World Health Organization’s Post

This is a noteworthy initiative by the World Health Organization to educate and raise awareness about a shift in medical practice. With advancements in science and technology, personalized treatments are becoming more available. The emphasis on integrating genomic information into healthcare decisions is a significant step towards preventive measures that could reduce the impact of genetically predisposed conditions and contribute to improving quality of life moving forward. #precisionmedicine #genomics #omics #personalisedmedicine #moleculardiagnostics #NGS

There's a bit of a "grossness" about the image below. I get it. I got it...it's hereditary. I don't talk online about my PKD much, but here it is. For those of us who have it, we have to manage all kinds of stuff we eat. Low sodium, low protein (which is really really hard, btw), low potassium, low phosphorus. AND drink water.. ALOT. I happen to be on a drug called Jynarque which helps to stop the growth of more cysts. Even still, my kidneys are huge. Actually so is my liver (see, when you have PKD, you also have cysts in your liver) That's why we have something called PKD belly...so yeah, I'm not preggers (that would be biblical at my age, lol). I'm pretty self-consious about it TBH. And, because of the size of, aforementioned organs, I get out of breath easily. Ugh. You might ask, "well what about getting a transplant?" As my nephrologist says, "it's better to keep a bad kidney as long as possible than to have a transplant." But truth is, one day, and we don't know exactly when that day will be (1 year, 2, 3??) I will need one, and living donors are WAY better than, well, you know, dead ones. So, if you're in the position to offer a kidney to a loved one who needs it today, Do It. Thanks for reading my long post.

🔊 Today is PKD Awareness Day—a day to shine a light on polycystic kidney disease (PKD), the 4th leading cause of kidney failure. PKD is a common genetic condition that impacts families by causing the uncontrolled growth of fluid-filled cysts in the kidneys. By raising awareness and educating others about PKD, we can inspire hope and drive meaningful action. Greater awareness means more resources for vital research and a faster path to a cure for future generations. 👉 Join the fight against PKD! Share this post, support research initiatives, and help spread the word. Together, we can make a difference! #PKDAwareness #EndPKD #KidneyHealth PKD Foundation

Today is Rare Disease Day. Did you know there are more than 6000 rare diseases? And 70% of genetic rare disease has childhood onset? Today is a great day to (further) educate yourself, raise awareness, and advocate for those with rare disease. I’m proud to work in a field where I can help individuals and families receive a diagnosis that will help inform decision-making, direct therapies/treatments, offer research opportunities, connect with supports, and raise awareness. #RareDiseaseDay #GeneDx #Awareness

Misconceptions about Sickle Cell Disease can lead to stigma and misinformation, creating unnecessary challenges for those affected, which is why It's important to raise awareness and educate our communities about this genetic, non-contagious condition. By sharing accurate information, we can build understanding, support, and empathy for those with Sickle Cell Disease. Let's come together to dispel myths and promote a more informed and compassionate society. #sicklecellawareness

Today is PKD Awareness Day—a day dedicated to spreading awareness and educating others about polycystic kidney disease, the 4th leading cause of kidney failure. PKD is one of the most common genetic diseases that primarily runs in families, causing uncontrolled growth of fluid-filled cysts in the kidneys. Help the PKD Foundation today by educating the world about PKD by visiting: https://lnkd.in/gZaeNJxp Increased awareness leads to greater involvement, more resources for essential research, and, ultimately, accelerating a cure for future generations. #PKDAwarenessDay #endPKD

Did you know that diagnosing a rare disease often takes many years, leading to a deterioration in health in all aspects and quality of life? I invite you to read the following post. #rarediseaseday #rarediseaseawareness

Rare diseases are much more interconnected with many other conditions and diseases than we can anticipate. #Rarediseasesday #DataBeasts #rarediseaseawareness #Rarediseases #dataanalytics #bioinformatics #sun4tech

As we commemorate World Rare Disease Day today the 29th February, we are reminded of the difficulties and challenges faced by the people and the families of those affected by rare diseases.   Rare Disease Day is the globally-coordinated movement on rare diseases, working towards equity in social opportunity, healthcare, and access to diagnosis and therapies for people living with a rare disease.   Just over 70% of rare diseases are of genetic origin. Here at Genseq, we recognize the need for access to high quality genomic services for timely diagnosis and therapy development. Genseq are committed to striving to create a service that aids in bridging these gaps in access for patients living with a rare disease. #raredisease #rarediseaseday #rarediseaseawareness

Did you know?💡Millions of people worldwide lack information about their rare disease. Improving access to information is crucial for diagnosis and treatment, research, patient empowerment, and support networks for people with rare diseases and their family's. It is a problem that Geneyx Genomex Ltd. and other companies are working to resolve. 🌍🌎🌏Join us to raise awareness about rare diseases. #PersonalizedMedicine #rarediseaseawareness #GeneticResearch #HumanGenetics #MolecularBiology