A WOMAN claims to have survived an entire year without a pulse. <\/p>\n
Sofia Hart is kept alive by plugging herself into the mains when she's at home, then running on battery power while out of the house. <\/p>\n
\n<\/p>\n
The 30-year-old has irreversible dilated cardiomyopathy (IDC) – a type of heart disease where one side is weaker, which can cause heart failure. <\/p>\n
She is awaiting a transplant. But to help keep blood pumping around her body in the meantime, she uses a life-saving left ventricular assist device\u00a0(LVAD). <\/p>\n
This requires electrical power, or two "very heavy" batteries, and being unplugged could kill her. <\/p>\n
Sofia said in a TikTok video: "I run off batteries, literally, and I don't have a pulse. <\/p>\n
<\/picture>MIRACLE <\/span><\/p>\n
<\/picture>LIFT OFF <\/span><\/p>\n
"I'm a human without a pulse. It's true. I'm not making it up.<\/p>\n
"I am on a device – I guess you can just call it a life support device – called an LVAD and it pumps to the left side of my heart.<\/p>\n
"I had open heart surgery at the end of November to implant the device that's inside of me that basically hugs my heart.<\/p>\n
"It's on a continuous flow."<\/p>\n
<\/picture>‘DO NOT EAT’ <\/span><\/p>\n
<\/span><\/p>\n
<\/picture>STEP TO IT <\/span><\/p>\n
<\/span><\/p>\n
<\/picture>SWEET ONE <\/span><\/p>\n
<\/span><\/p>\n
<\/picture>HAZARD ALERT <\/span><\/p>\n
<\/span><\/p>\n
Despite her twin sister Olivia being born with the same condition, Sofia only discovered she had IDC in the summer of 2022 while working on a horse farm.<\/p>\n
Usually upbeat and full of beans, she began to notice her energy levels slump.<\/p>\n
"It was a fatigue that I can't really describe," she told PEOPLE. <\/p>\n
"I wasn't tired in my brain, but my body was so tired and I was out of breath even from driving."<\/p>\n
Initially, she suspected she might have Lyme disease (transmitted by infected ticks), as she could have easily been bitten while outdoors with the animals.<\/p>\n
But after tests at a walk-in clinic and a conversation with Olivia, she learned the true cause of her symptoms. <\/p>\n
Until her transplant, Sofia has to connect to a wall outlet to charge her LVAD, nicknamed 'Janis' after her favourite singer Janis Joplin, which can make it tricky to move around. <\/p>\n
Sofia, who grew up in Martha's Vineyard and now lives in Boston, Massachusetts, US, said: "That cord is pretty long, and I have mastered living in places where I can get around on that cord."<\/p>\n
When she does leave the house, she is "battery powered" – and always carries a spare set just in case. <\/p>\n
Dilated cardiomyopathy is\u00a0a progressive, usually irreversible, disease which impacts the heart's ventricles and lower and upper chambers, according to the American Heart Association. <\/p>\n
It usually begins in the left ventricle – the heart's main pumping chamber – and the muscles begin to stretch and become thinner. <\/p>\n
The problem can then spread, meaning the muscles don't contract normally and the blood can't flow as it should. <\/p>\n
As the heart becomes weaker, heart failure can occur. The most common symptoms include shortness of breath and fatigue. <\/p>\n
<\/picture>THAT'S LIT! <\/span><\/p>\n
<\/picture>SEE EU THERE <\/span><\/p>\n
Dilated cardiomyopathy is estimated to affect around one in 250 people, the British Heart Foundation says. <\/p>\n
It is most common in adults under the age of 50, and is the leading cause of heart transplantation. <\/p>\n
\n
\nSource: Read Full Article<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"