The way you handle today is enough, whatever that looks like. #ALS

You’re allowed to acknowledge what today looks like without downplaying it. #ALS

Your experience is part of a wider story that deserves recognition. #ALS

I don’t want to be inspirational. I want to be understood. #ChronicallyIll

You bring something unique to the world that ALS cannot erase. #RareDiseaseCommunity

Explore the details on how a wearable robotic glove is helping a man living with ALS regain his hand function and grip: https://bit.ly/4wADf8w #ALS #RoboticGlove #LivingWithALS #ALSNewsToday #Bionews

Your worth isn’t measured in tasks, energy, or output. #ALS

Strength can exist without movement, effort, or action. #ALScommunity

There is value in every way you show up #ALSsupport

Today holds space for you exactly as you are. #ALSCommunity

How you show up today is shaped by things most people never see. #RareDiseaseCommunity

You’re moving through something complex, and it’s okay if your emotions are, too. #ALS

Some moments carry a kind of meaning that only you can define. #ALS

Today is Chronic Disease Day: https://bit.ly/4vYCkyV Living with ALS often means adapting to changes that affect everyday life, from mobility and communication to routines and independence. #ChronicDiseaseDay #ALS #LivingWithALS #ALSAwareness #ALSNewsToday #BioNews

The way you process today belongs entirely to you. #LivingWithALS

The everyday, challenging moments, such as repositioning in bed, bathing, and waiting for help with the restroom, can be some of the hardest parts of this disease. Your experiences during these times are recognized within this community. #ALS

You know your needs best: https://bit.ly/4h9yLRE #ALS #AmyotrophicLateralSclerosis #PatientAdvocacy #ALSNewsToday #Bionews

Caregivers do a thousand invisible things every day. We see you and send a virtual hug your way 🫂 #ALSCaregiver

For parents with ALS: the love you show your kids, even if it comes across differently, still reaches them. #ALS

Families living with ALS learn to manage fear, love, and responsibility all at once. It takes a community’s support, along with immense love and strength. #ALS

A promising advance in ALS research: https://bit.ly/4vmmjlg #ALS #AmyotrophicLateralSclerosis #ALSResearch #BrainComputerInterface #AssistiveTechnology #BioNews

Your body is carrying something far heavier than most people understand. This community acknowledges every hurdle you're going through. #ChronicIllness

Your effort counts, even when the outcome looks different than before. #RareDisease

Joy may look different now, but it still matters. #ChronicLife

Families adjusting to ALS build new routines constantly. It’s not easy work, and it’s okay if it feels messy or imperfect. #ALS

You deserve moments of ease wherever they can be found. Wishing you some gentleness today. #ALS

It’s understandable if your thoughts move in directions you didn’t expect. #ALS

Your way of navigating today doesn’t have to look like anyone else’s. #ALS

The impact you’ve had on people is woven into their lives in lasting ways. #ALSCommunity

A legacy isn’t built from accomplishments, it’s built from how you make people feel. #SpoonieSupport

Post-rest can still feel exhausting when your body doesn’t recover the way it used to. #ChronicFatigue

Some connections leave a mark that time can’t undo. #RareDisease

Rest is productive. Some days with ALS don’t go as planned. Even getting dressed can feel overwhelming, and the simplest tasks may take every ounce of energy: https://bit.ly/4oXgBod #ALS #ALSAwareness #LivingWithALS #ALSNewsToday #Bionews

A former NFL star is turning his experience into a call for greater ALS awareness, earlier recognition of symptoms, and stronger support for research: https://bit.ly/4vJcGOD #ALS #ALSAwareness #RareDisease #ALSNewsToday #Bionews

Acts of kindness can echo for years #RareDiseaseSupport

“I’m tired” can mean far more than people realize.  #ALS

Living with ALS means learning to hold onto moments of hope, no matter how small: https://bit.ly/3QvULvt ALS can take away many of life’s simple pleasures, making it difficult to look ahead with excitement. #ALS #LivingWithALS #ALSCaregiver #ALSNewsToday #Bionews

Leave a ♥️ in the comments if you believe love doesn’t fade - it just changes shape and keeps moving forward #ALS

Purpose isn’t found, but rather revealed through the life we live  #RareDisease

Compassion is a thread connecting us to others. #ChronicIllnessSupport

New ALS clinical trial news: https://bit.ly/4vInEUy A first patient has been dosed in a European study evaluating an investigational therapy designed to target fat metabolism, an area researchers believe may play a role in ALS. #ALS #ALSResearch #ClinicalTrials #ALSNewsToday #Bionews

Love shows up in the small moments as much as the big ones. #ChronicIllness

Illness life: where “I’m fine” can mean “I’m doing my best to hold on.”  #ChronicIllness

Some days I mourn. Some days I find moments of peace. Often it’s both. #ALS

I used to live by goals. Now I live by what is possible. #ChronicIllnessWarrior

“Hearing from others who’d lived through those same emotions and could both normalize them and offer practical advice felt like the ultimate gift of empathy and compassion” -Juliet Taylor: https://bit.ly/44bgFI2 #ALS

“Each of us develops our own means of coping with heartbreak” -Juliet Taylor: https://bit.ly/4a8B2cF #ALS

This experience has many layers, and you’re navigating them the best way you can. #ALS

Adult children need support too: https://bit.ly/4ePr3JV When a parent is living with ALS, adult children often find themselves balancing careers, relationships, parenting, caregiving, and the emotional weight of watching someone they love change. #ALS #ALSCaregivers #ALSNewsToday #Bionews

How you process things may change from day to day, and that’s completely normal. #ALS