🌟 Join Us in the Fight Against Cystic Fibrosis! 🌟 Every breath is a gift, and together, we can make a difference in the lives of those battling cystic fibrosis. Join our fundraising campaign to support the Cystic Fibrosis Foundation and help us find a cure for this life-threatening genetic disease. 💪 💙 Why Should You Get Involved? Cystic fibrosis affects thousands of individuals and their families worldwide, and we're on a mission to make their lives better. By participating in our fundraiser, you can: 1️. Raise awareness about cystic fibrosis. 2️. Fund vital research for new treatments and a cure. 3️. Support programs that improve the lives of those living with CF. 🤝 How You Can Help: 📣 Spread the Word: Share this post to your timeline, stories, and with friends and family. 💰 Donate: Contribute whatever you can to help us reach our fundraising goal. 🎁 Every donation, no matter the size, brings us one step closer to a world without cystic fibrosis. Together, we can make a positive impact and provide hope for those affected by CF. Let's breathe life into the fight against cystic fibrosis! 💨💙 Donate now: Click Link Below!!!!!!!!!!
Malcolm Profit Jr.’s Post
More Relevant Posts
-
🌟 Making Waves of Change: Supporting the Cystic Fibrosis Foundation! 🌟 As part of my selection into the 2024 class of Nashville’s Top 30 Under 30, I am excited to partner with the Cystic Fibrosis Foundation to raise crucial funds for research, advocacy, and support programs for individuals battling cystic fibrosis (CF). Cystic fibrosis is a genetic disease that affects the lungs and digestive system, posing significant challenges to those living with it and their families. But with your help, we can make a tangible difference in their lives. Here's how you can get involved: 1. Donate: Your contribution, no matter the amount, directly impacts the lives of those affected by CF. Every dollar raised brings us closer to breakthroughs in treatment and ultimately, a cure. Please consider donating to the cause via the link below. 2. Learn More: There are a number of helpful resources available to learn more about cystic fibrosis, including cff.org, which has a vast library of guides, articles, etc. 3. Spread Awareness: Share this post with your network to raise awareness about cystic fibrosis and the critical work being done by the Cystic Fibrosis Foundation. Together, we can educate others and inspire action. Thank you all for your support and commitment to making a difference!
Kevin's Fundraising Page at Nashville's Top 30 Under 30
finest.cff.org
To view or add a comment, sign in
-
I am being honored by the Cystic Fibrosis Foundation at a special event recognizing outstanding professionals in my community. In accepting this distinction, I have committed to raise money to help the Foundation realize its mission of curing cystic fibrosis (CF) and providing all people with CF the opportunity to lead long, fulfilling lives. My personal goal is to raise over $10,000 to help CF stand for Cure Found. Any and all donations are greatly appreciated. If you are unable to donate financially, please pass my campaign along to your friends, family, and coworkers. Please help me meet my fundraising goal by making a donation. By supporting my fundraising efforts, you have an opportunity in your lifetime to be part of ending this disease. Please consider joining us and help make medical history. Nearly 40,000 people in the United States have cystic fibrosis: a progressive, genetic disease that affects the lungs, pancreas, and other organs. Sixty years ago, children with CF usually did not live long enough to attend elementary school. Today, because of Foundation-supported research and care, the median survival age of people with CF is over 50. Working alongside the CF community, the CF Foundation has fostered the development of more than a dozen CF treatments and helped add decades of life for people with CF. Yet, many people with CF do not benefit from existing therapies. Our vision is a cure for every person with cystic fibrosis – a life free from the burden of this disease – and we will not leave anyone behind. #50finest2024 #PGH50Finest **Many companies will match donations so make sure to talk to your employer about matching your amount!!** https://lnkd.in/eyEpz2nG
To view or add a comment, sign in
-
Senior Digital Specialist at G7 Entertainment Marketing and Nashville Junior Chamber President. Entertainment marketer, digital native, content creator, collaborator and storyteller.
Can't believe it's been 7 whole weeks since I started 30 Under 30! And 2 weeks since my 27th birthday! While the new friends and professional development are a huge bonus, the most important and fulfilling part of this program is fundraising for Cystic Fibrosis Foundation - Tennessee Chapter. It would mean the world to me to see you at one of my upcoming events (June 18th happy hour at Ole Smoky or the celebration on August 10th!), but I would be especially grateful if you would donate to my campaign and help me reach my $5,000 fundraising goal. Might I suggest $30 to celebrate my Top 30 Under 30 status or $27 for my 27th? Maybe $300 to celebrate the fact that I have 3 more years of being under 30 left? Some more info on CF and the foundation: Nearly 40,000 people in the United States have cystic fibrosis: a progressive, genetic disease that affects the lungs, pancreas, and other organs. Sixty years ago, children with CF usually did not live long enough to attend elementary school. Today, because of Foundation-supported research and care, the median survival age of people with CF is over 50. Working alongside the CF community, the CF Foundation has fostered the development of more than a dozen CF treatments and helped add decades of life for people with CF. Yet, many people with CF do not benefit from existing therapies. Our vision is a cure for every person with cystic fibrosis – a life free from the burden of this disease – and we will not leave anyone behind.
Hannah D.P.'s Fundraising Page at Nashville's Top 30 Under 30
finest.cff.org
To view or add a comment, sign in
-
Psoriatic arthritis isn’t just a disease – it’s a daily battle for millions like Dedra. But with your help, we can change that. NPF is leading the charge in research for psoriatic disease, funding breakthrough projects that bring hope to those in need. Dedra’s journey is proof that together, we can make a difference. Join us in the 2024 Spring Match Challenge. Your donation will be matched dollar for dollar, up to $50,000, doubling its impact! Let’s rewrite the story of psoriatic disease. Donate now and be a part of Dedra's journey towards a brighter future! https://ow.ly/NoaU50RvbNx
To view or add a comment, sign in
-
-
Did you know that people can live perfectly healthy lives with just one kidney? Living kidney donation is when a healthy person (donor) chooses to give one of their kidneys to someone who needs it (the recipient). If you are over the age of 18 and in good health you can be considered as a living kidney donor. There are several tests you will need to go through to make sure you are healthy enough to donate and that your kidney is a suitable match for the intended recipient. You will not be able to donate if you have had cancer, or if you have diabetes, heart disease or a condition affecting your kidneys. You have the right to change your mind about donating at any time, right up until the operation itself. You can find out more about donating a kidney here: https://lnkd.in/eFCuXpPt
To view or add a comment, sign in
-
-
These remarkable kids, with their unparalleled zest for life, remind us of the beauty in diversity and resilience. If you've had the pleasure of meeting Aidan, you'll know first-hand what I mean! ✨ Support KSF's ground-breaking research and help turn the possibility of therapeutic treatment into reality: https://bit.ly/3SXHkl4
Commemorate this special Leap + Rare Disease Day by making a donation in support of life-changing treatments. We are relentlessly pursuing brighter futures by following our strategic, 2-year, $3.5M plan - LEAP! LEAP is the roadmap to treatments for Kabuki syndrome. This rare disease has no cure nor specific treatments, but we are an active, bold, joyful community fueled by science that shows Kabuki syndrome can be treated! LEAP with us and donate today: https://lnkd.in/gH2wj4Bx
To view or add a comment, sign in
-
-
Imagine waking up at 7am, and the first thing you have to do is put on your vest and start nebulizing for 30 minutes. During those 30 minutes the vest is vibrating at a high frequency which separates mucus from the airway walls and allows you to cough up and clear the mucus. It’s now 7:30am, and you continue with your day… But wait, it’s 11:00am, and you must do the 30 minute process all over again. Now it’s 4pm, and you have to do the process all over again... And again one last time at 10pm before you go to bed…. This is the reality for Will Corcoran, who I had the pleasure of meeting during a Cystic Fibrosis discussion. Will was diagnosed with Cystic Fibrosis (CF) when he was just 3 months old. He is now 26 years old and spends more than 2 hours a day doing his breathing treatments. Although CF presents different for everyone, there is one thing for sure, we need to find a cure! I was recently selected for the 2024 Milwaukee’s Finest Campaign. With this honor comes the responsibility of raising money for the fight against Cystic Fibrosis (CF). CF is an inherited, life-threatening disease that affects the lungs and digestive systems of nearly 50,000 children and adults in the United States. People with CF are living into their 30s, 40s and beyond. There is no cure, but there is a lot of hope! Please help us in our fight to make “CF” stand for “Cure Found”. You can help by: - Donating using the following link (please use the donate button NOT the buy tickets button): https://lnkd.in/gsrtZshs - Donating via Venmo (@Emma-Futoransky) or - Donating in the form of a check (if this is the preferred option, please DM me) Thank you for your time and generosity!
Emma's Fundraising Page at Hops for Hope
finest.cff.org
To view or add a comment, sign in
-
5 Days left and any donation helps! There is still time to purchase tickets! How your donation helps: Families never receive a bill from St. Jude for treatment, travel, housing or food — so they can focus on helping their child live Treatments invented at St. Jude have helped push the overall childhood cancer survival rate from 20% to more than 80% since it opened in 1962. And we won't stop until no child dies from cancer. St. Jude shares the breakthroughs it makes, and every child saved at St. Jude means doctors and scientists worldwide can use that knowledge to save thousands of children. Join us! Together we can help St. Jude change the world.
Events for St. Jude
fundraising.stjude.org
To view or add a comment, sign in
-
This October, I’ll be doing my personal best to raise funds to support The Heart Foundation. I’m going to walk at least 126 km (3 marathons) to raise funds for heart disease research that will help save lives. My fundraising has been kickstarted with such generous donations. In the past week I have welcomed Shauna Jarrett, June Young, Evonne Atallah and Carolyn Hough MAICD as new supporters. Plus an intriguing secret admirer!! 😍 Thank you for your trust, your motivation and your great generosity. Every donation makes that dawn immersion in the mist, fog, freezing cold and sunrise worth it. You join David DonaldsonAlida StanleyYvonne C. Margot Bain and family as my Heart S/Heroes. Heart disease is the leading cause of death in Australia, and I want to do something to support the thousands of Aussies whose lives are impacted by this disease every single day. I invite others amongst you to join me and help save Aussie 🇦🇺 🌏 hearts and contributing to life saving heat disease research 💚 💛 by making a donation to my page. https://lnkd.in/gA_7BBp5 $40 could pay for a researcher to isolate blood cells, which can then be used to study blood clots. Understanding blood clots and how these clots can be removed or prevented, is key to treating heart attack and stroke. $50 could cover the cost of basic tools researchers need to grow heart cells, such as syringes, test tubes, and flasks. $100 could pay for a DNA test that can help determine genetic factors to identify people at high risk of heart disease. $200 could pay for a pipette: essential for dispensing microlitres (0.001ml) of liquid for experiments.
To view or add a comment, sign in
-
-
Cystic Fibrosis Fighters like Steph are simply asking for the one thing we all take for granted - time. More time to hope that one day, she and the thousands of others like her who can't take the life-saving treatments currently available might be able to experience that "deep breath" of relief once a cure is found. Steph's story moved me deeply, the conflicting feelings of joy and despair watching others with CF blaze forward while you feel left in the dust waiting for your turn. But her story, like the history of cystic fibrosis itself, is a story of metamorphosis, of transforming hopelessness into a drive for change and relentlessly chasing that brighter tomorrow. While we've seen miraculous developments in the cystic fibrosis community over the last few years, we are simply not done yet. Help us drive out CF once and for all! Visit https://lnkd.in/gpZ3m3Ya 💙 Every donation goes directly to the Cystic Fibrosis Foundation, Georgia Chapter, funding critical research for CF treatments. #cysticfibrosis #UntilItsDone
To view or add a comment, sign in