Finding YOUR way

If you or someone you love has Lyme disease, or chronic Lyme disease, you are probably very aware of how debilitating it can be both physically and mentally. And then there's all the confusion. The tests are vague. The "official" (CDC) take downplays everything. You don't actually look sick. The ones that do agree that… Continue reading Finding YOUR way

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Chronic Lyme pt9 – And the months went on…the other symptoms

Brain fog. Yep, I had that. It felt like “pregnancy brain,” only way worse. Sometimes it was embarrassing. I was so dingy! Sometimes it was frustrating. I couldn’t read anything. By the time I finished a page, I’d have to start over because I already forgot what I read. And sometimes it was dangerous. I… Continue reading Chronic Lyme pt9 – And the months went on…the other symptoms

Chronic Lyme pt8 – And the months went on…and there was pain

As generally easy as the treatment was, the months were not. My pain multiplied and escalated. I still experienced the strange “bone” pain, but it spread to other parts of my body to the point that there were days that I couldn’t even pinpoint where it hurt. It felt like everywhere. There were times when… Continue reading Chronic Lyme pt8 – And the months went on…and there was pain

Chronic Lyme pt7 – The rules and other annoyances

The treatment itself wasn’t horrible. Once I figured out timing, it was pretty streamlined and easy. But the rules were constant trouble. Don’t get the CVC entrance area wet. Any contaminated water getting inside the opening could cause a massive infection. At this point in my life, I was engaged and was growing out my… Continue reading Chronic Lyme pt7 – The rules and other annoyances