The Power Of Unburdened Truth

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There are times we don’t talk about my sarcoidosis for weeks at a time. It’s almost as if my disease has just become part of the fabric of our lives. There is little need to discuss it. It is, after all, a known quantity in our lives. I am sick. What else is there to say? Why should we dwell. When all is said and done, we don’t need words to know the impact sarcoidosis has had on me and on us, the loss of income, the slower pace of life, the ease with which I now cry and feel helpless and ineffectual because my lungs burn in a fiery blaze, a blistering ache every time I take a breath and my body writhes in unexpected and mysterious discomfort for reasons no doctor seems to understand and, always at the most inconvenient of times.

Tonight for the first time in quite awhile, we did talk about it. I talked about it. I admitted a rarely spoken ugly fact about living with a chronic disease. I said that it’s hard. I said that I hate it. I don’t like to say these things. I feel like when I do, I give the disease power over me, power I loath to feed that horrible ogre who took up unwelcome residence inside my flesh and organs, my bones and limbs. I do hate it though and that’s the simple truth of the matter.

There are things about becoming persistently unwell that actually make you appreciate life in deeper and more profound ways. Time changes because you realize how much of it you wasted when you were well and worried about stupid, mundane, often petty things, stuff beyond your control, outside of your grasp, the injustice of things not going your way. What I know now because of my sarcoidosis, is that most things don’t turn out as planned and that this is meant to part of the adventure of life, not something to fret over. The unplanned events in life are what build our character because they are what shape us through the choices we make about how we face them.

I am grateful for the knowledge about life that I have gained from being knocked out of the rat race, the constant chase for the next best thing. I no longer have the drive or the need to be the best at everything I do or in the know about every stupid latest fad or fashion. Instead, I find my life of forced simplicity to be an unexpected blessing. There is ease in it. It does give me pause to be still and know that life is not only fleeting, it is profoundly short and when every breath you take is literally painful, well, this just gives you a better understanding of life and death, how the two are intertwined and cannot be unwoven from each other. There is a humanity and a humility that comes with the knowledge that death is forever chasing life. This is a little secret that can only be understood once your very being has been threatened by the mayhem of disease.

Most of the time, in my acute awareness that life is a fragile momentary passage of time on this insanely beautiful planet and, despite the unyielding stumbling blocks of life inside an uncooperative skin, I choose to be grateful. I choose to focus on contentment rather than disappointment. I seek serenity instead of worry. I long for peace instead of disturbance. However, I would be remiss and even a liar, if I didn’t once and awhile admit, despite my abhorrence to the fact that I loath to acknowledge it, having this disease is hard and I do hate it.

So tonight, I let the floodgates open but, only a crack. I released the burden of the all too often unvoiced reality about life with a chronic health condition. I admitted that I feel weary sometimes. I disclosed my loneliness and insecurities. I shed light on the ugly sorrow of a body burdened by disease but I only did this so that these demons cannot swallow me whole. Sometimes the only time the truth can hurt you is when you’re not honest. Feelings are only as powerful as you allow them to be. I do grieve and this disease does make me sad but when I am honest, when I acknowledge my broken heart and liberate myself from being mostly stoic and strong and outwardly fearless in the face of constant uncertain health, I am better able to appreciate the simple joy that is life and I am free to continue living with grace and acceptance of what is rather than what will never be.

7 thoughts on “The Power Of Unburdened Truth

  1. Sheila R. Dorris

    Lisa, today I was having a day that left me feeling defeated in my struggles. I was feeling sad and broken. Then I was feeling selfish since I should be feeling grateful for the blessings in life that I do have. So in trying to feel better, I looked for quotes of inspiration in hopes that I would once again feel like I am of worth.

    In reading your blog, learning a bit more and realizing the physical pain with which you are plagued, I felt so sad that I do not have a magic wand with which to wave and take your pain away. I hate that you suffer like you do. Yet I also admire your strength and your unselfish ways in which you educate, share, motivate, and inspire others.

    “There is a humanity and a humility that comes with the knowledge that death is forever chasing life.” Lisa Curry

    Yes, we are faced with challenges all along our paths in this journey we call life. You motivate me Lisa, your bravery kicks me in the butt! Your honesty and strength help me to realize I could face adversity and take it on, head on. Today after an emotionally rough day, I realized I need to stand up and face my demons. You are much braver than I Lisa and a hero as someone with who I look up to for inspiration. Now I also want to share an inspirational quote with you…

    “In Japan, broken objects are often repaired with gold. The flaw is seen an a unique piece of the object’s history which adds to its beauty. Consider this when you feel broken.”

    Lisa, I know you suffer and at times might not feel whole, or right. Yet please know that while I am sooooo sad that you suffer physically, your writing that blossoms from the challenge you face, continually moves and inspires me. Thank you for sharing your pain, your insight, your complete being. I love you just as you are and only wish I could take away your pain, help you feel better, plus prove to you that by far, you are still a shining star! MUCH LOVE!!! 💖 Sheila

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    1. Oh Sheila – You are too kind and give me too much credit. I’m glad you like the blog though. And, I’m sorry you are having a tough time too. Please don’t worry about me re: my health…I have accepted it for what it is and I deal with it the best that I can. It is what it is…Much love to you too my dear friend!

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      1. Sheila R. Dorris

        You deserve very special accolades Lisa, you are an angel on earth! I wish I could take the pain away for you, with each of your burning breaths. I am soooooo sad that you deal with this extraordinary challenge and I pray for a cure. I will send you further thoughts through our private communications!

        MUCH LOVE! 💖

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  2. Mortimer

    thank you for your blog. i’ve been through a year and a half of testing and found out it’s in my heart. not my lungs which made it so hard to figure out. probably in my nervous system too-still testing that one. about to embark on the hard part of this. apparently 8 months of prednisone was “short”!

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    1. I’m sorry for what you are going through. This is a tough disease and the treatments for it can almost be worse! Although when it messes with your heart, you really can’t avoid treatment. Hang in there! I’m not on pred. I’m on methotrexate. Pred didn’t work for me at all, which is another thing that makes this disease crazy…Not only does it not present itself the same way for all of us, we don’t all respond to the so called available treatments the same way…maddening…Hang in there…Slowly but surely…you’ll learn to live with this thing.

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      1. Mortimer

        Thank you! The internet has made living with these things easier. It’s a blessing to find others with the same issues even if we’re not all exactly alike. Thank you for your blog!

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