At the age of 32, a young woman who had “too much skin” on her body died.

I was 32 years old There was a rare obstacle. Hannah betAn “exciting” young woman who became a true example of her attitude when faced with her illness, He died..

Hannah became known for her suffering Harlequin-type fish scaleA rare, hereditary, incurable disease that appears throughout the skin and often as associated large, thick scales. Facial malformations and other physical abnormalities.

An example of facing pain

A young woman who lived in Norfolk, England, was born with this Hereditary disorders This is a fertility rate of 1 in 300,000 and the body makes too much skin.

About 50% of babies born with this disease die within the first few months, Hannah passed the test and lived a fulfilling, happy and affectionate life.

Unfortunately, he died of cancer on May 18th at the age of 32. mirror..

“I still can’t believe he’s gone. I feel like I can’t breathe because I want to see her once in a while“Her sister said. Lucy Betts35 years old, who Suffering from the same condition.. He added, “It’s a roller coaster with great emotions. It’s really difficult.”

In this sense, the woman explained that she and Hannah had to do Strict and intense routine Every day to prevent his hardened skin from cracking.

This included bathing every morning, scraping off excess skin layers, and moisturizing regularly throughout the day. I emphasized the middle.

By sharing the illness, the bond between them became very close and strong. Together, they experienced many things that no one else could explain. Each of them knew exactly how the other person felt...

“He has been with me for the past two years. My life revolved around her.. We were very fortunate to have her in our lives. Everything has improved a lot, “she said.

And I will affectionately explain in detail. “She made me laugh like no one else could. She loved everything that was pink and shimmering. I always remember her smile.. She was very affectionate and she loved all beings. She was honest. Ask Hannah if you want to know if her ass looked big. “

upon attitude His sister is her illness Facial expressions of othersLucy emphasized that the young woman would not hesitate to tell her to leave if she heard someone talking about them in the wrong language,

Hannah too Cerebral palsyLived in a bungalow of public housing, posted mirror,

He was diagnosed in February 2021 T-cell lymphomaHe had to undergo chemotherapy and immunotherapy.

A year later, in February of this year, he was admitted to James Paget Hospital in Great Yarmouth because he had a contract with Covid.

He recovered from the virus, but sadly died of cancer last week..

Emotional farewell to his family

The girl’s parents, Yang and Clive Betts, paid tribute to her and described her as follows: “Exciting” women..

“”She will sadly miss many people.. He inspired so many people. He never stopped smiling. Music was Hannah’s greatest passion. She liked to sing and dance, “she said.

On his side, Clive (66) added: We are very proud of her“.