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Posted 2/28/2017 12:15 AM (GMT 0)
Since I didn't properly introduce myself (I just got right into it) here goes: (I'll sign each post with this so people can comment)

_________________________________________

IgG via IgeneX 31-IND, 41++, 58+
IgM via IgeneX 31+, 41-IND

HSV1, CMV (like most adults over 40 except mine are active and not asymptomatic)

current symptoms: night sweats, depression, insomnia, restless leg syndrome, sleep apnea, vascular pain in both armpits, multiple migrating neuropathic myalgias, tachychardia, high blood pressure, emotional lability irritability, sore spot on head

tick bite over 10 years ago with Erythema Migrans rash inner thigh mt. biking tick area
outdoorsy athletic person most of my life, likely have other co-infections just haven't found them all yet.

Post Edited (borrelioburgdorferii) : 2/28/2017 1:33:10 AM (GMT-7)

Posted 2/28/2017 12:29 AM (GMT 0)
Formal welcome bb....new to lyme ,lyme lingo thread etc etc ...
ya borrelia always brings buddies ..

consider rife ,bvt ,mhbot herbal adjucts ...
Posted 2/28/2017 1:12 AM (GMT 0)
band 58 is thought to be a European strain.

Band 31 is pretty much lyme specific (except for rarely cross-reacting with a few viruses)

You've got enough there to back up symptoms consistent with LD.
Posted 2/28/2017 2:32 AM (GMT 0)
Ha bluelyme I didn't get your humor until now, yeah Bb always brings 'friends'

Bee venom therapy is fascinating.

And Girlie I know right? I have more symptoms than I mentioned, had swollen joints, and I had a phantom ankle sprain that hurt just like I had rolled it during sports, totally lymey, stiff neck cracks all the time, and forget about the neuro problems I've had, brain fog, inordinate fatigue, do like 2 household chores then I'm totally exhausted. Looking normal on the outside but inside feel like warm garbage.

Schaller believes the 31 band is one of the "fingerprint bands". I have a website where I write about some of it when I have enough clarity and energy..

www.borreliaburgdorferi.space

I wanted to put all my best links there when I get the chance, it's still a work in progress.

Debating whether or not to get a Skype consult with an LLMD (for clinical research studies/doctor referrals, possibly disability worst case scenario) --seems like most who get SSI don't come off it, so it's like a loss of hope, a relief, or a commitment thing, I'm still ambitious and think I can self-treat it though.
Posted 2/28/2017 3:21 AM (GMT 0)
Looks like you got a good handle" on it ...
Posted 2/28/2017 3:58 AM (GMT 0)
Herpes 1 is not a lyme co-infection. It's something you already had, like most humans do.
Posted 2/28/2017 3:50 PM (GMT 0)
BB- you can go to your profile and create a signature line that will appear at the bottom of every post and put a link to your website in there.

Welcome! I'm so glad you found us. There are actually quite a few of us that self treat for numerous reasons.
Posted 2/28/2017 4:41 PM (GMT 0)
borrelioburgdorferii welcome!! I love your site.

here is one you should research - Unlocking Lyme by Dr. Rawls. This book is awesome and really works in conjunction with Buhner.

Just a thought for you.
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