Adult CF Lost

sreedsage

New member
Adult CF Lost It has been along time since I have felt the need or the desire to state my feelings about being and adult with CF. I have felt like an outsider most of my adult life in reguards to CF due to the medical and social comunity and the disease itself. I live in a place were there is not much help or concern about CF and the concerns are all geared toward children. If you are lucky enough to reach adult hood the nearest help is 5-6 hours away and you are banned from the local CF center.

With that said, I have been in search of adults (with or without CF) who have the same concerns, frustration, anger, sorrow, infomational, and sense of humor just to talk to and maybe some day fit in. My last hospital stay I found this site and most of the now banned members (and others who are still here ) encouraged me to be the adult with CF that I am. Not only in ways of "nice tell me what I want to hear" but in realistic heartfelt "Pull your head out of your ass and deal with it" encouragement!! Although it sometimes is not pleasent to hear the truth and reality it is necessary otherwise your just a visitor sitting at the kids table being excluded from the reality of adulthood. Finally a place where I could speak my mind, heart and soul, only to find out this is not true.

To live in a world of "nice and corret" is a delusion. We live in a world of reality and as adults with CF we have the right to be frustrated, angry to the point of hostility, loving, caring and genuinly sorry for some of our outbursts of frustration. I hope all who read this know that words can cut like a knife but can be healed with the same passion that made the words so sharp.
 

sreedsage

New member
Adult CF Lost It has been along time since I have felt the need or the desire to state my feelings about being and adult with CF. I have felt like an outsider most of my adult life in reguards to CF due to the medical and social comunity and the disease itself. I live in a place were there is not much help or concern about CF and the concerns are all geared toward children. If you are lucky enough to reach adult hood the nearest help is 5-6 hours away and you are banned from the local CF center.

With that said, I have been in search of adults (with or without CF) who have the same concerns, frustration, anger, sorrow, infomational, and sense of humor just to talk to and maybe some day fit in. My last hospital stay I found this site and most of the now banned members (and others who are still here ) encouraged me to be the adult with CF that I am. Not only in ways of "nice tell me what I want to hear" but in realistic heartfelt "Pull your head out of your ass and deal with it" encouragement!! Although it sometimes is not pleasent to hear the truth and reality it is necessary otherwise your just a visitor sitting at the kids table being excluded from the reality of adulthood. Finally a place where I could speak my mind, heart and soul, only to find out this is not true.

To live in a world of "nice and corret" is a delusion. We live in a world of reality and as adults with CF we have the right to be frustrated, angry to the point of hostility, loving, caring and genuinly sorry for some of our outbursts of frustration. I hope all who read this know that words can cut like a knife but can be healed with the same passion that made the words so sharp.
 

sreedsage

New member
Adult CF Lost It has been along time since I have felt the need or the desire to state my feelings about being and adult with CF. I have felt like an outsider most of my adult life in reguards to CF due to the medical and social comunity and the disease itself. I live in a place were there is not much help or concern about CF and the concerns are all geared toward children. If you are lucky enough to reach adult hood the nearest help is 5-6 hours away and you are banned from the local CF center.

With that said, I have been in search of adults (with or without CF) who have the same concerns, frustration, anger, sorrow, infomational, and sense of humor just to talk to and maybe some day fit in. My last hospital stay I found this site and most of the now banned members (and others who are still here ) encouraged me to be the adult with CF that I am. Not only in ways of "nice tell me what I want to hear" but in realistic heartfelt "Pull your head out of your ass and deal with it" encouragement!! Although it sometimes is not pleasent to hear the truth and reality it is necessary otherwise your just a visitor sitting at the kids table being excluded from the reality of adulthood. Finally a place where I could speak my mind, heart and soul, only to find out this is not true.

To live in a world of "nice and corret" is a delusion. We live in a world of reality and as adults with CF we have the right to be frustrated, angry to the point of hostility, loving, caring and genuinly sorry for some of our outbursts of frustration. I hope all who read this know that words can cut like a knife but can be healed with the same passion that made the words so sharp.
 

sreedsage

New member
Adult CF Lost It has been along time since I have felt the need or the desire to state my feelings about being and adult with CF. I have felt like an outsider most of my adult life in reguards to CF due to the medical and social comunity and the disease itself. I live in a place were there is not much help or concern about CF and the concerns are all geared toward children. If you are lucky enough to reach adult hood the nearest help is 5-6 hours away and you are banned from the local CF center.

With that said, I have been in search of adults (with or without CF) who have the same concerns, frustration, anger, sorrow, infomational, and sense of humor just to talk to and maybe some day fit in. My last hospital stay I found this site and most of the now banned members (and others who are still here ) encouraged me to be the adult with CF that I am. Not only in ways of "nice tell me what I want to hear" but in realistic heartfelt "Pull your head out of your ass and deal with it" encouragement!! Although it sometimes is not pleasent to hear the truth and reality it is necessary otherwise your just a visitor sitting at the kids table being excluded from the reality of adulthood. Finally a place where I could speak my mind, heart and soul, only to find out this is not true.

To live in a world of "nice and corret" is a delusion. We live in a world of reality and as adults with CF we have the right to be frustrated, angry to the point of hostility, loving, caring and genuinly sorry for some of our outbursts of frustration. I hope all who read this know that words can cut like a knife but can be healed with the same passion that made the words so sharp.
 

sreedsage

New member
Adult CF Lost It has been along time since I have felt the need or the desire to state my feelings about being and adult with CF. I have felt like an outsider most of my adult life in reguards to CF due to the medical and social comunity and the disease itself. I live in a place were there is not much help or concern about CF and the concerns are all geared toward children. If you are lucky enough to reach adult hood the nearest help is 5-6 hours away and you are banned from the local CF center.
<br />
<br />With that said, I have been in search of adults (with or without CF) who have the same concerns, frustration, anger, sorrow, infomational, and sense of humor just to talk to and maybe some day fit in. My last hospital stay I found this site and most of the now banned members (and others who are still here ) encouraged me to be the adult with CF that I am. Not only in ways of "nice tell me what I want to hear" but in realistic heartfelt "Pull your head out of your ass and deal with it" encouragement!! Although it sometimes is not pleasent to hear the truth and reality it is necessary otherwise your just a visitor sitting at the kids table being excluded from the reality of adulthood. Finally a place where I could speak my mind, heart and soul, only to find out this is not true.
<br />
<br />To live in a world of "nice and corret" is a delusion. We live in a world of reality and as adults with CF we have the right to be frustrated, angry to the point of hostility, loving, caring and genuinly sorry for some of our outbursts of frustration. I hope all who read this know that words can cut like a knife but can be healed with the same passion that made the words so sharp.
<br />
 
6

65rosessamurai

Guest
Sometimes words cut so deep that a scar is left behind and never totally healed...

I just hope you are right in the idea that hurtful words can be healed, especially when someone can swallow their pride and say "I'm Sorry" and "Forgive Me".

At this point, I haven't seen those words yet, but am hoping....
 
6

65rosessamurai

Guest
Sometimes words cut so deep that a scar is left behind and never totally healed...

I just hope you are right in the idea that hurtful words can be healed, especially when someone can swallow their pride and say "I'm Sorry" and "Forgive Me".

At this point, I haven't seen those words yet, but am hoping....
 
6

65rosessamurai

Guest
Sometimes words cut so deep that a scar is left behind and never totally healed...

I just hope you are right in the idea that hurtful words can be healed, especially when someone can swallow their pride and say "I'm Sorry" and "Forgive Me".

At this point, I haven't seen those words yet, but am hoping....
 
6

65rosessamurai

Guest
Sometimes words cut so deep that a scar is left behind and never totally healed...

I just hope you are right in the idea that hurtful words can be healed, especially when someone can swallow their pride and say "I'm Sorry" and "Forgive Me".

At this point, I haven't seen those words yet, but am hoping....
 
6

65rosessamurai

Guest
Sometimes words cut so deep that a scar is left behind and never totally healed...
<br />
<br />I just hope you are right in the idea that hurtful words can be healed, especially when someone can swallow their pride and say "I'm Sorry" and "Forgive Me".
<br />
<br />At this point, I haven't seen those words yet, but am hoping....
 

Mockingbird

New member
We do have the right to speak our mind on this site. However, we also have to recognize other people have the right to reject our opinion.

This is the way I see it. Certain people with strong opinions often speak their mind on this site. However, when they're not listened to, that offends them and they resort to verbal attacks and harassment. It isn't about wanting to help people at that point; it's about wanting to be right.

I know what I'm taliking about because I used to be one of those people. I once wrote about it here: <a target=_blank class=ftalternatingbarlinklarge href="http://forums.cysticfibrosis.com/messageview.cfm?catid=19&threadid=22606&highlight_key=y&keyword1=whom%20do%20they%20spite">http://forums.cysticfibrosis.c...om%20do%20they%20spite</a>.

There's no problem with speaking your mind, heart and soul, and we do have a right to be frustrated and angry, but we don't have a right to take it out on others or to hijack threads with our opinions just because we think we're right. It's all outlined in the cysticfibrosis.com code of conduct (There's a link to it at the top of each topic and thread).
 

Mockingbird

New member
We do have the right to speak our mind on this site. However, we also have to recognize other people have the right to reject our opinion.

This is the way I see it. Certain people with strong opinions often speak their mind on this site. However, when they're not listened to, that offends them and they resort to verbal attacks and harassment. It isn't about wanting to help people at that point; it's about wanting to be right.

I know what I'm taliking about because I used to be one of those people. I once wrote about it here: <a target=_blank class=ftalternatingbarlinklarge href="http://forums.cysticfibrosis.com/messageview.cfm?catid=19&threadid=22606&highlight_key=y&keyword1=whom%20do%20they%20spite">http://forums.cysticfibrosis.c...om%20do%20they%20spite</a>.

There's no problem with speaking your mind, heart and soul, and we do have a right to be frustrated and angry, but we don't have a right to take it out on others or to hijack threads with our opinions just because we think we're right. It's all outlined in the cysticfibrosis.com code of conduct (There's a link to it at the top of each topic and thread).
 

Mockingbird

New member
We do have the right to speak our mind on this site. However, we also have to recognize other people have the right to reject our opinion.

This is the way I see it. Certain people with strong opinions often speak their mind on this site. However, when they're not listened to, that offends them and they resort to verbal attacks and harassment. It isn't about wanting to help people at that point; it's about wanting to be right.

I know what I'm taliking about because I used to be one of those people. I once wrote about it here: <a target=_blank class=ftalternatingbarlinklarge href="http://forums.cysticfibrosis.com/messageview.cfm?catid=19&threadid=22606&highlight_key=y&keyword1=whom%20do%20they%20spite">http://forums.cysticfibrosis.c...om%20do%20they%20spite</a>.

There's no problem with speaking your mind, heart and soul, and we do have a right to be frustrated and angry, but we don't have a right to take it out on others or to hijack threads with our opinions just because we think we're right. It's all outlined in the cysticfibrosis.com code of conduct (There's a link to it at the top of each topic and thread).
 

Mockingbird

New member
We do have the right to speak our mind on this site. However, we also have to recognize other people have the right to reject our opinion.

This is the way I see it. Certain people with strong opinions often speak their mind on this site. However, when they're not listened to, that offends them and they resort to verbal attacks and harassment. It isn't about wanting to help people at that point; it's about wanting to be right.

I know what I'm taliking about because I used to be one of those people. I once wrote about it here: <a target=_blank class=ftalternatingbarlinklarge href="http://forums.cysticfibrosis.com/messageview.cfm?catid=19&threadid=22606&highlight_key=y&keyword1=whom%20do%20they%20spite">http://forums.cysticfibrosis.c...om%20do%20they%20spite</a>.

There's no problem with speaking your mind, heart and soul, and we do have a right to be frustrated and angry, but we don't have a right to take it out on others or to hijack threads with our opinions just because we think we're right. It's all outlined in the cysticfibrosis.com code of conduct (There's a link to it at the top of each topic and thread).
 

Mockingbird

New member
We do have the right to speak our mind on this site. However, we also have to recognize other people have the right to reject our opinion.
<br />
<br />This is the way I see it. Certain people with strong opinions often speak their mind on this site. However, when they're not listened to, that offends them and they resort to verbal attacks and harassment. It isn't about wanting to help people at that point; it's about wanting to be right.
<br />
<br />I know what I'm taliking about because I used to be one of those people. I once wrote about it here: <a target=_blank class=ftalternatingbarlinklarge href="http://forums.cysticfibrosis.com/messageview.cfm?catid=19&threadid=22606&highlight_key=y&keyword1=whom%20do%20they%20spite">http://forums.cysticfibrosis.c...om%20do%20they%20spite</a>.
<br />
<br />There's no problem with speaking your mind, heart and soul, and we do have a right to be frustrated and angry, but we don't have a right to take it out on others or to hijack threads with our opinions just because we think we're right. It's all outlined in the cysticfibrosis.com code of conduct (There's a link to it at the top of each topic and thread).
 

Brad

New member
I hear Ya Shawn....

I have been on cf site that seem to right me off
because they think I have lived long enough.
At least thats the way I was made to feel just because I am Lucky enough
to grow older with cf.
They fail to realize that it took a lot of fighting,
a fight over and over every day.

I realize that the people who made me feel this way have lost
someone to CF.
I come from a family of 5 children, 4 of us have cf.
My oldest cf brother passed from cf and My only
Non CF sibling was killed in an accident when He was just 16.
So, I know there pain.

I have found a Adult Cf center now myself, they just
started seeing adults,So I am told.


I understand ....
 

Brad

New member
I hear Ya Shawn....

I have been on cf site that seem to right me off
because they think I have lived long enough.
At least thats the way I was made to feel just because I am Lucky enough
to grow older with cf.
They fail to realize that it took a lot of fighting,
a fight over and over every day.

I realize that the people who made me feel this way have lost
someone to CF.
I come from a family of 5 children, 4 of us have cf.
My oldest cf brother passed from cf and My only
Non CF sibling was killed in an accident when He was just 16.
So, I know there pain.

I have found a Adult Cf center now myself, they just
started seeing adults,So I am told.


I understand ....
 

Brad

New member
I hear Ya Shawn....

I have been on cf site that seem to right me off
because they think I have lived long enough.
At least thats the way I was made to feel just because I am Lucky enough
to grow older with cf.
They fail to realize that it took a lot of fighting,
a fight over and over every day.

I realize that the people who made me feel this way have lost
someone to CF.
I come from a family of 5 children, 4 of us have cf.
My oldest cf brother passed from cf and My only
Non CF sibling was killed in an accident when He was just 16.
So, I know there pain.

I have found a Adult Cf center now myself, they just
started seeing adults,So I am told.


I understand ....
 

Brad

New member
I hear Ya Shawn....

I have been on cf site that seem to right me off
because they think I have lived long enough.
At least thats the way I was made to feel just because I am Lucky enough
to grow older with cf.
They fail to realize that it took a lot of fighting,
a fight over and over every day.

I realize that the people who made me feel this way have lost
someone to CF.
I come from a family of 5 children, 4 of us have cf.
My oldest cf brother passed from cf and My only
Non CF sibling was killed in an accident when He was just 16.
So, I know there pain.

I have found a Adult Cf center now myself, they just
started seeing adults,So I am told.


I understand ....
 

Brad

New member
I hear Ya Shawn....
<br />
<br />I have been on cf site that seem to right me off
<br />because they think I have lived long enough.
<br />At least thats the way I was made to feel just because I am Lucky enough
<br />to grow older with cf.
<br />They fail to realize that it took a lot of fighting,
<br />a fight over and over every day.
<br />
<br /> I realize that the people who made me feel this way have lost
<br /> someone to CF.
<br /> I come from a family of 5 children, 4 of us have cf.
<br /> My oldest cf brother passed from cf and My only
<br /> Non CF sibling was killed in an accident when He was just 16.
<br /> So, I know there pain.
<br />
<br /> I have found a Adult Cf center now myself, they just
<br /> started seeing adults,So I am told.
<br />
<br />
<br /> I understand ....
<br />
<br />
 
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