Mandy Sellars, British Woman with Gigantic Legs/Feet, Suffering Proteus Syndrome (Pictures)
Posted Sep 20, 2008 by Lindsay Britney
Russian woman Svetlana Pankrtova stunned the world for her longest legs of any woman recognized by Guinness World Records. British woman Mandy Sellars now also attracted the similar international attention for her own (gigantic) legs, but apparently the latter is not as lucky as the former.
Mandy Sellars (pictured here), 33, from Lancashire of England, may be suffering from an extremely rare disease called Proteus syndrome [wikipedia] that left two of her legs weighing 92-98kg out of total body weight about 130kg. What’s the worse, the abnormal legs never stops growing, and one day, they may have to be amputated.
Excerpts From ABC News
….
Sellars is 33 years old and weighs 285 pounds [129kg]. Her upper torso is a petite size 8 and accounts for only about 70 or 80 pounds [31~36kg] of her weight. The rest is in her legs and feet.
“When I was born, there was a noticeable difference between my upper body and my lower body,” Sellars said. “They didn’t actually expect me to live further than about a few, a few days or so.”
A Tough Job for the Shoemaker
Throughout her childhood, the growth of her legs continued to outpace the rest of her body until she could no longer move on her own. She walks now with the aid of crutches and drives a specially equipped automobile.
Near her home in northwestern England, Sellars goes to a private shoemaker. Her right foot is 16 inches [41 cm] long and 7 inches [18 cm] wide, and her legs are of differing lengths because the left foot — a club foot, 11 inches [28 cm] long — faces backward.
So the fittings are delicate. It takes weeks of trial and error to produce the final molds for a pair of boots, and they will cost around $4,000 — money she has to raise because she is unemployed.
….
Because her condition remained such a mystery, she often seemed to be on the edge of disaster. In college, she was once suddenly paralyzed because of a blood clot that required 10 weeks of hospitalization. When a plastic surgeon tried liposuction to reduce the bulk in her legs, more tissue grew back than had been removed.
“In my mind, the condition has a mind of its own,” Sellars said, “because whatever you take away grows back bigger and bigger.”
…It was through the Internet that she finally began to get a clue about what her condition might be. A friend of hers came across the site of an organization in Great Britain called the Proteus Syndrome Foundation U.K.. That finally led to a diagnosis, one that Sellars had been waiting years to receive. The unusual growth of her legs and knees was common to people with Proteus syndrome
“This is a very rare disorder. Certainly, less than one in a million,” said Dr. John Graham, director of clinical genetics at Cedars-Sinai Medical Center in Los Angeles. “Proteus syndrome is named for the Greek God who could change his form. And because it was such an apt description of how these individuals rapidly change form from appearing relatively normal as young children to this startling overgrowth, the name has remained with the disorder ever since then.”
The most famous case of Proteus syndrome in history was that of Joseph Merrick, also known as the Elephant Man, who died in 1890 and was the subject of a well-known movie about his life.
…
Thinking AheadSellars lives independently in a home that has been only slightly modified for her, but even common household tasks — fixing a cup of tea — can be exhausting. She visits a nutritionist, hoping she can lessen the effects of Proteus syndrome through diet, but so far, it hasn’t helped. She has been told that eventually she may need to amputate her legs. She’s already considering how she will live her life then and has even thought about entering the London Marathon as a wheelchair racer.
“I’d love to do that,” Sellars said, “and hopefully then be able to wheel myself and train hard enough to be able to do that, and raise money for charity that’s helped me.”
Update: An interview with AOl Health in May, 2009, Mandy Sellars explained a bit about her condition. The AOL report said, “Reliant only upon government and delivery services, she lives alone and has no caretakers to help her out of bed in the morning, do the wash or scrub the dishes — activities that take her hours instead of minutes.”
We sympathize with Ms. Mandy Sellars so much! Sellars is suffering from the agonies that we normal people usual impossibly suffer. We are impressed by her optimistics on the future life. Wish her all the best!
#Permalink Tags: Disease, Foot, Health, Leg, Mandy Sellars, Proteous Syndrome, UK, Woman






January 5, 2009 at 10:03 pm
I do not understand why a decent Plastic Surgeon has not come out to offer to debulk her legs. A Good plastic Surgeon could remove half the useless bulk in each leg while leaving usable muscle tissue and bones. As it is, these legs are sucking the life out of her.
January 17, 2009 at 8:18 pm
Hey Mandy this is the muscle man Terrence Freeman from the state of Alabama in the USA. Do you remember chatting on email with me about a year or so ago?? I had lost your email and would LOVE to chatt with you once again. Can you give it to me again?
Thanks
Terrence
February 9, 2009 at 5:42 am
Mandy, I saw you on TV last night. Your story touched my heart. You have such a sweet spirit. I just had to write you this morning. I am Mother of 2 grown sons and 3 grandchildren. You are amazing women. I admire you for getting you degree. I know it was not easy. God has blessed me so much and I would love to e-mail and snail mail with you.
I do want to get to know you and know the outcome of your plight. I know God has sent me to you for a reason. You hang in there, things change daily and a Doctor my come along that can help you. I know you want to still be able to walk. I will keep you in my prays. You on line friend. Barbara Sutton
April 9, 2009 at 2:03 pm
Hi Mandy.
you are still a beautiful lady! I have watched your story on tlc and was touched by your nature, may god continue to watch over you… you are an inspiration to everyone!
April 12, 2009 at 4:54 pm
Does your condition affect your sex life?
April 13, 2009 at 5:56 am
Henry, you are such an indifferent and obnoxious person!
June 8, 2009 at 11:45 am
dear mandy:
i just want let you know that you are not alone, we are more than ten thousand people praying for you. i belive in Jesus that he will put peace in your hart. we love you!! filipenses 4:13
July 14, 2009 at 2:41 am
Mandy, can you please contact me by email please. I would like to email you personally. Can you get it from here. Thank you . Do get back to me as soon as you can Regards. Tricia
July 14, 2009 at 4:55 pm
Mandy I don’t know how to contact you – I have some probable positive help Please contact me ASAP I give you permission to obtain my email address from this source.
Regards Tricia.
July 29, 2009 at 5:49 am
Mandy did you see my comments above or if anyone who knows and can contact her please convey the above message to her..
Thanks Tricia
August 1, 2009 at 7:03 am
Mandy – I feel so sorry for you! People should not have to be staring
at you or be laughing at you either. I get stared at to and talked about and laughed at! I just ignore them people! They are so dumb!
Wait until they have a bad illness. You are so young to be having this
happen to your legs!
I have a medical illness also. And no Doctor wants to do any surgery
or any operation on my bad back!
October 19, 2009 at 5:51 pm
Hi Mandy!
My husband and I just saw your story last night and were so touched and awed by you. You are a remarkable and beautiful woman, going through so much. Our son was born with a club foot, his left also, and with surgery and castings, he is walking and running. Seeing you made us both wish with all our hearts there was something that could be done to help you. I could understand your decision against the amputation, I am certain I would have done the same if it were me. I just want you to know that we are humbled by your courage and strength. Please consider us friends who will keep you in our thoughts and prayers.
Love,
Monica and Rob