Re: I'm new too !!!!

[Guest guest]

Colleen

i live in Langhorne Bucks County

Pink Joyce IPF 3/06 Pennsylvania

Donate Life Listed 1/09 inactive 4/09

www.transplantfund.org---

Subject: Re: I'm new too !!!!To: Breathe-Support Date: Sunday, April 12, 2009, 5:42 PM

Colleen, Do you mean Springfield Delaware County or Springfield Montgomery count?I live in Montgomery county..Blue Bell near Norristown, but know both Springfields!

Z 65, fibriotic NSIP/05/PA

And “mild†PH/10/07 and Reynaud’s too!!

No, NSIP was not self-inflicted…I never smoked!

Potter, reader,carousel lover and MomMom to Darah and Sara

“I’m gonna be iron like a lion in Zion†Bob Marley

Vinca Minor-periwinkle is my flower

Colleen McCloud wrote:

Hi Kay,

I live in Springfield south of Philadelphia.

From: Beverly Romich <kayromich (AT) yahoo (DOT) com>To: Breathe-Support@ yahoogroups. comSent: Saturday, April 4, 2009 9:02:08 PMSubject: Re: I'm new too !!!!

Hi colleen, I'm new too, I also live in pa. I live close to harrisburg, where are you from?? Kay R.52.ipf.09, PA

From: Colleen McCloud <colleen_mccloud@ yahoo.com>To: Breathe-Support@ yahoogroups. comSent: Saturday, April 4, 2009 9:59:22 AMSubject: Re: I'm new

Sher,

Great to hear from you.. I only use this account on the weekend... WOW!! 430 emails from this group. looks like I have some catching up to do.. Its comforting to read thatI'm not going to die next month. I was diagnosed with PF and a slew of autoimmune and MCD's.. On and off a transplant list.. O2 24/7 than off O2 for almost a year and back on again... Let me muddle through these email I'm sure I"ll learn lots and have many questions.

Colleen

PF 2007 from PA

From: Sher Bauman <bofus (AT) wbcable (DOT) net>To: Breathe-Support@ yahoogroups. comSent: Friday, March 27, 2009 1:17:46 PMSubject: Re: I'm new



Yes Colleen... welcome to our Air Family as Peggy named us.

Check out the files, lots of info there and even photos!

Tell us in what State you live and do you have family to support you?

I'm Sher and I was dx (diagnosed) three years ago and remained stable until lately.

Many here have lived with our disease for 10 years and more so don't be afraid you're going to die next month.

What you call breathlessness we here on the board call short of breath (SOB). And many are on O2, each need it differently in different amounts.

When you write please add your name and State so we can remember who you are.

I'll be watching for your posts.

MamaSher; 70, IPF 3-06, OR. NasturtiumsDon't fret about tomorrow, God is already there!

I'm new

I am 42 and was diagnosed with PF about 2 years ago I’d like to connect with people who know what breathlessness is and learn from them