Jon

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Jon, I feel so lucky and blessed to have met both you and Teri. You are a great couple. I know this stupid disease isn't easy at all for anyone dealing with it. We can only do the best we can each and every day. One thing is for certain, you (we) have a whole group of people behind you (us) supporting you (us) in any way they can. Can't you feel the LOVE? I sure can. Happy New Year. Make 2008 Great! Love, LeanneJON wrote: JoyceYou are

such an inspiration to me. This Disease has really taken its toll on My body and especially my MIND, You seem to let it affect you so little. I truly wish I were that strong. I thought I had it bad until the trip to Chattanooga. I was upset using My 02 on 2 liters pulse. Being on a continous 8 or 10 just blows my mind. Needless to say when I got home from that trip I started taking it to work and said to heck with what people might say. Everyone in Chattanooga was a breath of fresh air and gave me some hope. I would just like to say thank you to all on this site, sometimes words spoken here makes dealing with this a little easier. THANK YOUHAPPY 2008 EVERYONEJon M IPF May 06 > <http://www.smileycentral.com/?partner=ZSzeb001_ZSXXXXXX37> Happy New> Year to all of you. This begins my 11th year

(since biopsy) with the> hateful PF. It begins my third year with all of you. What a blessing> you have been. I pray to the Father, through his precious son, that> this year brings us all health and peace. I love you all.> > Hugs, Joyce D.> PULMONARY FIBROSIS/LUPUS 1997 BRONCHIECTASIS 2004 INDIANA> 2 COR. 12:10 ....when I am weak, then I am strong.> > > > > > > > <http://smiley.smileycentral.com/download/index.jhtml?partner=ZSzeb112_Z\> SXXXXXX37 & utm_id=7920>>

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