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#Guillain Barre Syndrome
vaccinelaw · 1 year
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If you filed a vaccine injury claim and lost, you are not alone. Over the past 10 years, the U.S. Court of Federal Claims (the “Vaccine Court”) has dismissed thousands of claims under the National Vaccine Injury Compensation Program (VICP). In fact, since Congress established the VICP in 1988, the Vaccine Court has dismissed more claims than it has compensated. 
Read More:- https://vaccinelaw.com/lawyer/2021/07/18/Vaccine-Court/What-are-Your-Options-if-You-Lost-Your-Vaccine-Injury-Claim_bl42633.htm
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heardatmedschool · 2 years
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“Please, take these patients out of the trauma box.”
About Guillain-Barré patients.
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didanawisgi · 2 years
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disabledsysboxes · 1 month
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Autoimmune - 4
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drrohitgupta · 6 months
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Guillain Barre Syndrome is a rare but serious neurological condition that requires prompt medical attention and intervention. With the appropriate treatment and management strategies, patients with GBS can achieve significant improvement and regain function. Early recognition of symptoms and timely initiation of treatment are critical for optimizing outcomes in individuals affected by GBS.  Dr. Rohit Gupta stands out as one of the best Doctor for Guillain Barre Syndrome in India. With a stellar reputation in the field of neurology, Dr. Gupta brings a wealth of knowledge and expertise to the table.
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mcatmemoranda · 1 year
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Definition and pathogenesis – The acute immune-mediated polyneuropathies are classified under the eponym Guillain-Barré syndrome (GBS). The acute polyneuropathy of GBS is triggered when an immune response to an antecedent event cross-reacts with shared epitopes on peripheral nerve (molecular mimicry).
●Antecedent triggers – Most patients report an antecedent infection or other event in the four weeks prior to GBS. Upper respiratory tract infection and gastroenteritis are the most common infections, and Campylobacter jejuni gastroenteritis is the most commonly identified precipitant of GBS.
●Epidemiology – GBS occurs worldwide with an overall incidence of 1 to 2 cases per 100,000 per year. The incidence increases by approximately 20 percent with every 10-year increase in age.
●Clinical features – The typical clinical features of GBS include progressive and symmetric muscle weakness with absent or depressed deep tendon reflexes. Patients may also have sensory symptoms and dysautonomia.
•GBS symptoms typically progress over a period of two weeks. If the nadir is reached within 24 hours or after 4 weeks of symptom onset, alternative diagnoses must be considered.
•GBS is a heterogeneous syndrome with variant forms that may be identified by distinguishing clinical and pathologic features. Acute inflammatory demyelinating polyneuropathy is the most common form of GBS. Common variant forms include acute motor axonal neuropathy, acute motor and sensory axonal neuropathy, Miller Fisher syndrome, and Bickerstaff brainstem encephalitis.
●Diagnostic evaluation – The initial diagnosis of GBS is based on the clinical features consistent with the syndrome: acute onset of progressive, mostly symmetric muscle weakness, and reduced or absent deep tendon reflexes. The clinical diagnosis of GBS is confirmed if cerebrospinal fluid (CSF) and electrodiagnostic studies show typical abnormalities.
•CSF findings in patients with GBS is an albuminocytologic dissociation consisting of an elevated CSF protein (typically 45 to 200 mg/dL [0.45 to 2.0 g/L]) with a normal white blood cell count (typically <5 cells/mm3 but may be elevated up to 50 cells/mm3).
•Electrodiagnostic studies may show prolonged or absent F waves and absent H reflexes, increased distal latencies and conduction blocks with temporal dispersion, significant slowing or absent response on nerve conduction velocities, and reduced recruitment or denervation on needle electromyography of weak muscles.
•Laboratory testing is performed for all patients to screen other common causes of acute weakness. We reserve ganglioside autoantibody testing for patients with symptoms suggestive of a variant form of GBS. Neuroimaging is typically used for patients with atypical symptoms to exclude alternative etiologies.
●Differential diagnosis – The differential diagnosis of GBS includes chronic inflammatory demyelinating polyneuropathy, other acute polyneuropathies, and diseases of the spinal cord, neuromuscular junction, and muscle. Patients with features atypical for GBS should be evaluated for alternative sources to symptoms.
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qdnurses · 1 year
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Mnemonic For Understanding Guillain-Barré Syndrome: GBS
G - Gradual onset of weakness, often beginning in the legs   B - Body's own immune system attacking the nerves   S - Symptoms include muscle weakness, tingling, and in severe cases, paralysis  
Guillain-Barré Syndrome (GBS) is a rare but serious autoimmune disorder that often comes on quickly, following a minor infection such as a lung or stomach bug. It leads to muscle weakness that can evolve into severe nerve dysfunction.
The "gradual onset of weakness" encapsulates the first hallmark of GBS: a weakness that often starts in the legs and moves upward. The "body's own immune system attacking the nerves" serves as a reminder of the autoimmune nature of the condition. Lastly, "symptoms" emphasizes that, in addition to muscle weakness, GBS can present with tingling and, in severe cases, complete paralysis.
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brahmhomeo · 2 years
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Guillain Barre syndrome (GBS)
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willowreader · 3 months
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A huge study of #LongCovid in South Korea and Japan shows a pronounced increase of Guillain-Barré syndrome, cognitive deficit, insomnia, anxiety disorder, encephalitis, ischemic stroke and mood disorder. Reduced by vaccination.
Posted by @ danibeckman on X
A super important study published today. They looked at 10 million people in Japan and 12 million in South Korea.
The long-term risk of neuropsychiatric events following COVID-19 was higher than the risk in both the general population and those with another respiratory infection. Guillain-Barré syndrome had the highest hazard ratio post-COVID-19 diagnosis, followed by cognitive deficit, insomnia, anxiety disorder, encephalitis, ischaemic stroke, mood disorder, and nerve disorder.
This list of neurological symptoms is way too diverse and complex! What's is going on? Viral persistence? Autoimmunity? General neuroinflammation? So many questions...
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redheadgleek · 2 years
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I really wish my tummy would feel better.
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vaccinelaw · 1 year
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The CDC uses a three-stage approach to evaluate vaccine safety. Of course, this oversimplifies the process a bit. Within each of these stages, there are numerous intermediate steps, and multiple agencies and clinical researchers are involved in determining whether a vaccine should be released for widespread use in the United States. Contact our top vaccine injury lawyers.  
Read More:- https://vaccinelaw.com/lawyer/2020/06/01/Centers-for-Disease-Control-and-Prevention/When-Does-the-CDC-Consider-a-Vaccine-E2809CSafeE2809D_bl40225.htm
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healthcareporium · 2 months
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Guillain-Barre Syndrome is a rare but serious autoimmune disorder in which the body's immune system mistakenly attacks the peripheral nerves. This condition can lead to muscle weakness, numbness, and in severe cases, paralysis.
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didanawisgi · 2 years
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vijayananth · 7 months
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mauryaayurveda1 · 7 months
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At Maurya Hospital in Kerala, We provide ayurveda, Physiotherapy and other alternative medical care to treat patients with Guillain Barre syndrome.
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geeknik · 9 months
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My end of the year review is a hopeful look towards 2024 because 2023 will go down as the worst follow-up to a bad year ever.
August 2022, Dad passes.
November 2022, Wife t-boned in an Oklahoma City intersection; diagnosed with a traumatic brain injury.
15 January 2023, I am transported by ambulance and admitted to the hospital for trouble breathing & walking. 🚑 I am diagnosed with Influenza A and Pneumonia which was the trigger for a rare condition called Guillain-Barré Syndrome. It’s where the immune system decides the peripheral nervous system is the enemy and attacks those nerve endings. 🦠
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Medically induced sleep, ventilator, feeding tube, PIC line.
23 January 2023, wake up on a ventilator and find I am completely paralyzed from the neck down. 🥺 While I was asleep, I was treated for ventilator pneumonia, had a blood transfusion and 5 rounds of plasmapheresis. Basically, they replaced my icky blood plasma with nice fresh plasma from the blood bank. 🩸
26 January 2023, extubated and off the ventilator for about 3 hours when I suffer cardiac arrest and briefly die. 10 chest compressions plus a shot of something and I’m back on the ventilator when I wake up again. 💀 They said I had carbon dioxide poisoning, which caused the cardiac arrest. Now there is talk of a possible tracheotomy if my body refuses to tolerate being off the ventilator. That would have meant shaving off my 13 year beard. And being moved to a long term care facility. I’m against all of these ideas. 🤬 Months after my release, the nurse manager of the ICU assured me that shaving off the beard would have been absolutely avoided. 😍
A week or so later, they remove the ventilator once more, but this time, thank fuck, my body remembers how to breathe. I’m starting to regain movement in my fingers and toes and then I can lift my arms and legs. The nerve pain is un-fucking-bearable.
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I’m awake! And still bearded! Huzzah! 🎉
15 February 2023 left the ICU, transferred to an inpatient rehabilitation hospital right next door, where I, in my 40s, have to learn how to walk again.
15 March 2023 A very long and exhausting 30 days later I go home with a walker but within a week or so I’m pretty much walking on my own. During my time in the rehab hospital we discover I am incredibly allergic to Lyrica. 🫠 I won’t go into detail but let’s just say it was the worst bad trip ever.
I lost ~40 pounds on the ICU diet. Fast forward to today and I’m about 90-95% of where I was a year ago although I still have a lot peripheral nerve pain, balance issues, and I’m always tired. Thankfully the nerve pain is nothing like it was in the ICU.
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My beard and I going through some things.
In the end, I am incredibly lucky to have the love and support of my wife, my mom, my sister, my nieces, and of course my Internet hooligan friends, and last but definitely not least, my #spiderSilk🕷️🕸️ family, there to help me persevere and make a speedier than expected recovery. ❤️‍🩹
I am hopeful that 2024 will be the year I shrug off GBS for good. 🤙🏻
I’m not crying, you’re crying.
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