#alsnexus search results
We're incredibly proud of Dr. Daragh Heitzman for being recognized as one of @ALSassociation's ALS Heroes at #ALSNexus! š Honored for his exceptional impact through advocacy, research, and compassionate care. Congratulations, Dr. Heitzman! š bit.ly/3JQdjCM
We are thrilled to share that our very own Daniel Barvin, VP of Operations and Patient Advocacy, has been honored with the ALS Hero Award at this yearās #ALSNexus! This award recognizes individuals making a profound impact on the ALS community, and Daniel does just that everyā¦
We are on the ground at #ALSNexus! This event brings together researchers, advocates, industry leaders, and people living with #ALS, all working towards changing the future of ALS. At Coya, we're proud to contribute to this mission and look forward to collaborating, learning,ā¦
We proudly joined ALS leaders from around the globe at the @alsassociationās 2025 #ALSNexus Conferenceādriving progress toward making a meaningful difference in the ALS community. #TeamMTPA
Team Coya will be in Dallas on August 11-14 attending #ALSNexus hosted by the @alsassociation. We look forward to engaging in stimulating discussions and networking with leaders changing the future of #ALS! Send us a note at [email protected] if you would like to connect!ā¦
We had the privilege of hosting #ALS patient advocate and author @AndreaLytlePeet for a Meet the Author event at #ALSNexus 2025. Thank you to Andrea, her care partner Annie, and all who attended this thoughtful discussion on what it means to live with ALS.
This week, we are excited to present a poster on preclinical data from our lead ASO development candidate, TRCN-1023, and the Phase 1/2 clinical trial outline at #ALSNexus. The poster will be presented by CMO Irina Antonijevic on Wednesday evening's poster session, 4-6:30PM CDT.
Joining leaders at #ALSNexus 2025 in Dallas next week to dive into the latest ALS research, treatments & clinical progress! Excited to connect w/ leaders fighting for a cure. šŖJoin the effort: event.alsnexus.org/event/beb97dacā¦ #EndALS
At #ALSNexus hosted by the @alsassociation to present our research on neuronal aging and TDP-43 mislocalization! My talk will be tomorrow morning in the "Emerging Science" session, and I will also be at poster #3 tomorrow evening š¬
"Losing to the Letters," a beautiful new collaboration between Mikey Stone, who is living with ALS, and Frankie Torres, who lost her father to ALS. We are excited to premier this #song via livestream from #ALSNexus on TikTok and Instagram. Stay tuned for more updates!
At the @alsassociation #ALSNexus, we were proud to highlight caregiversā vital role in #ALSCare + share our fully remote #ClinicalTrial for #ALS. We're proud to stand with a community that wonāt give up on better care, better treatments, and a better future.
At #ALSNexus, our Focusing on Increasing Social Connection and Quality of Life session shared findings from a national ALS Focus survey that found half of people living with ALS reported feeling lonely and the top barriers to social connection were: worry, guilt, time, andā¦
That's a wrap on our first session of #ALSNexus. The session, Progress and Potential: Looking Back and Envisioning the Future, was a powerful conversation with members of the ALS community about ALS treatments, care and what the next era of ALS research and support will lookā¦
Thank you to everyone who joined us at the #ALSNexus conference! Your participation made it a truly inspiring event. Let's continue to work together to create a world without ALS!
We have exciting news! Thanks to our generous sponsors, virtual registration for #ALSNexus is now FREE for people living with ALS and their caregivers! We're grateful for the support that makes this possible and hope youāll join us. Register today to attend ALS Nexus:ā¦
We are so excited to welcome everyone to ALS Nexus! We look forward to sharing the inspiring keynotes, insightful panels and so much more. Whether you are joining us online or in-person make sure to share your Nexus experience by tagging us. #ALSNexus
QurAlis' CSO Dan Elbaum and Sandy Hinckley, vp and head of discovery, took the #ALSIceBucketChallenge at the #ALSNexus conference to help continue to raise awareness and support for ALS research with the goal of discovering and developing new treatments and ultimately a cure.ā¦
We're incredibly proud of Dr. Daragh Heitzman for being recognized as one of @ALSassociation's ALS Heroes at #ALSNexus! š Honored for his exceptional impact through advocacy, research, and compassionate care. Congratulations, Dr. Heitzman! š bit.ly/3JQdjCM
We had the privilege of hosting #ALS patient advocate and author @AndreaLytlePeet for a Meet the Author event at #ALSNexus 2025. Thank you to Andrea, her care partner Annie, and all who attended this thoughtful discussion on what it means to live with ALS.
At the @alsassociation #ALSNexus, we were proud to highlight caregiversā vital role in #ALSCare + share our fully remote #ClinicalTrial for #ALS. We're proud to stand with a community that wonāt give up on better care, better treatments, and a better future.
Canāt let a little sinus infection get your girl down š¤¦š»āāļø #noitssnot #heralsstory #alsnexus #babewithamobilityaid #alshero @alsassociation @HerALSStory
Iāll share more with yall soon, just know that Tuesday was one of the best nights in the history of ever š„° #alshero #alsnexus #heralsstory #babewithamobilityaide #sunnystrong @alsassociation @HerALSStory
We proudly joined ALS leaders from around the globe at the @alsassociationās 2025 #ALSNexus Conferenceādriving progress toward making a meaningful difference in the ALS community. #TeamMTPA
We are thrilled to share that our very own Daniel Barvin, VP of Operations and Patient Advocacy, has been honored with the ALS Hero Award at this yearās #ALSNexus! This award recognizes individuals making a profound impact on the ALS community, and Daniel does just that everyā¦
At #ALSNexus, our Focusing on Increasing Social Connection and Quality of Life session shared findings from a national ALS Focus survey that found half of people living with ALS reported feeling lonely and the top barriers to social connection were: worry, guilt, time, andā¦
Congratulations to our Hero Award winners! We would like to give a huge thank you to Chris Spaulding, Daniel Barvin, Sunny Brous, and Dr. Daragh Heitzman. Your contributions are an inspiration to the ALS community. #ALSNexus
We are on the ground at #ALSNexus! This event brings together researchers, advocates, industry leaders, and people living with #ALS, all working towards changing the future of ALS. At Coya, we're proud to contribute to this mission and look forward to collaborating, learning,ā¦
At #ALSNexus hosted by the @alsassociation to present our research on neuronal aging and TDP-43 mislocalization! My talk will be tomorrow morning in the "Emerging Science" session, and I will also be at poster #3 tomorrow evening š¬
That's a wrap on our first session of #ALSNexus. The session, Progress and Potential: Looking Back and Envisioning the Future, was a powerful conversation with members of the ALS community about ALS treatments, care and what the next era of ALS research and support will lookā¦
We are so excited to welcome everyone to ALS Nexus! We look forward to sharing the inspiring keynotes, insightful panels and so much more. Whether you are joining us online or in-person make sure to share your ALS Nexus experience by tagging us. #ALSNexus
This week, we are excited to present a poster on preclinical data from our lead ASO development candidate, TRCN-1023, and the Phase 1/2 clinical trial outline at #ALSNexus. The poster will be presented by CMO Irina Antonijevic on Wednesday evening's poster session, 4-6:30PM CDT.
Team Coya will be in Dallas on August 11-14 attending #ALSNexus hosted by the @alsassociation. We look forward to engaging in stimulating discussions and networking with leaders changing the future of #ALS! Send us a note at [email protected] if you would like to connect!ā¦
Joining leaders at #ALSNexus 2025 in Dallas next week to dive into the latest ALS research, treatments & clinical progress! Excited to connect w/ leaders fighting for a cure. šŖJoin the effort: event.alsnexus.org/event/beb97dacā¦ #EndALS
"Losing to the Letters," a beautiful new collaboration between Mikey Stone, who is living with ALS, and Frankie Torres, who lost her father to ALS. We are excited to premier this #song via livestream from #ALSNexus on TikTok and Instagram. Stay tuned for more updates!
Mark your calendars! Chief Medical Officer Dr. Eric Anderson is speaking at @alsassociation #ALSNexus conference, joining a powerful conversation on one of the most over-looked forces in #ALS care: family caregivers. Learn more: vist.ly/328qx #Caregivers
We have exciting news! Thanks to our generous sponsors, virtual registration for #ALSNexus is now FREE for people living with ALS and their caregivers! We're grateful for the support that makes this possible and hope youāll join us. Register today to attend ALS Nexus:ā¦
We are thrilled to share that our very own Daniel Barvin, VP of Operations and Patient Advocacy, has been honored with the ALS Hero Award at this yearās #ALSNexus! This award recognizes individuals making a profound impact on the ALS community, and Daniel does just that everyā¦
We're incredibly proud of Dr. Daragh Heitzman for being recognized as one of @ALSassociation's ALS Heroes at #ALSNexus! š Honored for his exceptional impact through advocacy, research, and compassionate care. Congratulations, Dr. Heitzman! š bit.ly/3JQdjCM
We had the privilege of hosting #ALS patient advocate and author @AndreaLytlePeet for a Meet the Author event at #ALSNexus 2025. Thank you to Andrea, her care partner Annie, and all who attended this thoughtful discussion on what it means to live with ALS.
At #ALSNexus hosted by the @alsassociation to present our research on neuronal aging and TDP-43 mislocalization! My talk will be tomorrow morning in the "Emerging Science" session, and I will also be at poster #3 tomorrow evening š¬
We are on the ground at #ALSNexus! This event brings together researchers, advocates, industry leaders, and people living with #ALS, all working towards changing the future of ALS. At Coya, we're proud to contribute to this mission and look forward to collaborating, learning,ā¦
Joining leaders at #ALSNexus 2025 in Dallas next week to dive into the latest ALS research, treatments & clinical progress! Excited to connect w/ leaders fighting for a cure. šŖJoin the effort: event.alsnexus.org/event/beb97dacā¦ #EndALS
Team Coya will be in Dallas on August 11-14 attending #ALSNexus hosted by the @alsassociation. We look forward to engaging in stimulating discussions and networking with leaders changing the future of #ALS! Send us a note at [email protected] if you would like to connect!ā¦
Thank you to everyone who joined us at the #ALSNexus conference! Your participation made it a truly inspiring event. Let's continue to work together to create a world without ALS!
At #ALSNexus, our Focusing on Increasing Social Connection and Quality of Life session shared findings from a national ALS Focus survey that found half of people living with ALS reported feeling lonely and the top barriers to social connection were: worry, guilt, time, andā¦
We are so excited to welcome everyone to ALS Nexus! We look forward to sharing the inspiring keynotes, insightful panels and so much more. Whether you are joining us online or in-person make sure to share your Nexus experience by tagging us. #ALSNexus
At the @alsassociation #ALSNexus, we were proud to highlight caregiversā vital role in #ALSCare + share our fully remote #ClinicalTrial for #ALS. We're proud to stand with a community that wonāt give up on better care, better treatments, and a better future.
This week, we are excited to present a poster on preclinical data from our lead ASO development candidate, TRCN-1023, and the Phase 1/2 clinical trial outline at #ALSNexus. The poster will be presented by CMO Irina Antonijevic on Wednesday evening's poster session, 4-6:30PM CDT.
We are excited to attend ALS Nexus, hosted by the @ALSassociation in Dallas, next week! We will share research on underrepresentation and bias in ALS research and care. Join us and register today at alsnexus.org. #EndALS #ALSNexus
@Synapticure team 100% in on the #Icebucketchallenge at the #ALSNEXUS conference this morning. So much ā¤ļø
QurAlis' CSO Dan Elbaum and Sandy Hinckley, vp and head of discovery, took the #ALSIceBucketChallenge at the #ALSNexus conference to help continue to raise awareness and support for ALS research with the goal of discovering and developing new treatments and ultimately a cure.ā¦
We have exciting news! Thanks to our generous sponsors, virtual registration for #ALSNexus is now FREE for people living with ALS and their caregivers! We're grateful for the support that makes this possible and hope youāll join us. Register today to attend ALS Nexus:ā¦
This morning, members of the Packard Center team and friends participated in the 10th Anniversary ALS Ice Bucket Challenge at the @ALSassociation Nexus Conference. What a great way to start the day! #ALSNexus
That's a wrap on our first session of #ALSNexus. The session, Progress and Potential: Looking Back and Envisioning the Future, was a powerful conversation with members of the ALS community about ALS treatments, care and what the next era of ALS research and support will lookā¦
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