Thanks for the website. It seems to have a lot of potassium in it (53% daily allowance which is higher than I have ever seen in any supplement).
I wish Biopure put the amount of the ingredients on their website, so we could compare. It would save a phone call.
Take care. Lee
-------------------- "The race has already been won." Posts: 74 | From midwest | Registered: Dec 2009
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cactus
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posted
Thanks for all who've been helpful on the nut/seed allergy issue.
GiGi - thanks for writing and asking them.
I don't doubt that chemicals can play a part in many nut alleric individuals' reactions.
My son's allergy is specific to the protein contained in the nuts or seeds - which is evident from his specific testing & from cross-reactivity among other items containing similar proteins [Sigh].
Did they mention anything about the specific proteins? (dreaming here) ...I will see what I can learn using some translating engines, and ask some German friends for their assistance as well.
Whatever the answer on the protein issue - my son is of the age that "outgrowing" allergies is still a possibility - so anything that may help him on that path is well worth investigating.
Seek - yes - his allergist may (or may not) be skeptical about water drops - as a Western doc. And as parents we would be concerned about "testing" to see where he is, in regard to his allergy.
But since we are all on the same page with regard to total avoidance of his allergens, I think I know how we would approach measuring any progress - which is simply an extension of how we will monitor his sensitivity levels from here on out.
CAP RAST (IgE) testing until the numbers are low enough to warrant a skin prick test - in the office.
If a skin prick test is negative (hoo ray!) we would then plan for an in-office food challenge - in which the kiddo would try miniscule amounts of the food in question - while being monitored.
And of course - because of the life-threatening aspect - I think we would always keep epipens on hand.
My goal here is not necessarily that the kiddo be able to gobble down an organic peanut butter sandwich, but more the assurance that he can live, travel, and function without this constant fear that the person in front of us in the check out line has recently eaten mixed nuts (or even a burger bun with sesame seeds) - thus possibly exposing my contact and inhalation sensitive son to a life-threatening episode.
Thanks, all, for the input on this - and any more thoughts or ideas are very welcome!
-------------------- �Did you ever stop to think, and forget to start again?� - A.A. Milne Posts: 1987 | From No. VA | Registered: May 2005
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GiGi
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posted
Just a quick comment before I get busy with my life off Lymenet:
Phosphorus is proving to be very important. It is one of the key ingredients in the Matrix Electrolytes. The subject was discussed at length at the recent Dr.K. seminar and I am sorry I cannot give you the whole lecture here. But I think it is important enough - and that's why I am posting it here. Til later.
Posts: 9834 | From Washington State | Registered: Oct 2000
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posted
Phosphorus is needed to remineralize our teeth and bones! Good one Gigi. I forgot I had tow bottles of Matrix. Rebreaking them out.
Posts: 462 | From Newnan, GA | Registered: Aug 2004
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GiGi
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posted
The 3 day seminar was named "Lyme and Other Chrnoc Infections As The Underlying Cause of Chronic Illness" and you would know everyone of the invited guest speakers as capacities in their field.
All. as Dr.K., are treating hundreds of chronically ill, especially Lyme patients and Autism which usually involves Lyme.
Hobo, here is more on phosphorus and why it is so important considering malabsorption in general and low mineral content of most grown foods today).
ASD children often have low kidney lab markers (BUN, GFR) that just would not improve... phosphorus may be the key. Phosphorus often quickly reduces the needs for high B6 (in KPU, seizure disorders, sleep, etc.). Phosphorus is needed for the conversion of B6 to P5P - taken orally it is reduced to B6 by a phosphatase in the gut and still requuires phosphorus to create the active form. Phosphorus is also needed for ATP production in the mitochondria. Taken in the cocktail, it fulfills most phosphorus needs. You can buy phosphorus in different products, if you wish. Whatever suits best.
Now I am off..........
Take care.
Posts: 9834 | From Washington State | Registered: Oct 2000
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Cass A
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posted
Dear Friends,
Just now being able to catch up a bit.
In addition to the usual holiday blitz, my mother passed away at my home three days before Christmas. She had been doing poorly for some time, and at her 90th birthday party in November announced that she wasn't going to live another year. We're all dealing with it, as she was a great lady and a true friend to each of literally thousands of people over the years.
I sent in my after-8th-round specimen to AI in early December. I'd been having more and more pre-seizure feelings, and then had (according to my husband) a full seizure overnight once again. He said it was briefer and less violent than the last one. But, since, I've been really having a bad time with the pre-seizure feelings, which pretty much take over my whole body.
I'd been hoping for my next round of drops to arrive. No show. So, I emailed Herr Grundmeyer last night, and he emailed me back saying they'd just been sent off.
So, as you can imagine, the recent posts from GiGi relating to phosphorus are very timely for me!!
I checked the electrolyte I take very often (Electrolyte Stamina from Trace Minerals Research), and it has no listing for phosphorus in it, so whatever the content, it is quite low.
I also checked another electrolyte product I've used a lot in the past--Emergen-C--which is a drink mix that's high in Vitamin C as well as electrolytes. However, it has only 24 mg per serving, which is 2% of the daily value, according to the package.
I've been having to take massive amounts of B-6 just to stave off the seizures, so it's out to the vitamin store for me TODAY to get some phosphorus!!
My thanks again to Gigi!!!
Best,
Cass A
Posts: 1245 | From Thousand Oaks, CA | Registered: Feb 2007
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posted
Gigi, My babesia seems wors ethan the Lynme. What does one do for that while on AI?
Posts: 462 | From Newnan, GA | Registered: Aug 2004
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I hope adding phosphorus helps with the seizure activity.
Posts: 88 | From Toronto | Registered: Nov 2009
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GiGi
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posted
Cass A, Wishing you will have this wonderful memory of your Mother forever.
Hobo, why call it "my" babesia? You are inscribing this possession into your DNA and it may be yours forever, whether you actually have it in physical form or hold on to the memory only forever. We create our own reality by the way we think.
I had Babesia and all other co-infections = Lyme. To this day I couldn't tell you which one caused certain pains. It could be from your dental situation; it could be caused by any of the neurotoxins the microorganisms leave behind.
You will be way, way ahead of the game if you are able to clean up some of the allergies, and repair your teeth. Nothing is more toxic than what the dead teeth/root canals drip into your system as long as they are left there. It took about 4 month before I started to get better after my root canals were carefully removed. I gradually moved up and up.
From what I have heard from my doctor over the last ten years, it is important to clean up teeth, mold in home, parasites, and then the microorganisms don't stand a chance. And you are doing AI, which clears the road to be successful with the rest of the problems, if any remain. Your teeth sound like a stumbling block and it is difficult to make everything else work as long as these remain.
That's just my experience, and listening to Dr.K. lectures the last few days, this is the way he approaches Lyme because the major problems are out of the way and this is what he has found works best. Clean up the body/terrain and the very intelligent microorganisms will give in.
I prayed a lot too, but I figured God also gave me a brain to use and do what is necessary.
Please all remember that a very important part of the Rehydration Cocktail is the protein/amino acids and sugar part that are necessary to take the electrolytes where they are needed in the cell. This is a more recent development in Dr.K.'s approach - and works a lot better than simply taking electrolytes as it has been done for many years.
They have also found that not just any phosphorus works equally well. Besides the complete Biopure electrolytes, "Angstrom Minerals Liquid Phosphorus" works well also for the kidney to repair. I have the amounts somewhere if interested.
I was told that I would probably look ten years younger if I stayed on the Rehydration a couple of months! Will do - at my age anything is appreciated!!!
Got to go.
Posts: 9834 | From Washington State | Registered: Oct 2000
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linky123
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posted
Gigi,
Thank you for the advice.
Linky
Posts: 2607 | From Hooterville | Registered: Apr 2009
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posted
The oral suregon wants me on 5000 units of D3. Anyone take this? I may live down south but I', rarely in the sun. My bad I know. Just confuseed about what the Pro Marhsall Protocal people keep saying.
Plus, ain't gonna be sunny here for a bit. It's like 19 degrees in ATL.
Posts: 462 | From Newnan, GA | Registered: Aug 2004
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So sorry about your mom's passing. my mom passed a few days later. i don't think we can ever be prepared for the depth of the loss. for me, it reverberates thru and thru.
Sounds like your mom left a beautiful legacy which is worth celebration.
i hope you can keep the seizures at bay. aliyah
Posts: 830 | From Colorado | Registered: Mar 2005
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posted
Hobo, the subject of D3 is controversial... MP folks say it is bad yet other LLMDs recommend. Sorry I don't have an answer for you.
Posts: 88 | From Toronto | Registered: Nov 2009
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GiGi
Frequent Contributor (5K+ posts)
Member # 259
This is the basis of discussion at last Lyme and Chronic Dis seminar I have talked about before:
Vitamin D3 (it's a hormone - give at bedtime/sleepy) - It's controversial in Lyme (see Marshall Protocol)
75 IU/pound of body weight daily. Anti-inflammatory, supports bones, theeth and facial development, anti-viral and anti-bacterial (TB, etc.) Important for many functions of the immune system www.mercola.com Goal is t get blood levels to 80 or more (25-OH form of D3) Any brand name seems fine Carlsons and Biotics Research (Bio-D-mulsion Forte = 2000 i.u. per drop) both work very well and are available in drops.
We take varying 5000 i.u. to less, according to testing. When we don't get out of the house, it is 5,000 i.u. I have taken it for several years in varying amounts - whatever tests, and sometimes I forget it....
Comment by Dr. K.: Marshall protocol worked for only one of the patients that tried it and that person actually had sarcoidosis. He was testing it out several years ago for a number of people and nobody benefitted.
The Marshall protocol scared the daylights out of me - how much more unnatural can you get? We a re not cave people. The more natural light I get, the better I feel. We pulled the whole ceiling in our family room out - glass 2/3 of the total room and it is the best room in the house. But day-and sunlight is not always easy to come by in this northern hemisphere.
Take care.
Posts: 9834 | From Washington State | Registered: Oct 2000
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runner21
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posted
I just got my D levels tested and i was way high..so i am going to back down the doseage. i am still testing for viruses..so i think i must be an exception to this rule. i agree about the marshall protocol..how much more unnatural can we get with this one?
Posts: 1118 | From jacksonville,fl usa/santa rosa ca | Registered: Dec 2001
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I sent my first test samples in to AI and am so excited to receive the drops!
Meanwhile I've been researching some of the things that Dr. K has suggested I take as part of my protocol as I wait for them to arrive at CMC. In particular, I'm wondering if anyone has taken the Phospholipd Exchange? I am concerned about my kidneys after reading that it is really EDTA. I took the heavy metal challenge this summer at CMC and my kidneys hurt terribly during the procedure and after. I do not want to hurt them further and think they may be weak.
Anyway, just wondering your experiences and your thoughts in regards to kidney protection. I am thinking about asking about Reliinex?
Thank you!
Posts: 78 | From Washington State | Registered: Dec 2009
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ukcarry
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posted
Cass A, so sorry to hear about your mother: my condolences.
posted
Started Round Two and I am having a rough go of it. It seems like most of my symptoms right now are emotional with indigestion. I'm panicking, raging, and confused -- hard not to fear Lyme overlay.
These symptoms started brewing softly the day before I began Round Two. Now that I'm two days into the new drops the emotions are like a hail storm non-stop.
I'm taking one drop three times a day at this point. Staying home and trying to be gentle.
Anyone else experience something like this?
wiserforit
Posts: 273 | From Banks of the Hudson | Registered: Nov 2008
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posted
Wiser, what did your round 2 report say? If emotional blockages were found in this round, this could be causing an outpouring of feelings.
I experienced similar during my round 3. Panic attacks, crying jags -the works. I just tried to "roll with it" and rest a lot. It does pass, as the blockages clear.
Take care of yourself!
Posts: 88 | From Toronto | Registered: Nov 2009
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Round 2 report said that everything had cleared from Round 1 except the chemicals found under 6.1.
I felt the emotional stuff literally brewing days before the Round 2 drops came in. I had so many emotional blockages on Round 1; maybe it was just slow to hit?
Thanks for the well wishes. This is truly a roller coaster ride!
Best of the best to you,
wiserforit2
Posts: 273 | From Banks of the Hudson | Registered: Nov 2008
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NanaDubo
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posted
Wiser - factors that have been corrected means that we can begin to move through them. I wish it meant "poof, it's all gone" but it doesn't.
Things can begin to heal now, whether it's emotions, the gut, whatever. Somethings will take time.
Many of us have cried a river as old traumas have popped up in our faces, vivid dreams that do not seem like dreams at all but a healing of old wounds.
Try to go with the flow as they say.
None of this built up over night and so..... you know the rest.
Just know your body and soul are working very, very hard and be kind to yourself.
lightparfait
Frequent Contributor (1K+ posts)
Member # 22022
posted
Wiser... the emotions and cleared things I liken to a river that has been dammed up for a very long time.
The beginning of the waterway is cleared for you...the debris is moving...with some wild rapids and other calm waters!
In the beginning the emotions were like a wild river rafting trip for me! Keep the flow happening, and it gets clearer and calmer over time.
There are other dams down stream that will be cleared next.
...and do "go with the flow" as Nana says! And hang on for the ride! lp
Posts: 1009 | From NJ | Registered: Aug 2009
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lightparfait
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posted
Cass A...
My condolences as well to you with the loss of your mother. My prayers are with you at this time.
Let us know how the phosphorus is working. lp
Wiser,
a suggestion...you may want to try a little journaling of your symptoms as you move through the rounds.
This helps me remember when I am going through something, or aids me in remembering old ailments that are resurfacing on the drops. It is a very healing and therapeutic exercise!
As I write, I also get a sense of what I am learning about myself through the process. Going through this has been healing on many levels.
Posts: 1009 | From NJ | Registered: Aug 2009
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linky123
Frequent Contributor (1K+ posts)
Member # 19974
posted
Aliyalex and Cass,
So sorry for your loss. I lost my Mom five years ago, and still miss her every day.
Take care and God bless you both.
Posts: 2607 | From Hooterville | Registered: Apr 2009
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posted
NanaDubo and Lightparfait, thank you for your kind words and thoughts!
I feel like Meryl Streep in that movie "River Wild" about white-water rafting now! Thanks for the imagery. Journaling sounds like a wonderful idea too.
Today, some of the anxiety calmed down and I suddenly became really, really creative. I started a lot of projects for tutoring children and went on to a community project. WOW! Normally I would have been too mentally exhausted to do this. It comes in waves.
I am curious to see what images sleep will bring tonight.
Thanks for the replies. They always help with grounding.
Best regards,
wiserforit2
Posts: 273 | From Banks of the Hudson | Registered: Nov 2008
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At $31 a bottle, it's significantly less expensive than the BioPure, which is now $50.
Hard to know how much phosphorus is in any of them.
I know Dr. K only sells *the best stuff* but I wonder if another brand might be good enough.
For now, I'm using the ConcenTrace minerals I have on hand.
GiGi, do you know the purpose of the baking soda in the rehydration cocktail? Is it for alkalizing the drink? I really hate the taste and saltiness of the baking soda and have a hard time getting it down, despite adding orange juice, protein powder, maple syrup, etc.
Could I use less than 1/4 tsp?
Or, I wonder if I could substitute some of the AlkaBase powder (supplement) I have. It foams up like baking soda, but the taste is not as harsh.
Thanks! Nutmeg
Posts: 386 | From WA state | Registered: May 2005
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NanaDubo
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posted
I use Biopure Matrix minerals but not in the rehydration cocktail. That calls for electrolytes.
Thank you for the corrections. I realize now that I looked at the wrong product. So Matrix electrolytes, not Matrix minerals. Big difference.
Also happy to know about BioPure, since I did think it was his company, so I apologize for incorrect assumption & spreading misinformation. I'm informed now!
I will get the electrolytes and try this again.
One more question...could I use full-fat plain yogurt instead of milk or milk analog? That's what I've always used in my shaker smoothies--I enjoy the thickness it brings to the drink.
Thanks, Nutmeg
Posts: 386 | From WA state | Registered: May 2005
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posted
Guys, I know this is off topic, but I know some of you are on the KPU protocal, so I wanted to ask.
I don't have either of heh two telltale symptoms - poor dream recall and spotty nails. Thus, I wonder if I should bother with the test.
The results seem amazing of people getting better so quickly makes me want this to be a part of teh puzzle.
Posts: 462 | From Newnan, GA | Registered: Aug 2004
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NanaDubo
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posted
If it were me, I would wait until I got further along with AI and see what happens.
Can always get the test.
Posts: 1129 | From Maine | Registered: Feb 2008
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Scroll to page 37 listing the major symptoms of HPU/KPU. There are a lot more than two.
But I agree with Nana, it's a lot better to wait than choosing to crash for several month before the major dysregulations are corrected with AI. KPU knocks at the deposits of toxins, and via AI we know that we are allergic to a whole number of them which invites the body to a battle to push them out --- and why battle and why suffer. I am not sure that KPU is needed after AI is complete and the body starts to properly regulate again. Don't know, but am very suspicious, if we have the patience to let that happen. I suppose it depends on how bad a person feels. I do not test positive for KPU and am releasing metals with AI by the tons, something I have never been able to do to that degree. My husband is now, since bottle #10, doing KPU and is releasing metals, slower, but releasing them, and most importantly -- doing KPU without crashing, which is important because of age. Organs need to be treated kindly and crashing is tough on the system.
I know you will make the right decision. Taking the KPU test doesn't hurt. Be sure you are off the KPU related supplements several days before you do the test.
Take care.
Posts: 9834 | From Washington State | Registered: Oct 2000
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GiGi
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Member # 259
posted
Nutmeg, the proven recipe calls for certain liquids. Not smoothies or yoghurt which probably take a lot longer for digestion than watered down milks. I go strictly by the rules because I have learned that he knows what he is talking about. He also does not hesitate to "recall" something, when he finds out it is not working as well as he wanted it to.
With that in mind, Dr. K. mentioned that he finds Biosil working better than the Jarrosil. I think I had posted about this earlier.
Take care.
I had posted a larger text, but was in the process of adding to it when the lights went out and computer black. So I lost it. You probably saw parts of it as indicated by your response.
Posts: 9834 | From Washington State | Registered: Oct 2000
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I didn't use a store-bought smoothie, just plain unsweetened yogurt, watered down. I will stick with the original recipe now, and wait to get started until I can get the electrolytes in.
Maybe I will just use my protein powder, since I don't drink milk, and also try almond or soy milk occasionally.
I made a note about the Biosil instead of Jarrosil, but have not tried that yet.
Thanks again. I appreciate all your thoughtful replies to everyone.
Nutmeg
Posts: 386 | From WA state | Registered: May 2005
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posted
I was wondering the same thing hobokinite. Do you all still take probiotics?
I started my first round yesterday and so far so good. I haven't noticed anything yet. I was really nervous about starting.
I've been reading or should I say trying to read this thread. I'm still trying to figure out if we need to take our suppliments or not. I really hate to quit my magnesium and a couple of other things but I want to do what is best. I know the less the better.
Another thing, I've always been severely constipated and I have to take something every day. Should I still take that or see what AI can do in that dept? I'm also taking Dr. Schulze's super food. I'm assuming it would be OK to still take that?
Sorry for the questions. I know the answer is here somewhere. I promise I have been reading and have found answers to some of my questions. There's just so much info here, it's overwhelming to my lyme brain.
Sapphire
Posts: 495 | From KY USA | Registered: Dec 2004
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NanaDubo
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posted
Yeast/fungus attach to the metals to protect us from them. When regulations take place and the metals start releasing so do the other things.
This past month I have experienced metal release, fungal die-off, metal release, fungal die-off, etc., etc.,
Fun? No. Rewarding? Yes. Patience is a virtue. I need this tattooed to my forehead!
Posts: 1129 | From Maine | Registered: Feb 2008
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posted
Ha! I think this is the longest running post on Lymenet. It needs a search button to find all the good bits of wisdom said here I already have forgotten!!!!
Waiting for my sixth AI batch.
Posts: 462 | From Newnan, GA | Registered: Aug 2004
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lightparfait
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Member # 22022
posted
I would not recommend anyone to do the KPU test yet if already started A.I. Basically to save money and time and to avoid being tempted to start too many protocols at once.
As I believe you will need to retest after the A.I. anyway to see if you still have it! Just more money on tests, although having the information is always interesting. Sometimes too much info is overload for me! I get confused and tend to want to start things before their time.
I tested for KPU in the beginning of my A.I. treatment, and I have a strong positive...but am now waiting to finish my A.I. before doing any treatments for KPU. Waiting is not easy for a pro-active person!
But as I reflect back on my healing history...when I wait for the right timing, healing happens more quickly and orderly.
As I have experienced many regulations with the A.I. already, there is a chance I may not need to do the protocol at all after A.I. We will see.
I will retest both urine and ART testing at that time. I spoke with my ND just yesterday about this and she agrees...as I am feeling well, why rock the boat now. We will retest later.
But as far as my daughter, she was recommended to start on core by my ND who understands her unique situation. We are all different, and have varying degrees of symptoms and ability to follow protocols.
So I recommend KPU testing after your major regulations happen with the AI!
Posts: 1009 | From NJ | Registered: Aug 2009
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lightparfait
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posted
Nana...interesting that we have many similar things happening together.
I am having loads of yeast/fungus and metal release too!
Knee pain is still gone!!!!!
But my hair is going wacky...a weird symptom I believe of something releasing through my folicles...my hairdresser sees it too!
My hair is parting in odd places all over my head...and not laying flat like normal...just hard to manage and odd looking at the roots! I have a shorter cut...so I look like a punk rock star now instead of my normal bob... smooth sleek look!
Anyone else have this?
Posts: 1009 | From NJ | Registered: Aug 2009
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NanaDubo
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posted
Bad hair day = metals coming out through hair folicles.
Glad your knee is hanging in there.
Yes, we do seem to run a similar pattern - more evidence that things DO happen with AI.
Sorry about your attempt to relay this on a different thread. I am having a hard time biting my tongue (fingers) on that one Posts: 1129 | From Maine | Registered: Feb 2008
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GiGi
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Member # 259
posted
LP, my husband has this. He has had snowwhite hair, totally smooth and the fullest head of hair ever. White for many many years. We have been going to the same hairdresser for longr than that! Ever since AI, his hair goes in episodes of frizzy on some parts that she has a hard time to keep within the haircut. She remarks about it He also now has some black hair coming through that I had never seen before.
He definitely is releasing metals as indicated in his Doctor's Data hairtest. Not quite as much as I am releasing yet, but we have since adjusted his mineral replacement because his mineral reserves showed as very low, probably affected by poor absorption due to the wheat/leaky gut problem wbich takes time to heal.
The release of metals through my hair is enormous. I had never been able to release toxic metals that was needed until I started AI. I did not have any food allergies, but metal allergies, and a sound mineral reserve (good minerals).
Goes to show you - we eat the same food every day and lead the same lifestyle - and our inherited burden was vastly different - he had 3 miasms, I had none.
If you had a hairtest done before too long, you would probably find a reason. When toxic metals appear in the hair, the metals are on their way out of the body. It is a test that DK frequently does because if properly interpreted, it tells a lot. If the zinc etc shows in the hair along with some others, KPU is a factor.
I can report about myself that I have not heard a sore throat in fifty years followed all within one day and night the release of a bucketful reqquiring a box of kleenex - all within 24 hours. I sound like I had a cold for a week, but havent. Strictly a release from top of head to end of neck. Eyes, nose, mouth/throat. I used to tell Dr. K. my head feels like it is clamped in a vice; or the other one "I am wearing three bathing caps, all two sizes too small". This feeling left after I got over Lyme in early 21st century, but this release never happened until almost a year of AI. We started in January.
So you have a partner with frizzy hair! He is really a super guy and you would like him. The frizzyness sort of comes and goes from one month to the next.
Take care.
Posts: 9834 | From Washington State | Registered: Oct 2000
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posted
Well, I spoke too quickly this morning. I am definitely feeling something now. I can't really contribute it to AI for sure though.
My head feels like Gigi described in the above post. Feels like it's in a vise. I have blurry vision, too. I just feel so sick all over. When I get up I feel like I'm going to pass out and get sick to my stomach.
I get this or similar stuff from time to time so I can't say it's the AI but I had been feeling so much better. I'm just going to bed and gonna hang on for the ride.
Sapphire
Posts: 495 | From KY USA | Registered: Dec 2004
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posted
Hi all, just wanted to report that our 11th bottles arrived today after the slow holidays' mail.
Our just turned 7 yr. old grandson is showing the amazing amount of 15 chemical substances after 6 rounds of AI, plus various amts. of biological and energetic blockades. He has already cleared most of his eczema and is improving in other areas but still has much more to go.
Posts: 67 | From northeast | Registered: Feb 2006
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posted
Just a note. I got the bad root canal tooth pulled this morning. Seemed to go okay., Having a bit more EMF symptoms than usual, but I guess that is from the stress of it all. Thank God it is done and it went out easy. He got all of it nothing left. There was root near the sinus but he got it!
I'm still numb so no idea if it will hurt or not.
Thanks guys for your help and prayers.
Cheers,
Michael
Posts: 462 | From Newnan, GA | Registered: Aug 2004
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GiGi
Frequent Contributor (5K+ posts)
Member # 259
posted
Clancy, it is still amazing to me how a child is able to accumulate all this toxin. So glad he is coming along well.
We are also waiting for bottle #11 and will compare notes!
Hobo, get a good long rest - and may your body continue healing.
Posts: 9834 | From Washington State | Registered: Oct 2000
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The
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