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This is a pretty cool survey that Christine Miserandino posted on her page! I love it! I think it gives us some insight into her journey! It would be cool to see all of your answers! Feel free to post them in the comments!
A lot of people may not understand what you are going through or the battles that you face on daily basis. This maybe something fun that you post to your social media accounts along with your answers! It will bring awareness to your disease and inform friends and family about your battle! Also, if you have not checked out Cristine Miserandino's Spoon Theory, YOU NEED TO! I believe she accurately describes what spoonies face every single day! My mom and I love it so much, we have a framed poster in our house! Hope you enjoy it as much as we do! -Jess
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There are so many vaccines out there that some times it's hard to know what you should and shouldn't get. One of the most important things about being a Lupus patient is that you need to be your own advocate! Don't be afraid to ask your doctors their opinion and even get a second opinion! Don't forget....no one knows your body like you do!
Here's an article that Christin Miserandino shared that provides some insight in vaccines and Lupus patients! -Jess |
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