Dr. Pretorius discusses the organ shortage for transplantation. He evaluates the organ donation after circulatory death (DCD) option to expand the organ pool in heart transplantation. Watch the DeBakey Bytes video below to learn more https://lnkd.in/gcGnAkPC or click the link below for the full-length presentation. https://lnkd.in/gqKtj6FT
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Organ transplantation shortage!! Dr. Pretorius evaluates the organ donation after circulatory death (DCD) option to expand the organ pool in heart transplantation. Watch the DeBakey Bytes video below to learn more https://lnkd.in/gv_QcMe5 or click the link below for the full-length presentation. https://lnkd.in/gP3mpQvW
Donation after Circulatory Death: A Surgical Perspective (Victor Pretorius, MD, Erik Suarez, MD)
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Vice Chair for Clinical Affairs and Strategy; Director, Interventional Psychiatry and Co-Director, OCD Surgical Program; Chief, CU Medicine Outpatient Psychiatry
In this episode of Transplant Talks, we explore the remarkable journey of Barbara Gould, who, after a grueling battle with COVID-19 received a life-saving liver transplant from Casey Czerpak, a selfless living donor. We talk about their moving journey, the challenges they faced, and how their experience deeply affected their families, highlighting the incredible impact of organ donation. Join us to discover their inspiring tale of hope, resilience, and the powerful connection forged through this act of kindness. https://lnkd.in/ggqRihV5
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Growth Leader | Client Partnership | B2B & B2C Marketing | Business Development | Strategy | Living Liver Donor | Literacy Advocate
𝐋𝐢𝐯𝐢𝐧𝐠 𝐋𝐢𝐯𝐞𝐫 𝐃𝐨𝐧𝐨𝐫 𝐀𝐜𝐭𝐢𝐨𝐧 𝐏𝐥𝐚𝐧 With the commitment to donate behind me and a transplant date scheduled for early January, there's nothing left but preparation and strengthening mind, body and resolve. Here's to getting after it: ✅ 𝐅𝐨𝐫 𝐭𝐡𝐞 𝐛𝐨𝐝𝐲 - 🏋️ - I'm pretty much doing everything Dan Go recommends out here on the platform. If you haven't discovered his content, check him out at 𝐡𝐭𝐭𝐩𝐬://𝐰𝐰𝐰.𝐥𝐢𝐧𝐤𝐞𝐝𝐢𝐧.𝐜𝐨𝐦/𝐢𝐧/𝐝𝐚𝐧𝐟𝐨𝐮𝐧𝐝𝐞𝐫/ Steps, water, good eating, lifting, stretching, resting, breathing. He has the playbook that will help my body withstand the trauma of the donation surgery through recovery. Following Dan may do you some good, as well. ✅ 𝐅𝐨𝐫 𝐭𝐡𝐞 𝐦𝐢𝐧𝐝 - 🧘 - I'm practicing what Rick Rubin recommends in 𝘛𝘩𝘦 𝘊𝘳𝘦𝘢𝘵𝘪𝘷𝘦 𝘈𝘤𝘵, which is to dial into what the universe is offering in the form of "Source" and living a creative life wherever possible. Oh, and a good daily dose of the stoics is helping too. ✅ 𝐅𝐨𝐫 𝐭𝐡𝐞 𝐫𝐞𝐬𝐭 𝐨𝐟 𝐮𝐬 - 🌎 - I'm eager to talk with anyone who's curious about organ donation - living or deceased donation. For example, more than 100,000 Americans are awaiting lifesaving organ transplants today. 🔊 👁 📌 🔎 Check out 𝐰𝐰𝐰.𝐮𝐧𝐨𝐬.𝐨𝐫𝐠 to learn more about the US organ donation system. You can also be sure to register to be an organ, eye and tissue donor at 𝐰𝐰𝐰.𝐝𝐨𝐧𝐚𝐭𝐞𝐥𝐢𝐟𝐞.𝐧𝐞𝐭. For international friends, please inquire into your local/regional organ donation organizations. The organ transplant supply gap is truly global. #beanorgandonor #unos #donatelife #thegoodgrind #livingdonor
UNOS | United Network for Organ Sharing | US Organ Transplantation
https://unos.org
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Under the Human Tissue Act 1983, you can give written consent to the removal, after your death, of tissue from your body for transplant to the body of a living person or for other therapeutic, medical, or scientific purposes. You can also decide that, after your death, your body will be donated to science. In this blog, we explore common questions related to organ and tissue donation after death, together with how body donor programs work. https://bit.ly/3F0upbX #monavalelawyers #estateplanninglawyers #advancecaredirectives #organdonation #tissuedonation #bodydonorprograms
Can I donate my body, organs or tissue upon my death?
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Your Donation Can Help Me To Undergo Bone Marrow Transplant
Your Donation Can Help Me To Undergo Bone Marrow Transplant
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Did you know plasma can be used to create life-saving medicines? Plasma-derived medicines treat patients with immunodeficiencies, neurological disorders, shock, burns and more. They’re also used in operating rooms around the country for transplant and surgical patients. By donating plasma at CSL Plasma, you can help tens of thousands of people around the world. #DoTheAmazing #DonatePlasma Learn more about plasma and how your donation can make a difference. Watch this video: https://bit.ly/3RFWBag
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Game-changing clinical trial results offer new hope for children with relapsed paediatric high-grade glioma (pHGG) 🌟 Currently, treatment for children with pHGGs is surgery followed by chemo and radiotherapy but despite this, two-year survival rate is less than 35%. Promising results from a phase 2 clinical trial, led by Dr Darren Hargraves from Great Ormond Street Institute of Child Health, have shown a dramatic improvement in overall survival for children with relapsed or recurrent pHGG. Read more ➡️ https://bit.ly/47Ima0m #Research #BrainTumourResearch #RaisingAwareness #Charity #BrainTumours
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NF2 is for life, an unwavering companion. It defies the boundaries of time, refusing to be confined to mere moments. There is no cure, no magic wand to erase its presence. Instead, there is resilience, determination, and a shared journey among those who navigate its complexities. Please support our research by donating to #ENDNF2 https://lnkd.in/ezPZxY2P
As we approach NF2 Awareness Day on May 22, it’s heartwarming to see the efforts to raise awareness and support research for this condition. Real people affected by NF2 are sharing their journeys, shedding light on the challenges they face, and inspiring hope for better understanding and treatments. These personal stories serve as powerful reminders of resilience, courage, and the importance of community. By sharing their experiences, these individuals contribute to a collective effort to improve the lives of NF2 patients and their families. We are each affected differently & people with NF2 are affected by Brain Tumours, Spine Tumours, Optical Tumours, Deafness, Blindness, Epilepsy, vocal chord paralysis, mobility problems, chronic pain, cataracts, facial palsy ... & much more! Today we meet Sarah whose NF2 journey is blighted by chronic pain. " I had surgery to remove a large vestibular schwannoma in 2003, and a spinal meningioma in 2022. I still have tumours remaining in my head and spine, and I live in fear of bad MRI results. I have so much pain every day. It's exhausting. " NF2, is a lifelong genetic condition, that weaves itself into the fabric of existence, unyielding and unrelenting. There is no middle or ending to any of our stories. Surgery, radiosurgery, and chemotherapy—are the only options we have. Yet, they come at a cost. Their impact reverberates through the delicate pathways of nerves, often leaving behind scars of lost function. NF2 is for life, an unwavering companion. It defies the boundaries of time, refusing to be confined to mere moments. There is no cure, no magic elixir to erase its presence. Instead, there is resilience, determination, and a shared journey among those who navigate its complexities Please consider donating to research, sharing your story & raising awareness. You can donate here to our research https://lnkd.in/euWUGuTS #endNF2 #NF2awareness #NF2Schwannomatosis #schwannomatosis #NF2support #nf2 #nf2family #nf2warrior #LetstalkNF2 #nf2charity #nf2cure #nf2treatment #nf2gene #nf2chromosome22 #nf2trials #nf2awarenessday #nf2journey #StrongerTogetherAgainstNF2
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As we approach NF2 Awareness Day on May 22, it’s heartwarming to see the efforts to raise awareness and support research for this condition. Real people affected by NF2 are sharing their journeys, shedding light on the challenges they face, and inspiring hope for better understanding and treatments. These personal stories serve as powerful reminders of resilience, courage, and the importance of community. By sharing their experiences, these individuals contribute to a collective effort to improve the lives of NF2 patients and their families. We are each affected differently & people with NF2 are affected by Brain Tumours, Spine Tumours, Optical Tumours, Deafness, Blindness, Epilepsy, vocal chord paralysis, mobility problems, chronic pain, cataracts, facial palsy ... & much more! Today we meet Sarah whose NF2 journey is blighted by chronic pain. " I had surgery to remove a large vestibular schwannoma in 2003, and a spinal meningioma in 2022. I still have tumours remaining in my head and spine, and I live in fear of bad MRI results. I have so much pain every day. It's exhausting. " NF2, is a lifelong genetic condition, that weaves itself into the fabric of existence, unyielding and unrelenting. There is no middle or ending to any of our stories. Surgery, radiosurgery, and chemotherapy—are the only options we have. Yet, they come at a cost. Their impact reverberates through the delicate pathways of nerves, often leaving behind scars of lost function. NF2 is for life, an unwavering companion. It defies the boundaries of time, refusing to be confined to mere moments. There is no cure, no magic elixir to erase its presence. Instead, there is resilience, determination, and a shared journey among those who navigate its complexities Please consider donating to research, sharing your story & raising awareness. You can donate here to our research https://lnkd.in/euWUGuTS #endNF2 #NF2awareness #NF2Schwannomatosis #schwannomatosis #NF2support #nf2 #nf2family #nf2warrior #LetstalkNF2 #nf2charity #nf2cure #nf2treatment #nf2gene #nf2chromosome22 #nf2trials #nf2awarenessday #nf2journey #StrongerTogetherAgainstNF2
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