Nonprofit supporting patients & families affected by urea cycle disorders. Working to advance research, improve care & raise awareness that saves lives #NUCDF
Joined February 2025
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National Urea Cycle Disorders Foundation (NUCDF) retweeted
We’re proud to share that PNRI postdoc Shradha Suyal, PhD has received the 2025 Cynthia Le Mons Fellowship from @NUCDF! 🎉 Her #research in Dr. Aimée Dudley’s lab is uncovering how genetic changes cause arginase 1 deficiency, a rare #ureacycledisorder.
Thank you NUCDF! 💙
NUCDF has awarded the 2025 Cynthia Le Mons Fellowship to @SuyalShradha, PhD, a postdoctoral fellow at @PNRIGenetics. Suyal works with Aimée Dudley, PhD @YeastGenetics, studying urea cycle disorders #UCDs
nucdf.org/news.html/article/…
NUCDF has awarded the 2025 Cynthia Le Mons Fellowship to @SuyalShradha, PhD, a postdoctoral fellow at @PNRIGenetics. Suyal works with Aimée Dudley, PhD @YeastGenetics, studying urea cycle disorders #UCDs
nucdf.org/news.html/article/…
Information is now available from the second session of our TeleECHO series. You can find recordings and other details here: nucdf.org/about-ucd/echo-cli…
The next session will take place on September 16. Register at the link above.
Have you become an official member of NUCDF yet? Your annual membership directly helps us fulfill our mission of supporting those with UCDs and continuing research/education with the ultimate goal of a cure for UCDs. Become a member: nucdf.org/about/donate/nucdf…
Time is running out to register for the 2025 Virtual Conference!
Register here so you don't miss out: nucdf.org/news-and-events/ev…
#virtualconference #nucdf #ureacycle #ureacycledisorder #ureacycledisorders #metabolicdisorders #geneticdisorders #raredisease #rarediseases
It’s hard to believe we’re talking back to school already, but it’s nearing that time! School can be a nerve-racking place and time for children with UCDs (and their parents). We’re here to support you. See our back-to-school resources here: nucdf.org/resources/ucd-guid…
Resources from NUCDF’s second session in the new clinician education series, Urea Cycle Disorders ECHO: The Essentials, are now available!
Find everything here: nucdf.org/echo
#teleecho #echo #nucdf #ureacycle #ureacycledisorder #ureacycledisorders
We love hearing from you. If you’d like to share images of you and your family enjoying the summer or celebrating a special life event, send them our way so we can share them (with your permission, of course) in our e-newsletter or on our social media.
nucdf.org/about/tell-your-st…
Become a member of the National Urea Cycle Disorders Foundation and help us in our fight against UCDs.
Join here: nucdf.org/about/donate/
If you haven’t joined our private UCD support group yet, we invite you to join and be a part of the community. Ask questions, interact with other UCD families, share stories, and provide support. Join here: facebook.com/groups/18206297…
Clinicians, it’s not too late!
You still have time to sign up for the next session in our ECHO series, “Urea Cycle Disorder ECHO: The Essentials,” scheduled for Tuesday, July 1, 5-6:30 pm ET.
Details here: nucdf.org/about-ucd/echo-cli…
We want to hear from you to help us shape our upcoming virtual conference.
Take the survey here: nucdf.org/conference-topics/…
#nucdf #virtualconference #ureacycle #ureacycledisorder #ureacycledisorders
Medical Advisory Board member Andrea Gropman, MD, is ALL IN on metabolic disorders.
Read the full article here:
stjude.org/research/progress…
#metabolicdisorders #metabolicdisorder #metabolic #health #ureacycledisorders #ureacycle #ureacycledisorder #childrenshealth #nucdf
What is one piece of advice you would give someone newly diagnosed with a UCD?
#ucd #ureacycle #ureacycledisorder #ureacycledisorders #raredisease #rarediseases #metabolicdisorders #geneticdisorders
