Mary’s Musings
![Why We Celebrate Rare Disease Day](https://images.squarespace-cdn.com/content/v1/5e39ecb01a207c2bf6a92bdd/1707418771810-B50AJD988PCJHXY9GVCW/11.png)
Why We Celebrate Rare Disease Day
Once a year, on February 28th, we pause to celebrate Rare Disease Day and our rare girl, Jessa; doing our small part to bring awareness to many rare diseases worldwide!
![Health Update: Jessa's Journey with Juvenile Dermatomyositis](https://images.squarespace-cdn.com/content/v1/5e39ecb01a207c2bf6a92bdd/1604353626125-AG3XJIWK15VSO3M0BF1W/123337634_2838463619721548_2192267645399882019_n.jpg)
Health Update: Jessa's Journey with Juvenile Dermatomyositis
An update on Jessa’s health journey with JDM and the results of her recent auto anti-body test results.
![2014: The Year of Unplanned Changes (Our Journey to Auto-Immune Diagnosis)](https://images.squarespace-cdn.com/content/v1/5e39ecb01a207c2bf6a92bdd/1601409243896-FW25CY0V3XM5DF4I54SA/Screen%2BShot%2B2020-09-29%2Bat%2B12.44.54%2BPM.jpg)
2014: The Year of Unplanned Changes (Our Journey to Auto-Immune Diagnosis)
We rang in 2014 knowing that our family was heading for some big changes; including a major career change for husband and our third baby’s arrival. What we didn’t know was that both of our daughters would be diagnosed with rare auto-immune diseases.
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