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krisgabes

New member
Just joined

Hello, I'm Kristen and I'm new to this site. I am 22 years old and I was diagnosed w/ CF at 4 months old due to failure to thrive. I live in NY and I'm so excited to finally meet others with CF! I'm a social work major and I'm in my senior year of college. I have a wonderful boyfriend who has been by my side for 3 years, and I have the most fantastic supportive family anyone could ask for. I think that about covers it. I'm looking forward to meeting all of you!
 
K

krisgabes

New member
Just joined

Hello, I'm Kristen and I'm new to this site. I am 22 years old and I was diagnosed w/ CF at 4 months old due to failure to thrive. I live in NY and I'm so excited to finally meet others with CF! I'm a social work major and I'm in my senior year of college. I have a wonderful boyfriend who has been by my side for 3 years, and I have the most fantastic supportive family anyone could ask for. I think that about covers it. I'm looking forward to meeting all of you!
 
K

krisgabes

New member
Just joined

Hello, I'm Kristen and I'm new to this site. I am 22 years old and I was diagnosed w/ CF at 4 months old due to failure to thrive. I live in NY and I'm so excited to finally meet others with CF! I'm a social work major and I'm in my senior year of college. I have a wonderful boyfriend who has been by my side for 3 years, and I have the most fantastic supportive family anyone could ask for. I think that about covers it. I'm looking forward to meeting all of you!
 
K

krisgabes

New member
Just joined

Hello, I'm Kristen and I'm new to this site. I am 22 years old and I was diagnosed w/ CF at 4 months old due to failure to thrive. I live in NY and I'm so excited to finally meet others with CF! I'm a social work major and I'm in my senior year of college. I have a wonderful boyfriend who has been by my side for 3 years, and I have the most fantastic supportive family anyone could ask for. I think that about covers it. I'm looking forward to meeting all of you!
 
K

krisgabes

New member
Just joined

Hello, I'm Kristen and I'm new to this site. I am 22 years old and I was diagnosed w/ CF at 4 months old due to failure to thrive. I live in NY and I'm so excited to finally meet others with CF! I'm a social work major and I'm in my senior year of college. I have a wonderful boyfriend who has been by my side for 3 years, and I have the most fantastic supportive family anyone could ask for. I think that about covers it. I'm looking forward to meeting all of you!
 
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GirlyGirl

New member
Hello All

Please forgive me if I have post incorrectly....still learning.

I am a partner of someone living with cf. We have a son together.
We are African American and I am seeking other African American or minority individuals with cf.
I see that this community seems to have a good bit of members and was just hoping to connect.

I have read some of the post and have learned a little more already. Up until 4 years ago I never heard of CF. But today at the hospital I surprised myself at the ability to speak to the various staff members about my partner's condition with ease! (My partner is currently in the hospital, doing ok)

Looking to connect
Girly Girl
 
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GirlyGirl

New member
Hello All

Please forgive me if I have post incorrectly....still learning.

I am a partner of someone living with cf. We have a son together.
We are African American and I am seeking other African American or minority individuals with cf.
I see that this community seems to have a good bit of members and was just hoping to connect.

I have read some of the post and have learned a little more already. Up until 4 years ago I never heard of CF. But today at the hospital I surprised myself at the ability to speak to the various staff members about my partner's condition with ease! (My partner is currently in the hospital, doing ok)

Looking to connect
Girly Girl
 
G

GirlyGirl

New member
Hello All

Please forgive me if I have post incorrectly....still learning.

I am a partner of someone living with cf. We have a son together.
We are African American and I am seeking other African American or minority individuals with cf.
I see that this community seems to have a good bit of members and was just hoping to connect.

I have read some of the post and have learned a little more already. Up until 4 years ago I never heard of CF. But today at the hospital I surprised myself at the ability to speak to the various staff members about my partner's condition with ease! (My partner is currently in the hospital, doing ok)

Looking to connect
Girly Girl
 
G

GirlyGirl

New member
Hello All

Please forgive me if I have post incorrectly....still learning.

I am a partner of someone living with cf. We have a son together.
We are African American and I am seeking other African American or minority individuals with cf.
I see that this community seems to have a good bit of members and was just hoping to connect.

I have read some of the post and have learned a little more already. Up until 4 years ago I never heard of CF. But today at the hospital I surprised myself at the ability to speak to the various staff members about my partner's condition with ease! (My partner is currently in the hospital, doing ok)

Looking to connect
Girly Girl
 
G

GirlyGirl

New member
Hello All

Please forgive me if I have post incorrectly....still learning.

I am a partner of someone living with cf. We have a son together.
We are African American and I am seeking other African American or minority individuals with cf.
I see that this community seems to have a good bit of members and was just hoping to connect.

I have read some of the post and have learned a little more already. Up until 4 years ago I never heard of CF. But today at the hospital I surprised myself at the ability to speak to the various staff members about my partner's condition with ease! (My partner is currently in the hospital, doing ok)

Looking to connect
Girly Girl
 
S

Sevenstars

New member
Oh, that is interesting. As you may know by now, there are very few African Americans that have CF - just not in the gene pool really. I did meet two girls at my Children's Hospital here many years ago (in Pittsburgh), twins, and they both had CF. I wonder how they are doing today. Anyway, welcome to the site. <img src="i/expressions/face-icon-small-smile.gif" border="0"> I hope your partner's stay goes well.
 
S

Sevenstars

New member
Oh, that is interesting. As you may know by now, there are very few African Americans that have CF - just not in the gene pool really. I did meet two girls at my Children's Hospital here many years ago (in Pittsburgh), twins, and they both had CF. I wonder how they are doing today. Anyway, welcome to the site. <img src="i/expressions/face-icon-small-smile.gif" border="0"> I hope your partner's stay goes well.
 
S

Sevenstars

New member
Oh, that is interesting. As you may know by now, there are very few African Americans that have CF - just not in the gene pool really. I did meet two girls at my Children's Hospital here many years ago (in Pittsburgh), twins, and they both had CF. I wonder how they are doing today. Anyway, welcome to the site. <img src="i/expressions/face-icon-small-smile.gif" border="0"> I hope your partner's stay goes well.
 
S

Sevenstars

New member
Oh, that is interesting. As you may know by now, there are very few African Americans that have CF - just not in the gene pool really. I did meet two girls at my Children's Hospital here many years ago (in Pittsburgh), twins, and they both had CF. I wonder how they are doing today. Anyway, welcome to the site. <img src="i/expressions/face-icon-small-smile.gif" border="0"> I hope your partner's stay goes well.
 
S

Sevenstars

New member
Oh, that is interesting. As you may know by now, there are very few African Americans that have CF - just not in the gene pool really. I did meet two girls at my Children's Hospital here many years ago (in Pittsburgh), twins, and they both had CF. I wonder how they are doing today. Anyway, welcome to the site. <img src="i/expressions/face-icon-small-smile.gif" border="0"> I hope your partner's stay goes well.
 
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