A newlywed ageing at twice the normal rate is refusing to let her condition slow her down.
At 30-years-old, Challi Muguira is one of the oldest surviving people with progeria in the world.
Progeria is a rare genetic disorder characterised by premature ageing, growth delay, short stature, small face and hair loss.
Challi, from Baton Rouge, Louisiana, has a rare form, which was so unusual that it took doctors 16 years to formally diagnose her.
Her form of progeria is different from the classic form and she does not age at quite the same rate, but is still mistaken for someone who is decades older.
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After meeting her partner online, Challi tied the knot with the love of her life in November 2017.
“I like being different. It’s affected my life in more of a positive way and I want to help people, especially kids like me,” Challi told Barcroft TV.
“Progeria is a rare ageing disorder. Normally the kids that have it pass away by the time they are 10 to 15.
“I have a very moderate case but I was told at a very early age that it would be a miracle if I would live to be 30 years old, so I am obviously doing well, compared to what I thought I was ageing, I am not ageing as fast.
“I do have the features of someone who has progeria – I have very prominent eyes, very thing nose, very thin hair and you can tell by looking at me that I don’t look 30.”
Challi first showed signs of the condition at just two-years-old when she fell off of her bicycle and her mother realised her fingers had started to club.
She was taken to the the doctors, but it took another 14 years before Challi was given the diagnosis of progeria.
She said: “The diagnosis itself was lots of doctors offices. Eventually one doctor sent us to a children’s hospital and from there I got a very good doctor.
“He had one of his classes do a study on just me and the class were actually the ones who diagnosed me. There are a lot of things that you learn about yourself during the process and I learned a lot.
“At 16 years old you don’t want to hear that you are ageing faster but I learned a lot. There are things that you kind of have to accept and I had amazing doctors along the way.”
The newlywed found it difficult to accept her different appearance at first, but later used it to her advantage to get served at 18-years-old.
Challi said: “It’s hard when you’re 15-years-old and people think you’re 30, that was rough. Even when I was younger people would think I was 21, I was only 18, I could drink at an early age, it was fun – it came in handy.”
However, she also found herself being targeted by bullies at school for her appearance.
After Challi left school, she finally found someone she could truly connect with romantically, her now-husband Tony.
She explained: “Tony and I met on a dating site. I liked talking to him, I enjoyed it and I like that fact that when you talk to somebody like that, they can’t judge you based on what you really look like. They are only judging the person they get to know.
“I think I loved him the moment I met him. I knew from way in the beginning that I wanted a life with him.”
Tony, who is legally blind, bonded with Challi immediately and neither of them have looked back since.
Tony said: “We support each other. We bring out the best in each other. We try, a lot of the time, to goof off and take each other’s minds off of it.
“We sit down and talk and remind each other that it’s not that bad.
“Being with Challi changed my perspective on a lot of things. She is just one in a million!”
Eighteen months into their relationship, Challi and Tony tied the knot in a ceremony attended by their closest friends and family.
Challi said: “My wedding was perfect. There was everything I could dream of.
“Walking down the aisle, and seeing Tony, I was so nervous, so nervous, but as soon as I got to him I was like, this is it – my whole life is about to change.
“It was the happiest day of my life.”
Despite the lack of certainty about her life expectancy, Challi is determined to live each day to the fullest and refuses to allow her condition to hold her back.
She said: “As far as how long I’m gonna live, no one knows. There is going to be a point where my life will be shortened and I know that.
“It has taken me a long time to come to terms with it and it’s actually easier to live with it now that I am happy and I have somebody who loves me.
“If I could tell anybody one thing about progeria, it would be that it’s not always negative. If you can see the positive in it, you’ll have a great life.”
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