Toby Cochran explaining how important it was to illustrate emotions in the animated film, LUKi & the Lights. Hear more in eps 101, "Animated Film, LUKi & the Lights: Helping Children Understand ALS/MND."
Listen: https://t.co/zC1H5CSdgO @ALSnederland@iamalsorg@alshoneybadgers
There are so many incredible organizations out there and Honeybadger Liz wants to highlight those organizations during #ALSAwarenessMonth!
Check back each day to learn a little more about the organizations and people that are helping us #endALS
We love to see our honeybadgers roar!
Sign up at the link below to listen to @boaflouncer's discussion with Prince George's County Office of Human Rights!
https://t.co/AAAnoTMrAn
Who are The Honeybadgers?
We are dedicated ALS advocates that have joined forces to collaborate & support each others ideas.
We face the fight against #ALS with the same ferocity that has made the honeybadger famous, never losing sight of our goal to #endALS
Join us!
The ALS Office Hours program kicks off tomorrow at 1 ET! Members of the ALS and research communities will be hosting the zoom each Friday to provide a safe place for people to find reliable and accurate information!
For more information, please visit https://t.co/0fkkAKjaKZ
The ALS Office Hours program is back!!
Connect with members of the ALS and scientific communities to find answers to your questions and connect with resources. No registration or sign up necessary!
For more information, please visit https://t.co/5qn1uXpN5j
Our Honeybadgers are showing the world that nothing can stop a #honeybadgerheart!
Way to go Mary!
Keep showing us all how to #RAWR!
https://t.co/vdoGoByS3N
Misdiagnosis is common when going through a diagnostic journey, which can lead to unnecessary procedures and lost time.
Please visit https://t.co/YsDkkxWryQ to learn more.
#endALS#rawr
Today members of the genetic ALS community will be participating in an educational panel for the National Society of Genetic Counselors at 1 PM ET
It's open to the public, it's free, and you can register here: https://t.co/8RXHxoGc2T
#endALS#rawr
On Jan. 31st at 10 AM Pacific Time, members of the genetic ALS community will be participating in an educational panel for the National Society of Genetic Counselors.
It's open to the public, it's free, and you can register here:
https://t.co/8RXHxoGc2T
Each week, honeybadger advocates from around the country hold a zoom roundup to discuss the projects that are important to them and brainstorm ways to support each other.
We know that there is strength and power in numbers.
What are your passion projects? Let’s chat!
#endALS
Who are The Honeybadgers?
We are a dedicated group of ALS advocates that have joined forces to collaborate and support each others ideas.
We face the fight against #ALS with the same ferocity that has made the honeybadger famous, never losing sight of our goal to #endALS
Looking for an easy way to help the #ALS community? How does a night at the movies sound?!?!
100% of ticket sales will go to Team Drea. That makes our honeybadger heart happy!
⭐️ONE NIGHT ONLY⭐️
On 1/17 at 51 @RegalMovies theaters, witness the incredible story of the 1st person with ALS to do a marathon in all 50 states! Celebrated as “one of the great discoveries of 2023," it is “a joyous ride we all need to take.” Trailer/tix: https://t.co/NCRYdMw1f7