Welcome to the CAPOS blog. you are awesome! Thank you for taking five, ten minutes reading my blogs! I appreciate YOU!

CAPOS is a unique syndrome with five equally complex symptoms: CLICK HERE to find out more


Made my first buck!

Hey folks!

That is right!  I made my first buck!  Took me 2 years, but I made a cool dollar!

I won’t see that buck, or any other bucks I may earn, until 2119!  I’ll be 151!  Yikes!

WordPress won’t payout any funds until it reaches $100!  I got a long way to go!  $99 dollars on my blog, put more up, pass it around, monetize my blogs!  Before blogging becomes a thing of the past!

Are libraries still as popular a dive as they once were?

Catch ya later!

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From the blog

About the author

Craig MacLean is DeafBlind with ataxia, a rare condition called CAPOS. He & his wife of 22 years have two sons, the oldest of which has CAPOS as well.

Craig uses American Sign Language to communicate. He is an avid writer, friend, Hot Wheel collector and intervenor advocate.

Craig sits on many committees, boards and associations as a DeafBlind rep. He graduated university with a BA in psychology in 2000.