Comments on: Every time I mention cystic fibrosis, take a shot. http://thespohrsaremultiplying.com/doctor-schmoctor/every-time-i-mention-cystic-fibrosis/ Thu, 09 Feb 2012 09:41:27 +0000 hourly 1 http://wordpress.org/?v=3.3.1 By: Memphislis http://thespohrsaremultiplying.com/doctor-schmoctor/every-time-i-mention-cystic-fibrosis/#comment-192 Memphislis Wed, 30 Apr 2008 01:33:00 +0000 http://thespohrsaremultiplying.com/?p=183#comment-192 Well I (obviously) couldn't see the picture when I left you the earlier comment. Man, you can tell how tiny Maddie is with the perspective of her seat. What a doll. Well I (obviously) couldn’t see the picture when I left you the earlier comment. Man, you can tell how tiny Maddie is with the perspective of her seat. What a doll.

]]> By: Gemini Girl http://thespohrsaremultiplying.com/doctor-schmoctor/every-time-i-mention-cystic-fibrosis/#comment-191 Gemini Girl Tue, 29 Apr 2008 13:27:00 +0000 http://thespohrsaremultiplying.com/?p=183#comment-191 Keeping my fingers crossed!<br/><br/>They tested neve twice for CF. First in the NICU, then when she had already been discharged. I doubt maddie has it since you are not a carrier. I def feel like i understand how pissed off you are about always being asked- since cf is quite the scare. <br/><br/>so glad she is doing well and is laughing! I want to mush her! Keeping my fingers crossed!

They tested neve twice for CF. First in the NICU, then when she had already been discharged. I doubt maddie has it since you are not a carrier. I def feel like i understand how pissed off you are about always being asked- since cf is quite the scare.

so glad she is doing well and is laughing! I want to mush her!

]]> By: Kristin.... http://thespohrsaremultiplying.com/doctor-schmoctor/every-time-i-mention-cystic-fibrosis/#comment-190 Kristin.... Tue, 29 Apr 2008 11:51:00 +0000 http://thespohrsaremultiplying.com/?p=183#comment-190 I don't know how she manages to get cuter each day, but she does! We're keeping our fingers crossed for good news today. I don’t know how she manages to get cuter each day, but she does! We’re keeping our fingers crossed for good news today.

]]> By: Memphislis http://thespohrsaremultiplying.com/doctor-schmoctor/every-time-i-mention-cystic-fibrosis/#comment-189 Memphislis Tue, 29 Apr 2008 11:34:00 +0000 http://thespohrsaremultiplying.com/?p=183#comment-189 I know how you feel about the CF tests. My best friend's daughter (now 8 1/2) was tested and tested as a baby, each time with a negative result. Turns out, she is extremely allergic to milk AND soy products, and the CF symptoms she was having were a reaction to the formulas. You guys are still in our prayers each day. When do we get a picture of Maddie in her Bumbo? I know how you feel about the CF tests. My best friend’s daughter (now 8 1/2) was tested and tested as a baby, each time with a negative result. Turns out, she is extremely allergic to milk AND soy products, and the CF symptoms she was having were a reaction to the formulas. You guys are still in our prayers each day. When do we get a picture of Maddie in her Bumbo?

]]> By: Bec http://thespohrsaremultiplying.com/doctor-schmoctor/every-time-i-mention-cystic-fibrosis/#comment-188 Bec Tue, 29 Apr 2008 08:54:00 +0000 http://thespohrsaremultiplying.com/?p=183#comment-188 She's such a cutie pie!<br/><br/>I can't imagine how frustrating it must be for you to have to deal with the CF thing over and over like this. They seem determined to chew up money for unnecessary tests don't they?<br/><br/>I hope the scan goes well. She’s such a cutie pie!

I can’t imagine how frustrating it must be for you to have to deal with the CF thing over and over like this. They seem determined to chew up money for unnecessary tests don’t they?

I hope the scan goes well.

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