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‘I’M NORMAL!’

Brave woman with thousands of tumours on her skin reveals how she refuses to hide condition

Gail Applegren has had neurofibromatosis her whole life and despite her illness being confused for a 'contagious disease', she refuses to hide it

A BRAVE woman with thousands of tumours all over her body refuses to hide them, despite her condition being confused for a ‘contagious disease’.

Gail Applegren, 57, from Edmonton in Canada, has battled with neurofibromatosis her whole life but believes the disorder makes her ‘special’ and ‘unique’.

 Gail Applegren speaks frankly about her rare skin condition that means she has thousands of benign tumours all over her body
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Gail Applegren speaks frankly about her rare skin condition that means she has thousands of benign tumours all over her bodyCredit: Caters News Agency

Up until the age of 12, Gail only had one large tumour on her chest and ‘café au lait’ spots before the ‘bumps’ on her body began to vastly multiply.

Growing up, Gail says bullies would tease her but even as an adult she claims people have asked her not to swim in public pools, touch fruit and have even shied away from sitting next to her on planes.

But that hasn’t stopped the former social worker proudly showing off her ‘bumps’ to educate others about her illness.

She said: “I cannot even guess how many bumps I have. They are in the thousands and thousands.

 Gail is married to Tim, who also suffers from neurofibromatosis
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Gail is married to Tim, who also suffers from neurofibromatosisCredit: Caters News Agency
 Gail's condition increased in severity from the age of 12
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Gail's condition increased in severity from the age of 12Credit: Caters News Agency

“My entire torso has wall-to-wall bumps. There are so many they are growing on each other or out of each other.

“When I look on my stomach and others range from the size of my first of my stomach and one on my back and tall bone that was twice my fist size.

“I don’t cover up, I wear sleeveless shirts and tops. I’m a regular person, I laugh and cry, like you or anybody else.

“When I look in the mirror, I don’t see neurofibromatosis, I see Gail looking back at me.

 She and husband Tim both met through support groups for sufferers of their disease
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She and husband Tim both met through support groups for sufferers of their diseaseCredit: Caters News Agency
 Despite her condition, Gail insists she is a normal person
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Despite her condition, Gail insists she is a normal personCredit: Caters News Agency
 Gail refuses to hide her illness and wears short sleeve tops
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Gail refuses to hide her illness and wears short sleeve topsCredit: Caters News Agency

“I see my smile and my bright eyes, that’s the way I’ve always been.”

Gail says she relishes people asking questions about neurofibromatosis.

She said: “I love people asking about it, I want to tell them. Seeing me it’s very obvious that I don’t look like a lot of other people.

Prior to 2010, Gail believed she was ‘too busy’ for love until meeting Tim, but the pair are not celebrating their fourth wedding anniversary.

 The brave lady says she loves it when people ask about her illness
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The brave lady says she loves it when people ask about her illnessCredit: Caters News Agency
 When Gail looks in the mirror, she does not see her illness - she sees herself
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When Gail looks in the mirror, she does not see her illness - she sees herselfCredit: Caters News Agency

Despite the couple having to contend with pain from the disorder, they try not to let it negatively affect their lives.

“I live every day to the fullest,” said Gail “as I get older the more complications I have with NF but I’m a happy and active person.”

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