PriorityWorkforce, Inc.’s Post

When you give to charities, you participate in changing lives. We want you to know exactly how your dollars are being used. Read our blog to see exactly how far your dollars go in another person’s life: https://lnkd.in/eqP8b6WS #Health #Ontario #Canada #Toronto #Charities #HealthCharities #Fundraising #Donation #NonProfit

Every blood donor is a lifesaver, but when it comes to children with thalassemia, you’re their only hope. Be the reason they smile, thrive, and dream. Sign up today to make a lasting impact (http://bit.ly/bloodbridge) —because giving blood is more than a donation; it's a lifeline. . . #bloodwarriorsindia #thalassemiafreefuture #blooddonationday #healtheducation #patientempowerment #thalassemiaprevention #medicalprogress #blooddonor #socialresponsibility #healthinitiative #charity #thalassemiaawarenessmonth #nonprofitorganization #healthandwellness #medicalinnovation #thalassemiaresearch #blooddrive #donateblood #savealife #thalassemiacommunity #bloodwarriors #thalassemiafighters

We often invest significant amounts in celebrations, yet we might overlook the importance of a simple Thalassemia test, which can have a profound impact on our lives. Before entering into a relationship, consider getting tested for Thalassemia—it's a small step that can prevent future challenges and ensure a healthier life. Take action today and make a difference by donating to support Thalassemia patients. Your contribution can help provide essential care and awareness. Donate now: https://lnkd.in/fV9-px5 #ThalassemiaAwareness #SupportThalassemiaPatients #DonateForACause #HealthcareForAll #MakeADifference

Whether you have an official AGM for charity giving or a good social rep who organises charity collection pots – we would love you to consider us as your next Charity of the Year, or at your next event, no matter how small. Like many charities, we rely on individual donations to fund our research, We’re a very small charity and we are ENTIRELY volunteers, who are patients, family, friends, or carers of someone living with NF2. Everyone has lived experience of NF2. What do we do? We increase awareness of NF2 related schwannomatosis (NF2) connect patients for support and offer hope to patients and their families and ultimately to fundraise to develop treatments or a cure for NF2. Our beneficiaries, in the UK, about 1000 people are affected by NF2 (incl. 330 children). At the present time only 40% of children are diagnosed in childhood. We need to ensure the physical and emotional wellbeing of these children as they grow up without the need for invasive surgeries or treatments that may rob them of their nerve functions one at a time. Or why not hold an event to benefit us, there are lots of ideas that will allow you to raise money for us. Let us know if you can help us in any way, or if you could nominate us to your employer or indeed if you run a business yourself, Or do you want to support someone who works with you who has NF2? We would LOVE to talk to you about how you can help us change the lives of those with NF2 related Schwannomatosis. Please message or email us clare@nf2biosolutions.org or joanne@nf2biosolutions.org Thankyou. #endNF2 #NF2awareness #neurofibromatosistype2 #schwannomatosis #NF2support #nf2 #nf2family #nf2warrior #LetstalkNF2 #nf2charity #nf2cure #nf2treatment #nf2gene #nf2chromosome22 #nf2trials #nf2diagnosis #nf2lifeexpectancy #nf2prognosis #nf2research #nf2ismyteam #nf2awarenessday #nf2journey #StrongerTogetherAgainstNF2

Meet Elizabeth, our Board President at the Endo Forward Foundation! 💛 In this video, she shares her excitement about where some of the funds raised during NTX Giving Day will go—and it’s all about pushing forward education and awareness for endometriosis. For Elizabeth, this mission is personal. After spending 14 years searching for answers and being told by over 40 doctors that everything she was going through was “normal,” she finally learned the truth—it wasn’t normal, and she had endometriosis. That’s why she knows firsthand how critical it is to spread education and awareness about this disease. With the funds from NTX Giving Day, we’ll be creating educational resources, raising community awareness, and pushing for better care so that no one has to go through what Elizabeth and so many others have endured. Your support is helping us break the cycle of misdiagnosis and misinformation, and it’s changing lives. Thank you for standing with us. Together, we’re making sure every Endo Warrior has the knowledge and care they need. 💛 Donate Here: https://lnkd.in/gfseREfv #northtexasgivingday2024 #endometriosissurgery #endometriosissupport #patientadvocate #endoforwardfoundation #endosupport #nonprofitlife #EffEndo #endometriosiswarrior #nonprofit #endometriosisawareness #makingadifference #youmatter #chronicillnesswarrior #endostrong #dallas #texasnonprofit #dfwnonprofit #austin #austinnonprofit

To my family and all my friends. For 30 days, this September I've challenged and accepted to run 60 miles. It's an average of 2 miles per day. I've started my 60-mile challenge. The more miles I record per day the less time for completion. I’m helping raise money for Crohn’s & Colitis UK! Support me at the fundraising link: https://lnkd.in/e4uNrgGR Please donate as much as you can: Want to join me in supporting a good cause? I'm raising money for Crohn's & Colitis UK and your contribution will make an impact, whether you donate a lot or a little. Anything helps. Thank you for your support. I've included information about Crohn's & Colitis UK below. Crohns Disease and Ulcerative Colitis are the two main forms of Inflammatory Bowel Disease, affecting more than 500,000 people in the UK. Yet it is largely a hidden disease, and one that causes stigma, fear and isolation, its thought that many people with the condition go undiagnosed and suffer in silence.  MN Akhtar•31 August 2024 Crohns Disease and Ulcerative Colitis are the two main forms of Inflammatory Bowel Disease, affecting more than 500,000 people in the UK. Yet it is largely a hidden disease, and one that causes stigma, fear and isolation, its thought that many people with the condition go undiagnosed and suffer in silence. #uel #rdsbl #uk #research #PhD #crohnsandcollitis #fundraising #donate #donation #nhs #fyp #goodcause #reels #shorts #tiktok

What are common myths surrounding living liver and kidney donation? Candice Coghlan, Education and Outreach Coordinator at the Centre for Living Organ Donation gives you an insight into the common myths surrouding living organ donation. Want to learn more about the Centre for Living Organ Donation and how to become a living donor? Visit livingorgandonation.ca #kidneydonation #livingorgandonation #livingdonor #beadonor #showyourscar #commonmyths #mythorfact #resources #centreforlivingorgandonation #organ #donate #givelifeuhn

🧠 Today is #WorldMSADay, a crucial time to raise awareness about a disease with a misdiagnosis rate as high as 20%. ⚕️ Multiple System Atrophy (MSA) is a progressive neurodegenerative disorder affecting the central and autonomic nervous systems. It causes movement difficulties, balance and coordination issues, and autonomic dysfunction. The disease progresses rapidly, leading to increased disability and often necessitating walking aids. 👁️ A crucial aspect of #MSA is eye movement dysfunction, caused by degeneration in brainstem structures that control eye movements. Diagnosing MSA is particularly challenging: 🩺 MSA is categorized as an atypical parkinsonian syndrome due to its resemblance to Parkinson's disease. It’s frequently misdiagnosed as Parkinson's or progressive supranuclear palsy, complicating research efforts across all three conditions. 🩺MSA presents in two distinct forms: MSA-P (parkinsonian type) and MSA-C (cerebellar type), each with unique clinical features, progression rates, and treatment responses. These 2 forms are hard to distinguish. New research highlights the potential of eye movement monitoring to revolutionize MSA diagnosis and care. It offers the ability to: 🔬Improve diagnostic accuracy, reducing the need for unnecessary invasive tests 🔬Enhance patient selection for clinical trials, ultimately speeding up the development of new treatments 💪Today, let's raise awareness and work towards better outcomes for those living with MSA. Bas Bloem Marcel Verbeek Bart van de Warrenburg Multiple System Atrophy Trust Mission MSA International Parkinson and Movement Disorder Society National Organization for Rare Disorders #biomarkers #neuroscience #eyetracking

🔬 10 years ago, PURA Syndrome was discovered. Today, on PURA Syndrome Awareness Day, we reflect on the progress that has been made but also acknowledge the urgent need for more research. There is still no treatment and no cure. As we mark this decade of discovery, we ask for your support. Raising awareness and funding is crucial to advancing research that can lead to life-changing breakthroughs for families living with PURA Syndrome. Every contribution counts – whether by sharing information, making a donation, or simply amplifying the voices of those in the PURA Syndrome community. Together, we can fuel momentum towards a treatment and a cure. Learn more and donate at jackstomorrow.org. #PURASyndrome #JacksTomorrow #PURASyndromeAwarenessDay

On this Organ Donation Day, let's recognize the importance of every degree when it comes to saving lives. Actipod by ZedBlox is dedicated to maintaining the right temperature for organs, ensuring the gift of life is preserved with precision and care. Every organ counts, and so does every degree. Together, let's make a difference. #OrganDonationDay #GiftOfLife #OrganPreservation #Actipod #ZedBlox #SavingLives #OrganDonationAwareness #PrecisionCare #LifeSavingTech #DonateLife #TemperatureControl #HealthcareInnovation #MedicalAdvancements #PreserveLife #OrganDonor #DonateOrgans