Jamie Lederer @JamieLedererNP
ILD Nurse Practitioner. Wife. Mom of two. Philadelphia sports lover. Former ICU Nurse. tweets are my own Joined November 2019-
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September is pulmonary fibrosis awareness month. As the month kicks off I can’t help but take time to think about the many patients and their family members I have had the privilege to work with over the last 8 years working in this specialty. #pfmonth
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There’s still time to join us today at 1 pm. register at us02web.zoom.us/webinar/regist…
If you work with patients who have advanced lung disease take some time to listen to the new episode of the @ats Breathe Easy Podcast with guest @CAJonesMD. He shares some great info and approaches to palliative care and hospice for patients breatheeasy.transistor.fm/episodes/lever…
This Philly girl is one hundred percent a Philadelphia Eagles fan (the rest of our ILD & Sarcoid team can attest to this)…but it is pretty awesome to see that Houston Texan Tavierre Thomas will be wearing @StopSarcoidosis cleats for @NFL #MyCauseMyCleats
Congrats and welcome! Come join us in ILD clinic….it’s the best clinic.
Congrats and welcome! Come join us in ILD clinic….it’s the best clinic.
We are kicking off the @PFFORG 2023 summit with our Nurse and Allied Health session. #pff #pulmonaryfibrosis #pffsummit #ild
Imagine an oxygen company telling you they can not give you oxygen supplies so you can leave your home…this happens to my patients. Please ask your congressional leaders to pass supplemental oxygen reform. Visit this link to send a message to Congress. a.lung.org/eoZrWsZ
Do you see patients with cough or shortness of breath? Please take a moment and check out this video - you may come across a patient with #ILD …@ThreeLakes_TLF and @accpchest want you to have the tools to recognize this rare diagnosis youtube.com/watch?v=kAmlfX…
Do you see patients with cough or shortness of breath? Please take a moment and check out this video - you may come across a patient with #ILD …@ThreeLakes_TLF and @accpchest want you to have the tools to recognize this rare diagnosis youtube.com/watch?v=kAmlfX…
Jamie Lederer retweeted
We’ve joined 23 other patient, professional, and industry groups to demand changes for how oxygen is provided. We know that access remains a huge issue, and that’s why we’re petitioning Congress. Read our latest blog post and sign the petition: ow.ly/1z2i50N2z9f
Jamie Lederer retweeted
A group photo of the attendees of the first-ever Pulmonary Fibrosis Stakeholder Summit at the end of the first session! And the presentations and discussions were great! Thanks to all sponsors @nih_nhlbi, @ThreeLakes_TLF @PFFORG! #CurePF #ScienceMatters #PFStakeHolderSummit2022
So excited to spend virtual time with so many amazing #pulmonaryfibrosis researchers and providers today and tomorrow. What a privilege to be a part of the #PFStakeHolderSummit2022
So excited to spend virtual time with so many amazing #pulmonaryfibrosis researchers and providers today and tomorrow. What a privilege to be a part of the #PFStakeHolderSummit2022
What a great resource for our patients on oxygen! @PennPulmonary 👀
What a great resource for our patients on oxygen! @PennPulmonary 👀
Jamie Lederer retweeted
No one has to live with pulmonary fibrosis alone. The PFF has a network of 150+ support groups across the U.S. that you can join today. Joining a support group can boost your mental health and help you learn about living with this disease. Visit www. pulmonaryfibrosis.org/supportgroups
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