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Thank you!

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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Afraid
May 11

May 11 Afraid

Nat Rosen

Can-cern

Pain In
May 4

May 4 Pain In

Nat Rosen

The Aspiration

Others
Apr 27

Apr 27 Others

Nat Rosen

“Wing” Person

Eyes
Apr 20

Apr 20 Eyes

Nat Rosen

Still Don’t Know

Eye
Apr 13

Apr 13 Eye

Nat Rosen

Don’t Know

Commuting
Apr 6

Apr 6 Commuting

Nat Rosen

Drive timing

Hockey
Mar 30

Mar 30 Hockey

Nat Rosen

And Cancer

Orphan
Mar 23

Mar 23 Orphan

Nat Rosen

Worth it

Different
Mar 16

Mar 16 Different

Nat Rosen

What’s it all about

Missing . . .
Mar 9

Mar 9 Missing . . .

Nat Rosen

. . . Dr. Strair

Oscar 2025
Mar 2

Mar 2 Oscar 2025

Nat Rosen

Supporting Cast

Life Insurance
Feb 23

Feb 23 Life Insurance

Nat Rosen

Call Big Lou

Family Day
Feb 16

Feb 16 Family Day

Nat Rosen

Celebrate

Scheduling
Feb 9

Feb 9 Scheduling

Nat Rosen

Carpe Day-em

Support
Feb 2

Feb 2 Support

Nat Rosen

Services

In-Canceration
Jan 26

Jan 26 In-Canceration

Nat Rosen

Medical Prison

Prep
Jan 19

Jan 19 Prep

Nat Rosen

Let’s get ready to Chemooooo!

Tragedy
Jan 12

Jan 12 Tragedy

Nat Rosen

Magnitude

Stress
Jan 5

Jan 5 Stress

Nat Rosen

Worry-Washing

SCT / HrBD
Dec 29

Dec 29 SCT / HrBD

Nat Rosen

Happy Re-Birth Day (12/29/17)

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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