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Pulmonary Fibrosis Support Group
A community of patients, family members and friends dedicated to dealing with Pulmonary Fibrosis, together.
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08/07/2010 01:50 PM
MAEMAE

HELLO THERE!!!

I am a new member and not too sure how this all works. I have been given the diagnosis of IPF. I found out 2 years ago. It is a scary situation and an unsure one. This summer is being especially difficult because of the heat and humidity. I live in Louisiana, so that should let you know how bad the heat etc. is. Smile Anyway, HELLO to everyone and I am hoping I can manage to use this site for communication with you all.

BLESSINGS, JACKIE Smile

Reply

08/07/2010 11:36 PM  Top
tony36
tony36
 
Posts: 1319
Group Leader
I'm an Advocate

Hi Jackie and welcome to our group. I am so sorry that you have to deal with IPF. It is not a pleasant disease and as you say the heat and humidity this year adds to your troubles. Are you on Oxygen?

Keep in touch,

Tony

Tony 36 Cared for Brid, my wife.
(Note: I speak as a carer. Please do not take anything I say as medical advice. I am not a doctor).

Previous discussions I participated in:
Hi and thanks in advance
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