In this task, you are given a text of many news articles seperated by special token "|||||". Your task is to summarize them.
Q: Tweet with a location 
  
 You can add location information to your Tweets, such as your city or precise location, from the web and via third-party applications. You always have the option to delete your Tweet location history. Learn more ||||| (CNN) As lawmakers push to get a health care bill through the Senate, one New Jersey mom is speaking out. 
  
 Alison Chandra's son, Ethan, was born with heterotaxy syndrome, a rare genetic disorder in which organs form on the wrong side of the body. 
  
 "Heterotaxy syndrome literally means different arrangement," Chandra told CNN. "Any of the internal organs can be malformed, missing, multiplied or misplaced." 
  
 "Ethan was born with nine congenital heart defects and he has two left lungs. Five or so spleens of dubious function, his liver and his gallbladder are down the middle of his body along with his heart, and then his stomach is on the right instead of the left side," she said. 
  
 On Friday, she tweeted her son's latest hospital bill and it went viral. 
  
 "It seems fitting that, with the #TrumpCare debate raging, I got this bill in the mail today from Ethan's most recent open heart surgery," she wrote 
  
 It seems fitting that, with the #TrumpCare debate raging, I got this bill in the mail today from Ethan's most recent open heart surgery. pic.twitter.com/pyUE2UxbWW — Ali (@aliranger29) June 24, 2017 
  
 I'll save you some math; without insurance we would owe $231,115 for 10 hours in the OR, 1 week in the CICU and 1 week on the cardiac floor. pic.twitter.com/CQ9OjOsFX8 — Ali (@aliranger29) June 24, 2017 
  
 Chandra also added up what their bill would have been without insurance: "Without insurance we would owe $231,115 for 10 hours in the OR, 1 week in the CICU and 1 week on the cardiac floor," she said in a followup tweet. 
  
 With lawmakers pushing a new health care bill to the Senate floor, the health care debate has become personal for Chandra. 
  
 "I didn't follow politics before November. I was overseas for both of President Obama's elections," Chandra said. "I have been shocked at how loudly each side yells about their specific talking points. It paints these issues as black and white when they are anything but that." 
  
 "It seems like our kids are being reduced to a line in a budget," Chandra said. "No one seems to realize there are real people behind it." 
  
 The new bill also raises some fears for Chandra and her family. 
  
 "My fear is that this bill comes into play and suddenly essential health benefits are no longer covered, like hospitalization, prescription medications," said Chandra. "He will rely on prescription medications for the rest of his life. He is functionally asplenic and will need to take prophylactic antibiotics the rest of his life to prevent and protect against sepsis, a huge risk of death for our kids in the heterotaxy community." 
  
 Since posting Ethan's medical bill on Friday, the tweet has been viewed over 73 thousand times. 
  
 "That is why I like to tell our story. Maybe you hadn't thought of this side before. You don't picture a 3-year-old with all these fees." 
  
 "Never in a million years did I think this would happen," Chandra said of her posts. "As a mother with a kid who has disorder you feel alone. I have now found a community of other heterotaxy families and the community is just so excited that heterotaxy is a word that is being spoken about on a national level. I am really hopefully this will lead to more awareness and maybe that mom who receives a heterotaxy diagnosis won't feel so scared." 
  
 But the mother of two says at the end of the day, the medical bills mean so much more. 
  
 "To see him go from a kid who lost his breath after going up a few steps to a kid who can hike by myself, be able to keep up with his sister and his friend, that is what that medical bill gave us and that is priceless to me." 
  
 "We just want him to be a kid." ||||| Tweet with a location 
  
 You can add location information to your Tweets, such as your city or precise location, from the web and via third-party applications. You always have the option to delete your Tweet location history. Learn more |||||
A: 
A New Jersey mother has given an adorable face to the healthcare debate in a viral Twitter thread detailing her toddler son’s rare genetic disorder and the costs it could incur should ObamaCare be repealed. Alison Chandra’s foray into the debate began Friday, when she posted a photo of her son’s latest hospital bill alongside the words, “It seems fitting that, with the #TrumpCare debate raging, I got this bill in the mail today from Ethan's most recent open heart surgery.” According to CNN, her son Ethan was born with a rare genetic disorder called heterotaxy syndrome, which causes organs to form on the wrong side of the body. Chandra also tweeted the bill’s tally, $231,115, which was almost entirely covered by her insurance provider. Chandra’s thread, which shows photos of Ethan in the hospital and playing after recovery, struck a chord on Twitter; her first tweet was liked by more than 81,000 and shared more than 53,000 times. "It's been kind of crazy, honestly,” she told BuzzFeed News, “but I'm hoping that I can be a clear voice for our community and for kids like Ethan who stand to lose so much from this bill." The mother of two added that if Ethan’s coverage is taken away or given caps, the family would have to sell its home and move to Canada, where her husband is from. Meanwhile, Chandra says the healthcare debate has given her 4-year-old daughter political aspirations. "She told me recently that when she becomes president she's going to make sure that everyone can go to the doctor when they need to.”