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#Pnes Reel by @alanasepilepsymission - Non Epileptic Attack Disorder ….. Not all seizures are epilepsy 🧠

Unlike epileptic seizures, NEAD is a, often subconscious, reaction of the nervous
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@alanasepilepsymission
Non Epileptic Attack Disorder ….. Not all seizures are epilepsy 🧠 Unlike epileptic seizures, NEAD is a, often subconscious, reaction of the nervous system, not a structural brain malfunction. The attacks are not done on purpose or faked. They are the nervous system going into survival mode 🧠 Symptoms can look like epilepsy: ✨Shaking of arms or legs ✨Falling ✨Losing awareness or consciousness ✨Going blank ✨Stiffening But unlike epileptic seizures, NEAD is not caused by abnormal electrical activity in the brain 🧠 It is often linked to: ✨Psychological stress ✨Past or present trauma ✨Anxiety or depression ✨Sometimes physical injury It’s the brain’s way of “shutting down” to cope with something overwhelming. Diagnosis is made through video-EEG monitoring, which shows no abnormal electrical discharges during an episode 🧠 Treatment focuses on psychological therapies like Cognitive Behavioural Therapy (CBT), helping people understand triggers and regain control 🧠 👉🏻Awareness matters. 👉🏻Compassion matters. 👉🏻Believing people matters. Because hidden conditions deserve understanding too 💜 #NEAD #PNES #EpilepsyAwareness #SeizureAwareness #HiddenDisability AlanasEpilepsyMission
#Pnes Reel by @stellarflower16 - The term "pseudoseizures" is outdated and no longer used in the medical field.
"Pseudo" means fake or false, which made many people believe that these
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@stellarflower16
The term “pseudoseizures” is outdated and no longer used in the medical field. “Pseudo” means fake or false, which made many people believe that these seizures were “not real” but that’s far from the truth. Today, the correct name is Psychogenic Non Epileptic Seizures (PNES) or Psychogenic Non Epileptic Episodes (PNEE). They may look similar and mimic epileptic seizures on the outside, but they’re not caused by abnormal electrical activity in the brain. Instead, PNES are a response to psychological or emotional stress, the brain’s way of expressing overwhelming distress through the body,ect. PNES are real, serious, and involuntary. They just come from a different origin than epileptic seizures. Changing the language matters it reduces stigma and reminds people that these episodes deserve understanding, compassion, and proper medical care. 💜 #seizures #seizuresawareness #pnes #fyp #epilepsywarrior
#Pnes Reel by @erinmichaelam - I'm done hiding it. It's something I can't control so I'm being raw and making this post. I just self discharged after spending 33 days admitted in ho
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@erinmichaelam
I’m done hiding it. It’s something I can’t control so I’m being raw and making this post. I just self discharged after spending 33 days admitted in hospital and been in and out of hospital for a while before that. As some of you are aware, I have been showing symptoms of ‘extreme anxiety’ (doctors words) for years now. I’ve had test after test and they all came back clear. Heart monitor, constant observations taken, 24 hour eeg, results all clear. The seizures. The fainting episodes. The tremors and temporary paralysis. The fatigue. Sickness after sickness. ‘It’s not epilepsy’ those words are a blessing but als a curse. I’m glad, knowing that my seizures are ‘safe’ and don’t damage my brain (seudo/functional pnes seizures). However it means it can’t be controlled by medication. It’s chronic, there is no cure. Therapy relieves some symptoms, but it’s something that changes seriousness based on external factors such as stress, anxiety, hyperactivity etc which all come with my diagnosis of autism (awaiting an adhd diagnosis). FND (functional neurological disorder) can stroke at any time and ruin your life completely. I’m sharing this post to raise awareness of what I have been going through on a daily basis. I’m truly thankful for all of the people who have stuck by my side and supported me throughout my diagnosis. I’ve met some truly incredible people and I’ll forever be in debt to them. @jess.stri @thornberry.fae #fnd #functionalneurologicaldisorder #pnes #awareness #iceskating
#Pnes Reel by @glammedbychelly_ - Hello loves for years. I've been embarrassed to show myself like this, but I wanna share my story. This was recorded two years ago. I still suffer wit
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@glammedbychelly_
Hello loves for years. I’ve been embarrassed to show myself like this, but I wanna share my story. This was recorded two years ago. I still suffer with seizures I was diagnosed with PNES. And I do have stage 2 brain cancer (grade 2 glioma) I got a call last week and I will start treatment. I’m not sure what treatment, but I want to share my journey with you and share my full story and how all of this started and hopefully be able to help someone going through something similar. You are not alone Jesus loves you! #braincancer #grade2glioma #seizures #PNES #ᴊᴇsᴜsʟᴏᴠᴇsʏᴏᴜ
#Pnes Reel by @epilepsyseen - Some of my
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📸 Source: @ chronically.lindsay on TikTok
All credit are reserved for their respective Owners
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💥Want credit or removal?👉 DM @ fixpost
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@epilepsyseen
Some of my - 📸 Source: @ chronically.lindsay on TikTok All credit are reserved for their respective Owners - 💥Want credit or removal?👉 DM @ fixposts - - - - #epilepsyjourney#epilepsysurgery#disabilityawareness#seizure#pnes#epilepsywarrior#seizurefree#epilepsyawarenessday#epilepsypositivity#seizuredisorder#epilepsywarriors#epilepsi#epilepsyeducation#epilepsylifestyle#epilepsysurvivors#nonepilepticseizures#epilepsias#epilepsyphotochallenge#seizurestrong#medicationsideeffects#sudepawareness#epilepsylivesmatter#epilepsyaware#epilepsyinmotion#epilepsiarefractaria#epistemic
#Pnes Reel by @_rockyandash_ - In 2021, I was hospitalized for 45 days after the gun violence I experienced. I started having dissociative episodes where I became unable to move my
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@_rockyandash_
In 2021, I was hospitalized for 45 days after the gun violence I experienced. I started having dissociative episodes where I became unable to move my body or respond to stimuli. I could not pull myself out of these episodes on my own so if I wasn’t found by someone, I would be in a catatonic dissociative state for several hours. I lost gaps of time. I would convulse and sometimes hyperventilate. I lost my vision. I couldn’t feel pain or extreme temperatures. I scratched myself without being aware of my actions as a subconscious attempt of grounding myself. I felt so detached that I felt out of my body or like I was living in a video game because nothing was real. I lost the ability to speak and control my body’s movements. I saw a Neurologist while hospitalized out of state because they believed I was having psychogenic non-epileptic seizures. I had an MRI of my brain, an EEG, tons of labs done, and nerve conduction testing. I was told that I have “weird brain activity, but not seizure activity”. I went on believing I was only experiencing psychosomatic dissociation when my c-ptsd was triggered. These episodes have put me in dangerous situations from me having to pull off on the side of the highway moments before becoming unresponsive, to losing my ability to communicate with police and EMS in emergency situations, to passing out because it took someone so long to find me. I was asked by Mayo Clinic to record a dissociative seizure because I wasn’t able to describe them and recently I have had dissociative episodes unrelated to trauma. My therapist helped me do this by allowing me to record one of our sessions. Ever since I watched the video back, I have felt super self-conscious from making fun of my t-rex arms to my double chin when my teeth are chattering and more. I’ve had friends on Instagram ask about my non-responsive dissociative episodes but I realized that how I feel during the episodes is different from how they look. 👇🏼👇🏼👇🏼 Continued in comments 👇🏼👇🏼👇🏼
#Pnes Reel by @dileowellnessfarm - I began my #fnd and #pnes journey in March. It's gotten progressively worse but it won't beat me. I'll be back.
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@dileowellnessfarm
I began my #fnd and #pnes journey in March. It’s gotten progressively worse but it won’t beat me. I’ll be back.
#Pnes Reel by @epilepsygrew - 💜🧠 no hate please #e
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📸 Source: @ chronic_bad_ass on TikTok
All credit are reserved for their respective Owners
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💥Want credit or removal?👉 DM @
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@epilepsygrew
💜🧠 no hate please #e - 📸 Source: @ chronic_bad_ass on TikTok All credit are reserved for their respective Owners - 💥Want credit or removal?👉 DM @ fixposts - - - - #disabilityawareness#seizure#pnes#epilepsywarrior#seizurefree#epilepsyawarenessday#epilepsypositivity#seizuredisorder#epilepsywarriors#epilepsi#epilepsyeducation#cerebralpalsy#epilepsyadvocate#seizurememes#walktoendepilepsy#seizurefreedom#seizuresupport#seizuredisorders#epilepsystrength#athletesvsepilepsy#epilepsysurvivor#epilepsynow#epilepsymonitoring#epilepsyfoundationofamerica#epilepsywalk#temporallobeepilepsy
#Pnes Reel by @epilepsyhold - … literally no one is safe forgot to post this for epilepsy awareness month last month but
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📸 Source: @ scratchyscalp on TikTok
All credit are reser
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@epilepsyhold
… literally no one is safe forgot to post this for epilepsy awareness month last month but - 📸 Source: @ scratchyscalp on TikTok All credit are reserved for their respective Owners - 💥Want credit or removal?👉 DM @ fixposts - - - - #epilepsystrong#seizureawareness#epilepsyjourney#epilepsysurgery#disabilityawareness#seizure#pnes#epilepsywarrior#seizurefree#epilepsyawarenessday#epilepsypositivity#seizuredisorder#epilepsywarriors#epilepsyfacts#infantilespasmsawareness#epilepsyresearch#1in26#seizurememes#walktoendepilepsy#seizurefreedom#seizuresupport#seizuredisorders#epilepsystrength#athletesvsepilepsy#epilepsysurvivor#epilepsynow
#Pnes Reel by @kimberly_corban (verified account) - I am absolutely mature enough for the name of this diagnosis.
#PNES #nonepilepticseizures
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@kimberly_corban
I am absolutely mature enough for the name of this diagnosis. #PNES #nonepilepticseizures
#Pnes Reel by @xopaigealexandra - As someone who's lived my entire life with seizures let me be the one to tell you, they never get easier. They're scary every single time.

I'm beyind
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@xopaigealexandra
As someone who's lived my entire life with seizures let me be the one to tell you, they never get easier. They're scary every single time. I'm beyind frustrated. It's been years. Not only that but.. nothing happened that triggered it. NOTHING. Thankfully I caught myself on the couch and was able to make a call before the lights went out. Came-to, to Oscar licking my face to try and wake me up. But the truth is, nothings new. This is my life. This has always been my life. This will always be my life. Nothings new. Nothings new. Nothings new. Thankful for my village that shows up when I need them & especially Robert for carrying me through my hard days. ♥️🙏🏼 I'm sad. #PNES #FND #spoonie #psychogenicseizure

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