The reality of Fibromyalgia is not only that people don’t know much about it unless they have it, but there are many who don’t even believe the condition is real.
Imagine your body is on fire. Imagine every time you take a step, it feels like the ground beneath you is littered with Legos. LEGOS people! Imagine if the mere act of walking from your car to your desk caused such exhaustion, you could sleep for a day. Sounds pretty terrible, right?

Now add in that there’s no way to prove what you are feeling is real. Every single test has come back negative. (And you’ve taken hundreds of tests.) Imagine that amid the fatigue, chronic pain and hypersensitivity, as you try to convince yourself to press on, you overhear people talking about how they are “over your Fibro” and how much you complain about your pain. Imagine hearing that all of your suffering is something you made up in your head.

Here are 25 Things People Without Fibromyalgia Should Know About People With Fibromyalgia.

If you know someone with Fibro and want to understand them better,Are you a Fibro warrior? Share this post to spread awareness and understanding.

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  1. Give gentle hugs please, my skin hurts
  2. I can sleep all day and still feel like I just ran a marathon
  3. When i’m tired, let me sleep

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    4. If i cancel my plans with you, don’t be mad, I already feel bad

    5.If i went out last night, I need a day to recover, its ok, it was worth it

    6.When I’m in a flare, leave me alone in a dark room (but check in), it makes me feel good

    2016-05-11-1462984758-4690477-husbandtime.jpg7. Every morning is a tough morning

    8. Your friend with Fibro that has no pain doesn’t make me feel any better

    9. “You should exercise” My work day is my exercise

    2016-05-11-1462984842-7957909-Joyride.jpg10. Certain foods make me flare-up (ie) peppers of any kind, sugar, caffeine

    11.Yes, diet matters but in flare mode, all bets are off

    12.Because of Fibro, I get to spend more time with my husband

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    13. Bright lights, loud noise and too many smells over-load my senses and make me nauseous

    14. My day, week and month are carefully planned to accommodate my Fibro

    15. Yes, my face is swollen, no I didn’t gain 5 pounds overnight. (I’m flared!)

    16. I have 3 different sizes of clothes in my closet to accommodate flare vs. non flare days

    17. I play hide and go seek with the elements, too cold, too rainy, too hot, too much sun

    18. To you, car rides are joy rides. To me, they’re a painful roller coaster ride.

    19. Going to the doctor makes me mad, it’s a reminder of my condition

    20. Some days it’s Ok to let my Fibro win, it reminds me that this is a marathon, not a sprint.

    21. I can get moody, you would be too if you were in pain all the time, be patient with me

    22. I can tell your mood as soon you walk in the room because my Fibro/spidey-senses are tingling

    23. There are no no-pain days but my low-pain days are my happy days

    24.Because of Fibro, the mandated down-time gives me the opportunity to write this blog, and I’m grateful

    25. Because of Fibro, I’ve become part of a strong, supportive community that reminds me I’m never alone

    Part of my mission is to bring the Fibromyalgia Survivor community together to offer real support and encouragement to one another. You can be part of this movement by sharing your story too. What do you want people to know most about how your Fibro affects you? Tell us in the conversation below.

    Disclaimer: I am not a doctor. All information presented should be regarded as friendly advice and opinions based on my own experience and research. I am not making an attempt to prescribe any medical treatment and the information contained in this blog is not intended to replace a one-on-one relationship with a doctor or qualified health practitioner.

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