How social media helps awareness with Megan Loden




The Rare hour with Christopher Velona show

Summary: <p>Megan is changing how rare disease families interact. With the help of social media, Megan's spin on the day-to-day lives of rare diseases has us laughing a bit more. You can see in her Instagram reels as she tells the truth through deadpan humor. </p> <p>You will like this creator for sure on today's show!</p> <p><br></p> <p>Megan is a mom to twins — identical 18-year-old girls — and a 14-year-</p> <p>old son. She, her husband, and her kids live just outside of Phoenix. She is</p> <p>a writer, caregiver, and mom. Maybe most importantly, Megan is also</p> <p>an advocate for rare diseases and rare disease caregiving. She feeds</p> <p>her soul with her career and works at ANGEL AID CARES uplifting</p> <p>other caregivers. She is currently the chair of the Arizona Angioma</p> <p>Community Alliance and treasurer of the HOD Association in her “free”</p> <p>time. Follow her on Facebook, or Instagram, or check out her website!</p> <p>meganloden.com</p> <p>Facebook:</p> <p>https://www.facebook.com/megan.loden.5?ref=bookmarks</p> <p>Instagram:</p> <p>https://www.instagram.com/megan.loden/</p>