Introducing myself

L

Lukesmommy

New member
I've been lurking here for a couple of weeks now. My six week old son has CF. He was diagnosed through newborn screening and genetic testing. As you all know it was a huge blow when we found out, but things are getting better. I love coming to this site and reading what everyone has to say. I would like to think that I am handling the truth pretty well, but at the same time I also have my moments where it feels as though my whole world has crashed around me. It is very inspiring to read everyone's stories, it gives me hope to read about people who have the same mutations as Luke. I feel very fortunate that we found out as early as we did. Well, I'm not sure what else to add at this point but I am very glad I found this site, I really think that I will need it and the support I see that so many people have found here.

-Jen
 
L

Lukesmommy

New member
I've been lurking here for a couple of weeks now. My six week old son has CF. He was diagnosed through newborn screening and genetic testing. As you all know it was a huge blow when we found out, but things are getting better. I love coming to this site and reading what everyone has to say. I would like to think that I am handling the truth pretty well, but at the same time I also have my moments where it feels as though my whole world has crashed around me. It is very inspiring to read everyone's stories, it gives me hope to read about people who have the same mutations as Luke. I feel very fortunate that we found out as early as we did. Well, I'm not sure what else to add at this point but I am very glad I found this site, I really think that I will need it and the support I see that so many people have found here.

-Jen
 
L

Lukesmommy

New member
I've been lurking here for a couple of weeks now. My six week old son has CF. He was diagnosed through newborn screening and genetic testing. As you all know it was a huge blow when we found out, but things are getting better. I love coming to this site and reading what everyone has to say. I would like to think that I am handling the truth pretty well, but at the same time I also have my moments where it feels as though my whole world has crashed around me. It is very inspiring to read everyone's stories, it gives me hope to read about people who have the same mutations as Luke. I feel very fortunate that we found out as early as we did. Well, I'm not sure what else to add at this point but I am very glad I found this site, I really think that I will need it and the support I see that so many people have found here.

-Jen
 
L

Lukesmommy

New member
I've been lurking here for a couple of weeks now. My six week old son has CF. He was diagnosed through newborn screening and genetic testing. As you all know it was a huge blow when we found out, but things are getting better. I love coming to this site and reading what everyone has to say. I would like to think that I am handling the truth pretty well, but at the same time I also have my moments where it feels as though my whole world has crashed around me. It is very inspiring to read everyone's stories, it gives me hope to read about people who have the same mutations as Luke. I feel very fortunate that we found out as early as we did. Well, I'm not sure what else to add at this point but I am very glad I found this site, I really think that I will need it and the support I see that so many people have found here.

-Jen
 
L

Lukesmommy

New member
I've been lurking here for a couple of weeks now. My six week old son has CF. He was diagnosed through newborn screening and genetic testing. As you all know it was a huge blow when we found out, but things are getting better. I love coming to this site and reading what everyone has to say. I would like to think that I am handling the truth pretty well, but at the same time I also have my moments where it feels as though my whole world has crashed around me. It is very inspiring to read everyone's stories, it gives me hope to read about people who have the same mutations as Luke. I feel very fortunate that we found out as early as we did. Well, I'm not sure what else to add at this point but I am very glad I found this site, I really think that I will need it and the support I see that so many people have found here.

-Jen
 
A

AbbysMama

New member
Jen,

Welcome to the site! We're glad that you are here and hopefully will have more to share with you. If you don't mind me asking, what are your son's mutations? That will help folks be able to help you with specific questions you might have and give insight to how things are progressing.

Again, welcome! We're sorry you have to be here, but are delighted that you found us for support. This place is wonderful.

Em
 
A

AbbysMama

New member
Jen,

Welcome to the site! We're glad that you are here and hopefully will have more to share with you. If you don't mind me asking, what are your son's mutations? That will help folks be able to help you with specific questions you might have and give insight to how things are progressing.

Again, welcome! We're sorry you have to be here, but are delighted that you found us for support. This place is wonderful.

Em
 
A

AbbysMama

New member
Jen,

Welcome to the site! We're glad that you are here and hopefully will have more to share with you. If you don't mind me asking, what are your son's mutations? That will help folks be able to help you with specific questions you might have and give insight to how things are progressing.

Again, welcome! We're sorry you have to be here, but are delighted that you found us for support. This place is wonderful.

Em
 
A

AbbysMama

New member
Jen,

Welcome to the site! We're glad that you are here and hopefully will have more to share with you. If you don't mind me asking, what are your son's mutations? That will help folks be able to help you with specific questions you might have and give insight to how things are progressing.

Again, welcome! We're sorry you have to be here, but are delighted that you found us for support. This place is wonderful.

Em
 
A

AbbysMama

New member
Jen,

Welcome to the site! We're glad that you are here and hopefully will have more to share with you. If you don't mind me asking, what are your son's mutations? That will help folks be able to help you with specific questions you might have and give insight to how things are progressing.

Again, welcome! We're sorry you have to be here, but are delighted that you found us for support. This place is wonderful.

Em
 
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