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" Attacking her personality "
Really VERY funny.
GLTA longs..
What a great post Learning...
" Nader Pourhassan PhD, I salute you valiant efforts ! I give you extreme credit for trying against extraordinary odds , to bring leronlimab to market "
And imo there were valiant efforts..Thank you Dr NP !!!!
All the best to our leronlimab !!
And good luck mostly to all of us , present and future patients !!!!!
All imo.
GLTA longs.
To me the most scary is testimony of Dr Buchhaults from last September to SC Senate .. Video Below...
Really scary with this DNA contamination inside of lipid nano-particles delivered inside our cells .
I don't know , but some scientists saying, like here , it may produce lethal autoimmune diseases , or severe cancers in some in the future ..
My best friend , also a physician , retired December 2022 , started to develop symptoms soon after , about May 2023 diagnosed with ALS , the bulbar type , the fastest progressing..
She is not doing well now.
There is no more lethal autoimmune disease then ALS . My friend had 3 Pfizers before ..
Is it a connection , we don't know , I am thinking to contact Dr Buckhaults if possible to check for it.. He think I believe it is possible..
But to me the video below is scary. and many scientists discovered the same..
Of course I do ..
It is happening to all of us ...
If that was a reason it is fine , but we had to many leronsaline here , so as you understand we little sensitive.
Thank you for explaining..
GLTU.
The name is ...leronlimab !!!!!.. try to learn if you are on CYDY message board !!!!
All imo.
GLTA longs,,
I believe VERY strongly WE ALL could benefit from leronlimab..
This politics in medicine , what a pity !!!
All imo.
GLTA longs..
I see your post , great.
Yes , as those drugs reduce obesity , and fat itself producing inflammation , they reducing generally inflammation ,
But they may produce very often side effects,
Not a very serious side effects are,
-diarrhea
-constipation
-nausea
-vomiting
-hair loss
-abdominal pain .
But then we have also this VERY severe side effects,,
-severe low blood sugar
-PANCREATITIS
-intestinal blockage
-kidney failure .
-thyroid CANCER
-gallstones
-suicidal thoughts or behaviors...
It is OK , I will stay with stronger anti-inflammatory without ONE serious side effect , ...leronlimab..!!!!
Also this is not good for acute diseases, like for egc cytokine storm in severe covid, or other severe diseases .
Leronlimab full effect is in about 50-53 hrs..
All IMO.
GLTA longs
OMG , thank you .
Yes the name is leronlimab !!!
Thank you !!!!!!!
GLTA longs
First , speak with me with respect , as I try to speak with you .
Don’t be a wise guys , or this conversation is over !
Yes they said , at the end we didn’t apply because FDA told us ..
Don’t even try ..
And I believe this was true , as after that we had 2 hit letters from FDA against CYDY ..
All imo .
GLTA longs
And you know what Grip it ,??
If only FDA will give us an EUA for critical as they should ..
He could have Nobel ...
All imo ..
GLTA longs
And we also know that results are accurate from reports of many doctors , and of our CEO , and I for one trust him !!!
And most probably they will be peer reviewed and published within months .. ..
So what is the problem ???
All imo
GLTA longs
You know Grip it ,….
That was a big discovery , until then everyone thought Long Covid is hyper immunity .
And many patients received steroids or other immunosuppressant for a treatment ..
But not !!
It is not proper for all , we know this after our study !!
And we see how leronlimab is working here !!
For leronlimab is not that important if hyper or hypo ..
Leronlimab is a great immune - modulator !!!
Works in both situations !!!
All imo
GLTA longs
Yes , this was peer reviewed and published paper.
What that mean . from internet..
" Peer review is the process whereby doctors evaluate the quality of their colleaques work in order to ensure that providing standards of care are being met "
The reason to have a peer review..
" To maintain the integrity of science by filtering out invalid or poor quality articles "
Is it important ..??
" The best way to check the accuracy of research "
GLTA longs
Yes Grip it , this is our study with leronlimab and Long Covid which Dr Otto Yang from UCLA peer reviewed and published.
Yes leronlimab is a GREAT drug..
This WAS peer reviewed and published !!!!!!!
https://www.uclahealth.org/news/some-cases-long-covid-19-may-be-caused-abnormally-suppressed
All imo.
GLTA longs..
And please ask any patient in our Long Covid study.
I believe , all except one did great when on leronlimab.
In some symptoms were back after 8 weeks of treatment , when leronlimab was stopped ...
But then we know , with immune problems some patients will need treatment for weeks , some for months and some for YEARS !!
All imo.
GLTA longs.
American Researcher Claim That Immune Downmodulation Contributes To Long COVID And That Treatment With Leronlimab Helps ..
https://www.sciencedirect.com/science/article/pii/S016344532400080X
GLTA longs
JustDaTruthB ..
First , congratulation for becoming a moderator here , we hope you will be here for a long time ..
We desperately need the truth !!!!!
🙏🙏
And no , I don't think anything will be explain , this was few years ago ..
Things just happen here , or they just don't happen !!
Who will explain ? FDA ??
Some of the FDA employee , I understand , think this is better then a “ housewife “
All the best to our drug …
All imo
GLTA longs ..
You copied one sentence from my post and answer me here ...
"We don't need to learn from it " .. I posted
You answered to me ..
"You must certainly do , You need to learn "
If you ONLY didn't try to change my post , you will
bring here my next statement in my post .
"We don't need to learn from it , for the future , guilty should not pay,
Is that what you think ??".....this is what I said.
So why to manipulate my post a wrong way ??
Why ??
All imo.
GLTA longs .
" Do you think FDA is paying other countries not to use the drug also "
At the time when the first hit letter came from FDA there was already debate going on in Philippine Parliament ( or Congress ??)..the same week.
If to give EUA to ivermectin and leronlimab, also talks were going in India.
The hit letter stopped all ... it is interesting to think what a timing from FDA..
all imo.
GLTA longs.
Here is the interview with Mr Moses , other link didn't work.
About 8,15 he is starting to talk about his Covid experience,,,and MIRACULOUS leronlimab..
https://www.stairwaytoceo.com/episodes/from-dreamer-to-drink-magnate-with-bill-moses-founder-and-ceo-of-flying-embers
Monroe , I was afraid my son will not last to next day , when he called me 2 hrs after his first shot of leronlimab , and told me he is feeling better , his oxygen is improving , and 26 hrs later he was discharged home on 3-4 L of oxygen..
The son of former President of Philippines called leronlimab a WONDER drug , after it saved his father life ,
and Mr Bill Moses ,
calling leronlimab a MIRACULOUS drug.
My old post with his interview below....!!!
YES , leronlimab is working !!!!!!!!
************************************************************
misiu143
Re: None
Saturday, March 11, 2023 6:36:12 AM
Post# of 231290 Go
And here is an interview with another grateful to leronlimab patient.. How nice to read this , and how sad that leronlimab was not allow to save more lives during this pandemic..
Interesting interview , when patient admitted to UCLA , Bill Moses , The Founder and CEO of Flying Embers ...
Admitted with severe bilateral Covid pneumonia , they gave him EVERYTHING without help , became severe/critical , on high flow oxygen , refused ventilator ,
so he said goodbyes to his family , wife and children , when suddenly Dr Otto Yang came to his room and proposed LERONLIMAB .
Dr Otto Yang treated many severe/critical Covid patients with leronlimab in UCLA , and said few times in the past ,
" Not every patient is improving with leronlimab , but MOST do.."
and lets not forget , he is talking about the most severe/critical patients , when nothing else worked ...
Patient took leronlimab , and VERY fast got better , and then went home , and he is an another person who like many other lucky patients , when leronlimb was given to them when nothing else was working , calling leronlimab a
" MIRACULOUS " drug.
It is truly a miraculous drug , I had a chance to observe this myself..!!!!!
and a drug without one serious side effect ..
Leronlimab is really miraculous to the lucky who could receive it.
This patient is so grateful to leronlimab, and Dr Yang , for saving his life at the last moment ..
If only ALL patients have this choice , how many less Americans will die ..
Probably we talking hundred thousands ....
How very sad , how very tragic this is..
Click on below link , ...
Then listen to this video.. ,
He start at 8:29 talking about his Covid experience...
https://www.stairwaytoceo.com/episodes/from-dreamer-to-drink-magnate-with-bill-moses-founder-and-ceo-of-flying-
**********************************************************************
All IMO>
GLTA longs
Yes moderators , please sticky this post ..
Now price is , 0.163—0.165 , by July 4 prediction is will be under 0.10 ..
Let’s see the experts , how accurate they are .
Thank you ..
All imo
GLTA longs
I know , that’s how some things maybe looking …
And I don’t know , I don't think , but I don’t know ..let’s the court figure this out !’
But is court always right ???
I know some things for sure .,
Dr NP had as much of excitement about leronlimab as all of us longs , he really wanted it to succeed , he knew it is saving lives ..
But the things happened preventing that ..
And I always will be grateful to Dr NP to allowed me leronlimab for my son , as at first Dr Kelly refused .
If you are really a woman , and if you are a mother , you will know my feeling ..
leronlimab given only because of Dr NP , saved my son live !!!’
Yes !!!
All imo
GLTA longs
No , if you will only come here as a friend , and not the attacker , we could have a great conversation .
Many , if not all made some mistakes here , different mistakes in a different degree ,
but don’t try to tell me our leronlimab is a saline , or whatever your associates are calling it ..
If you only could understand , what possibilities this drug has to help all us humans , with so many diseases , some very serious without help now ..
You will be on my side on this message board .
All imo
GLTA. Longs
If you will be knowledgable doing studies yourself , you will know
Missing clinical data which must be included in the report .
Is not the same as we dont have a good clinical data .
But because it was missing we don’t have accepted BLA ..
And this is why , at least one of the reason , imo we suing Amarex !!!!
Do not mean , we don’t have a good results !!!
All imo
GLTA longs
So what that means to you that FDA calling patients on the ventilators and ECMO a subgroup .
Is that mean that it is not important to us if they die or not .
As a physician I dont understand this .
All imo .
GLTA longs
You are right , I know only what the company telling us , and we know company is suing Amarex .
And I believe when Dr Arman , and Dr Jay telling all shareholders that results didn’t change , I believe this to be true .
You accusing me on the public message board that I lie ,
And you doing that not once , but in most of your posts ..
Are you sure that I lie ??
Are you saying Dr Arman and Dr Jay also lie ??
All imo
GLTA longs
We know for sure few questions ,
---What mistakes Amarex did , if any.
---How this affect our results ,
---How this affect progress of CYDY ....
And we know answers to those questions ..
--Mistakes were many , and important ....
So we suing now Amarex ...
--Results didn't change.
So as Dr Jay said even on the last CC , we preparing right now , our studies to send for peer review and then to publish them , they that good !!!!!!
-- progress of the company was affected very badly .
This is why we suing Amarex now.
And don't tell me about your smartness and successes , I can see what you are doing for living...
there is a reason you are here , for years now bashing penny stock , and insulting shareholders here , day and night ...haha
Is it 5.95 , or a different number now..?? ..or why you doing that , if not 5.95..
And please don't tell me because you trying to help all of us , and save new investors !!!!!!
All imo.
GLTA longs
Yes , everyone who know anything about CYDY heard Dr Jay or Dr Arman telling us.
Amarex did many mistakes , but in our situation no matter what mistakes they did , our results didn't change ,
We had now 3 independent auditing done for our studies , and all 3 came to the same conclusion.
Mistakes were made , results are correct.
Probably because it is not possible really to make mistakes looking at the blood tests from a different labs , and see changes of the viral load in HIV .
Or count how many died in critical Covid .
There is nothing in between , or someone died , or they didn't ..
Our studies were straight forward ...
It is ALWAYS good to know what is going on before we post !!!!!!
All imo.
GLTA longs.
Yes FDA , many things you told Americans in the last few years , you must walk back now.
https://www.zerohedge.com/political/fda-settles-ivermectin-case-agrees-remove-controversial-stop-it-post#google_vignette
All imo.
GLTA longs .
So you saying Dr Arman , and Dr Jay are lying to all the shareholders righ now ??
GLTA longs
All the results of our studies are accurate and will be peer reviewed and publish .
This is according to recent information from Dr Arman and Dr Jay
Are they lying to us ????
GLTA longs .
According to Dr Arman , and Dr Jay , all the results , of all studies are accurate .
are you saying they lying to us …
GLTA longs
It is funny you said that Monroe in your previous post.
But after thinking a little I should be also grateful to shorts , bashers , and FDA as to what happened until now ..
They allowed me to become a really big shareholder . Never dreamed of so many shares before .
So true , instead to be upset I need to start to be grateful to them .
But now I am done ( I think …:)) ) with averaging , let’s progress now .
I am waiting when all our studies will be peer reviewed , and published .
We had some beautiful results in HIV combo , critical covid , long COVID , cancers , and Nash .
And as Dr Arman said in the past. and now Dr Jay ..
No matter what happened with the studies , who did them , results are accurate .
I guess it is an easy statement ,
In combo HIV. results go by a blood test of viral load ,
critical Covid by mortality .
One can’t change a blood tests from different labs , and one can’t change mortality , or one died or didn’t .
So we are very sure about all these results , and let’s publish them asap ..
I don't know why this was not done in the last 2 years already .
But it is what it is now .
Go Dr Jay .
All imo
GLTA longs .
How can you even say that , how many died needlessly doesn't matter ,??
We don't need to learn from it , for the future , guilty should not pay.,
Is that what you think ??
All imo.
GLTA longs..
Tmac ,let me give you little more details about LL , and the results of our CD12 critical.
So , half life of leronlimab given SC is 10 days. We know at what point it is no longer in the system..
Knowing from Dr Patterson tests of our critical patients in Montefiore that in these severe /critical Rantes are still high at 2 weeks.
CYDY , with Dr Jay being at this time an interim CMO , presented FDA with a protocol for these patients .
4 weekly injections with leronlimab , then primary endpoint at 28 days.
Injections , 4 doses ,
at..
0, 7, 14 , 21 days , and then Primary Endpoint at 28 days.
Protocol was proper and logical.
But no , FDA refused to approve this way , they commented that VIRAL disease don't need 4 injections , but 2 will be enough , they approved only 2 weekly injections , at 0 and 7 days , but then refused to move Primary endpoint to 14 days , and left it at 28 days ..
First , since when severe/critical Covid is a Viral disease .
No , this is an immune disease , immune dysregulation..
But even with 2 injections only , results of the study were very impressive , showing what a great drug leronlimab is , and how many lives it could save, and showing all the patients were under-treated !!
With injections at 0 and 7 days results below.
At 7 days --78 % of mortality benefit ABOVE any other drugs .
At 14 days-- 82% mortality benefit !!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!
At 21 days -- 50%
At 28 days --31%
We can see clearly here that when drug was in the system results showing how great this drug is .
But after drug was withhold from these patients on the ventilators and ECMO , mortality benefit started to go down, As it could be expected..
But even at 28 days when there was nothing of leronlimab left in the system , still after the 2 doses there was 31% mortality benefit ,
I am sure these patients are very happy.
There was not one serious side effect , in contrary LL arm showed less side effects then SOC drugs only , which telling us LL helping with side effects from other drugs.
And FDA couldn't analyze all this ?? , they only look at 28 days , and wrote in the hit letter ,
They said...We will not look at some subgroups.
Why not FDA ?? those are Americans dying on the ventilators and ECMO , without one good drug approved for immune stage of the disease .. Why not to analyze carefully to see what is saving their lives..??
Why not ??
I was lucky , I knew what to ask for my son , I was invested here , in contrary to FDA I analyzed carefully the results , I read news how many critical surviving with leronlimab , I knew it is saving lives ..
but how many knew ???
All imo.
GLTA longs.
Yes , I agree at the time FDA wrote this in their hit letter , even though our results in critical at 2 weeks , when drug was in the system , showed the BEST results from any other drug, It showed it is saving many lives..
Remdesivir was TRENDING in mortality , leronlimab was saving lives , and it should be given EUA during this pandemic , when millions were dying without good drug ..
It should have EUA , probably with phase 4 .
But then if we have a VERY good saving lives drug , then by law vaccine will need more research and no EUA for them could be given ,
Was that the only reason I don't know ,
But this is my VERY strong opinion , from what I saw was happening during this pandemic,
HCQ , ivermecting was withhold from us as people were dying.
I am surprised entire USA is not screaming loudly as their love one died alone.
Leronlimab was given to over 100 patients , severe/critical , as compassionate or RTT.
Patients when everything else failed , there was not one serious side effect , and most of them survived ,
and FDA knew all this.
What was the reason to attack this small company with a great drug , instead of helping them to save lives ???
All imo.
GLTA longs.
For sure I understand , and know statistic better , then you understand medicine …
And thankfully patients do not go to a statistician for a medical advice .
Within months this study should be peer review , and publish , and results appreciated by ALL doctors .
All imo
GLTA longs ..
Grip it , investment is one thing , and effectiveness is another .
This is a very unusual drug , and if only FDA will give it EUA after CD12 critical showing 82% mortality benefit above any other drugs , and not one serious side effect , during pandemic , with not one good drug approved for immune stage of COVID ,
hundred thousands could be saved .
So please . You may say anything about investment , but don’t say anything about effectiveness if you don’t understand what is happening in medicine here .
All imo
GLTA longs