Tyler Robinson Foundation’s Post

Supporting **Liv Like a Unicorn** can bring immense relief and joy to families facing such tough times. Here’s how you can get started: ### Steps to Give to Liv Like a Unicorn: 1. **Visit Their Website:** Go to the charity’s official website where you can find more information about their programs and impact. 2. **Find the Donation Page:** Look for a “Donate” button or a dedicated donation page. 3. **Choose Your Donation Method:** Most websites offer multiple ways to give, such as one-time donations, monthly giving, or even sponsoring specific projects. 4. **Fill in Your Information:** You’ll need to provide your contact information and choose a payment method (credit card, PayPal, etc.). 5. **Submit Your Donation:** Review your information and submit your donation. ### Other Ways to Support: - **Fundraise:** Set up a fundraising campaign to engage your community and amplify your impact. - **Share and Advocate:** Spread the word on social media or within your circles to raise awareness about the charity. - **Volunteer:** Offer your skills and time for events or administrative support. ### Benefits of Giving: - **Direct Impact:** Your donation can help cover medical bills, provide emotional support, and create moments of joy for the children and their families. - **Community Support:** Being part of a supportive community can bring hope and strength to those in need. - **Tax Benefits:** Many donations to registered charities are tax-deductible. ### Thank You for Your Generosity: Giving to a cause like **Liv Like a Unicorn** has a profound impact, not only on the children and families but also on spreading hope and kindness in the world. Your generosity can make a real difference. 🌈✨

Miracles start with a belief in the impossible. After relapsing twice, Emily Whitehead’s doctors gave her just weeks to live. Refusing to give up, her parents enrolled Emily in a clinical trial where she became the first pediatric patient to receive CAR T-cell therapy. It was her only chance at survival, and it worked. Now a college student, Emily has remained cancer-free and is considered cured. Her miraculous journey from patient to survivor is featured in the award-winning documentary “Of Medicine and Miracles,” available to stream for a limited time. Make More Miracles Watch online. Then give so more patients like Emily can live. The purchase of a ticket to watch “Of Medicine and Miracles” does not benefit the Foundation. We invite you to match your ticket purchase (or give more generously) with a donation to the Foundation. Your gift will help us support families fighting childhood cancer and raise awareness and funding for advanced therapies like immunotherapy. https://lnkd.in/ekGjBkNR Jolt Penn Medicine, University of Pennsylvania Health System Stand Up To Cancer Children's Hospital of Philadelphia The Parker Foundation Robin Honan Ross Kauffman #OfMedicineandMiracles #DrCarlJune #EmilyWhitehead #BreakthroughAward #CancerResearch #LeukemiaTreatment #CARTherapy #MedicalMiracle #HealthcareHeroes #ScienceAndHope #BreakthroughInCancerCare #PediatricLeukemia #CARTcell #SU2C

Please join me and be one of the first to follow the NEW Saving Sophie Linked In Page.

This organization is very important to me. If your company has an interest in donating it can be done at the link below.

Approximately 500 children aged 0-19 are diagnosed with a brain tumour each year. That’s nearly 10 children each week. Tom's Trust celebrates investment into brain tumour research and this news from the Government, NIHR, the Tessa Jowell Brain Cancer Mission (TJBCM), research funders and other collaborating charities is positive. Brain tumours are the biggest cancer killer of children and adults under 40. We know that 62% of children who survive a brain tumour live with life-long disabilities (such as blindness, hearing loss, lost motor-function or learning disabilities). We need to act now and do all we can to improve the care and prognosis of those facing a brain tumour diagnosis. Read more: https://ow.ly/PJaL50ROWOM

➡ ➡ ➡ RWJBarnabas Health and Rutgers Cancer Institute, Tara Pisano McCabe MSN, RN, FNP-BC, AOCNP, is one of the best #oncology APPs in the business (and a bonafide #lymphoma expert). 🙌 🙌 🙌 And kudos to her on being a #bonemarrow donor! This is not only important but potentially life-saving! #marrowregistry #bonemarrowtransplant #stemcelltransplant #lifesaving

September is Childhood Cancer Awareness month to raise awareness of childhood cancers and how childhood cancer affects families. For this year, A Month of Movement aims to encourage you to move more for the month of September and raise vital funds for research into children’s cancers as you go. Move an extra 30 minutes for 30 days with your children this month. I know school has started but that is all the more reason to move more with your children. You can do 30 minutes at once, break it up into two 15-minute activities or three 10-minute activities. This will be good for you AND good for your children! What are some easy ways that you can get your family to move this month? Write your ideas in the comments. #childhoodcancerawareness #amonthofmovement

Please take a few minutes to read our buddy, Sam’s story. Then head over to pcflv.org to read them all from our 30 Days, 30 Stories series! #pcflv #pediatriccancer #september #awareness

The reality is extremely difficult, but there’s hope ✨  Here are 5 statistics about pediatric brain tumors we think are important for raising awareness! 1️⃣ It's the leading cause of cancer-related deaths: Brain tumors are now the leading cause of cancer-related deaths in children under 15. 2️⃣ There are 4,000 diagnoses each year: Approximately 4,000 children in the U.S. are diagnosed with a brain or central nervous system tumor annually. 3️⃣ There is a high survival for some brain tumors: Children with low-grade gliomas have a 5-year survival rate around 90%, but it varies by tumor type and location. 4️⃣ There are brain tumors that are incurable at diagnosis Diffuse Intrinsic Pontine Glioma (DIPG), for example, is one of the deadliest, with a 5-year survival rate of less than 1%. 5️⃣ It is the 2nd most common childhood cancer, and #1 most common tumor found in children: Brain tumors make up 25% of all pediatric cancers, second only to leukemia. 🌟 At the Childrens Brain Tumor Project, we’re dedicated to transforming the future for kids battling aggressive brain tumors. Our focus is on finding a cure and improving their quality of life through cutting-edge research. We’re here to give families hope and healing. 💛 You can help us on this journey! Whether through donations or getting involved, your support brings us closer to a cure. Together, we can make a lasting impact! 🌈 Click the link here to learn more about our 'Do Something' https://lnkd.in/epEWyNS5 #curechildhoodcancer #pediatricbraintumors #CBTP #braintumorresearch

After many months of hard work, it was fantastic to see so many from across the research community, research funders, and industry, coming together at yesterday's brain tumour research roundtable to consider how to drive progress and make a success of these new NIHR (National Institute for Health and Care Research) funding opportunities. Many of the attendees present yesterday had already been incredibly generous with their time and expertise in helping to shape what these new initiatives look like, and it was particularly poignant to be bringing them all together just two days after the anniversary of Dame Tessa Jowell's death from glioblastoma 6 years ago, to discuss how to make a step change for brain tumour patients through research.   Key points I took from the roundtable discussions:   👉 Patients, and their needs and experiences, must guide everything we do 👉 In taking a collaborative approach, and bringing together the expertise not only of those in the room but of the people in their networks, we can be more than the sum of our parts and drive faster progress 👉 There is a need to build capacity on a number of fronts, and it is up to everyone to extend the ladder to make that happen 👉 Partnership between industry and academia provides an opportunity to de-risk this space for industry and to enable better asset selection 👉 Regional variation in availability and accessibility of trials (and trial-enabling services like WGS) must be eliminated 👉 The impact of good quality care, support and rehabilitation for brain tumour patients should not be underestimated, and there is a need for research to identify the best approaches   It was clear that the work of the Tessa Jowell Brain Cancer Mission, over the 6 years since its formation, has brought together the brain tumour research community who now stand ready to move forward in a cohesive and collaborative way to capitalise on the outputs of all the efforts so far. I am particularly grateful to the wonderful Nicky Huskens and Andrew Wright, who have been key partners in the development of the roundtable and the new initiatives, and who I know will continue to play a crucial role in ensuring their success. Thanks also to NIHR colleagues Robert Gray, Claire Gregory and Richard Buchanan who put their well-oiled wheels into swift motion to develop the details of the treatment and care funding calls, which I am excited to see the launch this of later this summer.   No doubt there will be challenges which must be overcome as this work moves forward, but it was heartening to hear several participants highlight that if we can get this right for brain tumours, it can provide a model for other rare cancers and rare diseases, providing an opportunity to improve treatment and care for many more patients.