What most teenagers dream of is to go to college, travel the world, and have many friends. 12-year-old Taylor Smith, of Johnson City, Tennessee, was no different. This girl spent her days around her family and friends and loved watching a lot of Doctor Who.
Smith outlined these plans in a letter she wrote to her future self in April 2013. The letter was placed inside a box in her room with the instruction “To be opened by Taylor Smith on April 12, 2023 only (unless said otherwise).”
Unfortunately, she didn’t live long enough to see whether those dreams would be accomplished. Just months after she wrote that letter, Taylor died of complications from a sudden onset of pneumonia.
Her parents, Tim and Mary Ellen Smith, were heartbroken. They couldn’t believe their girl was forever gone.
One day, as they were sorting through her possessions, they found the letter. As it touched them deeply, they decided to share it online and give others some solace.
As she shared her daughter’s letter, Marry Ellen wrote: “I can’t physically resurrect her, I can’t bring her back, but
I’m so grateful people have been inspired by her story.”
Below is Taylor’s letter and the words she wrote to herself.
Dear Taylor,
How’s life? Life is pretty simple right now (10 years in your past). I know I’m late for you, but as I’m writing, this is early, so; congratulations on graduating high school! If you didn’t, go back and keep trying. Get that degree! Are you (we) in college? If not, I understand. We do have pretty good reasoning, after all.
Don’t forget, it’s Allana’s 11th birthday today! Sheesh, 11 already? In my time, she just turned 1! I didn’t get to go to that party though, because I was in Cranks, Kentucky for my first mission trip. I’ve only been back for 6 days!
Speaking of, how’s your relationship with GOD? Have you prayed, worshipped, read the bible, or gone to serve the lord recently? If not, get up and do so NOW! I don’t care what point in our life we’re in right now, do it! He was mocked, beaten, tortured, and crucified for you! A sinless man, who never did you or any other person any wrong!
Now, have you gone on any more mission trips? Have you been out of the country yet? How about on a plane?
Is Doctor Who still on the air? If not, what regeneration did they end it with? You should go watch some Doctor Who! Later though, you gotta finish reading your own words of wisdom!
Do you have your own place yet? If we’re in college, what are we majoring in? Right now, I wanna be a lawyer.
Have you been to Dollywood recently? Right now, their newest attraction is the Wild Eagle. It’s so fun!
Also I think I’m going to sell my iPad and buy an iPad mini, Don’t forget to tell your kids that we’re older than the tablet! Attached I also have a drawing of an iPad, so you can show them.
Well, I think that’s all. But remember, it’s been 10 years since I wrote this. Stuff has happened, good and bad. That’s just how life works, and you have to go with it.
Sincerely, Taylor Smith
Beautiful words from an angel who was taken away from her family too soon!
If you were touched by Taylor’s words as much as we were, please share this story in her memory.
“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.”
© Chuy, El hombre lobo / Chuy, The Wolf Man / Facebook
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.
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