Hello again, and thanks Truthquester for the reply.
Well it appears that I have been introduced to Mr Herxheimer after all, but first a little history.
I am male 54 yr old, slim, fit and active.
Have suffered Ulcerative colitis for 8 years which has been somewhat dormant for 4 years but has never left my side although its currently now steering my life for me.
Have suffered atrial fibrillation for 16 years, I’ve had 5 radio frequency catheter ablations or pulmonary vein isolation (PVI) as they are called currently, all fruitless.
Drugs for AF have no effect whatsoever and I have a thick light coating on my tongue that nothing will remove.
So after 7 days of brushing my teeth and gums thoroughly, gargling as well to get some experience at mixing/handling etc, my tongue is now squeaky clean which is a very encouraging sign.
I am also applying the spray bottle technique to a dark spot on the base of my neck and another spot to my upper abdomen to see what may happen, all as per the formulas in the Health Recovery Manual, both of these processes performed morning and night for the full 7 days.
On the eighth day bang, very severe pain throughout the abdomen, also a not quite egg size lump like a blockage on the right hand side of the lower abdomen, thankfully gone now, vomiting, constipation, then diarrhea, chills, known joint pain much worse than ever before not to mention all the new pains throughout the body, including burning through the kidneys, peripheral vision very poor and body very weak, oddly enough no headache.
I’m not going to sugar coat it the pain was horrendous, I’ve had kidney stones twice before, the last was 2 months ago and the pain was right up there with them. My son can confirm this as he found me curled up and almost screaming from the pain.
This continued for 18 or so hours then the intensity began to fade. It is now 3 days after the incident and the pain through my abomen is still quite bad and penetrating through to my spine then spreading across the lower back to all of that kidney area on both sides and still have the chills, the pain is not constant but that surging gastro type of effect.
Needles to say I havent taken MMS since the morning of the incident and did take VIT C during the worst of it, I have come prepared. I normally suffer AF once a week or so for 10 to 12 hours, sometimes more but my heart has been in a AFIB virtually constantly since the episode which has made it all the more difficult although it has ceased as I am writing this, It appears my insides are in complete chaos.
Anyway, I am giving myself a 7 day rest from any MMS to try to get as close as possible to my usual poor health Ha Ha. I intend to then commence the starting protocol and work my way up as indicated although this time I think I will use the HCI as it may be more suitable to my UC difficulties. I will endeavour to update any worthy progress over the coming month.
I dont think I am seeking any advice unless something is obviously wrong, maybe just venting to others who understand my predicaments.
My family are very supportive also.
Regards
OtB