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Content provided by Cystic Fibrosis Podcast and Jerry Cahill. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Cystic Fibrosis Podcast and Jerry Cahill or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://ro.player.fm/legal.
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Cystic Fibrosis Podcast 246 - Dealing with Post-transplant PTLD

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Content provided by Cystic Fibrosis Podcast and Jerry Cahill. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Cystic Fibrosis Podcast and Jerry Cahill or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://ro.player.fm/legal.
The You Cannot Fail Rare Disease podcast series was created so that the Boomer Esiason Foundation can shine a spotlight on other people and organizations in the rare disease community. In the second episode, Swapna Kakani discusses dealing with post-transplant lymphoproliferative disorder after her small intestine organ transplant. In June 2014, after checking a few things off of her bucket list, Swapna decided that she was ready to have a small intestine transplant and to deal with the complications that often accompany an organ transplant. Tune in to learn more about Swapna’s transplant journey. This video podcast series was made possible through an unrestricted educational grant from Atara Bio to the Boomer Esiason Foundation.
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71 episoade

Artwork
iconDistribuie
 
Manage episode 286969781 series 2420625
Content provided by Cystic Fibrosis Podcast and Jerry Cahill. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Cystic Fibrosis Podcast and Jerry Cahill or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://ro.player.fm/legal.
The You Cannot Fail Rare Disease podcast series was created so that the Boomer Esiason Foundation can shine a spotlight on other people and organizations in the rare disease community. In the second episode, Swapna Kakani discusses dealing with post-transplant lymphoproliferative disorder after her small intestine organ transplant. In June 2014, after checking a few things off of her bucket list, Swapna decided that she was ready to have a small intestine transplant and to deal with the complications that often accompany an organ transplant. Tune in to learn more about Swapna’s transplant journey. This video podcast series was made possible through an unrestricted educational grant from Atara Bio to the Boomer Esiason Foundation.
  continue reading

71 episoade

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