A Catamenial Pneumothorax anonymous support group with information on diagnosis, treatment, symptoms, along with personal stories and experiences with Catamenial Pneumothorax. You're not alone.
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Members Sharing the Experience "I Have Catamenial Pneumothorax"
5 Members
Related Groups to "I Have Catamenial Pneumothorax"
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This Experience at a Glance
Story highlights
These snippets show some of the most common themes mentioned in this experience's stories:
These snippets show some of the most common themes mentioned in this experience's stories:
- "After a chest tube was inserted and didn't repair the problem, they did a procedure called pleurodesis..."
- "I am desperately searching for help and answers to stop this before it happens again..."
- "Five days after returning home I was readmitted to the hospital with a double pnemothorax and fluid..."
And the Story Awards Go to...
Most Popular: I Have Catamenial Pneumothorax
Most Recent: I Have Catamenial Pneumothorax
Statistics:
40% of people who have this experience are in their forties, 40% are in their thirties, and 20% are in their teens.
You may cite any I Have Catamenial Pneumothorax statistics, provided you link back to this page
Check out this group's What Is It Like To Have Catamenial Pneumothorax guide, where people with this experience share their tips and hints.
Members said this page is also related to:
Do You Have Catamenial Pneumothorax? , What is it like to Have Catamenial Pneumothorax? ,Have Catamenial Pneumothorax personal stories, Have Catamenial Pneumothorax personal experiences
Other experience groups that have been combined into this group include: None yet.
Other experience groups that have been combined into this group include: None yet.
This is an experience group where everyone says: I Have Catamenial Pneumothorax. It features support, personal stories and experiences, advice, chat, talk, forums, videos, pictures and resources from real people, just like you.
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