A reminder during #UndiagnosedChildrenDay #ACTA2 #MSMDS #VSMC 📌Multisystemic Smooth Muscle Dysfunction Syndrome Symptoms 📌 🇪🇦Síndrome Multisistémico de Disfunción del Músculo Liso

ACTA2 Alliance @Acta2Alliance

2 months ago

A reminder during #UndiagnosedChildrenDay #ACTA2 #MSMDS #VSMC 📌Multisystemic Smooth Muscle Dysfunction Syndrome Symptoms 📌 🇪🇦Síndrome Multisistémico de Disfunción del Músculo Liso

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@Bptkramer @EricRoselliMD Biomarkers in MSMDS recently published here! Helps monitoring and preventing for aortic events soon after birth #EyesCheck #DilatedPupils #ACTA2 #AATS2024 👁️ x.com/acta2alliance/…

ACTA2 Alliance @Acta2Alliance

2 weeks ago

@Bptkramer @EricRoselliMD Biomarkers in MSMDS recently published here! Helps monitoring and preventing for aortic events soon after birth #EyesCheck #DilatedPupils #ACTA2 #AATS2024 👁️ x.com/acta2alliance/…

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“Research on rare diseases like these,” Dr. Musolino says, “is only possible by working together with patient families {...}” #CommunityImpact #ResearchMatters #MSMDS #ACTA2 #VascularDiseases @GeneStrokeLab Full article by @MassGeneralNews 📰giving.massgeneral.org/stories/develo…

Look out for number 8! 🧬 #MYH11 #MYLK #AATS2024 #Aortic2024 #ACTA2 #MSMDS #SmoothMuscle

Benjamin Kramer, DO, MS @Bptkramer

6 days ago

Look out for number 8! 🧬 #MYH11 #MYLK #AATS2024 #Aortic2024 #ACTA2 #MSMDS #SmoothMuscle

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Let's than a week to dive into the cutting-edge world of #MSMDS research with @DiannaMilewicz and Dr. Murdock! 📝Register now to hear about lab findings and the ongoing clinical trial for new therapeutic approaches bit.ly/Milewicz_Update @JohnRitterFdn #ACTA2 #research #SMDS

👱‍♀️ Introducing Dixie, a vital support within our community! #MSMDS #MeetTheTeam #ACTA2 #RareDisease

Exciting news with @MarkELindsay & @GeneStrokeLab! 👶MSMDS is being diagnosed earlier than ever, thanks to community efforts 🧬Gene therapy offers hope, and small molecule research expands possibilities 📝Natural History Study: enrol now! #ACTA2 #vascular bit.ly/ResearchMSMDS

The aorta, previously categorized as a vessel, is now recognized as an independent human organ! Read more on our website about what this groundbreaking news means for aortic medicine: gadacanada.ca/news/2024/3/12… #thinkaorta #aortaed #lds #marfan #acta2 #aorta @MACAorta

🥳A big THANK YOU to everyone who donated, shared, and reached out!! Togheter we can make this dream of the gene therapy for MSMDS come true 💪 Cheers to big dreams!!💚 #ACTA2 #genetherapy #MSMDS #geneticdisease #ultrarare

@PhilKonieczny "Ale jak to zrobia" pytaja sie niektorzy?Ano tak to zrobia,ze ci zablokuja wszystkie konta w bankach w PL i sam im oddasz dostep do twoich kont krypto,zebys mogl czynsz za mieszkanie zaplacic i chleb karta w Biedrze.Mlodzi zatesknia za PiS,ktory jako jedyny w UE blokowal #acta2

Happening now: "State of Research" talk by Dr. Musolino and Dr. Lindsay. Come along! facebook.com/share/S4WrXaTx… #msmds #acta2 #RareDiseaseDay #smoothmuscle #actin #genetherapy #genetherapies #biotechnology

Celebrate the gift of time this February 29th and donate to contribute to our gene therapy #MSMDS #ACTA2 ➡️Pick one of the 'rare' amounts we propose in the image if you don't know how much to give! #foreverthankyou #RareDiseaseDay #RareDisease #genetherapy bit.ly/donation_gene_…

Every MSMDS patient is a fighter💪 Not only today #RareDiseaseDay2024 Tomorrow #firstofmarch, they will continue fighting, being the reason behind the 1st systemic gene therapy for a severe genetic vascular disease. Help them here: bit.ly/donation_gene_… #ACTA2 @GeneticAll_UK

#RareDiseaseDay #Facts With so very few cases around the world, MSMDS is not a disease known by many doctors. For most of the patients, a common issue is having to speak about their disease in detail over and over again when seeing new doctors. bit.ly/donation_gene_… #ACTA2

📲Scan and join the team that wants to create a brighter future for #geneticdiseases. There's no better way to celebrate #RareDiseaseDay2024! 🪇 bit.ly/donation_gene_… #RareDiseaseDay #RareDisease #Geneticsmatters #Donations #helpinghand #Dosomethinggoodtoday #acta2 #msmds

🕵️‍♂️🕵️ You will only find one MSMDS patient in 131 million people nowadays... and if/when that happens, they will be able to 💚thank you💚 for contributing today to the gene therapy they need. Right here 👉 bit.ly/donation_gene_… #acta2 #msmds #genetherapy #RareDiseaseDay2024

Our MSMDS heroes, united now for a gene therapy. Make a donation today … and join the team!🦸‍♀️🦸🦸‍♂️🦸‍♂️🦸🦸‍♀️ bit.ly/donation_gene_… #acta2 #msmds #genetherapy #RareDiseaseDay2024 #RareDisease

🗓️Save the date! 👥On #RareDiseaseDay Dr. Musolino and Dr. Lindsay will be providing an update on the state of MSMDS research and the development of a gene therapy. Stay tuned for the registration link! @GeneStrokeLab @MarkELindsay #RareDiseaseDay2024 #ACTA2 #genetherapy

⏳We have 10 days leading up to Rare Disease Day 2024, on February 29th. 🤲Can you help us raise money to support treatments for MSMDS during these TEN DAYS? All funds can go into our PayPal account: bit.ly/donation_gene_… Feel free to share! #acta2 #msmds #RareDiseaseDay