Layers of Lyme- Down to my Mycoplasma

Hey guys,

It's been a while since I have posted. I am doing really well and wanted to share my experience for Mycoplasma and how I am doing with it.

I think of Chronic Lyme as layers. First I treated for Babesia and Lyme, then Bart and Lyme and though still on treatments for these I am happy to report that I am much better (normal emotions, cognition, no Bart numbness or pains), but now experiencing Mycoplasma- which I think will be my most challenging- (if that is possible to say).

I am pretty sure that I grew up with partially treated Lyme and suffered chronic immune impairment with recurring colds, sinusitis, bronchitis- which always responded to Biazin or Azityhromycin.

In 2003 I self diagnosed myself with Lyme (pos Western Blosts) and chronic Mycoplasma. I became miraculously immune competent treating myself with Samento, which I took for 4 years. Until being bit in 2007.

Now I have been on treatment for one year- and only symptoms remaining are fatigue and Mycoplasma (recurring chest infections). It is frustrating to be facing this again but I am determined to rid myself of the recurring infections.

I have improved using Azithromycin and Doxycycline. I was told that these 2 should be used together for chronic Mycoplasma. It is working so far-- but am looking for other protocols. I am determined to get beyond this.........?Lymecycline ?Cipro

I recently had all of my amalgams removed (which improved my dental pain and cognitive/emotional symptoms). Now I am thinking of doing a biofilm protocol.

I am planning to see Dr J (SC) before taking my PICC line out......any way any of you with similar problems? Success with chronic Mycoplasma?