CFers over 40

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LMG453

New member
I'm curious to know how many Cfer's there are over 40 on this website. Also, if you could share at what age you were diagnosed and what your PFT's are.  My husband is 43. He was diagnosed at 9 months. His PFT's are 54.
 
L

LMG453

New member
I'm curious to know how many Cfer's there are over 40 on this website. Also, if you could share at what age you were diagnosed and what your PFT's are. My husband is 43. He was diagnosed at 9 months. His PFT's are 54.
 
L

LMG453

New member
I'm curious to know how many Cfer's there are over 40 on this website. Also, if you could share at what age you were diagnosed and what your PFT's are. My husband is 43. He was diagnosed at 9 months. His PFT's are 54.<BR>
 
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lizlas

Guest
<P>Hi:</P>
<P> </P>
<P>Im 51...diagnosed with CF 45 (in 2005)...FEV currently 96%.....</P>
<P> </P>
<P>DF508</P>
<P> </P>
<P> </P>
<P> </P>
 
L

lizlas

Guest
<P>Hi:</P>
<P></P>
<P>Im 51...diagnosed with CF 45 (in 2005)...FEV currently 96%.....</P>
<P></P>
<P>DF508</P>
<P></P>
<P></P>
<P></P>
 
L

lizlas

Guest
<P><BR>Hi:</P>
<P></P>
<P>Im 51...diagnosed with CF 45 (in 2005)...FEV currently 96%.....</P>
<P></P>
<P>DF508</P>
<P></P>
<P></P>
<P></P>
 
I

Icklerose

New member
I am 45 years old, live in Scotland with my Husband. I was diagnosed at 6 weeks old, I am pancreatic sufficient, my genotype is Delta F508 and A455E and i am also a mum of 1 son aged 24 <img src="i/expressions/face-icon-small-smile.gif" border="0">
 
I

Icklerose

New member
I am 45 years old, live in Scotland with my Husband. I was diagnosed at 6 weeks old, I am pancreatic sufficient, my genotype is Delta F508 and A455E and i am also a mum of 1 son aged 24 <img src="i/expressions/face-icon-small-smile.gif" border="0">
 
I

Icklerose

New member
I am 45 years old, live in Scotland with my Husband. I was diagnosed at 6 weeks old, I am pancreatic sufficient, my genotype is Delta F508 and A455E and i am also a mum of 1 son aged 24 <img src="i/expressions/face-icon-small-smile.gif" border="0">
 
A

azdesertrat

New member
Hello!
I'm 47, diagnosed at birth.
According to the CF Foundation I don't matter any more because I got so bad I needed a double-lung transplant. I received my miracle on June 16, '05.
While my trans didn't go as well as we wanted I am still alive & kickin'...
I've had quite a few complications including losing a bit more than half of my right donated lung.
That was on Oct. 19 '09.
I've done pretty good since then, other than quarterly bouts with pseudomonas.
All our best to you & yours, 'Pat'.
 
A

azdesertrat

New member
Hello!
I'm 47, diagnosed at birth.
According to the CF Foundation I don't matter any more because I got so bad I needed a double-lung transplant. I received my miracle on June 16, '05.
While my trans didn't go as well as we wanted I am still alive & kickin'...
I've had quite a few complications including losing a bit more than half of my right donated lung.
That was on Oct. 19 '09.
I've done pretty good since then, other than quarterly bouts with pseudomonas.
All our best to you & yours, 'Pat'.
 
A

azdesertrat

New member
Hello!
<br />I'm 47, diagnosed at birth.
<br />According to the CF Foundation I don't matter any more because I got so bad I needed a double-lung transplant. I received my miracle on June 16, '05.
<br />While my trans didn't go as well as we wanted I am still alive & kickin'...
<br />I've had quite a few complications including losing a bit more than half of my right donated lung.
<br />That was on Oct. 19 '09.
<br />I've done pretty good since then, other than quarterly bouts with pseudomonas.
<br />All our best to you & yours, 'Pat'.
 
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