AP 8 months = Feeling absolutely bloody awesome!!!

[Pauyen]

Hi Kathy,

– First suffered mild joint pain around Feb 2009, which only got more painful and affected more and more joints as time went on, used 3 – 8 Panadeine to get through each day.

– Massive swelling/mobility issues occurred approximately in July/August (One day the left knee just blew up the size of a volley ball, the right followed a few weeks later).

– Diagnosed in November 2009, put on prednisolone, then Celebrex and Plaquenil.

– Heard of AP around Aug/Sept 2010, started late in Jan 2011… (I see now it’s also at the 9 months mark when I started this thread, not 8 as the title says 😉 )

So about 2 years and 9 months… in the scheme of things…not really all that long I guess. Seemed like forever when in the middle of it all.

Cheers,

Paul

[lynnie_sydney]

I’m always curious about how folks that have had disease longer respond to the AP therapy.

Kathy – my symptoms started in 1987 and I started AP in 2003. My original testimonial from 2007 is here:

https://www.roadback.org/index.cfm/fuseaction/community.display/display_id/490.html

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)

[Author]

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