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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

Hello everyone! I am continuing to raise money for EndoFound as I train for the NYC Marathon, and I would be so grateful for donations of any amount. If I don’t raise my minimum amount, I pay for the rest out of pocket, so anything helps! Bonus if your company offers donation matching ☺️ The Endometriosis Foundation of America is a non-profit organization that strives to increase disease recognition, provide advocacy, facilitate expert surgical training, and fund landmark endometriosis research. Without their efforts, it may have taken me longer to discover the signs and symptoms of endometriosis, which lead to my own diagnosis almost 3 years ago. Endometriosis is very common, with about 1 in 10 women experiencing this disease (200 million women worldwide). It is in the top 20 most painful conditions. There is, on average, a 7-10 year delay in diagnosis, and is one of the leading causes of infertility. Endo is often found in the pelvic cavity but has also been found in the kidneys, lungs, diaphragm, and brain. It can cause a wide range of symptoms and is considered a whole-body disease that can greatly reduce quality of life in those who have it. We need more research and advocacy for endometriosis so we can reduce the amount of time it takes to diagnose and treat it. Please consider donating to be part of this change! Anything helps!

October 10 is DAF Day!   Donor Advised Funds are enormously popular charitable giving vehicles—known for their ease and flexibility. Through a Donor Advised Fund, individuals can make a charitable contribution, receive an immediate tax deduction, and then recommend grants from the fund over time. Many donors have established Donor Advised Funds to streamline their giving and maximize their impact to Cystic Fibrosis Canada.   Donor Advised Funds are for individuals at every stage of their charitable giving journey—whether you’re just getting started in philanthropy, looking to expand your giving, or creating a legacy gift.   Learn more about the benefits of Donor Advised Funds below. Connect with me to discuss making a gift to Cystic Fibrosis Canada / Fibrose kystique Canada through your fund.

More businesses with big customer reach and retail presence should do this..

Learn more about the benefits of Donor Advised Funds below!

For many patients it can feel like RP has them rather than the other way around. That's not ok. Our research initiatives let patients with RP know that someone is truly in their corner. You can join us by helping fund the next wave of research today. Together, we can find better treatments and maybe, one day, a cure. Give Now: https://lnkd.in/d9Erv-T #autoimmunedisease #raredisease #donate

Check out Josh Gormley, Senior Plumbing Designer, on the RCCS Pigeon Talk Podcast below! He has been involved with Rofeh Cholim Cancer Society (RCCS) for 5 years and you can learn more and how to support on Josh's page. #engineering #engineers

We're extremely excited to present to you the new DT38 logo! ⭐️ We hope you like it! If your'e a user of the DT38 logo, please let us know and we'll send you the new one! #WeAreDT38 #DT38UK #DT38Aus #Charity #RaisingAwareness #TesticularCancer #SelfChecking #AwarenessDownUnder

🧠 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

We hope you all have enjoyed a successful start to the new year and are preparing for Race for a Reason just as we are. Across its history, Race for a Reason's roots tie back to raising money and awareness for the Cystic Fibrosis Foundation, specifically with the two charities Sean's Pals and Lilly's Sunshine. To give a more in-depth description of our beneficiaries and information about the disease, Kevin Abrams '98 has provided a letter to give us all a better understanding. Both current MBA/MSA classes have come together and created the idea for the first annual "Race for a Reason Fundraising Challenge" which will take place this upcoming Saturday, February 17th in efforts to raise $10,000 for the Cystic Fibrosis Foundation. Currently, have raised over $4,300! The rules behind this challenge are simple: The classes will compete in an O'Malley Cup Competition to see which class can raise the most money for their respective reason. The Class of 2024 will be representing Sean's Pals, while the Class of 2025 will be representing Lilly's Sunshine. All donations to each team will go straight to each charity, which ultimately donates to the Cystic Fibrosis Foundation. The classes will have to find the most creative ways to raise money with all of these events occurring between 9 AM - 5 PM. How to Donate and follow along: If you are feeling inclined, the link to donate is attached directly below! Any amount will help as it can be any dollar that finds the cure. If you would like to give to a specific class, you can select it in the drop-down menu when donating. If you do not want to choose, the donations will be split between the classes/charities! Although the physical efforts will be occurring from 9 AM - 5 PM, the donation link is open now! Our goal of raising $10,000 is lofty but can be achieved through your help. https://lnkd.in/epqxrMD7 To follow along, tune into @ohiosportsad and @ohioraceforareason on Instagram to see all the efforts being made! Thank you for all you do. Go Bobcats!