Today is World Fragile X Day. Fragile X syndrome (FXS) is the most common form of inherited developmental disability worldwide. There is no cure for FXS, but an early diagnosis with a genetic blood test can still help. #WorldFragileXDay#FragileXSyndrome https://t.co/LBOFggzOvc
We're raising money for #FRAXA starting next week for an early #worldfragilexday celebration!!
We've got a lot of collabs with a lot of wonderful people, + a whole #pokemon tournament planned!
Please 🔁 and 💙 so we can spread the word!!!
July 22nd is #WorldFragileXDay! Today is a powerful reminder of how #geneticresearch fuels understanding and hope. At CAN, we’re committed to uncovering how Fragile X and autism intersect, and advancing science that supports every brain. 💡
CarolinaEast Medical Center is joining over 400 locations worldwide that are going teal on July 22 for #WorldFragileXDay, showing our support for individuals with #FragileXsyndrome. FXS is the most common inherited cause of autism and intellectual disabilities worldwide. 💚💙
Tomorrow, July 22 is #WorldFragileXAwarenessDay. QurAlis joins the global #FragileX syndrome (#FXS) community to celebrate individuals living with FXS and families and friends impacted by FXS, as well as raise awareness as we advance research toward finding effective #precisionmedicine treatments and ultimately a cure. FXS is a rare, genetic #neurologicaldisease that is the leading inherited form of intellectual disability and a known cause of #autism. There are no disease-modifying therapies currently available for FXS.
On #WorldFragileXDay, we’re honored to amplify Ashley’s voice – a dedicated advocate for her son, Sebastian, and the entire #FragileX syndrome (FXS) community.
At Harmony Biosciences, stories like theirs are at the heart of our mission. Guided by empathy and driven by science, we remain committed to advancing meaningful therapies for those impacted by rare neurological diseases like #FXS: https://t.co/CWrapesVVi
#FragileXSyndrome
#FXSAwareness
#RareDisease
#CaregiverVoices
#Neuroscience
#Biosciences
#Pharma
Today, on World Fragile X Awareness Day, we are proud to spotlight our partners at @FRAXAresearch Foundation, who are helping lead research and support for the #FragileX community. As Holly Roos, community services director at FRAXA, reminds us: “When we come together, whether to raise awareness, support research, or show up for families, beautiful things happen.”
#FragileXAwareness #FRAXA #WorldFragileXDay,
July 22 is Fragile X syndrome awareness day. By lighting up landmarks and monuments around the world, the hope is to shine light on the need for research and a cure. #RareandReady#FragileX@FRAXAresearch@NFXFoundation
City Hall will be lit up in teal and blue tonight in recognition of #WorldFragileXDay.
Fragile X syndrome is a genetic disorder caused by a gene on the X chromosome shutting down.
@worldfxday recognizes families impacted by Fragile X.
Learn more: https://t.co/3HIJJr2iuW
TEAL | For World Fragile X Day!
"World Fragile X Day celebrates families impacted by Fragile X and highlights advancements of research to find effective treatments and ultimately a cure. On World Fragile X Day we shine a light on Fragile X by illuminating monuments and landmarks around the world. We gather with friends and family to celebrate loved ones who shine in the face of Fragile X" (FRAXA Research Foundation)
@worldfxday@FRAXAresearch
HPCL has always been at the forefront, supporting diversity & inclusion, having touched over 32 lakh beneficiaries under our #CSR initiative during FY 2023 24.
We have championed the cause of supporting disabilities of various kinds and today, we have coloured our iconic Petroleum House building #Green to support the cause of spreading awareness towards Fragile X syndrome on National Fragile X Awareness Day, today.
#DeliveringHappiness #HPTowardsGoldenHorizon