Tag Archives: Lyme

23 Ways to Imagine What It’s Like to Have Lyme Disease

This article was featured on The Mighty.

Dealing with Lyme Disease can be challenging enough based on the complex symptoms alone.

What makes it ten times more challenging, though, is the fact that (for most with Lyme Disease) our symptoms are invisible. Continue reading

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To the Passenger who Called Me A Slut

I don’t even know what you said in full, the wind disrupted the sound waves as your words were on their way from your mouth to my ears.

“Slut village?” “This isn’t Slut Village?”

Whatever you said, it initially made me chuckle. Receiving catcalls and obscenities is something I’d expect in my college town. And something that did happen often while I was in college, not because of how I acted, or how I dressed, but because men are men and that’s all. Continue reading

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Never Give Up Working With Your Hands

“You look more youthful.” The words hit me with surprise. 

Here I was, gripping a beast of a camera, one on loan from a good friend. I wanted to cry with the pain its weight brought to my arthritic fingers and wrists. But instead, I beamed with happiness. A youthful sort of happiness, as my husband pointed out. Continue reading

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Beyond Me: How Many More Will Suffer?

I am not the only person suffering from chronic Lyme disease. And chances are, I am not the only person you know who has it.

Have (or how have) you been touched by Lyme disease?

Perhaps you have a friend who has Lyme. Or a sibling, parent or child. Or multiple siblings or children. Perhaps you don’t know anyone personally, but have friends or relatives who do. Continue reading

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You Know You Have Fatigue When…

In high school French, I remember learning a lot of funny sounding words. My friend Rachel (Sylvie) and I created a list of favorite French words. At the top of my list was “raplapla,” an onomatopoeia meaning “worn out; tired; exhausted; fatigued.”

Over a decade later, I find it interesting that one of my favorite sounding French words has become the soundtrack of my life.  Continue reading

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So Let’s talk about symptoms

I have chronic Lyme disease, but I also have several Lyme co-infections and numerous other health complications because of these.

Because of the complexities of Lyme disease, and my own complex situation in particular, I tend to be rather vague when writing about my illness. There are so many topics to be covered, a vast number of subcategories within the category of Lyme disease.  Continue reading

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Change is in the air

The green tree leaves are changing to vibrant red hues. The air is crisp. (I could see my breath the other day.) As the sunny skies turn gray here in the Pacific Northwest, my mind turns to the changes ahead. With these atmospheric changes, there are changes in my health. Continue reading

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“What does Lyme feel like?” by Lori Dennis, MA,RP

I stumbled across the below post last week via a Facebook support group that I’m in (for people with Lyme disease).

I don’t read others’ Lyme stories, blogs or articles as often as I’d like – for many reasons. Why? I’m interrupted by my toddler. The pain from typing overwhelms. Or blurry vision sets in. (And the list goes on). Continue reading

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Why I don’t easily Trust Doctors

A little story. Or intelligent rant, as my husband puts it.

I had my blood drawn the other day. (Lucky me.) Upon exiting, I was given the choice of using tape versus a bandage to cover the blood. Ironically, I wasn’t given the choice of needle used for the procedure.  Continue reading

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Don’t mess with the sleeping baby

Have you ever been pulled over on a five-lane interstate with a sleeping baby in the back? I haven’t… until today.

Before this unfortunate encounter, I spent an entire two hours in my car, putting my toddler to sleep and then making sure he stayed asleep. He needed it bad. Continue reading

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