139.4K
ALThese hugs get more wobbly and have become more effort for Eric, but it’s effort worth expending, one day we will wish we could do this again.🤍
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#als #fuckals #alsawareness #love #hug
@alliecbrunner
High Volume
#Als
Смотрите 5.2M Reels видео о Als от людей со всего мира.
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AY子供と遊んでみた#als #車椅子 #難病
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BRA true professional @kjeansonne @nathanjeansonne #als #onwardforward #love #thejeansonne7 #motorneurondisease
@brianjeansonne
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LIThree years into their marriage she was diagnosed with ALS.
Most people with ALS live only about 2 to 5 years after diagnosis. Twenty years is incredibly rare.
ALS is one of the most devastating diagnoses a person can receive. Your mind remains clear and you understand everything happening, but little by little your body stops responding.
In many ways it’s the opposite of Alzheimer’s. With Alzheimer’s the pain is often hardest on the family watching someone slowly disappear. With ALS, everyone feels the weight of it together.
And yet somehow this couple has found a way to fill their lives with love, patience, and quiet joy.
Twenty years later he is still by her side. Lifting her, dressing her beautifully, brushing her hair, carrying her wherever she wants to go. And her smile says everything.
If you don’t watch the whole video, at least go to the moment when they are in the field of yellow flowers. He makes a halo for her head out of the flowers, holds her in the middle of the field, and later sits with her in his lap placing flowers around her face while she laughs. 🌼
The love between them comes through this video so beautifully.
Sometimes the most extraordinary love stories are the quiet ones where someone simply never stops showing up.
I wish everyone could feel loved like this. He truly seems like an angel on earth. ❤️
Music by me
Video source Reddit
#ALS
#Love
#Caregiving
#TrueLove
#Humanity
#LoveStory
@lisageng
1.3M
HAWhat we really wish for is a cure for ALS #Handicrap #handicap #crew #wheelchair #humor
@handicrapcrew
366.9K
ALWe need your help to find a cure! Visit ALS.org
#als #alsawareness
@als
337.7K
BRHere’s to 23 years and many more @kjeansonne #als #anniversary #love
@brianjeansonne
340.4K
NA❤️ @brianjeansonne #love #onward #als #bald #
@natejeansonne
1.1M
DOThis film brought me to tears. Check out “For Love And Life: No Ordinary Campaign” on @primevideo to learn about Brian’s miraculous fight against #ALS 🙏🏼 #forloveandlife #primevideocreator
@doctor.mike
36.7K
MNAt 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...
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#mnd #als #mndassoc #mndassociation #fundraising
@mndassoc
112.2K
UNThe three words you never want to hear changed my life completely.
You have ALS
#liveuntilyoudie #alsawareness #terminalillness #apositivelife #inspiringwomen
@unsteadyandready
89.4K
DA16 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
@darin_nakakihara
✨ Руководство по #Als
Instagram содержит 5.2 million публикаций под #Als, создавая одну из самых ярких визуальных экосистем платформы.
#Als — один из самых популярных трендов в Instagram прямо сейчас. С более чем 5.2 million публикаций в этой категории, создатели вроде @handicrapcrew, @doctor.mike and @brianjeansonne лидируют со своим вирусным контентом. Просматривайте эти популярные видео анонимно на Pictame.
Что в тренде в #Als? Самые просматриваемые видео Reels и вирусный контент представлены выше.
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Исследовать Als#al banat#al dente spaghetti#al pacino antalya#comidas para llevar al trabajo#jordi al nino#lisa su and al pacino#how did al capone get his scar#al jazeera news english