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In a message dated 11/13/2001 6:00:52 PM Central Standard Time,

MsMystic1@... writes:

> OK, another one - I just love it when you guys get technical and all this

> talk about the size of men's *members* made me laugh and smile.....so how

> does DS affect a woman? I know fat has a lot of hormones, so as you lose

> weight, do you lose your libido? OR do you get even more fiesty? Inquiring

> minds want to know! When answering this, also tell us how old you are or

> if

> you are pre or post menapausal or just a young, sexy thang! :-) Carole

>

>

38 years old, premenopausal---more able to act on a very healthy sex

drive---over and out.

Dawn--South Suburban Chicago area

Dr. Hess, Bowling Green, OH

BPD/DS

4/27/00

www.duodenalswitch.com

267 to 165 5' 4 "

size 22 to size 10

have made size goal

no more high blood pressure, sore feet, or dieting

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  • 8 years later...

Barbara, I realize that your post

was for Bruce.

But I've been told that there are at least 200

forms of PF!

Z fibriotic NSIP/05

Z 65, fibriotic NSIP/05/PA

And

“mild†PH/10/07

No,

NSIP was not self-inflicted…I never smoked!

Potter,

reader,carousel lover and MomMom to Darah and Sara 

    

“I’m

gonna be iron like a lion in Zionâ€Â  Bob Marley

Vinca

Minor-periwinkle is my flower

 

 

barbara carr wrote:

 

ore

barbara

jean

From: barbara carr <bjcarr2004 (AT) sbcglobal (DOT) net>

Subject: Re: Re: Question

To: Breathe-Support

Date: Wednesday, January 20, 2010, 7:48 PM

 

Bruce

I want to address this to you.  Not sure this is the correct way. 

Diagnosis Pulmonary Fibrosis in June 09 on NAC:

Diagnosed by pulmonary function test. cat scan and bronch

biopsy.  My only symptoms are shortness of breathe and slight cough and

runny nose. I have a oxcimeter and my oxygen falls when I

am exerting (walking, cleaning, etc.)  Went through Pulmonary rehab and

tolorated it well. Learned correct

breathing excercises etc. I have had very few problems, no colds, chest

pains = tiredness yes'  I have just repeated my pulmonary function test

and it had improved from about 45 to 65 I believe.  Cat scan still

shows fibrosis and he wants a lung biopsy this spring to see what type

of PF I have.  He did put me on predisone starting at 40 and tapering

to 5 in three months to see the results of a repeat Pulmonary Function

test. He also put me on Advair.  I have a sister who has PF and is on

oxy 24/7 and not good at all.  I asked him if that is what he could see

for me and he said not necesarily He said there are 5 kinds

of pf and he wants to find out what I have  thus the biopsy. I have

never heard of different kinds if Pulmonary Fibrosis   could you fill

me in        barbt] Re: Question

To: Breathe-Support@ yahoogroups. com

Date: Wednesday, January 20, 2010, 4:51 PM

 

Peggy

You're so cute and funny....I love following this:

1-Read the information about your heating pad.

2-Mine says don't use it in oxygen enriched area.

3-I've been using it in the area for 4 years.

4-Be careful

Now, I'm just wondering... ..why read the information? lol....

I'm with you though. I'd use it and be careful. Basically they tell us

not to use anything around oxygen. I know an electric razor is one.

Well, I do. I realize there is danger of a spark and problem and if so

I'll get on the move out. It's just like cooking and some of the other

things. They issue warnings to the extreme to cover their liability but

if we followed them all, we'd end up living in bubbles.

I'm glad the nebulizer and the morphine both help you. Every time I read

one of your posts I just look hoping you're feeling comfortable and

looking for the smile in your voice. You seem to be balancing things

very well and using the morphine in a way for it to help with the least

so that you're relieved of pain but having fun.

So, have you run over anyone yet with the Hoveround? Been back out? How

is feeling today? I hope better. For him to let it knock him out of

action, I know he was feeling pretty miserable.

>

> Hi , I do understand the SOB in your chest. I have had that

for a

while. It started with a feeling that I couldn't get enough air even

though my sats were mid 90's

> I have quite a bit of that now and am using a nebulizer with

albuterol. That helps, then when it is muscle spasms I use the morphine.

I am pretty sure what you are experiencing is an advancement of this

monster.. My Dr. told me when my sats are good and my heart rate is

good, we know my heart is good.. It's the disease.. It can

> be very scary. The only way I know to help is to get really quite

and

try to breathe easy for 5 minutes or so. I am that way about all the

time now. I also turn my 02 up a little. I am about out of numbers on

this regulator.

> I don't realize it because it is now my norm. "I HATE THIS

DISEASE."

>

> Read information about your heating pad. Mine says don't use in

oxygen

enriched area... LOL I have been doing it for at least four years. Just

be careful.

> I may be having a rough time breathing but I am having fun with my

go

fast....... I have to get pics but I have to get dressed---boooo.

> lol Take care my friend

>

>

>

> Love & Prayers

> Peggy

> IPF, 2004

>

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