Wes Osborne’s Post

🚵♂️ Meet one of our returning riders: Terri Gelberg! Terri shared with us why she rides for Team CHIbra: "I am proud to ride with Team CHIbra once again, recognizing the vital importance of supporting research for hyperinsulinism. This ride is especially meaningful for me to ride alongside, and honor, Dr. Charles Stanley. Dr. Stanley's groundbreaking work significantly advanced the understanding and treatment of hyperinsulinism during his career. By supporting this cause, we continue to build on his pioneering efforts, honor his legacy, and make a difference!" You can support Terri's fundraiser for HI research at https://lnkd.in/eXEiFPGa 🚲️ The Million Dollar Bike Ride is tomorrow, June 8 in Philadelphia, PA, and for the 11th year, we are raising funds for congenital hyperinsulinism research! ‼️ 💙 Your donations to CHI this month will go even further - The University of Pennsylvania will match the first $30,000 of our donations. CHI is raising funds to address the critical need for research for diagnostic tests to increase timely diagnosis of HI, tools for better management, new treatments, and, one day, a cure. #hyperinsulinism #raredisease #congenitalhyperinsulinism #hypoglycemia | Hyperinsulinism | Congenital | HI | Hypoglycemia | Rare Disease

Fundraising can be challenging but critical to ensuring program services are delivered. Understanding what matters to your donors and having open conversations with them about the need and your desired outcomes is the key to success.

Day 7 of the #47Challenge: it’s ok to fail. In fact, as we all know, there’s often more to learn from failure than success. For example: 🎾 Clotilde Iaia-Polak & I challenged ourselves to hit the ball back & forth 47 times. We failed once. Twice. This clip is from our 3rd try. We only made it to 39…. arrr… But here’s the silver lining: 🐈 39 happens to be the number of chromosomes in the male calico cat - also called “Klinefelter” cat as it has an extra X chromosome, and is “XXY” just like millions of “Klinefelter” humans. 🐴 In fact, many of our animal friends can have an extra chromosome! Did you know horses usually have 64 chromosomes (32 pairs), but researchers in Spain just discovered some have a 65th #Klinefelter horses! WHY DOES THIS MATTER? Because at My XXY | Chromodiversity Foundation we believe DNA differences are not disorders - just part of the natural diversity of life. That’s why we talk about #Chromodiversity, not “syndromes”, and work hard to #depathologize the language of genetics. 👧🏻🧒👦🏽👶🏾🧒🏼 SUPPORT KIDS WITH DIFFERENCES - My fundraising goal is $470. If you haven’t sponsored me yet, click here to donate: donate: https://gofund.me/64ab5e7b - Or create your own 47 challenge— head over to https://lnkd.in/dGqE3HQu set up your fundraiser. #eXtraordinarYeXperiences #eXtraordinarYkids #ItsInOurDNA

Legacy events are an essential part of the stewardship toolkit -- they're an opportunity to showcase the transformational power that legacies have had and inspire others to follow suit ➡️ They also can cement supporters' trust in your cause to use their money wisely; by examining what impact their gift could make in the long run. Should be a useful webinar with a brilliant panel! 💡

🩸 Together, We Can Stop Thrombosis! 🩸 Thrombosis affects millions worldwide, and it can strike without warning. But with greater awareness, research, and education, we can reduce its impact. Your donation to World Thrombosis Day helps to spread the word to prevent this life-threatening condition. Every dollar brings us closer to saving lives. Join us in the fight against thrombosis by donating today: https://lnkd.in/eVQN-XYF

🌟 Exciting News & A Call for Support! 🌟 After a refreshing family holiday where I focused on connecting my kids with their relatives, I’m back on LinkedIn with a purpose-driven challenge. At The Transformation Group, we’re fortunate to align our professional values with meaningful causes. I’m thrilled to announce that I’ll be supporting our primary charity partner, Tour de Cure Australia, by taking on a personal challenge: running 50km to raise funds for cancer research with Suncorp Group the sponsor of the event. Having recently completed a 450km cycling challenge, this run feels like a different kind of uphill battle without the luxury of training. The cause hits close to home as my wife’s family has recently faced a heartbreaking loss due to cancer. This run is dedicated to all the families affected by this disease, and I’m committed to giving it my best shot despite my fears of injury (currently dealing with two strained calf muscles so can't run more than 8k). Here’s where I’d deeply appreciate your support: Donations: Every contribution helps us get closer to a cure. Training Tips: With only 2 weeks to prepare, any advice on running, nutrition, or injury prevention would be incredibly valuable. Moral Support: Just knowing you’re cheering me on would mean the world! Feel free to contribute or share your insights via the link below. Let’s come together to make a difference! https://lnkd.in/gRajRPQ2 - team of 1 Thank you for your support and encouragement! #CharityChallenge #CancerResearch #RunningForACause #SupportAndDonate #MakeADifference

Hydration with Heart is in full effect today...

Day 4: Fundraising Focus – The AMF 3 Peaks Challenge An incredible and demanding adventure that will see the team climb the three highest mountains in Scotland, England, and Wales: 🏔️ Ben Nevis (1,345 meters) – The tallest mountain in the UK, located in the Scottish Highlands. 🏔️ Scafell Pike (978 meters) – The highest peak in England, found in the stunning Lake District. 🏔️ Snowdon (1,085 meters) – The highest mountain in Wales, towering over the beautiful Snowdonia National Park. ...over 3,000 meters of elevation – all in less than 24 hours. It’s a physical test, but the real goal is much greater: to raise crucial funds to support families facing Neuroblastoma. Why this matters: Neuroblastoma is a rare and aggressive cancer that primarily affects children, often those under the age of five. For families impacted by this devastating disease, every bit of support counts. The money raised through this challenge will go directly to helping AMF provide vital financial assistance and emotional support. Each donation will help families struggling with the emotional, physical, and financial burdens of battling Neuroblastoma. From supporting treatment costs to providing essential resources, your generosity will make a real difference for those in need. Together, we can make a powerful impact! Join the team or donate here: https://lnkd.in/eQfMGc8C #neuroblastoma #neuroblastomasupport

Today, Barry Falke, our CEO, took time to give the gift of life, and he doubled his effort by giving a Power Red donation for the first time! Thank you, Barry! A Power Red donation allows you to safely donate two units of red cells during one appointment maximizing your impact! Red cells from a Power Red donation are given to trauma patients, newborns, emergency transfusions during birth, people with sickle cell anemia and anyone suffering from blood loss. Ideal types to give a Power Red: O+, O-, A- or B- Learn more about maximizing your donation by giving Power Reds: rcblood.org/3JYQQjA Power Red= Double Your Impact 🩸🩸

Cystic fibrosis is a rare, life-shortening, genetic diseasefound in about 30,000 people in the U.S., which causes persistent lunginfections and limits the ability to breath over time. Those living with thisdisease are moms, dads, sisters, brothers, daughters, sons, friends, andco-workers – all struggling each day just to breathe and live normal, healthylives. Sixty years ago, most children with cystic fibrosis did notlive long enough to attend elementary school, but thanks to Foundation-basedresearch and care, many people with CF are now living into their forties –achieving milestones once thought not possible, such as attending college,pursuing careers, and having a family of their own. While there has been significant progress in treating thisdisease, there is still no cure and too many lives are cut far too short. Byparticipating in CF Climb, I am helping add tomorrows to the lives of all peopleliving with CF today.   Please make a difference and support me by donating to my CFClimb fundraising campaign today! https://lnkd.in/deqRwQZb