The power of a word: my new diagnosis & other stories
Alecia Hancock
Nonprofit Consultant. Digital Marketing. Social Media. Storyteller. | GAICD.
You may have seen on my?Facebook Page?that last week I was diagnosed with?fibromyalgia. It was definitely a surprise. I’ve already had a few autoimmune diseases for several years and lately it’s been a struggle.??
Let me get really, real here because I know you like the full truth.?
It’s not been just ‘a struggle’. It has really, really sucked.?
I’ve had headaches for 2-3 weeks at a time that pain killers don’t touch.?
I’ve been so tired that I can sleep 10 hours a night and have a two-hour nap most days.??
I got tachycardia (small bursts of fast or out of rhythm heart beats) and was referred to a cardiologist.?
I developed tremors in my hands, and I found it difficult to hold a cup of water without it looking like a scene from Jurassic Park.?If the tremors and my joint pain was bad, I had trouble cutting my own food.?
I have pain in my left lung if I breathe in deeply. I get joint pain in my elbows, wrists, knees, shoulder, and neck.?
I’d pretty much stopped exercising because it’s been too painful.?
I also?had?to admit my challenges to those around me and ask for a lot more help. Which is something I find HARD.??
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But that is NOT what this email is about. It’s about the power of a word. Because I was surprised by how much one word could carry so much loaded meaning to me, and to others.?
I struggled with getting another new ‘word’ to add to my list of diagnoses.??
I left my doctor’s office with a script, a scribbled word on a piece of paper and a link to a website to read up on the condition.
Then when I shared the diagnosis with a few people in my inner circle, the response took me by surprise. Both people I told looked puzzled and said something along the lines of: “but you do know?fibromyalgia?isn’t real?”?
I really had no idea how to respond. I felt confused and oddly embarrassed.?
At the end of the day, for me the word doesn’t really matter. What matters is that I have a new medication and it’s helping. I am feeling more and me every single day.?
But the lesson here is that words can have such power. A single word can be laden with so many different layers of emotion and mean different things to different people.?
?I thought this was a timely reminder to me, and you, to think about the words we use and the impact they have – both positive and negative.?
You want people to react emotionally to your words. But you don’t want a throw away comment to have unintended emotional fallout. Your words have power – use them wisely.?
Sub-Editor
1 年Thank you for writing this, Alecia! Fibro is such an awful, misunderstood illness so it certainly helps to get the validation and roadmap of a diagnosis. I’m sorry you’re experiencing this. Always here if you want to chat with someone who’s knows the journey. Gentle hugs to you xx
Recruitment | Consulting
1 年Thanks for sharing Alecia Hancock, what I can say, from someone who suffers auto immune disease too, it’s very real for many people, so be kind. ??????
Positioning & Community Engagement Ideation for Advocates of Purpose, Ambitious Leaders & Teams ?? Personal Connection for Professional Influence ?? LinkedIn Strategist, Speaker & Trainer ?? Perth Pool Guide & Quest
2 年Invisible doesn’t mean not real! I know it can be debilitating for some and needs management. People’s reaction is usually about them and their filters and bias. I was recently diagnosed with ADHD, which explains so much. Some replied with ‘sorry to hear..’ which I found odd as I don’t see it as a positive or negative, it just is. I dislike labels but identifying it means I can work through my challenges. Ignorance is no excuse for dismissiveness.
Seeking my next opportunity | Fundraising Professional | DEI&B advocate | Public speaker | Pastry chef
2 年Thank you for sharing Alecia - having invisible illness and disability does suck big time. It's nice to see someone be so open and honest about it
Autism Dad
2 年i am AutismDad ,BUT ALL SO HAVE ..BOTH ..M.E .AND FIBRIOMAGIA ..Migraines very badly 5 migraines a day .if Pain is too bad i am then Vomiting all over .People never see the every day EFFECTS.MARK