Making a Living Abroad With Lupus and a Laptop
- Added May 11, 2019
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When I was diagnosed with lupus in 2016, I had no idea what was next for me. I really felt that my life was over. A career I loved that was very physical was something I could no longer do. Unlike many people in the workforce who hate their jobs, I loved my chosen career. So to have to walk away from it because my battle has been filled with aggressive symptoms, I had to learn how to work with what was now happening in my life and my body. I share some ways I manage to cope and make a living while rotating in and out of the hospital on average 4 times a year.
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When I was diagnosed with lupus in 2016, I had no idea what was next for me. I really felt that my life was over. A career I loved that was very physical was something I could no longer do. Unlike many people in the workforce who hate their jobs, I loved my chosen career. So to have to walk away from it because my battle has been filled with aggressive symptoms, I had to learn how to work with what was now happening in my life and my body. I share some ways I manage to cope and make a living while rotating in and out of the hospital on average 4 times a year.
Check out Amoya's video where I get the spidey tingles mentioned in the video :-) https://youtu.be/sj1tScGoZ_0
If you would like to contribute to my ear collection, here is my wishlist: https://amzn.to/30bTD0U
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