https://twitter.com/realLizUSA
Liz Harrington Retweeted
Rising serpent Flag of United States
@rising_serpent
·
10m
He was with actual first responders.
Dave Catanese
@davecatanese
· 5h
Former President Trump — absent from the 20th anniversary 9/11 ceremony in his own city.
Dan ScavinoFlag of United StatesEagle
@DanScavino
Replying to
@DanScavino
Shows pictures of POTUS Trump with first responders in NY!
What????
https://www.youtube.com/watch?v=39WrSskl3XE
They're actually disecting a FROG on Newsmax right now!
Dear Lord help this woman right now in need of healing Father! God thank you that we can be healed because Jesus Christ himself nailed to the cross with him ever sickness, illness and disease!! Thank you Lord! We speak complete healing over this woman right now that she will be able to get up and walk right out of that hospital on her own accord! Thank you Lord for all of us that hear this prayer will stand together in Faith (believing) in your power and Love, Agape, perfect Love, that you Father God will never fail us! Thank you for anwering this Anons prayer right now!
In Jesus' Holy name, Amen!
>CreutzfeldtJakobDisease
Creutzfeldt–Jakob disease
From Wikipedia, the free encyclopedia
Not to be confused with Variant Creutzfeldt–Jakob disease.
Creutzfeldt–Jakob disease
Other names Classic Creutzfeldt–Jakob disease[1]
Practneurol-2016-001571f02.jpg
Magnetic resonance image of sporadic CJD[2]
Pronunciation
UK: /ˌkrɔɪtsfɛlt ˈjækɒb/ KROYTS-felt YAK-ob, US: /- ˈjɑːkoʊb/ - YAH-kohb[3]
Specialty Neurology
Symptoms
Early: memory problems, behavioral changes, poor coordination, visual disturbances[4]
Later: dementia, involuntary movements, blindness, weakness, coma[4]
Complications Aspiration pneumonia due to difficulty coughing
Usual onset Around 60[4]
Duration 70% die within a year of diagnosis[4]
Types Sporadic (mutation), Familial (heredity), Iatrogenic (acquired), Variant (Infection)[4]
Causes Prion[4]
Risk factors Having at least one living or deceased ancestor with the disease (in case of hereditary CJD)
Diagnostic method Based on symptoms and medical tests after other possible causes are ruled out[4]
Differential diagnosis Encephalitis, chronic meningitis, Huntington's disease, Alzheimer's disease[4]
Treatment Supportive care[4]
Medication For pain relief: Morphine, Methadone
Prognosis Universally fatal[4]
Frequency 1 per million per year[4]
Creutzfeldt–Jakob disease (CJD), also known as subacute spongiform encephalopathy or neurocognitive disorder due to prion disease, is a fatal degenerative brain disorder.[4][1] Early symptoms include memory problems, behavioral changes, poor coordination, and visual disturbances.[4] Later symptoms include dementia, involuntary movements, blindness, weakness, and coma.[4] About 70% of people die within a year of diagnosis.[4] The name Creutzfeldt–Jakob disease was introduced by Walther Spielmeyer in 1922, after the German neurologists Hans Gerhard Creutzfeldt and Alfons Maria Jakob.[5]
CJD is caused by a type of abnormal protein known as a prion.[6] Infectious prions are misfolded proteins that can cause normally folded proteins to also become misfolded.[4] About 85% of cases of CJD occur for unknown reasons, while about 7.5% of cases are inherited from a person's parents in an autosomal dominant manner.[4][7] Exposure to brain or spinal tissue from an infected person may also result in spread.[4] There is no evidence that sporadic CJD can spread between people via normal contact or blood transfusions,[4] although this is possible in variant Creutzfeldt–Jakob disease.[8][9] Diagnosis involves ruling out other potential causes.[4] An electroencephalogram, spinal tap, or magnetic resonance imaging may support the diagnosis.[4]
There is no specific treatment for CJD.[4] Opioids may be used to help with pain, while clonazepam or sodium valproate may help with involuntary movements.[4] CJD affects about one per million people per year.[4] Onset is typically around 60 years of age.[4] The condition was first described in 1920.[4] It is classified as a type of transmissible spongiform encephalopathy.[10] Inherited CJD accounts for about 10% of prion disease cases.[7] Sporadic CJD is different from bovine spongiform encephalopathy (mad cow disease) and variant Creutzfeldt–Jakob disease (vCJD).[11]
https://en.wikipedia.org/wiki/Creutzfeldt%E2%80%93Jakob_disease
Forgot the link!
Hold on!!!
Found this too in same link above…
=Cannibalism= has also been implicated as a transmission mechanism for abnormal prions, causing the disease known as kuru, once found primarily among women and children of the Fore people in Papua New Guinea.[29] While the men of the tribe ate the muscle tissue of the deceased, women and children consumed other parts, such as the brain, and were more likely than men to contract kuru from infected tissue.[citation needed]
Are they trying to give us their own disease - kuru, cjd, from cannibalism???
👀
(recalling the video of killary shaking her head back and forth like the possessed witch she is!)
No, not through the food, through the VAX!!!
Follow the links back to the post re what they've found in people who've been vaxxinated - CJD!!!