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Reels en Tendencia

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#Mnd Reel by @als (verified account) - Get ready with @rarewithmikey ALS turns even the smallest tasks into big challenges. Today is Global ALS/MND day. A day to recognize the challenges t
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AL
@als
Get ready with @rarewithmikey ALS turns even the smallest tasks into big challenges. Today is Global ALS/MND day. A day to recognize the challenges that people living with ALS all over the world face. Your donation can help change how people with ALS live and support the search for a cure. Donate today! #als #globalalsmndday #mnd #alsawareness #makealshistory #grwm #morningroutine
#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 @alliecbrunner (verified account) - I share this to show Eric's first visible symptoms, the ones that pushed him to start advocating for answers. Many people can experience these symptom
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AL
@alliecbrunner
I share this to show Eric’s first visible symptoms, the ones that pushed him to start advocating for answers. Many people can experience these symptoms and have something entirely different. But for him, the combination of all of them pointed us toward ALS. . . . . . . #als #alsawareness #endals #alsadvocacy #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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DA
@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 @als (verified account) - Physical Therapy with @leannesklavenitis Physical therapy can be challenging for anyone living with ALS. Leanne is from Australia and she is working
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@als
Physical Therapy with @leannesklavenitis Physical therapy can be challenging for anyone living with ALS. Leanne is from Australia and she is working hard to make sure she can continue to live life to the fullest. Her story echoes that of so many others across the globe. By supporting the ALS Association you can help fund critical research projects that can help make ALS a livable disease until we find a cure. Make a donation in recognition of Global ALS/MND Day. #als #globalalsmndday #mnd #alsawareness #makealshistory #physicaltherapy
#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 @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 @mndassoc (verified account) - "It's taking a long time, given that Charlotte unfortunately doesn't have time…" As her father Bob explains, Charlotte first showed symptoms of motor
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@mndassoc
“It’s taking a long time, given that Charlotte unfortunately doesn’t have time…” As her father Bob explains, Charlotte first showed symptoms of motor neurone disease (MND) when she was pregnant…her son is now 3, yet Charlotte is still waiting for vital housing adaptations. People with MND don’t have time to waste on red tape and paperwork. Write to your councillor - link in our bio. 🔗 __________________________ #MND #MNDAssoc #UnlockTheDoor #HousingCampaign #MNDAssociation
#Mnd Reel by @ed_slater (verified account) - Winter is a crap time especially when you're in a wheelchair, getting outside in the sun is much easier, even if you're in a hole. I've got this lit
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@ed_slater
Winter is a crap time especially when you’re in a wheelchair, getting outside in the sun is much easier, even if you’re in a hole. I’ve got this little exercise machine and it feels good to be able to be outside doing any sort of exercise. Keep moving forward. #keepmovingforward #als #mnd #livingwithmnd
#Mnd Reel by @mdaorg (verified account) - People living with ALS/MND around the world, like Brooke Eby, don't have time to wait. This disease is relentless. But so is the Muscular Dystrophy As
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@mdaorg
People living with ALS/MND around the world, like Brooke Eby, don’t have time to wait. This disease is relentless. But so is the Muscular Dystrophy Association. Global #ALS research is severely underfunded, and progress depends on urgent action from all of us. Together, we can #EndALS. 👉 TAKE ACTION: Share this post and donate at MDA.org/EndALS #MND #EndALSwithMDA #ALSResearch #ALSMNDWithoutBorders #GlobalALSAwarenessDay
#Mnd Reel by @darin_nakakihara (verified account) - Watch my 2-year ALS journey - from 2 days before diagnosis, to 1 year later, to today, when I can no longer speak. This is my unfiltered progression w
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@darin_nakakihara
Watch my 2-year ALS journey — from 2 days before diagnosis, to 1 year later, to today, when I can no longer speak. This is my unfiltered progression with amyotrophic lateral sclerosis (ALS) — also known as Lou Gehrig’s disease, motor neuron disease (MND), or Charcot’s disease. Two years ago, I was teaching, walking, and talking. One year later, my speech began to fade. Today, I rely on assistive tech to communicate — but my story isn’t over. This video captures the physical decline, emotional fight, and the lesson I never expected: the world is full of kind people. I’m sharing this to raise awareness and show what ALS/MND really looks like — not just the science, but the humanity. For newly diagnosed patients, caregivers, and families: you’re not alone. This disease takes your movement and your voice, but not your hope or your heart. You’ll see: – A clip from before diagnosis – My 1-year update and changes in speech/mobility – Today’s reality: no voice, but still finding joy I made this video for anyone affected by ALS, MND, Lou Gehrig’s disease, or Charcot’s disease — and anyone who believes in strength through community. Please share this to help spread awareness and connect with others who need to see they’re not fighting alone. Subscribe for more honest updates on life with ALS/MND — covering progression, adaptive tech, and the pursuit of joy even when life slows down. #ALS #MND #LouGehrigsDisease #MotorNeuronDisease #CharcotsDisease #ALSprogression #ALSawareness #disability #wheelchairlife #hope #inspiration #GoFindSomeJoy Even when you lose your voice, your story still has power.
#Mnd Reel by @bbcnewsni (verified account) - A Belfast actor, who won high praise for playing Richard III in a wheelchair, is hoping a new clinical trial drug will help him in his fight against M
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@bbcnewsni
A Belfast actor, who won high praise for playing Richard III in a wheelchair, is hoping a new clinical trial drug will help him in his fight against Motor Neurone Disease (MND). Michael Campbell, also known as Michael Patrick, was diagnosed with the terminal disease in February 2023. MND, is usually life-shortening and there is currently no cure, but treatment can help manage the symptoms. 📲 For more on this story, and other news from BBC NI, click the link in our bio. #bbcnewsni #northernireland #motorneuronedisease #mnd

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📹 Los videos verticales de alta calidad (9:16) funcionan mejor para #Mnd - usa buena iluminación y audio claro

✍️ Descripciones detalladas con historia funcionan bien - longitud promedio 601 caracteres

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