Things that have no place in fights against terminal illness or infectious virus:
Politics
Racism
Turf fights
Things that belong:
Science
Facts
Remembering that we are all in these fights together.
Sometimes in the fight vs ALS, no good deed goes unpunished.
Be grateful for things in your toolkit.
You don't have to take a therapy just because it's approved.
It's good that people at least have the choices they have.
Choices.
My few cents.
ALS is a disease. It is a terminal disease.
I have ALS.
And my doctors tell me that it will kill me soon. Someday they may be right. But not today or tomorrow or even next week.
Right now, I am living with ALS. More alive and grateful every day than the last.
Bringing this up again, @alsaindiana ... Given the terrible loss of life that service-related ALS has taken. it makes so much sense to have an ALS-awareness & remembrance aspect to https://t.co/k1fp3SeDgr Please in 2020! Thank you. @500Festival#500MEMservice@ims
This week we turn our eyes and hearts to Leah Darling an angel/Social Worker at the ALS VA Clinic. Leah is a tireless advocate and friend to the individuals and families living with ALS. She is an incredible... https://t.co/xhhV3UP693
Did you know that there are more than 400 Hoosiers impacted by ALS? Join our movement to help raise funds to support our local programs, cutting edge research, and advocate those Hoosiers living with ALS!
HOW?... https://t.co/KeW6CUFkC0
On this #VietnamWarVeteransDay I honor my husband who fought in a fight he never wanted to be in. He survived that fight but is now in the fight of his life with no suitable weapons against an enemy he cannot conquer - the beast called #ALS.
#EndALS#DefeatALS#FundALS
We spend every day looking forward to tomorrow as we believe that tomorrow will somehow be better.
What if today—this moment—is as good as it gets? And even if it isn’t, what if we acted like it is?
Celebrate the mundane while dreaming of the possible.
#IAMALS
I don't post much, especially personal things, but I can't keep quiet about this. I've lost too many friends to #ALS and my husband is living with it. I'd love to wake up one day & see that a cause and a cure are here. Not in my lifetime but in my children's? #DefeatALS#FundALS
When was the last time you told your loved ones how much you love them? Today, we’re launching a campaign to raise #ALSAwareness & bring more love to the world. Watch: https://t.co/FehIxCaUny. #ALS#MND#VoiceYourLove
There is no hope until there is. Today, I AM ALS launches. Today, we have more hope that a cure will be found. Together, we can. Join us: https://t.co/01Uu5ktCXa
We have a drinking game that includes words like "promising," "exciting," "breakthrough," etc. We have now officially added a phrase -- "never b4 a more exciting time in ALS research" (and its variants).
Please modify your habits accordingly.
It started when he couldn’t grasp a pen.
Diagnosed with ALS at 37, former Obama staffer hopes to use campaign skills to raise funds for a cure. https://t.co/NBtL1j9bDK (via @byalisonbowen)
After watching her late father battle #ALS, Tess created a documentary on his journey with the disease. For teens & young adults like her, the power of art can help those impacted by ALS tell their stories. Submit to #AlsoUs by 1/22 for the chance to work with a creative expert.