Latest posts tagged with #ALSAWARENESSMONTH on Bluesky
A Quebec father who’s been diagnosed with ALS is planning a cross-country journey in his motorized wheelchair to raise money and awareness.
Visit www.ctvnews.ca/montreal/art... to read more.
#als #alsawarenessmonth #canada #quebec #ctvnews
#ALSAwarenessMonth is a reminder of the urgent need for progress.
Dr. Lorne Zinman and Kelli Maguire, who lives with ALS, spoke with CTV about the new Garry Hurvitz Brain Sciences Centre and the integrated care available through the Yuval & Lori Barzakay Brain Health Clinic.
bit.ly/3ZieLD0
June is #ALSAwarenessMonth — a time to raise awareness about amyotrophic lateral sclerosis, a devastating neurodegenerative disease.
Dr. Erik Pioro is launching a research program to accelerate the development of therapies that could slow or stop ALS.
Read the full story:
#ALSAwarenessMonth day 31. Last day!
ALS has been known for 150 years and there is still no cure. Effective treatments are limited. Thankfully research funding has been increased but ALS needs more!
#ALS #findacure #takeabreath
www.iamals.org/research-fun...
Not rushed. Not confusing. Not a dead-end. Just real care, real answers, and real people who understand.
Looking for support? Call (855) 255-5917 or visit synapticure.com
#ALSAwarenessMonth #EndALS #ALSCommunity #IAMALS #PatientStories #VirtualCare
#ALSAwarenessMonth day 26
(I got behind again!)
This is one way funds raised for ALS are used. Research and drug trials!
www.prnewswire.com/news-release...
"These Moments are the Gifts; don't miss the Moments that Matter." Adam Soldati is battling ALS & Fighting to Live ❤️ 🙏
Real talk about Adam's journey since receiving his ALS diagnosis 15 months ago. More to come in The B1G Story from BTN. #BoilerUp #ALSAwarenessMonth www.youtube.com/watch?v=wQ3M...
It’s Week 4 of ALS Awareness Month and we’re spotlighting the caregivers—the family, friends, and partners who show up every day.
Our caregiving resource highlights ways to reduce burnout, care for your own well-being, and feel less alone.
Explore it here: tinyurl.com/bdkkjrem
#ALSAwarenessMonth
During #ALSAwarenessMonth we are highlighting some of the symptoms of ALS that you should be aware of.
ALS gradually prohibits the ability to:
🔴 Speak
🔴 Swallow
🔴 Walk
🔴 Grasp objects
🔴 Move
🔴 Breath
Find out more at alsa.org
May is #ALSAwarenessMonth. ALS is a disorder that affects the function of nerves and muscles.
Over 6,000 people in the U.S. are diagnosed with ALS each year.
Find out more at ALSA.org
#ALSAwarenessMonth day 28
Research is promising!
www.genengnews.com/topics/drug-...
#ALS #bobertswarriors #takeabreath #ALSawareness
#ALSAwarenessMonth day 25
Do not cut funding for ALS! This disease needs more research not less!
www.instagram.com/reel/DJ7ZMXi...
#ALSAwarenessMonth day 24. Brooke Eby Is awesome for sharing her story and letting people see ALS in real life
fb.watch/zOgnZkcWR5/
During #ALSAwarenessMonth, in my Disney way, I convey ALS through Ben's experience, as well as how it affected me as his #caregiver.
We must fight this regime's reckless and severe budget cuts to research for ALS and other diseases.
pixiedustforcaregivers.com/2025/05/24/o...
During #ALSAwarenessMonth, in my Disney way, I convey ALS through Ben's experience, as well as how it affected me as his #caregiver.
We must fight this regime's reckless and severe budget cuts to research for ALS and other diseases.
pixiedustforcaregivers.com/2025/05/24/o...
#ALSAwarenessMonth day 21
www.alstogether.org
The headquarters for all affected by ALS. Patients, family and caregivers.
ALS patient sitting in the sin surrounded by dogs
#ALSAwarenessMonth
Protecting the queen.
🤍
Charlene 12-5-49 ~ 5-29-15
#ALSAwarenessMonth | Gene therapy is shaping the future of ALS treatment. 🧠
🎙️ Listen to Prof. Dame Pamela Shaw discuss groundbreaking insights in our exclusive podcast episode:
🎧👉 buff.ly/dipCRgG
#GeneTherapy #ALSResearch #Neurology #Neuroscience #ALS #MedSky
#ALSAwarenessMonth day 19
One way to get involved and help is to volunteer your time! There are so many wonderful organizations in addition to #ALSAssociation .
#ALSAwarenessMonth day 18 (I got behind!)
For so many this disease has advanced a lot before a definitive diagnosis is made!
#findacure #ALSawareness #thereishope
Custom features can be the difference between being able to communicate or not.
Bridging Voice specializes in customizations—like our “Translate” button, letting users type in one language and speak in another—instantly. Explore what’s possible.
#ALSAwarenessMonth #ALS
This week, we're highlighting how smart customizations—like layout tweaks, eye movement adjustments & better error correction—can make communication smoother, faster & less tiring.
See what we do: bridgingvoice.org/innovations
#ALSAwarenessMonth #pALS #AssistiveTechnology
Every person with ALS has different needs—and their communication tools should reflect that.
At Bridging Voice, we believe customization is key to helping pALS communicate more effectively. 💬
#ALSAwarenessMonth #AssistiveTechnology #BridgingVoice #pALS
#ALSAwarenessMonth Day 17
Someone with ALS may experience:
Air “hunger” (gasping, labored breathing) with an without activity
Fatigue
Frequent yawning or sighing during the day
Waking in the morning with a headache
Awakening frequently during the night
Difficulty lying flat
#TakeABreath
It’s #ALSAwarenessMonth, (Day 16) and there’s no better time to double your impact!
It’s a powerful way to boost your support and help fund critical care, support, and advocacy for #ALS Visit doublethedonation.com/alsnetwork to check if your employer participates in a matching gift program.
#ALSAwarenessMonth day 14! How did I miss it!
The Muscular Dystrophy Association is a leading organization dedicated to fighting ALS. MDA has a long history of funding ALS research and supporting the ALS community through various initiatives like care centers, advocacy efforts.
