Tag Archives: CDC

United for Medical Freedom

A woman stands with an umbrella, rain steadily dripping above her head. She holds a sign: “My child, my right.” Pushing a stroller with two young ones, she makes her way closer to the front to hear the speaker.

A man in overalls steps in place to keep warm. He grins as we catch eyes. Passion emits from the microphone, and he is the first to applause. 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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GoFundMe: Locked With Lyme Q&A

GoFundMe: Locked With Lyme Q&A

1. Tell me about the treatment you are undergoing: Who, what, where: when?
I will be traveling to Coeur d’Alene, ID to see Dr. Tony Smith for his LymeStop Program. I have three appointments spread over the course of almost one week (December 15-20).

Dr. Smith is an experienced healer, who specializes in chiropractics. He developed a unique way of treating Lyme using magnetic therapy. The magnets are used to trigger the body’s immune system to heal itself. 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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