@freelancehack@freelancehack@G_Insider Oh, and in case it wasn't already obvious from my profile picture, I'm not a member of the Tribe๐. My birthday is Halloween, so I guess Dan Lee has provided motivation as to this year's costume.
@freelancehack I can assure you, I've received zero funding for https://t.co/DnQP4zpLJb. I'm just a local Fort Wayne resident, born and raised. Perhaps CEO Dan Lee is more fearful of acknowledging grassroot opposition to Wall Street investment analysts.
https://t.co/RjPo8immLo
My bunica's (grandma) return to our family's Romanian roots, Ernea, Sibiu, Romania, just prior to her (familial) ALS diagnosis. Our family is affected by 'the Balkan' SOD1 variant, L144F/L145F.
https://t.co/3r5rNX5l8O
@LisaLegacy4ALS@alsassociation@Jeanc9orf72 Especially in the context of pre-symptomatic individuals with gene mutation with FDA approved treatment, where the expectation of likely future treatment. Analyzing by size (# of full time employees), where health care costs are more spread out the larger the employer.
In honor of Veterans Day, I'm sharing a video interview of my paternal grandfather, Richard B. Olson. My grandfather fought for our country during WWII, in the Battle of the Bulge.
This was recorded when I was in middle school.
https://t.co/ANQgIIpCxf
@RunningMama0522 I have both Ecowitt (Bluetooth) and Plaid (ZigBee) sensors that I use throughout my house, lawn, and garden. The ZigBee ones are hit and miss on connectivity. The Ecowitt ones have been much more consistent. ZigBee requires a ZigBee router while Ecowitt is proprietary as well.
Weird flex, but this is the most successful houseplant that I've grown. I'm proud of it and have to share. I bought it from Wally World in the Spring of 2021, when it was around a foot tall. The smart soil moisture sensor is a recent addition but has been extremely helpful!
ALS in its most advanced stages changes not only your perspective on life but the core essence of who you are. When I lost my ability to walk during my first year of symptoms, I was still concerned of my new image as a disabled person and how I was seen by society. I bought a fancy wheelchair and tried to continue with my life as normally possible. Fast forward six years later, I am writing this post with my eyes, hooked to a ventilator. It's been three years since I had real food or heard the sound of my voice. The questions I ask myself now have drastically changed. Instead of being concerned of my image, I'm more concerned with my relationship with God. Furthermore, I ponder about my place in this universe rather than in society. Before, I lamented over fading relationships, whereas now I'm at peace being by myself. The glamour and noise of galas, award ceremonies, film screenings, and fundraising walks doesn't intrigue me as much as finding that moment of silence where time seems to stand still. Lastly, realizing how much love you leave this world with will ultimately determine your legacy. #ALSAwarenessMonth