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Hi Ismith,thanks for writing I feel like a wimp after reading about

some of the people here. I have not responed to any others post but I

have read a few.looks like I found a careing place even tho most of

us wish we did not have to be,I am a little shy so it is kinda hard

for me to write sometimes.

I wish Dr's would and could take a few mins to listen maybe we would

be feeling a lot better.

I used to work for Mead Paper in Atlanta Ga. and I was working with

heated glue,Not relizeing that it was messing with my insides.

(i am not the smartest person in the world) i had to make a liveing

regardless.i was around the glue for about 12 yrs. there and 5 years

at a simular place.So i know now what caused my lungs to be so bad.

hope you are having a great day.

Ruth

-- In Breathe-Support , " lsmith7892006 "

wrote:

>

> Sorry you had to look for us but glad you found us. Welcome. Feel

> free to come and go as you please and unload your thoughts and

fears

> as you need. GP docs really don't understand. Mine recently

> referred to my disease as ARDS even though he has a copy of my

biopsy

> and knows exactly what its name is, not ARDS. Even my pulmo has a

> difficult time understanding. I told him I can feel it when it is

> going to act up. He says there are no nerve feelings in the lungs

> and that is not possible. But I do feel it.

>

> Please take care of yourself in the sweltering heat and humidity

over

> there.

>

> S, Lubbock, TX

> NSIP w/PF 12/2006

>

>

> > > > >

> > > > > You're welcome, Grandma. There's plenty of us here who

also

> > > are

> > > > grands. This is a good place to learn about fibrosis and

> > > associated

> > > > diseases. It' been my school for a few months now. I'm

about

> to

> > > > finish grade school, and look forward to moving on to high

> > > school. I

> > > > am very ambitious and hope to get my PHD some day.

> > > > > Jack

> > > > > 79/UIP - IPF/06/005 Maine

> > > > >

> > > > >

> > > > > looking for information &

friends

> > > > >

> > > > >

> > > > > hi Everyone,just wanted to drop in and say hello.I have

> read

> > > some

> > > > of

> > > > > your post and found them very interesting. Hope you

didn't

> > mind.

> > > > > I was introduced to PF years ago. I am on oxygen.

> > > > > I can tell my breathing is getting a lot worse.

> > > > > My dh has had COPD for years, and i have been takeing

care

> of

> > > him.

> > > > > So if i get really bad then we will be in bad shape.

> > > > > This computer is the only friend I have to the out side

> > > world.I'm

> > > > not

> > > > > really good on it but i do like to visit and learn what I

> can.

> > > > > Thanks for shareing with me,

> > > > >

> > > >

> > >

> >

>

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Welcome, Ruth!

I am so glad you found this place too. I have been here about a month and found everyone to be real patient and kind. I have asked many questions I know have been answered over and over, but people will still take the time to give me a personal answer. No one has made me feel like an idiot yet, although the meds I'm taking are making me not quite myself on just about everything. I hope to get to know you better through your posts!

(PF ,Sjogren's Apr.'08)age 52>> Sorry you had to look for us but glad you found us. Welcome. Feel > free to come and go as you please and unload your thoughts and fears > as you need. GP docs really don't understand. Mine recently > referred to my disease as ARDS even though he has a copy of my biopsy > and knows exactly what its name is, not ARDS. Even my pulmo has a > difficult time understanding. I told him I can feel it when it is > going to act up. He says there are no nerve feelings in the lungs > and that is not possible. But I do feel it.> > Please take care of yourself in the sweltering heat and humidity over > there.> > S, Lubbock, TX> NSIP w/PF 12/2006> > > > > > >> > > > > You're welcome, Grandma. There's plenty of us here who also > > > are > > > > grands. This is a good place to learn about fibrosis and > > > associated > > > > diseases. It' been my school for a few months now. I'm about > to > > > > finish grade school, and look forward to moving on to high > > > school. I > > > > am very ambitious and hope to get my PHD some day.> > > > > Jack> > > > > 79/UIP - IPF/06/005 Maine> > > > > > > > > > > > > > > looking for information & friends> > > > > > > > > > > > > > > hi Everyone,just wanted to drop in and say hello.I have > read > > > some > > > > of > > > > > your post and found them very interesting. Hope you didn't > > mind.> > > > > I was introduced to PF years ago. I am on oxygen.> > > > > I can tell my breathing is getting a lot worse. > > > > > My dh has had COPD for years, and i have been takeing care > of > > > him. >

> > > > So if i get really bad then we will be in bad shape.> > > > > This computer is the only friend I have to the out side > > > world.I'm > > > > not > > > > > really good on it but i do like to visit and learn what I > can.> > > > > Thanks for shareing with me,> > > > >> > > >> > >> >>

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thanks ,

I hope I can say no one has made me feel like an idiot after a

month.

I have had lots of welcomes, which has made me feel good.

thanks for the reply and I look forward to hearing from you often.

Ruth

> & gt; & gt; & gt; & gt; & gt;

> & gt; & gt; & gt; & gt; & gt; You're welcome, Grandma. There's plenty of

us here who

> also

> & gt; & gt; & gt; are

> & gt; & gt; & gt; & gt; grands. This is a good place to learn about

fibrosis and

> & gt; & gt; & gt; associated

> & gt; & gt; & gt; & gt; diseases. It' been my school for a few months

now. I'm

> about

> & gt; to

> & gt; & gt; & gt; & gt; finish grade school, and look forward to moving

on to high

> & gt; & gt; & gt; school. I

> & gt; & gt; & gt; & gt; am very ambitious and hope to get my PHD some

day.

> & gt; & gt; & gt; & gt; & gt; Jack

> & gt; & gt; & gt; & gt; & gt; 79/UIP - IPF/06/005 Maine

> & gt; & gt; & gt; & gt; & gt;

> & gt; & gt; & gt; & gt; & gt;

> & gt; & gt; & gt; & gt; & gt; looking for

information & amp;

> friends

> & gt; & gt; & gt; & gt; & gt;

> & gt; & gt; & gt; & gt; & gt;

> & gt; & gt; & gt; & gt; & gt; hi Everyone,just wanted to drop in and say

hello.I have

> & gt; read

> & gt; & gt; & gt; some

> & gt; & gt; & gt; & gt; of

> & gt; & gt; & gt; & gt; & gt; your post and found them very interesting.

Hope you

> didn't

> & gt; & gt; mind.

> & gt; & gt; & gt; & gt; & gt; I was introduced to PF years ago. I am on

oxygen.

> & gt; & gt; & gt; & gt; & gt; I can tell my breathing is getting a lot

worse.

> & gt; & gt; & gt; & gt; & gt; My dh has had COPD for years, and i have

been takeing

> care

> & gt; of

> & gt; & gt; & gt; him.

> & gt; & gt; & gt; & gt; & gt; So if i get really bad then we will be in

bad shape.

> & gt; & gt; & gt; & gt; & gt; This computer is the only friend I have to

the out side

> & gt; & gt; & gt; world.I'm

> & gt; & gt; & gt; & gt; not

> & gt; & gt; & gt; & gt; & gt; really good on it but i do like to visit

and learn what I

> & gt; can.

> & gt; & gt; & gt; & gt; & gt; Thanks for shareing with me,

> & gt; & gt; & gt; & gt; & gt;

> & gt; & gt; & gt; & gt;

> & gt; & gt; & gt;

> & gt; & gt;

> & gt;

>

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Hi Zena,

thank you, I never expected so many welcomes. I am so thankful I

found this board. Now to dig my heels in and find out all I can about

this disease. The Dr's never take the time to explane things. Maybe

thay think we are suppose to be as smart as they are. I don't know.

I just hope I can make someone feel as good as you people have made

me feel.

Ruth

> > > > > > >

> > > > > > > You're welcome, Grandma. There's plenty of us here who

> > also

> > > > > are

> > > > > > grands. This is a good place to learn about fibrosis and

> > > > > associated

> > > > > > diseases. It' been my school for a few months now. I'm

> > about

> > > to

> > > > > > finish grade school, and look forward to moving on to high

> > > > > school. I

> > > > > > am very ambitious and hope to get my PHD some day.

> > > > > > > Jack

> > > > > > > 79/UIP - IPF/06/005 Maine

> > > > > > >

> > > > > > >

> > > > > > > looking for information &

> > friends

> > > > > > >

> > > > > > >

> > > > > > > hi Everyone,just wanted to drop in and say hello.I have

> > > read

> > > > > some

> > > > > > of

> > > > > > > your post and found them very interesting. Hope you

> > didn't

> > > > mind.

> > > > > > > I was introduced to PF years ago. I am on oxygen.

> > > > > > > I can tell my breathing is getting a lot worse.

> > > > > > > My dh has had COPD for years, and i have been takeing

> > care

> > > of

> > > > > him.

> > > > > > > So if i get really bad then we will be in bad shape.

> > > > > > > This computer is the only friend I have to the out side

> > > > > world.I'm

> > > > > > not

> > > > > > > really good on it but i do like to visit and learn what

I

> > > can.

> > > > > > > Thanks for shareing with me,

> > > > > > >

> > > > > >

> > > > >

> > > >

> > >

> >

>

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Guest guest

Hi Zena,

thank you, I never expected so many welcomes. I am so thankful I

found this board. Now to dig my heels in and find out all I can about

this disease. The Dr's never take the time to explane things. Maybe

thay think we are suppose to be as smart as they are. I don't know.

I just hope I can make someone feel as good as you people have made

me feel.

Ruth

> > > > > > >

> > > > > > > You're welcome, Grandma. There's plenty of us here who

> > also

> > > > > are

> > > > > > grands. This is a good place to learn about fibrosis and

> > > > > associated

> > > > > > diseases. It' been my school for a few months now. I'm

> > about

> > > to

> > > > > > finish grade school, and look forward to moving on to high

> > > > > school. I

> > > > > > am very ambitious and hope to get my PHD some day.

> > > > > > > Jack

> > > > > > > 79/UIP - IPF/06/005 Maine

> > > > > > >

> > > > > > >

> > > > > > > looking for information &

> > friends

> > > > > > >

> > > > > > >

> > > > > > > hi Everyone,just wanted to drop in and say hello.I have

> > > read

> > > > > some

> > > > > > of

> > > > > > > your post and found them very interesting. Hope you

> > didn't

> > > > mind.

> > > > > > > I was introduced to PF years ago. I am on oxygen.

> > > > > > > I can tell my breathing is getting a lot worse.

> > > > > > > My dh has had COPD for years, and i have been takeing

> > care

> > > of

> > > > > him.

> > > > > > > So if i get really bad then we will be in bad shape.

> > > > > > > This computer is the only friend I have to the out side

> > > > > world.I'm

> > > > > > not

> > > > > > > really good on it but i do like to visit and learn what

I

> > > can.

> > > > > > > Thanks for shareing with me,

> > > > > > >

> > > > > >

> > > > >

> > > >

> > >

> >

>

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Guest guest

Hi Zena,

thank you, I never expected so many welcomes. I am so thankful I

found this board. Now to dig my heels in and find out all I can about

this disease. The Dr's never take the time to explane things. Maybe

thay think we are suppose to be as smart as they are. I don't know.

I just hope I can make someone feel as good as you people have made

me feel.

Ruth

> > > > > > >

> > > > > > > You're welcome, Grandma. There's plenty of us here who

> > also

> > > > > are

> > > > > > grands. This is a good place to learn about fibrosis and

> > > > > associated

> > > > > > diseases. It' been my school for a few months now. I'm

> > about

> > > to

> > > > > > finish grade school, and look forward to moving on to high

> > > > > school. I

> > > > > > am very ambitious and hope to get my PHD some day.

> > > > > > > Jack

> > > > > > > 79/UIP - IPF/06/005 Maine

> > > > > > >

> > > > > > >

> > > > > > > looking for information &

> > friends

> > > > > > >

> > > > > > >

> > > > > > > hi Everyone,just wanted to drop in and say hello.I have

> > > read

> > > > > some

> > > > > > of

> > > > > > > your post and found them very interesting. Hope you

> > didn't

> > > > mind.

> > > > > > > I was introduced to PF years ago. I am on oxygen.

> > > > > > > I can tell my breathing is getting a lot worse.

> > > > > > > My dh has had COPD for years, and i have been takeing

> > care

> > > of

> > > > > him.

> > > > > > > So if i get really bad then we will be in bad shape.

> > > > > > > This computer is the only friend I have to the out side

> > > > > world.I'm

> > > > > > not

> > > > > > > really good on it but i do like to visit and learn what

I

> > > can.

> > > > > > > Thanks for shareing with me,

> > > > > > >

> > > > > >

> > > > >

> > > >

> > >

> >

>

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