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After development, my husband and I went to the first date of 50k

After development, my husband and I went to the first date of 50k

For a woman, she is like “50 first dates in real life” every day.

Nesh Pillay, 34, suffered a brain injury that led to amnesia and forgot who she had a daughter or boyfriend.

Her story is likened to the plot of films like The Vow or 50 First Date, and is now the subject of a documentary series titled “50,000 First Dite: A True Story” which will premiere on Amazon Prime 2 Video from the 11th month.

One day after the nap, Pillay woke up and then lost her memory. jam press/@pillay.nesh

She told Jam Press, adding that she “blowed away” and she “comes,” far away. ”

“But most importantly, the most important part of it is raising awareness.”

Since sharing her journey on social media, she said people have told her that they “feel” because they have experienced similar life events.

“That was incredible humility,” she said.

“It’s the kind of story I wish I could have when I was young, and it’s an honor to know that I can be someone else’s voice now and I won’t take it easily.”

“It’s the kind of story I wish I was young, and it’s an honor to know that I can be someone else’s voice now and I won’t take it easily,” she said. Jam Press/NESH PILLAY
She doesn’t remember who her boyfriend is. Jam Press/NESH PILLAY

In 2022, Toronto-based Pillay woke up from a nap and experienced memory loss and could not recognize her partner, Johannes Jakope, 32, and did not remember her. Little daughter.

She mistakenly thought Yakopu for a ride-hailing driver many times and completely forgot about her child, which she always called “children.”

“I called my daughter a “child” and I thought it was a shocking experience for her,” Pirey recalls. “I would say ‘Do I have children? I don’t know how to take care of the children!’ ”

Pillay has suffered head injuries in the past and believes that recent head trauma may have caused amnesia, although she has no memory of it. The denerologist’s travel confirmed that she suffered from a concussion and could experience multiple seizures, resulting in memory loss.

“I’ve only retained about 20% of my new memories – if you ask me what I did two days ago, I might just stare at you, hoping for a prompt.”

But she gradually recovered – Jacob was always by her.

“My health changes every day, so when people ask me about my condition, it’s hard to answer.”

“Sometimes, I feel almost normal, sometimes I can’t get up, so I can’t have a conversation.”

The couple is now engaged in March last year and welcomes their son. Jam Press/NESH PILLAY
Their love story compares to “50 First Time Datings”. Jam Press/NESH PILLAY

Still, when he helped her take care of her, she fell in love with Jacob again and even learned how to weave her hair.

“Anyway, I always knew he was a safe space. He was still the one I chose to go to a doctor date or help me take a shower with me,” she said.

“It’s natural that even in my brain state, I want to marry him.”

Yakop finally made a suggestion – although she was unable to legally agree due to her condition at first – the two welcomed their son in March 2024.

“So many people call our story 50 first dates or vows, I see the similarities – after all, I did fall in love with him for the second time and probably would do it for the rest of my life.” She explained.

Pillay, who suffers from side effects such as headaches and tremors, is still looking for treatments to “make life easier”.

“I also hope the documentary shows that real life is not a movie, it’s messy, uncertain and imperfect, it’s OK,” she said. Jam Publishing House/Main Video/Peacock Lane Entertainment
“Anyway, I always knew he was a safe space. He was still the one I chose to go to a doctor date or help me take a shower with me,” she said. Jam Publishing House/Main Video/Peacock Lane Entertainment

The documentary series is a meeting with neuroscientists at the University of Toronto, who she articulates her condition, which she says is “exciting” but also “terrifying.”

“I brought these results to multiple neurologists to try to piece together the treatment plans,” she explained. “Unfortunately, we still don’t know the human brain, so now, it feels a lot like putting Italy in the face of the world.” Throw the face on the wall, hoping something sticks to it.”

She said she opened up on the movie “spent a lot” but she did “really happy”.

“For a long time, my diagnosis was so unclear because my diagnosis was so, and I know some doctors didn’t believe me completely,” she explained.

“I also hope the documentary shows that real life is not a movie – it’s confusion, uncertainty and imperfection, it’s OK.”

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