What was intended to be a joke ended up being one of the greatest gifts a mother could ever have from her son.
An Arizona guy grew out his hair for over three years in order to give it to his mother, who lost her hair due to radiation treatment.
Matt Shaha declared, “It makes perfect sense.” “In the first place, she gave me the hair.”
Melanie Shaha battled a benign brain tumor for many years.
She remarked, “I had surgery twice, in 2003 and 2006, for a pituitary tumor that was recurrent and benign brain tumor.”
After two successful surgeries to remove it, she was prescribed radiation in 2017 when it reappeared.
“I inquired with my doctor, ‘Will my hair fall out?’” and they replied, “No.”
She lost her hair three months later.
A TWO-DAY WEEK…
She remarked today, “When you don’t have hair, you stand out like a sore thumb and kind people can say things that make you cry.” “Looking sick bothers me more than actually being sick.” At the store, I’d want to fit in rather than stand out.
Shortly after Melanie started experiencing hair loss, her son, who is 27 years old, made a joke one day about growing his hair out and getting a wig for her.
I began working with Matt Shaha a year ago, and he is one of the most giving people I have ever met. Among the original…
Even though Melanie’s son was receiving such a nice offer, she didn’t want to burden him with it.
But Matt had a different perspective. For the next 2.5 years, he let his hair grow out. He went to his mother’s house with a few coworkers when his hair was at the right length, and they chopped it off.
I began working with Matt Shaha a year ago, and he is one of the most giving people I have ever met. Among the original…
Melanie remarked, “We were so excited that we started crying when they started cutting.”
He even paid the $2,000 to have the wig created when the time came.
The mother and son team discovered a wigmaker who created a lighter and more comfortable wig by hand-stitting the hair. Melanie had the wig trimmed and styled as soon as it arrived.
“It’s the first time I’ve seen my mom look like that since she lost it, so it’s been about four years,” Matt remarked upon seeing her in it.
Melanie, smitten with her new appearance, conceded that surpassing her son’s present would be difficult. “It definitely fills your heart.”
Melanie is very happy! Look at her expression! Matt is even grinning broadly. For them both and their families, I adore this.
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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