Real life rag doll: Stunning model with rare muscle condition means she goes floppy like a rag doll

A stunning model has a rare muscle condition causing her to go weak and floppy at any moment – just like a RAG DOLL.

Clare-Alana Ford, 23, from Hayling Island, Hampshire, suffers from a bizarre condition that makes her body go limp and weak without warning.

The incurable condition, often nicknamed the rag doll disease, can cause Clare-Alana to lose all control of her voluntary muscles, such as those in her legs and arms.

But despite her rag doll condition – known as myasthenia gravis – brunette Clare-Alana has managed to forge a successful modelling career.

Clare-Alana Ford, 23, has a rare muscle condition causing her to go weak and floppy at any moment

Clare-Alana Ford, 23, has a rare muscle condition causing her to go weak and floppy at any moment

Clare-Alana said: “Sometimes I will go to put my hair up and suddenly my arms will just go limp and flop down to my side.

“I’ve been walking along the road before and my legs will just give way, and there’s nothing I can do.

“It’s a condition that improves with rest so I have to talk breaks when I’m doing activity.

“It sounds strange but it’s just like a rag doll.

“It can be difficult as I get very tired, but I refuse to be a slave to my condition.

“I love modelling and I’ve been able to be successful despite my health issues.

“I’ll always do my best and I’ll never let it affect how well I do on a shoot.

“I won’t let my condition define me.”

Clare-Alana said: "People can be quite insensitive at times because of their ignorance about the condition and I'm often mistaken for being lazy which is very upsetting."

Clare-Alana said: “People can be quite insensitive at times because of their ignorance about the condition and I’m often mistaken for being lazy which is very upsetting.”

Clare-Alana began to model at the age of 17 – just as she began to experience her unusual symptoms.

Shea said: “A friend of mine was looking for people to model some dresses for a show during London Fashion Week.

“I thought it sounded like fun, so I told her I’d do it.

“But at around the same time I started to get very tired easily and weak for no reason at all – I was terrified I’d fall over on the runaway in front of everyone.

“I was very active and I did ballet, so I thought I was just doing too much.

“I was nervous but I loved the experience of modelling, and I decided to embark on it professionally.

“Then I remember once my legs just totally gave way and I felt like a weight was pushing down on me and I couldn’t get up.

“At first the doctor told me it was growing pains, but I knew it was something more so I pushed for further tests.

“Eventually I was diagnosed with myasthenia gravis – I’d never even heard of it before.

“It was very scary and such a shock to be diagnosed with something so foreign to myself, and something that even medical professionals knew little about, but I was determined to carry on with my life as normal.”

Despite her condition Clare-Alana has managed to forge a successful modelling career

Despite her condition Clare-Alana has managed to forge a successful modelling career

Clare-Alana has continued to model, and even had surgery last year in the hope of treating her condition.

She said: “I had surgery in July 2013 to remove my thymus gland, as there is some evidence that this can help kick start the condition into remission and aid symptoms.

“It can take up to three years to see improvement so I have a little while yet.

“For now I’m taking medication and I’m trying not to let it affect me too much.

“It can be hard as the condition is invisible, so often people don’t realise if I’m having a particularly bad with it.

“People can be quite insensitive at times because of their ignorance about the condition and I’m often mistaken for being lazy which is very upsetting.

“Stress can play a big factor in worsening the symptoms so I try to stay cool and not let things affect me too much.

“Sometimes I’ve had to pass up jobs as I’ve been ill – I had the opportunity to model for Harrods but I was too unwell to accept it, and I turned down the chance to model in Thailand as I was having surgery.

“My agency is based in London so traveling back and forth can sometimes be daunting and scary – the idea of facing the tube on a casting day is mortifying for me with all the stairs and the crowds.

“It’s hard sometimes to miss out on things, but it just makes me more determined to get better.”

Now, Clare-Alana has become a successful model, and hopes to move to Los Angeles to further her career.

The incurable condition, often nicknamed the rag doll disease, can cause Clare-Alana to lose all control of her voluntary muscles

The incurable condition, often nicknamed the rag doll disease, can cause Clare-Alana to lose all control of her voluntary muscles

Clare-Alana said: “Shortly after I was diagnosed with the condition I flew out to America to have a break from it all.

“I loved the lifestyle out there and I ended up meeting lots of successful and celebrated people involved in the modelling and entertainment industry.

“It made me realise that I could still have fun and be me, regardless of the condition.

“Now, I’m in the process of applying for my US via and continuing my modelling career.

“I won’t let anything hold me back.”

Ruth Ingledew, CEO of Myasthenia charity, Myaware, said: “Myasthenia Gravis is a neuromuscular condition which affects the transmission of messages from nerves to muscles.

“The brain can tell a muscle that it wants to, for example, lift up an arm, but the more the message tries to get through, the message gets weaker and weaker, until eventually the arm can’t lift up anymore.

“Initially it can affect the facial muscles so often people are misdiagnosed with a stroke.

“We don’t know what triggers myasthenia gravis, but women tend to be diagnosed in their 20s and 30s, whilst men are diagnosed in their 40s and 50s – our figures suggest that there around 10 to 12,000 people with the condition in the UK.

“In the past, myasthenia gravis could be fatal, but these days there are medications that work very well, and people can go on to lead happy, normal lives.

“If people want any support or information about the condition, we have a great website and a Facebook page that sufferers of all ages will find useful.”

For more information visit www.myaware.org.