BridgeBio’s Post

A recent study argues for the implementation of nationwide screening for homozygous familial hypercholesterolemia (HoFH) in the United States. Read the full article here ⤵️ #HoFH #HomozygousFamilialHypercholesterolemia #CardiovascularDisease

Understanding Phobias A phobia is an uncontrollable, irrational fear of certain objects, situations, or activities. This intense fear can lead to avoidance and even panic attacks. Phobias can start in early childhood, often appearing between ages 15 and 20. Both men and women can be affected, though men are more likely to seek treatment. Phobias may be caused by genetic and environmental factors, sometimes linked to a bad first encounter with the feared object or situation. Learn more about phobias at https://lnkd.in/dNE4Vp4T.

Next chapter! Looking forward to catching up with you, Erin! So excited to continue to connect with others - breaking down the barriers that I faced while sharing knowledgeable experiences creating additional channels to provide community advocacy support by sharing these stories about the rare disease journey. In the United States, rare diseases and conditions are those that affect fewer than 200,000 people. Not sure where we would be today without people who have supported us like Mark Dant guiding us and taking us in. #globalgenes #positivelyrare Danae' Bartke Eileen Novins Masciale #lds2024 #hcuawareness2024 #genetics #aortaed #lowprotein #undiagnosis #rarex2 #traverse #brainboost #clinicaltrials #chiari #syndrome EveryLife Foundation for Rare Diseases

Today, on May 16th, we recognize Hereditary Angioedema (HAE) Day, a crucial day dedicated to raising awareness about this rare and potentially life-threatening genetic condition. HAE patients often face significant challenges, from severe swelling episodes to the constant uncertainty about when the next attack might occur. At CSL Behring, we are committed to transforming the lives of those affected by HAE. Our cutting-edge treatments and dedication to innovative research have been pivotal in improving the quality of life for patients worldwide. We understand the critical need for effective management and the impact that advanced therapies can have on reducing the burden of this condition. We are proud to be at the forefront of HAE care, providing technologies that not only alleviate symptoms but also empower patients to lead fuller, more active lives. Our mission is to ensure that every patient has access to the best possible care and support. On this Hereditary Angioedema Day, let's stand together in support of the HAE community, acknowledging their strength and resilience. Let’s continue to drive forward with passion and purpose, making a tangible difference in the lives of those who depend on us. #HAEDay #HereditaryAngioedema #CSLBehring #HAEAwareness #PatientCare #InnovativeHealthcare #IWorkforCSL #DrivenbyOurPromise

May 16 is #HAEDay. While it seems like there is a “day” acknowledging everything nowadays, this one is particularly special to me and my colleagues at CSL Behring. Why? Because hereditary angioedema (HAE) can be a fierce and unpredictable disease. Imagine living life feeling like a ticking time bomb, with almost no notice on when or where a swelling attack could occur. And when it does, the best-case scenario is that it sidelines your day, and in the worst case, it sends you to the hospital. AT ANY TIME.   HAE is estimated to affect 1 in every 40,000–50,000 people globally. So on a day like today, I reflect with pride that the company I work for creates hope for people living with HAE. Our portfolio of plasma-derived and recombinant therapies gives them a sense of control over an otherwise uncontrollable situation. Whether their day was a trip to the grocery store, or a trip to Paris, they can be more prepared and enjoy more of what life has to offer. Isn’t that what we all want?    I honor those living with HAE today and every day. #IWorkforCSL #DrivenbyOurPromise 

🔥LER's new course from leading expert Laurel Wilson will amaze and inspire you!🔥 ⭐ An awe-inspiring explanation of how human milk affects genetic expression ⭐ ➡️ How an infant's first food activates or silences genes to determine lifelong health ➡️ How these changes can be inherited by future generations ➡️ Why this makes access to human milk a powerful force in healing the cumulative effects of oppression, racism, and marginalization → https://vist.ly/uyin

With the Goal of Assessing Epigenetic Variance. How cool would it be to assign identical twins controlled environments . Twins can be fraternal (dizygotic) or Identical (monozygotic) Unlike identical twins, the Genes involved in the formation of Fraternal twins can be inherited. Fasication & Conjoined polyembryony in plants is another story all together! Panama Red x NL Two sets of Twins ! 😂 or one set of Twins, and a Seedling 🌱, with 3 Radicals 🤷♂️. From each set Hoping for a ♂️ and a ♀️ 🧪👨🔬

Ever wondered if IBS runs in your family? 🤔 It turns out, there's a higher chance of having IBS if a parent or sibling has it. Twins, especially identical ones, share a particularly strong likelihood of both having IBS. But here's the twist – it doesn't necessarily mean there's a genetic inheritance. Family members often live in the same environment, munch on similar grub, and even share the same colonic bacteria. 🏡 So, is IBS a family affair for you? Share your thoughts in the comments below! 👇 https://buff.ly/2ChKJ81 #FamilyHealth #IBSInsights #CuriousMinds

October is Down Syndrome Awareness Month! This is a special time to promote acceptance, raise awareness, and celebrate the abilities and achievements of individuals with Down syndrome. Let's work together to educate others about this genetic condition and show our support. Looking for ways to get involved? Here are 10 impactful things you can do this month: https://lnkd.in/g-qf_CHg #DownSyndromeAwareness #DownSyndromeAwarenessMonth #CelebrateAbilities #InclusionMatters

TPCA joins the global celebration of World Down Syndrome Day! Today, we recognize individuals with Down syndrome and do our part to raise awareness.   Down syndrome is one of the most common genetic variations and occurs in approximately one in every 770 live births in the United States. It is a naturally occurring chromosomal arrangement, being present across racial, gender or socioeconomic lines. According to the CDC, there are three types of Down syndrome: Trisomy 21, Translocation Down syndrome, and Mosaic Down syndrome. Learn more about Down syndrome, by visiting https://lnkd.in/evvNKJ3. #WorldDownsyndromeDay #EndtheStereotypes