@patrickstoner How can you possibly get the reel rolling on a new bio-pic? Lou Gehrig. Nothing could bring more awareness to ALS, than a movie: featuring a famous actor as Lou Gehrig. My dad passed from ALS 8 years ago. My hubby diagnosed with ALS 4 years ago.
@JohnKruk watching Phils. Hubby has ALS. Hoping to make it to Phillies ALS game. Maybe meet you! How about a new biopic Lou Gehrig. Better than the ice bucket
@JohnKruk@Coombsie77@bendavisnbcs John Kruk- I’m not good with X. Watching the phils now. We love you!!!
Hubby has ALS. How about a new biopic Lou Gehrig
@bsw5020 You guys have put yourselves out there. Thank you. So very happy for you. I know you are not without your daily conflicts. These daily conflicts are the undoing of the average ALS pals and CALS. I can hardly get enthused when I’m paying out our entire retirement fund for care-
@dantate2 Remaining an advocate for ALS, after PALS has passed can be draining. My dad passed from ALS 7 years ago. I never wanted to see those 3 letters ever again. Then my husband was diagnosed with ALS 3 years ago. I’m back to slay this beast.
@sarahkarpar My husband never went back to his office again, after a second opinion confirmed ALS in January 2021. He was an owner in the business, so they worked it out. He fatigued easily, and didn’t want to go back.
@Markbedwell11 As my husbands caretender, it takes me, at the very least, 26 minutes to get my thoughts together, make a cup of coffee- which I take directly back to the bedroom, before I get him up
@bsw5020 That’s excellent. My pals continues with PT 2x week, NeuroFitness, in Wilmington DE. He can’t walk, but PT is the highlight of his week. According to JIMMO settlement Medicare must pay. @neurofitness
@ChrisCoons please keep fighting for NurOwn. I know you have been effected by ALS. My dad passed from als 7 years ago. My husband was diagnosed 3 years ago.
@sarahkarpar Don’t fall. Don’t fall don’t fall. Don’t fall. Next time you will bash your face. Don’t take any chances. Update and implement your toolbox
@sabrevaya We are riding in the same sinking ship. A spouse caregiver is quickly burnt out. Medicare is required to pay for caregivers when an individual is home bound and is receiving either nursing care, PT, OT or ST at home. It’s not happening. Need Medicare advocacy. Need more PCAs