Mahogany Geter, a 24-year-old aspiring model, was born with a rare condition that left her with a 100-lb leg. After a lifetime of facing difficulties, Geter’s life changed forever when she was offered a chance to model, starting her off on a journey of spreading the message of body positivity to others.
Bright Side found her story inspiring and a great example of how beauty can be found everywhere, and wanted to share Geter’s story of self-love with you.
She was born with a rare condition.
Mahogany Geter, a resident of Tennessee, was born with a rare condition that left her with a left leg that weighs 100 lb. The condition, known as lymphedema, can cause excess fluids to collect in the soft tissue of the body and lead to swelling. For Geter, her entire left side of the body is impacted by this, but only her leg is the most visible.
Geter was diagnosed with the condition right after she was born, and it made it extremely difficult for her to walk. “It drains my energy, of course, because it’s an extra 100 pounds,” she said. The condition makes her more susceptible to contracting fibrosis, and the only way to manage it is through physiotherapy and massages to drain the excess fluid in her leg.
She had a difficult time growing up.
The model talked about how she faced many difficulties growing up: “I’ve been through a very depressed state because you’re a little kid, and you have a bunch of grown adults staring at you.” She would receive many unwarranted comments from others and was teased throughout her childhood. “I will say it probably can affect you more mentally and emotionally,” she revealed.
“As a child, I never felt pretty. I felt ugly, like a freak of nature, and cried in private so many times,” said Geter. She had been suggested surgery by many doctors, but she turned it down every time, stating that in some other, more severe cases, surgery hadn’t completely gotten rid of the growth. Instead, she chose to accept herself as she was.
She began her modeling journey in 2017.
Geter’s life changed forever in 2017 when she was spotted by a photographer while she was working at Walmart. Initially thinking it was fake, the young woman eventually agreed to let the photographer take pictures of her. “I was like, ’I’m getting older now, maybe it’s time I start putting my full body out there,’ and hopefully me doing that can help somebody else,” she said.
This one opportunity catapulted Geter’s career as a model. Following this, she was featured in a viral YouTube video that amassed over 10 million views. Her presence on Instagram and other social media platforms has also increased. “Mainly, I’ve gotten a lot of positive responses, and the ones I like the most are that it helps people that also feel low about themselves,” she said.
She aims to help others embrace their unique bodies.
Despite her increased presence on the internet resulting in some Internet trolls, Geter has remained positive throughout, saying, “People have been so nice and supportive of me online. It isn’t all trolling and negativity.” She has remained consistent in spreading body positivity and encouraging others to be more comfortable in their bodies.
Geter is committed to her dream of becoming a model. “If I ever make it big, I want to buy my mother a house and take care of my family, then I’ll do everything I can to raise awareness of lymphedema to pay it back to everyone who has ever shown me kindness.” She continues to use her condition to inspire others to celebrate their differences as well.
Her journey has inspired many.
Although Geter’s journey has been hard, she has learned to accept herself and vows to spread this attitude to others. “For the longest, I felt so low about myself, but once I got older and with loads of support from the online lymphedema community and my mom who is my inspiration, I realized how beautiful I am. Not only looks, but as a person.”
What part of Mahogany Geter’s journey resonated with you the most? Do you have any advice for those that struggle to accept their bodies? Share it with us.
Preview photo credit lymph.goddess23 / Instagram, lymph.goddess23 / Instagram
“She’s a real Thumbelina” – Meet the girl who’s only 99cm tall and defied all the odds
Kenadie Jourdin-Bromley, a Canadian child from Ontario, seemed ordinary at first glance.
She had high hopes for the future, loved sports and drawing, and went to school.
Nonetheless, one characteristic set Kenadie apart from her peers: her diminutive height of 99 centimeters.
Reports state that when Kenadie was born in February 2023, she weighed a mere 2.5 pounds. Her condition was quickly diagnosed by doctors as an uncommon form of cardiovascular disease, thought to affect only 100 people globally. The nurses dubbed her “Thumbelina,” quite fittingly.
Regretfully, Kenadie had slim chances of surviving.
According to reports, the girl’s condition can lead to complications like delayed mental development, respiratory issues, and digestive issues. Doctors at the hospital where the girl was born were concerned that she wouldn’t have much time to live due to her brain injuries.
Understandably, her parents were devastated. In order to give their little girl a name in case she passed away, they chose to christen her on the day of her birth.
“We thought we were going to take her home to die, because that’s what the doctors told us,” mom Brianne explained to Barcroft TV back in 2016.
Still, as the days went by, Kenadie steadfastly refused to give up. After she triumphed over all the challenges and hardships, her parents were able to dream again that she would survive. It was nothing less than a miracle for them.
Many years later, Kenadie still astounds everyone she encounters. She is only 99 centimeters tall, her arms and legs are still immature, and she struggles to learn new things, but she is a content young girl who enjoys life to the fullest.
Kenadie reportedly enjoys bowling and ice skating. Above all, she makes people happy that she meets.
“Kenadie makes me laugh. She’s very empathetic – if you hurt your finger she comes and gives you a hug. She’s got an infectious laugh that makes you want to laugh along with her,” Kenadie’s assistant Jessica Putnam mentioned to Barcroft TV in 2016.
Naturally, Kenadie and her family face many new challenges in their lives. Despite her loved ones’ best efforts to take each day as it comes, the young girl is continuously dealing with medical issues.
“My hope for Kenadie’s future– my biggest hope for her– is I want her to be happy. I want her to smile and be successful. If we can get through today, then we’ll see about tomorrow,” her mom said.
We are happy to share Kenadie’s inspiring story!
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