I’m Dying To Tell You Podcast with Lorri Carey
@LorrisPodcast
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Midwest Momma & Wife. ALS Warrior for 20 years. Host of I’m Dying To Tell You Podcast. Living Faith Over Fear. Instagram: imdyingtotellyoupodcast
Joined February 2020
New Episode! Jake Popyura opens up about life as a 39-year-old musician with ALS, finding dark humor in his diagnosis, and how his band lifts him—sometimes literally—onto stage. A powerful reminder of adaptation & resilience. Listen: @HerALSStory #mnd
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Jill Brattain mentions a study that shows veterans are 6-10 times more likely to be dx with ALS, depending on the military job. This is one reason why Jill can't walk away from this fight! Hear more: "Life After ALS: A Journey of Healing and Hope" #als.-
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Coming up -@HopOnACure's Harmony for Hope, 10/18 in Atlanta! A singer-songwriter concert with TOP talents! Can't attend, but wanna purchase a ticket for someone living with ALS to go, that would be AMAZING! .All event, ticket & sponsorship info here:
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In my recent episode of I'm Dying To Tell You Podcast, I chat with four remarkable women as they share how they found joy, community, and purpose after losing their loved ones to ALS. LISTEN LINKS:.or .@ALSTDI .#ALSawareness
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Super excited to be part of the Host Committee for Harmony for Hope! 🌻Last year was a blast! The evening is a unique night of live music & fun bringing us together to fund ALS research through @HopOnACure. 🎟️ Tickets: .Thx for checking it out! #als
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NEW EPS!."Life After ALS: A Journey of Healing and Hope".Here I chat with 4 amazing women who have each lost someone to ALS, yet show it’s possible to build a meaningful life that honors both past relationships and present possibilities. 🎧Listen: @ALSTDI
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That’s a wrap!!! Mile by Mile - All for those who cannot & the work being done at @ALSTDI 💜 If you wanna support, here’s my page: Thank you for the donations on my behalf & the encouragement to keep pushing through!! Great big hugs!
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Grateful to be featured here by The Jeff Weber Always Lifting Spirits Foundation! I love their mission and the grace with which they carry it out! Thank you for this and all you do!💜.Link to article on my journey: @ALSunitedOhio #als
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Add 9 for today!.“200 Miles in 25 Days”.Participating in ALSTDI’s Tri-State Trek. If it’s on your heart to support my trek & research at ALSTDI, here is link to my page. Thx for the donations so far!! .💜.@ALSTDI @iamalsorg #als
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Meet John Rieder, front office @Reds! One guest in “Love, Legacy & Lou Gehrig Day: A Team Effort Against ALS”. Hear how his family’s loss leads to making MLB’s Lou Gehrig Day the most inclusive, inspiring & impactful event every year!Listen: .@iamalsorg
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I’ve set a goal of 200 miles in 25 days in this year’s Tri State Trek! I hope my efforts help fund ALS research at @ALSTDI 💜.Create your own goal to meet by 6/30 & Join My Team: Or Support Me: @Catrike .@iamalsorg #endals #als
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Thank you @iamalsorg for making it Easy Peasy to find out what’s happening at ALL @MLB ballparks for Lou Gehrig Day, June 2nd!
iamals.org
Learn more about Lou Gehrig Day and all the events that I AM ALS is hosting in partnership with Major League Baseball (MLB) teams around the country.
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Eleven Years = Eleven Swallows! So happy to celebrate Andrea Lytle Peet living with ALS for 11 years. She inspires me EVERY SINGLE DAY to “Go On, Be Brave!” Big love to my friend & IDTTY guest, Andrea!! @TeamDreaFdn @ALSTDI @HerALSStory @iamalsorg #als
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Honored to be the keynote speaker at an @iamalsorg Empathy Dinner, created & hosted by my friend Deb Winters. Grateful to be a part of this beautiful ALS awareness event! More about ALS Empathy Dinners: #ALSishere #SoAreWe #ALS @marshall_health #iamals
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New Episode!.Each guest has lost someone to ALS, yet surprising ALS families with accessible vans, wheelchair ramps, lift chairs & patient care! You kinda gotta hear it to believe it, so here are some listen links: or @iamalsorg
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