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Ron has PKD

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Ron Luccarelli, is a 61-year-old man from New Jersey. He has a genetic kidney disorder called PKD, Polycystic Kidney Disease. The same disease that took his mom and runs throughout his family. Ron had to take out his kidneys because of the disease and he survives solely because of dialysis. He goes to dialysis four days a week, four hours a day for years, cleansing his blood, but the clock is ticking. Ron is badly in need of a living kidney donor for a kidney of blood type B+, O  or any for paired exchange. Ron needs your help, he needs a miracle to save his life!
 
Do you have the desire to be an angel? If you answered yes, please call the Johns Hopkins Transplant Center at:410-614-9345 Case # Ron1957. Save 1 Person. Save The World.

Kathy has ESRD

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Katherine (Kathy) Malone is a 45-year-old woman from the southwestern suburbs of Chicago. She was diagnosed with ESRD (End Stage Renal disease) in 2017. Kathy was diagnosed with Type 1 diabetes in childhood, Kathy also has a long family history of cardiac issues.  When Kathy had heart surgery in 2016, she was told  losing kidney function might be a side effect of the surgery.  Although Kathy's kidneys did not return 100 percent, following the open heart surgery, they did bounce back fairly well and remained stable for a while. That was until Kathy noticed her legs and face were swollen.  That day she went to the nurse and told her something wasn’t right. After testing, the nephrologist said, “You need a kidney. You’re going on dialysis.” Now, Kathy Malone desperately is in need of a living kidney donor.

Do you have the desire to save a life? If you answered yes, please contact her husband Kevin Malone on 708-289-6049. For more details please visit https://kathyneedsakidney.info. Save 1 Person. Save The World.

Father of 2 in need of a living liver donor

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Adam Mandel from Florida suffered from colon cancer and beat that unfortuntately it has now spread to his liver. Doctors say that Adam now needs a liver transplant. Adam is registered at a hospital in Cleveland Ohio for the transplant. A liver transplant could ensure that the cancer will not spread. The more time that goes by, the more likely the cancer can progress. Adam is the proud father of two young girls and wants to be around to see these young ladies grow up. Did you know the liver is the only organ in the body that regenerates itself after 6 to 8 weeks?

Do you have B or O blood and have the desire to save a life? If you answered yes, please contact the kidney matchmaker at This email address is being protected from spambots. You need JavaScript enabled to view it. or call 917-627-8336. Save 1 Person. Save The World.

Devora Needs Help With her Heart!

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Devora is only 18 years old and her heart literally hurts. Devora was born with a rare heart defect: the flow of blood from her heart to both her lungs - where it fills with oxygen to feed every cell in her body- is mostly blocked. Surgeries have kept her breathing with the help of a tube but now that she's a grown lady, the tube no longer is sufficient. This young lady needs a larger tube to keep her breathing and alive. Devora is drowning, fatigued by smaller efforts, spending more time in bed and her skin and fingernails are becoming bluer due to lack of oxygen. Devora's parents’ hearts are breaking watching their child gasp for air. 

 

 

Devora must have that last final operation to implant the adult-size life-giving tube -they have just a few months before she reaches the point where nothing will save her anymore. The cost of the operation is more than $150,000. This amount is more than what her parents have despite using their last penny and asking friends and family for support. To learn more call 972-53-416-7951. Donate online at www.atov.org/donate. Save 1 Heart. Save The World.

 

 

 

 

Baby Needs Your Prayers

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Eliana Cohen is daughter of Shani Levi Cohen and Ariel Cohen from Miami, Florida. Eliana, wasn’t hitting her developmental milestones. At age 1, she was misdiagnosed with hypotonia -reduced muscle tone- but when physical therapy wasn’t improving her condition, her family went back to a neurologist to find answers. The Cohens finally discovered that Eliana has an incredibly rare condition called spinal muscular atrophy (SMA) type 2, that will keep her from being able to walk and could significantly reduce her lifespan. There’s a new FDA-approved “miracle drug” called Zolgensma that could help this sweet girl lead a healthy life. A one-time transfusion helps deliver the missing cells children with SMA Type 2 lack but the drug has to be administered before the age of 2. Unfortunately, the Cohens’ insurance company won’t pay for the drug, which costs $2.2 million, a jaw-dropping amount. 

The family miraculously raised the money but now requires your prayers for it to work. Do you want to save a life? If you answered yes, find out more here: https://thechesedfund.com/esther/save-eliana