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Thank you very much. My wife is very familiar with the website.

My youngest sister had Lyme Disease in the late 1990s. Very, very ugly disease. She had Bell's Palsy in conjunction with the Lymes. It took months and months to get a diagnosis. She wore a continuous IV for a long time. The medicine it took to arrest the disease is literally poison.

She still suffers lingering effects.

[reformedliberal]

We call it Lyme’s Fog. The people we know who have a relapsing/remitting form of it do suffer long term cognitive deficit.