z35W7z4v9z8w I Won’t Apologize for Having Fun While Chronically Ill - Cannabis Connection

I Won’t Apologize for Having Fun While Chronically Ill










When I was six, I was hospitalized with Rocky Mountain spotted fever. At the hospital, I was encouraged to get out of bed, get dressed and spend as much time as possible in the playroom. I brought magazines and books back to my room to read and played with other kids who were up and about on the pediatric floor. There was a girl in the next room with leukemia, and we made faces and waved to each other through our shared window. The fact that I was able to play didn’t mean I wasn’t sick enough to be hospitalized. It meant that regardless of my illness, I was a child with the same needs and wants as other children.





Yet, with adults, the same concept doesn’t seem to hold true. Whenever ill people do — well, anything — it’s taken as “proof” that we’re bluffing about our condition. Many of us are confronted by complete strangers on a regular basis when we go out in public, on everything from using parking placards to requesting ADA accommodation at events. We’re challenged more by people we know, who should really know better.

After I became ill, I decided to go to my favorite theme park one day. I didn’t do much; it was a very sedentary experience. I posted a photo of myself on one of the rides on Facebook with my germ mask on backward, slept for days to recover from my adventure, and didn’t think much of it. A few days later, my Mom called me about it. A “family friend” had seen the photo and was furious about it. She’d apparently complained to several people that if I was at a theme park, I was obviously well enough to be working and was pulling some sort of scam. It had gotten back to my mother.

I promptly unfriended and blocked the person, but their actions stayed with me. For most of the next year or so, whenever I posted a photo of myself doing anything fun, I looked over my shoulder. I always made a point of describing how sick I was and how I’d needed to rest, and how tired I was afterward. I felt the need to qualify what I was doing; to verify that I was still ill, and to remind everyone that there was more to the truth than what was visible in the photo. Someone’s ignorance and unkind judgments had made me feel guilty about enjoying my life to the best of my ability and upset my mom, and that was unconscionable.


It often seems that there’s no real way for chronically ill people to win this battle. Hostile individuals who don’t want to believe that you’re really ill will find fault with anything you do. There’s no way to appease them, regardless of how you live your life.






Some chronically ill people are able to exercise, some are not. Some of us are encouraged to be physically active in some way to help us maintain function (I have a series of physical therapy exercises to do every day to help with some specific orthopedic issues, for instance). Yet, if you’re seen being physically active in any way, it’s taken as a sign that you’re not sick after all. Society likes to applaud those Olympic athletes who fight through their illness or disability to compete. If you fight through your illness or disability to do something physical sometimes, such as a 5K or dance performance, it may be seen as proof that you’re a fraud.

It’s widely accepted that having a strong, supportive network of friends and family is helpful to those who have chronic illness. We’re told that for our own well-being, we should get out of the house once in a while. However, if we dare to go out in public with friends or do something fun occasionally, again, some will believe we’re not sick. And if we spend one afternoon at the movies now and again, it somehow equates to being able to spend 40 hours a week, 50 weeks a year, at work.

If you live alone or don’t have a lot of support, you still have to take care of daily tasks, but something as simple as buying your own groceries might actually be seen as proof you’re able-bodied.
If you are too exhausted or hurting too much to shower, do your hair or dress up you’ve let yourself go; if you go out with makeup and styled hair, well, you’re obviously not sick because you don’t look sick.

If you post photos on social media where you’re looking well people will think you’re not ill; if you post photos of yourself undergoing treatment, you’ll be accused of being an attention seeker.

If you tell someone about the progressive course of your illness, you’re faking it because your Aunt Edna’s son’s niece had the same condition and she’s fine now.

Social media photos and observations of chronically ill people smiling and looking “normal” or doing errands have even been used to deny or remove disability benefits, which is quite possibly the most troubling thing of all. It’s hard to understand that disability determination specialists, doctors and government benefits administrators — people who supposedly are knowledgeable about a wide range of health conditions — don’t accept the concepts of good days, payback and invisible illnesses that do not always have linear trajectories.

Nobody ever seems to consider what’s happening outside and around that Facebook photo they’re snarking about. The fact that it might have been the first time in weeks that chronically ill patient got to do something really fun eludes them. They don’t realize how much those activities cost in terms of pain, fatigue and reduced function. They look at one photo or one Facebook status about one day and think they’re an expert on your life.







I’m not sure what these people think we’re supposed to do every day. We have incurable chronic illnesses. We often spend most of our time either at home or in treatment as it is. We’re often exhausted and in a lot of pain. If we’re not able to work full time, are we supposed to forgo any and all moments of joy, distraction, social interaction or enjoyment? Will that help us in any way? Being sick is extremely hard for many of us. It’s even harder when hurtful, judgmental types decide that illness should invalidate the fact that we have the same needs as anyone else. Instead of telling chronically ill individuals to shake off comments and accusations, maybe the onus should be on these hecklers to refrain from making them and mind their business. Is it really that hard to leave other people alone?



Eleanor Roosevelt once said: “Do what you feel in your heart to be right — for you’ll be criticized anyway.” I’ve taken those words to heart when it comes to interacting with others about my chronic illness. I am no longer particularly nice when I’m confronted by impromptu judges. Every once in a while someone honestly doesn’t understand, and politely and succinctly explaining a few things helps them. More often, though, they’ve already come to their own conclusions and nothing I say is going to put a dent in their hostility. I won’t waste my time trying to justify myself to random strangers and mean-spirited acquaintances who have appointed themselves judge and jury of my life.

I can’t stop others from thinking whatever they want about me. However, I can and do refuse to comply when someone demands apologies, guilt or justifications from me for getting out of the house once in a while. Anyone who decides that chronic illness somehow invalidates my needs as a person — including my needs for happiness and socialization — isn’t getting an iota of my concern.
I Won’t Apologize for Having Fun While Chronically Ill I Won’t Apologize for Having Fun While Chronically Ill Reviewed by Admin on 07:48:00 Rating: 5

20 comments:

  1. I could not agree more. I have Arnold Chiari Malformation and P.O.T.S. and can not work. And I have a handicap placard. The looks I get from people because you can't see my illness. I just want to smack them.

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  2. I have AIP; Acute Intermittent Porphyria. It's genetic and rare. I also have Complex PTSD due to multiple rapes and a badly damaged thigh from the last encounter. I limp badly and the pain is constant.
    I work 3 days a week, 10 hrs a day, sleep for a full day to recover then slowly get my home chores done so I can do it again. My pain usually starts to recede on my last day off. On that day, I try to do something fun. Go to a gallery or museum - where oeople whisper loudly how I wouldn't be panting if I took better care if myself.
    If a sharp noise makes me jump, I'm told to get over it. If I don't get startled, well the attack wasn't that bad or didn't actually happen or I'd be worse right?
    An AIP attack can hit anytime. If the timing is inconvenient, then I'm faking it to get out of something.

    I'm fortunate in that I have a good support system and a boss who understands. Still, those who judge really need a month in these shoes. Then let's see if they're brave enough to spend a life here.

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    1. You are a rock star!!

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  3. well written but i have to ask what morgan freeman has to do with your post? he didnt write it. his pic shouldnt be used to draw readers

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  4. I, too, am wondering why Morgan Freeman's photos are in this article.

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    1. Yeah, it made me think I was reading about Morgan's childhood illness.

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  5. His photo is there because he has an "invisible" chronic illness, fibromyalgia. It should have been mentioned in the article to explain why his photos were used but they must have assumed everyone knew the connection.

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  6. Like me he has fibro, they prob used his face cos hes well know for having this condition. it sucks.

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  7. Well said. Shared and explained. Horrible when you don't feel like you can enjoy little snippets of what you used to do without feeling guilty. The conditions are bad enough to deal with. Totally emphathose and hear you. So glad you wrote this x

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  8. Very well put,I have a extremely hard job but I need to eat make my car payments put a roof over my head and so on,but when I push myself through my day with that fake smile,that's why people don't believe,but they are not with me on day's I cry in my car on the way home,working during peak at UPS just drains me,FMLA is what has helped me keep my job,and I'm lucky enough to have a great pain management doctor,bad back also I hope I live long enough to retire,so I can grow my own mary jane and have a good day every day!

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  9. Fibromyalgia is REAL and it's PAINFUL ALL DAY EVERY DAY. Yes, you get up and put one foot in front of the other and get on with your day. You don't sleep , you hurt all over but you keep moving. It's not fun to live with for sure and we do the best we can with what we have.

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  10. Don't judge what you can't see or feel...
    PERIOD

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  11. I have Fibromyalgia and serves on the PWD committee at work to make our work place more accessible to all PWD. During one of our meetings I mentioned that the resistance settings on the automatic doors are set too high which causes me severe, acute pain since it feels like my shoulder is being ripped from its joint when I have to pull on the door to open it. Would you believe that the COO of our company responded with the nasty comment that maybe I should rather gym regularly, then I'd be strong enough to open the doors and I'll loose some weight too, which wouldn't be a bad thing either. I was having a hard time that day and the guard in front of my mouth was on strike, so I responded that maybe I should rather rip his heart out through his ribcage just to prove how strong I really am. I can tell you, that didn't win me any friends and I decided I didn’t really care either way.

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  12. These words are so wise and on point. Millions of us live with a disease that can bring out horrors that no one can see, but because we look normal they can't understand.

    The face of an invisible and chronic illness is a cruel one.

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  13. So much this. :D And my conditions don't stop me for one second either.... and I don't care what anyone thinks. I've wasted enough of my life doing that.

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  14. Story of my life. So when I finally say I don't feel well it's like just having a splinter. It's not like I stayed awake all night because my hips and back were too painful or charley horses in a number of muscles or my blood sugar is plummeting for no reason. My family has had to literally revive me because my blood sugar was in the 30's. I had to work until hospitalized, when my husband left me with 4 children. My bro. And sis. sued me when my parents died so lost my home and belongings. Fighting Dr.s over treatment options I need! Taught the physical therapist because I could not do certain excersises because of muscles and COPD. NOT from smoking! Had to fight to be able to still take only half my pain meds. Sometimes I just must collapse. I'm 60 but feel like 80. I look like I'm 50. That's a problem too. You don't want people to feel sorry. You want them to help just to be kind! Yes. This is cruel.

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  15. Brenda kline burger23 December 2016 at 07:22

    I represent all of us with Behcets Disease and/or Gastroparesis or other auto immune diseases which have challenged our lives in many ways. THANK you Morgan for posting this, it helps all of us striving for just one normal day. Bless you.

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  16. Like alo if us, I too suffer from an invisible illness, CRPS. Unlike many I am lucky to live in Australia where we all have access to medical treatment at no or little cost.
    As traumatised as I was from the accident which left me 5 years in a wheelchair, unable to walk, I was determined to be independent. I modified the car, I took myself into town to shop, have my hair and nails done etc.
    My pain on a daily basis is so bad that I often wake up crying after reliving the crash in my dreams, angry at that the truck driver who hit my car for not killing me. Yet on the outside, I make sure that I look as healthy and able as I can. I take pride in my appearance, I smile and I contribute to my community as much as I can....yet come to my home uninvited, on the days I don't have on my mask, you can find me so bad that even my husband has to ask if a gentle hug would be too painful.
    I look quite a bit younger than I am, am now able to walk on crutches and start every day with gratitude exercises and meditation to make sure that my brain's neuro pathways don't strengthen in areas of negatively but strengthen those neuro pathways that enforce that I am not my disease. I am not Complex Regional Pain Syndrome, I am a person who can still contribute, love, laugh, make a positive difference to many. I am a person whose body defied medical options, shocked Drs who still don't understand why I am alive, let alone walking after being told I never will...
    To those who want to label me as sick or healthy, take a ticket, get in line. I am me, I am not my body but a living being trying my best every day. I don't care what you think, just remember, never judge a book by it's cover. Those who count support me, those who don't count, I don't listen to. By all means, if you are honestly interested why this disease is said to be the most painful condition on the planet, I might give you the facts, not to have you feel sorry for me but to understand that many of us suffer in silence, struggle yet will not give up.

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  17. Can't add much more other than to say I unfortunately relate only too well. xx

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