⏳ Just days left in 2024! Let’s end the year by making an impact. Support the “Half a Million to Beat VWM”’Every donation brings us closer to life-changing breakthroughs.
Join us now: https://t.co/uY4oPqeVqx 💙
#BeatVWM#EndOfYearGiving#MakeADifference#findacureforvwm
Shoutout to Run for Nash for supporting our fight against Vanishing White Matter (VWM) Disease! Sending a VWM t-shirt to Dr. Bonkowsky as we work toward raising $500K for life-changing research. Every donation matters.
💙 Donate: https://t.co/IBVYlOowHl
“If you want to run far, run together. We are all in this together- let’s help get ourselves to the finish line!
You can help! …share your story with your friends/supporters/influencers…
Every dollar matters!
Dr. Josh Bonkowsky, a VWM researcher and clinician, is trying to reach 500,000 feet of running elevation gain by midnight Dec 31,2024
#findacureforvwm#halfamilliontobeatvwm#VWMResearch
Learn more: https://t.co/uY4oPqenAZ
FDA's new Operation Warp Speed initiative for rare diseases has accepted San Francisco-based biotech @calico's investigational drug ABBV-CLS-7262 for neuro in partnership w/ AbbVie as 1 of <10 in START pilot. Calico/AbbVie's eIF2B activator fosigotifator https://t.co/6zluHIPzYi
Shout out to our rockstar doctors, researchers who continue to research and give families HOPE!
Thank you! - ULF Board of Directors Treasurer, Donna Skwirut
#findacureforvwm
VWM Families Foundation
Last week we did a story on a missing laptop from the SLC Airport. It had important medical information and the woman desperately needed it back. Yesterday, I got a call from the person who got it by mistake. What a happy ending! @KSL5TV at 5 and 6.
https://t.co/Vkqo2xaj8L