DAY TEN 📌📌📌 SCD is a genetic disorder caused by inheriting abnormal haemoglobin genes from both parents. It is not a punishment or curse, but rather a biological condition. Warriors, ignore those cultures or those saying that SCD is a result of a curse or punishment. Do you still hear these kinds of statements? If yes, what do you do/what is your response? 🤔 Tell us in the comments. 👇 Like, comment and share this to educate your circle!!! 💪🏻 See you tomorrow! 😊✌️ #nextgenerationinitiative #mythsvsfacts #scdmythsvsfacts #scdmyths #scdfacts #sicklecellawareness #sicklecelladvocacy
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Planning for the future starts with knowing your DNA. Our Extended Carrier Screening offers peace of mind by identifying genetic risks before they become realities. With DNA-based testing, we help individuals and couples understand their risk of having children with severe inherited genetic disorders. Absolute DNA offers a range of carrier screening options, testing up to 420 genes linked to common inherited conditions like Cystic Fibrosis, Spinal Muscular Atrophy, and Fragile X Syndrome. Our comprehensive and highly accurate tests empower prospective parents to make informed reproductive decisions. Take control of your family's future today. Discover the power of knowledge with Absolute DNA. #absolutedna #dnatesting #health #carrierscreening https://lnkd.in/gbXYh56f
🔬 Explore Extended Carrier Screening with Absolute DNA 🔬
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Is anxiety genetic? #anxiety #hypnotherapist #hypnosis #anxietysupport #anxietyhelp #anxietyrecovery #anxietyhealing #blushing https://lnkd.in/dYWyGY_r
Is Anxiety Genetic?
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Today is Undiagnosed Children's Day where we spread the word about what it means to be affected by a syndrome without a name (SWAN)/undiagnosed genetic condition. Learn more : https://bit.ly/3PVzNCI #PINKathon #EarlyDiagnosisSavesLives
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#NiemannPick is a rare, fatal and progressive genetic disorder in need of safe and effective treatment options. Learn more: https://bit.ly/44t6U5P #NiemannPick #NPC1 #RareDisease
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T1D Level 27 🇮🇩 IKADAR | PERSADIA | Diabetes Initiative Indonesia 🌏 NCD Diarist - NCD Alliance | #dedoc° voices | Blue Circle Voices - IDF | ISPAD Ambassador
Diagnosed with cardiomyopathy in 2018. As a person living with multiple NCDs, the condition is confusing in my early diagnosis and adjustment needed towards my daily routine, especially on doing workouts. No run, just walk, in order to keep a less increase heart rate or I would be at risk for cardiac arrest. ❤❤❤ #cardiomyopathy #type1diabetes #asthma #multipleNCDs
Knowing if you have an inherited type of #cardiomyopathy is important because it can impact the risk for other family members. Genetic testing can help other family members to know if they also have a genetic predisposition and help protect them. Earlier this week, we heard Hannah's story of being diagnosed with hypertrophic cardiomyopathy (HCM). Watch now to hear from Hannah's older sister, Bethany. It’s time to take notice of cardiomyopathy. You or a loved one could unknowingly be at risk. #ThinkCardiomyopathy #CardiomyopathyAwareness #Cardiomyopathy2024 #ThinkCM
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Today, on World Hemophilia Day, let's share information on this rare genetic disorder affecting blood clotting. Join us in spreading awareness and supporting those living with hemophilia. Here are some vital tips for healthier living with this condition. #WorldHemophiliaDay #RareDisease #BleedingDisorder #HemophiliaAwareness #PreventiveCare #AsterBangalore #AsterHospitals
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Some people are diagnosed with MDS due to the activities linked to it, while others inherit through genetic conditions. This post highlights the causes of MDS through linked activities and genetic conditions. Despite the challenges, there are ongoing advancements in research and treatment options, offering hope for those affected by this condition. Together let's fight this battle and help those who are battling with MDS! #MDS #MyelodysplasticSyndromes #CancerAwareness #CancerTreatments #SSO #SSOSingapore #SingaporeSocietyOfOncology
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Hemophilia is a genetic bleeding disorder. People with hemophilia bleed for longer than normal because their blood does not contain enough clotting factor, or the clotting factor doesn’t work properly. Clotting factors are proteins in the blood that help control bleeding. Hemophilia is usually inherited, meaning that it is passed from parent to child through the parent’s genes. Genes carry messages about the way the body’s cells will develop. They determine a person’s hair and eye colour, for example. In people with hemophilia, the genes responsible for the production of clotting factors are altered or changed. As a result, their body will either not produce sufficient or any clotting factor, or the clotting factor it produces does not work properly. Visit: https://lnkd.in/deHQE7fb #WorldHemophiliaDay2024 #Knowmore #EdenGardens
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World Retinitis Pigmentosa Day raises awareness about a group of genetic disorders that cause retinal degeneration and vision loss. This day promotes education, support, and research to improve the lives of those affected by this condition, aiming for early diagnosis and potential treatments. #WorldRPDay, #RetinitisPigmentosa, #VisionLoss, #RPawareness, #SupportRP, #GeneticDisorders, #EyeHealth, #RPResearch, #BlindnessAwareness
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X-chromosome genetic disorders inheritance explained Haemophilia - a disorder in which blood doesn't clot normally. When blood can't clot properly, excessive bleeding \(external and internal\) occurs after any injury or damage. Symptoms include many large or deep bruises, joint pain and swelling, unexplained bleeding, and blood in urine or stool. Treatment includes injections of a clotting factor or plasma. Youtube video: https://lnkd.in/dAD6YRrx \#nikolays_genetics_lessons
X-chromosome genetic disorders inheritance explained
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6moIt is neither punishment nor a curse