3 Sites for a Crohn's Expat in Beijing

 Crohn's disease in Chinese is 克罗恩病 Kè luó ēn bìng.

In 2018 I packed my bags and moved to Beijing. It was an easy choice for the trip of a lifetime, but it was so hard to find any information about what life was like for a Crohn's Expat. I spent 3 months before departure researching: local hospitals, IBD doctors, medications, and insurance and trying to find out any information about life as a Crohn's patient in China.

Here are some useful sites I found to help you start planning your travels:

*The Beijinger - a Beijing Directory and news source

https://www.thebeijinger.com/

  • I found addresses for local hospitals - some places listed fees and included reviews

  • It's not always up-to-date and you occasionally have to try a few variations of search terms to find where you are looking for but this was the best directory available.

Crohn's and Colitis UK - for insurance information

https://www.crohnsandcolitis.org.uk/about-crohns-and-colitis/publications/insurance-ibd

  • Health Insurance - I could not find an affordable provider who covered my Crohn's as it came under pre-existing conditions.

  • I opted for Travel Insurance - I was covered to fly back home or receive emergency medical treatment if I went to hospital. I did end up flying back home a couple times.

IBDPassport - for IBD hospitals around the world

https://www.ibdpassport.com/

  • I was able to find hospitals in my area of Beijing with an IBD doctor

  • Some hospitals also listed medications they had available (my biggest concern) like Azathioprine.

While this list is by no means exhaustive, these sites were a great starting point for planning. My two years were challenging and fun, and no two hospital visits were ever the same. Having these as a reference point before departure made travelling a lot easier for me.

If you know of any other websites let me know in the comments.

~J


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