CF Calendar

[Guest guest]

HI,

ARE WE TALKING ABOUT THE TOBI CALENDER OR SOMETHING ELSE, WE LOVED OUR TOBI

CALENDER LAST YEAR.

AMY MOM TO NATHAN 2.5 WITH CF

Re: CF Calendar

I Skeffington's mom definitly want at least 1. If the CF Foundation

picks it up, I'll try to get mpre.

Thank you for doing all the hard work, I am sure that it will show your hard

work.

judy ('s mom)

[Guest guest]

In a message dated 10/20/2003 7:58:31 PM Central Daylight Time, bevd@...

writes:

Yes, It is much smaller (kinda the regular size ).They are very pretty . I

didn't take one but they were handing out like flies at the conference.

SOOOOOOOOO ask your clinic to get the rep to bring some for them to pass

out.

If I can get some , I'll post that I have them. it is early for me to get

them BUT the centers should now or soon.

LOVE & HUGS, grandmomBEV

So is anyone on here in the calendar this year? Deb A

[Guest guest]

In a message dated 10/20/2003 8:52:49 PM Central Daylight Time, bevd@...

writes:

I think their are but for the life of me I cant remember who. If they are

reading the posts, maybe they will let us know. There are quite a few

..Smaller pictures, not as much story about them.

LOVE & HUGS< GRDMBEV

Well, I hope they do it is always neat to be able to actually see the people

we have been talking to. I can't wait to see one. Let me know when you get one

or if you have some to said out. Thank Grandma Bev. Deb A

[Guest guest]

I think their are but for the life of me I cant remember who. If they are

reading the posts, maybe they will let us know. There are quite a few

..Smaller pictures, not as much story about them.

LOVE & HUGS< GRDMBEV

Re: CF Calendar

In a message dated 10/20/2003 7:58:31 PM Central Daylight Time,

bevd@...

writes:

Yes, It is much smaller (kinda the regular size ).They are very pretty . I

didn't take one but they were handing out like flies at the conference.

SOOOOOOOOO ask your clinic to get the rep to bring some for them to pass

out.

If I can get some , I'll post that I have them. it is early for me to get

them BUT the centers should now or soon.

LOVE & HUGS, grandmomBEV

So is anyone on here in the calendar this year? Deb A

[Guest guest]

I told everyone I would post to the list as soon as I heard from the

CF Foundation about my calendar. Unfortunately they came up with

several reasons why they did not want to put their logo on the

calendar and endorse it on their website. The main reason they gave

me was they needed a written consent from each person in the

calendar, they did not let me know this until 5 minutes ago and I

turned the calendar in to them 3 weeks ago. I am a little

disappointed but not surprised, they were dragging their feet getting

back to me. Oh well,

Still, I put this thing together and I for one am very proud of it.

I know everyone who is in it or has their child featured in it are

very eager to get their hands on one. I meet with my printer today

and I will give him the " go ahead " with the final print. This means

they should be in my hands in 10 days. I have already received

several e-mails requesting them, but for everyone else who may not

know about the calendar allow me to explain a little.

It is a simple 12 month calendar for 2004 featuring a person with CF

on every month. It has a picture and a caption about each person.

There is some information provided on the calendar about CF to

promote awareness. I printed 1,000 copies and am selling them for

$15 each. I was going to send all of the proceeds to the CFF but now

I am going to collect all the money and divide the grand total to

other smaller foundations. There are several people who have

approached me with very worthwhile causes. ALL of the money will go

to families affected by cf in the form of a scholarship for school,

money to buy medications, or help pay for bills due to hospital

stays. I made this calendar to help make a difference in my

daughters life and the lives of everyone else effected by CF. I

wanted her to know that she is not alone, she is not quite 2 and I

thought a calendar would be an excellent way to show her there are

other people out there just like her, that have to go through some of

the same things she does. We live in a small town and there is no

one else with CF in our community. There has only been 2 children

with cf go through our public school system in the past 15 years, so

I thought this would also be good for raising awareness in

communities like ours.

IF you are interested in recieving a calendar or a couple!! Send a

check or money order to:

402 Yale Street

Mexico, MO 65265

I will keep everyone posted on how sales are doing and how much we

will be able to donate to the different organizations. I know it's a

small step, but every little bit counts (in my eyes at least)

Thanks to all who supported the calendar and to everyone who was in

it or had their child in it. I hope you love it as much as I do!!!

Mom to Princess Madeline 1.5 wcf, and one due May 10th!!

[Guest guest]

,

Will these arrive in time for Christmas? Does the $15 cover postage?

Thanks,

Gale

>

> I told everyone I would post to the list as soon as I heard from

the

> CF Foundation about my calendar. Unfortunately they came up with

> several reasons why they did not want to put their logo on the

> calendar and endorse it on their website. The main reason they

gave

> me was they needed a written consent from each person in the

> calendar, they did not let me know this until 5 minutes ago and I

> turned the calendar in to them 3 weeks ago. I am a little

> disappointed but not surprised, they were dragging their feet

getting

> back to me. Oh well,

> Still, I put this thing together and I for one am very proud of

it.

> I know everyone who is in it or has their child featured in it are

> very eager to get their hands on one. I meet with my printer today

> and I will give him the " go ahead " with the final print. This

means

> they should be in my hands in 10 days. I have already received

> several e-mails requesting them, but for everyone else who may not

> know about the calendar allow me to explain a little.

> It is a simple 12 month calendar for 2004 featuring a person with

CF

> on every month. It has a picture and a caption about each person.

> There is some information provided on the calendar about CF to

> promote awareness. I printed 1,000 copies and am selling them for

> $15 each. I was going to send all of the proceeds to the CFF but

now

> I am going to collect all the money and divide the grand total to

> other smaller foundations. There are several people who have

> approached me with very worthwhile causes. ALL of the money will

go

> to families affected by cf in the form of a scholarship for school,

> money to buy medications, or help pay for bills due to hospital

> stays. I made this calendar to help make a difference in my

> daughters life and the lives of everyone else effected by CF. I

> wanted her to know that she is not alone, she is not quite 2 and I

> thought a calendar would be an excellent way to show her there are

> other people out there just like her, that have to go through some

of

> the same things she does. We live in a small town and there is no

> one else with CF in our community. There has only been 2 children

> with cf go through our public school system in the past 15 years,

so

> I thought this would also be good for raising awareness in

> communities like ours.

> IF you are interested in recieving a calendar or a couple!! Send a

> check or money order to:

>

> 402 Yale Street

> Mexico, MO 65265

>

> I will keep everyone posted on how sales are doing and how much we

> will be able to donate to the different organizations. I know it's

a

> small step, but every little bit counts (in my eyes at least)

> Thanks to all who supported the calendar and to everyone who was in

> it or had their child in it. I hope you love it as much as I do!!!

> Mom to Princess Madeline 1.5 wcf, and one due May

10th!!

[Guest guest]

,

I will send the addresses in the mail, its not important that they get out right

now.

Thanks,

judy