What started as a joke turned into one of the most amazing gifts a mother could ever receive from her son.
Matt Shaha, from Arizona, spent nearly three years growing out his hair to make a wig for his mother, Melanie, who lost her hair after receiving radiation treatment.
“It’s a no-brainer,” Matt said. “She gave me the hair in the first place.”
Melanie had been battling a benign brain tumor for years. She had two surgeries in 2003 and 2006 to remove the tumor. But in 2017, when the tumor came back, she had to start radiation treatment.
“I asked my doctor, ‘Will I lose my hair?’ and they said ‘No,’” Melanie said.
But three months later, she did lose her hair.
“It’s hard when you don’t have hair. People can say things that hurt your feelings,” Melanie told Today. “I don’t mind being sick, but I mind looking sick. I’d rather blend in at the store.”
Not long after Melanie started losing her hair, her 27-year-old son Matt jokingly said he would grow out his hair and make a wig for her.
Even though Melanie thought it was a sweet offer but didn’t want to burden him, Matt was serious about it. He spent the next two and a half years growing his hair long enough to make a wig.
When Matt’s hair was long enough, he and a few coworkers went to his mom’s house to cut it off. Melanie said, “We were super pumped, and when they started cutting, we bawled.”
Matt even paid $2,000 to have the wig made. They found a wigmaker who hand-stitched the hair to make it lighter and more comfortable. Once the wig was delivered, Melanie had it cut and styled.
“Seeing her in it was the first time I had seen my mom look like that since she lost her hair, so it’s been about four years,” Matt said.
Melanie loved her new look and felt deeply touched by her son’s gift. “It sure fills your emotional cup,” she said.
Look at the joy on Melanie’s face! Even Matt is beaming with happiness. I love this for both of them and their family.
Please share this heartwarming story.
Celine Dion Faces ‘Unimaginable’ Medical Crisis: New Documentary Reveals All!
Celine Dion is giving fans an honest look at her life with stiff person syndrome.
In a new documentary, the famous singer experiences a scary medical crisis during a physical therapy session, and it’s all caught on camera.
In 2022, Dion revealed she had been diagnosed with stiff person syndrome. In the documentary, “I Am: Celine Dion,” she shares that she had been dealing with symptoms of this rare, progressive neurological disorder for 17 years.
“I need my instrument. And my instrument was not working. So we started to elevate the medicine,” Dion, 56, said after struggling to hit certain notes during her 2018 and 2019 tours.
Though she completed her 2018 tour, Dion had to postpone several dates from her 2019 tour due to the “common cold” before the pandemic shut it down.
Her tour resumed in 2022, but she had to keep canceling and rescheduling shows. It wasn’t until she announced her diagnosis that she officially canceled the rest of her appearances.
“I can’t lie anymore,” Dion says in the documentary. “From a sinus infection to an ear infection to whatever. Sometimes I would point my microphone toward the audience, and I would make them sing it. There are moments where I cheated and I tapped on the microphone like it was the microphone’s fault.”
LONDON, ENGLAND – JULY 05: Celine Dion performs live at Barclaycard Presents British Summer Time Hyde Park at Hyde Park on July 05, 2019 in London, England. (Photo by Samir Hussein/Redferns)
In the documentary, there’s a part where Dion shows a very personal moment. She’s lying on a massage table doing exercises for her physical therapy when her foot suddenly starts to cramp. Soon after, her whole body tightens up and she can’t move or talk to the people around her.
The camera keeps recording as another person from her medical team rushes in with a nasal spray called benzodiazepine. They give it to Dion, who’s in so much pain that she’s crying, even though she can’t move. It’s really hard to watch this part of the video.
Once the spasms have subsided – they typically last anywhere from 30 minutes to an hour – Dion is able to sit up and speak.
“Every time something like this happens, it makes me feel so embarrassed,” she says. “I don’t know how to express it, you know, to not have control over yourself.”
Her physical therapist speculates the attack was brought on by being “overstimulated” from an earlier singing session.
“If I can’t get stimulated by what I love, then I’m going to go on stage, and you’re going to put the pulse oximeter on me and turn me on my back?” she wonders.
Dion hopes that one day soon she’ll be able to return to the stage.
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