Great Article on Accessible RVing

https://wheelchairtravel.org/resources/wheelchair-accessible-rv-motorhomes/

Mile 6

CRPL
Clandestine Racing Powerchair League

I’m going to break the first rule of CRPL, and talk about it. What is CRPL? Illegal nighttime powerchair racing; that’s what it is! It’s sweeping the nation, in a whisper– you just don’t know cuz we don’t talk about it, just saying.

I had the distinct pleasure of taking on the trash talkin, I mean the incomparable Maceo (Comon) Carter! Meg and I also had the pleasure of meeting his beautiful family, wife Maya and their three boys. Before I reveal the winner of the CRPL throw down (me), I want to share our visit with them.

Again, Meg and I had planned on meeting them our first trip, but alas we were overcome by events. Not this time!

We were greeted by Maya with their youngest in her arms. After the initial pleasantries we chatted about? I’ll give you a few guesses. The wheelchair race? No. Kids? No. ALS? Bingo! Makes sense, right!

We shared the extreme challenges of caring for someone with ALS and maintaining the household. While also navigating the constant loss ALS generates. Compounding the challenges for their family is the fact they left family to pursue a more responsive clinical support network. COVID has only added to the feeling of isolation for the entire family. Maceo shared candidly that he is simply tired of the relentless and insatiable appetite of ALS; “just fucking tired”. The remainder of our conversation is, well, between two wheelchairs.

Now as for the powerchair race, watch the video!

J Reyes

3 responses to “Mile 6”

  1. Awesome as always 😊🤣🤣❤️

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  2. So just for curiosity sake is the conversation basically the same at each stop? All about ALS or are any of the visits just about sports and family and stuff? I know that ALS is what we all have in common but just curious. And when it does turn to ALS is their anything you guys have learned that can be shared with us all?

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    1. Actually the conversations are usually about life in general, work, kids, travel and so much more. I try and let our visits flow organically based on the individual and their family. I want to know who they are not their ALS. But you bring up a good point about sharing tips, I’m going to add a section to the website for that! Thank you

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