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Specific Lyme Symptoms In People That Have Lyme


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if this is going to casue any type of controversy i am sorry i dont want to do that hopefully it wont/// i tend to ask alot of questions becasue i am interested in peoples expericenes with pots since i am new to this....my aunt diane lyme disease as well and she had severe joint pain fevers......i know lyme can cause pots and autonomic problems., my question is for those who actually have lyme disease....what were your main symptoms fromw hen you think you got lyme until you took antibiotics? for example FEVER? JOINT PAIN? TREMORS? i wanna see if they compare at all to the way i felt when i first got ill until now....again please dont think im starting another lyme issue im just curious after reading the recent lyme post

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