Shawn Dunahue, CSL’s Post

DON'T FORGET this month's Live and Ticking! Wednesday 24th April at 4pm, listen to our latest webinar titled 'How Much Do You Know About High Blood Pressure?!' Register your interest below: https://lnkd.in/gRJD64ME #webinar #bhf #charity #information #support #liveandticking

Though there may not be a cure, there is hope! In May, we recognize ALS Awareness Month. ALS is a progressive disease in which a person’s brain loses connection with the muscles, slowly taking away their ability to walk, talk, eat, and eventually breathe. View the link below to find ways to get involved in spreading awareness throughout Pennsylvania! Find ways to help raise awareness for ALS in Pennsylvania:

🌟 Psoriasis Action Month: Uniting a Community, Empowering Individuals 🌟 Each August, the National Psoriasis Foundation (NPF) leads the charge in celebrating Psoriasis Action Month. This is a time to come together, share our stories, and act towards a future free from the burdens of this chronic condition. As part of the 125 million-strong global psoriasis community, you are not alone in this journey. Your experiences, your triumphs, and your challenges are shared by so many others who understand the realities of living with this disease. Remember, there is strength in the community. By coming together and supporting one another, we can overcome obstacles, celebrate the victories, and pave the way for a brighter, healthier future. This Psoriasis Action Month let's embrace the diversity of our experiences and the unity of our purpose. Together, we can create meaningful change. #PsoriasisActionMonth #NPF #ThisIsPsoriasis #PsoriasisAwareness #ChronicIllness For more information on ways to get involved, visit the National Psoriasis Foundation website at www.psoriasis.org.  

“When you start out in advertising you learn everything about the product. You read the manual, you go to the factory, you experience the items. Here we do the same thing with people. Everything we do at GOOD is about telling the truth. We have a lot of conversations with people. Whether it’s motor neurone disease, or people experiencing homelessness for Crisis, or any other kind of charity that we work with – we listen.” Bryn Attewell, GOOD's Executive Creative Director, chats to Marketing Beat about our latest work with Motor Neurone Disease (MND) Association, the process of creating the campaign and the importance of authentic storytelling. 📰 Read the full feature here: https://lnkd.in/escwKWeb

May 1st marks the first day of #ALSAwarenessMonth. Amyotrophic Lateral Sclerosis, ALS, or Lou Gehrig's Disease, is a progressive neurodegenerative disease that affects cells in the brain and spinal cord, causing the brain to lose connection with muscles. As the disease progresses, a person will lose the ability to walk, talk, eat, and eventually breathe. There is currently no cure for ALS. You can learn more about #ALS from The ALS Association at https://lnkd.in/gz-W9kcd #ALSMonth #LouGehrigsDisease #Accessibility #ALSAwareness

🌟 Stop What You're Doing and Make a Difference Today! 🌟 Right now, you have the power to change lives. By registering with Salute to Life or contacting us to learn how easy it is to host a DoD Level Event, you can make an incredible impact for families in need. Hosting a drive is not only a fulfilling experience for you, but it’s also a beacon of hope for men, women, and children waiting for their life-saving match. Imagine being the reason a family like Baby Milena’s can finally find relief from the stress and heartache of battling a rare blood disease like Diamond-Blackfan Anemia. Here’s how you can help: Register with Salute to Life: It takes just a few minutes to become a potential bone marrow donor. Host a Drive: Contact us to see how easy it is to organize a DoD Level Event. We’ll guide you every step of the way. Your involvement can bring hope, healing, and independence to families facing incredible challenges. Don’t wait—take action now and be a hero in someone’s life. Let’s come together to support our fellow men, women, and children. Your simple act of kindness can make all the difference. #SaluteToLife #BoneMarrowDonor #HostADrive #LifeSavingHeroes #CommunitySupport #HopeAndHealing

World Sepsis Day 🌍 🗓 Date: September 13th, every year 📢 Hashtag: #WorldSepsisDay World Sepsis Day is observed on September 13th annually to raise awareness about sepsis, a life-threatening condition caused by the body's extreme response to infection. Established in 2012 by the Global Sepsis Alliance, it unites people worldwide to fight sepsis and highlight the importance of early detection and treatment. With sepsis causing 11 million deaths annually, accounting for one in five deaths globally, this day promotes action through awareness, research, and advocacy. Join the movement by spreading the word and supporting efforts to reduce sepsis-related deaths! https://lnkd.in/eBhvW3iU

Hello LinkedIn Community!🌟We're thrilled to share one of our blog post, "SES and The British Liver Trust Roadshow" shedding light on our impactful collaboration. In this blog, we delve into the heart of our partnership with the British Liver Trust, exploring the incredible journey of the roadshow and the meaningful impact it's making. 🤝 Dive into the details here: https://lnkd.in/ec3djUUJ 👉 Share your thoughts and join the conversation. How do you evision the future of community-driven initiatives for health and well-being?

Come Walk With Us! On May 4th, A3Access Advisors will be joining the Moving Day Walk in San Francisco to show our support for the Parkinson’s Foundation and those patients and caregivers impacted by Parkinson’s disease. Parkinson’s is very personal to me. Twenty-five years ago, my father passed after a two-decade battle with this horrible disease. It’s severely debilitating with no known cause, cure, or prevention. Impacting nearly one million Americans and 10 million people worldwide, Parkinson’s is second only to Alzheimer’s as the most prevalent neurodegenerative disease. While there is great science focused on treating and hopefully one day curing Parkinson’s, we are not there yet. We must do more to accelerate our efforts to identify treatment alternatives. The Parkinson’s Foundation is committed to making the lives better for those at risk and suffering from Parkinson’s by advancing research, improving access to care, and funding community programs. Their efforts on behalf of Parkinson’s families deserve our support! I’m hoping you will join us in making a difference. If you would like to join our team, or show your support, you can learn more here https://lnkd.in/ghP2QGA7.  

💔September marks Sickle Cell Awareness month and as you may know, Sickle Cell Disease is a devastating condition that affects millions globally, with a disproportionate impact on the Black community. It's not just a disease that affects individuals; it affects entire families. As someone with the Sickle Cell Trait myself, it was important for my wife and I to bring more awareness to this issue. Together, with Dorothy D., I produced a video a few years ago speaking to a Sickle Cell Warrior, Ronke and Sickle Cell advocate Adesayo Talabi to shine a light on the struggles faced by those living with the condition, their families, and the life-changing importance of blood donations. 🎥 Blood transfusions are a critical treatment for many living with this condition, and there's an ongoing need for diverse blood donors to support those affected. You can sign up here https://lnkd.in/eTKAyz3v 💉❤️ In the video, we also cover the importance of getting tested for the Sickle Cell Trait before starting a family, a simple but vital step in preventing future generations from being impacted by this painful disease. 👉 Please take a few moments to watch and share this video. Together, we can raise awareness, encourage more people to donate blood, and help fight the impact of Sickle Cell Disease. 🔗 Watch here: https://lnkd.in/ew4icHxr #SickleCellAwareness #DonateBlood #FamilyPlanning #HealthMatters