Social Intelligence 101:
If your friend is telling you about an accomplishment, do not try to one-up them by sharing an accomplishment of your own.
Tame your ego.
Sit back and actively listen.
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Storytelling 101:
Your readers need to be able to empathize with your main character, otherwise they will not continue reading.
Best way to make them empathize is by making your character relatable.
'How?'
By giving your character flaws.
Make them human.
Just to add on.
Your antagonist or villian should have a desirable quality.
For example: an evil villian that has a lot of riches.
Giving your villian some pros makes the reader root for your antagonist even more.
Face it, humans are drawn to flaws over perfection.
But a main character with negative traits & a villain with positive traits creates magic.
Counterintuitive, I know.
But you are creating friction.
You are sparking dual emotions in your readers.
This will make the readers go on an emotional roller coaster.
This is just one of the many principles of storytelling
If you like stories, then sign up for my email list: https://t.co/JjtGWxvwz4
I do storytelling emails where I take my readers onto a journey from my past
If you read carefully, you will leave with many lessons for life
Your readers need to be able to empathize with your main character, otherwise they will not continue reading.
Best way to make them empathize is by making your character relatable.
'How?'
By giving your character flaws.
Make them human.
Just to add on.
Your antagonist or villian should have a desirable quality.
For example: an evil villian that has a lot of riches.
Giving your villian some pros makes the reader root for your antagonist even more.
Face it, humans are drawn to flaws over perfection.
But a main character with negative traits & a villain with positive traits creates magic.
Counterintuitive, I know.
But you are creating friction.
You are sparking dual emotions in your readers.
This will make the readers go on an emotional roller coaster.
This is just one of the many principles of storytelling
If you like stories, then sign up for my email list: https://t.co/JjtGWxvwz4
I do storytelling emails where I take my readers onto a journey from my past
If you read carefully, you will leave with many lessons for life
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@franciscodeasis https://t.co/OuQaBRFPu7
Unfortunately the "This work includes the identification of viral sequences in bat samples, and has resulted in the isolation of three bat SARS-related coronaviruses that are now used as reagents to test therapeutics and vaccines." were BEFORE the
chimeric infectious clone grants were there.https://t.co/DAArwFkz6v is in 2017, Rs4231.
https://t.co/UgXygDjYbW is in 2016, RsSHC014 and RsWIV16.
https://t.co/krO69CsJ94 is in 2013, RsWIV1. notice that this is before the beginning of the project
starting in 2016. Also remember that they told about only 3 isolates/live viruses. RsSHC014 is a live infectious clone that is just as alive as those other "Isolates".
P.D. somehow is able to use funds that he have yet recieved yet, and send results and sequences from late 2019 back in time into 2015,2013 and 2016!
https://t.co/4wC7k1Lh54 Ref 3: Why ALL your pangolin samples were PCR negative? to avoid deep sequencing and accidentally reveal Paguma Larvata and Oryctolagus Cuniculus?
Unfortunately the "This work includes the identification of viral sequences in bat samples, and has resulted in the isolation of three bat SARS-related coronaviruses that are now used as reagents to test therapeutics and vaccines." were BEFORE the

chimeric infectious clone grants were there.https://t.co/DAArwFkz6v is in 2017, Rs4231.
https://t.co/UgXygDjYbW is in 2016, RsSHC014 and RsWIV16.
https://t.co/krO69CsJ94 is in 2013, RsWIV1. notice that this is before the beginning of the project
starting in 2016. Also remember that they told about only 3 isolates/live viruses. RsSHC014 is a live infectious clone that is just as alive as those other "Isolates".
P.D. somehow is able to use funds that he have yet recieved yet, and send results and sequences from late 2019 back in time into 2015,2013 and 2016!
https://t.co/4wC7k1Lh54 Ref 3: Why ALL your pangolin samples were PCR negative? to avoid deep sequencing and accidentally reveal Paguma Larvata and Oryctolagus Cuniculus?