Join Rycon Construction on Thursday, July 18 at noon at Oxford Development Company’s 3 Crossings in Pittsburgh for the 2024 CEO Soak in support of The ALS Association. Rycon's own Heather Saxon, alongside executives from other local companies, will participate in a unique take on the ALS Ice Bucket Challenge to raise critical funds and awareness to combat this devastating disease. Support Heather with a donation or to learn more about ALS and this year’s CEO Soak by clicking here: https://lnkd.in/eqZa9U9q #ryconnection #2024ceosoak #ALSceosoak #ceosoakpittsburgh #fightagainstALS #ALSicebucketchallenge
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Progress is being made! Check out Sean’s video to learn more. 💜
Let's Find a Cure Please Join me this year in supporting Team Wilson's Purple Perks Posse in the Take Step walk to support the Crohn's and Colitis Foundations mission of find a cure for Crohn's. Donate at https://lnkd.in/gagdwt24 Donate by 5/9 and Team Wilson will match your donations up to $10,000. #crohnsdisease #ccf #TeamWilson #FindaCure #CrohnsWarrior #Takesteps #research #PurplePerksPosse Thanks everyone for your support, Sean, Erin, Briggs, Maggie, Dave and Jane Wilson
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Come and join the conversation on Hyperemesis Day!
🖥️ We're going live with our friends at Hyperemesis Ireland on International Hyperemesis Day, are you joining us? We will be discussing: • Recent insights in Hyperemesis research • Our charities successes for you the community • Our charities hopes for the future and upcoming projects Join us at 8pm on Wednesday 15th May over on instagram. #HopeForHG #HyperemesisGravidarum #PregnancySickness
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Founder, NKH Crusaders, Fierce Patient advocate and proud rare disease parent. Project Manager IQVIA
"🎉 Join our event: Colorado Day Blitz for NKH Research! This entire month, we're focused on supporting vital research to treat Nonketotic Hyperglycinemia. Help us reach our $35,000 goal. Every donation made will be matched, doubling your impact! 🚀 Learn more and donate here: bit.ly/CODAYBLITZ #NKHBlitz #FundraisingEvent #MatchedDonation"
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Join us and Purple Perks Posse (Erin Wilson, Sean Wilson, Maggie, Briggs, Jane, and Dave) at Take Steps! As our largest fundraising campaign, Take Steps helps to accelerate the progress of breakthrough research just like the new wearable device Sean mentions in his video. Check out his video below for one incredible example of the #TakeStepsEffect
Let's Find a Cure Please Join me this year in supporting Team Wilson's Purple Perks Posse in the Take Step walk to support the Crohn's and Colitis Foundations mission of find a cure for Crohn's. Donate at https://lnkd.in/gagdwt24 Donate by 5/9 and Team Wilson will match your donations up to $10,000. #crohnsdisease #ccf #TeamWilson #FindaCure #CrohnsWarrior #Takesteps #research #PurplePerksPosse Thanks everyone for your support, Sean, Erin, Briggs, Maggie, Dave and Jane Wilson
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#Glaucoma is the 2nd leading cause of blindness in the world according to the WHO. The Glaukos Charitable Foundation is making an impact by donating over 6,200 devices to underserved glaucoma patients spanning 45 countries. Learn 4 key facts about glaucoma: https://lnkd.in/gZD9m_b7
Across the globe, we're advancing the treatment of ophthalmologic diseases. The Glaukos Charitable Foundation provides patients in need with access to meaningful, safe, and long-term eye care. Learn more about our philanthropic efforts at https://bit.ly/3tCs0So #Glaukos
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Education
Have you heard of APS ACTION?? APS ACTION stands for AntiPhospholipid Syndrome Alliance For Clinical Trials and InternatiOnal Networking, and they are a team of researchers working on finding better TREATMENT and a possible CURE for APS! The APSFA believes in APS ACTION's mission, and we are one of its sponsors. To learn more about APS ACTION, click this link: apsaction.org. Don't forget that for the remainder of JUNE, 50% of donations to APSFA will go to APS ACTION! Donate to the APSFA at apsfa.org/donate. #AntiphospholipidSyndrome #APSAwareness #GoBurgundy #APSMaatters
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A diverse #blood supply saves lives! Blood #donations from diverse donors are crucial to meeting the needs of all patients, including those with rare blood types. Learn more about why diversity in blood donations is so important: https://lnkd.in/eFeracDt #BloodDonation #DiverseDonorPool #Hemanext #PatientAdvocacy
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APDS is an underrecognized primary immunodeficiency (PI). The Immune Deficiency Foundation is running a series of walks to raise awareness of PIs like APDS and to support people living with them. For more information about the walks or to donate, visit walkforpi.org To learn more about APDS, download the Warning Signs of APDS at https://lnkd.in/gs2rftdg #WalkForPI #AllaboutAPDS
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How important do you think it is to raise awareness about marrow donation, especially within diverse ethnic populations? To learn more, listen to my podcast interview with Dr. Ronald Francois, Empowering Communities with NMDP and Raising Awareness for Marrow Transplants - https://rpb.li/YWV #healthandwellness #bonemarrow #donation
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How important do you think it is to raise awareness about marrow donation, especially within diverse ethnic populations? To learn more, listen to my podcast interview with Dr. Ronald Francois, Empowering Communities with NMDP and Raising Awareness for Marrow Transplants - https://rpb.li/YWV #healthandwellness #bonemarrow #donation
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3moCongrats Heather !!