LETTER TO PEOPLE WITHOUT CHRONIC PAIN


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Having chronic pain means many things change, and a lot of them are invisible. Unlike having cancer or being hurt in an accident, most people do not understand even a little about chronic pain and its effects, and of those who think they know, many are actually misinformed.In the spirit of informing those who wish to understand, these are the things that I would like you to understand about me before you judge me….Please understand that being sick doesn’t mean I’m not still a human being. I have to spend most of my day in considerable pain and exhaustion, and if you visit, sometimes I probably don’t seem like much fun to be with, but I’m still me–stuck inside this body. I still worry about school, family, my friends, and most of the time, I’d still like to hear you talk about yours too.Please understand the difference between “happy” and “healthy”. When you’ve got the flu, you probably feel miserable with it, but I’ve been sick for years. I can’t be miserable all the time. In fact, I work hard at not being miserable. So, if you’re talking to me and I sound happy, it means I’m happy. That’s all. It doesn’t mean that I’m not in a lot of pain, or extremely tired, or that I’m getting better, or any of those things. Please don’t say, “Oh, you’re sounding better!” or “but you look so healthy!” I am merely coping. I am sounding happy and trying to look normal. If you want to comment on that, you’re welcome.

Please understand that being able to stand up for ten minutes doesn’t necessarily mean that I can stand up for twenty minutes, or an hour. Just because I managed to stand up for thirty minutes yesterday doesn’t mean that I can do the same today. With a lot of diseases you’re either paralyzed, or you can move. With this one, it gets more confusing every day. It can be like a yo-yo. I never know from day to day, how I am going to feel when I wake up. In most cases, I never know from minute to minute. That is one of the hardest and most frustrating components of chronic pain.Please repeat the above paragraph substituting, “sitting”, “walking”, “thinking”, “concentrating”, “being social” and so on….it applies to everything. That’s what chronic pain does to you.Please understand that chronic pain is variable. It’s quite possible (for many, it’s common) that one day I am able to walk to the park and back, while the next day I’ll have trouble getting to the next room. Please don’t attack me when I’m ill by saying “But you did it before!” or “Oh, come on, I know you can do this!” If you want me to do something, then ask if I can.In a similar vein, I may need to cancel a previous commitment at the last minute. If this happens, please do not take it personally. If you are able, please try to always remember how very lucky you are–to be physically able to do all of the things that you can do.Please understand that “getting out and doing things” does not make me feel better and can often make me seriously worse.

You don’t know what I go through or how I suffer in my own private time. Telling me that I need to exercise or “do something to get my mind off of it” may frustrate me to tears and is not correct. If I was capable of doing some things any or all of the time, don’t you know that I would? I am working with my doctor and I am doing what I am supposed to do.Another statement that hurts is, “You just need to push yourself more, try harder…” Obviously, chronic pain can deal with the whole body, or be localized to specific areas. Sometimes participating in a single activity for a short or a long period of time can cause more damage and physical pain that you could ever imagine.Not to mention the recovery time, which can be intense. You can’t always read it on my face or in my body language. Also, chronic pain may cause secondary depression (wouldn’t you get depressed and down if you were hurting constantly for months or years?), but it is not created by depression.Please understand that if I say I have to sit down/lie down/stay in bed/or take these pills now, that probably means I have to do it right now – it can’t be put off or forgotten just because I’m somewhere, or am right in the middle of doing something.

Chronic pain does not forgive, nor does it wait for anyone.If you want to suggest a cure to me, please don’t. It’s not because I don’t appreciate the thought and it’s not because I don’t want to get well. Lord knows that isn’t true. In all likelihood, if you’ve heard of it or tried it, so have I. In some cases, I have been made sicker, not better. This can involve side effects or allergic reactions. It also includes failure, which in and of itself can make me feel even lower.If there were something that cured, or even helped people with my form of chronic pain, then we’d know about it. There is a worldwide network (both on and off the internet) between people with chronic pain. If something worked, we would know. It’s definitely not for lack of trying. If, after reading this, you still feel the need to suggest a cure, then so be it. I may take what you said and discuss it with my doctor.If I seem touchy, it’s probably because I am. It’s not how I try to be. As a matter of fact, I try very hard to be normal. I hope you will try to understand. I have been, and am still, going through a lot. Chronic pain is hard for you to understand unless you have had it. It wreaks havoc on the body and the mind. It is exhausting and exasperating.Almost all of the time, I know that I am doing my best to cope with this and live my life to the best of my ability.

I ask you to bear with me, and accept me as I am. I know that you cannot literally understand my situation unless you have been in my shoes, but as much as is possible, I am asking you to try to understand in general.In many ways, I depend on you – people who are not sick. I need you to visit me when I am too sick to go out…Sometimes I need your help with the shopping, cooking or cleaning. I may need you to take me to the doctor or to the store. You are my link to the normalcy of life. You can help me to keep in touch with the parts of life that I miss and fully intend to undertake again, just as soon as I am able.I know that I asked a lot from you and I do thank you for listening, it really does mean a lot.

8 thoughts on “LETTER TO PEOPLE WITHOUT CHRONIC PAIN

  1. Shari mintzer

    Written wonderfully. from a sufferer I find out so difficult to explain to those who have no clue and often don’t want to because so much sound like a complainer. This is so well put and hope many read and truly understand what this says. Thank you for speaking for so many of us

    Reply
  2. Just me

    Very well stated. I have stomach problems in addition to other (physical) issues. One day I can feel perfectly normal ~ or MY “normal” ~ where I feel well enough to eat a somewhat normal meal, such as a burger or a piece of chicken. The next day I can be so sick at my stomach, I’m sitting on the porcelain queen hovering over a trash can.

    Reply
    1. Just me

      And unfortunately, I’m not given advanced warning/notice. I can wake up and feel fine but 20 minutes later it can hit. And unfortunately, when it hits, it can last anywhere from a few minutes to a couple of weeks. I felt GREAT Wednesday, but was in the bed early Monday night, ALL day Tuesday, then again back in the bed ALL day Thursday and slowly warmed up to sipping on some chicken broth Friday (but it took about 4 hours to start to feel somewhat decent ~ not even “normal”. I can’t make plans because 9.5 out of 10 times I’m going to have to cancel….not because I want to, but because I’m either in pain, sick, nauseated, but usually it’s all of those combined. After decades of taking pain medication, it’s certainly not a wonder drug. At best, I hope that the meds will help me to feel better but I’m lucky to keep things at bay. It’s frustrating and depressing because people don’t understand. I’m not “lazy”. I’m sick. But it’s the kind of “sick” that one cannot “see”. And no one understands because, unless they have lived through it, there’s no way for them to understand. You think I LIKE being in the d*mn bed?? Hell no! I miss working. I miss my social life. I miss going on dates with my husband. Speaking of, we went out for a “date night” maybe about 2 1/2 – 3 years ago on a Thursday night. I was in SO MUCH PAIN I thought I needed to go to the ER, but if I go to the ER all they want to do is run the same tests I’ve had done over the past six years, tell me to follow up with a specialist and won’t give me anything for pain. And the cost for this is approximately $1,500. So I suffered all weekend and finally started to feel better late that Sunday night. Lesson was learned! Doc said for me to just puree’ my food. Uhm, a pureed steak just doesn’t sound too appealing! I’d just like to eat a normal meal without throwing it up or being in pain or the other couple of things that happen. There’s only so much soup one can eat!

      Reply
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