Traveling with MdDS can be scary or difficult, but it doesn't have to be when you try my travel hacks and coping tips! What a trip!
In this 3rd and final video in this series I discuss what worked, what didn't, things I'd do differently, and how to enjoy what you can while traveling with a chronic illness. It's so easy to allow fear of increasing symptoms to hold us back from doing things we enjoy, which can then cause us to feel like shells of the people we once were. Living with a rare and chronic illness that is at times completely debilitating, can cause us to feel robbed of the lives we've worked so hard to build. As we learn to accept our new normal, it's important to remember that our illness doesn't define us. We are often times still capable of doing many of the things we enjoy, we just have to find new ways to do them, and new ways to find that joy.
Please be sure to leave me a comment down below if you're a fellow MdDS warrior, and feel free to share some travel success tips! Let's help each other find ways to live our life to our fullest, if we're all going to be stuck on this party boat, we might as well rock it.
If you missed the other 2 videos on this mini series, you can catch them right here!
https://youtu.be/lyf12U1m5Mk
https://youtu.be/dfb2oxZd8Pw
Interested in my other videos about Mal de Debarquement Syndrome?
Help spread awareness with videos in this playlist! Mal de Debarquement Syndrome:
https://www.youtube.com/playlist?list=PLlqn9Hl_BwDN3lXCDszCVfVgeZorwKVHc
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https://www.facebook.com/LifeRocksMdDS/
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https://twitter.com/_Life_Rocks?s=09
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https://instagram.com/_life_rocks_?igshid=uhti0y8c7hrd
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