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#024 - Living With: Pigmented Villonodular Synovitis (PVNS)

#024 - Living With: Pigmented Villonodular Synovitis (PVNS)

Released Monday, 12th April 2021
Good episode? Give it some love!
#024 - Living With: Pigmented Villonodular Synovitis (PVNS)

#024 - Living With: Pigmented Villonodular Synovitis (PVNS)

#024 - Living With: Pigmented Villonodular Synovitis (PVNS)

#024 - Living With: Pigmented Villonodular Synovitis (PVNS)

Monday, 12th April 2021
Good episode? Give it some love!
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Hey everyone! In this week's episode, I'll be talking to Lauren about what it's living living with PVNS. It's a rare diseases where only about 10 in a million get it, so we're lucky to have her on to talk about what struggles she faces with having PVNS and surgeries she needs to go through, and the risks she might face in the future. 

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Even if you're not on an iPhone, just click this link here!

CONTACT ME;

If you want to be a guest on the show, please send me an email with a short biography about yourself and what you have to;[email protected]

(you can also email me letting me know how I can improve this podcast, and what you might want to hear more or less on the show as well!)

Twitter; @robert_bednarz

Instagram; @thepatientwillseeyounow

Facebook; fb.me/thepatientwillseeyounow

 

Logo made by David Falcone, find him here;https://www.davidfalcone.com/

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