15% of the world population suffers from a form of tinnitus. 20% of those with tinnitus are severely disabled. 1% of tinnitus patients attempt suicide. Traditional evidence-based approaches have failed to develop any treatments for tinnitus. That’s why it’s time for a new medical research approach: War on Tinnitus. The goal is to find a solution for tinnitus in 3 to 5 years. To reduce and ideally abolish the sound. We aim to raise funds to cover the total cost of the ‘War On Tinnitus’ research project: €345.000 for the first two years of the 4-year research period. Help us win the war against tinnitus! Go to www.tinnitusfree.eu #tinnitus #tinnitusresearch #tinnitusawareness #tinnituscure
TinnitusFree Foundation’s Post
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Great way to end this conference- with a full exploration and discussion of different perspectives on prolonging grief disorder.
At #EGC2024, Maarten Eisma, Martin Lytje, fiona tuomey (HUGG), and Manuel Fernández Alcántara will form our plenary panel discussion, 𝗣𝗿𝗼𝗹𝗼𝗻𝗴𝗲𝗱 𝗚𝗿𝗶𝗲𝗳 𝗗𝗶𝘀𝗼𝗿𝗱𝗲𝗿: 𝗘𝘅𝗽𝗹𝗼𝗿𝗶𝗻𝗴 𝗣𝗲𝗿𝘀𝗽𝗲𝗰𝘁𝗶𝘃𝗲𝘀. The topics they'll cover include an overview of Prolonged Grief Disorder (PGD) its impact on children, the neuroscience of PGD, and its impact on everyday life. We're looking forward to this panel discussion and welcoming everyone to Dublin this November. Register for #EuropeanGriefConference. Early bird tickets on sale now 👉 https://lnkd.in/eCgfbXY4 -- Irish Hospice Foundation, Det Nationale Sorgcenter, Royal College of Surgeons in Ireland (RCSI)
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September 7th is World Duchenne Awareness Day! At Muscular Dystrophy Canada, we're committed to ongoing initiatives that support individuals and families affected by Duchenne muscular dystrophy (DMD), working to make a meaningful impact on their journey. DMD Masterclass: We provide healthcare professionals with advanced training on the latest clinical and research developments in DMD. Duchenne Canadian Journey Mapping: We are mapping out the experiences of those with DMD and their families, from early symptoms to diagnosis, steroid use, and beyond, highlighting their present-day challenges. GrowDMD Transition Study: We collaborate with families to understand their transition from pediatric to adult care, aiming to improve the support available to youth with DMD across Canada. Detect Duchenne - Diagnosis Experiences Survey: We’ve launched a survey to capture insights into the diagnosis experiences of both children/youth and adults with DMD. The survey is available in English: Children/Youth: https://lnkd.in/eDSDDpHz Adults: https://lnkd.in/eWJMPvxq
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Deputy Director at Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Endometriosis affects 1 in 10 women during their reproductive years. That is 190 million women globally who encounter signficant pain, nausea, fatigue, mental health symptoms, and potentially infertility. Most women wait 7 to 10 years to be diagnosed and require surgery for a definitive answer. We're looking to change that equation. NICHD launched a new initiative today to move rapidly to diagnosis and advance biomarkers - the link is below https://lnkd.in/eQGqhiVW!! Society for Women's Health Research (SWHR) American College of Obstetricians and Gynecologists (ACOG) Endometriosis Foundation of America - can you help spread the word? #femtech #biomarkers #womenshealth #endometriosis #NICHDimpact
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🌟Consortium Partner Spotlight: Murdoch Children’s Research Institute🌟 Our partnership with the Murdoch Children's Research Institute (MCRI) - Australia's largest child health research centre – strengthens our efforts to revolutionise childhood cancer care. Ranked among the top three globally for paediatric research quality and impact, MCRI's commitment to improving child health is unparalleled. MCRI’s co-location with two of our other consortium partners - The Royal Children's Hospital and University of Melbourne – facilitates researcher-clinician collaborations from bench to bedside. By supporting collaboration amongst our 8 consortium partners, we aim to accelerate the translation of research breakthroughs into clinical practice, to benefit children with cancer locally and globally. #VPCC #ChildhoodCancerCare #ChildhoodCancer #CancerResearch #PaediatricOncology #Collaboration #MakingADifference
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Managing Director at TrainAbility | Disability Equality Trainer | Disability Advocate and Campaigner | wheelchair user | stroke survivor. Helping companies and their ERG's succeed and achieve their potential.
This is Multiple Sclerosis (MS) Awareness Week, and it is a dedicated period aimed at raising awareness about multiple sclerosis, a chronic autoimmune condition that affects the central nervous system. Over 130,000 people are affected by MS in the UK and each year nearly 7,000 people are newly diagnosed. Celebrating MS Awareness Week is crucial to help increase understanding and knowledge about MS within communities, reducing stigma and misconceptions surrounding the condition. Secondly, it provides an opportunity to highlight the importance of research into MS, as well as advancements in treatment and care. Increased awareness often translates into more funding and resources allocated towards research efforts aimed at finding a cure or more effective treatments for MS. And finally, MS Awareness Week serves as a platform for individuals living with MS to share their experiences, connect with others facing similar challenges, and advocate for improved access to healthcare, employment opportunities, and other support services. Celebrating MS Awareness Week is not just about raising awareness—it's about empowering individuals affected by MS, fostering understanding and support within communities, and driving positive change towards a world where everyone living with MS can lead full and fulfilling lives. Famous people living with MS include: Christina Applegate, Jack Osbourne, Jamie-Lynn Sigler and Selma Blair, to name a few, but it can affect anyone. If you want to learn more, check out https://lnkd.in/epUhmzMz and get involved #MultipleSclerosis #LearnMore #NervousSystem #AutoImmune #Brain #SpinalCord #BlurredVision #InclusionMatters #Balance #Learn #MSSociety
Here for everyone with MS
mssociety.org.uk
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CEO & Physiotherapist at Muscle Craft Physiotherapy | Professional Speaker | Master of Ceremonies Talent
Empowering voices, raising awareness. 💛 Today, and every day, we stand with all those impacted by endometriosis. To commemorate this, we've uploaded an Endometriosis video on our Youtube channel. Click the link in our bio for this video. Let's keep fighting for understanding, support, and breakthroughs. #EndometriosisAwareness #EndoWarriors #StrengthInSolidarity #physicaltherapy #physiotherapy #physiotherapist #jamaicanphysiotherapist #rehabilitation #pelvicfloor #pelvicfloorphysio #pelvicfloorphysicaltherapy 🎗️💪🏼
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More than 1 billion people in the world live with unaddressed vision impairments of some sort, and Seva Foundation, a global nonprofit eye care organization that works with local communities around the world, is looking to combat that. A recent paper from the organization says that, when prioritized, eye health could yield $36 in benefits for every $1 spent, meaning every dollar spent on refractive error or cataract correction produces $36 in benefits. This is 6 times greater than the typical $6 return seen in other development interventions. The 2 highest returns outside eye care were seen in nutrition and noncommunicable diseases, which were at 13 to 1 and 9 to 1, respectively. Read More: https://ow.ly/gkV550QVunt
The value of sight: Unveiling the economic returns of eye care
ophthalmologytimes.com
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🚀 New episode out now! Prof. Dr Sandra Juul dives into the HEAL trial's findings and strategies for supporting neurodevelopment in asphyxiated infants. Tune in to learn about this important topic here: https://lnkd.in/dzpTaPfp #NeonatologyNow #NeonatalCare #NICU #HEALstudy
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Chief Clinical Officer, Emerging Neurotech Strategy, leading neuro clinical evidence and cutting-edge neurotech innovation 🧠
💡 Well stated JoJo Platt 📢 Keep #NeuroTech and innovative #brain 🧠 research alive and well by letting your local Congress 🇺🇸 members know the 40% grant 💰 cut from the #NIH Brain Initiative has not gone unnoticed… see below 👇 for details #Neurotechnology #neurotech #Brain #bci #ai #innovation #neuromodulatiin #neurospine #neurotumor #gbm #neuropharma
NIH BRAIN Initiative funding has been cut. No. It's been brutalized. I'm not sure if you know this, but no one at NIH, including all of our favorite staffers, can do anything to intervene. It's up to US to reach out to our members of congress and members of the appropriate committees to pressure them to reinstate - if not this year, then at least for next year. The other challenge is that congress won't know that we care unless we TELL THEM WE CARE. So please, take a moment to help me help you. Find your congressional members here https://lnkd.in/gZP_nfaR and HHS (federal budget appropriations) and maybe some of our new high-profile investors in neurotech can reach out via their networks 🤷♀️
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🧠 𝗦𝗲𝗽𝘁𝗲𝗺𝗯𝗲𝗿 𝗶𝘀 𝗕𝗿𝗮𝗶𝗻 𝗔𝗻𝗲𝘂𝗿𝘆𝘀𝗺 𝗔𝘄𝗮𝗿𝗲𝗻𝗲𝘀𝘀 𝗠𝗼𝗻𝘁𝗵! 🧠 This month, we shine a spotlight on brain aneurysms and the importance of early detection and education. A brain aneurysm can be a life-threatening condition, but awareness and knowledge can play a crucial role in prevention and management. Let’s work together to spread knowledge and support those affected by brain aneurysms. Also, consider making a donation to the Brain Aneurysm Foundation to support brain aneurysm research. #BAF #1in50 #StopThePop #BrainAneurysm #Scan2Save #BAFAdvocacy
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