Michigan LYME Information

[Woods1977]

Hi Friends

[frenchmoxie]

Hi,

I’m in Michigan and have been looking for someone to help treat my Lyme/coinfections, so thank you for posting this information. Also, wondering if you’d be willing to private message me the name of doctor(s) you see in Michigan? Thank you so much!

[Woods1977]

Hi Frenchmoxie,

I sent you a reply- but it seems to be stuck in my “outbox”. Please let me know if you receive my response! Otherwise, feel free to reach me at woods_1977@yahoo.com

[lynnie_sydney]

woods, all – in this system all PM’s sit in the sender’s outbox until recipient picks them up – doesn’t mean they haven’t gone, just not been opened yet 😀

Be well! Lynnie

Palindromic RA 30 yrs (Chronic Lyme?)
Mino 2003-2008 100mg MWF - can no longer tolerate any tetracyclines
rotating abx protocol now. From Sep 2018 MWF - a.m. Augmentin Duo 440mg + 150mg Biaxsig (roxithromycin). p.m. Cefaclor (375mg) + Klacid 125mg + LDN 3mg + Annual Clindy IV's
Diet: no gluten, dairy, sulphites, low salicylates
Supps: 600mg N-AC BID, 1000mg Vit C, P5P 40mg, zinc picolinate 60mg, Lithium orotate 20mg, Magnesium Oil, Bio-identical hormones (DHEA + Prog + Estrog)

[Woods1977]

Thanks Lynnie! I didn’t know… I assumed it didn’t get sent. 🙂

[Author]

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