Posted 7/13/2019 1:56 AM (GMT 0)
Hi everyone, I'm new to the forum and to the LD world. Just a little background... I had been reading a lot about Lyme in my research around my hypothyroid disorder and adrenal fatigue I developed after my son was born Oct 2014. I believe my hypo started Sep 2016, and I was diagnosed Jun 2018. In Sep 2018 I found out about my underlying low cortisol and low iron (amongst other low nutrients) and bottom line had to begin healing my adrenals (with Adrenal Cortex and other supplements) before I could up my T3 medication to where I now DON'T have fatigue, low temps, brain fog, etc. During that time of my online research I was running into info about Lyme and sending it to my friend with MS and my friend with Fibromyalgia.
Ironically, on Mon 6/17/19 I started to develop a rash around a lesion on my chest. Just 2 days prior I had been at a park here in the Atlanta area, and my son and I had been pulling down some low-hanging Kudzu (invasive Asian vine that chokes out native trees.) In hindsight that wasn't a great idea. As the rash grew over the next couple of days and was circular (with no central clearing) I knew not to mess with that and contacted a local LLMD (that I got from ILADS) and was in her office on Mon 6/24, one week after the rash started to develop. She wanted to start with Western Blot through LabCorp, as well as Mycoplasma IgG/IgM and Rocky Mountain Spotted Fever IgM. That blood draw was the next day Tue 6/25.
Two weeks later on Thu 7/11 I was back in her office for my results. I had 1 band: IgM band 23. My understanding from this and another forum is 23 is indicative of Lyme. But she said not only do we not know what strain (of Borrelia?) it is, nor which co-infections I might have, but also that there are different "most effective" treatments for each. She also said this bite/rash might not be when I actually got the infection and that there isn't a particular timeframe when IgM turns to IgG... some people can have IgM for a long time she said.
Let me stress that I have had NO symptoms besides the rash since getting the rash and being in that park. She said she could start treating me right away (I think with Doxy), but of course I would need retesting to see if it's working... because I have no symptoms. She does use IgeneX, but it's not her first choice anymore after getting one or more false negatives with them. After learning first hand (at a seminar by the founder) about Armin Labs in Germany and their multi-pronged testing, including the EliSpot, she now recommends that as the premier testing in the world. It shows you exactly which strain(s) you have and the coinfections. From their website: "In the complexity of tick-borne and opportunistic infections, we are specialized in T-cellular tests (EliSpot), B-cellular tests (IgA, IgM and IgG-antibodies), and NK cell tests (CD57, CD56) for several bacterial, viral, parasitic, and fungal infections." It is pricey for the comprehensive test (basically checking all the boxes.) I'm not sure how much cheaper it may be if you order it directly from Armin, but I just assume have her guidance, the phlebotomist she uses to insure it gets to Germany (following all instructions), her interpretation and her recommended treatment.
This is what is making me nervous... am I waiting too long for treatment?? My blood draw for Armin will be Wed 7/17, and at the moment I have no idea how long it will take to get the results, although from another forum post I don't think it will be too long. (I will ask my doctor when I pick up the kit on Mon.) On the one hand I want to know what infection(s) I have before messing that up with antibiotics, but on the other hand I'm starting to worry I'm missing my window for potentially being cured of it before it takes hold in my body. Any thoughts?