Multiple Myeloma - Survival Rate Statistics by Hospital
  • Home
  • Higher Risk Myeloma
  • Myeloma Blog
  • Myeloma Specialists Listing
  • Doctor Submissions
  • Contact Us

When Myeloma Awareness Month Falls Every March - DOES ANYONE HEAR US??

2/21/2014

7 Comments

 
March is Multiple Myeloma Awareness month, but how does a disease which effects just 20,000 people in 315,000,000 or just .0063 percent of the people in the USA annually, get any attention or awareness?  Breast cancer has 232,340 newly diagnosed annually or 11 times more cases but just 2 time more deaths.
Picture
Everyone knows about breast cancer and should, but few if anyone other than those effected by myeloma have heard of multiple myeloma. It is therefore really important we work together, or we will not be heard. 

We have some outstanding organizations that have helped to create awareness, raise funds, and spearhead drug development. Organizations like the IMF (International Myeloma Foundation), MMRF (Multiple Myeloma Research Foundation), and LLS (Leukemia & Lymphoma Society), and they do the best they can to get the word out, however somehow the average life expectancy remains at just 4 years for the third straight year in a row based on the statistics provided by the National Cancer Institute. In March of 2012, I wrote an article headlined "Why Do People Die From Multiple Myeloma? Lack of Awareness!!!", where I was trying to understand how multiple myeloma specialists had patient survival of 10 years of more but the average for all patients remains at just 4 years. To read the article CLICK HERE.  
 
We also have a number of selfless, generous patient advocates, which include Mike Katz, Pat Killingsworth, Jennifer Ahlstrom, Lizzy Smith, Cynthia Chmielewski, Jack Aiello, Suzierose, Matt Goldman, Nick Van Dyk, Danny Parker, Cure Talk and Beacon contributors,  et. al, who work tirelessly to get the word out and raise awareness, all while fighting this disease.  We recently got the Tom Brokaw Bump (not a new dance) from his selfless and brave announcement of his condition.  Google searches and views of my site doubled and tripled the week of Tom's announcement, but are now back to previous levels.  It remains up to the selfless and knowledgeable myeloma advocates and myeloma organizations to continue their outreach efforts because each of these advocates know that a knowledgeable myeloma patient  who has a MYELOMA SPECIALIST on their team will outlive the average life expectancy by a factor of 2 to 4, or 8 to 16 years vs. the current average of 4 years.  And this 6 years of extra life for the 80,000 myeloma patients represent 480,000 years of life, and another 120,000 years of life with each new year of newly diagnosed.    

I question some of the recent headlines in the news lately, but only because I think they need to add some fine print.  Some of the headlines are:

Tom Brokaw's Multiple Myeloma Cancer and His Hopeful Future ...

Brokaw's multiple myeloma called incurable but treatable - USA Today

Tom Brokaw Diagnosed With Cancer, Prognosis Encouraging

Tom Brokaw reveals cancer diagnosis; doctors are 'optimistic' - CNN ...


These are all accurate, but only with some qualifiers.  For reasons I have yet to understand completely, the prognosis for the average patient is for them to live an average of just 4 years with 20% dying in the first year, and this is not too hopeful, encouraging, and optimistic.   The qualifying fine print should therefore read, the future is hopeful, encouraging, and optimistic if Tom has a skilled multiple myeloma specialist on his team, (he does). He goes to a facility that does genetic testing and is extensively involved in clinical trials (he is), is at a facility that tracts survival statistics and knows the results for every type of treatment in use at their facility (they do), is a low risk case which is 85% of cases based on genetic testing (I have no idea what his risk factors are).  And, finally some of the most skilled myeloma specialists have stated they believe a minimum of 10% to 40% of their patients will be effectively cured using currently approved drug combinations and a protocol including induction, transplant, consolidation, and then maintenance, or in one case no transplants. 

One way for YOU to help with Myeloma awareness is by getting this message out to your facebook, twitter or other social media contacts.  You may not know someone with myeloma 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 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


7 Comments

Tom Brokaw has Multiple Myeloma - Thank You for Making it Public!  You May Have Just SAVED LIFE!

2/13/2014

0 Comments

 
I have the utmost respect and admiration for Tom Brokaw as a broadcaster and just a person who seems to be a great and caring human being.   I was shocked to hear of his diagnosis, and can say "I know how he felt".  How would anyone feel when they are told that they have an incurable blood cancer with an average life expectancy of just 4 years as reported by the National Cancer Institute.  For one thing, you often have it for a while, before it is diagnosed, and have fatigue, constant infections, bone damage, kidney, and other organ damage, or any number of symptoms that may be treated, but as yet not diagnosed as caused by multiple myeloma.   

Then when you are diagnosed,  usually by a local oncologist, he may believe he has the skill and expertise to treat this disease.  This is one of the biggest mistakes often made by the myeloma patient, and is the reason I wrote the article "Improved Multiple Myeloma Life Expectancy in FIVE IMPORTANT STEPS."  Tom Brokaw has accomplished the two most important steps by finding a multiple myeloma specialist, someone who is skilled in this complex and deadly disease.  And it is because of this skill, knowledge, and familiarity with the nuances of myeloma that the myeloma specialist's patients live 2 to 4 times longer than the average.  They will live 8 to 12 years or longer and some 15 to 30% will be CURED.

Picture
I truly thank Tom for the strength and courage to make his diagnosis public. We hear so many stories of cancer patients being shunned by people they thought were their friends, the loss of job opportunities, or not being selected for promotion or plum assignments, or to be pitied, and viewed as a "Dead Man Walking".  

So why do I say that Tom just may have SAVED LIFE.  For one thing because multiple myeloma is an orphan disease with only 20,000 people diagnosed nationally, few have heard of it, not many doctors are really skilled at treating it, and drug companies seldom put money into drugs for myeloma because there are so few customers, and the customers won't be customers for very long (4 year average life expectancy).  So if someone of Tom's status becomes active, more people find out about multiple myeloma, the best way to treat it and where to get it treated, and fund raising goes up for more research into finding the ultimate cure. Some examples of some people who have had a huge impact on multiple myeloma are:

Sam Walton of Walmart - Not so much that he had the disease, but was lucky enough to have Dr. Bart Barlogie of MD Anderson as his doctor.   Dr. Barlogie went on to start the first Myeloma Intitute in the World in Little Rock, Arkansas, where many of the first innovations in treatment have been developed.  

Susan Novis, Brian Novis, and Dr. Brian Durie -  Susan Novis's husband Brian was diagnosed with mutiple myeloma and this trio started the IMF (International Myeloma Foundation).   The IMF has been on a mission, a mission to improve the lives of myeloma patients. With over 196,000 members in 113 countries worldwide, the IMF is the oldest and largest organization dedicated to finding a cure for myeloma. http://myeloma.org/Main.action

Kathy Giusti - Identical twin sisters Kathy Giusti and Karen Andrews founded the MMRF after Kathy was diagnosed with multiple myeloma.  The MMRF relentlessly pursues innovative means that accelerate the development of next-generation multiple myeloma treatments to extend the lives of patients and lead to a cure.  They have collected over $300 million dollars to fund research into a cure.

http://www.themmrf.org/

So Tom, we welcome you to a select group of people who no one in their right mind wants to join.  Thank You Again, Good Luck, and May God Bless your family's myeloma journey.  

For more information on multiple myeloma survival rates and life expectancy  go to the web site www.myelomasurvival.com, or you can follow me on my twitter account at: https://twitter.com/grpetersen1 

0 Comments

Cure vs. Control for Multiple Myeloma - Dr. Vincent Rajkumar, One of Mayo Clinic's Myeloma  "DREAM TEAM", Discusses This Vigorously Debated Subject

2/9/2014

2 Comments

 
***Now that the broadcast has aired, I believe we just had one of the best Myeloma Cure Panel Broadcasts yet presented.  To listen to a rebroadcast CLICK HERE.***

Mark your calenders for what I believe will be one of the best Myeloma Cure Panel Broadcasts yet presented.  Dr. Vincent Rajkumar will be discussing the subject of Cure vs. Control for Multiple Myeloma at 5:00 pm EST on February 26th.  For instructions on how to listen or to ask your questions on air CLICK HERE.

The subject of CURE vs. CONTROL  for multiple myeloma has been a vigorously debated subject for a very long time.  Dr. Rajkumar had been a proponent of the Control Treatment Philosophy and ten years ago, when few if any people believed that myeloma was curable, control was overwhelmingly the majority view.  But maybe "The Times They Are A-Changin".  More and more doctors are now saying the big C word, CURE. 

I mention the Myeloma "Dream Team" because I believe Mayo has assembled a world class team of medical professionals for the primary purpose of fighting multiple myeloma.  In the current Olympic charged atmosphere, I remember the first time the USA assembled the best NBA basketball players, the first DREAM TEAM which resulted in a gold medal performance.  Mayo's improvement in survival rates is nothing short of miraculous. The Mayo Clinic Medical Edge Video from July 11, 2011 states that their 3 year survival has improved from 29% to close to 90%. When compared to the SEER rate of 55.6% you are at least 3 times more likely to survive three years under their care than at the average of all facilities that report their data to the National Cancer Institute.
PictureDr. Vincent Rajkumar a Member of Mayo's Myeloma DREAM TEAM!
With a group which includes Dr. Vincent Rajkumar, Dr. Robert Kyle, Dr. Martha Lacy, Dr. Shaji Kumar, Dr. Asher Chanan-Kahn, Dr. Vivek Roy, Dr. Rafael Fonseca, Dr. Keith Stewart, and Dr. Craig Reeder, it truly is a Myeloma "DREAM TEAM", and we have the Michael Jordan for this broadcast.

Not wanting to put Dr. Rajkumar on the spot, but hold onto your hats, because we have an Olympic level performance in the making. You can view his exceptional bio if you CLICK HERE. If you would like to see a 2011 Blood Journal article by Dr. Rajkumar on this subject CLICK HERE.

For more information on multiple myeloma survival rates and life expectancy  go to the web site www.myelomasurvival.com, or you can follow me on my twitter account at: https://twitter.com/grpetersen1 



P.S. - As you may have heard Tom Brokaw of NBC has been diagnosed with Myeloma and will be getting his treatment at Mayo. Tom, welcome to a great group of people that no one wants to join.  You are in excellent hands at Mayo. May God Bless your myeloma journey.  View a blog post on Tom Brokaw CLICK HERE.

2 Comments

I Am Off To See The Wizard, The Wonderful Wizard of Arkansas!!! -  Time For My Annual Visit To Be Prodded, Poked, Punctured and a New Test MRD (Minimal Residual Disease)

2/1/2014

16 Comments

 
I can hardly believe that it has been 8 years since my diagnosis with dialysis dependent kidney failure, and then found out this was the good news.  The bad news, which I found out later was the kidney failure was caused by a cancer of the bone marrow called multliple myeloma.  I was first treated at Mayo Jacksonville and then went on to do a modified off protocol version of the UAMS-MIRT University of Arkansas Myeloma Institutes TT3 (Total Therapy 3) program.   So now I return once a year to see if my complete remission  continues.  In the first week in February I will have blood drawn, a 24 hour urine analysis, MRI, PET scan, and a bone marrow biopsy, and a new test called MRD or Minimal Residual Disease test.
PictureBart the Wonderful Wizard of Arkansas
The bone marrow biopsy is usually the one test that most people dread. I have found that if I have a fentanyl lollypop 30 minutes prior to the procedure, I don't have that much discomfort.  If you actually want to find out what the nurse is doing back there during the biopsy you can see a video of the process if your CLICK HERE.

However this time I am more apprehensive of the new MRD test. All the current tests for light chains, lesions, bone marrow biopsy, M spike, etc. have always indicated that I was in CR.  The MRD test is a far more sensitive test,  and will be able to see if there are any myeloma cells left in my system.  So a MRD negative result would confirm that my disease is under control based on the most sensitive tests yet available for multiple myeloma diagnostics.  And a positive result would just SUCK.   Other diseases use a MRD test to determine if a patient's treatment has been successful, and when or if it should be changed.  MRD is used for acute lymphoblastic leukemia (ALL), and MRD status is one of the most powerful predictors of disease-free and overall survival for children with ALL.  The promise for myeloma is that we are able to use this test in the same manner.  The International Myeloma Foundation has developed
 a program called the Black Swan Initiative intended to use a test for MRD with enough sensitivity that a MRD negative result would define a multiple myeloma cure and develop  treatment protocols that can achieve this goal.

So now I am off to see the Wizard (Bart Barlogie).   I like Bart, respect their program and the people at UAMS but as I have found, "There's no place like home, there's no place like home!"

For information on the UAMS MIRT myeloma program from a patient's perspective you can CLICK HERE, or go to Nick's Myeloma Blog which gives a detailed explanation of the program as Nick goes through it day by day if you CLICK HERE.


Added after my checkup at UAMS


So how did my visit go.   For a little reference, where did I start out in Feb of 2006.  I was fatigued, and a checkup which showed dialysis dependent end stage kidney failure, which at the time with myeloma had a three month life expectancy.  My bone marrow was 90% myeloma cells, I was anemic, few platelets, five lytic lesions on my chest, low red and white blood cell counts, and in the emergency room for 5 days of continuous dialysis with a special filter to remove the light chains that were clogging my kidneys.

The result of my current tests, blood tests showed a normal hemogram, improved creatinine, normal liver function, CD4 counts recovering, light chains within normal levels, bone marrow biopsy with no morphological evidence of myeloma, MRI and PET scan showed no lytic lesions or infection, CT bone density did show osteopenia in my spine and I will start low-dose Zometa.  

And the MRD test by 8-color flow cytometry was negative.  YEA!!!!   The statement from Dr. Bart Barlogie  "Thus, the patient qualifies for the highest level of complete remission." YEA!!!  With a final few jokes and laughs, and as always a hug for me and my wife, we bid farewell to The Wonderful Wizard of Arkansas.

For more information on multiple myeloma survival rates and life expectancy  go to the web site www.myelomasurvival.com, or you can follow me on my twitter account at: https://twitter.com/grpetersen1 


16 Comments

    Author

    Gary R. Petersen
    [email protected]
    CLICK HERE for my myeloma journey

    ©2012 All Rights Reserved

    Categories

    All

    Archives

    January 2025
    August 2023
    March 2023
    October 2022
    February 2021
    October 2020
    September 2020
    August 2020
    May 2020
    April 2020
    March 2020
    February 2020
    January 2020
    December 2019
    September 2019
    August 2019
    July 2019
    June 2019
    May 2019
    March 2019
    February 2019
    January 2019
    December 2018
    November 2018
    October 2018
    August 2018
    June 2018
    May 2018
    April 2018
    January 2018
    November 2017
    October 2017
    September 2017
    August 2017
    May 2017
    April 2017
    March 2017
    February 2017
    January 2017
    December 2016
    October 2016
    September 2016
    August 2016
    July 2016
    June 2016
    May 2016
    April 2016
    March 2016
    February 2016
    January 2016
    December 2015
    November 2015
    October 2015
    September 2015
    August 2015
    July 2015
    June 2015
    May 2015
    April 2015
    March 2015
    February 2015
    January 2015
    December 2014
    November 2014
    October 2014
    September 2014
    August 2014
    July 2014
    June 2014
    May 2014
    April 2014
    March 2014
    February 2014
    January 2014
    December 2013
    November 2013
    October 2013
    September 2013
    August 2013
    July 2013
    June 2013
    May 2013
    April 2013
    March 2013
    February 2013
    January 2013
    December 2012
    November 2012
    October 2012
    September 2012
    August 2012
    July 2012
    June 2012
    May 2012
    April 2012
    March 2012

    RSS Feed

Web Hosting by iPage