Happy Anniversary to us....

[Guest guest]

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

[Guest guest]

Leanne... thanks to you for being here for us. I can only guess the amount of time you must put in for the board's behalf.

I'm sure grateful I found you the same day I was dx! Online is not a good way to find out I have a fatal disease but finding the board next, was indeed a good thing.

God Bless you!

MamaSher; 71, IPF 3-2006, OR.Don't fret about tomorrow, God is already there!

Happy Anniversary to us....

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 (AT) pulmonaryfibrosis (DOT) org. 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 1/03Executive Director of the Pulmonary Fibrosis FoundationOwner Breathe Support Groups

[Guest guest]

Happy Anniversary to USSSS.. THANK YOU OUR WONDERFUL LEADER.. I think I said this every year but AGAIN how wonderful I think-- know you are to have thought about all we lost hurting people with this disease. You have indeed created our Air Family.We all owe you so much from our hearts for bringing us together, sharing information with us.. you are SUPER. I honestly love you so much. Love & Prayers, Peggy Florida, IPF/UIP 2004"I believe that friends are quiet angels who lift us to our feet, when our wings have trouble remembering how to fly." 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 (AT) pulmonaryfibrosis (DOT) org. 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

[Guest guest]

To US!

This Forum has been important to us in so many ways & as a 'Global' member I feel very grateful that it fills a HUGE void to for of us living in countries where resources are scant & scattered.

Special TA to Leanne & Beth! Know that your efforts are deeply appreciated!

To my much loved Air Family...you make my journey all the better for being so openly shared. My family thanks you too 'cos it means I don't bend their ears nearly so much!

in Oz

>> 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>

[Guest guest]

,

Your words echo what I wish I had thought o say - I second 's comments to our Forum

and a special thanks again to Leanne & Beth -

Dorothy Reinecke Fayetteville, GA

66 - DX VATS 7/05 - UIP 7/05

From: Breathe-Support [mailto:Breathe-Support ] On Behalf Of grangi49Sent: Saturday, November 07, 2009 8:58 PMTo: Breathe-Support Subject: Re: Happy Anniversary to us....

To US!

This Forum has been important to us in so many ways & as a 'Global' member I feel very grateful that it fills a HUGE void to for of us living in countries where resources are scant & scattered.

Special TA to Leanne & Beth! Know that your efforts are deeply appreciated!

To my much loved Air Family...you make my journey all the better for being so openly shared. My family thanks you too 'cos it means I don't bend their ears nearly so much!

in Oz

>> 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>

[Guest guest]

What would we do without out this board. Leanne and Beth Thank You both so much. Marcia

[Guest guest]

ditto

Pink Joyce R (IPF 3/06) IFA 5/09 Pennsylvania

Donate Life Listed 1/09 Inactive 4/09

www.transplantfund.org---

Subject: Re: Happy Anniversary to us....To: Breathe-Support Date: Sunday, November 8, 2009, 3:18 AM

What would we do without out this board. Leanne and Beth Thank You both so much. Marcia

[Guest guest]

I joined on 17th oct 2007.

So happy 2nd Anniversary to me!

Thank you all and Beth and Leanne for this wonderful group.

Geeta

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> Subject: Re: Happy Anniversary to us....

> To: Breathe-Support

> Date: Sunday, November 8, 2009, 3:18 AM

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> What would we do without out this board. Leanne and Beth Thank You both

so much.   Marcia

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