When your concern for my chronic FM pain shows up as frustration

#ThisIsChronicIllness #InvisibleIllness

In the last 10 years that I have been living with FM, I can positively say that I have heard/seen the gamut of reactions about my life with pain……disbelief, shock, encouragement, concern, feeling of being resigned, anger, frustration and finally impatience. The frustration shows up as a borderline rude question: “will you ever say that you are without pain?” or “will you ever get better?”

The answers in my mind range from, “Gee, why yes, as soon as they find a cure for it” to a mental flip/showing them the bird but because I know the intent behind this Q, I either say that I have to live with it or make a joke out of it – that FM and my life are 2 parallel but ever present tracks in my life and I am in the middle of it. Sometimes I just flat out lie and say that I am OK, when I am actually not. And I come out of the conversation feeling hurt and in more pain than before.

I know that you are genuinely concerned about my health and feel bad that I am in pain everyday…you know what,  I appreciate and am thankful for your concern. But when my answer is not what you expected, your concern turns into something I don’t deserve. Remember these things when I say I AM FINE, or its PAIN AS USUAL:

  • It means that I am managing my pain the best way I know

Not everyone chooses to take prescription meds for their pain because of several reasons. I was on a cocktail of them until I realized that they were doing me more harm than good and hence I quit ALL of them cold-turkey. Now apart from a regular painkiller here and there, I don’t take any prescription meds and hence can feel the full-blown effects of FM pain. Imagine any pain you were in, say you stubbed your toe and it is throbbing. The throbbing might last for a couple of hours max. Now imagine incessant throbbing, tingling, nerve pain, stiffness, burning and much more ALL over your body , ALL the time and multiply it by 100 times or 1000, that’s what I feel. But I am ok with feeling this pain as it is A CHOICE that I made to be fully coherent and not be a zombie that these meds were turning me into. If you can’t understand my reasons, then don’t question it and tell me that it is my fault that I am in pain.

  • It means that I am actually struggling with it but putting on a what passes as a cheerful and brave front  

Chronic FM pain is a real pain in the you-know-where and when it is visited by its old friends – migraines and depression, it gets even more difficult to deal with it all. But when when you are in fact not only experiencing overall body pain but also having a migraine attack and feeling depressed, things can get out of control real fast. But when you have duties to fulfill, you recognize your symptoms for what it is, keep an eye on it like an outsider and get on with your life doing the best you can. And the best might be just getting through the basics today to going all out tomorrow. It means that I might never be healthy but that is not going to come in my way of being happy and at peace

  • It means that I am taking it one day at a time and just because I did something yesterday doesn’t mean I can do it in the today

This is the one thing that most people have trouble believing. People have come up to me and said: “But I saw you yesterday in XYZ,” or “You celebrated ABC last month but now you are saying you cannot do DEF,” or something similar. Well sometimes I end up pushing myself or not pacing that I pay the price and sometimes I chose to sit out so that I don’t pay the price. It all comes down to the choice of whether you want to do something today that you end up in bed or worse get a flare-up for the next week or so (OR) sit it out so that you can carry on with those daily activities – lunches packed, homework checked – even if they are routine and seem drab but are absolutely necessary.

  • It means that I know that you are impatient and view my pain as an annoyance and as something that I got because of something I did

If I had put away a quarter for every time I heard that “I am imagining it,” or “I should keep myself so occupied that I forget it,” or “I am not active enough hence I am in pain,” or “I am strong thats why God has given me this,” and so on and so forth, I would actually have a good amount to pay for a year’s tuition of my Masters.

Would you ever walk up to someone suffering from life-threatening illnesses or serious injuries and ask them the questions that you ask me in a frustrated and impatient tone? No of course not. Because you can see it and know that the person is either going to be cured or not and in your eyes, you can’t put me in either box so I am automatically imagining and not doing enough to get better. Guess what, people thought about these life-threatening illnesses the same way they do about FM.

I know I am in limbo with my condition and I know it is difficult for you to see me in pain but when your expression of concern shows up as anger or worse frustration, it not only hurts me, it majorly pisses me off because in addition to dealing with my pain, I now have to make sure that I sugarcoat the truth just so that you feel that I am feeling alright, when in reality I am working really hard to get through each day. And do stop right there when you tell me that God only tests those who are strong or some nonsense like that. I know and firmly believe that God is not sitting up there, wherever there is, with a spreadsheet of things to hand out to the strongest.

Like my high school teacher told our class once: “if you don’t have anything good  to say, just zip it.” You think your words are comforting but they are anything but and please spare me your oh-so-wise worldly knowledge.

  • It means that the pain is here to stay but it does not DEFINE who I am

Living with pain for 10+ years is a lifestyle change. I plan ahead to the smallest detail possible, knowing in the back of my mind that I might have to cancel or not be a part of it at the last minute. The planning helps me identify any possible hurdles, alternatives and look at every activity as a milestone. It helps me be in touch with the person I was and still am, highlighting those things I cherish and those that are unnecessary and helped me cut off all the unnecessary baggage – both emotionally and physically.

laks tattoo
My ink

Remember every person you see with an invisible illness is actually fighting with a smile – fighting to fall asleep when they are in fact wide awake, fighting to stay asleep when the pain wakes them up every couple of hours, fighting to wake up and get on with their day, fighting the pain every step of their way and finally fighting the most important fight – being their own advocates and creating awareness when all they want is to have a single day without pain – Cos that’s who they are – warriors fighting their own battle and looking for just a bit of understanding and kindness ~ Lakshmi

 

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10 Comments Add yours

  1. So well put! Sending you gentle hugs and positive vibes ❤

  2. jcrohnie715 says:

    Love your tattoos and the quote at the end! Stay strong and keep fighting on!

  3. Reblogged this on and commented:
    My fellow fibro warrior Lakshmi wrote a great blog earlier this week and I wanted to share. Two especially good points I wanted to highlight:

    ” I know that you are genuinely concerned about my health and feel bad that I am in pain everyday…you know what,  I appreciate and am thankful for your concern. But when my answer is not what you expected, your concern turns into something I don’t deserve.”

    “Would you ever walk up to someone suffering from life-threatening illnesses or serious injuries and ask them the questions that you ask me in a frustrated and impatient tone? No of course not. Because you can see it and know that the person is either going to be cured or not and in your eyes, you can’t put me in either box so I am automatically imagining and not doing enough to get better.”

  4. Fibronacci says:

    Beautifully put! Thank you for this post. 🙂 Really enjoying your blog btw. Happy to meet another grad student with FM!

  5. kate1975 says:

    You are so correct when you write that people don’t know what box to put us in and that then they blame us for what we endure and judge us for all the choices we make. I hate being disbelieved and judged. I’m sorry that you go through that. More compassion, empathy, and civility would be wonderful.

    Good and healing thoughts to you.

    Kate

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