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About The Canswer Man:

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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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Trials
Mar 17

Mar 17 Trials

Nat Rosen

Clinicaltrials.gov

This . . .
Mar 10

Mar 10 This . . .

Nat Rosen

. . . is why

Patient
Feb 25

Feb 25 Patient

Nat Rosen

Pushy or Pushover?

Blood
Feb 18

Feb 18 Blood

Nat Rosen

Hemoglobin level

Alive
Feb 11

Feb 11 Alive

Nat Rosen

Natural Selection

5  Stars
Feb 4

Feb 4 5 Stars

Nat Rosen

Medical “Michelin” Rating

Sphere
Jan 28

Jan 28 Sphere

Nat Rosen

Big Blue Marble

Shovel-ry
Jan 21

Jan 21 Shovel-ry

Nat Rosen

Thank You !

CIPN 101
Jan 14

Jan 14 CIPN 101

Nat Rosen

Next “Steps”

New
Dec 31

Dec 31 New

Nat Rosen

Twenty Twenty-Forward

Study
Dec 17

Dec 17 Study

Nat Rosen

Pay it forward

Afraid
Dec 10

Dec 10 Afraid

Nat Rosen

The real risk

Holi-does
Dec 3

Dec 3 Holi-does

Nat Rosen

Festive focus

Acupuncture
Nov 26

Nov 26 Acupuncture

Nat Rosen

What have I got to lose?

Masking
Nov 19

Nov 19 Masking

Nat Rosen

Comfortable

Gamification
Nov 12

Nov 12 Gamification

Nat Rosen

Guess Who?

Volun-cheer
Nov 5

Nov 5 Volun-cheer

Nat Rosen

The Power of Internship

Courage
Oct 29

Oct 29 Courage

Nat Rosen

Mark Herzlich

Clarification
Oct 22

Oct 22 Clarification

Nat Rosen

Sniffling, not suffering

Annoyed
Oct 15

Oct 15 Annoyed

Nat Rosen

But Alive

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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