The power of a word: my new diagnosis & other stories

The power of a word: my new diagnosis & other stories

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.??

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.?

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

Chantelle O'Sullivan

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. ??????

Jo Saunders

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.

Patricia Scheetz

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

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

回复

要查看或添加评论,请登录

Alecia Hancock的更多文章

社区洞察

其他会员也浏览了