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When Clone Force 99, a.k.a. The Bad Batch, scored their own spinoff after being introduced early on in Star Wars: The Clone Wars Season 7, they were joined by Omega, a female clone of Jango Fett who, like Boba Fett, ages at a normal rate. Omega’s come a long way during her time with Hunter, Wrecker, Echo and the late Tech, and with Star Wars: The Bad Batch’s third and final season about to begin, Michelle Ang, who voices Omega, opened up to CinemaBlend about the young character’s evolution in Season 3. Additionally, if Omega is ever played in live-action, Ang provided some advice to the hypothetical actress who’d take over the role.<br/><br/>During my chat with Ang, I pointed out how in The Bad Batch Season 1, Omega was a sheltered child who was finally got to experience freedom for the first time when the title group took her off Kamino and brought her along on their travels. Then in Season 2, we watched Omega become a capable soldier who could handle herself in the field much better. So regarding Season 3, I asked the actress what she thinks is the biggest way Omega has evolved for this new batch (pardon the pun) of episodes.
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ARIFUL MIX FUN
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Palli Gram TV
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Scores of sick and starving pelicans have been found along the coast of California in recent weeks, with many dying as rescue centers become overwhelmed. Over 100 pelicans have been rescued so far that were anemic, dehydrated and weighing only half of their normal weight. The cause of the pelicans becoming sick is unclear but they appear to be starving despite abundant marine life off the coast. Wildlife experts have noted a similar event occurred in 2022. Rescue centers are focused on caring for the birds until they can recover and return to the wild.
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ARIFUL MIX FUN
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Real Life Review
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Shinchou Yuusha: Kono Yuusha ga Ore Tsueee Kuse ni Shinchou Sugiru<br/><br/>There is a popular saying: \
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ARIFUL MIX FUN
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ARIFUL MIX FUN
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A mum who was told she was “cruel” for having her son after he was born with a rare severe cleft lip says it has never held him back.<br/><br/>Zac Coates, now 18, was born with Tessier cleft lip and palate – a condition which is caused by facial tissues not joining up properly during development.<br/><br/>It left Zac with severe facial disfigurement on his ride side and he had no eye lid which left him blind in his right eye.<br/><br/>Mum, Joanne Lythgoe-Frank, 58, was “shocked” when she first saw her son but raised him to accept his differences.<br/><br/>Zac has undergone 16 surgeries to help restructure his face and is now a happy and healthy 18-year-old who is hoping to go to university to study film production in September.<br/><br/>Zac, who lived in Cyprus for 17 years, has dealt with stares and comments such being called a “monster” – but he hasn’t left his difference hold him back.<br/><br/>Joanne, a part-time receptionist, living in Faringdon, Oxfordshire, said: “My initial reaction was shock at the extent of it. <br/><br/>“It was different to what I expected – a lot more severe.<br/><br/>“I’ve never hidden Zac away to be an over protective mother.<br/><br/>“I tried to instil in Zac – ‘you are different but to embrace it and be proud of your differences’.<br/><br/>“It’s made him into a confident young man.<br/><br/>“On TikTok I was told how cruel a mum I was because I let my child be born.<br/><br/>“Zac lives a normal life. He’s educated, confident his differences haven’t hindered him in life.”<br/><br/>Joanne, who is originally from Manchester, was living in Cyprus when she fell pregnant with her second child Zac.<br/><br/>At 22 weeks pregnant she was told he had a cleft anomaly and asked if she wanted an abortion.<br/><br/>She said: “That for me was never an option.”<br/><br/>Joanne started getting a high blood pressure and developed severe preeclampsia at 24 weeks along.<br/><br/>She was rushed for an emergency C-section and Zac was born on February 24, 2006, weighing 1lbs 5oz.<br/><br/>Joanne said: “I remember being told ‘your little boy isn’t going to survive – he’s got issues. Maybe it’s better he doesn’t’.<br/><br/>“I came round hours later and got taken down to see him.<br/><br/>“Zac’s face was all bandaged up.<br/><br/>“It was deemed something you hide away in Cyprus.”<br/><br/>Joanne was told Zac had a 20 per cent chance of survival and she didn’t see her little boy properly until she was able to get him flown over the UK two weeks later.<br/><br/>There he was diagnosed and Joanne was able to hold him for the first time.<br/><br/>She said: “I didn’t see him without bandages until I came back to the UK.<br/><br/>“They offered for me to hold him. My instincts were he was about to die.<br/><br/>“They put him down my bra and he was there for hours.”<br/><br/>Zac was discharged after six months in hospital but had his first surgeries at nine months old to repair his palate and his lip.<br/><br/>Since then he has been back and forth to the UK for further surgeries to reconstruct his face.<br/><br/>He had a recent surgery in October 2023 to reconstruct his cheek – by using bone from his skull.
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ARIFUL MIX FUN
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ARIFUL MIX FUN
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