Tag Archives: late stage lyme disease

A New Year’s Letter to My Decade-Younger Self

Dear Self,

You think it’s pretty crazy that it’s already two-thousand-and-seven, don’t you? You wish you could have accomplished more in this last year, but you’re sitting down with pen and paper, eager to write out a full list of all the amazing things you want to accomplish in the new year.

After an hour of journaling right before bed, your hand writing at awkward angles as you use your pillow for a desk, you come up with something like this.
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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On Turning 30

I’m feeling older than I did a year ago. My body is less forgiving of simple, basic movements –turning to check my blind spot, putting my toddler into the baby carrier, standing on my feet for more than a minute…

I find myself quoting the words of King David: “How long, O Lord…?” 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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