revolutionary improvements.
Breast Cancer: Was it new drugs, new procedures, imaging, or breakthrough surgical methods that made such improvements? No it was awareness of the need for self examination and mammograms, and the great promotional and awareness work of advocates like Susan Komen and Breast Cancer ads everywhere.
Colon Cancer: It was the same thing here with advocates like Katie Couric, and improved awareness of the need for Colorectal Cancer Screening. Screening has gone up significantly which should result in an excellent improvement in survival because polyps are removed before they become phase 3 or 4 colorectal cancer cases. The big news here is that the rate of new cases per 100,000 population has dropped by 34% from 58 to 38 per 100,000. This represents 25,917 fewer colorectal cancer deaths each year.
I could go on, however we can learn from this success in other cancers. The UK's National Health Service has noted that 20% of myeloma patients die in the first two months after diagnosis, in the US one third of patients die in the first two years, 25% of patients are diagnosed more than 306 days after going to the family practitioner for the first time, the majority of patients are treated by a local hematologist/oncologist without a myeloma specialist as part of their treatment team, and in a study in the UK 97% of the population had never heard of multiple myeloma.
What could be done? I am no marketing expert, however it would seem we have a visibility issue. No one knows we exist. I often say you can not improve that which you do not measure, but maybe our biggest hurtle is that myeloma patients, family practitioners(GP's), oncologists, and the general population "Don't know what they don't know!" , and the general public and GP's will continue to not know until we find ways to get awareness up from 3% to more like 90%+. We need a major "Public Service Myeloma Awareness Campaign." I am coming to the belief that the numbers will not change until the general population and family practitioners know the symptoms, and oncologists know that they need a myeloma specialist on the treatment team. Otherwise, unless something changes, nothing will change!
Without a major Public Service Awareness Campaign our best approach is for EACH of us get this message out to our facebook, twitter or other social media contacts and give it to our family doctors. You may not know someone with myeloma symptoms but your contacts might, and you may just help to SAVE LIFE! Just Click the Twitter and Facebook icons at the end of this post. The United Kingdom's National Institue of Health has put out a pamphlet for family doctors, just CLICK HERE. World renowned myeloma specialist Dr. Edward A. Stadtmauer of the University of Pennsylvania has a web based educational program for general practitioners and it should be required reading CLICK HERE.
The Symptoms of Multiple Myeloma can include:
In about one-third of patients, multiple myeloma is detected before symptoms appear through routine blood tests that show elevated levels of immunoglobulin proteins.
Good luck and may God Bless your Cancer Journey. For more information on multiple myeloma survival rates and treatments CLICK HERE and you can follow me on twitter at: https://twitter.com/grpetersen1
Everything which has been accomplished seems to be the right things, however if the results do not improve, I can only think we are not pushing the right buttons to improve results in a Revolutionary not Evolutionary manner. Might we be missing the things which when accomplished would improve results in a Revolutionary way?
Let us look at the history of other cancers to see what in fact has caused their Revolutionary improvements.
Breast Cancer: Was it new drugs, new procedures, imaging, or breakthrough surgical methods that made such improvements? No it was awareness of the need for self examination and mammograms, and the great promotional and awareness work of advocates like Susan Komen and Breast Cancer ads everywhere.
Colon Cancer: It was the same thing here with advocates like Katie Couric, and improved awareness of the need for Colorectal Cancer Screening. Screening has gone up significantly which should result in an excellent improvement in survival because polyps are removed before they become phase 3 or 4 colorectal cancer cases. The big news here is that the rate of new cases per 100,000 population has dropped by 34% from 58 to 38 per 100,000. This represents 25,917 fewer colorectal cancer deaths each year.
I could go on, however we can learn from this success in other cancers. The UK's National Health Service has noted that 20% of myeloma patients die in the first two months after diagnosis, in the US one third of patients die in the first two years, 25% of patients are diagnosed more than 306 days after going to the family practitioner for the first time, the majority of patients are treated by a local hematologist/oncologist without a myeloma specialist as part of their treatment team, and in a study in the UK 97% of the population had never heard of multiple myeloma.
What could be done? I am no marketing expert, however it would seem we have a visibility issue. No one knows we exist. I often say you can not improve that which you do not measure, but maybe our biggest hurtle is that myeloma patients, family practitioners(GP's), oncologists, and the general population "Don't know what they don't know!" , and the general public and GP's will continue to not know until we find ways to get awareness up from 3% to more like 90%+. We need a major "Public Service Myeloma Awareness Campaign." I am coming to the belief that the numbers will not change until the general population and family practitioners know the symptoms, and oncologists know that they need a myeloma specialist on the treatment team. Otherwise, unless something changes, nothing will change!
Without a major Public Service Awareness Campaign our best approach is for EACH of us get this message out to our facebook, twitter or other social media contacts and give it to our family doctors. You may not know someone with myeloma symptoms but your contacts might, and you may just help to SAVE LIFE! Just Click the Twitter and Facebook icons at the end of this post. The United Kingdom's National Institue of Health has put out a pamphlet for family doctors, just CLICK HERE. World renowned myeloma specialist Dr. Edward A. Stadtmauer of the University of Pennsylvania has a web based educational program for general practitioners and it should be required reading CLICK HERE.
The Symptoms of Multiple Myeloma can include:
- Bone pain and skeletal fractures, including compression fractures of the spine, which can cause severe pain, particularly in the back. A backache that lasts for months can be a signal that multiple myeloma is affecting bones in the spine and/or the ribs.
- Frequent infections, especially bacterial infections of the respiratory and urinary tracts, which occur because the immune system is weakened.
- Fatigue, weight loss, and general discomfort caused by anemia (insufficient red blood cells).
- Nausea, vomiting, altered mental state, depression, and headache, caused by abnormally high calcium levels in the blood (hypercalcemia).
- Loss of kidney function, leading to fatigue, buildup of fluid in the lower limbs, nausea, and vomiting.
- Bruising, rashes, nosebleeds, vision loss, headache, dizziness, and peripheral neuropathy (numbness, tingling, and burning pain in the extremities) caused by blood that has thickened (a condition called hyperviscosity) due to high levels of protein.
- Shooting pains in the arms and legs caused by a tumor in the spinal column pressing on nerves.
In about one-third of patients, multiple myeloma is detected before symptoms appear through routine blood tests that show elevated levels of immunoglobulin proteins.
Good luck and may God Bless your Cancer Journey. For more information on multiple myeloma survival rates and treatments CLICK HERE and you can follow me on twitter at: https://twitter.com/grpetersen1
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