Feb. 26, 2025

Fruitful Conversations with Michelle fruhschien

Fruitful Conversations with Michelle fruhschien

Relationships can be complicated especially without patience, communication, and understanding. On this week's episode join me and medical mom Michelle Fruhschien as we discuss her journey from teaching English, switching to Special Education, to finding out her daughter was diagnosed with Jordan's Syndrome an incredibly rare genetic disability. We also discuss the importance of encouraging children to ask questions, to include, and respect members of the disability community at a young age, the importance of recognizing each individuals unique needs and celebrate the milestone. We here at the Sit Down Stand Show would like to send a special thank you to the hardworking people at Jordan's Guardian Angels for providing support and resources to families affected by Jordan's Syndrome we'd also like to wish Hailey Fruhschien a very happy 5th Birthday For more information regarding Jordan's Syndrome or how you can follow along on the Fruhschien family's journey click the links below and until next time Keep Calm and Roll On ⁠https://jordansguardianangels.org⁠⁠https://mamabearforrare.com⁠⁠https://instagram.com/mamabearforrare⁠https://www.facebook.com/share/19tbXr5BaZ/?mibextid=wwXIfr⁠This episode is sponsored by Community Living Trent Highlands and Job Quest ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠https://www.clth.ca⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ To support The Sit Down Stand Out Show please consider leaving a 5 star review or checking out our merch store here. ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠https://www.rollingdragonmedia.com⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ #rarediseaseawareness#medicalmom#disabilitycommunity#inclusion

 

Until next time Keep Calm and Roll on.

Michelle fruhschien Profile Photo

Michelle fruhschien

Advocate, special educator, mom

Hi! I am Michelle, wife, special educator, advocate, and mom to two children. Noah, 7.5 and Hailey who will be 5 in February. My advocacy journey truly started when Hailey was born, but became a calling when she was 8 months old and diagnosed with an ultra rare disease called Jordan's Syndrome.