How do you figure out which symptom goes to which infection ?

All the symptoms are almost the same for Lyme, Bartenella, Babesia, Yeast infection, and Mycoplsma, all of which I either Have or probably have going by symptom lists. Lyme ,Mycoplasma, and yeast showed up on tests but some symptoms get better with certain treatments. Bartenella treatments seem to help pain in feet and legs. so figure that is from Bart. Started babesia treatment and than had to stop because didn't have money for all supplements I needed last pay day and Babesia was 40 dollars so went with out for two weeks and some symptoms got worse like sweats and stomach pain and chills so think that my be babesia.

Trying to figure out what to treat and which supplements are necessary is very difficult for me . I also can not tell If I'm having new symptoms, flair, Herx , reaction to supplements, allergy to some thing. How does everyone deal with all this. My doctor isn't even sure what is going on. Not llmd But lyme friendly and has other patients with lyme, but not one who has been sick for as long as me. they are trying to help since I can not get to or afford a llmd. I'm on my own for much of this. They give me almost any med I ask about or any test I ask for. They won't treat for Babesia because test came back negative twice. But they will treat for Bartenella because the drugs are just bacterial infection drugs and they can issue me these because I am showing bacterial infections on test. I'm completely on my own with babesia for now.

I found this helpful
http://www.lyme-symptoms.com/LymeCoinfectionChart.html

It's from the New to Lyme section. Note that for each infection you need to scroll past all the infections to see the second half of the symptoms for each infection. They start again alphabetically.

That's why you need a protocol like the one I'm on. Because who knows what they've accumulated over the years and, yes, the symptoms do overlap.

No, no $$$.

It's just the way I am. I'll never forget when I first joined healingwell 3 years ago. I was so excited about finally finding the root cause of my 'ms' I wanted to share with the ms forum.....well, after 3 posts I started getting emails from moderators and not nice responses from the ms mod..... Telling me to stay in the Lyme forum and off the ms one!

That didn't feel right to me. Why? Because if I'd have known about Lyme I wouldn't have had to suffer for 9 years with a misdiagnoses and my life would be totally different now. I was only trying to help and it just seems like people should be given options/facts and they can make their own decisions on how to proceed.

Bottom line....I don't want people to suffer because I know how that feels and I'm feeling better and want them to feel better too :)

you can always follow buhners protocol for babesia...