HCU Network America @HCUAmerica
The mission of HCU Network America is to help patients with #Homocystinuria and related disorders manage their disease and to find a cure. #HCUNetworkAmerica linktr.ee/hcuna United States Joined March 2017-
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Join our host, Ben of the HC&U: A Homocystinuria Podcast, and our guests Melanie, Shaina & Julie as we dive into a lively discussion on their experiences navigating their child's diagnosis & treatment! ➡️ Register: bit.ly/WHAD2024 or stream live on Facebook #WHAD2024
Meet our May #HCUHero, Brooklyn from Montreal! 💙 You can read her full story here: ➡️ hcunetworkamerica.org/brooklyn/ #patientstories #lowproteindiet #medicalformula #raredisease #classicalHCU #homocystinuria #HCU #HopeConnectsUs #lgbtqia
Check out this webinar, brought to you by @GlobalGenes! 🔹Topic: Coping Skills for Caregivers 🔹Date/Time: Thursday, May 9 at 3:00 pm EST ➡️ Register here: bit.ly/3xTF2N5
🌎 World Homocystinruias Day (#WHAD2024) 🌎 is coming, and we've got all sorts of excitement planned! 🎟️ Our virtual raffle kicks off May 10 & will feature some awesome prizes (TBA soon!) Register to watch the live stream discussion: ➡️ bit.ly/WHAD2024
We're excited to have almost 1⃣0⃣0⃣ patients enrolled in our Homocystinurias Data Collection Program! Join the global movement 🌎 Head to ➡️ homocystinuria.rare-x.org to register & get started! #research #treatment #homocystinuria #cobalamindisorders #severeMTHFR #HCU @RARE_X_
Join our community's own Liz Carter! She'll be a panelist on a webinar this Thursday called "Charting the Future: Exploring Trends in Family Leadership for Systems Change", brought to you by @ExpectHealthOrg ! ➡️ Register here: bit.ly/3UBXBhx
📣 Exciting news! 📣 The Acappella Natural History study is now enrolling ages 1-4 with Classical HCU! You may be able to receive payment for your time and travel if your child participates in this study. ➡️ For more info, visit hcuconnection.com
We are only 2 months away from our #MovingMountains Family Conference in Aurora, Colorado! 🏔️ We've got an epic speaker lineup, incredible breakout sessions, an amazing KidZone program, and of course a #lowprotein menu! Join us! ➡️ To register, visit: bit.ly/hcuconference2…
Now accepting request for proposals! Find more information ➡️ bit.ly/24HCURFP Deadline to submit is June 25, 2024. @RareDiseases @GlobalGenes @RARE_X_ @SIMDtweets @gmdi
New episode of the HC&U: A Homocystinuria Podcast out NOW!🎙️ ➡️ Catch it on Spotify, Apple Podcasts, iHeart, or Amazon Music! Or hcunetworkamerica.org/hcu-podcast/ #podcast #raredisease #advocacy #lowprotein #advocacy #research #diagnosis #homocystinuria #HCU #HopeConnectsUs
This exciting event, hosted by PKU Organization of Illinois, is open to anyone with an IEM and their families! 🎣 🛶⛺️ IEM campers are FREE and family members are just $10 each! ➡️ Learn more/register here: bit.ly/3TKWdJc
We've got an epic speaker lineup for our #MovingMountains2024 Homocystinuria Family Conference! 🗻 We're excited to welcome Thomas McCorvie, PhD! Dr.McCorvie will share some exciting information about his latest research on Classical HCU! Join us! ➡️ bit.ly/hcuconference2…
World Homocystinurias Day is coming! Get your t-shirt in our Bonfire (one for classical, cobalamin, and severe MTHFR) through April 25 to receive in time for #WHAD2024 on May 18! 👕 bonfire.com/store/hcu-habe…
🚨 TONIGHT @ 7 pm ET! 🚨 Join HCU Network America on & meet with leaders of @flokhealth (formerly PKU News). We'll talk about programs like Family Camp, the flok app, & take any questions you may have for the flok team. ➡️ Register: bit.ly/3Tp7jmY #flokhealthapp
We invite you & your colleagues to submit a poster abstract for the 4th HCU Patient-Expert conference. Trainees are encouraged to submit. Accepted poster presenters must register for the symposium & be present. ➡️ Email [email protected] for further details!
World Homocystinruias Day (#WHAD2024) is happening in 1 month!! 🎉 This year's theme is 'Help Navigate the Maze', & we've got all sorts of excitement planned - virtual raffle, a live panel discussion, tshirt sale & more! The fun starts in May - keep your eyes peeled 👀
Thx to the experiences shared by caregivers in our homocystinurias Rare-X DCP, we have more insight into the quality of life of our pediatric patients. Complete the Quality of Life Survey by 5/20/24! Head to ➡️ homocystinuria.rare-x.org to get started! @RARE_X_
We've got an epic speaker lineup for our #MovingMountains2024 Family Conference! 🗻 We're excited to welcome Sagar Vaidya, MD, PhD, VP of Clinical Development @ Travere Therapeutics to share updates on Pegtibatinase. Join us - Register here: ➡️ bit.ly/hcuconference2…
Happening this Saturday! Our Pizza Party get-together at Blaze Pizza in Charlotte, NC! 🍕🍕 We hope to see you there!!!
🚨 Exciting opportunity alert! 🚨 Are you someone who: 🔹 Benefits from 1:1 coaching? 🔹 Wants guidance in identifying advocacy goals? 🔹 Desires extra support in building relationships with legislators? Learn more: bit.ly/3VX57o7
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19 Followers 116 Following@OnceUponAGene Yes! But also for kids, please pause and consider if this is a photo they'd want on the internet or for others to see when they're older. So many medical journals have embarrassing photos and that's dehumanizing. 💚
Companies: Please show real pics of our #RareDisease kids. Not a happy/laughing/rolling in the grass fam clearly hitting your DEI ✔. Most of our kids can't even do the pincher grasp in those pics of kids holding toys. Show real rare kids. We need to 👀 them and so does the 🌎
We got to connect with the wonderful folks from @HCUAmerica at the ACMG conference not too long ago. Tune in to learn more about the impactful work they're doing. #ACMG #HCUNetworkAmerica #ACMGMtg24 #MedicalGeneticsAwareness #Genetics #Genomics #PatientWorthy #ClinicalGenetics
Interesante artículo que tiene el interés de orientar en la deficiencia de 5-10 meteniltetrahidrofolato sintetasa (MTFS; OMIN 604197) , como valorar la dosis adecuada de de 5MTHF #EnfermedadesRaras @ACIMET_MMA @Aecom_EIM @HCUAmerica @AEGHgenetica @pelendinez @AderleL @senep_es
Let's not wait and see; let's offer Exome Sequencing today! #RareDisease #GeneticTesting #CerebralPalsy #RareEpilepsies
We see you!! Thank you #LouisvilleKy #BigFourBridge #RareDiseaseAwareness
This week was Rare Disease Week & members of our HCU community were busy advocating & spreading awareness! 💙 How did YOU celebrate #RareDiseaseDay2024? Drop pics or let us know in the comments! 👇 #RareDiseaseWeek #RareDisease #RareDC2024 #homocystinuria #HCU #HopeConnectsUs
Este artículo revisa el desarrollo actual de la #terapia #génica viral y no viral para #EnfermedadesRaras hepáticas; def. del ciclo de la urea, acidemias orgánicas, enf. de Wilson, glucogenosis Ia, PKU y MSUD @RRelagh @GA1Familia @ACIMET_MMA @Glucogenosis @Aecom_EIM @HCUAmerica
Couldn’t resist! @HCUAmerica @RareRevolutionM @RareAdvocacy @GlobalGenes @mariashriver 🦓
Learning! So proud of these young, courageous leaders. @rarelikeher @G17Esiason @_OurOdyssey_ @sportssammy05 @lilannalaurent #danaebartke @HCUAmerica @LDSFoundation @MarfanFdn #GretchenMacCarrick @MgrDantastic @ConquerChiari @OnceUponAGene #SwapnaKakani #meganhilt
Hi, everyone! As Patient Engagement Consultant for Taylor Kane Consulting LLC, I’ve had the opportunity to work with numerous companies in the rare disease space, with a focus on helping them harness their relationships with the rare disease community.🧵
Excited to be at #ACMGMtg24 and visit with @HCUAmerica and Dr. Kim Chapman
Thank you @RepMcGovern for advocating on the House floor today for the 2.7 million Americans with gastrointestinal or inherited metabolic disorders who rely on #medicalnutrition. It's #TimeforMNEA
I introduced the Medical Nutrition Equity Act with @RepRutherfordFL so families impacted by inherited metabolic diseases or gastrointestinal conditions can access the specialty food and formula they need to live their lives to the fullest. Congress should pass it NOW!
CurePDE has started a youtube channel. For the first webinar we discussed the work within the #PDE and #CHARLIE consortiums. It is such an honor to collaborate with patient and advocate groups like CurePDE, @OrganicAcidemia, and @HCUAmerica youtube.com/@CurePDEFounda…
Best way to explain @HCUAmerica #RareDiseaseMonth Enlighten me. It’s just a way of life for some. Why do you think you have to eat a high protein meal? Just the opposite.
There are millions of kids with Rare Diseases. What keeps you going? Early morning before the day begins, … 🙏 🍀 ✨! Day 2 : @HCUAmerica Danae +everyone who works tirelessly for others. #patientcentric #lowprotein Not just about tacos and burritos all the time. 😘
🎉 Exciting news! I'm so happy to announce that I've been awarded an EPSRC New Investigator grant! 🚀 I'll be seeking a talented post-doctoral researcher in the new year - please spread the word!🌟 #AcademicTwitter #NewInvestigator
Exciting to share this weekend new data from improvements to the SYNB1353 fermentation process! Proud of our team's commitment to optimize this potential treatment for #HCU. Check it out: loom.ly/Qi620sE . #synbio #syntheticbiology #homocystinuria #inbornerrors
@IhabFathiSulima I believe besides putting Marfan syndrome as the first differential diagnosis, we should consider a condition called Homocystinuria regarding his scoliosis. The complications of pectus excavatum, are of course, related to the compression to heart and lungs. There are two ➡️
At the recent #SSIEM2023 meeting, we presented a satellite symposium on our investigational product in development for classical homocystinuria that is now available online at bit.ly/49DUvPE. #InRareForLife #classicalHomocystinuria #HCU #SSIEM
Immensely thrilled that this is popular and privileged to have worked with @JIMD_Editors @FroeseLab on my maiden podcast performance. Of course this is all down to the most beautiful and fascinating cobalamin/B12! x.com/jimd_editors/s…
In the our most popular podcast of 2023, Dr @FroeseLab is joined by @TheYueLab to discuss cobalamin, crystallography and consuming raw liver. Soundcloud: soundcloud.com/user-109006120… Audible: audible.co.uk/pd/The-complex… Or search for Complex cobalamin wherever you listen #JIMDpodcasts