New to the CF club: DX at 43...

A

Aspiemom

Guest
Wow, I was dx at age 43 at JH, also! Do you see Dr. B? I LOVED him! <img src="i/expressions/heart.gif" border="0">(We moved to GA in early 2007 and I miss him and his staff terribly!). My nurse there told me that as a late dx I am going to have to change my thinkings on things. Growing up not knowing about the CF, I hadn't been proactive about my health and there was so much I didn't know about, that early dx know, so S. would try to get things in to my thick head that things would not be like they'd always been.

I was dx w/ bronchiectisis at age 28, too. When I finally got the CF dx so much made sense to me. I had Pulmonary Dr. Sonye D. at JH before the dx and she was wonderful and very compassionate when she broke the news and explained the basics to me. She kept asking me "Are you OK? Are you going to be alright?" because I felt such shock to find out I had something so severe and HAD HAD IT ALL ALONG. She had basically rendered me speechless. But I told her the RELIEF was so nice and I was grateful for the dx so we knew what we were dealing with after all of those years.

Emotionally, it's very hard to come to terms with. Sometimes I've gotten upset at all of the drs. who mis-treated me, missed the dx, who probably made things worse for me now. But the others questions I don't do. You can't change things in the past, so I don't bother myself with whatifs and make myself crazy.

One of the hardest things for me to deal with, with the late dx, is my husband didn't know this when he married me and I've had the idea ever since the dx that he wouldn't have married me. This wasn't what he bargained for and he seems resentful of the financial burden and the many things I can't do. He won't admit it, but I certainly get that feeling and it hurts. So many on here, their husbands KNEW what they were getting into and still did it, which really spells out l-o-v-e for me.

So, <i>do you see Dr. B? Isn't he WONDERFUL</i>!!!!!!?????
 
A

Aspiemom

Guest
Wow, I was dx at age 43 at JH, also! Do you see Dr. B? I LOVED him! <img src="i/expressions/heart.gif" border="0">(We moved to GA in early 2007 and I miss him and his staff terribly!). My nurse there told me that as a late dx I am going to have to change my thinkings on things. Growing up not knowing about the CF, I hadn't been proactive about my health and there was so much I didn't know about, that early dx know, so S. would try to get things in to my thick head that things would not be like they'd always been.

I was dx w/ bronchiectisis at age 28, too. When I finally got the CF dx so much made sense to me. I had Pulmonary Dr. Sonye D. at JH before the dx and she was wonderful and very compassionate when she broke the news and explained the basics to me. She kept asking me "Are you OK? Are you going to be alright?" because I felt such shock to find out I had something so severe and HAD HAD IT ALL ALONG. She had basically rendered me speechless. But I told her the RELIEF was so nice and I was grateful for the dx so we knew what we were dealing with after all of those years.

Emotionally, it's very hard to come to terms with. Sometimes I've gotten upset at all of the drs. who mis-treated me, missed the dx, who probably made things worse for me now. But the others questions I don't do. You can't change things in the past, so I don't bother myself with whatifs and make myself crazy.

One of the hardest things for me to deal with, with the late dx, is my husband didn't know this when he married me and I've had the idea ever since the dx that he wouldn't have married me. This wasn't what he bargained for and he seems resentful of the financial burden and the many things I can't do. He won't admit it, but I certainly get that feeling and it hurts. So many on here, their husbands KNEW what they were getting into and still did it, which really spells out l-o-v-e for me.

So, <i>do you see Dr. B? Isn't he WONDERFUL</i>!!!!!!?????
 
A

Aspiemom

Guest
Wow, I was dx at age 43 at JH, also! Do you see Dr. B? I LOVED him! <img src="i/expressions/heart.gif" border="0">(We moved to GA in early 2007 and I miss him and his staff terribly!). My nurse there told me that as a late dx I am going to have to change my thinkings on things. Growing up not knowing about the CF, I hadn't been proactive about my health and there was so much I didn't know about, that early dx know, so S. would try to get things in to my thick head that things would not be like they'd always been.

I was dx w/ bronchiectisis at age 28, too. When I finally got the CF dx so much made sense to me. I had Pulmonary Dr. Sonye D. at JH before the dx and she was wonderful and very compassionate when she broke the news and explained the basics to me. She kept asking me "Are you OK? Are you going to be alright?" because I felt such shock to find out I had something so severe and HAD HAD IT ALL ALONG. She had basically rendered me speechless. But I told her the RELIEF was so nice and I was grateful for the dx so we knew what we were dealing with after all of those years.

Emotionally, it's very hard to come to terms with. Sometimes I've gotten upset at all of the drs. who mis-treated me, missed the dx, who probably made things worse for me now. But the others questions I don't do. You can't change things in the past, so I don't bother myself with whatifs and make myself crazy.

One of the hardest things for me to deal with, with the late dx, is my husband didn't know this when he married me and I've had the idea ever since the dx that he wouldn't have married me. This wasn't what he bargained for and he seems resentful of the financial burden and the many things I can't do. He won't admit it, but I certainly get that feeling and it hurts. So many on here, their husbands KNEW what they were getting into and still did it, which really spells out l-o-v-e for me.

So, <i>do you see Dr. B? Isn't he WONDERFUL</i>!!!!!!?????
 
A

Aspiemom

Guest
Wow, I was dx at age 43 at JH, also! Do you see Dr. B? I LOVED him! <img src="i/expressions/heart.gif" border="0">(We moved to GA in early 2007 and I miss him and his staff terribly!). My nurse there told me that as a late dx I am going to have to change my thinkings on things. Growing up not knowing about the CF, I hadn't been proactive about my health and there was so much I didn't know about, that early dx know, so S. would try to get things in to my thick head that things would not be like they'd always been.

I was dx w/ bronchiectisis at age 28, too. When I finally got the CF dx so much made sense to me. I had Pulmonary Dr. Sonye D. at JH before the dx and she was wonderful and very compassionate when she broke the news and explained the basics to me. She kept asking me "Are you OK? Are you going to be alright?" because I felt such shock to find out I had something so severe and HAD HAD IT ALL ALONG. She had basically rendered me speechless. But I told her the RELIEF was so nice and I was grateful for the dx so we knew what we were dealing with after all of those years.

Emotionally, it's very hard to come to terms with. Sometimes I've gotten upset at all of the drs. who mis-treated me, missed the dx, who probably made things worse for me now. But the others questions I don't do. You can't change things in the past, so I don't bother myself with whatifs and make myself crazy.

One of the hardest things for me to deal with, with the late dx, is my husband didn't know this when he married me and I've had the idea ever since the dx that he wouldn't have married me. This wasn't what he bargained for and he seems resentful of the financial burden and the many things I can't do. He won't admit it, but I certainly get that feeling and it hurts. So many on here, their husbands KNEW what they were getting into and still did it, which really spells out l-o-v-e for me.

So, <i>do you see Dr. B? Isn't he WONDERFUL</i>!!!!!!?????
 
A

Aspiemom

Guest
Wow, I was dx at age 43 at JH, also! Do you see Dr. B? I LOVED him! <img src="i/expressions/heart.gif" border="0">(We moved to GA in early 2007 and I miss him and his staff terribly!). My nurse there told me that as a late dx I am going to have to change my thinkings on things. Growing up not knowing about the CF, I hadn't been proactive about my health and there was so much I didn't know about, that early dx know, so S. would try to get things in to my thick head that things would not be like they'd always been.
<br />
<br />I was dx w/ bronchiectisis at age 28, too. When I finally got the CF dx so much made sense to me. I had Pulmonary Dr. Sonye D. at JH before the dx and she was wonderful and very compassionate when she broke the news and explained the basics to me. She kept asking me "Are you OK? Are you going to be alright?" because I felt such shock to find out I had something so severe and HAD HAD IT ALL ALONG. She had basically rendered me speechless. But I told her the RELIEF was so nice and I was grateful for the dx so we knew what we were dealing with after all of those years.
<br />
<br />Emotionally, it's very hard to come to terms with. Sometimes I've gotten upset at all of the drs. who mis-treated me, missed the dx, who probably made things worse for me now. But the others questions I don't do. You can't change things in the past, so I don't bother myself with whatifs and make myself crazy.
<br />
<br />One of the hardest things for me to deal with, with the late dx, is my husband didn't know this when he married me and I've had the idea ever since the dx that he wouldn't have married me. This wasn't what he bargained for and he seems resentful of the financial burden and the many things I can't do. He won't admit it, but I certainly get that feeling and it hurts. So many on here, their husbands KNEW what they were getting into and still did it, which really spells out l-o-v-e for me.
<br />
<br />So, <i>do you see Dr. B? Isn't he WONDERFUL</i>!!!!!!?????
 

DarbSkull

New member
Hey Juliet. I was diagnosed at 29 and was quite relieved to finally find out what was up. The whole long, drawn out story is <a target=_blank class=ftalternatingbarlinklarge href="http://blogs.cysticfibrosis.com/index.cfm?month=8&year=2007">here</a> if you are interested. Welcome to the club!
 

DarbSkull

New member
Hey Juliet. I was diagnosed at 29 and was quite relieved to finally find out what was up. The whole long, drawn out story is <a target=_blank class=ftalternatingbarlinklarge href="http://blogs.cysticfibrosis.com/index.cfm?month=8&year=2007">here</a> if you are interested. Welcome to the club!
 

DarbSkull

New member
Hey Juliet. I was diagnosed at 29 and was quite relieved to finally find out what was up. The whole long, drawn out story is <a target=_blank class=ftalternatingbarlinklarge href="http://blogs.cysticfibrosis.com/index.cfm?month=8&year=2007">here</a> if you are interested. Welcome to the club!
 

DarbSkull

New member
Hey Juliet. I was diagnosed at 29 and was quite relieved to finally find out what was up. The whole long, drawn out story is <a target=_blank class=ftalternatingbarlinklarge href="http://blogs.cysticfibrosis.com/index.cfm?month=8&year=2007">here</a> if you are interested. Welcome to the club!
 

DarbSkull

New member
Hey Juliet. I was diagnosed at 29 and was quite relieved to finally find out what was up. The whole long, drawn out story is <a target=_blank class=ftalternatingbarlinklarge href="http://blogs.cysticfibrosis.com/index.cfm?month=8&year=2007">here</a> if you are interested. Welcome to the club!
 

Juliet

New member
Hi everyone, Thanks for the very insightful comments. Yes, I've seen Dr. B but also a new doc up there Dr. S. He's such a great doc too! I really appreciate the way they take the time to explain things and answer all my Qs. And I come armed with lists. <img src="i/expressions/face-icon-small-wink.gif" border="0">

I was dx with Bronchectisis as a teenager. I was pretty sick as a kid a few times a year, then after I got married I had a pretty healthy spell for about 10 years. Actually when I was pregnant I was the healthiest I've felt in most of my life. Other than being tired and REALLY hungry for like the wierdest things. <img src="i/expressions/face-icon-small-smile.gif" border="0"> It's only been the past few years that I've had several bouts of lung crud and started really pushing the docs to get to the bottom of it all.

I think my Mom has taken my DX far harder than me. She's gone through an emotional rollercoaster for sure. And she keep apologizing. As if she picked the genes!?!??? I know there really isn't much that they could have done differently for me growing up. When I got sick my illnesses were always treated promptly. My Mom always had lots of food for us kids (I didn't have that failure to thrive thing!) and with her Irish upbringing and loving to cook lots of German food (for my Dad) we had lots of healthy and homegrown foods with high calorie gravies and stuff. I was slender as a kid (not now though!) but certainly not underweight, so I'm sure that kind of diet helped! Mom is a survivor of Breast & Colon cancer so when I told her about my DX I'm sure it really stirred up all those same feelings and thoughts about mortality.
 

Juliet

New member
Hi everyone, Thanks for the very insightful comments. Yes, I've seen Dr. B but also a new doc up there Dr. S. He's such a great doc too! I really appreciate the way they take the time to explain things and answer all my Qs. And I come armed with lists. <img src="i/expressions/face-icon-small-wink.gif" border="0">

I was dx with Bronchectisis as a teenager. I was pretty sick as a kid a few times a year, then after I got married I had a pretty healthy spell for about 10 years. Actually when I was pregnant I was the healthiest I've felt in most of my life. Other than being tired and REALLY hungry for like the wierdest things. <img src="i/expressions/face-icon-small-smile.gif" border="0"> It's only been the past few years that I've had several bouts of lung crud and started really pushing the docs to get to the bottom of it all.

I think my Mom has taken my DX far harder than me. She's gone through an emotional rollercoaster for sure. And she keep apologizing. As if she picked the genes!?!??? I know there really isn't much that they could have done differently for me growing up. When I got sick my illnesses were always treated promptly. My Mom always had lots of food for us kids (I didn't have that failure to thrive thing!) and with her Irish upbringing and loving to cook lots of German food (for my Dad) we had lots of healthy and homegrown foods with high calorie gravies and stuff. I was slender as a kid (not now though!) but certainly not underweight, so I'm sure that kind of diet helped! Mom is a survivor of Breast & Colon cancer so when I told her about my DX I'm sure it really stirred up all those same feelings and thoughts about mortality.
 

Juliet

New member
Hi everyone, Thanks for the very insightful comments. Yes, I've seen Dr. B but also a new doc up there Dr. S. He's such a great doc too! I really appreciate the way they take the time to explain things and answer all my Qs. And I come armed with lists. <img src="i/expressions/face-icon-small-wink.gif" border="0">

I was dx with Bronchectisis as a teenager. I was pretty sick as a kid a few times a year, then after I got married I had a pretty healthy spell for about 10 years. Actually when I was pregnant I was the healthiest I've felt in most of my life. Other than being tired and REALLY hungry for like the wierdest things. <img src="i/expressions/face-icon-small-smile.gif" border="0"> It's only been the past few years that I've had several bouts of lung crud and started really pushing the docs to get to the bottom of it all.

I think my Mom has taken my DX far harder than me. She's gone through an emotional rollercoaster for sure. And she keep apologizing. As if she picked the genes!?!??? I know there really isn't much that they could have done differently for me growing up. When I got sick my illnesses were always treated promptly. My Mom always had lots of food for us kids (I didn't have that failure to thrive thing!) and with her Irish upbringing and loving to cook lots of German food (for my Dad) we had lots of healthy and homegrown foods with high calorie gravies and stuff. I was slender as a kid (not now though!) but certainly not underweight, so I'm sure that kind of diet helped! Mom is a survivor of Breast & Colon cancer so when I told her about my DX I'm sure it really stirred up all those same feelings and thoughts about mortality.
 

Juliet

New member
Hi everyone, Thanks for the very insightful comments. Yes, I've seen Dr. B but also a new doc up there Dr. S. He's such a great doc too! I really appreciate the way they take the time to explain things and answer all my Qs. And I come armed with lists. <img src="i/expressions/face-icon-small-wink.gif" border="0">

I was dx with Bronchectisis as a teenager. I was pretty sick as a kid a few times a year, then after I got married I had a pretty healthy spell for about 10 years. Actually when I was pregnant I was the healthiest I've felt in most of my life. Other than being tired and REALLY hungry for like the wierdest things. <img src="i/expressions/face-icon-small-smile.gif" border="0"> It's only been the past few years that I've had several bouts of lung crud and started really pushing the docs to get to the bottom of it all.

I think my Mom has taken my DX far harder than me. She's gone through an emotional rollercoaster for sure. And she keep apologizing. As if she picked the genes!?!??? I know there really isn't much that they could have done differently for me growing up. When I got sick my illnesses were always treated promptly. My Mom always had lots of food for us kids (I didn't have that failure to thrive thing!) and with her Irish upbringing and loving to cook lots of German food (for my Dad) we had lots of healthy and homegrown foods with high calorie gravies and stuff. I was slender as a kid (not now though!) but certainly not underweight, so I'm sure that kind of diet helped! Mom is a survivor of Breast & Colon cancer so when I told her about my DX I'm sure it really stirred up all those same feelings and thoughts about mortality.
 

Juliet

New member
Hi everyone, Thanks for the very insightful comments. Yes, I've seen Dr. B but also a new doc up there Dr. S. He's such a great doc too! I really appreciate the way they take the time to explain things and answer all my Qs. And I come armed with lists. <img src="i/expressions/face-icon-small-wink.gif" border="0">
<br />
<br />I was dx with Bronchectisis as a teenager. I was pretty sick as a kid a few times a year, then after I got married I had a pretty healthy spell for about 10 years. Actually when I was pregnant I was the healthiest I've felt in most of my life. Other than being tired and REALLY hungry for like the wierdest things. <img src="i/expressions/face-icon-small-smile.gif" border="0"> It's only been the past few years that I've had several bouts of lung crud and started really pushing the docs to get to the bottom of it all.
<br />
<br />I think my Mom has taken my DX far harder than me. She's gone through an emotional rollercoaster for sure. And she keep apologizing. As if she picked the genes!?!??? I know there really isn't much that they could have done differently for me growing up. When I got sick my illnesses were always treated promptly. My Mom always had lots of food for us kids (I didn't have that failure to thrive thing!) and with her Irish upbringing and loving to cook lots of German food (for my Dad) we had lots of healthy and homegrown foods with high calorie gravies and stuff. I was slender as a kid (not now though!) but certainly not underweight, so I'm sure that kind of diet helped! Mom is a survivor of Breast & Colon cancer so when I told her about my DX I'm sure it really stirred up all those same feelings and thoughts about mortality.
 

DarbSkull

New member
I know what you mean Juliet. Telling my mom was easily the hardest part of my diagnosis, especially when it meant my twin sister probably also had CF (she was diagnosed a year later).
 

DarbSkull

New member
I know what you mean Juliet. Telling my mom was easily the hardest part of my diagnosis, especially when it meant my twin sister probably also had CF (she was diagnosed a year later).
 

DarbSkull

New member
I know what you mean Juliet. Telling my mom was easily the hardest part of my diagnosis, especially when it meant my twin sister probably also had CF (she was diagnosed a year later).
 

DarbSkull

New member
I know what you mean Juliet. Telling my mom was easily the hardest part of my diagnosis, especially when it meant my twin sister probably also had CF (she was diagnosed a year later).
 

DarbSkull

New member
I know what you mean Juliet. Telling my mom was easily the hardest part of my diagnosis, especially when it meant my twin sister probably also had CF (she was diagnosed a year later).
 
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