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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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"Compliance"
May 14

May 14 "Compliance"

Nat Rosen

Worth repeating

Being Masked
May 7

May 7 Being Masked

Nat Rosen

The kids are alright

Why I . . .
Apr 30

Apr 30 Why I . . .

Nat Rosen

Mission Accomplished

Press Release
Apr 23

Apr 23 Press Release

Nat Rosen

Nat for Natera Oncology

Science
Apr 16

Apr 16 Science

Nat Rosen

Greetings from AACR

Ongoing
Apr 9

Apr 9 Ongoing

Nat Rosen

Winning the long-term war

Diet
Apr 2

Apr 2 Diet

Nat Rosen

Tips and Tricks and Treats

Traveling
Mar 26

Mar 26 Traveling

Nat Rosen

Back on the road again

Stigma
Mar 19

Mar 19 Stigma

Nat Rosen

It's time we woke up

Oscar
Mar 12

Mar 12 Oscar

Nat Rosen

The Os-can-cer goes to . . .

Co . . .
Mar 5

Mar 5 Co . . .

Nat Rosen

Cold or Covid?

Couture
Feb 26

Feb 26 Couture

Nat Rosen

Hospital habiliments

QoL
Feb 19

Feb 19 QoL

Nat Rosen

Quality of life choices

Super Bowl
Feb 12

Feb 12 Super Bowl

Nat Rosen

My epic battle

Free
Feb 5

Feb 5 Free

Nat Rosen

My turn will come

Tricky
Jan 29

Jan 29 Tricky

Nat Rosen

The deceptive ways of cancer cells

Rebound
Jan 22

Jan 22 Rebound

Nat Rosen

Call me Mr. Anomaly

SKOL
Jan 15

Jan 15 SKOL

Nat Rosen

Some Keys of Life

Positive
Jan 8

Jan 8 Positive

Nat Rosen

Case # 101,006,703

Resolve . . .
Jan 1

Jan 1 Resolve . . .

Nat Rosen

. . . To do nothing

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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