So it’s #ALS awareness month & this tweet only got 6 retweets. How am I supposed to raise awareness if only 6 people care enough to retweet awareness tweets! How do I reach more people & then get them to care about this HORRIBLE disease? @alsassociation@iamalsorg@MDA_Advocacy
You’ve seen us in NYC at Times Square, you’ve seen us in Chicago on the Magnificent Mile ... and now this May we are taking the ALS revolution to DC!
Click the link to help us honor you or your loved one who has or had #ALS on the National Mall in DC! https://t.co/aLgGYt5KLP
@skalpakoff I went on a date with @petpam10 to see #lostcitymovie. I love that you are living with, like me, #ALS. So many choose not to. Next week we will see #ambulancemovie.
Get out and live !! #endALS!
Hi everyone. I wanted to update you on my "I have ALS" sign/sticker. My friend Lauren took my idea of a few emojis and came up with this. What do you think? Do you understand? What would you do if you didn't know me and saw this on my wheelchair? #ALS#endALS@iamalsorg
#EmergencyPreparedness, do you have a #MediAlert bracelet or something similar?? Always wear it upside down on the left wrist! Because the Paramedic is always on the left, 🚑 even in the helicopter 🚁and needs to read it, not you! 😀 #EndALS
@bsw5020 I lost my Aunt to Covid at the end of the year and my Mom to dementia 6 weeks later. They were fighters till the end. I will fight like them, even I use a vent!
#endALS
In the last 2 days I’ve received a lot of DMs asking what @synapticure is.
It is a company built on the crazy idea that the ALS care you receive should not be based on your zip code.
Say what? Sandra and I explain below. Find out more at https://t.co/lWeuv4aUj5.