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Thank you!

About The Canswer Man:

IMG_1728-1 (dragged).jpg

A simple man with a simple plan: Kick the Big "C" with a cocktail of family/friend love, unapologetic laughter and a dash of Nat-titude.  And if I'm lucky, maybe even one of my odd-servations will help with YOUR situation.

Please join me on my selfish/selfless journey --- to infinity, and beyond!

How To Follow Along

Submit your e-mail in the form at the left to stay up-to-date on all Canswer Man posts. They'll come right to your inbox when I publish.

Thanks,

-TCM

 

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Reinforcements
Sep 5

Sep 5 Reinforcements

Nat Rosen

Calling in the Chemo Cavalry

Duality
Aug 28

Aug 28 Duality

Nat Rosen

My bifurcation situation

New Dr. S
Aug 21

Aug 21 New Dr. S

Nat Rosen

New beginnings - same coverage

Pain
Aug 14

Aug 14 Pain

Nat Rosen

I prefer the term: discomfort

System
Aug 7

Aug 7 System

Nat Rosen

Paper work - or not work

Hmmm . . .
Jul 31

Jul 31 Hmmm . . .

Nat Rosen

Why NOT me?

Balance
Jul 24

Jul 24 Balance

Nat Rosen

Risk / Reward

Connectivity
Jul 17

Jul 17 Connectivity

Nat Rosen

Physiological and pharmaceutical interdependence

Stat
Jul 10

Jul 10 Stat

Nat Rosen

The weight of waiting

Numbers
Jul 4

Jul 4 Numbers

Nat Rosen

Living in the digital age

Time
Jun 26

Jun 26 Time

Nat Rosen

Friend or foe?

Blame
Jun 19

Jun 19 Blame

Nat Rosen

I’ll see you in court

Sand Man
Jun 12

Jun 12 Sand Man

Nat Rosen

Fuzzy feeling feet

EHR
Jun 5

Jun 5 EHR

Nat Rosen

A new acronym

Remembering
May 30

May 30 Remembering

Nat Rosen

Sacrifice by choice

Aging
May 22

May 22 Aging

Nat Rosen

Older, but any wiser?

Dr. S 2.0
May 15

May 15 Dr. S 2.0

Nat Rosen

New and Improved?

Weight
May 8

May 8 Weight

Nat Rosen

Too much?

Mr. Nat-ural
May 1

May 1 Mr. Nat-ural

Nat Rosen

Keep on truckin’

Anybody
Apr 24

Apr 24 Anybody

Nat Rosen

Indiscriminate

Load More
 
                             My "life" with Multiple Myeloma

                             My "life" with Multiple Myeloma

Disclaimer - The choice of my blog name is not in any way intended to imply that I alone possess the answers to all of the questions that are inevitably bombarding your brain. Quite the opposite.

Every dimension of your disease is unique to you, so I encourage you and your Personal support team to ask as many questions as you want (write them down, trust me - you'll forget).  And if your Medical support team doesn't have the time or patience for your rightful inquiries, then I can tell you one thing - you need a better Medical support team.

Seek information, embrace your disease, and work hard to understand as much as you can about what is being done to help you. It makes you a better player on BOTH teams, and adds to the quality of your journey/outcome.

 

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