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Linda Evangelista says she's been left 'permanently deformed' by fat-reduction procedure

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Linda Evangelista says she's been left 'permanently deformed' by fat-reduction procedure

Linda Evangelista has claimed she has been left "permanently deformed" following a fat-reduction procedure.

The 56-year-old star - who was one of the world's most famous supermodels in the 1990s - has revealed she has stepped out of the public eye and alleged that popular procedure CoolSculpting left her "brutally disfigured".

She wrote on Instagram: "Today I took a big step towards righting a wrong that I have suffered and have kept to myself for over five years.

"To my followers who have wondered why I have not been working while my peers' careers have been thriving, the reason is that I was brutally disfigured by Zeltiq's CoolSculpting procedure which did the opposite of what it promised.

"It increase, not decrease, my fat cells and left my permanently deformed even after undergoing two painful, unsuccessful, corrective surgeries.

"I have been left, as the media has described, 'unrecognisable.' "

Linda also said she has developed paradoxical adipose hyperplasia (PAH) which is said to be a " very rare but serious side effect" of the fat-freezing procedure, according to Heathline.

Referencing a lawsuit, she continued: "I have developed Paradoxical Adipose Hyperplasia or PAH, a risk of which I was not made aware before I had the procedures.

"PAH has not only destroyed my livelihood, it has sent me into a cycle of deep depression, profound sadness, and the lowest depths of self-loathing.

"In the process, I have become a recluse. With this lawsuit, I am moving forward to rid myself of my shame, and going public with my story.

"I'm so tired of living this way. I would like to walk out my door with my head held high, despite not looking like myself any longer."

CoolSculpting - the brand name for cryolipolysis, which uses cold temperatures to reduce fat deposits - is also known as body contouring, and has been approved by the U.S. Food and Drug Administration.

Zeltiz - which is a subsidiary of Allergan - markets and licenses devices used for such procedures.


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