Time for a coffee enema

Yesterday was a bad day for me.  The brain fog and fatigue was quite debilitating.  I have also noticed that for the past couple of day, the minor cramp in my liver area has become more prominant.  I hope it is an indication of increased stress on the organ due to the need to remove toxins resulted from the Bionic 880 treatment.  If that is the case, it is no surprise that I am feeling as crappy as I was yesterday.

I'm boiling a pot of coffee as I'm typing now for my first coffee enema in a long time.  Generally I try to avoid coffee enemas because of the mess that it creates.  But I think my recent liver cramp warrants the hassle this time.  Hopefully that would help clear some of the toxins from my liver so I would be in a better shape for my Bionic treatment this afternoon. 

Day after my 4th Bionic treatment

Had my 4th Bionic treatment yesterday (3rd at 100%). Again, not much of an adverse reaction today, but I've learned to accept that this process will probably take longer than 6 sessions to clear the Lyme as common for people who visited Dr. W in Germany. As noted previously, this could be due to:

1. the lack of use of the live vials,
2. the use of the Desbio nosodes instead of the S-P nosodes that Dr. W uses, and
3. the lack of post-treatment support IVs.
   

I have, however, already made an appointment with my LLMD after my scheduled 6th Bionic treatment at 100%. I will see if the Bionic has made a dent in my Lyme infection at that time. If not (the possibility of which I am bracing myself for), I will continue the Bionic treatments using the S-P nosodes from Germany, which would remove one of the variables for keeping the treatments from working.

Patience needed?

Thanks to the comments from Sixgoofykids on my last post, I was reminded of the patience that I need in this treatment process. Six was under the care of Dr. W in Germany and learned from the horse's mouth that the treatment would take longer to work without the live borrelia vials that are used at Dr. W's clinic. Having heard that, I don't feel so bad that I didn't quite herx or improve as quickly as I had hoped. The "miracle cure" that I had in mind for the Bionic 880 wasn't so realistic an expectation after all, at least not without the live vials.

I guess I'll have to bug Lady X for longer than I previously anticipated. I can't emphasize enough on her graciousness.

This morning, I'm not feeling too bad. Brain fog is there but not too debilitating. My extremities were extremly cold throughout yesterday and last night, and I eventually went into a hot bath to bring my body temperature back up in the evening. I did feel a bit of a headache after the hot bath, which was not usual for me. Perhaps my immune system was working to kick some Lyme butts bugs?

The day after treatment

Today, the day after my 3rd treatment with the Bionic (2nd at 100% power), I have not noticed any significant worsening of symptoms.  My brain fog is just as usual (no improvement compared to pre-treatment).  As such, this deviates from my previous two treatments following which I had noticeable increase in symptom intensity.  

I do wish to report that for the last week or so, I have been having an abnormal sensation in my liver / right kidney area.  It is not unpleasant, but it rather feels like a minor cramp that is barely noticeable.  It also comes and goes, rather than being a constant sensation.  

I was tested positive energetically for Lyme affecting my liver, so I don't know if my body is going after the Lyme infection there and deal with the brain later.  Wishful thinking perhaps?  But it is not inconceivable that the body exercises such intelligence once the immune system is rectified by the photons.  

As it stands, I really don't know what to make out of the Bionic treatment thus far, but I'll definitely stick with it for at least 6 sessions at 100% power.  I have also made an appointment with my LLMD to get tested on his Vega machine for Lyme after the 6th treatment, so I'll know if the Bionic did anything for me at all even if I don't feel it.

I have ordered the Borrelia Burgdorferi nosodes from Staufen-Pharma today.   Those are the exact same nosodes that Dr. W uses for his patients in Germany.  I really should have ordered them before I started treatment on the Bionic, instead of using the Desbio ones; but I'm in a rush to get well so I dove right into it with the Desbio nosodes.  Anyway, if things don't improve after a few more treatments, I would consider switching to the S-P nosodes and see if they make a difference.  It is always good to have a Plan B.

Another thing that came to mind regarding the effectiveness of the treatment as I administered it would be the use of vials with live Borrelia samples by Dr. W on his patients in Germany.  That is the one thing that I don't have the luxury of having when administering the treatments on myself at Lady X's place.  Perhaps the lack of the live sample vial on the solar plexus would take the treatment longer to produce results?  

I am not going to quickly write off this treatment as another one that I fail to respond to.  After all, I have only really had 2 treatments so far with nosodes that are frankly less than ideal.  There are simply too many success stories from fellow Lyme sufferers who's been to Germany and came back Lyme-free.  This is the most promising treatment modality that I have come across yet, and I am not changing my opinion unless I have made sure I've done everything correctly as Dr. W would.  

It is an experiment with my own body to say the least.  But then again, isn't that true with so many other treatments that I have explored so far?  Salt/C, MMS, ozone, IRT, etc... So this process is not foreign to me in any way.

My 3rd Bionic 880 Treatment

Had my 3rd Bionic 880 treatment today; my 2nd at 100% power.  

Not much to report on the treatment itself, other than the fact that I have transferred my nosodes from my fat clear vials to skinnier ones that Lady X got from eBay.  The skinnier vials are similar in size to the original amber vials that the Desbio nosodes came in.  

The reason for the transfer is so the vials could all stay closer to the center of my body (at the solar plexus), rather than being spreaded out like a belt across the bottom of my chest.  Hopefully the treatment would work better that way.

I will see if my brain fog and other symptoms get worse tomorrow.  If so, that would be a clear pattern of the Bionic 880's effect after each treatment day so far.  

On another note, I received a Lyme disease wristband from Lady X today similar to this one:

I'll make sure I wear it if I ever go camping again to remind myself and others of the reality of Lyme disease out there.