We are a team of veterans, caregivers, and families who are fighting ALS. We encourage, connect, support, and advocate for veterans with ALS, a 100% service-connected, 100% fatal motor neuron disease. Join us in our fight to #endALS.
The VA final decision for accessing Relyvrio now better aligns with the FDA's criteria and will afford meaningful access for many. This is an important decision. We will continue to advocate for access so that no barriers remain for Vets living with ALS. https://t.co/3sP1ES5qgh
"If these soldiers were dying in the field ...
we would leave no stone unturned.
We would use the best existing resources
to make sure they had whatever they needed to survive"
~ #GenMik#Thanksgiving#Thanksgiving2022#VeteransDay#ALS
https://t.co/fyreATfwQO
@johnfeal2
Dear ALS community,
We have waited years for NurOwn to come before the FDA for approval. Given the FDA's recent decision on NurOwn, @iamalsorg and other organizations wrote a letter to the FDA requesting an AdComm for NurOwn.
Make your voice heard today: https://t.co/K8YWFwm9cV
Widow Truth: Gonna have a win today. I am meeting with the Central TX VA Leadership to have what I am calling an exit interview. Discussing how to find a path foward for equality in care for ALS veterans they serve. @AlSvets#ALSveterans#Tomstroops#ALSwidow
The @iamalsorg Community Outreach Team offers the Tim Lowrey #ALS Panel Series to bring in a virtual panel discussion to groups, classes, association, organizations, or clubs. https://t.co/SweTUwEZ7P
Last year, our team and .@iamalsorg’s Community Support team worked together to create a suicide awareness and intervention campaign. This website is one result of our actions: https://t.co/W8YsV3lQYi
https://t.co/kYfjKJSVSC
I AM ALS shares the frustration and disappointment felt by the ALS community today. Read our full statement regarding the FDA's refusal to file.
https://t.co/5uiCogl7BV
Did you know veterans are more than twice as likely to be diagnosed with #ALS than civilians? RT this to spread awareness https://t.co/jFE7KoesAY @repSlotkin @chriscoons, @murkowskiS
The IAA Veterans Team raises awareness about veteran-specific ALS issues, educates the public, connects veterans with resources to improve their quality of ALS care and accelerate the development of and access to treatments and cures. @ALSvets
https://t.co/C272wohpvz
It's with great sadness and broken hearts that we announce @sandymorris333 our namesake and precious friend is no longer with us. We vow to continue the fight in her honor.
Opinion: Inspired by the Denver Principles, written in 1983 by people living with AIDS, the Morris ALS Principles aim to map out the ALS community's social contract with professionals and organizations focused on the disease. https://t.co/STLTGtozjH
Dear ALS Key Opinion Leaders,
Thank you for asking if people with lived ALS experience are welcomed and involved before saying "yes" to speaking engagements. #endALS