Re: 1 year old with CF

[Guest guest]

Hi Sara, my 2 year old, also named Zachery, was just diagnosed 2 weeks ago.

Unlike your Zachary he had no symptoms at birth so I can not help you there.

I am not sure of our Zacks mutations yet. But we did endure 2 years of him

being treated for everything other than what was really wrong with him. It

is a relief to finally be being treated for the true problem.

Welcome to the group. These people really are alot of help.

Christal

Mom of Tristan 6ncf, Zack 2wcf and Ki'a 4monthscf?

[Guest guest]

Hi there, I am glad all is well .It does sure make a difference when the DX

is finally made & you start off with the right things to take & do. Bless

you & all your precious family

LOVE & HUGS, grandmomBEV

Re: 1 year old with CF

Hi Sara, my 2 year old, also named Zachery, was just diagnosed 2 weeks ago.

Unlike your Zachary he had no symptoms at birth so I can not help you there.

I am not sure of our Zacks mutations yet. But we did endure 2 years of him

being treated for everything other than what was really wrong with him. It

is a relief to finally be being treated for the true problem.

Welcome to the group. These people really are alot of help.

Christal

Mom of Tristan 6ncf, Zack 2wcf and Ki'a 4monthscf?

[Guest guest]

In a message dated 3/7/2003 3:14:24 PM Central Standard Time,

dwson2@... writes:

> Sara

You were very smart to get retested. I have two girls with CF and my oldest

was not diagnosed until she was 6 years old. Early detection is the best

because there is so much out there to help our kids. You will learn so much

from this group. We are glad you are here!! Because this is the best place

for information and a great place to vent too. Ask any questions you have

because there are a lot of people on here with years of experience. Where do

you live? Deb A