If you or a loved one has been diagnosed with pulmonary sarcoidosis, you must be clear about diagnosis and treatment for the condition. To get the clarity you deserve, you have to become an advocate. That means you’ll also need to know which questions to ask, where to find additional resources, and how to build a community.
Below we’ve created a reference list that may help make your road to advocacy just a bit easier. Questions to Ask Your Doctor
Below we’ve created a reference list that may help make your road to advocacy just a bit easier. Questions to Ask Your Doctor
- How are my lungs impacted by my pulmonary sarcoidosis and how severely are they affected?
- What information did you use to determine that I have pulmonary sarcoidosis?
- What are the symptoms and signs that I should watch for on a day-to-day basis?
- How will you determine whether I require treatment or not for my pulmonary sarcoidosis?
- What are changes I can make with my lifestyle that can help me feel better?
Pulmonary Sarcoidosis Resources:
- Foundation for Sarcoidosis Research
- American Lung Association – Living with Sarcoidosis
- Life & Breath’s Sarcoidosis Planner
- Inova Lung Sarcoidosis Patient Education Handout
- Mount Sinai – Sarcoidosis Program
References
You Might Also Like:
Exercise
5 Heart-Pumping Workouts to Kickstart Your New Year
The new year is often a time for fresh starts and resolutions – start yours with these heart-healthy exercises.
NOWINCLUDED
January 16, 2025
Healthy Eating
Post Holiday Detox Diet and How to Stick to It
A post-holiday detox diet isn’t about punishing yourself or giving up everything you love. It’s about fueling your body with what it needs to feel good again. Learn more.
NOWINCLUDED
January 15, 2025
