November is a time to honor the unwavering strength, compassion, and dedication of caregivers who stand by those living with ALS. Caregivers are the heart of the ALS community, offering not only daily support but also hope and love. #callingallcaregivers https://t.co/UmFRnC7XAL
I am super excited to share that I am an official employee at I AM ALS!!! I am looking forward to continuing my efforts to raise awareness for ALS. https://t.co/qzbmWUSYeR
EyeGaze technology allows people living with ALS the opportunity to continue to communicate, create, and retain independence through the use of their eyes. Join us on 8/22/24 6:30pm ET to learn more. Sign up here https://t.co/vPSIPQGLuG
@BridgingVoice has a free, upcoming training on the therapeutic value of scleral contact lenses for people with #ALS using #eyegaze computers. Register to join the free Zoom training Aug. 20 at https://t.co/mZrj0DQ1U4. Hope to see you there! #BridgingVoice#aac
The Write Stuff Team is looking for creative people to join them! If you've been impacted by ALS and have ever used writing to share or process your feelings, you would make a great addition to the group. @iamalsorg
https://t.co/nKK7BfIqmd
Get ready for the next I AM ALS Eyegaze by tuning into @BridgingVoice’s free webinar, “Eye Health: Seeing is Achieving,” today at 3 p.m. ET.
Experts will discuss the impact of #eyegazetechnology on your eyes and how to keep them healthy.
Register at: https://t.co/EtoI7hFv7O
Looking to support I AM ALS but short on time? They have an easy way for you to get involved and make a difference. Check out the link.
https://t.co/7JDblqMAa9
@ScottsFight Kurt needed some extra O2 in his life, too. Like other ALS issues, it's not a one size fits all diagnosis. Glad you are cozy and getting some rest.
📷 VETERANS!!! I AM ALS needs your help! 📷 Are you a Veteran receiving home care? Are you about to reach your 65% expenditure cap for non-institutional care alternative programs?
Please share your story. Together, we can make a difference!
📷 https://t.co/uiFyqbz1oN
I took 60 seconds out of my day to help ALS patients access the promising therapies they need. You can be an advocate too! Join me by going to the link below and sending your representative and senators a message. https://t.co/WybJRHw4p7
Please join us in asking Congress to pass the Elizabeth Dole 21st Century Veterans Healthcare and Benefits Act. Our Veterans with ALS need help THIS YEAR so they can remain at home with their families for their care. https://t.co/bEwi25xwsa
Lou Gehrig Day is coming up sooner than you think! Head to our landing page to find an event in your neck of the woods (and make sure to order your swag, too!) https://t.co/X8K5HPZoGK