🌟 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
Salute to Life, C.W. Bill Young / Department of Defense Marrow Donor Program’s Post
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"🎗️ On #WorldCancerDay, let's stand together in solidarity with those fighting, survivors, and the loved ones lost. 💙 Let's raise awareness, support research, and foster hope for a cancer-free world. Together, we can make a difference. 🌍💪 Visit:- https://lnkd.in/dU85VUYN #ilovenehlia #nehliarealtors #nehlia #CancerAwareness #FightTogether"
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"🎗️ On #WorldCancerDay, let's stand together in solidarity with those fighting, survivors, and the loved ones lost. 💙 Let's raise awareness, support research, and foster hope for a cancer-free world. Together, we can make a difference. 🌍💪 Visit:- https://lnkd.in/gU-NNs7F #ilovenehlia #nehliarealtors #nehlia #CancerAwareness #FightTogether"
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Our Team Needs Your Support for Step Up for Stroke! This June, we're participating in March of Dimes Canada's Step Up for Stroke fundraiser, and we need YOUR help to make a real impact! We're raising money for the After Stroke program, which provides crucial support to stroke survivors and their families. Our team created a recipe book with 89 recipes. Donate now and receive an electronic copy of our cookbook! Here's how YOU can be a part of our team's success: ✅ Donate to our team page: Link below ✅ Every contribution, big or small, helps stroke survivors regain independence. Want to get even more involved? Share our team page with your network and spread the word! Together, let's Step Up for Stroke and help survivors thrive! #StepUpForStroke #MarchofDimesCanada #StrokeRecovery
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Our Team Needs Your Support for Step Up for Stroke! This June, we're participating in March of Dimes Canada's Step Up for Stroke fundraiser, and we need YOUR help to make a real impact! We're raising money for the After Stroke program, which provides crucial support to stroke survivors and their families. Our team created a recipe book with 89 recipes. Donate now and receive an electronic copy of our cookbook! Here's how YOU can be a part of our team's success: ✅ Donate to our team page: Link below ✅ Every contribution, big or small, helps stroke survivors regain independence. Want to get even more involved? Share our team page with your network and spread the word! Together, let's Step Up for Stroke and help survivors thrive! #StepUpForStroke #MarchofDimesCanada #StrokeRecovery
Mandi Shelswell - Step Up for Stroke 2024
marchofdimes.akaraisin.com
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ChatGPT 4 recognized | Google: Top Global Patient Blood Management Influencer | Top Global Anemia Influencer | Documentary Producer | Global Chief Creative Officer |
For decades, #Harlem has made every attempt to protect its heritage, culture, and real estate value as part of New York City. But something has moved into the community that they never saw coming: #anemia. Many residents experience symptoms like #fatigue, cold feet or hands, and emotional exhaustion leading to #burnout, never realizing that these may be early warning signs of anemia or iron deficiency. We hope awareness of what is currently affecting the community is addressed with early detection. #Children, expecting #mothers, adolescent girls, and mid-to-senior women are most at risk and make up a major portion of Harlem's population. We hope this issue is highlighted during Black Health Matters 2024 Harlem Week sponsored by Sanofi this year. If successful, maybe anemia will move to another address. If not, keeping your doors locked won't help. We would love to do what we can. Please don't send us donations; awareness is more valuable to us. We are confident that NYC Health + Hospitals are on your side in this fight. Please look for the Anemia insignia the next time you visit a medical center, or ask your doctor about their thoughts on anemia awareness. We are confident that all major NYC medical centers are working hard to fight this spread of anemia and its symptoms with early detection. The Anemia insignia is the most valuable way to show you care for the community.
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Née Hanratta | Making connections and building meaningful relationships across East Anglia to help turn science into a reality
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
Live & Ticking
bhf.org.uk
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🌟 Let’s raise awareness for Rare Disease Day! Every year, on the last day of February, the world comes together to shed light on the struggles and triumphs of those living with rare diseases. It's a day to highlight voices that often go unheard, to stand in solidarity with individuals and families facing extraordinary challenges, and to ignite hope for a brighter future. Rare diseases affect millions worldwide, yet they are often overlooked due to their rarity. This day is our opportunity to change that narrative, to educate ourselves and others, and to advocate for better resources, treatments, and research. Together, we can make a difference. Whether it's sharing stories, donating to organizations dedicated to rare disease research, or simply wearing or sharing to show your support, every action counts. Let's paint the world in the vibrant colors of awareness, compassion, and unity. Join us on Rare Disease Day and let's make a difference💙 #RareDiseaseDay #ShowYourRare #CareAboutRare
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https://lnkd.in/eq9ZwEBU This is the second webinar in our fatal cases series. Please do sign up on the link below to learn more about to support bereaved families through the coronial process.
The Coronial process: Supporting bereaved families and professionals
events.irwinmitchell.com
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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.
Parkinson's Foundation: Keep on Moving!
secure3.convio.net
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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
May is ALS Awareness Month
tips.amramp.com
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