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


I’m back!

Hi there!

It is mid February and I haven’t posted a lot…

There are a few reasons for that:

I got some new hardware for my iPad, including a new keyboard, and stand,

Then, the iPad itself had a crack, then many cracks, then spider webs of cracks appears!

I had to order a replacement.

When that arrived, a piece of the charging cord, a tiny minuscule bit, broke off inside the charging port, and I couldn’t charge it.

So, I took it back to Apple Store, five minutes later, the Genius guy, named Fang BTW, used tweezers to get the tiny piece of shit out!

Now, the iPad is fixed and I can go forth and blog!

I am also waiting for a “table” to put the iPad on, so that it is higher and closer to me. So that I am not scrunched over like a wilting flower!

All these improvements will make blogging for accessible, comfortable and worthwhile!

Once I have everything together, I’ll take some photos and share!

Thank you for reading!

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.