Designated prayer time for Aubrie

[Guest guest]

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This is a beautiful email from on Cystic-L. If you choose to read, great.

If not, please read this part:

12 NOON DAILY. Please pray/meditate/send good thoughts/whatever you do

for Aubrie. She is recovering from lung transplant and has pneumonia

and is really in need of healing.

This will be most appreciated by Aubrie, her husband, and all

her friends and family.

Love,

Lenora

PS: I don't think it matters what time zone you participate in. If we

all do it in our own zone, it will be like a 4-hour wave of prayer!

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>Date: Tue, 10 Dec 2002 17:31:32 -0500

>Reply-To: Crowe heaven_scent_angel_forever@...>

>Sender: Cystic Fibrosis Discussion CYSTIC-L@...>

>

>Subject: [CYSTIC-L] Designated prayer time for Aubrie

>To: CYSTIC-L@...

>

>What a year its been in the cystic-l community. WE have lost many and yet

>seen many successes in mile stones that the friends on this list have made.

>From weddings to birthdays to even baby showers celebrating the new lives

>of those who had children, one thing is for sure.. The year has been full

>of many changes. As a group we rejoice in our fourtunes and cry when things

>arent doing well along with those who are suffering. Although we cant be

>with them all each in person, somehow we each are affected by one anothers

>lives even though we know one another sometimes only through the medium of

>the internet. One of my favorite things this year was the wonderful

>opportunity I got to share spending time with our famous Grandma Bev. She

>really is an angel here on earth. Its funny how people whom we never met

>face to face can become family members within an instant. I can tell you

>all that if ever given the chance to meet her your life will truly never

>again be the same because the warmness she shares with us each daily online

>pales in comparison to the wonderful woman she truly is in real life. I can

>honestly say that this woman is one of my favorite people in the world, he

>desire and willingness to go the extra mile for someone else makes me yearn

>to become more like her daily with my own life.

>

> So much have I realized how much the group here means to me that I cant

>imagine how my life was before I met each of you. And I think each of us

>feels the same to some extent... When we hear about a transplant we all

>attentively wait for the updates. When someone goes to the prom or gets out

>of the club,or found " the one " as a family we wait for all the details and

>get excited for them.

>

>Right now I feel so strongly about the events plaguing and Aubrie and

>the holiday season. Perhaps it brings back memories for me when we were all

>watching our email boxes about kate and Jims transplant experience.But

>whether you have been touched physically by aubrie and chris's lives or

>like me you watch even though you dont know them please keep them in

>prayer. Even though Ive never met them Im attentively seeking out the

>latest and it reminds me of how us as a group were when Kate was going

>through her transplant story. PErhaps we are so concerned because we face

>the same trials with our own lives, or perhaps its because we personally

>feel connected to them because we share in an illlness that only those

>touched with cf can feel. In showing our support for another friend dealing

>with transplant trials named Aubrie GAhman please join me daily at 12 noon

>for prayer for her, and their families. Although we cant be there

>for them in the physical form, our warm thoughts and prayers can make a

>difference!

>

>Sincerely,

> Crowe

>24pwcf and now praying about full time missions

--

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