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Finally, after five months of neurological symptoms the third Neurologist is going to treat me for lyme disease based on my CF result and presented symptoms. I have been given oral antibiotics and have been told IV will commence next week. My symptoms are light, sound, touch over-sensitivity. Tinnitus, burning skin. Body tremors and spasms. Loss of cognitive skills, eye movement, disassociation and insomnia. Has anybody had iv or oral medication? Did it stop any of your symptoms?
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