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No Respect!  Myeloma Patient's Don't Even Get Credit For Dying!  Do The Myeloma Math.

2/29/2016

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This a subject I have thought of writing about for a very long time.  When we lost Pat Killingsworth recently it brought it back front and center for me.  Pat has had a 9 year battle with a rare presentation of multiple myeloma.  In the end he died from a brain aneurysm, aggravated by a rare form of blood disorder called TTP, and TTP was most likely caused by the chemotherapy from his myeloma fight.  He was admitted into the hospital with kidney failure.  So what was on his death certificate, kidney failure, brain aneurysm, TTP, or complications from chemotherapy, or complications from multiple myeloma.  Well, it was listed as a brain aneurysm. I am fairly certain Pat would say he died from complications due to myeloma.  This would be important to him because funding for the NCI(National Cancer Institute) uses lives lost in there allocation of funds.   So if Pat, a myeloma patient and fervent myeloma advocate, can not be considered part of the myeloma death statistics then who can.  Let's take a look at the math.  The National Cancer Institute reported the following:

  • Estimated New Cases in 2015 -  26,850 
  • Estimated Deaths in 2015        -  11,240

This would suggest the cure rate would be (26,850-11240)/26,850  =  58%, however the long term survival of myeloma patients is only 10 to 15%.  It can therefore be deducted myeloma deaths are under-reported by over 43%.  Because the most likely causes of death for myeloma patients is  pneumonia, infection, and bleedouts, these could easily be on the death certificates of many myeloma patients.  So if cure was 15%, then the number of deaths would be closer to 22,822.   Why is this important for the myeloma patient community?  The NIH (National Institute of Health) and NCI (National Cancer Institute) use deaths, and lost years of life by cancer type to rationalize the research spending for the NCI research projects.  The more deaths and  lost years of life the more spending for that form of cancer.  A study by the NIH tries to rationalize spending to the number of lives lost and years of life lost by cancer and you can read it if you CLICK HERE.  A summary slide is shown below. 


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The way to read the graph is that for prostate cancer, NCI funds three times more than the YLL(years of lost lives due to prostate cancer) can justify.  It also shows myeloma gets about 8/10 of what it should get based on its reported YLL, but we know myeloma deaths are being underrepresented.  If represented correctly the myeloma spending falls to about 1/2 of what is justified by its real YLL.   Great for leukemia which 2.2 times what its YLL would justify or lymphoma, which gets 1.4 times what its YLL would justify.  But as is the title of this post, "Myeloma Gets No Respect".  This graph shows how out of balance the spending is to the lost years of life by cancer type, and I hope the NCI uses this study to better balanced spending.  In addition, the deaths should be computed by taking the newly diagnosed number and subtracting out the projected cure rate.  Most other cancers seem to closely follow this formula when you look at the reported newly diagnosed and deaths shown on the NCI SEER web site.

We spend $124 billion on cancer treatment each year and fund the NCI with just $5 billion.  To me this is penny wise and pound foolish.  Maybe we should be funding everything at 3 times the current average funding instead of cutting anything.  That would just be $15 billion, and one would expect a much larger reduction in cancer treatment cost to offset this in the longer run.   That would mean myeloma would end up with 7 times the current amount if everyone got their YLL share.  Wishful thinking,
dreamer, yes, but reasonable and logical. 


For more information on multiple myeloma CLICK HERE and you can follow me on twitter at: https://twitter.com/grpetersen1

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Today Is A Very Special Double Anniversary!  Married For 46 Years, and 10 Years Since My Myeloma Diagnosis. By Gary Petersen   

2/27/2016

4 Comments

 
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Today is a very special day for me in two ways. First, 46 years ago today, February 27th is when my lovely wife Anita and I were married.  So that was one of the best days of my life. 

It was also one of the worst days of my life, in that 10 years ago today on my wedding anniversary, I was informed I had Stage 3 mutliple myeloma with end stage renal failure.  My daughter, who was an editor on the medical  desk of the Wall Street Journal, researched myeloma and talked to some myeloma specialists.  She found the average life expectancy of myeloma was published at just 3 years, but end stage dialysis depended kidney failure made it very high risk with an average life expectancy of just 3 MONTHS.  I was treated by a myeloma specialist at both Mayo and UAMS.  Today is also a happy day for my myeloma journey because I have been MRD (minimum residual disease) negative for two years, and I have lived beyond  my prognosis by 9 years and 9 months. 


So I hope and pray we all can beat the averages, and find the cure.  And as always, may God Bless your myeloma journey/ Gary Petersen editor@myeloma survival.com

For more information on multiple myeloma go to the web site www.myelomasurvival.com or you can follow me on twitter at: https://twitter.com/grpetersen1

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Pat Gave Us His All, And Continues To Do So With An Outstanding Survival School!

2/24/2016

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Pat's Beach Party Memorial is now Pat's Myeloma Survival School, and before he so tragically left us, he put together an outstanding program for the newly diagnosed and long term myeloma survivor.  As only Pat could do, he has lined up some of the best and most knowledgeable myeloma doctors and patient advocates to present the World of Myeloma According to Pat.

The newest and most up to date treatment for myeloma will be presented by Dr. Guido Tricot.  He has been a leader in the myeloma treatment since his days at UAMS.  His program has resulted in estimated life expectancy 2 to 3 times the average published by the National Cancer Institute.  He was also Pat's doctor and was able to get Pat into sCR. and will be able to discuss TTP, which was the rare blood disorder twice as rare as myeloma which caused Pat's brain aneurysm. 

Just so you all know this educational program is still very much alive, and although Pat's recent passing had all but eliminated new sign ups, they have started to pick up and we have 100 signed up, but still have 50 spots available.  

A draft of the Myeloma Survival School is as follows:

Dr Guido Tricot, MD, PHD-U of Iowa Hospital/Holden Comprehensive Cancer Center
"Total Therapy Demystified"
His Staff: 2 nurses will be speaking on "The Transplant Experience from a Nurse's Perspective"

Melanie House, PT, Clinical Specialist will be speaking on "The Physical Challenges of Myeloma from Diagnosis to Treatment"

Mary Doyle,(Pattie's Sister) Facility Administrator for Newport Richey Kidney Center will speak on "Protect Your Kidneys" Diet/Dialysis/Labs  She is also bringing Maria Ramos, Patient Liaison/Patient Care Technician with her.

Dr. Brian Van Ness, PhD, U of MN, speaking on "Promising New Drug Research".

John McKillip, DDS, U of Missouri College of Dentistry tells his transplant experience.

Dr Ryan Perkins, Oncologist from Ackerman Cancer Center in Jacksonville, speaking on "Innovations in Radiation Therapy".

Kim Alexander (Wife of Elijah Alexander-NFL) tells her story and her goal to duplicate Myeloma Patient support in every place Elijah played.

Tracy Bonds, RN, Amgen's Clinical Nursing Educational Team on "The Survivorship Deck: Four tests to keep you on top of things,"  together with Dave Visel

New FDA Approved Drug information

Caring for the Caregiver
How the MMRF and IMF can help-support available

Myeloma and food, Chi Gung, managing your oral meds

In addition, many myeloma advocates and Pat's friends will be there to meet and greet and provide you with their myeloma incites. Cynthia Chmielewsk, Nick Van Dyk, Danny Parker, Gary Petersen, Andy Sninsky,  Kimberly Alexander, Matt Goldman and more.

Pat and Patti would like no more than to have a full house, and even after death, Pat provides hope and a future for all of us in the myeloma patient community. PLEASE CLICK HERE TO SIGN UP.  And as always Feel Good  and Keep Smiling!


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Opps, Your Comments Have Not Been Publishing! 

2/23/2016

1 Comment

 
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So sorry to my readers.  I had been thinking I was publishing my comments from readers for a long time. However, the Weebly Blog system was updated and the old method of approval  did not work anymore.  I had over 40 comments that were not published.  I will be trying to catch up with the replies in the nest few days.  I  have been working to get this fixed with the web publishers for three weeks, and I think I can now approve the comments for publication.  I believe I finally understand how to publish them with the new system update so this should be in the past. 

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Pat Killingsworth's Memorial Myeloma Beach Party

2/22/2016

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Several people have asked me when and where will be Pat's funeral and memorial.  They have also asked how Pattie is doing and is there anything they could do.  Patti is doing as well as can be expected.  Pat married a kind, caring, and loving women, who is also very strong.  She is committed to follow through on Pat's Beach Party and in fact make it A Pat Killingsworth Memorial Party. This will be the only public memorial.  What can you do for Patti?  You can make sure you attend the Memorial Beach Party, and help Patti to continue Pat's efforts to support the MCRI (Myeloma Crowd Research Initiative).  For more information on how you can participate in the memorial I have provided the most recent post from Pat's blog below:

Countdown Has Begun!
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We would first like to thank everyone for the outpouring of thoughts, prayers and support during this time.  They mean more than you could ever know and we hold them close to our hearts every day.  As we move forward planning the event that was so important to Pat, your support gives us strength and purpose…to continue the fight. We know you would like to hear how Pattie is doing. There is a lot to take care of in this situation, so she is very busy taking care of them.  She is so grateful for all of you!  Even with all she has to do, she is making arrangements for this years’ event, to make it a success for all of you. She is an amazing gal!
We are now only 6 weeks away from this year’s Pat’s Myeloma Beach Party! Preparations are in full swing. As you all are aware, this year has a new meaning and is an important year to join us in Fernandina Beach, FL. Not only do we have some very special guest speakers, but we are honoring Pat Killingsworth- Author, Blogger, Patient Advocate and Friend. With this years’ special memorial to Pat, we are filling up fast! If you have not registered yet, please do so as soon as possible!  We have limited space and we do not want you to miss out.  To reserve your spot, click on this link:

Pat’s Myeloma Survival School 2016 Registration

In Honor of Pat, we are also giving the beach party a new name.  It will now be called “Pat’s Myeloma Survival School”.  We are excited about this as it holds a special tribute to Pat.
Don’t forget to join us for the Pat’s Myeloma Survival School 5K Beach Walk while you are there!  Remember, the proceeds go to CrowdCare Foundation to help pay for cutting edge clinical trials that are stalled due to lack of funding. To register, click on this link:

Pat’s Myeloma Survival School 5K Beach Walk 2016

For those of you that have people that would like to sponsor your walk, have them register with their name and put your name in the “Company Name” spot provided on the registration form.  They may also donate to Pat’s Myeloma Survival School 2016 or the Pat’s Myeloma Survival School 5K Beach Walk via Paypal. just go to

https://www.paypal.me/PKillingsworth

Add the persons name being sponsored in the “Notes” section.
We would like thank everyone for their support moving forward for this years’ event.  We couldn’t do this without you!
Never Forget…
Feel Good and Keep Smiling!

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A True Myeloma Hero, Pat Killingsworth Is Tragically Gone!

2/12/2016

1 Comment

 
I find it very difficult to write anything about Pat and his passing.  Each time I try, I find it hard to see the screen thru my tears. So I will just let all his friends and the myeloma patient community do it for me.  The following are just of a few of the tributes to Pat, who was my dear friend, Pattie's adoring husband, loved by his family, friends, and the entire myeloma patient community.

The MyelomaCrowd.com's Jenny Ahlstrom wrote a heartfelt goodbye to Pat in a post titled "Goodbye Dear Friend: A Tribute to Myeloma Advocate Pat Killingsworth"  To view CLICK HERE.

Just look at the over 130 comments on Pat's last two blog posts if you CLICK HERE, and HERE.

Cure Talks Priya Menon posted "Remembering Pat Killingsworth - Saying Good Bye to a Dear Friend
" -  CLICK HERE and the Cure Talks panel said there last goodbye to their beloved fellow panelist Pat if you CLICK HERE.

The MMRF Multiple Myeloma Research Foundation had a post you can see if you CLICK HERE.

Patient Power posted "The Loss of a Patient Power Friend" - CLICK HERE

Myeloma Teacher Cynthia Chmielewski posted - CLICK HERE

Dana Holmes Smoldering Myeloma Group -  CLICK HERE

The Myeloma Beacon had a post titled "Remembering Pat Killingsworth" which has over 60 comments- CLICK HERE

Matt vs Myeloma provided a blog post "Rest In Peace Pat Killingsworth" - CLICK HERE

The Florida Times Union's Jacksonville.com wrote in the Home/News - CLICK HERE

The IMF (International Myeloma Foundation) of which Pat was a Support Group Leader and a IMF myeloma ambassador provided a column in the IMF Myeloma Minute - CLICK HERE, Robin Tuohy wrote a post called "Keep Smiling My Friend" - CLICK HERE, and  a facebook post. - CLICK HERE

I could go on and on because Pat was one of the few people in the world that seemed to be loved by all.  Pat beat myeloma and was in sCR, and he will continue to be an inspiration to me and the entire myeloma patient community.  Please share some memories of Pat by viewing the attached video.

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Thirty Minutes Of Exercise A Day Keeps Cancer at Bay!  Up to a 50% Improvement!

2/7/2016

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A little over 2 years ago I wrote this post on the potential benefits of exercise on myeloma survival.   Pat Killingsworth had just completed a three part series that Danny Parker authored on the benefits of exercise on myeloma life expectancy, survival rate, and the probability of relapse.   I have found little data myself on the impacts of survival for blood and bone diseases like multiple myeloma, but Danny has gotten down into the nitty gritty of the impact of exercise on the biology of multiple myeloma.  You can read the entire series if you click on the following links:  PART1, PART2, & PART3. 

When I was going through my stem cell transplants, they were very insistent on making sure that we had at least 30 minutes of exercise every day.   And as any person who has gone through the SCT process, you really do not want to do much of anything, but obviously as noted by Danny and Pat, there are benefits from exercise that are extremely important to the patients long term survival. 


Do you know who this is on the left??  Because if you have multiple myeloma you are on average 69 years old and know that this is Jack LaLanne who was considered "The Godfather of fitness".  Jack died at age 96, well past the 46 year expected life expectancy for a male born in 1914.  Few of us will look like this, but the benefits of exercise does not require that you do any more than 30 minutes of exercise a day.

The majority of data on life expectancy, survival rates, and a reduction in the probability of relapse come from studies of the far more common forms of cancer.  And as could be expected, the rarer the disease the less data that is available.  I think that the data that Danny and Pat provide explains the biology of exercises benefits, and as a result we can hope that the experience from the studied cancers can transfer to multiple myeloma.  

So what do some of the studies for other cancers show.  Some of the more robust studies come in the area of breast cancer, and colon cancer.  You can do your own research on these cancers, however, I will provide a few examples.  

Dr. Meyerhardt, of the Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, is one of the country's leading researchers on the impact of lifestyle factors on cancer outcomes. He stressed that regular non-strenuous exercise can significantly improve survival in people recovering from colorectal cancer. Colorectal cancer recurrence or death was reduced by 49% in the people who regularly exercised. 

In 2005, Harvard researchers found that simply walking on a regular basis helped breast cancer patients. The study focused on about 3,000 women diagnosed with breast cancer who are part of the Nurses’ Health Study. Those who regularly walked three to five hours a week (or got comparable exercise) were 50% less likely to have a recurrence of their cancer than women who exercised less than an hour per week.

So, IF, and it is a big IF, we myeloma patients can obtain similar benefits  from exercise, then it is time for all of us to get moving, join a gym, walk, ride a bike, and any other activity that your physical limitations will allow.  Because a 50% benefit is a remarkable improvement to obtain without much cost or effort at all.  Recently, Myeloma Crowd has started a program to help all myeloma patients to get fit, and this program is call Muscles for Myeloma.  This program is designed to get you started on becoming fit to fight myeloma, and help fund a cure.  You can find out about this program if you CLICK HERE.

And as always, may God Bless your myeloma journey/ Gary Petersen editor@myeloma survival.com

For more information on multiple myeloma go to the web site www.myelomasurvival.com or you can follow me on twitter at: https://twitter.com/grpetersen1


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    Author

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

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