“This Makes Me Sick”: Newborn Twins Given Two Years To Live After Insurance Denies Them Treatment

Your account is not active. We have sent an email to the address you provided with an activation link. Check your inbox, and click on the link to activate your account.Eli and Easton Reed, diagnosed with spinal muscular atrophy after their birth on March 31, 2024, currently face a dire prognosis after the family’s insurance company denied, SMA refers to a group of hereditary diseases that can damage and kill specialized nerve cells in the brain and spinal cord .

“Time is of the essence with this … since they don’t have symptoms as of right now,” the twins’ mother, Amanda Reed, told He added: “The fact that their life is in somebody else’s hands, whether they get this treatment or they don’t, you know, then that’s somebody else’s choice and that’s hard to cope with that right now.”Type II begins to affect children between 6–18 months old. Children can sit independently but cannot walk.

On Tuesday , Kecia announced that the fundraiser had been stopped “with the great hope, the boys will be able to receive the medication soon.”

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“This Makes Me Sick”: People Stunned By Insurance’s Refusal To Cover Newborn Twins’ Medicine'The fact that their life is in somebody else’s hands, whether they get this treatment or they don’t, you know, then that’s somebody else’s choice, and that’s hard to cope with that right now.'
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