"We won't stop until every person on the planet knows what ALS is and no person on this planet suffers from the disease." Seems like a reasonable thing to fight for... Am I right? #ALS #iamals #WhyIFight

The FIRST-EVER drug guidance for #ALS has the potential to speed up the process of drug development, reduce costs and create incentives for the industry to enter the ALS market and develop new treatments. As Brian Wallach & I AM ALS said, it's not a cure, but it's a critical step:

Did anyone else see this?!?

If people knew that signing this petition for getting #ALS (Lou Gehrig’s disease) treatments through trials and to patients was easier than downloading an app, would they do it? Please sign and RT if you see this! #SaturdayThoughts iamalsorg.typeform.com/to/EYs4oV

You can help save lives. iamalsorg.typeform.com/to/EYs4oV #TeachSomethingIn5Words

With #ALS (Lou Gehrig’s disease) everyday is #NationalIceCreamDay! It’s helpful in keeping weight on, and it’s delicious! My dad’s favorite is rasp choc chip from Graeter's Ice Cream and I always keep it stocked. Please help us #endALS by signing this petition! iamalsorg.typeform.com/to/EYs4oV

I am a wife, mother, teacher, daughter, sister, counselor. I thought I did everything right. Went to college, grad school, got married, worked as a HS teacher, gave birth to a girl & boy. Then got diagnosed with #ALS. My #ALSplea is U.S. FDA to approve BrainStorm #NurOwn

Great strides in ALS research 5 years after Ice Bucket Challenge broke the internet: abcn.ws/2yKO3Ge

BrainStorm to Announce 2nd Quarter Financial Results and Provide a Comprehensive Corporate Update. Tuesday, August 13, 2019, at 8:00 AM EST Conference call Call-in numbers: 1-877-423-9813 International: 1-201-689-8573 ID: 13693394. $BCLI

For the first time, there are promising therapies in the pipeline for ALS - and patients should be able to access treatments that have a real chance of improving their lives. Innovative clinical trials, incl. the platform approach that Dr. Cudkowicz describes here, are critical.

So I was curious to see what the comments on this were like, and I was not disappointed. All but one of them are about #ALS. I love this community. 💕

We’re proud to fund I AM ALS to develop tools & build a movement that connects patients, caretakers, doctors, scientists, foundations, corporations + the public in the fight to #EndALS. Read more via People people.com/human-interest…

Thank you Biohub and I AM ALS for the great strides in elevating the conversation around #ALS and other rare diseases.

Amazing work, Brian! You SOOOOO deserve this! So so so excited for this and to see what you do next! 🙌🏻

Just picked up some Ben & Jerry's after our local ALSA chapter meeting where I met some great people. Now to find a spoon. #IceCreamForALS 😋

My good friend Tim McDaniel passed away last week. I’m so sad and shocked by how fast his #ALS progressed. In October he wheeled his daughter down the aisle... and now he’s gone.

We have clinic tomorrow and I know my dad needs a g-tube, but he’s worried if he gets one he won’t be able to get #NurOwn if/when it’s ready. Does anyone have any insights on that?? C Lebovits Mary Kay Turner @MattBellina3

Getting the g-tube presentation. Dad seems ok with it! Super relieved that he’s deciding to get one, but worried about the thought of surgery. His breathing isn’t great.

Whelp... we may have waited too long. Dr. is saying his breathing scores might be too low to be sedated for the procedure.