Spring Break...ing Free


Lisa Thompson • Mar 21, 2022

Ah, spring. I’m sitting on the front porch as I write this. The front porch of my little 1940's house becomes my second living room during the summer. I’m counting the days until I can get back out here on the regular! 


The sun is shining. The birds are singing, they’re exited too. And if you live in the Midwest, you know the smell of spring in the air…the fresh air smells a little like mud. It’s loamy. The snow has melted and the fertile soil is welcoming the first bursts of spring…I saw my first yellow crocuses today. The tulips, daffodils, and hyacinths aren’t far behind.  Soon the straw colored dead grass will give way to the fresh, green lawns of 2022.  The earth just seems to smile a bit more…and so do we as we get back outside and blow the dust off.

 

And with spring comes spring break, spring vacation, Easter vacation, spring holiday…whatever you choose to call it. Our family never really took spring vacations when I was a kid. As an adult, with a young child in school, and living in another state, my husband and I quickly learned that “spring break” was a thing.  An annual ritual.  Now that I'm solo, it’s still a bit of a yearly tradition for me so many years later.


For the last few years, I’ve flown off to Florida. Visiting a variety of friends, cities, beaches, and every once in a while, a theme park. This year, I procrastinated making my plans. “I don’t have the money,” or “I have too many things on the calendar,” or “work is too busy” or “should I spend the money”. When it comes right down to it…I’ve been afraid. Afraid to commit, afraid to plan. And what is procrastination? Yep…nothing but fear.


I’ve not taken a plane trip since my diagnosis. February, 2021 was my last flight. I was diagnosed a month later, so really, I was flying/traveling with Meniere’s, I just didn't know it's name yet.  Has anything really changed?  Part of me wants to say, “nothing really.” However, in my heart of hearts, I do know things have changed in the short span of a year.  My ears are far more unruly. They feel full or snap, crackle, and pop more than ever. My hearing has diminished in my left ear. I’m leaning in toward people with my "good ear" far more often. I notice the strange, dizzy, slightly off balance “hum” more regularly. Does that mean I'll never go anywhere ever again? 


Only a week ago it didn’t occur to me that I’d be going at all. I was just going to let spring break kind of float on by.  I was just going to let Meniere’s quietly sneak up and hold me back, make me afraid, and take something else from me.  I’d simply choose to do nothing...that was apparently my plan. 


Well, sometimes when you don’t have the guts to jump, the universe will just give you a little shove right off the high dive and into the deep end, just like the kid you knew in the third grade. Have you ever noticed that?  I happened to be looking at my calendar and staring back at me was a rather empty week coming up. Allegiant was still offering some really great fares, and friends were ready to welcome me with a place to stay and relax. And then, the unmistakable Karmic bomb dropped right into my lap. The On the Vertigo golf tournament, to raise awareness and funds for Meniere’s Disease research, is in April.  And wouldn't you know, it's going to be held only about 25 minutes from where I would be staying.


A bit of back-story…Discovering the book On the Vertigo: One Sick Man's Journey to Make a Difference  made a huge impact on me early in my Meniere’s journey.  It was the second book I read actually, when I was hungry for any information I could find.  I stumbled upon Steve Schweir and his book through an online support group when I was feeling quite overwhelmed  by the fear of my new diagnosis. Connecting with Steve and his brother, Dave, has allowed me, like so many others, to learn more about Meniere’s, to see the positive, to find more courage, strength, and humor as we live with this disease.  (He and his brother are funny guys.)


I simply couldn’t deny the time in my schedule, the invitation from friends, and the opportunity to meet a fellow Meniere's warrior and volunteer to help with the tournament. This was a clear message from the Universe! I believe God gives us signs. I believe in the flow of our lives, how situations present themselves. We can choose to not see, not hear, and keep trying to travel upstream...or we can participate and join with ease, you know, downstream.  God opens doors, and this door was being flung wide open for me to walk right through. 


Am I apprehensive? Yes. Do I fear an attack on the plane with every fiber of my being? Yes. Yet, I’m going to jump in.  None of us approach any new challenge or new situation in life without at least some preparation, right? This is no different. And hey, I’m a mom...we know how to be prepared for every scenario. If I’ve got 4 bottles of water, and what amounts to a Walgreen's pop-up in my carry-on, then so be it. If I find I don’t need any of the meds, even better!  I’ll be prepared regardless! That in itself will probably relax me.


As I sit here in the warm-ish sun, listening to the birds singing, I'm reminded that spring is a time when we can begin again. Come back to life.  Shake off those gray of the winter blahs.  We feel energized.  Invigorated.  What better time to conquer a fear or an insecurity, right?  What better time to emerge from that safe little cocoon of habits where our Meniere’s Disease can keep us?  We’re all different. Our symptoms are as unique as each one of us.  What is something unique to you, that you can try, even the littlest thing, to help you feel stronger? To help you conquer a fear you have? To enable you to take back a little bit more of your power?  To help you feel more independent?  For me, it’s grabbing my sun screen and getting on that plane!


With love and wishing you good balance.  Happy Spring!

My Dizzy Life


Bungalow style house
By Lisa Thompson 05 Sep, 2022
I love this home I’ve made for myself. And when I was first diagnosed, these walls were a refuge. A private place to be raw, to be angry, to be scared, to cry, to live my symptoms without anyone else having to see. To be safe.
Three people talking doing a podcast
By Lisa Thompson 18 Jul, 2022
Connection. We all crave it in our lives. Whether we’re volunteering, in a book club, a golf league, or sharing a video on Instagram. As we live with Meniere’s, we all need to find connections with others sharing this path…
Woman at desk working on a laptop
By Lisa Thompson 23 Feb, 2022
Here’s the weird thing, every time I looked at it or spent much time on any application, I felt a vague queasiness. A little dizziness. Just that little hum, you know the one. Especially when there was a lot of white on the screen, like emails. When I walked away or when returning to my older computer, the uneasiness subsided.
Four friends arms around each other at sunset
By Lisa Thompson 25 Jan, 2022
“You were fine…” ten minutes ago, yesterday, last month, last year. Pick one! And this week, for the first time since my diagnosis, I was labeled a “flake.”
Large jar with small pieces of folded paper inside
By Lisa Thompson 10 Jan, 2022
One of the things I’ve done for the past 2 years, is keep a “Jar of Moments.” Little slips of paper on which I write happy adventures, good times shared with family or friends, “ah-ha” moments, kindnesses that were extended to me over the months, when I made a new friend, things I did for others that made me feel lit up inside…you get the idea. On New Years Day, I dump them out and read them all.
happy woman in sunflowers with bubbles around her arms outstretched
By Lisa Thompson 06 Dec, 2021
Today is today. I can miss the moments in front of me, worried about what might happen, stewing and brewing up a lot of gunky feelings. Or, I can keep looking for what this is teaching me. Embracing it as part of who I am and seeing how this thing that is now my travel companion is sharing my journey…whether I like it or not. Knowing this helps me notice and experience life more fully.
overturned salt shaker
By Lisa Thompson 22 Nov, 2021
Whether you’re new to this whole Meniere’s thing or a veteran, one thing is certain…we’re all thirsty for knowledge. Why do our bodies do what they’re doing? Or not doing? What in the world can we do to control our symptoms? And what's all this talk about salt?
Woman looking out the window
By Lisa Thompson 15 Nov, 2021
All of us who live with Meniere’s often struggle with making plans. When newly diagnosed, we wonder if we’ll ever be able to enjoy family events, holidays, social occasions, or even a happy hour, ever again.
Lisa in purple dress
By Lisa Thompson 31 Oct, 2021
Welcome to MyDizzyLife.com. Thank you for visiting. My name’s Lisa and I was diagnosed with Meniere’s Disease in March, 2021.
Barometer
By Lisa Thompson 31 Oct, 2021
Throughout the summer and as the season begins to change, I'm reading a lot of posts from fellow Meniere’s warriors who are struggling with the weather right now. There are lots of fun things to do. Everyone wants to get outside…at least in the Midwest, because we’re all going to be hunkering down again once winter comes. That’s too soon, by the way!
More Posts
Share by: