Global EditionASIA 中文雙語Fran?ais
    Lifestyle
    Home / Lifestyle / People

    Changing perceptions

    By Zhang Zefeng | China Daily | Updated: 2017-11-29 10:26
    Share
    Share - WeChat

     

    Young volunteers in the campaign, I Invite You to Sleep, get together to help raise awareness for people with a sleep-related affliction. [Photo provided to China Daily]

     

    Ahead of the International Day of Persons with Disabilities, Zhang Zefeng talks to four young people with uncommon afflictions, who are working to raise public awareness of rare genetic diseases.

    Growing up with congenital heart disease and epilepsy, Pan Longfei had a fairly eventful childhood.

    Seeing doctors and taking medication were an indispensable part of his early life, and he was physically the smallest and weakest among his peers. Schools saw him as a risk and parents thought his condition was contagious, so Pan was elbowed out of schools about five times. It took him 10 years to complete primary school.

    Pan was also misdiagnosed with leukemia. Even when his peers started their journey to adulthood, he still hadn't started puberty, which brought him sneers and humiliation.

    "I always perceived myself as an alien," says the now 28-year-old.

    Even today, he still has social phobia.

    Until he was 23, no one realized that Pan had Kallmann syndrome, a rare genetic hormonal disorder that causes delayed puberty and infertility.

    Pan was thrilled to receive that diagnosis as the doctor said hormone replacement treatment is generally effective. However, for some others the diagnosis leads to despair and heartbreak.

    "Many patients try to commit suicide as they believe it's incurable and they will need lifelong medical treatment," Pan says.

    In 2014 Pan set up an online group, Kallmann, offering patients health consults, sex education and networking activities.

    Over the years, the group has morphed from a small group to a community of more than 2,800 members.

    To inspire the public to learn about Kallmann syndrome and other rare diseases, Pan began walking from place to place. Last year, he covered nearly 500 kilometers walking from the Inner Mongolia autonomous region to Beijing.

    In China, there are more than 140 rare diseases affecting 16.8 million people, of which 80 percent are genetic, according to Fudan University Research Center for Birth Defects. They often appear early in life and may be present throughout a person's life.

    Dec 3 is the International Day of Persons with Disabilities.

    1 2 3 4 Next   >>|
    Most Popular
    Top
    BACK TO THE TOP
    English
    Copyright 1995 - . All rights reserved. The content (including but not limited to text, photo, multimedia information, etc) published in this site belongs to China Daily Information Co (CDIC). Without written authorization from CDIC, such content shall not be republished or used in any form. Note: Browsers with 1024*768 or higher resolution are suggested for this site.
    License for publishing multimedia online 0108263

    Registration Number: 130349
    FOLLOW US
     
    性无码专区| 免费看又黄又无码的网站| 成年午夜无码av片在线观看| 最新中文字幕在线视频| 无码人妻精品一区二区三区99不卡 | 亚洲av日韩av无码黑人| 中文字幕一区二区三区精彩视频| 成年午夜无码av片在线观看| 伊人久久精品无码av一区| 日韩人妻无码精品无码中文字幕| 亚洲一级特黄无码片| 国产精品无码专区在线观看| 无码人妻少妇久久中文字幕蜜桃| 少妇性饥渴无码A区免费| 91天日语中文字幕在线观看| 日韩亚洲变态另类中文| 亚洲?v无码国产在丝袜线观看 | 午夜无码伦费影视在线观看| 无码H黄肉动漫在线观看网站| 色综合久久综合中文综合网| 人看的www视频中文字幕| 久久影院午夜理论片无码| 大学生无码视频在线观看| 久久亚洲精品成人av无码网站 | 狠狠噜天天噜日日噜无码| 日韩欧精品无码视频无删节| 无码国产色欲XXXX视频| 亚洲AV无码1区2区久久| 亚洲∧v久久久无码精品| 无码日韩精品一区二区免费暖暖| 亚洲欧洲精品无码AV| 亚洲AV无码国产精品色午友在线| 一本色道无码不卡在线观看| 亚洲韩国精品无码一区二区三区 | 亚洲va中文字幕无码久久| 亚洲永久无码3D动漫一区| 亚洲爆乳精品无码一区二区三区| 在线精品无码字幕无码AV| 无码少妇一区二区三区浪潮AV| 无码一区二区三区免费| 国产成人无码精品久久久免费|