Last weekend our team was proud to participate in The Terry Fox Foundation's #TerryFoxRun, an annual charity event dedicated towards raising awareness and funds towards #cancerresearch. We are thrilled to share that our team raised $8,306 for the Terry Fox Foundation! A heartfelt thank you to our dedicated team members, their families, friends, and the Vancouver community for your support. Terry Fox’s legacy of courage and determination continues to inspire our mission to develop innovative, multifunctional therapeutics for difficult-to-treat cancers. We were honored to join this event and help carry forward his vision. Learn more: https://lnkd.in/eJP6mAW #TerryFoxRun #DearTerry #TryLikeTerry
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Self-Published Author of “Killing Cancer with TILs”. Inspirational Speaker, Autologous CELL Therapy Proof Of Concept for Solid Tumors, Rare Melanoma Survivor Thriver & Advocate, Clinical Trial Volunteer, & Giver of Hope
I worked for almost 10 years for the Golf department at a private country club which were some of the best 10 years of my life from 2006-2016. The relationships I formed and the life lessons I’ve learned, have shaped me to who I am today and I’m forever grateful for those experiences. I mentioned this because I’d love to be playing in this tournament tomorrow, but I’m not but I’m hopeful for next year. As a #RareCancer survivor myself, I credit my cure to the therapy that actually eradicated my terminal #Cancer from a single one time #AutologousCellTherapy using my own #TIL or #TumorInfiltratingLymphoyctes. These type of novel #AdvancedCellTherapies which use a patient’s own specific cells to fight back the ones that go rogue and mutate, not only saved my life, but is also the same concept that is changing the future of #RareDisease. I do not work in philanthropy or the #CGT industry specifically but I do follow this space very closely. The world of #CellTherapy is so much more than just the cure for #SolidTumors or #HematologicCancers, but also the answer to autoimmune diseases like #RheumatoidArthritis and #Diabetes as well. The data is out there with studies and clinical trials. Over the past 4 1/2 years as I’ve been navigating survivorship and recovery, finding a sense of community has been more of a challenge than I thought it would be. I’ve never been in this position before so I didn’t know what to expect but I am mission focused. Instead of being disease focused, I have concentrated my efforts on treatment and therapy focused spaces which has led me to connect with the Emily Whitehead Foundation. As a needle in a haystack, it’s tough to find other needles and with so few, sometimes they are hard to find. Cheers to everyone playing in tomorrow’s tournament and God bless all the players and sponsors in their support for Teeing Off For T-Cells! ⛳️🏌️♂️ #CellTherapy #EndCancer #Melanoma #MetastaticMelanoma #MalignantMelanoma #MucosalMelanomaSurvivor #TIL #ClinicalTrials #TumorInfiltratingLymphocytes
We are teeing up for our 10th annual Tee Off for T-Cells tomorrow! Our 10th Annual Tee-Off for T-Cells golf tournament presented by CNB Bank is a family-friendly fundraising event in Philipsburg that supports families fighting childhood cancer and raises awareness and funding for advanced therapies like immunotherapy. The event has raised almost $450,000 over the last nine years, and your support can help make this the year we cross $500,000! Thank you to all of our 2024 sponsors for helping us #ActivateTheCure. You can still support this year's event by making a donation to the Foundation. https://lnkd.in/eu5wiKs
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Cancer Patient Advocate•TEDx Speaker•2x Cancer Survivor•Freelance Blogger•Keynote Speaker•Healthcare Influencer•Best-Selling Author
🚨Please help me in raising $200 to send an advocate to Washington D.C. with NCCS!!! 🎗️By raising funds, this campaign will help patient advocates join state representatives and lawmakers on Capitol Hill to disscuss important legislation for cancer patients and survivors. Without people advocating for patients, who will? #patientadvocate #policyadvocate #canceradvocate
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Every year Redwood throws an annual charity event, making it a point to prioritize not only giving back, but to spread awareness for different causes and organizations that have touched or affected our coworkers & colleagues. Particularly, my team, Cash Us If You Can, has chosen to support RUNX1 Research Program (RRP), as a member on our team and their family has been impacted by RUNX1-FPD (familial platelet disorder). What is this you might ask? Medically it is a hereditary hematologic malignancy syndrome associated with a pathogenic variant of the RUNX1 gene. And you might also ask, what does that mean? It means that this pathogenic variant affects the stem cells that produce blood cells, which results in the following issues and complications: A lower count of platelets and/or platelet dysfunction, bone marrow deficiencies, various skin disorders, excessive bleeding & bruising, and an increased risk of getting cancer & specifically blood-related cancers. If you are able, please consider making a donation toward my team’s goal. No amount is too small. Also, please feel free to share this post so that we can all advance awareness and provide a healthier & longer future for every person affected. Additionally, this year our fundraising teams were able to choose individual organizations to donate to versus one organization that was selected company wide. So that means there are many other organizations available to donate to as well on the link below. Please check that out if you have time. Thank you!! ❤️https://lnkd.in/gYR_wSY3
2024 Redwood Games
givebutter.com
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📣 September is #DesmoidTumorAwarenessMonth! Celebrate by sharing Ria's story to help raise #DesmoidAwareness. Visit DTRF.org/awareness for more ways to celebrate, educate, and raise funds for a cure this September. ✨ The desmoid tumor patient experience is vast and varied, but members of our community have one thing in common: they are not fighting this rare disease alone. The DTRF, a 501(c)(3) organization, is the only foundation in the U.S. dedicated to funding research for desmoid tumors. Our progress is accelerating! Learn more and help us keep the momentum going with a donation: https://bit.ly/givetodtrf #DTAM #desmoidtumorawareness #togetherwewillweekend2024 #DTRF #DesmoidTumorResearchFoundation #Desmoidian #DesmoidTumors #desmoidtumor #desmoidresearch #aggressivefibromatosis #desmoidresearch #familialadenomatouspolyposis #OrphanDisease #raredisease
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Over the last four years, I've donated my hair twice to support cancer patients. Each time, I’ve been reminded of the power of small actions in making a significant impact. Why I Do It: Restoring Confidence:A wig can truly help someone feel like themselves again during a challenging time. Building Community:It’s about connecting with those who are fighting cancer and showing them they are not alone. If you’re considering donating, I encourage you to take the plunge! Your hair could bring hope and joy to someone in need. Let’s spread awareness and inspire others to join this meaningful cause. Together, we can make a difference—one haircut at a time. #HairDonation #CancerSupport #CommunityImpact #MakeADifference
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A cancer diagnosis can be extremely stressful and the volume of information available on the internet can be overwhelming 💙 *Although Yes to Life does not endorse or recommend any of the practitioners or clinics featured in our Life Directory, they have all been handpicked by Yes to Life researchers after a careful process of vetting and reviewing. Visit our Life Directory on our website and via the link in the comments We are able to provide our services across the UK because of your donations. Consider donating to Yes to Life today! #yestolife #cancercharity #IntegrativeCancerCare #IntegrativeMedicine #cancersupport #cancercare #lifestylemedicine #ComplementaryMedicine #IntegratedHealth #IntegratedHealthcare #charityfundraising
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📣 September is #DesmoidTumorAwarenessMonth! Celebrate by sharing Kayla's story to help raise #DesmoidAwareness. Visit DTRF.org/awareness for more ways to celebrate, educate, and raise funds for a cure this September. ✨ The desmoid tumor patient experience is vast and varied, but members of our community have one thing in common: they are not fighting this rare disease alone. The DTRF, a 501(c)(3) organization, is the only foundation in the U.S. solely dedicated to funding research for desmoid tumors. Our progress is accelerating! Learn more and help us keep the momentum going with a donation: https://bit.ly/givetodtrf ✨ Online registration CLOSES TODAY for the annual "Together We Will" Weekend from Sept. 20-21 here: https://bit.ly/2024tww. In honor of DTAM, use the promo code TWW10 for 10% off! #DTAM #desmoidtumorawareness #togetherwewillweekend2024 #DTRF #DesmoidTumorResearchFoundation #Desmoidian #DesmoidTumors #desmoidtumor #desmoidresearch #aggressivefibromatosis #desmoidresearch #familialadenomatouspolyposis #OrphanDisease #raredisease
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Congratulations Barbara on completing your epic walk to raise awareness and funds for YOUNG TONGUES . You are a great ambassador for the charity and also in all your work raising awareness about Mouth Cancers. in 2022, the Mouth Cncer Foundation. UK published the following stats. It makes sobering reading. Latest figures show that 8,864 people in the UK were diagnosed with mouth cancer last year. The number of people in the UK getting mouth cancer has more than doubled (103%) in the last 20 years. The number of people in the UK getting mouth cancer has increased by more than a third (34%) in the last 10 years. More than two-in-three (68%) mouth cancers in the UK are diagnosed in men. Nearly two-in-three (64%) mouth cancers in the UK are diagnosed in the over 60s. Latest figures show that 3,034 people in the UK lost their life to mouth cancer last year. The number of people losing their life to mouth cancer in the UK has increased by 46% in the last 10 years. In fact the incidence of Tongue cancer in women under 45yrs is also on the increase and scientists do yet fully understand why. Sharing this post or supporting Young Tongues might save someone's life. Will you help?
CEO & Founder of peer to peer support charity The Young Tongues. Providing support services for those affected by tongue cancer aged 18-64 worldwide.
I have completed our epic challenge, through beautiful Jordan. 🥾🏜️🐪 In honour of the 700+ young tongue cancer patients and survivors and the 1000s, who haven’t found us yet. Please donate now: https://lnkd.in/eKfZYdAG #jordan #fundraising #fundraisingchallenge #petra #tonguecancer #tonguecancersurvivor
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The Eve Appeal is the leading UK national charity funding research and raising awareness into the five gynaecological cancers – womb, ovarian, cervical, vulval and vaginal. We were set up to prevent gynaecological cancers and save lives by funding ground-breaking research focused on developing effective methods of risk prediction, earlier detection and developing screening for all of the five gynae cancers. We have played a crucial role in providing seed funding, core infrastructure funding and project funding in addition to campaigning to raise awareness. The world-leading research that we fund is ambitious and challenging but our vision is simple: A future where gynaecological cancers are a disease of the past.
Fiona's fundraiser for The Eve Appeal
justgiving.com
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📣 September is #DesmoidTumorAwarenessMonth! Celebrate by sharing Jessica's story to help raise #DesmoidAwareness. Visit DTRF.org/awareness for more ways to celebrate, educate, and raise funds for a cure this September. ✨ The desmoid tumor patient experience is vast and varied, but members of our community have one thing in common: they are not fighting this rare disease alone. The DTRF, a 501(c)(3) organization, is the only foundation in the U.S. dedicated to funding research for desmoid tumors. Our progress is accelerating! Learn more and help us keep the momentum going with a donation: https://bit.ly/givetodtrf ✨ Don't forget to register for the annual "Together We Will" Weekend from Sept. 20-21 here: https://bit.ly/2024tww. In honor of DTAM, the promo code TWW10 for 10% off has been extended until Sept. 17th! #DTAM #desmoidtumorawareness #togetherwewillweekend2024 #DTRF #DesmoidTumorResearchFoundation #Desmoidian #DesmoidTumors #desmoidtumor #desmoidresearch #aggressivefibromatosis #desmoidresearch #familialadenomatouspolyposis #OrphanDisease #raredisease
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