National Urea Cycle Disorders Foundation
@nucdf.bsky.social
We support patients and families affected by urea cycle disorders, a group of rare genetic diseases. Working to advance research, improve care, and raise awareness that saves lives https://nucdf.org
#UCDs #RareDisease #CheckAmmonia
#UCDs #RareDisease #CheckAmmonia
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...
July 21, 2025 at 9:04 AM
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...
Excited to announce the 6th International Symposium on UCD Sept 2, 2025 | Kyoto, Japan (satellite to ICIEM)
Trainee abstract submissions encouraged — registration fee and travel awards available for select poster presenters. ucdc.rarediseasesnetwork.org/index.php/6t...
Trainee abstract submissions encouraged — registration fee and travel awards available for select poster presenters. ucdc.rarediseasesnetwork.org/index.php/6t...
June 26, 2025 at 12:25 AM
Excited to announce the 6th International Symposium on UCD Sept 2, 2025 | Kyoto, Japan (satellite to ICIEM)
Trainee abstract submissions encouraged — registration fee and travel awards available for select poster presenters. ucdc.rarediseasesnetwork.org/index.php/6t...
Trainee abstract submissions encouraged — registration fee and travel awards available for select poster presenters. ucdc.rarediseasesnetwork.org/index.php/6t...
We are pleased to announce that we are launching a two-year project to establish the NUCDF Partner Network and develop a roadmap for future research in urea cycle disorders #UCDs #PatientEngagement #OTC #CPS1 #ASA #ASS1
nucdf.org/partner-netw...
nucdf.org/partner-netw...
June 18, 2025 at 2:17 PM
We are pleased to announce that we are launching a two-year project to establish the NUCDF Partner Network and develop a roadmap for future research in urea cycle disorders #UCDs #PatientEngagement #OTC #CPS1 #ASA #ASS1
nucdf.org/partner-netw...
nucdf.org/partner-netw...
Clinicians, it’s not too late! Sign up now for the next session in our ECHO series, “Urea Cycle Disorder ECHO: The Essentials,” scheduled for Tuesday, July 1, 5-6:30 pm ET.
A registration link and the prior session recording are all available here: nucdf.org/echo
A registration link and the prior session recording are all available here: nucdf.org/echo
June 6, 2025 at 11:08 AM
Clinicians, it’s not too late! Sign up now for the next session in our ECHO series, “Urea Cycle Disorder ECHO: The Essentials,” scheduled for Tuesday, July 1, 5-6:30 pm ET.
A registration link and the prior session recording are all available here: nucdf.org/echo
A registration link and the prior session recording are all available here: nucdf.org/echo
Living with rare diseases like urea cycle disorders can be isolating. Finding a community can make all the difference.
Join Jill Drury as she shares inspiring stories of patients/caregivers finding hope through the National Urea Cycle Disorders Foundation.
rarerevolutionmagazine.com/cure-the-cycle
Join Jill Drury as she shares inspiring stories of patients/caregivers finding hope through the National Urea Cycle Disorders Foundation.
rarerevolutionmagazine.com/cure-the-cycle
June 3, 2025 at 10:16 AM
Living with rare diseases like urea cycle disorders can be isolating. Finding a community can make all the difference.
Join Jill Drury as she shares inspiring stories of patients/caregivers finding hope through the National Urea Cycle Disorders Foundation.
rarerevolutionmagazine.com/cure-the-cycle
Join Jill Drury as she shares inspiring stories of patients/caregivers finding hope through the National Urea Cycle Disorders Foundation.
rarerevolutionmagazine.com/cure-the-cycle
When we stand united, our Urea Cycle Disorders community speaks with a powerful voice — one that raises awareness, drives research, and fuels hope for a cure.
We’ve already come so far, but there’s still so much more to do, and your support is what powers progress.
Join us: nucdf.org/about/donate/
We’ve already come so far, but there’s still so much more to do, and your support is what powers progress.
Join us: nucdf.org/about/donate/
April 22, 2025 at 9:57 AM
When we stand united, our Urea Cycle Disorders community speaks with a powerful voice — one that raises awareness, drives research, and fuels hope for a cure.
We’ve already come so far, but there’s still so much more to do, and your support is what powers progress.
Join us: nucdf.org/about/donate/
We’ve already come so far, but there’s still so much more to do, and your support is what powers progress.
Join us: nucdf.org/about/donate/
We are partnering with Project Echo to host a new educational series for clinicians, Urea Cycle Disorders: The Essentials. Be sure to share this information with your colleagues so that they have an opportunity to attend!
Find details and a registration link here: nucdf.org/about-ucd/ec...
Find details and a registration link here: nucdf.org/about-ucd/ec...
April 16, 2025 at 8:53 AM
We are partnering with Project Echo to host a new educational series for clinicians, Urea Cycle Disorders: The Essentials. Be sure to share this information with your colleagues so that they have an opportunity to attend!
Find details and a registration link here: nucdf.org/about-ucd/ec...
Find details and a registration link here: nucdf.org/about-ucd/ec...
We’re revamping our membership opportunities! Now is your chance to be an official member of the National Urea Cycle Disorders Foundation.
You can join us and help our mission.
Find more information – and join – here: nucdf.org/donate/annua...
#nucdf #ureacycledisorders #rarediseases
You can join us and help our mission.
Find more information – and join – here: nucdf.org/donate/annua...
#nucdf #ureacycledisorders #rarediseases
April 7, 2025 at 12:42 PM
We’re revamping our membership opportunities! Now is your chance to be an official member of the National Urea Cycle Disorders Foundation.
You can join us and help our mission.
Find more information – and join – here: nucdf.org/donate/annua...
#nucdf #ureacycledisorders #rarediseases
You can join us and help our mission.
Find more information – and join – here: nucdf.org/donate/annua...
#nucdf #ureacycledisorders #rarediseases
Twenty-five years ago, there was just one medication option available. Today, we are pleased to see various choices for families, recognizing that a personalized approach is essential in meeting diverse needs.
More info here: nucdf.org/resources/uc...
More info here: nucdf.org/resources/uc...
April 6, 2025 at 10:29 AM
Twenty-five years ago, there was just one medication option available. Today, we are pleased to see various choices for families, recognizing that a personalized approach is essential in meeting diverse needs.
More info here: nucdf.org/resources/uc...
More info here: nucdf.org/resources/uc...
Twenty-five-year-old Maia Romero was born a healthy baby, but when she was 5 or 6 years old, Maia was diagnosed with ASA.
Read more:
nucdf.org/resources/ma...
Read more:
nucdf.org/resources/ma...
April 4, 2025 at 10:25 AM
Twenty-five-year-old Maia Romero was born a healthy baby, but when she was 5 or 6 years old, Maia was diagnosed with ASA.
Read more:
nucdf.org/resources/ma...
Read more:
nucdf.org/resources/ma...
🌟 A Journey Through Time: Celebrating Our History 🌟
💙 Join us over the next several weeks as we journey back through our organization's history to share with you the important milestones throughout the years. 💙
Let's start with the early years ⬇️
💙 Join us over the next several weeks as we journey back through our organization's history to share with you the important milestones throughout the years. 💙
Let's start with the early years ⬇️
April 2, 2025 at 12:01 PM
🌟 A Journey Through Time: Celebrating Our History 🌟
💙 Join us over the next several weeks as we journey back through our organization's history to share with you the important milestones throughout the years. 💙
Let's start with the early years ⬇️
💙 Join us over the next several weeks as we journey back through our organization's history to share with you the important milestones throughout the years. 💙
Let's start with the early years ⬇️
April is Urea Cycle Disorders Awareness Month! We will share important information about UCDs all month long and raise awareness about these disorders. Will you help?
April 1, 2025 at 9:25 AM
April is Urea Cycle Disorders Awareness Month! We will share important information about UCDs all month long and raise awareness about these disorders. Will you help?
We have been working to advance research, improve care & raise awareness that saves lives for people affected by urea cycle disorders #UCDs since 1988. Check out our many milestones: nucdf.org/our-history....
March 12, 2025 at 2:47 PM
We have been working to advance research, improve care & raise awareness that saves lives for people affected by urea cycle disorders #UCDs since 1988. Check out our many milestones: nucdf.org/our-history....
We will continue to share the importance of this unseen threat.
Delayed diagnosis of hyperammonemia can lead to neurological damage or death.
CHECK AMMONIA
#checkammonia #neurologicaldamage #hyperammonemia #nucdf #metabolicdisorders #geneticdisorders #ureacycledisorders #UCDs
Delayed diagnosis of hyperammonemia can lead to neurological damage or death.
CHECK AMMONIA
#checkammonia #neurologicaldamage #hyperammonemia #nucdf #metabolicdisorders #geneticdisorders #ureacycledisorders #UCDs
March 10, 2025 at 1:52 PM
We will continue to share the importance of this unseen threat.
Delayed diagnosis of hyperammonemia can lead to neurological damage or death.
CHECK AMMONIA
#checkammonia #neurologicaldamage #hyperammonemia #nucdf #metabolicdisorders #geneticdisorders #ureacycledisorders #UCDs
Delayed diagnosis of hyperammonemia can lead to neurological damage or death.
CHECK AMMONIA
#checkammonia #neurologicaldamage #hyperammonemia #nucdf #metabolicdisorders #geneticdisorders #ureacycledisorders #UCDs
Did you know?
There are 6,000+ identified rare diseases.
Help us celebrate #rarediseaseday and raise awareness for the 300 million people worldwide living with a rare disease, their families and carers.
#RareDiseaseDay #NUCDF #UCDs #metabolicdisorders #ureacycledisorders
There are 6,000+ identified rare diseases.
Help us celebrate #rarediseaseday and raise awareness for the 300 million people worldwide living with a rare disease, their families and carers.
#RareDiseaseDay #NUCDF #UCDs #metabolicdisorders #ureacycledisorders
February 28, 2025 at 6:04 PM
Did you know?
There are 6,000+ identified rare diseases.
Help us celebrate #rarediseaseday and raise awareness for the 300 million people worldwide living with a rare disease, their families and carers.
#RareDiseaseDay #NUCDF #UCDs #metabolicdisorders #ureacycledisorders
There are 6,000+ identified rare diseases.
Help us celebrate #rarediseaseday and raise awareness for the 300 million people worldwide living with a rare disease, their families and carers.
#RareDiseaseDay #NUCDF #UCDs #metabolicdisorders #ureacycledisorders
Be part of Rare Disease Week on Capitol Hill! Join virtually to learn about #raredisease policy priorities:
✅ "Rare Reels" documentaries highlighting powerful stories
✅ Legislative Conference (Tues 9-5 EST)
✅ Rare Disease Congressional Caucus Briefing (Wed 9-10 EST)
Watch at shorturl.at/NLcxO
✅ "Rare Reels" documentaries highlighting powerful stories
✅ Legislative Conference (Tues 9-5 EST)
✅ Rare Disease Congressional Caucus Briefing (Wed 9-10 EST)
Watch at shorturl.at/NLcxO
February 25, 2025 at 2:54 PM
Be part of Rare Disease Week on Capitol Hill! Join virtually to learn about #raredisease policy priorities:
✅ "Rare Reels" documentaries highlighting powerful stories
✅ Legislative Conference (Tues 9-5 EST)
✅ Rare Disease Congressional Caucus Briefing (Wed 9-10 EST)
Watch at shorturl.at/NLcxO
✅ "Rare Reels" documentaries highlighting powerful stories
✅ Legislative Conference (Tues 9-5 EST)
✅ Rare Disease Congressional Caucus Briefing (Wed 9-10 EST)
Watch at shorturl.at/NLcxO
Did you know?: 70% of genetic rare diseases start in childhood.
#rarediseaseday #raredisease #rarediseases #facts #nucdf
#rarediseaseday #raredisease #rarediseases #facts #nucdf
February 24, 2025 at 4:54 PM
Did you know?: 70% of genetic rare diseases start in childhood.
#rarediseaseday #raredisease #rarediseases #facts #nucdf
#rarediseaseday #raredisease #rarediseases #facts #nucdf
In honor of #RareDiseaseDay on Feb 28, @pnrigenetics.bsky.social is hosting a scientific symposium with Seattle Children's Research Institute + participants from University of Washington to celebrate the network of researchers, clinicians, and patient advocates in Seattle
pnri.org/rarediseased...
pnri.org/rarediseased...
February 21, 2025 at 4:53 PM
In honor of #RareDiseaseDay on Feb 28, @pnrigenetics.bsky.social is hosting a scientific symposium with Seattle Children's Research Institute + participants from University of Washington to celebrate the network of researchers, clinicians, and patient advocates in Seattle
pnri.org/rarediseased...
pnri.org/rarediseased...
October may officially be Check Ammonia Month, but we will continue to share this important information throughout the year in hopes that it can save even one life.
Know the signs and symptoms of hyperammonemia. This knowledge could literally save lives.
#checkammonia #hyperammonemia #highammonia
Know the signs and symptoms of hyperammonemia. This knowledge could literally save lives.
#checkammonia #hyperammonemia #highammonia
February 3, 2025 at 5:40 PM
October may officially be Check Ammonia Month, but we will continue to share this important information throughout the year in hopes that it can save even one life.
Know the signs and symptoms of hyperammonemia. This knowledge could literally save lives.
#checkammonia #hyperammonemia #highammonia
Know the signs and symptoms of hyperammonemia. This knowledge could literally save lives.
#checkammonia #hyperammonemia #highammonia
🔬 Why Research Matters for UCDs 🔬
Research is the key to finding better treatments and ultimately a cure for UCDs. Thanks to our supporters, we fund groundbreaking research into new therapies, diagnostics, and patient support systems.
👉 Want to help? Donate today!
nucdf.org/donate/donat...
Research is the key to finding better treatments and ultimately a cure for UCDs. Thanks to our supporters, we fund groundbreaking research into new therapies, diagnostics, and patient support systems.
👉 Want to help? Donate today!
nucdf.org/donate/donat...
January 31, 2025 at 8:56 PM
🔬 Why Research Matters for UCDs 🔬
Research is the key to finding better treatments and ultimately a cure for UCDs. Thanks to our supporters, we fund groundbreaking research into new therapies, diagnostics, and patient support systems.
👉 Want to help? Donate today!
nucdf.org/donate/donat...
Research is the key to finding better treatments and ultimately a cure for UCDs. Thanks to our supporters, we fund groundbreaking research into new therapies, diagnostics, and patient support systems.
👉 Want to help? Donate today!
nucdf.org/donate/donat...
Female carriers of #OTC (heterozygous females) face both symptoms and health risks at higher levels than previously thought. They should be monitored to reduce risks and possibly treated to address symptoms that may have gone unrecognized. Read more: nucdf.org/research-new...
January 28, 2025 at 4:31 PM
Female carriers of #OTC (heterozygous females) face both symptoms and health risks at higher levels than previously thought. They should be monitored to reduce risks and possibly treated to address symptoms that may have gone unrecognized. Read more: nucdf.org/research-new...
The siblings of individuals with UCDs can face significant emotional, psychological, and social challenges. We've developed a number of resources to help - check them out here: nucdf.org/resources/si...
#RareDisease #Siblings #UCDs
#RareDisease #Siblings #UCDs
January 21, 2025 at 4:18 PM
The siblings of individuals with UCDs can face significant emotional, psychological, and social challenges. We've developed a number of resources to help - check them out here: nucdf.org/resources/si...
#RareDisease #Siblings #UCDs
#RareDisease #Siblings #UCDs
We are excited to share our end-of-year review! Check out all we've done, from family conferences to fundraisers, new support resources to scientific conferences and so much more. Thanks to all who helped make 2024 a success!
76cc07341.flowpaper.com/YearinReview...
#UCDs #Raredisease
76cc07341.flowpaper.com/YearinReview...
#UCDs #Raredisease
January 17, 2025 at 3:20 PM
We are excited to share our end-of-year review! Check out all we've done, from family conferences to fundraisers, new support resources to scientific conferences and so much more. Thanks to all who helped make 2024 a success!
76cc07341.flowpaper.com/YearinReview...
#UCDs #Raredisease
76cc07341.flowpaper.com/YearinReview...
#UCDs #Raredisease
What are UCDs? Urea cycle disorders are eight related disorders caused by genetic mutations that lead to deficiencies in enzymes crucial to removing ammonia, a toxic byproduct of protein metabolism, from the bloodstream. Learn more: nucdf.org/about-ucd/wh...
January 8, 2025 at 2:46 PM
What are UCDs? Urea cycle disorders are eight related disorders caused by genetic mutations that lead to deficiencies in enzymes crucial to removing ammonia, a toxic byproduct of protein metabolism, from the bloodstream. Learn more: nucdf.org/about-ucd/wh...
NUCDF dollars at work: Grant funds equipment purchase for research into genetic diagnosis of urea cycle disorders @aimeedudley.bsky.social @pnrigenetics.bsky.social
nucdf.org/research-new...
nucdf.org/research-new...
January 3, 2025 at 3:11 PM
NUCDF dollars at work: Grant funds equipment purchase for research into genetic diagnosis of urea cycle disorders @aimeedudley.bsky.social @pnrigenetics.bsky.social
nucdf.org/research-new...
nucdf.org/research-new...