So sad. We’ve been living in very strange and dark times. False science and fake trials have been dictating medical rules, imposing experimental injections and blocking potential life saving drugs. The truth will prevail. Thanks for sharing your very important work.
"Otherwise, the case we’re constructing is a tautology: the experts are correct because the studies that the experts take seriously tell us that the experts are correct." This. So true (and not just in the medical field, but also in journalism).
I ponder about the prophylactic trial of Prof. Carvallo:
My intuition after digging up and down literature and experimenting through waves of CoV Flu RSV is :
* GLYCERINE is the active part.
We now pour 1ml to every filling of inorganic antiseptic and other nasal sprays (we diy to “need of the day”, other ingredients see below).
Sprays offering backdrip vent are also an excellent hygienic storage to store inhalative fluids, our supermarked / drugstore nasal sprays have 0.14ml per puff, and are corrosion resistant, can be opened by heating in boiled water for 40secs dipping it in to upper seal rim, no more, then pre-dilating one round by some soft-edged metal lever (bottle opener, pan table spoon in need) against pointing finger holding the rim, then jerk open. Prewarming seal before closing helps enhance gas tightness. Also drying vent hole by straw first blowing, then sucking, then filling hole with silicone fat enhances storage time of CIO2 against diffusion through the vent PTFE mesh membrane.
GSE+xylitol spray ie xylimed = xlear has more: 0.23ml/puff. It is not corrosion resistant and has no backdrip preventing valve, so new content needs to be self-preserving.
* Hygiene: Inorganic antiseptics as premedication in inhalative therapy:
Always spray some puffs of Na Hypochlorite 800ppm (oral or wound rinse) into inhaler head to sterilise it and also inhale it, if using inhalers in hospital or elderly care homes environment offering multiple resistant pathogens. Studies showed that even simulated inhalation (without touching mouthpiece by lips) resulted in 40% contamination of insides of inhaler head with hospital germs, just by normal handling, wow...
* Glycerine:
I assume the following principles of action, please add:
- Prebiotic (strong biome digests pathogens, weak gets infected by CoV and vax vector plasmides),
- slightly antiviral,
- enhances viscosity (prevents aerosols from forming, enhances barrier function; to be verified),
- drag-along helping substance: self-distributing medication (for right viscosity, to full upper respiratory tract)
- emulsifier (not distorting biome!): lVM gets resorbed ca. 5x if solved in glycerine (to be measured and compared to reference “taken on fat-containing meal” (assume 100%) vs. taken on empty stomach (1/5ths of resorption on fed).
As it is only slightly antiviral,
* enhance it by something or several agents being antiviral and acting orthogonally.
Like
* one inorganic antiseptic found:
I2 stab 100ppm,
- PVP-I 10% 1.5ml pH=6.5,
- NaHCIO 800ppm 1.5ml, best choice!,
- CIO2 <= 5ppm 2-5ml,
- H202 0.1-2% pH=6.5 ca.,
— do you find more?
* organic antivirals:
- propolis,
- cineol, inhaled traces 1/2 drop/24ml
- essences like oregano or thyme or thymol (crystaline, effective at 1ppm), or
- mustard essences (horseradish), ablento penetrate bacteria films just like the inorganic antiseptics due to low molecular size, so also diffusing into cells.
- allicin (garlic extract, micronised, also diffusing into cells, even systemically).
- salts also containing ++ charged metal ions like Mg++ or Ca++ are enhancing the mucosal physical barrier function by increasing surface tesion for 6 hours. See
We just use dead sea, stone, or artificial or natural Bad EMSer salz (a healing bath in DE, you will find similar natural salts anywhere; non-purified salt always has interesting properties :)
For compunding pharmacy: add a bit of CaCl2 to the NaCl like in trial
- grape seed extract (fluid: sold in glycerine). Very anti-oxidative, so incompatible with inorganic antiseptics, as opposed to glycerine itself
(Use - if available - glycerine from quality (bio) plant oil. It seems to make a difference. Will mix my GSE and propolis in good glycerine Infound from linseed bio oil mill now by myself next time. )
I reduced the harsh condition of the protocol in Prof. Carvallo’s preventive lVM in glycerine trial which ran like
“Take 5x a day 1 drop on tongue, Away from eat drink for 1 hour +-“
to … +- 1/4 hour distance, preferably after meals ir drinking. For “alternative” non-lVM antivirals, we take 2-3 drops.
(iota-carrageenan nasal spray, as he stated later, is nice, but not needed there. But it is a possible anti-viral add-on to glycerine anyways.
Production of iota-carrageenan Inhalable solution 0.15% in salt water:
Easy or difficult? : Solve or stir a clumps-free “thin pudding” eg by magnetic stirrer, produce a fine snow fall of the iota-carrageenan powder by placing fine-scale measured 0.15% eg 0.45g for 300g salt water on a fine sieve (metal gold mesh for coffee, or ring-stretched stockings’ nylon mesh, knock it on glass rim or brush till it has slowly and evenly distributed fallen through the slits wile stirring.
Just a proposal. Use any method for clump free pudding stirring. Sieving out clumps in viscuous fluids is challenging … knocking the sieve some time longer on the rim of a glass.
We also add
- 0.6-0.9% dead sea or stone salt and
- 9% Xylitol Birch sugar
- then Sterilise:
Heat to 100°C, close lid and gently start to shake shortly, let expanding air carefully evade several times till lid also has 100°C. After some minutes kept warm in clothg. Store in fridge. From time to time, add a few drops inorganic antiseptics. Choose the type you inhale with, see above.
For CDS CIo2 stay below 5ppm in sum for sure., using 1/600th (eg 1/2ml CDS in 300ml base solution would be MAX sum dose, I always only add 1/2 a drop of CDS=CIO2(aq) 0.3%=3000ppm. )
We store this ready mixed base solution for sprays and inhalation in the fridge.
We like to spray iota-carrageenan, as it also is caring nasal mucosa. :)
Since we discovered, GSE and cylitol helped resolve a 1 year anosmia after CoV infection, we just do a combo spray. For anosmia, you may want to include anti-allergics like chromolynium acid and azelastine or CPM.
In a glide gel, iota-carrageenan would also prevent chicken pox. Don’t laugh, we can buy this with iota-carrageenan readily available.
(I would accept iota-carrageenan as a wide-spread ingredient for “antiviral hygiene”, as it really does no harm. :)
We prefer 1x/day prevention: Discipline for prevention is THE limited resource, as modern hectic people (and my teen girls as well) have no time or mindfulness and stress/vax/smart phone adhd, and disciline seems the key factor.
Especially as the goal is that a boring “nothing” shall happen. Gosh! Unthinkable contra to the “performing” narrative.
Only possible with countries with strong anti-structural-corruption interventions working good, like Uttar Pradesh in India.
So discipline to “just take it” may even be a major prevention factor. Alone. Without even any “it”. Indicating personal stability and resilience. Hinting on a milieu no pathogen likes to hang around.
How to show?:
(Distributed meshed network private trials conducted under the radar of the establishment, using eg sensors attachable to a smartphone or bead LAMP quantitatively calibrated and running a DNA channel formreference, anyone can learn in a day, and only in late stage going public. Possible for all interventikns and remedies non-Rx.
We should constrain to those.
) ==>
Invent new forms of trials subverting the bias WHO GSP impeaches. )
Prevention is the earliest point of time for therapy! <=>
Strong prevention <==> Good therapy ?
:
If you come near 100% protection, I assume you also can expect high impact in early therapy. And vice versa.
Early therapy is the testing stone for this.
I want to come near to the question by observation first.
So any time you feel a sore throat and take some remedy, you should experience symptoms at least not worsening while taking it. If done till resolving, you won.
(My kids loose energy to stubbornly take things a week upon first relief, so my first question now is: how many things and how often per day are you willing to take?
Leading to the concept of personalised protocol: the base is the contract with your lazy or doubting ego. Sikencio, and dig it through.
This is why I recommend the “pool scenting” inorganic antiseptics (we use Sodium HypochIorite electrolytically proflduced and Cl2 free or ChIorine Dioxide) to them. Due to diffusion properties, taken topically eg by nasal spray eg preventively
“In 4 rounds in ca. one minute,
Breathing in, spray to nose, mouth to throat and one under the tongue.
It diffuses into the dead cells making up the upper derma of mucosa growing slowly up in the stable, and on top layer only, dissolve to set free mucilage and, if infected while living, enclosed produced viruses, ca 60k/cell, that then diffuse quickly (10mins) over mucosa against cilial flush in 10mins to nose tip, and down to lungs. Trained innate antibodies and defensines and barrier function prevent boundless infections, so normallly an infection is kept locally and not necessarily slides down to lungs, totally depending on 100s of factors making up “mucosal defense” including “natural immunity” by trained nK based innate antibodies mainly.
(As 1/5ths start in saliva glands, 4/5ths in throat ring, and only 1% elsewhere, for non-smokers ie happily fledging cilia hair cells.
For smokers, ciliae are paralysed, so infections start a bit more distributed, so spray and “breathing in” is ideally for smokers, but for non-risk non-smokers, gargling may suffice.
For vulnerables, prevention may be ideal by inhaling once eg in the evening and go to bed.
For symptoms sliding down from throat to vocal chords or tracheae, mostly, lungs are already infected, but keep viral load low: if out, take inorganic antiseptic or mixed spray and quickly and deeply inhale a puff from spray to mouth in direction of throat. Repeat eg 10x. Get some nebuliser (and if it is a moisturiser “lantern” so modern) and eg 800ppm NaHClO 1.5ml per session (0.8ml ok if run only while breathing in). Do it asap an on symptoms, if you like every 1/2 hour.
We inhaled everything except GSE (found no safety studies, I first have to dig up what some surfactant does to alveoli).
And I did not yet studied the art of micellar or liposomal (in sunflower based pure phospholipides) solving where huge therapeutic potential are to be expected from
- lvermectine,
- NicIosamide (especially both, systemically as topically, both best solved liposomally!)
- Progesterone.
- Hyalurone (short vhained): de-scars and refunctionalises.
The insane thing about the Together Trial is that it wasnt done Together!
Treatments were sequenced, yet all Ivermectin therapies Ive studied and adopted use a multi component protocol, which applies the omponents simultaneously. A sequenced approach is employed if the the symptomes worsen after the initial course, as done by Dr. Chatty in South Africa, or Tyson and Fareed, or McCullough in the US and so forth.
And have the PI's at Together released their data yet, like they said they would in August 2021?
Alexandros,
This series is a great public service. Thank you.
So sad. We’ve been living in very strange and dark times. False science and fake trials have been dictating medical rules, imposing experimental injections and blocking potential life saving drugs. The truth will prevail. Thanks for sharing your very important work.
"Otherwise, the case we’re constructing is a tautology: the experts are correct because the studies that the experts take seriously tell us that the experts are correct." This. So true (and not just in the medical field, but also in journalism).
- Glycerine + “something antiviral”?
- inhalatives?
- DIY multi-modal topical …
- prevention <=> therapy?
I ponder about the prophylactic trial of Prof. Carvallo:
My intuition after digging up and down literature and experimenting through waves of CoV Flu RSV is :
* GLYCERINE is the active part.
We now pour 1ml to every filling of inorganic antiseptic and other nasal sprays (we diy to “need of the day”, other ingredients see below).
Sprays offering backdrip vent are also an excellent hygienic storage to store inhalative fluids, our supermarked / drugstore nasal sprays have 0.14ml per puff, and are corrosion resistant, can be opened by heating in boiled water for 40secs dipping it in to upper seal rim, no more, then pre-dilating one round by some soft-edged metal lever (bottle opener, pan table spoon in need) against pointing finger holding the rim, then jerk open. Prewarming seal before closing helps enhance gas tightness. Also drying vent hole by straw first blowing, then sucking, then filling hole with silicone fat enhances storage time of CIO2 against diffusion through the vent PTFE mesh membrane.
GSE+xylitol spray ie xylimed = xlear has more: 0.23ml/puff. It is not corrosion resistant and has no backdrip preventing valve, so new content needs to be self-preserving.
* Hygiene: Inorganic antiseptics as premedication in inhalative therapy:
Always spray some puffs of Na Hypochlorite 800ppm (oral or wound rinse) into inhaler head to sterilise it and also inhale it, if using inhalers in hospital or elderly care homes environment offering multiple resistant pathogens. Studies showed that even simulated inhalation (without touching mouthpiece by lips) resulted in 40% contamination of insides of inhaler head with hospital germs, just by normal handling, wow...
* Glycerine:
I assume the following principles of action, please add:
- Prebiotic (strong biome digests pathogens, weak gets infected by CoV and vax vector plasmides),
- slightly antiviral,
- enhances viscosity (prevents aerosols from forming, enhances barrier function; to be verified),
- drag-along helping substance: self-distributing medication (for right viscosity, to full upper respiratory tract)
- emulsifier (not distorting biome!): lVM gets resorbed ca. 5x if solved in glycerine (to be measured and compared to reference “taken on fat-containing meal” (assume 100%) vs. taken on empty stomach (1/5ths of resorption on fed).
As it is only slightly antiviral,
* enhance it by something or several agents being antiviral and acting orthogonally.
Like
* one inorganic antiseptic found:
I2 stab 100ppm,
- PVP-I 10% 1.5ml pH=6.5,
- NaHCIO 800ppm 1.5ml, best choice!,
- CIO2 <= 5ppm 2-5ml,
- H202 0.1-2% pH=6.5 ca.,
— do you find more?
* organic antivirals:
- propolis,
- cineol, inhaled traces 1/2 drop/24ml
- essences like oregano or thyme or thymol (crystaline, effective at 1ppm), or
- mustard essences (horseradish), ablento penetrate bacteria films just like the inorganic antiseptics due to low molecular size, so also diffusing into cells.
- allicin (garlic extract, micronised, also diffusing into cells, even systemically).
All have low resistances danger.
- iota-carrageenan (only antiviral, quite perfectly though, leaves our biome unaffected). Inhalable.
- salts also containing ++ charged metal ions like Mg++ or Ca++ are enhancing the mucosal physical barrier function by increasing surface tesion for 6 hours. See
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7453358/pdf/S2633289220000095a.pdf
We just use dead sea, stone, or artificial or natural Bad EMSer salz (a healing bath in DE, you will find similar natural salts anywhere; non-purified salt always has interesting properties :)
For compunding pharmacy: add a bit of CaCl2 to the NaCl like in trial
- grape seed extract (fluid: sold in glycerine). Very anti-oxidative, so incompatible with inorganic antiseptics, as opposed to glycerine itself
(Use - if available - glycerine from quality (bio) plant oil. It seems to make a difference. Will mix my GSE and propolis in good glycerine Infound from linseed bio oil mill now by myself next time. )
I reduced the harsh condition of the protocol in Prof. Carvallo’s preventive lVM in glycerine trial which ran like
“Take 5x a day 1 drop on tongue, Away from eat drink for 1 hour +-“
to … +- 1/4 hour distance, preferably after meals ir drinking. For “alternative” non-lVM antivirals, we take 2-3 drops.
(iota-carrageenan nasal spray, as he stated later, is nice, but not needed there. But it is a possible anti-viral add-on to glycerine anyways.
Production of iota-carrageenan Inhalable solution 0.15% in salt water:
Easy or difficult? : Solve or stir a clumps-free “thin pudding” eg by magnetic stirrer, produce a fine snow fall of the iota-carrageenan powder by placing fine-scale measured 0.15% eg 0.45g for 300g salt water on a fine sieve (metal gold mesh for coffee, or ring-stretched stockings’ nylon mesh, knock it on glass rim or brush till it has slowly and evenly distributed fallen through the slits wile stirring.
Just a proposal. Use any method for clump free pudding stirring. Sieving out clumps in viscuous fluids is challenging … knocking the sieve some time longer on the rim of a glass.
We also add
- 0.6-0.9% dead sea or stone salt and
- 9% Xylitol Birch sugar
- then Sterilise:
Heat to 100°C, close lid and gently start to shake shortly, let expanding air carefully evade several times till lid also has 100°C. After some minutes kept warm in clothg. Store in fridge. From time to time, add a few drops inorganic antiseptics. Choose the type you inhale with, see above.
For CDS CIo2 stay below 5ppm in sum for sure., using 1/600th (eg 1/2ml CDS in 300ml base solution would be MAX sum dose, I always only add 1/2 a drop of CDS=CIO2(aq) 0.3%=3000ppm. )
We store this ready mixed base solution for sprays and inhalation in the fridge.
We like to spray iota-carrageenan, as it also is caring nasal mucosa. :)
Since we discovered, GSE and cylitol helped resolve a 1 year anosmia after CoV infection, we just do a combo spray. For anosmia, you may want to include anti-allergics like chromolynium acid and azelastine or CPM.
In a glide gel, iota-carrageenan would also prevent chicken pox. Don’t laugh, we can buy this with iota-carrageenan readily available.
(I would accept iota-carrageenan as a wide-spread ingredient for “antiviral hygiene”, as it really does no harm. :)
We prefer 1x/day prevention: Discipline for prevention is THE limited resource, as modern hectic people (and my teen girls as well) have no time or mindfulness and stress/vax/smart phone adhd, and disciline seems the key factor.
Especially as the goal is that a boring “nothing” shall happen. Gosh! Unthinkable contra to the “performing” narrative.
Only possible with countries with strong anti-structural-corruption interventions working good, like Uttar Pradesh in India.
So discipline to “just take it” may even be a major prevention factor. Alone. Without even any “it”. Indicating personal stability and resilience. Hinting on a milieu no pathogen likes to hang around.
How to show?:
(Distributed meshed network private trials conducted under the radar of the establishment, using eg sensors attachable to a smartphone or bead LAMP quantitatively calibrated and running a DNA channel formreference, anyone can learn in a day, and only in late stage going public. Possible for all interventikns and remedies non-Rx.
We should constrain to those.
) ==>
Invent new forms of trials subverting the bias WHO GSP impeaches. )
Prevention is the earliest point of time for therapy! <=>
Strong prevention <==> Good therapy ?
:
If you come near 100% protection, I assume you also can expect high impact in early therapy. And vice versa.
Early therapy is the testing stone for this.
I want to come near to the question by observation first.
So any time you feel a sore throat and take some remedy, you should experience symptoms at least not worsening while taking it. If done till resolving, you won.
(My kids loose energy to stubbornly take things a week upon first relief, so my first question now is: how many things and how often per day are you willing to take?
Leading to the concept of personalised protocol: the base is the contract with your lazy or doubting ego. Sikencio, and dig it through.
This is why I recommend the “pool scenting” inorganic antiseptics (we use Sodium HypochIorite electrolytically proflduced and Cl2 free or ChIorine Dioxide) to them. Due to diffusion properties, taken topically eg by nasal spray eg preventively
“In 4 rounds in ca. one minute,
Breathing in, spray to nose, mouth to throat and one under the tongue.
It diffuses into the dead cells making up the upper derma of mucosa growing slowly up in the stable, and on top layer only, dissolve to set free mucilage and, if infected while living, enclosed produced viruses, ca 60k/cell, that then diffuse quickly (10mins) over mucosa against cilial flush in 10mins to nose tip, and down to lungs. Trained innate antibodies and defensines and barrier function prevent boundless infections, so normallly an infection is kept locally and not necessarily slides down to lungs, totally depending on 100s of factors making up “mucosal defense” including “natural immunity” by trained nK based innate antibodies mainly.
(As 1/5ths start in saliva glands, 4/5ths in throat ring, and only 1% elsewhere, for non-smokers ie happily fledging cilia hair cells.
For smokers, ciliae are paralysed, so infections start a bit more distributed, so spray and “breathing in” is ideally for smokers, but for non-risk non-smokers, gargling may suffice.
For vulnerables, prevention may be ideal by inhaling once eg in the evening and go to bed.
For symptoms sliding down from throat to vocal chords or tracheae, mostly, lungs are already infected, but keep viral load low: if out, take inorganic antiseptic or mixed spray and quickly and deeply inhale a puff from spray to mouth in direction of throat. Repeat eg 10x. Get some nebuliser (and if it is a moisturiser “lantern” so modern) and eg 800ppm NaHClO 1.5ml per session (0.8ml ok if run only while breathing in). Do it asap an on symptoms, if you like every 1/2 hour.
We inhaled everything except GSE (found no safety studies, I first have to dig up what some surfactant does to alveoli).
And I did not yet studied the art of micellar or liposomal (in sunflower based pure phospholipides) solving where huge therapeutic potential are to be expected from
- lvermectine,
- NicIosamide (especially both, systemically as topically, both best solved liposomally!)
- Progesterone.
- Hyalurone (short vhained): de-scars and refunctionalises.
- DMS0 1%
The insane thing about the Together Trial is that it wasnt done Together!
Treatments were sequenced, yet all Ivermectin therapies Ive studied and adopted use a multi component protocol, which applies the omponents simultaneously. A sequenced approach is employed if the the symptomes worsen after the initial course, as done by Dr. Chatty in South Africa, or Tyson and Fareed, or McCullough in the US and so forth.
And have the PI's at Together released their data yet, like they said they would in August 2021?
Thank you.