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#Mnd Reel by @anaclarabutcher - The greatest honour of my life is to have him as my soulmate and I will fight everyday for him❤️‍🩹

#mnd #mndawareness #terminalillness
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@anaclarabutcher
The greatest honour of my life is to have him as my soulmate and I will fight everyday for him❤️‍🩹 #mnd #mndawareness #terminalillness
#Mnd Reel by @apexneuro - Results from a 2hr MND session…

From struggling to lift her arm, reduced wrist control and weakened grip ➡️ to being able to resist force and fully m
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@apexneuro
Results from a 2hr MND session… From struggling to lift her arm, reduced wrist control and weakened grip ➡️ to being able to resist force and fully move her arm, flip her hand over and back, and hold a glass with strength 💪🏼 “I held my coffee cup this morning! ☕️” All in just a few hours. #apexneuro #motorneuronedisease #ALS #ireland #uk #manchester #mnd #motorneuronediseaseawareness
#Mnd Reel by @mndassoc (verified account) - At just 26 years old, animal and outdoor loving Tamara received her MND diagnosis. 💔

Whilst Tamara's love of her animals remains unchanged, her abil
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@mndassoc
At just 26 years old, animal and outdoor loving Tamara received her MND diagnosis. 💔 Whilst Tamara’s love of her animals remains unchanged, her ability to go out into the yard and ride her horses has been taken from her. Here, Tamara and her mother Tracey share how her MND diagnosis has impacted their lives. Tamara’s story has touched not just us here at the MND Association, but many of her colleagues and friends. 🧡 Together, they have raised thousands in the fight against MND in Tamara’s honour, and we look forward to sharing more on this with you this week... ______________________________________ #mnd #als #mndassoc #mndassociation #fundraising
#Mnd Reel by @anaclarabutcher - We've spent more than £3500 getting Jonny seen and diagnosed privately whilst the NHS LAUGHED in our faces when we asked them to consider MND. They sa
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@anaclarabutcher
We’ve spent more than £3500 getting Jonny seen and diagnosed privately whilst the NHS LAUGHED in our faces when we asked them to consider MND. They said he had FND and told him to do physio which included a lot of heavy weight lifting which we now know is not allowed for MND patients. The NHS recommendations made him worse faster and we can’t change that but we can fight from now on. Jonny is my soul mate, best friend, love of my life and I will do ANYTHING in my power to fight for him even with this terminal desease and all help is appreciated 🥹❤️‍🩹 thank you for your support and prayers. I know God is with us. 🇧🇷Nós gastamos mais de £3.500 para que o Jonny fosse atendido e diagnosticado no sistema privado, enquanto o NHS riu na nossa cara quando pedimos para considerarem a possibilidade de ELA (Doença do Neurônio Motor). Disseram que ele tinha FND e recomendaram fisioterapia que incluía levantamento de peso pesado, algo que agora sabemos que não é recomendado para pacientes com ELA. As recomendações do NHS acabaram fazendo com que a condição dele piorasse mais rápido. Não podemos mudar o que já aconteceu, mas podemos lutar a partir de agora. Jonny é minha alma gêmea, meu melhor amigo e o amor da minha vida, e eu farei tudo que estiver ao meu alcance para lutar por ele, mesmo diante dessa doença terminal. Toda ajuda é muito bem-vinda. 🥹❤️‍🩹 Obrigada por todo o apoio e pelas orações. Eu sei que Deus está conosco. #mndawareness #mnd #mnddiagnosis
#Mnd Reel by @zalisteggall (verified account) - Did you know that every day in Australia, two people are diagnosed with Motor Neurone Disease (MND) and two people lose their lives?

I recently met w
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@zalisteggall
Did you know that every day in Australia, two people are diagnosed with Motor Neurone Disease (MND) and two people lose their lives? I recently met with Warringah locals Ron and Anna. Ron was diagnosed at just 35, and together they are raising two young children. Their story is deeply moving, and tragically they know of two other young men here in Warringah also living with MND. Across Australia, around 2,700 people are living with this cruel disease, with thousands of families impacted. The cost is already more than $5 billion a year and is projected to rise to $7.5 billion by 2025. That’s why I am calling on the government, alongside Ron, Anna and MND Australia, to fund a national MND database. We need this data to drive better treatment, prevention, and ultimately, save lives. Thank you to Ron and Anna for sharing their story with me, and for their extraordinary advocacy in the face of such heartbreaking challenges.
#Mnd Reel by @livewellsouthwest - Steve's inspirational story on living with MND. Working with our Speech and Language Therapy Team, he's trying cocktails with new technology and contr
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@livewellsouthwest
Steve’s inspirational story on living with MND. Working with our Speech and Language Therapy Team, he’s trying cocktails with new technology and controlling his world with his eyes. #mnd #mndawareness #speechandlanguagetherapy #manchesterunited #robburrow #inspirational
#Mnd Reel by @ed_slater (verified account) - Two codes. One cause.

I'm proud to bring the 745 Cross Code Rugby Game back - union vs league standing together to fight MND. Every ticket sold helps
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@ed_slater
Two codes. One cause. I’m proud to bring the 745 Cross Code Rugby Game back — union vs league standing together to fight MND. Every ticket sold helps families like mine and funds vital support. 📅 9th November — Kingsholm Stadium, Gloucester 🎟️ Tickets: 745game.org Let’s pack the stands and show what the rugby family can do. #745Game #RugbyFamily #MND
#Mnd Reel by @darin_nakakihara (verified account) - One year. Same disease. A very different voice.
This is what ALS sounds like after 12 months.
Every May 19, I'll document my voice-until I no longer c
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@darin_nakakihara
One year. Same disease. A very different voice. This is what ALS sounds like after 12 months. Every May 19, I’ll document my voice—until I no longer can. #ALS #VoiceProgression #GoFindSomeJoy #LouGehrigsDisease #TerminalIllness #ALSAwareness #BeforeAndAfter #OneYearLater #MND #VoiceBanking
#Mnd Reel by @bbc5live (verified account) - "We didn't let this disease take us over as a couple."
 
Lionesses great Steph Houghton spoke to 5 Live Breakfast about her husband's battle with moto
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@bbc5live
“We didn’t let this disease take us over as a couple.”   Lionesses great Steph Houghton spoke to 5 Live Breakfast about her husband’s battle with motor neurone disease   The former Bradford City defender Stephen Darby was diagnosed with MND in 2018. #BBCFootball #mnd
#Mnd Reel by @the_745game - Billy Twelvetrees speaking before last year's 745 game, reminding us what this is all about: unity, noise, and the fight to find a cure for MND.

We a
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@the_745game
Billy Twelvetrees speaking before last year’s 745 game, reminding us what this is all about: unity, noise, and the fight to find a cure for MND. We all have a part to play. See you at Kingsholm on the 9th November. Tickets in bio #745Game #FightMND #ForTheOnesWeLove
#Mnd Reel by @darin_nakakihara (verified account) - 16 months. One disease. And a reality that changes faster than anyone is prepared for.

In this video, I'm showing the progression of ALS (amyotrophic
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@darin_nakakihara
16 months. One disease. And a reality that changes faster than anyone is prepared for. In this video, I’m showing the progression of ALS (amyotrophic lateral sclerosis) over the past 16 months. What started as subtle weakness slowly turned into something much bigger. This is what living with Lou Gehrig’s disease really looks like day by day, month by month. ALS, also known as motor neuron disease (MND), is a progressive neurodegenerative disease that affects the nerve cells that control voluntary muscles. As the disease progresses, people living with ALS gradually lose the ability to walk, talk, eat, and eventually breathe independently. This video documents a very real ALS progression timeline. It’s not meant to scare people. It’s meant to show the truth about this disease so that more people understand what families and patients face every day. Awareness matters because ALS is still considered a terminal illness, and research, advocacy, and community support are desperately needed. For those who are newly diagnosed with amyotrophic lateral sclerosis, caring for someone with motor neurone disease, or supporting a loved one with Lou Gehrig’s disease, I hope this video helps you feel less alone. My goal is simple: to raise awareness about ALS, share the reality of living with this disease, and remind people that even in the hardest moments, it’s still possible to go find some joy. If you are part of the ALS community, a caregiver, family member, or someone trying to understand motor neuron disease, please share this video so more people can see what ALS really looks like. Awareness leads to understanding. Understanding leads to compassion. And compassion moves the world forward. #ALS #ALSawareness #LouGehrigsDisease #MotorNeuronDisease #MND #ALSAwarenessMonth #ALScommunity
#Mnd Reel by @bbc (verified account) - Kevin Sinfield says there will always be a Rob Burrow presence in Leeds.

Before Rob died in June, he recorded a new series of his BBC podcast.

With
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@bbc
Kevin Sinfield says there will always be a Rob Burrow presence in Leeds. Before Rob died in June, he recorded a new series of his BBC podcast. With his family's blessing, those episodes have been released. You can hear them on @bbcsounds #KevinSinfield #RobBurrow #MND

✨ Guida alla Scoperta #Mnd

Instagram ospita 2.2 million post sotto #Mnd, creando uno degli ecosistemi visivi più vivaci della piattaforma.

#Mnd è uno dei trend più coinvolgenti su Instagram in questo momento. Con oltre 2.2 million post in questa categoria, creator come @darin_nakakihara, @anaclarabutcher and @ed_slater stanno guidando la strada con i loro contenuti virali. Esplora questi video popolari in modo anonimo su Pictame.

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💡 I contenuti top ottengono oltre 10K visualizzazioni - concentrati sui primi 3 secondi

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