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Life & Breath Foundation
Home
About Sarcoidosis
Patient Resources
My Life & Breath Sarcoidosis Planner
Living Well
Monthly Webinars
Research Studies
Find a Sarcoidosis Physician
Personal Stories
Sarcoidosis FAQ
Store
Get Involved
How You Can Help
Fundraisers
Support Josh Polito
Birthday Fundraiser
Life & Breath Scholar
About Us
Our Vision
Our Board
Sponsors
In the News
Contact Us
Donate
Home
About Sarcoidosis
Folder: Patient Resources
Back
My Life & Breath Sarcoidosis Planner
Living Well
Monthly Webinars
Research Studies
Find a Sarcoidosis Physician
Personal Stories
Sarcoidosis FAQ
Store
Folder: Get Involved
Back
How You Can Help
Fundraisers
Support Josh Polito
Birthday Fundraiser
Life & Breath Scholar
Folder: About Us
Back
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View fullsize Balancing sarcoidosis and a 9–5 job isn’t easy. Fatigue can hit hard, even after a full night’s rest. And trying to explain flares to your boss or coworkers can leave you feeling misunderstood or judged.

Your energy has limits, and
View fullsize Behind every diagnosis is a story of strength and survival. The quiet courage it takes to face each day, the resilience built from every setback, and the hope that refuses to fade. Your journey matters  and it deserves to be seen, heard, and honored.
View fullsize Every journey with sarcoidosis is personal. There’s no race, no deadline, no “should be better by now.” Healing happens at your own rhythm. Give yourself permission to slow down, rest when needed, and honor where you are today. 

Pr
View fullsize
View fullsize You’re not imagining it. The side effects you feel are real. From prednisone moon face and methotrexate nausea to hair thinning and constant fatigue, living with medication side effects can be exhausting.

Your experience is valid, and you&rsqu
View fullsize Rest is not a setback. It is an essential part of healing. When you live with sarcoidosis or any chronic condition, pushing through exhaustion can do more harm than good. 

Recovery days allow your body to restore balance, reduce inflammation, and pr

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