iPhone app iPad app Android phone app Android tablet app More

Featuring fresh takes and real-time analysis from HuffPost's signature lineup of contributors
Lisa Copen

GET UPDATES FROM Lisa Copen
 

8 Ways to Annoy a Friend With a Chronic Illness

Posted: 09/10/2012 12:08 pm

Roughly half of the U.S. population lives with at least one chronic condition, such as diabetes, lupus, multiple sclerosis, chronic back pain, migraines, and others. So one would assume that most people know basic etiquette skills when it comes to what to say to one who is chronically ill.

For instance, we all know that you shouldn't kick the tire of a wheelchair someone is sitting in, so why is it okay to tell someone with an invisible illness, "You don't look sick to me."

Here are some ways to quickly annoy an ill friend, and possibly even destroy the relationship.

1.) Remark on her treatment. "I'd be sick too, if..."

"If I saw all those doctors ... sat around waiting rooms ... never had to get out of bed ... took all those medications..." "If I was as sick as you say you are I would be trying acupuncture, supplements, something natural." "Those doctors know how to cure you but they wouldn't make any money then."

2.) Tell her she needs to fight the disease.

When she makes a wise choice about her limitations and pacing herself, she doesn't need your motivational speech. For example, if she cancels plans on you, don't fire back with, "You are letting the disease win! You have to fight it. You have to want to be well! Be strong!"

3.) Get excited to go somewhere because you can use her disabled parking permit.

None of us wants these placards, and we use them on only the most painful days. If you are driving, we may ask you to drop us off and then park the car, so the spot can be saved for someone else who needs it. Don't insist to use it, jump out of the car, and smile haughtily at a passerby, and then brag to friends, "Guess where we got to park?"

4.) Say, "You are so lucky because..."

"You are so lucky because you don't have to work... You don't have kids. You are so lucky you don't have to travel." Or here is a common one, "You are so lucky to be diagnosed with this at such a young age." Um... okay.

5.) Tell her that her illness is caused by stress.

"You need to slow down, you need to cope better, you are under too much stress." Basically it sounds like you are saying, "Most people -- including myself -- can cope with stress fine, but you do so poorly at it, you've brought this disease on yourself."

6.) Call attention to her assistive devices.

"You don't really need that cane. I think you are relying on it too much." "Once you start to use a wheelchair, you will forget how to walk." "I am not going to push you, so if you want to ride you will need to just learn to drive a scooter." Her appearance is also up for grabs if you don't value the friendship. "I would just die if I had to wear those shoes. I love my heels too much." "Maybe if you put a little effort into your appearance you'd feel so much better."

7.) Tell her about the cure you heard about.

Trust me, she has already heard about it -- the water, the juice, the chocolate, the supplements, and yes, even the reindeer antlers and mushroom tea. You may feel the need to share what you have heard, but she will likely tune you out as "one of those people," especially if you tell her you are a distributor.

8.) Ask her how she is and then try to one-up her story.

"Oh, you don't know pain until you have had run a marathon." "You think you're tired? Try being a single mom, while working." "Oh, that is nothing! You won't believe what happened when my neighbor's brother's son had surgery!"

Watch your words. When you go to another country the culture and language is different. Words that you say at home may be considered impolite or even obscene. People have had different experiences and so they interpret your words differently. So it is in the world of the the ill.

When you tell a workout buddy, "Hey, don't give in. No pain, no gain, right?" they interpret it much differently than one who lives with a chronic illness.

Talk to your friend. Say, "I have realized there are times when I have said the wrong thing. Can you tell me some things that encourage you -- and what irritates you? I don't want to be one of those friends you would rather avoid."

It sounds corny, I know. A bit like an assignment a counselor would give you. But we all want to be acknowledged, validated, and understood. If you ask this, your friend may still fall over, but it will be out of her surprise, not because you insisted she leave her cane in the car.

Lisa Copen is the founder of Invisible Illness Awareness Week, celebrating their 10th year September 10-16, 2012. Join her at http://invisibleillnessweek.com for the 5-day free virtual conference and download a free 80-page ebook, "263 Tips To Do More Than Just Get By."

For more by Lisa Copen, click here.

For more on chronic conditions, click here.

 

Follow Lisa Copen on Twitter: www.twitter.com/lisajcopen

FOLLOW HEALTHY LIVING
 
 
  • Comments
  • 26
  • Pending Comments
  • 0
  • View FAQ
Comments are closed for this entry
View All
Favorites
Recency  | 
Popularity
photo
SandwichINK
Christian baby boomer in the Sandwich Generation
07:23 PM on 09/15/2012
Great tips on such an important subject. Whether it's an aging parent, a young grandchild, or a dear friend who is ill, they need our support and encouragement and support of their current treatment and doctor's advice. Thanks for another great resource, Lisa.
10:10 PM on 09/13/2012
Lisa, I've loved your attitude and activism since way back in the day. I think I've been with you through over at least three (maybe 4?) different social platforms, have received great advice to you, suggested some other options, reviewed your cookbook way back when I blogged, have never taken off my white "Invisible Illnesses; Visible Hope" rubber bracelet since I first got it, like 5 years ago maybe? And yes, to this day, I have people asking me what it means, which is a great way to get some I.I. activism into a conversation! I've introduced a lot more people to I I W again this week/year via fb and Twitter. I still think you are a super-woman! Go girl!

~Debby Polis Carter
+Fibromyalgia, stroke, Myofascial Pain Disorder, osteoarthritis, more herniated discs than one person should have, spinal stenosis; migraines, "pre-cancerous" lumps in my left breast; hiatal hernia, allergies to most everything that grows in Florida, cystic ovaries (which I'm hoping is over since I'm now post-menopausal-yay!), aphasia from my stroke and a rare blood clotting disorder to round up the pack! I think a lot of your writings reminded me we have the power to speak up as it is OUR body, to remember to keep humor in situations and to not give up, but to remember to keep everything in moderation. We adore you!!+
photo
HUFFPOST BLOGGER
Lisa Copen
06:19 PM on 09/15/2012
wow! what more could I ask for? thank you!! I so appreciate your support to me, personally, but also helping spread the word for all of those who suffer silently. And thanks for commenting on the article. All the comments help encourage other people more than the articles sometimes. Appreciate you! and so glad to hear of the bracelet!
photo
ellarceehill
carpe diem
06:46 PM on 09/13/2012
Sadly, others words, too often, are abusive to those of us who suffer. Freinds no longer become friends. And it becomes a choice sorely taken when discovering that we simply cannot continue abusive relationships, because it's too overwhelming when dealing with chronic health issues.

Oftentimes, we isolate. While trying to have an open heart and an open mind, it becomes futile to really have another (who does not suffer from any multitude of illnesses) understand. And that we are not trying to pull them down.We are just trying to function within our own means.

I suffer from multi-health disabilities that are chronic and would not wish this on anyone.

Thank you for this post, I wish more would take the time to read your words.
photo
HUFFPOST BLOGGER
Lisa Copen
06:24 PM on 09/15/2012
thanks for writing Ella. I know it can be so hard when people ARE abusive--words do hurt! You may enjoy the 2 workshops at Invisible Illness Awareness Week (google it) by Georgia and Leslie. Both talk about friendships- the good, the bad, how to cope, when to let go. Some excellent advice that i hope encourages you. Bless you. Keep taking one day at a time.
photo
ellarceehill
carpe diem
09:37 PM on 09/15/2012
Lisa, this is very enlightenting to even have discovered I not alone. Verbose controling remarks from others (without physical multiple maladies) can be toxic to our mind/body healing process. Particularly when we are on a path of serenity for that moment.

I've worked diligently to reach a point of serenity with myself and functioning within my daily routine and some small projects. Yet I've heard others may say, "You only work hard at sitting on your bed all day while I'm at work sweating it out on hard labor." At that point, I can only commend them on their own abilites to perform physical labor, step away, not pass judgement on others, and go about my journey.
Thank you for the good advice and kind words.
03:21 PM on 09/13/2012
I was once told "You aren't really sick. You are just putting on a good act to get attention." That was when I was "only" dealing with chronic pelvic pain from adhesions (scar tissue) tying my intestinal tract up in knots. Since then I have been diagnosed with fibromyalgia and several other auto-immune system disorders. Now I am again traveling the diagnostic treadmill to find the cause of soft tissue pain in both legs from the hip to the ankle. I wonder if that means I am now a better actress than I was 10 years ago. If so, then I should be auditioning for a film career. It would have to pay better than what I am getting now, since I have been unable to work for 12 years.
photo
HUFFPOST BLOGGER
Lisa Copen
06:25 PM on 09/15/2012
it sounds like through it all you have kept a sense of humor and that is vital! we've jokingly said we should dress up like how we FEEL for halloween, but that could be really scary!
10:29 PM on 09/15/2012
My bad days are those when "the only way I could hurt worse is if I were twins." Without my sense of humor I would go down that "dark road" of depression, and then the battle REALLY begins.
11:02 AM on 09/13/2012
As a person living with an invisible (and often unrecognized) illness, Lyme Disease, I can relate to many things in this article. Thank you for spreading the word and thanks to Lisa for communicating what so many of us want the world to know.
photo
HUFFPOST BLOGGER
Lisa Copen
06:26 PM on 09/15/2012
thanks, MamaRich. I know when you don't feel well just commenting is an extra step! Appreciate you taking your time and energy to let me know it touched you.
10:56 AM on 09/13/2012
Great article, Lisa. Thanks for all you do to raise awareness.
01:18 AM on 09/13/2012
Oh, the number of people who know nothing about lupus, but know how I should handle having it!
03:06 PM on 09/12/2012
Amen Lisa!! Especially #5 and #7...unfortunately, these are all too common. Thanks for helping to spread the awareness!
(from a young sufferer of spinal arthritis)
photo
ellarceehill
carpe diem
06:09 PM on 09/13/2012
So, so agree, with you on #5 & #7. Was told my anxiety is my pain . Then the sea salt cure for sweating due to severe colitis/infection which necrotised part of my colon. That I can just walk (with severe degenerative bone disease/O/A & R/A of the spine) . Or drink their special water, or take their special vitamins.Or put up and shut up.
Glad there's a place to go to where I don't have to listen to their cures for something they know nothing about.
Thank you for the article, and for others posting.It actually makes me feel not so alone.
photo
HUFFPOST BLOGGER
Lisa Copen
06:53 PM on 09/15/2012
seems like #5 and #7 have hit a lot of nerves. I've heard those two probably more often than all the rest, so I understand. "If you would just..." or "I probably shouldn't say anything but I think..." is how many people start their sentences when giving advice. It's so cliche it is becoming easier to laugh about over time.
01:55 PM on 09/12/2012
GO Lisa! I can't tell you how often I've heard most of these (or how many of the people who have said them no longer get to spend time with me . . . LOL)
01:41 PM on 09/12/2012
Thank you, thank you, thank you for this article!!! From a person living with lupus, lupus nephrits, fibromyalgia, and a host of other secondary conditions, I applaud you!!! I have been on disability for 12 years and was unable to have children due to chemotherapy for lupus. My life was forever changed because of it. Luckily, I still look pretty good despite my body being at war with itself. My pet peeve is when I tell people I have lupus, usually the first thing out of their mouths is: either "What is lupus?'' or "but, you don't look sick!" If I told these same people I had cancer, I am sure their reaction would be quite different. People living with invisible chronic illness don't wat pity but we do need a little understanding and support now and then! We may not look sick, but we are and we have had to learn to live the best life we can in spite of our illnesses.
photo
HUFFPOST SUPER USER
Alexandra Lawson
The cake is a lie.
04:24 AM on 09/13/2012
I can totally relate. I have fibro and I hate hate HATE getting, "But you don't *look* sick!" It drives me MAD.
photo
ellarceehill
carpe diem
06:15 PM on 09/13/2012
Totally agree, and identify with being misunderstood because I'm disabled . fanned/fav.
01:15 PM on 09/12/2012
As a person with several chronic conditions, I really take offense at those who are healthy acting as if it is some moral failing on my part causing my health issues. I have a very positive attitude, but some days comments like these cause me to just throw my hands up and want to give up.
photo
HUFFPOST BLOGGER
Lisa Copen
01:21 PM on 09/13/2012
yes, I think this is one of the hardest parts of illness. people really do believe that they have lived "perfectly healthy" lives --and even if they have not--they have obviously done better than you. This is, of course, completely ridiculous--I had barely ever taken more than a tylenol before I was diagnosed with rheumatoid arthritis at age 24, but it helps healthy people believe they do have some control over their life. Sadly, someday their world will be shaken--most people do live longer now, but we have many more chronic health conditions in those later years.
11:24 PM on 09/13/2012
Do medical schools and/or nursing schools teach the right attitudes for their patients? Has any study been done on the public?
04:12 AM on 09/11/2012
Thank you for this. Sadly, it probably won't help since it's one of those things that unless you have gone through it... you just have no idea. But I hope it does help.
photo
HUFFPOST BLOGGER
Lisa Copen
12:39 PM on 09/12/2012
Yes, I know it can be discouraging! Few will actually change the habits they grew up understanding, but it is nice, if you are the one who is ill, to be able to email and article like this to a close friend or family member. It makes it a little less of an "attack" of "YOU hurt my feelings!" into, "hmmm, just thought you would see how this explains how I feel." Warmly, Lisa
01:28 PM on 09/10/2012
Unfortunately, people don't know how to respond when someone is diagnosed with a chronic and/or life threatening injury or illness. Several friends asked me to provide some help in this area, which resulted in the post How to Respond When Someone is Ill or Injured http://healingwhole.blogspot.com/2011/07/how-to-respond-when-you-learn-that.html It is one of the most downloaded posts on my blog for those affected by chronic conditions "Healing Whole."