Patient Snapshot: 44 year old John Knighten

Posted on October 25 2012 by Pat Killingsworth | 1,022 views

Last month I flew west to speak to a support group in Spokane, Washington.  While I was there, I met an exceptional multiple myeloma survivor, John Knighten.

John shared at the meeting how he was preparing for the fight of his life–a tandem auto/allo transplant.  John is only 44 years old, yet he has endured so much.  John is a true multiple myeloma warrior.

John looks so “tough” in this picture–and he is.  But when you meet him in person, a more sensitive, compassionate side shines through.  And John is one of the most optimistic, bravest guys I think I have ever met!

After the meeting, I asked John two things:  If he would write a brief history, recapping his life since his myeloma diagnosis, and if I could follow his upcoming auto/allo transplant therapy and write about it  in real time.

One week later, I received an email from John.  In it I found a long and detailed account of his life up to now.  I emailed back, kidding about how he started his story “from my youth.”  But I think it’s interesting, so I’m going to post John’s story intact, with only a few minor edits.

Last week I featured a two part feature about Ken, a 76 year old, newly diagnosed patient:

Patient Snapshot: Ken from Florida

 

Patient Snapshot: Ken from Florida (Part Two)

 

I thought it would be interesting this week to balance things out by sharing a younger patient’s experience, too.  So here is Part One of John’s Patient Snapshot:

Pat.  I’m not exactly sure what you need as far as background, so I’ll try to start from my youth.   I was born in 1968 as the 11th of 12 kids–I guess if you’re looking for a stem cell donor the bigger the better.  My father died in 1973 of a brain aneurism.  He had a rather rough life, enlisting in the Marine Corps at the age of 16 in 1943 till 46.  He was recalled for the Korean war in 1950 as well.  My father saw quite a bit of combat so I’m sure he had what they now call delayed stress syndrome.  After my father’s death with government and church help, my mother got her nursing degree in approx. 3 years, and began a career as an RN with an orthopedic sub-specialty.

We moved to the Wenatchee, WA area in 1977 and mom began work at Deaconess Hospital in Wenatchee, who later were taken over by Central Washington Hospital.  We attended Eastmont School District and Church.  Through Church we met the Gary McLeod family, his wife, Norma Jean was one of my first Sunday school teachers. Gary a Deputy Sheriff with Douglass Co. took a liking to my family and over time became a sort of father figure to the younger brothers of our family.  Ultimately his children became as close as little brothers and sister to me.

School was reasonably easy for me.   I could have put more effort into it, but I’d say I was an above average student.  In High School, my effort wasn’t near what it could have been.  At times I focused on working to help support myself.

Money was always tight with a large family so if you wanted certain things, you had to help by working for some of them.  I found myself in the party crowd.

Sports wasn’t my big thing in High School, with the exception of wrestling.  Maybe it was some of the childhood fights with siblings and bullies helped to prepare for it.  That was my one sport ambition back then.  I also started developing an interest in a couple of career paths.  One was in the Marine Corps,  attributed to the father I barely knew and came to represent a way to learn more about his time in the Corps.

The other was in the Fire Service.  I had an older brother (who was also a Marine) who was a volunteer firefighter in the old family home of Kalama, WA.  I’d admire the shiny red trucks when we visited.  In High School a friend of mine asked for a ride to the Wenatchee Fire Dept. for his Explorer Scout meeting.  I don’t know if it was the full time paid status or the fire pole, but I joined up and won praise from my mother.  She always said when a fire started around town it couldn’t be me ’cause I was at the fire house!  Close to graduation I was leaning toward the fire science school in Tacoma, but father figure Gary talked to me about listening to all the times I talked about wanting to be a Marine.  He also stated that it was rare for too many 18-20 year old to be hired as Firemen or Cops, it would give me plenty of time to experience the Marine Corps.

I enlisted in  April of 86 on the delayed entry program with a enlistment date of 28 Dec 1990.  My Mom wondered why I had to wait that long.  I told her I needed to graduate and wait for an opening in my most desired field to open.  Without signing a 6 year enlistment my desired field of Crash Crew (military airfield firefighting) wasn’t guaranteed with a four year deal

After my time in the Marine Corps–and following the short term marriage to my first wife–I returned to Washington State to pursue my career as a firefighter.  I went into the Resident Firefighter Program with Pierce Co Fire Dist. 9.  They later consolidated with other departments and became part of Central Pierce Fire & Rescue just after I was hired by the Spokane Fire Department as a career firefighter.

I spent a year as a recruit firefighter, where my job would become permanent as long as I passed my recruit test.  I was assigned to Ladder Company 2.  In the majority of departments ladder and rescue crews tend to draw the more aggressive types.

After my promotion to Fire Equipment Operator I spent a year as a relief driver, filling in where the vacancies occurred and one year as the driver of Engine 8.  I enjoyed those 2 years, but I really wanted to get back on a ladder crew.  I made it onto ladder 4 in 2002 and also onto the technical rescue team assigned to station 4.  These were some of the best years of my fire career.  Until new year’s day of 2010.  I wasn’t feeling all that great when I left for duty, but I wasn’t going to pass up double time and holiday pay after Christmas. 

As the shift progressed my sore throat became worse and after bed time it was becoming more difficult to breath.  I finally realized I had no business being on duty and woke my Lt.  He saw how bad I looked and awoke our paramedics who said driving myself home wasn’t going to happen.   I refused to go by ambulance so the engine crew drove me 8 blocks to the nearest ER.  The ER staff looked me over and was surprised I was breathing on my own. They said I had epiglottitis, a bad throat infection and would need to be intubated soon.

Eventually I asked to be tubed.  I awoke a week later thinking I had dodged a bullet, but was told I had been diagnosed with Multiple Myeloma.  Thankfully my wife felt something worse was going on than a throat infection and finally convinced a pretty sharp doc to look over my case.  Looking at the numerous cases of pneumonia within the previous year and the anemia my primary overlooked, a bone survey was done and multiple lesions were found.

My local Oncologist felt I needed to go to the nearest center with a leading myeloma specialist,  so within two weeks of discharge from the hospital my wife and I made the 5 hour drive to the Seattle Cancer Care Alliance, made up of Fred Hutchinson Cancer Research lab, University of Washington Medical Center and Seattle Children’s Hospital.

I had my initial consult with Dr William Bensinger, who advised me he thought my age and otherwise good health, and based on statistics 2-3 matched family stem cell donors, he thought this would be my best chance for either the longest term remission, or even cure.  After checking in at SCCA, I told my assigned transplant doc that I wasn’t real comfortable with the risks of the donor transplant, so we made the decision to go with an autologous stem cell transplant instead.

I sailed through my auto transplant with only 5 total days inpatient.  I was discharged for home on day 28 post transplant.  By Jan 2010 I was released from light duty back to full duty on Ladder company 4, and I couldn’t have been happier… 

Ignorance can be bliss–especially for a multiple myeloma survivor!  I’m afraid that John’s myeloma journey would become far more difficult soon.  Tune-in for the second part of John’s story tomorrow.

And if any of  you would like to email me your myeloma stories, please do!  I know from experience that there are things we can learn from every patient’s story.

But if you do, think about emphasizing the parts of your journey that would be most helpful and inspirational to your fellow patients and caregivers.  Don’t get too bogged-down with the numbers.  And YES!  Caregivers are encouraged to write in, too! 

Feel good and keep smiling!  Pat

9 Comments For This Post

  1. Mark Says:

    Thanks to John for sharing his story. I would be curious if he could elaborate on why he was not comfortable with the risks of the early allo. I really viewed the allo as an opportunty. Both in terms of potential cure and the opportunity to avoid all the side effects and potential resistance to Revlimid/Velcade.

    When I was making my decision about the early allo, I basically looked at 2 scenarios. If I did not do the allo upfront, how would I feel when I relapsed, knowing I gave up my best chance at a potential cure. I then compared that to having some complications from the allo. I always thought I would feel worse about relapsing and not having done the allo as opposed to some side effects from the allo. I know I am definitely in the minority on that! Patients get side effects from the drugs we use for myeloma therapy. I also had no matched sibling donor and I did have a match on the Be The Match Registry. I may not have always been so fortunate to have a matched donor.

    I am really looking forward to Part 2.

  2. Pat Killingsworth Says:

    Hey Mark! Did you see the Beacon’s report about success of early allos a few days back? Add Velcade to the mix and cut-back on melphalan just a bit and I think docs may have a winner! Also, not sure why so many want to do tandems when stats are so mixed on that…

  3. Michelle Gillet Says:

    I am 43 abd very interested in hearing part two of what looks like to be a very interesting and informative story. Pat, I had a tandem. I did not choose to have 2. I has 1 but that only got me into vgpr, so tandem was my next option which thankfully got me into cr.

  4. Pat Killingsworth Says:

    Good to know, Michelle. My docs figured mine worked so poorly, why try again…

  5. John Knighten Says:

    Just wanted to answer Marks question. My wife and I being fairly new to the myeloma fight did alot or research and even found papers written by Dr Bensinger talking about how allo transplants were still considered experimental. It put enough doubt in my mind that when we checked in and met Dr Holmberg, we told her that we were not comfortable with the risks. If I knew what I know now, I’d probably have done the auto/allo combo at the beginning.

  6. Pat Killingsworth Says:

    Mark, did you have a tandem or simply an allo?

  7. Mark Says:

    John,

    All positive vibes and prayers going out your way as you go through this difficult time. I was curious how the allo was presented to you since I know Dr. Bensinger is one of the most most respected allo Doctors in the world. It sounds like it is what you read about the allo that made you hesitant about the procedure. While I know a lot of the myeloma Doctors say allos are “experimental” for myeloma patients, I do not buy it with respect to younger patients. There are 25,000 allos done annually for various disorders according to the Be The Match Registry. IMO a procedure done that often should not be called “experimental”. I would also point out that Robin Roberts is a big star and very valuable to ABC. Would they have had her go out and do an “experimental” procedure as soon as she was diagnosed with MDS? We basically have the same problem MDS patients do – our immune systems are not functioning properly.

    I think your story will be a very valuable one for younger patients to read. Thanks again for sharing and know that everyone is pulling for you to get through this.

    Mark

  8. Mark Says:

    Pat,

    I did a tandem auto-allo because my insurance company viewed allo first as “experimental”. They did pay for tandem auto-allo Reduced Intensity Conditioning. Since I did not have an extra $600k plus “handy” I did the tandem!

    It really did not help me out because my Doctor likes using a strong conditioning regimine right before the allo. I used 200 Melphalan for auto and 190 MEL plus high dose Fludarabine for the allo. I think the tandem concept was first used because the auto was the only way to get a patient into remission (or close to it) prior to Velcade and Revlimid. In my Doctors opinion it does not matter how you get to CR prior to the allo. I asked her after we found out that I would have to do the auto first if she would reduce the intensity of the conditioning for the allo since I would be getting high dose MEL. She replied the only thing that changes is that instead of a Velcade based regimine getting you to CR, hopefully high dose MEL will. If the auto did not get me to CR, I would have gone back to the Velcade/Doxil/DEX regimine before I did the allo.

    Mark

  9. Pat Killingsworth Says:

    I’m just curious about how an allo without preceding auto works. Maybe more of insurance issue than medical necessity?

6 Trackbacks For This Post

  1. Patient Snapshot Update: Our friend John | Multiple Myeloma Blog Says:

    [...] Patient Snapshot: 44 year old John Knighten [...]

  2. Patient Snapshot Update: Our friend John | Cure Talk Says:

    [...] a reminder, here are links to the two part story I wrote about John a couple of weeks back:Patient Snapshot: 44 year old John KnightenPatient Snapshot: 44 year old John Knighten (Part Two)  Here is part of an email John sent me a [...]

  3. mSMART, OS update and inspirational friends | Multiple Myeloma Blog Says:

    [...] Patient Snapshot: 44 year old John Knighten [...]

  4. mSMART, OS update and inspirational friends | Cure Talk Says:

    [...] Patient Snapshot: 44 year old John Knighten [...]

  5. Let’s hear from our readers! | Multiple Myeloma Blog Says:

    [...] Patient Snapshot: 44 year old John Knighten [...]

  6. Let’s hear from our readers! | Cure Talk Says:

    [...] Patient Snapshot: 44 year old John Knighten [...]

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