I was pretty active on social media for World Rare Disease Day, and I wanted to make sure that you got to see my posts too! If you aren’t already following me on social media, I would strongly suggest it. You can find me on both Instagram (@findinglifessilversun) and Twitter (@lifessilversun). I also have a Facebook page, specifically for my blog: facebook.com/FindingLifesSilverSun.
(All times typed in this post are provided in mountain time, which is my local timezone. I’m not sure what time stamps will display in the embeded posts, since I believe they will show your local time.)
Technically, I started my WRDD awareness the day before, on February 27th with this blog post, tweet, and Facebook post:
Then, I was having a high pain night. Since I was suffering from some painsomnia, I decided to go ahead and get the day started before I went to bed! (The Instagram post was done at 1:51am and the tweet was at 2:01am.)
After I was able to sleep, I decided that I wanted to use my social media presence to showcase some of the rare disease elements of my life.
Throughout the day, I also shared some of my fellow Chronic Illness Bloggers WRDD posts on my Facebook page! The posts are all fantastic and definitely deserve a read!
To see more social media posts, not from me, related to WRDD this year:
One of my Chronic Illness Blogger buddies, that I somehow missed sharing her post on WRDD: “Being a Zebra” by A Southern Celiac
What were some of your favorite things to come out of World Rare Disease Day? Personally, I absolutely loved seeing everyone come together and positively shout about rare diseases! I know I learned a lot this year, and I hope you did too!