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皮肤白癜风的早期症状潮州
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发布时间: 2025-05-30 16:06:52北京青年报社官方账号
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  皮肤白癜风的早期症状潮州   

CHULA VISTA Calif. (KGTV) - Arson investigators are looking into a fire that damaged a Mexican restaurant in Chula Vista late Thursday evening.The fire at Tacos Y Mariscos Imperial, located on 2490 Main Street, was reported at around 10:15 p.m., according to fire officials at the scene.Firefighters said the blaze started outside and quickly spread to the front of the restaurant.No one was inside the restaurant at the time of the fire.The cause of the fire is under investigation. 491

  皮肤白癜风的早期症状潮州   

Christine Hallquist's bid to become the first transgender governor in American history -- and the first trans person elected to any statewide position in Vermont -- will face its first electoral hurdle on Tuesday in the state's Democratic primary.If she wins Tuesday night, she will become the nation's first transgender gubernatorial nominee for a major political party.A former energy company executive, Hallquist is already a trailblazer. She was the first CEO to transition while in her job, according to the Victory Fund, a political action committee backing Hallquist and "dedicated to electing openly LGBTQ people" up and down the ballot. 653

  皮肤白癜风的早期症状潮州   

Chicken and waffles has become a pretty popular dish. Red Lobster is working to take advantage with a new lobster and waffles offering featuring Maine lobster and waffles made from the batter of the restaurant's Cheddar Bay Biscuits.Red Lobster announced the chain began serving the dish Monday and plans to continue for a limited time.   371

  

CHULA VISTA, Calif. (KGTV) - A new exhibit at the Chula Vista Library's Heritage Museum is telling the stories of the South Bay's Holocaust Survivors."History repeats itself, and if you don't recall it, then it's going to happen again," says Curator Sandra Scheller.The exhibit, "RUTH: Remember Us The Holocaust," focuses on Scheller's mother, Ruth. She survived three concentration camps before coming to Chula Vista. It also features 11 other survivors who called the area home over the last 70+ years.Scheller says only five survivors are left in the South Bay, and she wants to make sure no one forgets what they went through, or how they made Chula Vista a better place throughout their lives."This was a labor of love," Scheller says. "I've loved every second of it."The exhibit features photos of the survivors, artifacts from Jewish life before, during and after the Holocaust, and personal touches from Scheller's family. It includes replicas of the yellow stars her grandparents wore during World War II, clothing and even a tooth from her grandmother."She had to break this tooth out because it had some gold in it," Scheller explains. "The Nazis would have killed her for this gold."The exhibit opens Sunday, January 12 and will remain on display throughout the year. In addition to the exhibit, the museum plans to host speakers, movies, readings and other events about the Holocaust all year long.Scheller says she'll also give personal tours of the exhibit for schools.For more information on the new exhibit, click here. 1544

  

CHULA VISTA, Calif. (KGTV) - Jeff Miranda loved his job with the Border Patrol. His entire 17-year career was in San Diego County. Now, he’s battling a deadly disease that forced him into early retirement.Jeff and Liz Miranda live in Chula Vista. In early 2015, they started to notice something wasn’t right. “He was doing a presentation at work and all of a sudden, his voice just wouldn’t project,” Liz said.They then noticed fasciculation, which Liz described as small tremors throughout his body. His speech was also becoming increasingly slurred. “We had a feeling it was something neurological at this point,” Liz said.Several months later, they received the official diagnosis. It was ALS, or amyotrophic lateral sclerosis. It is also often called Lou Gehrig’s disease. It is a progressive neurodegenerative disease that affects nerve cells in the brain and the spinal cord, according to the ALS Association.“We were… somewhat psychologically prepared by the time he got officially diagnosed because we had already suspected it for a couple months,” Liz said.Liz said, however, it was heart stopping when they first found out ALS was a possibility. “Your mind [goes] a million miles an hour,” she said.Jeff, an avid cyclist and outdoorsman, is now confined to a wheelchair and uses eye gaze technology to communicate. “As horrible [as] ALS is and given that there is still no cure, I feel very lucky about today’s technology.This computer device and the chair didn’t exist before. Both devices have been an enormous help to me and my family,” he said.They have made modifications to their home, including a wheelchair ramp and lift. Liz said Jeff still has his sense of humor and is the same person cognitively. He joked that he charges five dollars for a ride in the wheelchair lift.“I think that sometimes people will see him and talk to me and ask me questions for him,” Liz said. “He can answer you. It just takes a second to respond.” There is currently no cure to the disease. The average survival time is 3 years, according to the ALS Association.About 20 percent of people with ALS live five years, 10 percent will survive ten years, and five percent will live 20 years or more.“I think on a whole, we want to continue living our life. It’s all about attitude really. We could be sitting here miserable and then we’d miss out on the time that we have,” Liz said.There was one moment during the interview that brought tears to the couple. That was when Jeff spoke about his wife’s support.“The real victims are my family and loved ones which has been my biggest struggle living with this disease. My wife has been the most positive person that I have ever met. Having her by my side always with a smile has given me enormous happiness and hope. She has always made me feel like the luckiest man in the world,” Jeff said, as his eyes started to well up.Jeff and Liz have been together for 24 years, meeting on their first day of college in Florida. They got married in 2001 and have two teenage daughters.The battle against ALS not only has emotional and physical impacts, but it is also taking a huge financial toll.Liz had to quit her job in order to take care of Jeff, who is now 100 percent dependent. They are worried about losing their home. Jeff has exhausted the remainder of his paid time off. His fellow Border Patrol agents have donated some of their time to help the family, but that is also soon running out.“We’ll have to leave California, which would be a snowball effect because we leave California, he leaves all his doctors. We lose all our friends and our family that are here, our support system,” Liz said.Liz said she reluctantly set up a GoFundMe page to help with expenses. “We’ve never had to ask for anything. Never wanted to, so that was very hard for us,” she said.Through the campaign, though, she discovered the kindness of both friends and strangers. She said the support “melts your heart.”“ALS has stolen my abilities to do the things I used to love, plus a million other things most people take for granted. But it will never steal what’s the most important thing in my life and that’s my family and friends,” Jeff said. 4190

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