I have been very open about living with endometriosis. Since my diagnosis, I have continued to travel the world, and even checked off dreams like the Mount Everest Base Camp trek, attending a friend’s wedding in India, riding the trains through Sri Lanka, and so much more. But through it all I try to be transparent that I travel with endometriosis – a chronic, incurable condition that affects my daily life. And of course, it affects how I travel.
I am so proud to bring you this post about traveling with endometriosis, with tips from seven endo warriors. Traveling is hard on anyone’s body, and when you have a chronic illness like endometriosis, it’s that much harder. I know a lot of people with endometriosis avoid travel, or feel limited in their travel options. Personally, one of my biggest passions in life is travel, and endometriosis became a big barrier to that. How could I avoid a flare? What could I eat? How do I deal with the pain? What products can help? There are so many questions when it comes to traveling with endometriosis. That’s why I reached out to these fellow endo warriors to share their best tips.
Just over a month ago, I was waking up from laparoscopy surgery between the starchy sheets of a Michigan hospital bed. Above the overwhelming nausea and the muzzy anaesthesia brain, I was given my results: endometriosis. Specifically, adhesions and bowel endometriosis