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Blood and plasma donor who saved more than 2 million babies dies at 88

Blood and plasma donor who saved more than 2 million babies dies at 88

Yahoo04-03-2025
(WJW) – James Harrison, a prolific blood and plasma donor for decades who helped save the lives of millions of babies in Australia, has died, according to the Australian Red Cross Lifeblood.
The organization made the announcement on Saturday, confirming that Harrison passed away in his sleep at the Peninsula Village Nursing Home last month. He was 88.
Nicknamed the 'Man with the Golden Arm,' Harrison was internationally known for saving more than 2 million babies by donating plasma more than 1,100 times since 1954, the organization said.
'James' plasma contained the rare and precious antibody, Anti-D, which is used to make the life-saving medication given to mothers whose blood is at risk of attacking their unborn babies,' Lifeblood said in a press release.
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According to the organization, Harrison had to undergo blood transfusions after lung surgery when he was 14.
With some encouragement from his father, Harrison started donating when he turned 18 and never missed an appointment until he retired at 81 years old, the organization said.
'James extended his arm to help others and babies he would never know a remarkable 1,173 times and expected nothing in return,' said Lifeblood CEO Stephen Cornelissen 'He continued to donate even in his darkest days, after the passing of his wife Barbara, who was also a blood donor, and helped inspire his career as a lifesaver.'
'He was also very proud to have saved so many lives, without any cost or pain. It made him happy to hear about the many families like ours, who existed because of his kindness,' his daughter, Tracey Mellowship, added on behalf of the family.
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According to the organization, researchers are now working to grow the antibody in their lab, nicknaming the project 'James in a Jar.'
'Using the blood of James and other donors, the team has successfully recreated and grown his antibody in the lab – with the hope it will one day help prevent Haemolytic Disease of the Foetus and Newborn, not just for pregnant women in Australia, but also worldwide,' the press release said.
Learn more about the research being done right here.
Copyright 2025 Nexstar Media, Inc. All rights reserved. This material may not be published, broadcast, rewritten, or redistributed.
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AngioDynamics Enrolls First Patient in AMBITION BTK Trial Advancing Treatment for Critical Limb Ischemia
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AngioDynamics Enrolls First Patient in AMBITION BTK Trial Advancing Treatment for Critical Limb Ischemia

BUSINESS WIRE)--AngioDynamics, Inc. (NASDAQ: ANGO), a medical technology company focused on restoring healthy blood flow in the body's vascular system, expanding cancer treatment options and improving patient quality of life, today announced enrollment of the first patient in the Randomized Study of the A uryon Atherecto m y System Used in Combination with Standard B alloon Ang i oplasty Versus S t andard Balloon Angioplasty Alone Treating I nfrapopliteal Lesi on s in Subjects with Critical Limb Ischemia B elow- t he- K nee (AMBITION BTK). AMBITION BTK is a prospective, multicenter, randomized controlled trial (RCT) designed to investigate the clinical safety and effectiveness of the Auryon Atherectomy System combined with standard balloon angioplasty, compared to balloon angioplasty alone, in treating infrapopliteal lesions in patients with Critical Limb Ischemia (CLI). The primary endpoint will be evaluated using a win-ratio approach, comparing the two treatment groups based on the following components in a hierarchical manner at 12 months: freedom from major amputation, freedom from clinically driven target lesion revascularization (CD-TLR), and primary patency. The RCT will include up to 224 patients at up to 30 sites. In parallel, a companion registry will enroll up to 1,500 additional patients who are ineligible for the RCT and are treated with the Auryon System above or below the knee. 'The enrollment of the first patient in the AMBITION BTK trial is a significant milestone in our commitment to advancing clinical evidence for the treatment of below-the-knee peripheral artery disease (PAD),' said Laura Piccinini, Senior Vice President/General Manager, Cardiovascular & International, AngioDynamics. 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The Auryon Atherectomy System is the first laser atherectomy system to efficiently treat any lesion type, any lesion length, at any lesion location, with minimal impact on vessel walls. 3,5,8,9 The Auryon Atherectomy System uses solid-state laser technology for the treatment of PAD and is FDA cleared with an indication for treatment, including atherectomy, of infrainguinal stenoses and occlusions, including ISR. 4,6 The Auryon System's targeted biological reactions minimize the risk of perforation and preserve the ability to vaporize lesions without thermal ablation. 3,5,8,9 The Auryon System uses a 355nm wavelength laser platform which enables the use of longer wavelengths and shorter pulses to produce a groundbreaking delivery of short UV laser pulses. 4 For more information, please visit About AngioDynamics, Inc. 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Acumen Pharmaceuticals Presents Studies Showing the Utility of a pTau217 Assay in Screening for a Phase 2 Alzheimer's Disease Trial and Validates Sabirnetug Oligomer-Selectivity, at the Alzheimer's Association International Conference (AAIC) 2025
Acumen Pharmaceuticals Presents Studies Showing the Utility of a pTau217 Assay in Screening for a Phase 2 Alzheimer's Disease Trial and Validates Sabirnetug Oligomer-Selectivity, at the Alzheimer's Association International Conference (AAIC) 2025

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Hyperfine Swoop ® AI-Powered Portable MRI System Demonstrates 100% Sensitivity for ARIA-E Detection in New Data Presented at the 2025 Alzheimer's Association International Conference
Hyperfine Swoop ® AI-Powered Portable MRI System Demonstrates 100% Sensitivity for ARIA-E Detection in New Data Presented at the 2025 Alzheimer's Association International Conference

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Hyperfine Swoop ® AI-Powered Portable MRI System Demonstrates 100% Sensitivity for ARIA-E Detection in New Data Presented at the 2025 Alzheimer's Association International Conference

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