Writings about Ataxia, being DeafBlind, family life. The best life can offer!


School…

Hello readers.
After a long and adventurous summer, boy was it profitable! Amen!
My sons have joined the phalnax of freshly laundered (or at least deodorized) kids, teens and young adults on their pursuit, willingly or not, of cranium enhancements!
My wife also returns to gainful employment, two months downtime is all done!
The First Day of school also prompts me, the ataxian who can’t work, to kickoff, for the 83rd time, my writing and blogging career.
I vow to you all that, by the end of this year, I will have a finished manuscript, and I’ll be blogging every day. I’ve got a new office too!
No more TicTok until noon, poker until 2, Candy Crush til dinner, then kaput…
Please join me in welcoming our younglings back to school, our academic staff back to work, our police officers who are handing out tickets to forgetful drivers.
Let’s have a great year!

Leave a comment

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.