Well, it’s been a year since the last Rare Disease Day!! Time is flying very quickly these days. If you’re new here, welcome!! My name is Sarah and this is my little space on the internet where I share about life post-bone marrow transplant.
Today is a day where everyone who has been affected by a rare disease in some way raises awareness. It’s a huge day for advocacy and sharing stories. I have previously shared my story on here in written form. But I have a surprise… (well some of you may know).
BUT…
I STARTED A PODCAST!!
This podcast is titled It’s a Rare Story. This podcast is all about sharing stories of people with lived experiences of rare diseases and disabilities. This has been on my heart to begin for almost the past year. I am so excited to launch it today on Rare Disease Day. Today we launched with a trailer and my story. I go through it all.
To see anything more about the podcast, there is a special “It’s a Rare Story” tab on this website for Achieve the Impossible Today. All the links are there. You’re able to listen to the show on Spotify, YouTube, and Apple Podcasts.
If you have a rare story with a rare disease and/or disability and would like to share, we would be more than happy to interview you! Reach out to us by emailing itsararestory@gmail.com.


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