You are using an out of date browser. It may not display this or other websites correctly.
You should upgrade or use an alternative browser.
You should upgrade or use an alternative browser.
Emma's CaringBridge Website
- Thread starter MargaritaChic
- Start date
M
mneville
Guest
I took our son Aidan out to U of M when Dr Warwick was there. It is a great center. Our son was diagnosed through newborn screen as well at 8 days old. Total shock just like you. He is three and a half now and amazing!!
I am finally going to make a caringbridge site for him. Enjoy your little girl and give yourselves time to adjust. I was like you- researching everything, talking to every person associated with CF, calling all over. I won't lie. I still do it to an extent, anything to get the best for our little guy. It sounds like you are off to a great start.
Megan,mom to Aidan 3 W/CF and Gavin, 7 months NO CF
I am finally going to make a caringbridge site for him. Enjoy your little girl and give yourselves time to adjust. I was like you- researching everything, talking to every person associated with CF, calling all over. I won't lie. I still do it to an extent, anything to get the best for our little guy. It sounds like you are off to a great start.
Megan,mom to Aidan 3 W/CF and Gavin, 7 months NO CF
M
mneville
Guest
I took our son Aidan out to U of M when Dr Warwick was there. It is a great center. Our son was diagnosed through newborn screen as well at 8 days old. Total shock just like you. He is three and a half now and amazing!!
I am finally going to make a caringbridge site for him. Enjoy your little girl and give yourselves time to adjust. I was like you- researching everything, talking to every person associated with CF, calling all over. I won't lie. I still do it to an extent, anything to get the best for our little guy. It sounds like you are off to a great start.
Megan,mom to Aidan 3 W/CF and Gavin, 7 months NO CF
I am finally going to make a caringbridge site for him. Enjoy your little girl and give yourselves time to adjust. I was like you- researching everything, talking to every person associated with CF, calling all over. I won't lie. I still do it to an extent, anything to get the best for our little guy. It sounds like you are off to a great start.
Megan,mom to Aidan 3 W/CF and Gavin, 7 months NO CF
M
mneville
Guest
I took our son Aidan out to U of M when Dr Warwick was there. It is a great center. Our son was diagnosed through newborn screen as well at 8 days old. Total shock just like you. He is three and a half now and amazing!!
I am finally going to make a caringbridge site for him. Enjoy your little girl and give yourselves time to adjust. I was like you- researching everything, talking to every person associated with CF, calling all over. I won't lie. I still do it to an extent, anything to get the best for our little guy. It sounds like you are off to a great start.
Megan,mom to Aidan 3 W/CF and Gavin, 7 months NO CF
I am finally going to make a caringbridge site for him. Enjoy your little girl and give yourselves time to adjust. I was like you- researching everything, talking to every person associated with CF, calling all over. I won't lie. I still do it to an extent, anything to get the best for our little guy. It sounds like you are off to a great start.
Megan,mom to Aidan 3 W/CF and Gavin, 7 months NO CF
M
mneville
Guest
I took our son Aidan out to U of M when Dr Warwick was there. It is a great center. Our son was diagnosed through newborn screen as well at 8 days old. Total shock just like you. He is three and a half now and amazing!!
I am finally going to make a caringbridge site for him. Enjoy your little girl and give yourselves time to adjust. I was like you- researching everything, talking to every person associated with CF, calling all over. I won't lie. I still do it to an extent, anything to get the best for our little guy. It sounds like you are off to a great start.
Megan,mom to Aidan 3 W/CF and Gavin, 7 months NO CF
I am finally going to make a caringbridge site for him. Enjoy your little girl and give yourselves time to adjust. I was like you- researching everything, talking to every person associated with CF, calling all over. I won't lie. I still do it to an extent, anything to get the best for our little guy. It sounds like you are off to a great start.
Megan,mom to Aidan 3 W/CF and Gavin, 7 months NO CF
M
mneville
Guest
I took our son Aidan out to U of M when Dr Warwick was there. It is a great center. Our son was diagnosed through newborn screen as well at 8 days old. Total shock just like you. He is three and a half now and amazing!!
I am finally going to make a caringbridge site for him. Enjoy your little girl and give yourselves time to adjust. I was like you- researching everything, talking to every person associated with CF, calling all over. I won't lie. I still do it to an extent, anything to get the best for our little guy. It sounds like you are off to a great start.
Megan,mom to Aidan 3 W/CF and Gavin, 7 months NO CF
I am finally going to make a caringbridge site for him. Enjoy your little girl and give yourselves time to adjust. I was like you- researching everything, talking to every person associated with CF, calling all over. I won't lie. I still do it to an extent, anything to get the best for our little guy. It sounds like you are off to a great start.
Megan,mom to Aidan 3 W/CF and Gavin, 7 months NO CF