CD4 and VL trends post-MMS discontinuation

Hello All,

As some people are talking about their CD4 / VL, I thought it might be any useful to share my data in this forum.

It is interesting to see on the attached sheet how my CD4 and VL have been changing. Its pattern is quite like what some others had already talked in the forum.

I was almost killed by Pneumocystis pneumonia in 2007, and was taking ARV drugs since then.

My quick history of MMS is;

Started taking MMS2 (4caps/day) on May 20, 2011.

Switched to MMS1 (Protocol 1000) on May 27, 2011, but

gave up on MMS1 in a week due to severe diarrhea.

and resumed taking MMS2 only.

Stopped taking ARV drugs on Sep.27, 2011.

Started taking MMS1 (P1000+DMSO) on Oct.26, 2011 and continued it for 5 weeks.

I had persistent dry coughing for weeks, but no fever or any other painful symptoms. I was just as active as usual after all, but it was somewaht like reviewing the pneumonia in 2007.

Maybe MMS was detoxificating the antibiotics left in my lungs since 2007??

No MMS2 during this P1000.

After the 5 weeks, in early Dec.2011, resumed MMS2 (2caps/day) and reduced MMS1 (to 6drops/1x/day) through today.

(currently no DMSO added… my kitchen is too cold for DMSO and it is frozen )

It’s been about three months since I completed P1000, and my CD4 still keeps going down as low as 182, as of Feb.16 2012.

Although my doctor is worried I could pick the pneumonia again (my doctor knows I don’t take ARV anylonger), I feel much healthier as tense muscles in my back and neck are relaxed and skin condition is improved.

Now I’m hoping my CD4 count kicks back again anytime soon (and VL goes down), but also have a feeling that detoxfication of ARV and any other chems / metals in my body will take lot more time.

Any questions or advice are welcomed.

Thank you !

Taka