Navy Dad Comes Home To Newborn Son, Turns To His Wife And Says Four Words Nobody Expected

Every time a loved one is sent overseas, military families deal with tremendous difficulties. For many families, saying goodbye—possibly for the final time—is an agonizing reality.

It’s a daunting idea to consider the possibility of never seeing each other again. Military troops must make life-or-death decisions while on duty and must count down the days until they can go home. Their families also struggle, juggling obstacles in daily life without the help of a loved one. Keeping in touch while serving overseas is still challenging, despite the availability of contemporary tools like video calls.

Lt. Michael Lemmons of the US Navy also experienced this. His wife gave birth to their son while he was stationed overseas. Lemmons related this story to twenty-seven other crew members who had not seen their babies born. They could not wait to see their new family members when they returned.

Lemmons’s face beams in a touching video when he sees his wife waiting for him on the dock. He finally gets to see his newborn kid as he rushes to her side. She holds their small, darling child in her arms.

Lemmons erupts, overcome with emotion, saying, “He’s perfect.” I’m grateful. He wanted to thank his wife for bearing with him through the ordeal of giving birth and for keeping the household running well. He recognizes the difficulties of being a single parent.

His wife started crying when she heard his sincere remarks. While her husband was serving the nation, she felt appreciated for all that she had done. Even though her efforts were less apparent, they were clearly important.

Lemmons and his wife held their newborn in their arms. Now that their family was complete, they could finally mend their relationship. Lemmons loved spending time with his wife and new baby because he knew he wouldn’t have this much time to spend at home and that he would soon have to serve again.

Supportive remarks were made on Lt. Lemmons’s heartwarming reunion on YouTube.

“My husband was aboard the US Bataan when they were deployed for ten and a half months,” a viewer shared. When they returned home, they had about 150 new fathers—and that number did not include the Marines.

What do you think of this Navy father’s sincere response upon seeing his newborn son?

“People Only Know Me as a Freak,” The Wolf Man Struggles to Find a Job Outside the Circus

Jesús Aceves has hypertrichosis, which makes his hair grow abundantly over his face and back. Because of his condition, he’s also known as The Wolf Man. But he’s tired of this alias and wants to live a normal life.

Meet Jesús Aceves, a 55-year-old man born with a condition called hypertrichosis, which means he has abnormal hair growth over his body, especially his face. Although married with kids, Jesús isn’t fully happy with his living conditions. He says he and his family suffer discrimination. In an interview, one of his kids mentioned, “People call me names, and they even tell their kids not to be my friends.”

He worked in the circus all his life, traveling through several cities. But now, he’s tired of being seen as a freak. As a consequence of years on the road, he’s been known as The Wolf Man.

Back home and not in the circus anymore, he’s facing another challenge: finding a “normal” job. He needs to support his family since his wife works in temporary jobs.

After several failed job interviews, he agreed to try something he had always avoided: shave his face. He relied on his family barber to transform him, even creating eyebrows and lashes.

The experience was difficult since the face is an extremely sensitive body area, but both he and his wife believed that simply by shaving, he would be able to find a job.

Jesús did several interviews, and it’s confident that now he’ll find somewhere to work besides the circus. If this happens, he must shave his face every 2 days.

Although rare, some conditions aren’t impossible to have. Luckily, people find a way to overcome the difficulties a rare condition brings and strive in life. Hannah Tyre, for example, was born with osteogenesis imperfecta, meaning that her bones break very easily. But her love for makeup made her an internet influencer, reaching millions of followers. We hope that, by reaching the mainstream media, people with genetic diseases won’t suffer more discrimination.

Preview photo credit A True Story / Youtube

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