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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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Age
Oct 8

Oct 8 Age

Nat Rosen

Just a number

Listen . . .
Oct 1

Oct 1 Listen . . .

Nat Rosen

. . . To Your Body

Heartwarming
Sep 24

Sep 24 Heartwarming

Nat Rosen

The quiet power of family

Growth
Sep 17

Sep 17 Growth

Nat Rosen

Floral portrayal; not my actual flowers

9/11/23
Sep 11

Sep 11 9/11/23

Nat Rosen

Remember

Writing
Sep 3

Sep 3 Writing

Nat Rosen

Labor of Love

Passed
Aug 27

Aug 27 Passed

Nat Rosen

The Vast Past

Anticipation
Aug 20

Aug 20 Anticipation

Nat Rosen

Coping with Hoping

Fog
Aug 13

Aug 13 Fog

Nat Rosen

Chemo Brain

Pivot
Aug 6

Aug 6 Pivot

Nat Rosen

Doctors’ attitude adjustment

Source
Jul 30

Jul 30 Source

Nat Rosen

What started this all?

Both
Jul 23

Jul 23 Both

Nat Rosen

Realistic and Optimistic

Gratifying
Jul 16

Jul 16 Gratifying

Nat Rosen

To help - I hope

Boring
Jul 9

Jul 9 Boring

Nat Rosen

Right where I want to be

Independence
Jul 2

Jul 2 Independence

Nat Rosen

Freedom every day

Sad
Jun 25

Jun 25 Sad

Nat Rosen

Worse than me

Supportive
Jun 18

Jun 18 Supportive

Nat Rosen

How can I help?

Somebody
Jun 11

Jun 11 Somebody

Nat Rosen

The helped or the helper

Family
May 28

May 28 Family

Nat Rosen

Combining Chemicals and Compassion

Sometimes
May 21

May 21 Sometimes

Nat Rosen

Just having a bad day

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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