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Kandungan disediakan oleh Christopher Velona. Semua kandungan podcast termasuk episod, grafik dan perihalan podcast dimuat naik dan disediakan terus oleh Christopher Velona atau rakan kongsi platform podcast mereka. Jika anda percaya seseorang menggunakan karya berhak cipta anda tanpa kebenaran anda, anda boleh mengikuti proses yang digariskan di sini https://ms.player.fm/legal.
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How social media helps awareness with Megan Loden

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Manage episode 339433194 series 3085162
Kandungan disediakan oleh Christopher Velona. Semua kandungan podcast termasuk episod, grafik dan perihalan podcast dimuat naik dan disediakan terus oleh Christopher Velona atau rakan kongsi platform podcast mereka. Jika anda percaya seseorang menggunakan karya berhak cipta anda tanpa kebenaran anda, anda boleh mengikuti proses yang digariskan di sini https://ms.player.fm/legal.

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.

You will like this creator for sure on today's show!

Megan is a mom to twins — identical 18-year-old girls — and a 14-year-

old son. She, her husband, and her kids live just outside of Phoenix. She is

a writer, caregiver, and mom. Maybe most importantly, Megan is also

an advocate for rare diseases and rare disease caregiving. She feeds

her soul with her career and works at ANGEL AID CARES uplifting

other caregivers. She is currently the chair of the Arizona Angioma

Community Alliance and treasurer of the HOD Association in her “free”

time. Follow her on Facebook, or Instagram, or check out her website!

meganloden.com

Facebook:

https://www.facebook.com/megan.loden.5?ref=bookmarks

Instagram:

https://www.instagram.com/megan.loden/

  continue reading

45 episod

Artwork
iconKongsi
 
Manage episode 339433194 series 3085162
Kandungan disediakan oleh Christopher Velona. Semua kandungan podcast termasuk episod, grafik dan perihalan podcast dimuat naik dan disediakan terus oleh Christopher Velona atau rakan kongsi platform podcast mereka. Jika anda percaya seseorang menggunakan karya berhak cipta anda tanpa kebenaran anda, anda boleh mengikuti proses yang digariskan di sini https://ms.player.fm/legal.

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.

You will like this creator for sure on today's show!

Megan is a mom to twins — identical 18-year-old girls — and a 14-year-

old son. She, her husband, and her kids live just outside of Phoenix. She is

a writer, caregiver, and mom. Maybe most importantly, Megan is also

an advocate for rare diseases and rare disease caregiving. She feeds

her soul with her career and works at ANGEL AID CARES uplifting

other caregivers. She is currently the chair of the Arizona Angioma

Community Alliance and treasurer of the HOD Association in her “free”

time. Follow her on Facebook, or Instagram, or check out her website!

meganloden.com

Facebook:

https://www.facebook.com/megan.loden.5?ref=bookmarks

Instagram:

https://www.instagram.com/megan.loden/

  continue reading

45 episod

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