Make Room For The Stuttering

The Stuttering ID Card

Posted on: April 11, 2016

Stuttering CardUp to this point, I’ve been quiet about the Stuttering ID Card that has been created by the Stuttering Foundation for people who stutter to carry in their wallet. This card was created in response to an incident that occurred at an airport where a person who stutters claims to have been detained because of her stuttering.

When I first heard about it, I did chime in on Twitter to say there is going to be hundreds of people who stutter coming through the airport in July for the annual conference of the National Stuttering Association. But I’ve been quiet since, as there has been no word from the airport about what happened and there is always two sides to a story.

The young woman has garnered a lot of attention in the stuttering community. She has written articles for the Huffington Post and was also featured in The Mighty.

Recently, I saw that the American Speech-Language-Hearing Association wrote about the ID card on their blog, The ASHA Leader.

So, now, two prominent organizations have advocated that people who stutter carry this card when going through customs at airports, to help explain that they stutter.

I wouldn’t feel comfortable carrying this card. I don’t need a piece of paper to state that I stutter. I can tell people that myself, if it becomes necessary. Sometimes, it’s very obvious that I stutter, sometimes not so obvious. There are times when I feel comfortable advertising that I stutter and times where I am not.

I’m curious. How do you feel about this? Would you carry this card with you when traveling?

 

1 Response to "The Stuttering ID Card"

When I first heard about the card, I wasn’t for it. I have to admit though, I almost downloaded one for when I travel to the conference because my stuttering has greatly increased. After giving it some thought though, I decided I didn’t need the card. I can tell people I stutter. I have flown many times and it has never been a problem. However, I am downloading one for my Tourettes since that is more of an issue.

Leave a Reply

Fill in your details below or click an icon to log in:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out /  Change )

Facebook photo

You are commenting using your Facebook account. Log Out /  Change )

Connecting to %s

Podcasts, Posts, Videos

Glad you're stopping by!

  • 713,317 visits

Monthly Archives!

Copyright Notice

© Pamela A Mertz and Make Room For The Stuttering, 2009 - 2022. Unauthorized use and/or duplication of this material without express and written permission from this blog’s author and/or owner is strictly prohibited. Excerpts and links may be used, provided that full and clear credit is given to Pamela A Mertz and Make Room For The Stuttering with appropriate and specific direction to the original content. Same protection applies to the podcasts linked to this blog, "Women Who Stutter: Our Stories" and "He Stutters: She Asks Him." Please give credit to owner/author Pamela A Mertz 2022.
Follow Make Room For The Stuttering on WordPress.com
%d bloggers like this: