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Patient Perspective: Living Well with Pulmonary Fibrosis | Charolette Saunders 

Pulmonary Fibrosis Foundation
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Pulmonary Fibrosis Foundation (PFF) Ambassador Charolette Saunders, presenting at the PFF Summit 2015: From Bench to Bedside, shares the story of her journey with idiopathic pulmonary fibrosis (IPF). Charolette has undergone a lung transplant and experienced a series of health obstacles. She now inspires others to take charge of their health and to live life to the fullest.

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17 окт 2016

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Комментарии : 19   
@lorismith5369
@lorismith5369 16 дней назад
Most real talk shared by PFF! We need more like her…. FIND OTHERS! How can we help? 💚💙💚💙❤️
@rhrocha2009
@rhrocha2009 Год назад
Awesome testimony!!
@trixie-bellfaith5380
@trixie-bellfaith5380 5 лет назад
How inspirational this dear lady is. Bless you.
@elcompamartinez2647
@elcompamartinez2647 4 года назад
I hope this WARRIOR still doing good!!!!
@lorismith5369
@lorismith5369 16 дней назад
YES 💙💚
@M11689
@M11689 3 года назад
Wow...now this is an amazing woman
@elcompamartinez2647
@elcompamartinez2647 4 года назад
I was diagnosed in 2010 and im feeling like nothing is worthed anymore!! Im almost 70 an dont know if i'll b elegible for transplant,,,, i was runing marathones and doing 50 miles bikerides untill 3 years ago . (THANKS GIVING DAY TODAY 2020) 😢
@sojournerhouse
@sojournerhouse 4 года назад
I am 70 too.
@pfforg
@pfforg 4 года назад
Hi Jose, We're sorry to hear of the difficult times you are facing. If you'd like to learn more about treatment options and support services that may be available to you, please contact our Patient Communication Center at 844.825.5733 or email pcc@pulmonaryfibrosis.org.
@TheWalterSamuel21
@TheWalterSamuel21 4 года назад
man you had a good run, we all have to die one day. you already beat the odds and apparently you did very well with pf. in your shoes i would not go for transplant, you might be taking a way that chance from a younger person, who could benefit way more from it.
@elcompamartinez2647
@elcompamartinez2647 4 года назад
@@TheWalterSamuel21 THINK WHAT EVER,,,,, BUT I WILL IGNORE YOUR CLASSIST RESPONSE,,,, I WONDER IF YOU, 'D THINK THE SAME IF IT WAS YOUR MOTHER IN MY PLACE 🤔🤔(future comments will be ignored)
@TheWalterSamuel21
@TheWalterSamuel21 4 года назад
@@elcompamartinez2647 If my mother was 70 I think I could live with her passing away, as I said we all have to go, one day. I wonder if you´d think the same thing if i was your son and some 70 year old got a transplant instead of me. checkmate. still best of luck, just my 2 cents.
@mom2tdks2012
@mom2tdks2012 5 лет назад
I have this and scared to death
@pfforg
@pfforg 5 лет назад
Hi Joanne, We understand how overwhelming a diagnosis of PF can be but you are not alone. Please call our Patient Communication Center at 844.825.5733 or email pcc@pulmonaryfibrosis.org.
@sojournerhouse
@sojournerhouse 4 года назад
Me too!
@sojournerhouse
@sojournerhouse 4 года назад
Me too.
@leavethelightsonpleasethec7154
How are you now?
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