Anonymous ID: 48e03a Oct. 1, 2021, 3:10 p.m. No.14701746   🗄️.is 🔗kun   >>1762

>>14701703

https://www.komen.org/

 

Look for pink to be aware… they used to be connected to Planned Parenthood on the down low.

In 2012 they supposedly disconnected ties. Although I bet they have shared funds somewhere

Anonymous ID: 48e03a Oct. 1, 2021, 3:12 p.m. No.14701762   🗄️.is 🔗kun

>>14701746

Forgot the other image- pink

Because you know- there’s 10000 genders

https://www.plannedparenthoodaction.org/pressroom/planned-parenthood-supporters-paint-country-pink

Anonymous ID: 48e03a Oct. 1, 2021, 3:16 p.m. No.14701775   🗄️.is 🔗kun   >>1811 >>1836 >>2000

>>14701688

Last bread friend anon made this meme.

Gather these teachers that are quitting and form co-op education groups.

Look up state law- you’ll be surprised how many homeschool groups there are! We homeschooled for 5 years and all grew very close as a family. Best thing we ever did for our family

 

Now doctors and nurses that are quitting need to form free state coalitions and then unite the free states for unvaxxed and free people commerce

Police and firefighters that quit need to form private free people’s security companies

See a pattern- let’s do this!

Anonymous ID: 48e03a Oct. 1, 2021, 4:10 p.m. No.14702131   🗄️.is 🔗kun   >>2147 >>2168

>>14702112

https://en.wikipedia.org/wiki/RIG-I

 

RIG-I (retinoic acid-inducible gene I) is a cytosolic pattern recognition receptor (PRR) responsible for the type-1 interferon (IFN1) response.[4] RIG-I is an essential molecule in the innate immune system for recognizing cells that have been infected with a virus. These viruses can include West Nile virus, Japanese Encephalitis virus, influenza A, Sendai virus, flavivirus, and coronaviruses.[4][5] RIG-I is structurally considered a helical ATP-dependent DExD/H box RNA helicase, that recognizes short viral double-stranded RNA (dsRNA) in the cytosol during a viral infection or other irregular RNAs (i.e., non-coding RNAs).[4][6][7] Once activated by the dsRNA, the N-terminus caspase activation and recruitment domains (CARDs) migrate and bind with CARDs attached to mitochondrial antiviral signaling protein (MAVS) to activate the signaling pathway for IFN1.[4][6] IFN1s have three main functions: to limit the virus from spreading to nearby cells, promote an innate immune response, including inflammatory responses, and help activate the adaptive immune system.[8] Other studies have shown that in different microenvironments, such as in cancerous cells, RIG-I has more functions other than viral recognition.[7] RIG-I orthologs are found in mammals, geese, ducks, some fish, and some reptiles.[6] RIG-I is in most cells, including various innate immune system cells, and is usually in an inactive state.[4][6] Knockout mice that have been designed to have a deleted or non-functioning RIG-I gene are not healthy and typically die embryonically. If they survive, the mice have serious developmental dysfunction.[6] The stimulator of interferon genes STING antagonizes RIG-1 by binding its N-terminus, probably as to avoid overactivation of RIG-1 signaling and the associated autoimmunity. [9]