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LOS ANGELES – The Trump administration announced on Monday that it would reconsider its decision to force immigrants faced with a life-threatening health crisis to return to their home country, a sudden move that provoked public outrage and was strongly condemned by the medical establishment.
On Aug. 7, the US Citizenship and Immigration Services, without a public notification, removed a "deferred action" program that allowed immigrants to avoid paying taxes. deportation while their relatives or themselves were undergoing vital medical treatment.
The agency, which is part of the Department of Homeland Security, sent letters informing those who had applied for a renewal, which immigrants must submit every two years, to no longer receive such requests. The letters indicated that immigrants had to leave the country within 33 days or risk deportation.
On Monday, the agency said in a statement that, while limiting the program was "appropriate," officials "would complete the workload on August 7".
According to the statement, no deportation proceedings were opened against those who received the letter. However, he did not specify whether he would continue to grant immigrants extensions to stay in the country or whether the program would continue after the processing of pending applications.
When asked for clarification, an agency official said the agency "is taking immediate corrective action to reopen pending cases for review."
"If a very limited version of deferred share will continue to be transmitted to U.S.C.I.S. is still in the study. More information will be forthcoming, "said the manager, who has only agreed to speak in the background.
Maria Isabel Bueso, 24, who has been involved in several medical studies, including a drug trial that resulted in treatment for her rare condition, causes dwarfism and other physical malformations. .
Without the drug, it was unlikely that Ms. Bueso and other people with the genetic disorder would live until adulthood. His doctor, Paul Harmatz, said that leaving the United States would cause him to fall sick quickly and die.
Upon learning that she had the chance to stay in California rather than returning to Guatemala, where the drug is not available and where she can not receive the required medical care, Ms. Bueso said, " It's amazing. It's great news to wake up.
After the Times featured Ms. Bueso in an article last week, she was invited to testify before Congress in the coming days. The outrage over the social media policy and several Democratic lawmakers, including House Representative Nancy Pelosi, have called on the Trump government to reverse its decision.
Ms. Bueso's lawyer, Martin Lawler, said: "It's not clear whether people will benefit from the appropriate extensions or whether people like Isabel will always live on the edge, fearing that the next expansion will not be granted when they find themselves in the middle of receiving medical treatment for their serious illnesses. "
Ms. Bueso, a longtime advocate of people with rare diseases, said she was considering lobbying Congress to find a long-term respite for patients. "We need to find a permanent solution so that families like mine do not have to go through this anymore," she said.
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