Stepping onto the ALS Rating Scale

Stepping onto the ALS Rating Scale
4.6
(52)

Oh, how I wish living with ALS weren’t so murky: We don’t know its cause, we don’t have a cure, and we measure symptom progression by way of 12 questions. I can’t do anything about the cause or cure, but I’m up on my soapbox (the one with the handicap rails, mind you) to voice my opinion about those darn questions.

For 20 years, a simple test has been used worldwide. The questions on the ALS Functional Rating Scale-Revised (ALSFRS-R) also are used in studies and clinical trials of potential treatments.

What is the problem?

My chief complaint is that the test is subjective and requires little demonstration of function or skills. With a possible high score of 48 points, ALS patients are predicted to lose one point per month over the course of their disease. Based on those expectations, my 120 months of living with ALS should put me in negative numbers!

I’ve decided the ALSFRS-R needs a few enhancements, which I’m happy to share with you.

Let’s add a degree-of-difficulty rating

As a newly diagnosed patient, my neurologist surprised me by asking about my handwriting, whether I could use a fork and knife, and whether I used the handrail when climbing stairs. But what about other skills?

When I was coaching and competing in gymnastics, certain skills were awarded extra points for degree of difficulty. We had the simple cartwheel, but being able to do it balanced on one hand was credited as slightly more difficult. And performing it in midair without the use of either hand earned the highest rating.

Let’s translate this system to ALS.

Handwriting? Using a fork and knife? How about extra credit for additional skills? I can still knit a colorful scarf and — when I have to — thread a needle and sew on a button.

Use the handrail when climbing stairs? That’s easy! How about awarding extra credit for ninja heroics when navigating badly placed grab bars in public restrooms?

How about points for risk, originality, and virtuosity when figuring out how to enter businesses or friends’ homes that are not easily accessible? Using back doors, loading ramps, and lifting and shoving a rollator over a brick walkway? I’ve done them all. And from the comments on my columns, most of my readers have, too.

Humor helps

You’ve probably figured out that I’m looking at the ALSFRS-R through a humorous lens. Having a sense of humor is something we need when facing the challenges of living with ALS.

And maybe in this murky world of ALS, my new scoring system has potential. Especially to measure our ability to successfully learn new ways to function. Let’s continue to learn, laugh, and live well while living with ALS.

***

Note: ALS News Today is strictly a news and information website about the disease. It does not provide medical advice, diagnosis, or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website. The opinions expressed in this column are not those of ALS News Today or its parent company, BioNews Services, and are intended to spark discussion about issues pertaining to ALS.

When Dagmar was diagnosed with ALS at the age of 59 in 2010, she tapped into her nearly 30 years of professional experience. She not only follows her own wellness and fitness advice but also inspires and teaches others to do the same. Dagmar is a patient columnist at BioNews, writing “Living Well with ALS.” In addition, she is one of the moderators for the ALS News Today Forum and writes a personal blog called “ALS and Wellness.” She lives in Arizona, enjoying finding humor in life’s situations, and spends her free time pursuing creative projects in fiber arts.
×
When Dagmar was diagnosed with ALS at the age of 59 in 2010, she tapped into her nearly 30 years of professional experience. She not only follows her own wellness and fitness advice but also inspires and teaches others to do the same. Dagmar is a patient columnist at BioNews, writing “Living Well with ALS.” In addition, she is one of the moderators for the ALS News Today Forum and writes a personal blog called “ALS and Wellness.” She lives in Arizona, enjoying finding humor in life’s situations, and spends her free time pursuing creative projects in fiber arts.

How useful was this post?

Click on a star to rate it!

Average rating 4.6 / 5. Vote count: 52

No votes so far! Be the first to rate this post.

As you found this post useful...

Follow us on social media!

We are sorry that this post was not useful for you!

Let us improve this post!

Tell us how we can improve this post?

4 comments

  1. Rosemary Kutschke says:

    Right on Dagmar! I have to think outside the box since my mobility and dexterity have been waning. It’s good for your brain too! So, even if it looks strange to someone, if it works for you Rock On! You are a an inspiration! The BEST ada Catholic Church is in Green Valley..St. Mary’s ! Added bonus is excellent family support close by!

  2. Mike says:

    Thank you for sharing!
    Hearing your stories, your positive outlook, trying to help others, we need more of that.

  3. Cate says:

    How about style and creativity points? Like the ability to open a jar by putting it under my arm and tipping it sideways? Or opening a zipper bag by holding one corner in my teeth? Using my rollator seat as a tea cart? I won’t share how I manage to put on a bra–but it’s creative! As always, Dagmar, you have me smiling and looking on the bright side.

Leave a Comment

Your email address will not be published. Required fields are marked *

Pin It on Pinterest

Share This