Japanese Baths, Gobs of Medical Research
& A Clear and Thorough List in Case One Still Doesn't Believe.
In my book, https://www.amazon.com/Vaccine-Injuries-Lies-Deaths-Resources/dp/B0BXNJLZF9/ref=sr_1_1?crid=D09TYTGEJJB9&keywords=deanna+kline+vaccine&qid=1682917844&sprefix=deanna+kline+%2Caps%2C123&sr=8-1, I have a chapter dedicated to a wonderful woman who suffered Rhabdomyolysis with many lab and liver changes and with severe diffuse pain for months after her second jab. I saw her often and treated her because she feared the hospital despite critical health concerns, and she fully recovered. Praise the Lord.
I’ve now seen 5 people with Polymyalgia Rheumatica (PMR) post their shots. I recently treated a woman with it who repeatedly told me “I am in hell”, “This is the worst pain of my life”, “Much worse than delivering a baby and it’s been months” and “I’d go to the hospital if I thought they could help me”. She began to have pain after her booster, which she initially tried to relieve w/ over the counters and acupuncture. She saw a specialist. The pain worsened and she was getting depressed from her loss of vitality and mobility and constant pain. I treated her. She returned and said “You are a healer!”, “How did you figure that out?”, “I feel great!”. Comments like this keep me from changing careers.
Her son died suddenly and unexpectedly a couple weeks after his booster, he was in his late 40s. Suspected massive MI. Autopsy not done. I asked her if she is willing to speak at a medical freedom event about her devastating pain and medical diagnosis and her devastating loss of her son.
She, like others I’ve asked, is barely getting her life back together. Some don’t want attention. Some are permanently injured, debilitated and homebound. Some are just too busy living their life now and want to forget all about the awfulness of it all.
Trust me, I can relate.. but people need to speak out for the lost lives, the disabled lives, to correct the lies, to tell the truth, and to work toward regaining many freedoms and preserving the few remaining.
Silence and selfishness, fear and complying and allowing censorship and widespread corruption is how we got here. Have you joined the fight for truth yet?
Whoops, sorry! Back to the matter at hand:
People, and recently, radio hosts and podcasters, ask me how I can relate certain diagnoses to the covid injections. It is pretty easy to do so.
The very nature of at least half of patient encounters has changed compared to pre-covid shot rollouts. Timelines and onset of symptoms, combined with uncharacteristic conditions for age groups and unusual or sudden patient complaints offer many clues. Trending and correlating lab changes and strangely high rates of incidence paint a new picture of patient findings en masse.
Of course some heart attacks and strokes and clots happen, but not to people in their teens - 40s. Not in such large numbers between 20-50. Not to the masses in such a short period of time! Don’t believe me? Check the real, raw data: https://www.theyliedpeopledied.com/the-book.html
Do not let the ‘news’ or your AI feed use nudge tech to train your brain into accepting this was always normal! We already let them rape minds, believe lies, and fuel fear erroneously. No more. Can you discern nudge tech? Can you identify lies?
So the Japanese here have discussed deaths in the bathtub and share proven harms post covid shots, including rhabdomyolysis and PMR, along with every subject matter/diagnosis in my book and far beyond it! So, when I get asked how I can be sure the vast majority of cases I investigate and see are jab related, I’m confident in my answer. Check these out:
Figure 1. Deaths while sitting in the bathtub after COVID-19 mRNA vaccination.
They go on to advise avoiding exertional exercise, alcohol, smoking and baths immediately post jab. They are not specific as to how long to avoid these things. They mention Singapore’s advice to avoid exercise as well.
I can’t fathom their abstract and conclusion! Despite all these jab reactions and possible death, they say they wanted to share this because rollouts for kids was on the way (this was published in May 2022) and to avoid these activities after your jab!
Table 1. Organ-specific diseases associated with the COVID-19 vaccines:
2.1. Cardiovascular Diseases
Various cardiovascular diseases have been reported to be associated with the COVID-19 vaccine. These include myocarditis and pericarditis [5,20,27,36,37,38,39,40,41], ACS [5,6,7,36], aortic dissection [5,6,34,35], vasospastic angina [36], Takotsubo cardiomyopathy [42], heart failure [5,7,27], arrhythmia [5,14,27,39,43], and pulmonary embolism [5,44] (Table 1). Stark et al. reported the interplay between inflammation cytokines and thrombosis in cardiovascular pathology [45]. The COVID-19 vaccine promotes inflammatory cytokine release [7,8,9,10] and can cause cardiovascular events, including myocarditis (inflammation), ACS (thrombosis), etc. Cardiovascular diseases are the most common causes of death after COVID-19 vaccination [5,6]. Hence, we created a flowchart of the differential diagnoses of chest discomfort and palpitation after COVID-19 vaccination (Figure 2). Myocarditis and pericarditis are reported to be more common in young males after the second vaccination. In male patients aged 12–15 and 16–17 years, the reported incidence is 162.2/million and 93.0/million, respectively [40]. Patients with myocarditis/pericarditis usually present 24–72 h post-vaccination [38]. In contrast, patients with ACS tend to be older in age and typically present 24 h post-vaccination [36]. Oster et al. reported that 98% of post-vaccine myocarditis cases showed an elevated troponin level [38]. Troponin is useful for screening post-vaccine myocarditis, but false negatives are possible, especially within 12 h of the vaccine or a few days later [46]. Electrocardiography and transthoracic echocardiography (TTE) have detected 72% and 17% of the abnormalities associated with post-vaccine myocarditis, respectively [46]. Therefore, diagnosis by multi-modality imaging, including cardiac magnetic resonance imaging and longitudinal strain measured by TTE, is important [37,41]. In cases where a definitive diagnosis is difficult due to the inability to perform multi-modality imaging, detailed follow-up is critical in any cases of suspected myocarditis/pericarditis. NSAIDs, colchicine, and steroid therapy are the standard treatments for myocarditis/pericarditis [27]. In severe cases, steroids may be effective in preventing cytokine release, autoimmunity, and eosinophilic myocarditis [20]. Colchicine, which has an inhibitory effect on the NOD-like receptor family pyrin domain containing 3 (NLRP3) inflammasome, which is associated with IL-1β (inflammatory cytokine) secretion [47], may be also effective for vaccine-associated inflammation [48].
Figure 2. A flowchart of the differential diagnoses of chest discomfort and palpitation after COVID-19 vaccination. ACS: acute coronary syndrome; AMI: acute myocardial infarction; UAP: unstable angina pectoris; FT4: free thyroxine; FT3: free triiodothyronine; TSH: thyroid-stimulating hormone.
2.2. Respiratory Diseases
Asthma attacks [49], diffuse alveolar hemorrhages [50], eosinophilic pneumonia [21], interstitial lung disease [51], and sarcoidosis [52] following COVID-19 vaccination have been reported (Table 1). Although the relationship between the COVID-19 vaccines and asthma attacks and interstitial lung disease is unknown, there have been reports of cardiac arrest after vaccination [34,35,49]. The deaths associated with respiratory disease are the third most common after cardiovascular and cerebrovascular disease [5]. Differentiating these cases from heart failure is important, especially in individuals who exhibit coughing and dyspnea.
2.3. Gastroenterological Diseases
Appendicitis [5,53], autoimmune hepatitis (AIH) [11,13], bleeding duodenal ulcer [6], intestinal obstruction/perforation [5], mesenteric ischemia [5], and pancreatitis [54] have been reported post-vaccination (Table 1). Some reported cases of AIH occurred secondary to autoimmune diseases such as primary biliary cholangitis [55,56].
2.4. Renal Diseases
Wu et al. reported that minimal change disease, IgA nephropathy, and vasculitis are common in post-vaccine renal disease. Other cases following COVID-19 vaccination include membranous nephropathy relapse, the acute rejection of a kidney transplant, IgG4 nephritis relapse, new-onset renal thrombotic microangiopathy, and scleroderma renal crisis [11,12] (Table 1).
2.5. Neurological Diseases
Garg et al. reported many diseases associated with COVID-19 vaccines [57], including acute disseminated encephalomyelitis [58], acute hemorrhagic leukoencephalitis [59], autoimmune encephalitis (AE) [60], Bells’ palsy [5,57], cerebral hemorrhage [61], cerebral infarction [6], cerebral venous sinus thrombosis [62], chronic inflammatory demyelinating polyneuropathy (acute-onset) [63], GBS [5,11,64], multiple sclerosis (MS) [65], myasthenia gravis (MG) [66], neuromyelitis optica spectrum disorder (NMOSD) [16], Parsonage-Turner syndrome (Neuralgic amyotrophy) [67], subarachnoid hemorrhage [6,68], thrombophlebitis [69], and transverse myelitis [70] (Table 1). The second most common cause of death after cardiovascular disease is cerebrovascular disease [5]. IL-6 causes blood-brain barrier dysfunction and enhanced leukocyte transmigration [71], leading to inflammation of the central nervous system. Moreover, IL-6 is also involved in producing anti-aquaporin-4 antibodies, and it has been reported that IL-6 has a higher level in NMOSD [72]. Intracerebral hemorrhages after vaccination due to central venous sinus thrombosis [68], vasculitis [61], and Moyamoya disease with Sjogren disease [73] have been reported. In cases of cerebral hemorrhage after COVID-19 vaccination, thrombosis, vasculitis, and autoimmune diseases should also be considered.
2.6. Skin Diseases
Alopecia areata (AA) [74], bullous pemphigoid [75], COVID arm (local injection site reaction) [76,77], eosinophilic cellulitis (Wells syndrome) [22], eosinophilic panniculitis [24], erythema multiforme [78], herpes zoster (skin, oral and facial palsy) [53,57,79,80], leukocytoclastic vasculitis [81], non-episodic angioedema with eosinophilia [23], psoriasis [82], Stevens–Johnson syndrome [83], subacute cutaneous lupus erythematosus [11,84,85], and urticaria [77] have been reported following COVID-19 vaccination (Table 1). AA is an autoimmune disease, and an increase in IFN-γ and inflammatory cytokines, including IL-6 and IL-1β, have been reported [86]. Eosinophilic cellulitis and panniculitis are thought to be type IV hypersensitivity reactions with an increase in IL-4 and IL-5 [24,87]. AA, eosinophilic cellulitis, and eosinophilic panniculitis have been reported not only after COVID-19 vaccination but also after SARS-CoV-2 infection [74,87]. The reactivation of herpes zoster has been reported after mRNA vaccination. The causes are thought to be the dysregulation of T cell function due to vaccine-induced immunomodulation [57].
2.7. Endocrine Diseases
Graves’ Disease [88,89], hypophysitis [90], hypothyroidism [88], thyroiditis (painful, silent, and subacute) [88,91], syndrome of inappropriate antidiuresis [92], and Type 1 diabetes mellitus [15] have been reported following COVID-19 vaccination (Table 1). Jafarzadeh et al. reported thyroid dysfunction following COVID-19 vaccination [88], and Yamamoto et al. reported a case of thyroid storm [14]. Therefore, the evaluation of the thyroid hormones after vaccination is important. It is thought that autoimmune diseases, including Graves’ Disease and hypothyroidism, are associated with cross-reactivity. Autoantibodies are produced by the cross-reactivity between thyroid tissue antigen and the SARS-CoV-2 spike proteins produced by mRNA vaccines [93].
2.8. Collagen Diseases
Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis [94], antiphospholipid syndrome (APS) [95], dermatomyositis (DM) [96], eosinophilic granulomatosis (EGPA) relapse [25], giant cell arteritis [97], polymyalgia rheumatica [98], rheumatoid arthritis (RA) [11], systemic lupus erythematosus (SLE) [99], and systemic sclerosis (SSc) [100] have been reported after COVID-19 vaccination (Table 1). Autoimmune diseases, including ANCA-associated vasculitis, DM, RA, SLE, and SSc, have been reported [11,94,99,100]. Jinno et al. reported systemic thrombotic events after vaccination in a patient positive for the antiphospholipid antibody. They also suggested that the vaccine may have triggered the onset of APS (second hit) (95).
2.9. Hematologic Diseases
Aplastic anemia [101], acquires hemophilia A [102], autoimmune hemolytic anemia [103], hemophagocytic lymphohistiocytosis [28], immune thrombocytopenia [104], and vaccine-induced immune thrombotic thrombocytopenia [105] have been reported after COVID-19 vaccination (Table 1). In each reported case, the main disease was suspected to be related to autoimmunity. Hematologic adverse reactions may not be easily diagnosed, especially if anemia progresses slowly or if the onset of symptoms is slow [103].
2.10. Others
Abnormal menstrual cycles (delayed menstruation or increased bleeding or pain) [106], anaphylaxis [44], gout flares [48], lymphadenopathy [107,108], rhabdomyolysis [109], shoulder injuries related to vaccine administration (SIRVA) [109,110], and Vogt–Koyanagi–Harada syndrome [19] have also been reported following COVID-19 vaccination (Table 1). SIRVA is an acute inflammation of the shoulder that causes substantial shoulder pain and a limited range of motion [109,110]. FDG uptake with positron emission tomography imaging, which suggests the inflammation of the deltoid muscle and axillary lymph nodes at the inoculation site, has been reported [107,108].
Funny how this long list is just like -but only some of- Pfizers own, which we only got to see after a court ordered release of their documents forced their hand. They wanted to hide the info for 75 years! And still, some trust!!
Consider reading the whole article, where they discuss higher risks in the naturally immune, of course, and the pathophysiology of how the adverse events are playing out in the body processes. More confirmation of my suspicions and what I saw in people and their labs and signs and symptoms,.. beautiful, previously healthy, fabulous people, over the last 2+ years.
You see the number in brackets in red, they refer to more medical research, and are at the end of the full article, found here:
Thank you