Chronic Pain: I found this on another... - My Fibro Community

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Chronic Pain

WhiteJambo profile image
5 Replies

I found this on another forum and thought it may help some people.

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 that 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, my 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 everyday. 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 sociable" 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 some things 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 than 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 that I do 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 worldwide networking (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 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 be understanding 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 you help me 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 have asked a lot from you, and I do thank you for listening. It really does mean a lot.

AUTHOR UNKNOWN

**********************************

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WhiteJambo profile image
WhiteJambo
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5 Replies
Walshy profile image
Walshy

Your life is a mirror image of mine, you have put it into words in a way I don't feel I could have done. It made me cry with empathy and understanding. Thank you

Glosgran profile image
Glosgran

Have copied and edited it slightly to suit my own situation to share with my own family & friends.

jan1022 profile image
jan1022

Oh my god this is exactly how I feel. everyone that has fibro needs to copy this and give it to those that don't understand what we go thru. sadly this is me now, where once I was healthy and able to do anything and did. I worked in factory I had a social life and when where and when I wanted. now I can't do much and the pain seems to get worse with each passing year. some days not sure if I can take any more of the pain. I also have degenerative bones in spine and nerve damage in legs and feet along with restless legs. unfortunately my guy doesn't get it. I think he thinks it's all in my head. the numbness in my feet make me unsteady but I also have stabbing and burning in my feet. every day seems like theres another pain to deal with. I have to go thru procedures on my back every other month or so. needles, injections,nerve blocks, etc. none of which works. lot of the time I have to go thru these without anesthesia as I can't find a driver. these are painful and hell. I'm 64 now and feel 94. I never looked my age and was always young at heart. now i'm over weight from all the steroids they put me on in 2008 [was always thin] I look in the mirror and wonder who that is. i'm now having trouble with my hair falling out. great I need something else . sorry to complain but my life has become so depressing this all started in 2008 and has gotten worse and worse. just doctors treatments, procedures, medicine and PAIN ALWAYS PAIN. tired always and sad. hope this finds the rest of you so much better and lot less pain jan

Floppymaud profile image
Floppymaud

Wow, right on the nail!! Wonderful insight into chronic related conditions, just how I feel on a daily basis.

jan1022 profile image
jan1022

so sorry to hear that I don't want anyone to suffer every day like me. I hope they find something that works soon as some days the depression gets the best of me and I wonder how much more I can go thru. god love you and I pray you have a happy pain free day

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