Skip to main content

A Word to the Support System

For most of us, there comes a time in life where basic functions become celebrations.  Where abilities that were once take for granted are now mountains we must climb.  Where often modesty and personal dignity step aside in the face of necessity.

These inevitable moments may arise after a surgery, when the recovering patient can finally use the restroom on his own instead of in a bedpan held by a nurse.  A new mother finds sweet satisfaction in the ability to shave her own legs after months of not seeing her own feet.  The simple words "yes" and "no," uttered from a stroke patient's mouth, brings victorious tears to everyone in the room.

Whether it's relatively short-lived or stems from a long-term illness, these experiences force us to look at ourselves - and the people around us - differently.  Others often surprise us with their "true colors," as it were.  The gruffest person we know could become our most attentive friend.  Those we thought would stand by us may drift away.  And through all this, our self-image is largely shaped into one of two categories: humility, or humiliation.

In my experience, much of the shaping factors are not the level of disability undergone, but how the people around you react to the situation.  Now, I'm not discounting personal responsibility and the choice each of us has to view their circumstances in an ultimately healthy or unhealthy way.  Regardless of the people around you, it is still a difficult internal battle.  But the people surrounding a sick person can often make the difference in how hard that battle has to be.

So if you are part of someone's support system, listen up!

Needing help for the most basic of functions, or fighting your own body to accomplish those tasks, is a humbling thing.  There's no way around it.  No one can go through this alone.  But often the most important help a person can receive is not physical assistance, but emotional support.

Before you stop reading because you're convinced you're not qualified, it's not actually that hard.  As a disability systematically chips away at a person's self-respect, what they need most is some of that dignity restored.  

Respect that person's triumphs, no matter how trivial it seems to you.  It took them the same amount of effort as it would take you to train for a footrace.  Celebrate with them; don't patronize them.

Believe them when they say they're ill.  Just because you can't see it doesn't mean they aren't in a load of pain, fatigue, etc.  Genuinely appreciate the struggle of trying to appear normal - often times specifically for you.  They want to be the least difficult for you they can be.  Treat them like the normal person they are underneath the disability and don't begrudge them the special accommodations they can't do without.

Humility connotes gratitude. Those with disabilities are well aware of what they are giving up. They do not have the option of whether to accept help. To have some of that dignity given back to them after having done nothing to earn it is one of the best feelings in the world.  Humility becomes a place of peace, love, and acceptance.

On the other hand, humiliation is synonymous with shame.  It strips away any remaining dignity a person has until nothing but a charred hull remains.  It robs them of hope, of worth, of meaning.  It is a place of despair.

Treating someone like their disability is fake or exaggerated is one of the most humiliating responses possible.  In the name of "treating them like they are normal," the people that are supposed to build a person up often heap a greater burden of guilt upon them.  While struggling to rise to unrealistic expectations, they are left with intense frustration and self-loathing in the inevitable face of failure.  They think they are letting their friends down, concluding that their illness has rendered them worthless in the sight of their loved ones.

Refusing to acknowledge the accomplishments that you take for granted, or worse, mocking them, hurts.  Getting dressed or brushing your hair aren't even tasks worth mentioning to you, but to your friend, that is the most they can do before having to take a nap.  Embarrassment at accomplishing so little as compared with societal norms just encourages withdrawal, not motivation to find something more to life than pain.


If you have never experienced such a humbling situation, it is pointless to ask you to treat someone like you would want to be treated.  The truth is, unless you have experienced it, you don't know.  It is next to impossible to imagine a mindset in which your life is a war with your own body when you have never been drafted into combat.  Far be it from me to judge your ignorance from the other side of the fence.

However, if you have read this far, you are no longer unaware.  We, the ill/disabled, have no delusions that you will fully understand us.  We often don't even understand each other, as we all have different battles.  

We do ask to be respected.  Respect that you don't understand.  Respect our effort.  Respect our needs.  And respect the simplicity of it: we are all, chronically or acutely ill, disabilities or in perfect health, just...people.

Comments

Popular posts from this blog

What Brought Me Home

I found the floors in my house today!   No, I'm not remodeling the floors.  We just cleaned up and vacuumed.  It's funny how much an afternoon of cleaning can affect you.  I began the afternoon completely anxious, upset, and honestly...mean.  Very mean.  I was overwhelmed and felt like throwing a temper tantrum on the floor - which would have been impressive since this was before I found it. But I don't wanna clean the house!! As I started cleaning, the transformation was marvelous.  As the house transformed, so did my mood.  I went from tantrum to dancing. Many people comment on the fact that a messy house makes them feel depressed, in a bad mood, etc.  However, I think it was something else that made my heart so light - or rather, some one .  So I would like to express my public thanks to... My Husband There are so many things I could say about my husband.  I love bragging on him.  He deserves so much mor...

Twenty-Five & Fabulous!

I am one quarter of a century old as of two days ago!  Spunk and sass have been my ever-present companions these past few days, and I am loving it!  Because you know what?  Sarah Brinson is a fabulous person! This may age me more than any birthday announcement could. Do kids still watch HSM these days? Sure, I'm still insecure.  Who isn't?  I'm an American woman who has access to the media.  I have no choice!  On a more serious note, I am fully aware of my sinfulness and selfishness, as well as my ignorance in many areas.   But I am saved by grace, so I may not deserve to be spunky, but Jesus says I can anyway because He already took care of my penance.  I mean, come on!  How awesome is that?!?!?  Jesus, Savior of the world , says that I am fabulous in Him,  I don't have to look like Sharpay, and I don't have to be perfect on the inside either.  He gives me His own heart so my sassy personality can be shown off to...

Enjoying Life After 23

I'd like to say that I finally found my writing materials that had been lost in the moving boxes, and that is why I am finally returning after my eight-and-a-half-month hiatus.  But in this age of technology and internet clouds, that can no longer be my excuse.  Food for thought in the examination of today's generation, but I digress. When I first started my short run at this blog last year, it was because I had never dared to plan or dream past age 23, and therefore had the feeling that, in a way, my life was over.  At least, my life as I had always imagined it was over.  I had just found out that bearing children - if that was even an option anymore - was unlikely without fertility treatments.  The only dream/goal I had allowed myself after age 23 was suddenly ripped out from under me and dangled somewhere ahead in the dark mist of the future, taunting me with the possibility that, even then, it was only a mirage. At the beginning of this blog, I ha...