Cogent is proud to launch a photo mosaic to recognize and celebrate those impacted by Mast Cell Diseases – from individuals living with a Mast Cell Disease, their family members, friends, and patient advocates, to healthcare providers and researchers. It takes a community to make a difference. For each unique picture uploaded, we will make a charitable donation to The Mast Cell Disease Society, Inc. Upload your photo at www.MastCellMosaic.com. The final mosaic will be revealed at the TMS MastCellCon Event in Indianapolis, IN, July 13-15th. #MastCellMosaic #MastCellDiseaseAwareness #SystemicMastocytosis
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🚵♂️ Meet one of our returning Team CHIbra's riders: Dr. Diva D. De León-Crutchlow! Diva is one of the foremost congenital hyperinsulinism experts in the world - she is the Director of the Congenital Hyperinsulinism Center at Children's Hospital of Philadelphia, a CHI Center of Excellence, and is the Lead Clinician of the CHI Collaborative Research Network. You can support Dr. De León-Crutchlow's fundraiser for HI research on her page: https://lnkd.in/ebB-qhbn 🚲️ The Million Dollar Bike Ride is on June 8 in Philadelphia, PA, and for the 11th year, we are raising funds for congenital hyperinsulinism research! ‼️ If you are interested in riding, you must register by June 2nd (see details on our website) ‼️ 💙 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
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September is #SickleCellAwarenessMonth. Join us as we raise awareness about #SickleCell disease, the challenges experienced by patients, their families, and caregivers, and how advancing SCD research can help change lives. Here are 3 ways to support: 1. Check out local events 2. Donate blood 3. Donate money And visit https://go.usa.gov/xFAdH to learn more about Sickle Cell Disease #SickleCellAwarenessMonth #Sicklecelldisease #sicklecellstories #Sicklecell #Chronicillness
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🚵♂️ 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
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Join us in raising awareness for Generalized Lymphatic Anomaly (GLA). Together, we can support those affected by this rare disease and promote hope for a brighter future. Learn more in our new Patient Guidebook (https://lnkd.in/eyPX6xNZ) and share with patients.💚 Be the Light: Illuminate Lives with Your Donation! (https://lnkd.in/ezuZUNAq) #RareDiseases #LymphaticDisorders #RareDiseaseWarrior #complexlymphaticanomalies #LGDAwarness #LymphaticAnomalies #RaisingAwareness #RareDisease #rarediseaseawareness #PatientAdvocacy #CLAawarness
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Did you know? Heart and circulatory disease kills more than 1 in 4 people in the Aneurin Bevan area. With your help, we can fund vital research, raise the quality of patient care and equipment that goes beyond what the NHS provides. Make a difference in the community today. https://lnkd.in/ejRbjpu6 #cardiology #fundraising #heartdisease #patientcare
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Highlighting these three phenomenal KIPP Capital Region Public Schools leaders (left to right: Brandi Langhorn - Assistant Principal, Chrisheena Hill - Principal & Kelsey Flood - Director of Students Support Services) today for their dedication and awareness in supporting the research and cure for Sickle Cell Disease (SCD). Sickle Cell Disease (SCD) is a group of inherited red blood cell disorders that affect hemoglobin, the protein that carries oxygen through the body, and can lead to severe problems, including stroke, eye problems, infections, and episodes of pain called pain crises. The Sickle Cell disease (SCD) affects more than 100,000 people in the United States and 20 million worldwide. Help us to bring awareness by donating to the cause for the expansion and outreach of programs to continue elevating the voices of the SCD community. All of the funds received go towards accomplishing our mission. https://lnkd.in/et6dCabw #awareness #sicklecelldisease #support #donations #helpacause #missiondriven
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When you can’t breathe, nothing else matters. The American Lung Association is celebrating 120 years of making an impact as the trusted champion of lung health. By raising funds through the 2024 Fight For Air Climb Orlando, we are able to continue the critical work needed to save lives by improving lung health & preventing lung disease. A donation of any size will make an impact. Can I count on your support? Your support will get us all closer to a world free of lung disease. Today, we are more focused than ever on our four strategic imperatives: to defeat lung cancer, create a tobacco-free future, champion clean air for all, and improve the quality of life for those living with lung disease. Make your mark on the future of lung health here >> https://lnkd.in/epTxzFrV
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💙💚 As OPOs are planning their content for 2024, we can help capture the stories of their donors and transplant recipients to educate and inspire their communities about the gift of life. These stories can be shared with hospitals, funeral home directors, medical examiners, active donor family cases, schools, BMVs and more. Learn more about how we help our donation and transplantation clients share their impact at https://bit.ly/44PmiZH. #OrganDonation #Transplant #TransplantProfessional #TransplantLogistics #DigitalMarketing
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Over the last several weeks, we have shared information relating to organ donation, and kidney disease in particular. This article provides a recap, information about what happens when you are an organ donor, and how you can become an organ donor. If you are already registered, THANK YOU! https://lnkd.in/gKTnaSx2 #fglcares #freshgreenlight #driversed #drivingschool #teendriver #organdonor #organdonation #beanorgandonor
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Coping with Crohn's disease and ulcerative colitis (collectively known as inflammatory bowel disease or IBD) can be extremely challenging and isolating. That's why I'm participating in Take Steps, the Crohn's & Colitis Foundation's largest nationwide fundraising campaign - to raise awareness and funds to accelerate the progress of breakthrough research and to support critical patient programs. Will you support me with a donation or join me in fundraising for Take Steps? Please help me reach my personal goal — because no one should face the challenge and uncertainty of IBD alone. Your donation to my fundraising efforts will help the Foundation invest in cures for the future, while providing support to patients today. https://lnkd.in/gtZ6b2aX
Help me take steps toward cures for Crohn’s disease & ulcerative colitis
takesteps.crohnscolitisfoundation.org
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