NanaDubo
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Member # 14794
posted
If everyone on this site has or had lyme, why would you be surprised that we all have a similar toxic load?
I think this is what sets the terrain enabling us to become so ill in the first place. Lyme is only a small part of it.
Syphillis and TB are miasms - inherited from who knows how long ago. The memory stored in DNA (not active disease in my understanding).
I suspect that like Scott, I may be looking at being finished up soon. I feel pretty normal these days. Hope it keeps up.
For a therapy/protocol/remedy that can go on up to a year - $500 and change is minuscule compared to many or most other things I've come across.
This one requires patience, patience, more patience and a big dollup of more patience. These people are working very, very hard for a small amount of money.
Posts: 1129 | From Maine | Registered: Feb 2008
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seekhelp
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Member # 15067
posted
Nana, did you have as many blockages as me when first starting?
Sometimes what's hard to assess is I recall you're doing 10,000,000 other treatment types in addition to AI, along with others like Scott F, Alv, and others. It's so hard to isolate a cause and effect when so many variables come into play.
I agree $500 in the big picture isn't that much compared to what most of us spent to get here. However, $500 times the number of failures, ripoffs, and more is hard to digest. It's frustrating to mentally feel conned at times, especially in front of family as the sick sucker who'll buy anything.
The worst part is it's $500 for a bottle of WATER. lol. My wife would want 25 cases of water for that price bottled. Paying for water is a crazy, crazy notion. lol.
Posts: 7545 | From The 5th Dimension - The Twilight Zone | Registered: Mar 2008
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NanaDubo
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Member # 14794
posted
Oh yes indeed.
Posts: 1129 | From Maine | Registered: Feb 2008
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NanaDubo
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posted
You will Ping!!
Seekhelp - I did NOT do 10,000,000 other treatments - actually there's quite a short list if you would like to have it.
And would you be the one to tell someone which stones not to overturn when wanting to get well?
Pretty big job.
Posts: 1129 | From Maine | Registered: Feb 2008
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seekhelp
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posted
I'm sorry, I must be mixing you up with someone else Nana. I was just throwing out the 10 million as humor. Sorry. I can't keep it all straight. I'd love to hear what you do to get/stay well as I always carefully watch those who hit remission as I'd love to be there too.
Of course, I would never tell someone what not to do. I can only speak from my personal viewpoint. With Lyme, or any other chronic illness, one can always fear it coming back, never feel they achieved perfect health, etc.
Sometimes, I just have a hard time understanding how much people put into this stuff with respect to supplements, alternative treatments, etc. when I hear they are doing quite well and decide to try another thing anyways. I think there's a point of diminishing returns. Do you drop $10k wondering if you can get from 97% health to 98%? Know what I mean? When you're at 5-10% health, cost becomes irrelevant. You're desparate.
I look at the big picture when making decisions.
Posts: 7545 | From The 5th Dimension - The Twilight Zone | Registered: Mar 2008
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SForsgren
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posted
Agree with NanaDubo. It's an inexpensive treatment.
If people are not sure it is right for them, don't do it. It makes no sense to start a new therapy when you don't believe it can help. That truly is a waste of money.
As for people seeing similar results, that isn't a surprise. We are all toxic. I have seen differences in results and the # of miasms in particular seems to correlate highly to how ill the person is in the ones I have seen.
-------------------- Be well, Scott Posts: 4617 | From San Jose, CA | Registered: Jul 2005
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posted
I guess my issue is that I have tried SO many treatments and I am still as sick as I was when I started 2 years ago... SO yes, you become frustrated, untrustworthy, and tired of it all...
I am not saying that I don't think it COULD work... but just that at this point in the game I don't know what I believe in anymore or what is ever REALLY wrong with me. I go to one of the TOP LLMD's...
So I guess I have put sort of a protective wall up... But only because I have been so let down.
-------------------- "You'll be surprised to know how far you can go from the point you thought it was the end" Posts: 946 | From Massachusetts | Registered: Apr 2008
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There is no way I could get 7 yrs of continuous antibiotics where I live and I don't have a boatload of money to come to the States where I would have no insurance. So I don't even want to get into the pathetic treatment available in Canada where they won't even accept a positive lyme test from the States.
Even if I could, there's no guarantee I would be recovered at the end of it, as some posting on lymenet have complained about has been the outcome for them.
Ping, you are fortunate if you feel you have recovered. Maybe AI can help improve your health even further, keep us posted.
Posts: 590 | From Canada | Registered: Oct 2007
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posted
I tried abx for about 6 months with an LLMD and I also did 6 months of the HORRID Marshall Protocol...
The 6 months on LLMD abx I had A lot of issues, constant yeast infections that would not go away with ANY measures, Organs felt weak, And a VERY close case of C-diff which I had to stop abx for 2 weeks.. It was not fun what was happening to me at THAT point but I don't want to get too graphic. I also became extremely suicidal because of the meds and lack of any sort of change or herx or improvement to show me something was happening.
At that point my LLMD's PA didn't know what to do with me.. and basically said that I needed IV but KNEW that my insurance didn't cover it and that I coudln't AFFORD it on my own. From that point I decided to stop ALL pharmacueticals and abx and started eating raw foods, juciing and taking herbs. From that I DID have some kind of imprvement... meaning I was no longer completely bedridden, I could walk myself to the bathroom and even got out of the house a couple of times.. Which I hadn;t done it 2 years.
I have started to get back to that point of being bedridden again all the time.. I am back seeing my LLMD but I STILL was NOT put on ABX because of what happened last time with my lack of respose and other problems.
I am also seeing an LLND who is trying to strenghen my body and systems and also has me on low doses of herbs.. Androgrpahis and Zhangs art... along with some nasty teas and homeopathy.
I see my LLMD in July.. It is the 1st time in a year taht I will have seen him as I ALWAYS saw the PA... He will probably want me on ABX but I don't think it is the ANSWER... not for someone who has been sick for as long as me... maybe if this was caught years ago.. I also do not think I have JUST lyme.. I think there are toxins, chemicals, mold and other issues that make my symptom picture so severe.
I intuitvely feel that ABX may not be the answer... at least not for the 3-4 years you speak of. I would do them if my Doc said... YOU NEED THEM OR ELSE... but I just dont think it is THE answer.
I have been to 3 different LLMD's... and of course as many of you may have experienced... MANY other doctors, practioners, healers, YOU NAME IT... I am SPENT!
And you are absolutely right Sfrosgren.... GIVING UP IS NOT AN OPTION.. I have two children and a Man I love dearly that has stayed by my side and sacrifced EVERYTHING to be here to take care of me... I would never give up. (even though sometimes it is hard and you want to)
Peace & Blessings to all of you, that we find the answers we are so despertaely seeking
(Sorry for spelling mistakes..)
-------------------- "You'll be surprised to know how far you can go from the point you thought it was the end" Posts: 946 | From Massachusetts | Registered: Apr 2008
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posted
Like I had said in previous post I am probaly one of the sickest here doing A1 . I have been diagnosed with M.S. 17 years and years later finaly was tested for Lyme +( Im in a wheelchair most of the time, I can walk short distance poorly with a walker due to horrible balance. I am doing no other therapy although I have tried countless over the years.I have been doing the A1 for three rounds now and while no, I am not up and running yet, 20 years or so of ezxema is finaly gone and my fingernails that never in my life grew this great I all contribute to A1. So for those two things alone I think the money has been woth it. Terri
Posts: 203 | From tipp city oh.45371 | Registered: Jul 2003
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posted
I think the results (slow but sure) of the guys who have been on it a few months seem promising. Is it the cureall? Hopefully just a missing link.
I cou'dn't cut and paste my test results but:
But Dysfuctions (red and yelows) in everything but 2.3.
No milk allergy showing (untrue I believe), Soy, wheat, gluten, Corn, all top 3 penicillins, botom 4 mucums, Lead, copper, mercury, nickle
9.1 =6, 9.2 + 9,
B;ocks in Sacrum and cocyx - this is really where I do have pain!
Pineal, Throid, Pancreas. Shocked that my tired adrenals showed fine. Enzymes.
bottom 3 gentic toxins. No other bac or virsus.
Posts: 462 | From Newnan, GA | Registered: Aug 2004
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seekhelp
Frequent Contributor (5K+ posts)
Member # 15067
posted
Hobokinite, that's a mirror of my report basically. Odd. THe spinal blockages are different a bit, but they have a symptom list so they can change it accordingly hypothetically. The impossible to detect items on a symptom list are showing up identical.
Scott, the idea you have to believe in a treatment to work is simply not true if it works. Tell a person going into allergic shock they are getting an epipen injection. If they don't 'believe' in it working, will it not?
I'm not saying attitude doesn't play a big part in health and recovery, but it's the not the end all be all.
I just wants facts, stats, other people's results, progress on therapy and hard data when making decisions. We are all sick obviously, but I'd expect you have to have many less blockages/issues when you're functioning at 95% most days, able to travel, and other normal activities compared to others here bedbound w/serious neuro issues. That's just common sense.
Posts: 7545 | From The 5th Dimension - The Twilight Zone | Registered: Mar 2008
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SForsgren
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posted
Hard data does not exist for every possible beneficial treatment. If someone is looking for absolute proof that AI works, it probably makes more sense to look for other treatment options where this proof exists - though I am not aware of too many of those when it comes to this disease.
As for my own AI, I showed just as many issues as others. I've still got road to travel. Am at about 80% compared to where I have been. And, I've been there in bed with serious neuro issues. Fortunately, that is not currently my reality.
Years ago, I learned that there are three key parts to this illness:
1) Toxins 2) Infections 3) Emotional trauma and conflicts
I think it is only when we incorporate work on all of these areas that we can get well. A focus on any one or any two alone often disappoints.
-------------------- Be well, Scott Posts: 4617 | From San Jose, CA | Registered: Jul 2005
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posted
I believe Scott's list is correct. I ahve been working on #3 for a long time now with prayer and counceling and stress reduction.
Posts: 462 | From Newnan, GA | Registered: Aug 2004
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lymeparfait
Unregistered
posted
Balance in all things is key.
I agree about the three parts, and while on AI, there is no way to avoid dealing with all three.
Everything comes to the surface, literally.
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lymeparfait
Unregistered
posted
Could anyone please go over their eye symptoms again. Anyone have twitching and trouble focusing on reading while on the drops? Daughter says her eyes twitch from side to side...not the eyelid twitches. This is new.
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ukcarry
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posted
I posted bit about my test results earlier in the thread; they are very close to Hobokinite's, eg:
Dysfunctions, exactly the same [ie all except 2.3]
Same food allergies and metals, penicillins, but one fewer mucor
9.1=6 9.2=9 [same]
Spinal blocks in 5of 6 areas [not Atlas]
Same gland dyxfunctions,ie pineal, thyroid, pancreas and enzyme too.
All 4 genetic toxins
I know it is hard not to be too suspicious of new treatments, especially when you've been losing money in lost wages and spending it like there's no tomorrow on trying to get well.
I waited a while to see what pioneering AIers reported for that reason, but I think it makes sense that we have similar results, as we share a similar illness status!
The cost of this is not prohibitive and AI have nothing to gain from sending out more and more drops, as the on-off price includes everything except postage.
I do understand too about hopes being dashed when you invest hope as well as cash in a therapy.
Yes, it's a gamble as to whether it will help, but as Scott says, if you're not getting better on your current protocol, you can only accept the status quo or try something else.
NanaDubo
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Member # 14794
posted
Lymeparfait - can't speak of the eyes specifically except they have been a source of discharging for me throughout this.
I did have the twitching thing back when I was on round three but it was my lip.
It started twitching (not visibly) the first day of round 3 and continued for two days pretty much non-stop. That was the end of it.
Posts: 1129 | From Maine | Registered: Feb 2008
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NanaDubo
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posted
Ping, one first remedy froze in my mail box and they said it was fine. Heat may be different, I'm not sure. Maybe a quick email to them?
Posts: 1129 | From Maine | Registered: Feb 2008
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lymeparfait
Unregistered
posted
I asked the same type of question about:
Heat Length of time between taking treatment vials xrays
And they said the water retains the energy information no matter the heat, the length of time, and the xrays and heat do not damage it.
I do think if heated too much, it would evaporate.
But they said, the information does not leave the water.
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GiGi
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Member # 259
posted
Posted by Seekhelp:
"I just wants facts, stats, other people's results, progress on therapy and hard data when making decisions. We are all sick obviously, but I'd expect you have to have many less blockages/issues when you're functioning at 95% most days, able to travel, and other normal activities compared to others here bedbound w/serious neuro issues. That's just common sense."
No, it is not just common sense. A friend of mine, fully functional like many people you see walking around when people watching, a little leg swing here, bad dull hair, acne blooming, overweight, old and fat, all these people already have a manifestation of things not right. You don't have to be in bed. I was hardly ever in bed because I had enormous will power to stay afloat. My friend came up with more than 30 dysfunctions (red x's and red numbers - not the graph charts) From all appearances, there is not a thing wrong with her.
It may surprise you that I have not had active Lyme Disease in over five years until I made the one stupid mistake - i.e. put the Bionic to my body setting off an avalanche of problems that nearly drove me out of my mind. Yet amazingly, I still came up with 25 errors on the first AI test. I expected that I would have a few dysregulations, but 25 --- never.
My husband who is since Bionic treatment unable to walk, while he was able to before the Bionic, and does not have Lyme any longer and was always borderline Lyme and questionable, still showed 33 errors on the first AI test. He never had any problems except movement disorders. No pain - can't move.
Many many further dysregulations are still found every time we test, following these first tests: They are identified as chemicals and similar substances. But the major findings are the blockages, the errors in the nervous system, the emotional blockades, and most of all the damage caused silently by the wheat to the overall system, the damage caused to the Autonomic Nervous System (ANS), synapses and all the different systems broken down that you find listed from 7 to 14.
A major impact is from the inherited toxins/miasms on 14.1 and from the inherited psychoenergetic conflicts. And of major importance 9.1, the Unresolved conflicts of present life. My husband had 3 of the miasms - I had none. I also had no food allergies.
I know that miasms under 14.1 are red flags that they find in the most serious diseases (not Lyme). It's wise to no longer have to deal with them. These are already recognized in the DNA right after birth, even before actual diseases manifest themselves.
Our son, who is on bottle #4 now, just dropped by and told us that this one is hitting him hard. So, thank God, it's working. I am just holding my breath to get all children, their wives and grandchildren on this.. Every grandchild has one or more allergies already. A hidden allergy can turn into a disaster in few years.
As I suggested a few weeks ago, it might help people to get a better understanding that this is not a scam and that it does work if you order the study which they published. It is a study on approx. 200 people that goes back to 2005 showing the results broken down by problem, male, female. Since it has very little English text on it, you can easily understand it by just looking up a few words in a dictionary.
I just would like to tell you that with the pharma at the watch, anybody making false propaganda as some of you suggest, people doing this would have one foot in jail. They very clearly explain who they are and what they do. They also recommend that a practitioner should be consulted. I would post the one study I have here, but it does not copy as clearly as the original they can send you by e-mail. I posted pieces of it a week or so ago.
If you cannot trust AI - please do not go into it. There are many moments where not much is happening and where you wonder - what now?; but there are many moments, all too many for us, where I absolutely understand that many changes are taking place.
The problem arises with the fact that the errors in the system, as they call it, are found in different layers. If all the errors were to appear at once in the same layer, most likely the body would not be in a position to respond to them and to compensate for them. That means then - they have to work through layer after layer which makes for the different bottles with new information.
At the moment they are working on my husband's balance problems - he falls out of the chair and cannot adjust himself --. While they are adjusting that error, another one that had been corrected now has gone worse and one feels everything is getting worse. It is literally section after section, bit by bit they have to work through, and it is up to the client to learn enough about the system to understand how and why and then to stick with it until nothing to correct can be found any longer. Of course, a dead body part is a dead body part. I am not expecting that in an 83 year old man everything can be fixed. As long as the basics are good, we are doing drops until they now longer find anything. Even a 3/4 life is better than that none. We still try to enjoy the day, the grandkids, the daily events and are thankful that we still have each other. We have not a thing to loose. With the changes that have already happened to me and my husband, cost is negligible.
At that point, when they no longer can find any errors in the system, the body should be fully regulating and can then start to take care of the backlog. The immune system can step in and finally direct the concert again -- something it was not able to do with an energetic base, DNA, messed up and gone haywire. Then all values shown on the first test should start to improve further and further. I am sure it will take time.
Looking at my own regulation pathways, they find an enormous chaos, because the system often went zig zag wrong direction when it had no other choice. I had 12 root canals that were constantly contaminating my body.
AI are not against taking medication when necessary. But If medicines are being taken all the time, the body is likely to continue running into the same errors, the same tracks, suggesting that everything is in order to make more of the same errors --often the ones that brought about the dysregulations in the first place. The system is being derailed - again and again.
If this note sounds disjointed, please note that I read and type here and there while doing a thousand other things in between. So please take it as is.
Take care.
Posts: 9834 | From Washington State | Registered: Oct 2000
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lymeparfait
Unregistered
posted
I was the one that had a "no", response for awhile, when wanting to begin.
The testing I used was ART with a ND. It is your own body energy that communicates. It is within and also as explained to me, in the energy field, light, outside your body. Where your long term memory is also believed to be stored.
It depends on how your phrase the questions. The therapy was always a "yes" when asked if it was good for my body. It could have meant that water was good for my body...it is a general statement.
You have to get good at phrasing the statements to get at the root of what you are searching for. And your regulation needs to be open to get the best response. Many on lymenet have helped me learn about this. I am still beginning.
I suggest you spend time on learning about this before beginning the drops. It will give you confidence in your intuition when you understand this and your body better energetically.
The "no" answer was when stating the AI therapy is beneficial for my body today. That my body would benefit in regulation with the therapy. I waited until I received the yes.Usually I go full steam ahead...but I waited.
There is always a reason for the no. It may even be an emotional reason. This is something for you to investigate. It was new to me, but amazing.
My ND had a strong intuitive feeling that I was harboring anger against someone. This was the day I had my no response as well. She left the room, and said to think about who this was and we will release it...
Well, after a minute, not feeling anger with anyone, I realized, I was actually angry at lyme disease and the whole nightmare it created in my life, and feeling like my life has been taken away. That my husband has lost his wife, and my kids have lost their happy and active mom. I was angry! But never verbalized it or realized it until that moment.
I was also trying to find the cure...the answer...and not stopping to enjoy anything until I had saved my family and myself from the terror of this disease. I was spending way too much time researching online. I was over the top.
This was an overwhelming emotional response and experience. She helped me release this anger, and my healing started to escalate at that time. I let it go. I have worked on other spiritual and emotional things since then, and have been healing physically with that release.
The AI therapy has even brought more of this out. And now I am more relazed, bu just dong this one therapy. (And not obsessively being on line.)
There were other things that were a yes on that day for me. Specifically chorella, and taking the KPU test. For me, at that time, I had just taken out my amalgam fillings, and my body was adjusting, along with moving out candida.
The KPU test proved I had kryptopyorria, and we began therapy. Since then I have gone off that therapy, (another whole story), but am doing the AI alone, until complete before beginning the KPU therapy, if needed after the AI.
It appears the my KPU may be cleared with the AI. That is to be seen. But I feel like my detox pathways are opening.
I also now have a biotenser that confirms for me what is right at any given time. It all is about how to phrase the statements. I rephrase my statements many times to make sure I get the correct yes or no. When I am lazy and only ask one way, I may get the wrong direction.
This takes practice. For important new tretments, I will always get tested with ART by a ND to confirm.
I use the biotenser for general things related to doses, and timing and extra needs.
I also test how many drops each of the three times of day. Also test when to take my next dose.
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lymeparfait
Unregistered
posted
Ping, Look for a pm...
Just ordered AI therapy for my other child without lyme symptoms...as I want both my kids to clear disregulations before they have a chance to pass them onto their unborn children...
That's how much I think this is working.
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GiGi
Frequent Contributor (5K+ posts)
Member # 259
posted
I mailed AI this morning re hot weather/drops. They wrote back --
Hallo Frau Gilberg,
ich glaube nicht, dass die Hitze einen Einflu� hat. Im letzten Jahr hatten wir viele Fl�schchen nach Italien, Ungarn, Jugoslavien und und und gesandt, wo es auch extrem hei� war. Niemand hat etwas beanstandet. Die Wirkung war auch vorhanden.
Gru�
Translated - this says, that they do not believe heat has an influence. Last year, they mailed many bottles to Italy, Hungary, Jugoslavia and and and, where it was also extremely hot. Nobody complained and the drops were effective.
Just a question: How can they savely deliver anything (besides paper) if they do not have some way of cooling systems in their vehicles?
You guys seem to worry way toooooo much. Relax and enjoy your day ---
Posts: 9834 | From Washington State | Registered: Oct 2000
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GiGi
Frequent Contributor (5K+ posts)
Member # 259
posted
Just a few thoughts:
"GiGi advised that it would be best to have amalgam removal after A.I."
I am sure that is not the only thing I said, and anyone looking at this sentence only, will misinterpret my comments on amalgams. Certainly I would not do the removal now, if I thought I needed to remove them to get better.
Some people are of the opinion that when the regulation is again up and running and the body recognizes all toxins, including toxic heavy metals, one may not need to remove amalgams. I do not know and I certainly do not want to make a blanket statement about AI and amalgam.
Dr. W. told me, also in writing, more than once, "biophotons take the metals out" . Heck no, they don't, not if the body does not recognize mercury as a toxin or others having a toxic effect. This belief and trust is what got my husband into worse troubles - we moved more metals into the sensitive places/CNS and he rapidly deteriorated to the point where he could no longer walk. Period.
One should not attempt to detox unless sure the immune system is not dysfunctional and can take on the task. In my opinion, many herxheimers during abx is nothing but shaking the toxic tree and trying to find a new spot to deposit the stuff. I am sure that's why symptoms continue and continue - neurotoxin symptoms in my mind cannot cannot be differentiated - to me they felt the same no matter what we were dislodging or whether we were killing this or that infection. After all, they are all hanging out in the same terrain.
I would not at this point attempt to move or kill any neurotoxins until we clear all errors. At that point, it is my belief that we will have an able body that can deal with the toxins much more readily. It took me a while to learn from Dr. K. that it is not the bugs that cause us the problems, but the dead debris and the neurotoxins they leave in the body. There are thousands of them.......
This is how I feel --- all of you may feel differently.
Posts: 9834 | From Washington State | Registered: Oct 2000
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Someone wrote a while back that they couldn't get the drops out of the bottle. You have to pierce the top of the spout (underneath the white cover) with a needle or pin.
---- Most said they were taking the drops directly into the mouth -- 5 drops 3x a day. Someone added drops to a little water. ----
You take homeopathics away from food, I'm thinking that would apply to this as well, but don't know for sure.
Posts: 590 | From Canada | Registered: Oct 2007
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posted
Yup, having a real histimine reaction to the drops. YARGGGGG
Posts: 462 | From Newnan, GA | Registered: Aug 2004
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GiGi
Frequent Contributor (5K+ posts)
Member # 259
posted
the tip of the bottle can be cut off with a sharp knife or razorblade - just about 1-2 mm or 1/16 ". I put the 5 drops in a small tiny glass and put a teeny bit of water in it - a teaspoon full is plenty. Then drink it. I am afraid to put them directly in the mouth - because more is definitely not better. You do not have to do the absorbing bit as with a homeopathic - it is not a homeopathic. It has no relation whatsoever to homeopathy - so I was recently told. A young man drank out the whole bottle one time and he slept the whole day! Sometimes if the reactions are too strong, nothing wrong with taking less. Like whispering the information to the body! Our times vary - sometimes before eating, somtimes in between. Sometimes after. If I took them too late before going to bed on the first couple of bottles, they would keep me awake. Just sort of an even distribution 3 times during the day. I never tasted anything but water.
That's the best part about it - what is easier to take than 5 drops of water?
We bless the drops as we take them. It's our ritual.
Hobo, the drops are totally fitted to your body, specifically. So I don't think they would send you anything you are allergic to. Let us know how you feel after a couple days. I definitely mark the bottles clearly, because my husband's definitely do not test energetically on me.
Enjoy the drops. They will work for you.
Posts: 9834 | From Washington State | Registered: Oct 2000
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posted
I must be a klutz or paranoid or both. I opened the tip witha pin. Pin was new in a package that I must have had for a whie. Then I notioced the pin looked dirty or discolored so I'm worrying that I ruined the batch.
Someone send for the straightjacket.
Posts: 462 | From Newnan, GA | Registered: Aug 2004
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ukcarry
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Member # 18147
posted
If you think you've been silly, Hobok.....I actually cut the tip off the protective cap this morning!
It's going to take a while for my heart symptoms and thyroid imbalance to improve, so I decided to try starting the drops, on the basis that I could stop if they made things worse......so far I'm doing a lot of swallowing.
So you and I are starting on the same day, Hobok! Good luck!
posted
What I thoughtw as an allergy seems to have lessened.
No idea if it is the heat/weather or the AI, but I am having tons of joint and muscke pain since starting it.
Blessing the drops and anything you put in your mouth seems a good idea.
Perhaps praying and commanding healing to all of our bodiues 3X a day is too. Says the guy who just overslept and missed chruch today.
Posts: 462 | From Newnan, GA | Registered: Aug 2004
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Any diea if AI has helped people with EI sesnativites or even EMF sensativities?
Thanks and blessings,
Michael
Posts: 462 | From Newnan, GA | Registered: Aug 2004
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GiGi
Frequent Contributor (5K+ posts)
Member # 259
posted
Hobo, what's EI!
There is hardly a chronically ill person today who does not have an EMF problem. I think the number is zero. I was at a Klinghardt seminar yesterday, and it is again and again the same story - toxins including EMF's starting with children to the oldies. The metal content in our body combined with the chemicals is simply too high in everybody with a chronic disease. If you add the infections into the equation, we don't need to wonder why we are sick.
AI addresses everything connected with chronic disease and is helping. Some may need more work later, some may not. It depends on the individual make-up. There is nobody on this board who does not have a half dozen other problems besides a Lyme infection.
We need to learn to relax and flow with this therapy. Foremost - because everything starts with the first thought. Good or bad biochemical reactions become second. And some may need 1-2 years, and some are great in a few months. Lifestyle and thought play a big if not only role. That is my take on it.
Take care.
Posts: 9834 | From Washington State | Registered: Oct 2000
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lymeparfait
Unregistered
posted
Carry,
I had the candida white tongue, and major candida on my gums...like cottage cheese stuck there.
Had to use a water pic power washing device to remove it.
don't know if it was the AI, as it happened at the time I started the AI, but had also just removed a metal amalgam, and had been detoxing for that purpose...so it's hard to tell.
Also, Hobo...I have had a major pain behind my right knee, at the beginning of round 3, chemicals. Never had a knee problem in that knee before, but had only one in my left knee for years. It was extremely painful for the two weeks of round 3.
I recently added a natural anti-inflamitory, Curcumen "enhanca"...and it helped the pain ease up in one day. Sprinkled it on my food two times a day, and after two days, the pain is gone, but still have swelling behind the knee.
Again, I don't know if it is AI related, but so glad others are sharing their symptoms so we can all compare. I am hoping it is AI, and things are just regulating...not escalating!
posted
Gigiu, EI means enviornemntal illness - super senative to chemicals, smells, etc.
Posts: 462 | From Newnan, GA | Registered: Aug 2004
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posted
Hi Gigi, Did DK talk about KPU Pyrrolia ? If so can you share please. Thanks Joyce
Posts: 905 | From Santa Cruz,Calif | Registered: Aug 2005
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SForsgren
Frequent Contributor (1K+ posts)
Member # 7686
posted
He will be speaking on it next week at LIA on Sunday morning.
-------------------- Be well, Scott Posts: 4617 | From San Jose, CA | Registered: Jul 2005
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posted
Thanks Scott, Wish I could be there. Please share if anything new. There seems to be a lot more about AI and KPU. I guess we are the pioneers again. Take care Joyce
Posts: 905 | From Santa Cruz,Calif | Registered: Aug 2005
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posted
Funny how no one showed chemcials at first. Perhaps it only shows the bigest culprits first and when they are gone, teh depper ones.
Posts: 462 | From Newnan, GA | Registered: Aug 2004
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posted
Pardon my spelling -- I have Lyme. Last sentance should have been THE DEEPER ONES.
Posts: 462 | From Newnan, GA | Registered: Aug 2004
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SForsgren
Frequent Contributor (1K+ posts)
Member # 7686
posted
Ping, your note is confusing. How can they send you the therapy without a saliva sample? The therapy is based on the sample.
-------------------- Be well, Scott Posts: 4617 | From San Jose, CA | Registered: Jul 2005
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Paying for water is a crazy, crazy notion. lol.
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