Thank you, to our GOH board for supporting this wonderful trial. Always leading the way. What's raised here stays here. 🖤💛 https://lnkd.in/eQQZYUHf
A Glimmer of Hope Foundation | The Symbol of the Cure’s Post
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Proud to lead the fight, but we can only do it with YOUR support! Get to know more about the BCRFA in this recent article from 256 Today: https://lnkd.in/gt-RSTNB #FundingRessearchSavingLives #BreastCancerResearch
BCRFA is on the front lines of Alabama's fight against breast cancer
https://256today.com
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Leicestershire County Council Candidate for Loughborough South | Trustee for Robert Bakewell Primary School | Proud Loughborough University Alumnus
There are around 10,500 new pancreatic cancer cases in the UK every year, that's 29 every day (2016-2018). Meaning it is the 5th biggest cancer killer in the UK with 9,000 deaths every year. Not to mention Pancreatic cancer has the lowest survival of all common cancers, with a five-year survival rate of less than 7%. More needs to be done. The U.K. government simply write people off every year with a lack of action on this specific cancer. It’s a failure that 80% (4 in 5) are diagnosed at stage three and stage four. With 1 in 2 people being diagnosed via an emergency, such as A&E. Pancreatic Cancer is rarely caught by a GP or at early intervention stages resulting in an extremely high death rate. Please do your bit and sign this petition. Pancreatic Cancer does not have to be a death sentence. Families don’t have to suffer like mine did. We can do more, we must do more.
Don't Write Me Off.
pancreaticcancer.org.uk
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Patients with rare disease are often more motivated to: 🤝Develop close-knit networks 📲Form Facebook groups 🏨Create non-profit organizations 💌Organize email blasts or newsletters How can these rare disease communities help you find determined participants and drive engaging research? Find out in the blog: https://bit.ly/43iGWCl #PatientCentricity #PatientEngagement #PatientRecruitment #ClinicalTrials #RareDisease
Rare Disease Research: Finding Participants and Driving Progress
https://medrio.com
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"Donate? Nah, you'll never know where the money ends up going". Not for your Movember donation. It was recently announced that a whopping CAD $53 million is invested in Canada. Grant funding and capacity building opportunities are provided to empower First Nations, Métis and Inuit-led organizations to develop, implement and evaluate innovative programs/interventions to improve First Nations, Métis and Inuit men’s social and emotional wellbeing (SEWB). It is one of 4 initiatives under Movember’s new Indigenous Social and Emotional Wellbeing Portfolio. Annual funding of up to CAD $300,000 per applicant is available for 3 years to improve SEWB among First Nations, Métis and Inuit boys and men in Canada. For those in my network with ties and links to the indigenous communities in Canada, please do share this information with said communities. https://lnkd.in/e9vs2Ca9. #Movember #MentalHealth #Fundraiser
Movember
ca.movember.com
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Link to my fund raising page
Jonathan's fundraiser for Clatterbridge Cancer Charity
justgiving.com
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Manager,Client Delivery |Co Chair, All-In Diversity Committee at Greenphire| VP Public Relations - Toastmaster at Greenphire | Duchennes Muscular Dystrophy Advocate
💚It is September!! Muscular Dystrophy Awareness month! 💚 We wear green! What is MD - Muscular dystrophies are a group of muscle diseases caused by mutations in a person’s genes. Over time, muscle weakness decreases mobility, making everyday tasks difficult. There are many kinds of muscular dystrophy, each affecting specific muscle groups, with signs and symptoms appearing at different ages, and varying in severity. link here for more information. https://lnkd.in/e2ea9G3T
September will mark MDA’s kick-off of National #MuscularDystrophyAwareness Month, to raise awareness and critical funds for families across the nation who are living with #MuscularDystrophy, #ALS, and related #neuromuscular diseases. Hundreds of events throughout the month support our mission to empower the neuromuscular disease community to live longer, more independent lives through advocacy, strategic funding to accelerate research and support for over 150 MDA Care Centers. We are also pleased to announce Board approval for $8.4 million in research grants to be announced in September. Donations to support our mission during the #30DaysOfStrength campaign may be made at MDA.org/30days Learn more:
Muscular Dystrophy Association Kicks Off 30 Days of Strength Campaign for National Muscular Dystrophy Awareness Month in September | Muscular Dystrophy Association
mda.org
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A community for those with skin conditions supporting the social, emotional, and spiritual impacts of living with visibly different skin
May 24 is National Don't Fry Day, a pivotal occasion to underscore the significance of sun safety in safeguarding our skin health. This annual event serves as a crucial reminder of the perils of sun overexposure and the imperative need for proactive protection to mitigate the escalating rates of skin cancer. Sun safety is not merely a one-day affair, but a daily commitment to nurturing your skin's well-being. The advice shared in this guide is instrumental in fortifying your defenses against UV radiation on National Don't Fry Day and beyond. Join us in advocating for skin health by embracing these sun-safe practices and spreading the word to empower others. https://buff.ly/2XoLUxG #acommunityforthosewithskinconditions #volunteer #causes #donate #change #activism #nonprofit #dogood #charity #fundraising #philanthropy #socialgood #madeamasterpiece #+perspective #skinconditions #communityforskinconditions #yourenotalone #yourskinisacanvas #extrodinary #diseases
National Council on Skin Cancer Prevention
https://skincancerprevention.org
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#WealthPilotCares – Giving back to our community is a core value at WealthPilot Financial. Each month we will be making a donation and highlighting a charity that is making an important difference in the world. In July, we supported Propel a Cure. Propel A Cure’s primary purpose is to raise funds for innovative research that will identify the underlying cause of Crohn’s disease, the first step in the development of a cure. https://bit.ly/3OurEDK
About Propel a Cure for Crohn's Disease
propelacure.org
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For anyone that has suffered from pushing the document and data regulatory boulder uphill, only to have to do it again the next day, same path, same grind, crying out in your head (because to do so at work would get you a visit from HR) "please, God!! There has GOT to be a better way than this!!" What's great about Accumulus Synergy: It's not regulatory operations business as usual. It's a creative, strategic, collaborative solution to the crushing boot of inefficiency in the typical regulatory process. Bravo and best of luck! This is clearly a space where creative innovation is needed.
Accumulus Synergy is excited to announce the launch of the initial version of our first-in-kind information and data exchange platform. https://lnkd.in/gif75xJb #industryassociation #nonprofit #regulatoryaffairs
Accumulus Synergy Launches Highly Anticipated Cloud-Based Platform
globenewswire.com
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Moving forward the transformation of the regulatory filing process globally
Accumulus Synergy is excited to announce the launch of the initial version of our first-in-kind information and data exchange platform. https://lnkd.in/gif75xJb #industryassociation #nonprofit #regulatoryaffairs
Accumulus Synergy Launches Highly Anticipated Cloud-Based Platform
globenewswire.com
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