Re: Happy Anniversary to us....

[Guest guest]

Leanne, I cannot imagine what my life would be like without the wonderful support of people on this board. I am so lucky to have found this support and plenty of life-long friends. The trips have been awesome!

I almost joined here in 2004 right before I had ARDs but I didn't until 2007. I found some notes where I had written down some info about NAC and some other info. I had even downloaded the info book on the compuiter and made it an icon on the desktop. I think it is still on Eddie's computer. Maybe he saw it when I was hospitalized for so long. After my dad passed away in Sept. 2006 of UIP/IPF, I know I came back on the computer and was looking around and I clicked on the icon that I had downloaded in June of 2004,

I am glad that I am here and I am glad that everyone is here that needs to be here.

Toodles!

Jane UIP/IPF 12/1998 Dalton, Georgia aka pianolady_musicgirl>> Hello all,> > Today is our anniversary. The Online Breathe Support Group started four years ago today.....we've come a long way babies! > > I'm glad that people are finding this forum helpful in dealing with this disease. I know that I personally have made life-long friends and I can't imagine what it would be like without them walking this walk with me. We are in this fight together. > > I'm sorry that I don't post as often as I would like to but still try to keep in touch and read the posts. > > Welcome to all the newbies...this is a great, great group of people who will help you with your questions and concerns because as we are fond of saying "we get it". There are a few of us who have been on the board pretty much since inception. > > This is our board. If you have any ideas or tips you'd like to share in how we can improve and be better, please feel free to contact me @ lstorch@... > > A special thanks to Beth who is the Moderator Extraordinaire...she devotes a lot of time and care to this board and I know she considers this group her/our air family. > > God bless you all and thank you for all the support I personally have received and the information that I have learned about pulmonary fibrosis. We learn most from each other because we are walking the walk daily.> > Leanne Storch - uip diagnosed 1/03> Executive Director of the Pulmonary Fibrosis Foundation> Owner Breathe Support Groups>