Salt in My Soul

Salt in My Soul

Mallory Smiths book, Salt in my Soul was published posthumously by her mother, Diane Shader Smith (husband Mark) after she died from CF at the age of 25 years old. Smith died after a double lung transplant. So many people have read her book. I bought it years ago, but was never able to read it. I have a mental block, lots of CF books sitting on my shelf that I can’t read. I am living this life, I am raising not one but two girls with cystic fibrosis. I didn’t think I could handle any of these books, but I bought them, and they sat on my shelf.

Serendipity happened to me, as it always does with CF related incidents. I was on a zoom webinar, got bored, and started looking at their Ads. One popped out at me: Lost Women of Science with NY Times reporter Katie Hafner. She did a four part series about Dr. Dorothy Anderson, who discovered in 1938, that CF existed. So for whatever reason, it seemed time to start reading all these books I had -- with my girls at 27 and 24 years old, it was time to delve into everything CF.

At this time Diane Shader Smith and Director, Will Battersby were debuting their film, Salt in my Soul. It was Mallory's story on film. It featured her videos, writings, her story. I didn't know what to expect, but after watching it I felt like Diane was my CF Mom Soulmate and I had to talk to her. That's where our story begins.

In this podcast you'll hear from Diane and Will. We talked about everything from Phage therapy that could have saved Mallory, to staying strong and pushing for more in the world of CF.

Will Battersby: @Battersby4Will

Film link: saltinmysouldoc.com

Diane Shader Smith: @dianeshadersmth

Trailer link: https://youtu.be/m5779DFldHA

Film: @SaltInMySoulDoc

More on phage therapy: @YalePhage

Salt in My Soul Website: https://saltinmysouldoc.com/

Like, subscribe, and comment on our podcasts!

Please consider making a donation: https://thebonnellfoundation.org/donate/

The Bonnell Foundation website:https://thebonnellfoundation.org

Email us at: thebonnellfoundation@gmail.com

Watch our podcasts on YouTube: https://www.youtube.com/@laurabonnell1136/featured

New: Shop our merchandise! https://thebonnellfoundation.org/product-shop/

Thanks to our sponsors:

Vertex: https://www.vrtx.com

Viatris: https://www.viatris.com/en

Read us on Substack: https://substack.com/@lstb?utm_campaign=profile&utm_medium=profile-page

Watch our trailer of Embracing Egypt: https://youtu.be/RYjlB25Cr9Y

Denne episoden er hentet fra en åpen RSS-feed og er ikke publisert av Podme. Den kan derfor inneholde annonser.

Episoder(211)

The Night Shift: Living with CF After Dark, Dr. Kimberly Canter

The Night Shift: Living with CF After Dark, Dr. Kimberly Canter

I Was Wide Awake for Dr. Kimberly Canter’s Presentation on Sleep and Cystic FibrosisI was wide awake during a presentation about sleep, but that’s exactly what happens when you hear Dr. Kimberly Cante...

21 Sep 43min

16 Years of Hope: Why the Bonnell Foundation’s Mission Matters

16 Years of Hope: Why the Bonnell Foundation’s Mission Matters

Hi everyone, The Bonnell Foundation’s mission has always been deeply personal. As we celebrate our Sweet 16 Night of Hope Gala on September 19th, it’s a perfect time to reflect on why this work matte...

14 Sep 15min

CF Care Around the World with Petrina Fraccaro

CF Care Around the World with Petrina Fraccaro

Friends for years and with CF as their connection, Laura and Petrina have figured out how to raise CF awareness across the world. How does cystic fibrosis care compare between Australia and the United...

7 Sep 36min

The Anomaly: living off donated organs and dark humor by Inka Nisinbaum

The Anomaly: living off donated organs and dark humor by Inka Nisinbaum

What would you do if you didn't know what your future held? For people living with cystic fibrosis, uncertainty is often a constant companion. Inka Nisinbaum faced one of the biggest unknowns of her l...

27 Jul 47min

Ireland's Rising Golf Star, David Howard, who happens to have CF

Ireland's Rising Golf Star, David Howard, who happens to have CF

Luck of the Irish.   Irish international amateur golfer David Howard  doesn't seem to need luck with all the talent he has. We had an inspiring conversation about chasing big dreams while living with ...

20 Jul 44min

CF Scholars: Stories of Determination

CF Scholars: Stories of Determination

Dreams and Determination: Meet four Inspiring students, Living with cystic fibrosis. One of the greatest joys of The Bonnell Foundation is helping young adults living with cystic fibrosis pursue their...

13 Jul 53min

Turning family loss into hope: Kate O'Donnell's story

Turning family loss into hope: Kate O'Donnell's story

I thoroughly enjoy doing my podcasts. It’s the one thing I truly miss from my television news reporting days — interviewing extraordinary people every single day. Through The Bonnell Foundation, I now...

6 Jul 44min

Jon Gay on Radio, Podcasting, and the Art of Storytelling

Jon Gay on Radio, Podcasting, and the Art of Storytelling

Jon Gay and I had a great time recording this podcast because we not only talked about podcasting, but also reflected on our years in the broadcast business and what people should know before starting...

29 Jun 48min

Populært innen Fakta

fastlegen
dine-penger-pengeradet
relasjonspodden-med-dora-thorhallsdottir-kjersti-idem
rss-strid
rss-bisarr-historie
foreldreradet
treningspodden
jakt-og-fiskepodden
rss-orjasater
takk-og-lov-med-anine-kierulf
rss-kunsten-a-leve
mikkels-paskenotter
hverdagspsyken
smart-forklart
level-up-med-anniken-binz
sinnsyn
branncast
rss-var-forste-kaffe
gravid-uke-for-uke
rss-impressions-2