Jump to content
RemedySpot.com

Re: University of Penn

Rate this topic


Guest guest

Recommended Posts

,

I'm so sorry that you are frightened. Please try not to be. Your son will be

at your side. Your family and we all will be, too, in spirit.

I think you really need this test, not because I suspect you have cancer,

but because an endoscopic ultrasound is a very good diagnostic tool which

will allow your physicians to take a very close look at your digestive tract

and the nearby organs. This way, they can look at your bile ducts and

pancreas in a way that they haven't before. You need some answers in order

to get some relief from your pain and bring you some peace of mind.

Here are some descriptions of the endoscopic ultrasound (EUS) procedure:

http://www.medicinenet.com/Script/Main/Art.asp?li=MNI & ArticleKey=6656

http://www.ncmedicaljournal.com/jan00/McGrath.htm

http://www.mayo.edu/mcj/gastro/endoultra.html

http://www.ucihealth.com/resource/chao%20cancer%20center/eus.htm

What do you mean the GI called after you cancelled the appointment? Which

appointment? Don't worry about anything he says. Just stay focused on the

upcoming test and appointment.

Please try to think of all of the important details of the events of the

last few months. You and your son may want to come up with a list of things

that happened and symptoms and all drugs that you were on before your first

attack and since. I know that they will have your medical record, but your

version of what happened may differ slightly. It won't hurt to add your

thoughts and questions.

Let me know what else you need.

----- Original Message -----

From: " Valued Compaq Customer " <ruf-caimi@...>

< egroups>

Sent: Wednesday, January 03, 2001 12:48 PM

Subject: [ ] University of Penn

> Hi Guy,

> Well they tell me all the test they took have come back normal. Doesn't

> mean 100% that there is no cancer. I have to go to the U. of P. next

> Tuesday for a Endoscopic Ultrasound. They know I have a dilated bile duct

> probably from somekind of blockage. I wasn't going to go but I made the

> appointment. The GI doctor called me yesterday after I canceled the

> appointment. He told me he knew I issues about school but I was putting

my

> education before my health. I know I don't like him and I think he thinks

> I am too old to be in school. Even my primary doesn't like him. This

> procedure is suppose to be a outpatient thing. I was told that when they

> did the ERCP, and I had to stay. My primary told me there is an 88%

> chance that there is no cancer. They even took lymph nodes and they were

> fine. My son told me if there is a cancer it is microscopic. The stint

> they put in is only good for two months after that there would be a

> horrible injection from it. No one told me that before it was done, I

> don't think I would have let them do it. The primary thinks they will

have

> to take it out before the procedure.

> Okay so I bummed, I keep thinking it could be worse and by God it does get

> worse. Nothing can be easy with me. I am glad that it will be done at

> the U. of P. Has anyone ever had this test. I'm scared, my son will be

> going with me, I don't think he would let anyone else take me.

> Me Mom

>

> Our websites: http://rheumatoid.arthritis.freehosting.net/

> http://www.rasupport.webprovider.com/

> Change subscription options:

>

>

Link to comment
Share on other sites

Me mom ,

I'm glad to hear that you made the appointment. I know you are scared, but

your really have to resolve this pancreatic problem. It is stopping you

from eating properly, and you will have other problems from not eating.

Maybe this will give you all the answers that you've been looking for. U

of Penn is a great hospital and you will be in good hands. I will keep you

in my prayers.

a

----- Original Message -----

From: Valued Compaq Customer <ruf-caimi@...>

< egroups>

Sent: Wednesday, January 03, 2001 1:48 PM

Subject: [ ] University of Penn

> Hi Guy,

> Well they tell me all the test they took have come back normal. Doesn't

> mean 100% that there is no cancer. I have to go to the U. of P. next

> Tuesday for a Endoscopic Ultrasound. They know I have a dilated bile duct

> probably from somekind of blockage. I wasn't going to go but I made the

> appointment. The GI doctor called me yesterday after I canceled the

> appointment. He told me he knew I issues about school but I was putting

my

> education before my health. I know I don't like him and I think he thinks

> I am too old to be in school. Even my primary doesn't like him. This

> procedure is suppose to be a outpatient thing. I was told that when they

> did the ERCP, and I had to stay. My primary told me there is an 88%

> chance that there is no cancer. They even took lymph nodes and they were

> fine. My son told me if there is a cancer it is microscopic. The stint

> they put in is only good for two months after that there would be a

> horrible injection from it. No one told me that before it was done, I

> don't think I would have let them do it. The primary thinks they will

have

> to take it out before the procedure.

> Okay so I bummed, I keep thinking it could be worse and by God it does get

> worse. Nothing can be easy with me. I am glad that it will be done at

> the U. of P. Has anyone ever had this test. I'm scared, my son will be

> going with me, I don't think he would let anyone else take me.

> Me Mom

>

> Our websites: http://rheumatoid.arthritis.freehosting.net/

> http://www.rasupport.webprovider.com/

> Change subscription options:

>

Link to comment
Share on other sites

M-M--

When I was looking into gastro referrals and my anemia

problems a year ago- after my GI doctor thought I had

Barrett's and my primary said I did not, I reviewed a

number of teaching hospitals. I went to Mayo because the

problem became more one of menstrual hemmorhagia and

clotting problems rather than GI bleeding. U of Penn is

one of the teaching hospitals my primary and I

considered when we thought it was more of a GI problem -

it is an excellent facility. I thought it might help if

you had one more person who told you how excellent their

rep - especially in the GI area -is. You are in my

prayers.

Hugs,

Link to comment
Share on other sites

Me Mom :

I am also glad you are having more testing done regarding your intestines.

Don't be afraid. The tests that they do are quite normal and they sedate you

so you will not feel anything. At least they may get to the bottom of the

problem. Please tell me what meds you are using for RA. My meds bothered my

stomach so so bad. It could perhaps be a combination of things. Good luck

and God Bless.

Jeannette

Link to comment
Share on other sites

M M :

88% chance of it not being cancer is quite high. 12% chance that it is

cancer is very low. Hold onto the positive. It is what gets us by and

creates less stress for us. You don't need any added stress to trigger RA

pain. I think it will work out good and that is my wish for you.

Jeannette

Link to comment
Share on other sites

Hi ,

I was suppose to go back to the GI specialist on Tuesday and I cancelled

the appointment. His nurse called to reschedule and I told her, I would

call her later. I didn't want to be rude to her, so I felt this was the

best way to leave it. Well two hours later the doctor called and left a

message on my machine to please call him. When I did they told me to call

back at the 2 they were eating lunch. I called at 2 and was told he left

for the day????????? In the mean time I was talking to my primary and he

knew how I wasn't going to go back to this doctor. He met up with him at

the hospital and explained things. The GI doctor called again and spoke to

me. That was how I knew the tests came back okay.

I just don't like him and I am tired of all his test having to be run two

or three times. I think he has made enough money off of me.

Me Mom

----------

> From: Matsumura <Matsumura_Clan@...>

> egroups

> Subject: Re: [ ] University of Penn

> Date: Wednesday, January 03, 2001 2:47 PM

>

> ,

>

> I'm so sorry that you are frightened. Please try not to be. Your son will

be

> at your side. Your family and we all will be, too, in spirit.

>

> I think you really need this test, not because I suspect you have cancer,

> but because an endoscopic ultrasound is a very good diagnostic tool which

> will allow your physicians to take a very close look at your digestive

tract

> and the nearby organs. This way, they can look at your bile ducts and

> pancreas in a way that they haven't before. You need some answers in

order

> to get some relief from your pain and bring you some peace of mind.

>

> Here are some descriptions of the endoscopic ultrasound (EUS) procedure:

>

> http://www.medicinenet.com/Script/Main/Art.asp?li=MNI & ArticleKey=6656

> http://www.ncmedicaljournal.com/jan00/McGrath.htm

> http://www.mayo.edu/mcj/gastro/endoultra.html

> http://www.ucihealth.com/resource/chao%20cancer%20center/eus.htm

>

> What do you mean the GI called after you cancelled the appointment? Which

> appointment? Don't worry about anything he says. Just stay focused on the

> upcoming test and appointment.

>

> Please try to think of all of the important details of the events of the

> last few months. You and your son may want to come up with a list of

things

> that happened and symptoms and all drugs that you were on before your

first

> attack and since. I know that they will have your medical record, but

your

> version of what happened may differ slightly. It won't hurt to add your

> thoughts and questions.

>

> Let me know what else you need.

>

>

>

> ----- Original Message -----

> From: " Valued Compaq Customer " <ruf-caimi@...>

> < egroups>

> Sent: Wednesday, January 03, 2001 12:48 PM

> Subject: [ ] University of Penn

>

>

> > Hi Guy,

> > Well they tell me all the test they took have come back normal.

Doesn't

> > mean 100% that there is no cancer. I have to go to the U. of P. next

> > Tuesday for a Endoscopic Ultrasound. They know I have a dilated bile

duct

> > probably from somekind of blockage. I wasn't going to go but I made

the

> > appointment. The GI doctor called me yesterday after I canceled the

> > appointment. He told me he knew I issues about school but I was

putting

> my

> > education before my health. I know I don't like him and I think he

thinks

> > I am too old to be in school. Even my primary doesn't like him. This

> > procedure is suppose to be a outpatient thing. I was told that when

they

> > did the ERCP, and I had to stay. My primary told me there is an 88%

> > chance that there is no cancer. They even took lymph nodes and they

were

> > fine. My son told me if there is a cancer it is microscopic. The

stint

> > they put in is only good for two months after that there would be a

> > horrible injection from it. No one told me that before it was done, I

> > don't think I would have let them do it. The primary thinks they will

> have

> > to take it out before the procedure.

> > Okay so I bummed, I keep thinking it could be worse and by God it does

get

> > worse. Nothing can be easy with me. I am glad that it will be done

at

> > the U. of P. Has anyone ever had this test. I'm scared, my son will

be

> > going with me, I don't think he would let anyone else take me.

> > Me Mom

> >

> > Our websites: http://rheumatoid.arthritis.freehosting.net/

> > http://www.rasupport.webprovider.com/

> > Change subscription options:

> >

> >

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

> Our websites: http://rheumatoid.arthritis.freehosting.net/

> http://www.rasupport.webprovider.com/

> Change subscription options:

Link to comment
Share on other sites

Hi a,

Thanks for your message. I am scared the primary told me there is an 88%

chance that there is no cancer. However, in my book that means there is an

12% chance that there is. I am glad I am going to the U. of P., I hear

only good things about it. My Rheumy called yesterday and wants to see me

soon. I was suppose to see him on the 29, but now I am going on Monday. I

know he is concerned that I am off of the Fosamax. I think he wants to

touch bases. I know he and the primary have been talking. He will be glad

I changed doctors, he told me he doesn't have a good working relationship

with the GI doctor I was going to. He had recommended that I change over a

month ago.

Hope you and are feeling better.

Me Mom

----------

> From: a <aA@...>

> egroups

> Subject: Re: [ ] University of Penn

> Date: Wednesday, January 03, 2001 9:54 PM

>

> Me mom ,

> I'm glad to hear that you made the appointment. I know you are scared,

but

> your really have to resolve this pancreatic problem. It is stopping you

> from eating properly, and you will have other problems from not eating.

> Maybe this will give you all the answers that you've been looking for.

U

> of Penn is a great hospital and you will be in good hands. I will keep

you

> in my prayers.

> a

>

> ----- Original Message -----

> From: Valued Compaq Customer <ruf-caimi@...>

> < egroups>

> Sent: Wednesday, January 03, 2001 1:48 PM

> Subject: [ ] University of Penn

>

>

> > Hi Guy,

> > Well they tell me all the test they took have come back normal.

Doesn't

> > mean 100% that there is no cancer. I have to go to the U. of P. next

> > Tuesday for a Endoscopic Ultrasound. They know I have a dilated bile

duct

> > probably from somekind of blockage. I wasn't going to go but I made

the

> > appointment. The GI doctor called me yesterday after I canceled the

> > appointment. He told me he knew I issues about school but I was

putting

> my

> > education before my health. I know I don't like him and I think he

thinks

> > I am too old to be in school. Even my primary doesn't like him. This

> > procedure is suppose to be a outpatient thing. I was told that when

they

> > did the ERCP, and I had to stay. My primary told me there is an 88%

> > chance that there is no cancer. They even took lymph nodes and they

were

> > fine. My son told me if there is a cancer it is microscopic. The

stint

> > they put in is only good for two months after that there would be a

> > horrible injection from it. No one told me that before it was done, I

> > don't think I would have let them do it. The primary thinks they will

> have

> > to take it out before the procedure.

> > Okay so I bummed, I keep thinking it could be worse and by God it does

get

> > worse. Nothing can be easy with me. I am glad that it will be done

at

> > the U. of P. Has anyone ever had this test. I'm scared, my son will

be

> > going with me, I don't think he would let anyone else take me.

> > Me Mom

> >

> > Our websites: http://rheumatoid.arthritis.freehosting.net/

> > http://www.rasupport.webprovider.com/

> > Change subscription options:

> >

>

>

> Our websites: http://rheumatoid.arthritis.freehosting.net/

> http://www.rasupport.webprovider.com/

> Change subscription options:

Link to comment
Share on other sites

Hi ,

I know this is a good hospital. Last Christmas night my brother received

his heart transplant at the U. of P.. He was treated great and of course

he still has to go back every other week. He is alive and well with the

heart.

Me Mom

----------

> From: k.j.choate@...

> egroups

> Subject: Re: [ ] University of Penn

> Date: Wednesday, January 03, 2001 10:48 PM

>

> M-M--

>

> When I was looking into gastro referrals and my anemia

> problems a year ago- after my GI doctor thought I had

> Barrett's and my primary said I did not, I reviewed a

> number of teaching hospitals. I went to Mayo because the

> problem became more one of menstrual hemmorhagia and

> clotting problems rather than GI bleeding. U of Penn is

> one of the teaching hospitals my primary and I

> considered when we thought it was more of a GI problem -

> it is an excellent facility. I thought it might help if

> you had one more person who told you how excellent their

> rep - especially in the GI area -is. You are in my

> prayers.

>

> Hugs,

>

>

> Our websites: http://rheumatoid.arthritis.freehosting.net/

> http://www.rasupport.webprovider.com/

> Change subscription options:

Link to comment
Share on other sites

Me Mom ,

Try to concentrate on the 88% and not the 12%. Stress and worry slow down

healing. It's hard sometimes to try staying positive especially when you

don't know what is wrong with you. 88% is a high number.

Being scared is normal. I can't wait for it to be over for you so you can

get back to living life and going to school.

(((hugs))))

a

----- Original Message -----

From: Valued Compaq Customer <ruf-caimi@...>

< egroups>

Sent: Thursday, January 04, 2001 8:12 AM

Subject: Re: [ ] University of Penn

> Hi a,

> Thanks for your message. I am scared the primary told me there is an 88%

> chance that there is no cancer. However, in my book that means there is

an

> 12% chance that there is. I am glad I am going to the U. of P., I hear

> only good things about it. My Rheumy called yesterday and wants to see me

> soon. I was suppose to see him on the 29, but now I am going on Monday.

I

> know he is concerned that I am off of the Fosamax. I think he wants to

> touch bases. I know he and the primary have been talking. He will be

glad

> I changed doctors, he told me he doesn't have a good working relationship

> with the GI doctor I was going to. He had recommended that I change over

a

> month ago.

> Hope you and are feeling better.

> Me Mom

Link to comment
Share on other sites

Thank you a, I just can't concentrate on anything. I just talked to my

son and he told me that since the brushings and small stuff came back okay

and that is a good sign. He also said that there could be stones there

that are very small and the other doctor couldn't pick it up. He also told

me that when he first started working after grad school he thinks he

interviewed the GI doctor I was seeing. He said he was arrogant. I told

him if I need a gastro doctor after Tuesday, I will go to the one his

father-in-law wanted me to go too. He is pleased with that decision, he

thinks I probably will need someone.

He also said that with all the drugs anyone with RA takes, their immune

system is very sensitive. This makes everything medically harder. I see

my primary tomorrow. Thank you for trying to help and you have.

Me Mom

----------

> From: a <aA@...>

> egroups

> Subject: Re: [ ] University of Penn

> Date: Thursday, January 04, 2001 9:15 AM

>

> Me Mom ,

> Try to concentrate on the 88% and not the 12%. Stress and worry slow

down

> healing. It's hard sometimes to try staying positive especially when

you

> don't know what is wrong with you. 88% is a high number.

> Being scared is normal. I can't wait for it to be over for you so you

can

> get back to living life and going to school.

> (((hugs))))

> a

>

>

> ----- Original Message -----

> From: Valued Compaq Customer <ruf-caimi@...>

> < egroups>

> Sent: Thursday, January 04, 2001 8:12 AM

> Subject: Re: [ ] University of Penn

>

>

> > Hi a,

> > Thanks for your message. I am scared the primary told me there is an

88%

> > chance that there is no cancer. However, in my book that means there

is

> an

> > 12% chance that there is. I am glad I am going to the U. of P., I hear

> > only good things about it. My Rheumy called yesterday and wants to see

me

> > soon. I was suppose to see him on the 29, but now I am going on

Monday.

> I

> > know he is concerned that I am off of the Fosamax. I think he wants to

> > touch bases. I know he and the primary have been talking. He will be

> glad

> > I changed doctors, he told me he doesn't have a good working

relationship

> > with the GI doctor I was going to. He had recommended that I change

over

> a

> > month ago.

> > Hope you and are feeling better.

> > Me Mom

>

>

>

> Our websites: http://rheumatoid.arthritis.freehosting.net/

> http://www.rasupport.webprovider.com/

> Change subscription options:

Link to comment
Share on other sites

Hi Jeannette,

With all you have been going through, it is nice of you to think of me.

The meds I am on just for the Ra, are predisone, metho pill form but I have

ask to go on the injection. I have learned from this group that this will

by pass my stomach. Folic acid I was on clinoril but that was stopped.

Remicade that has been stopped too. Druggist tells me that is the drug

that is the culprit. Darvocet is the really bad days. Alluvial at night,

I couldn't sleep so they gave me that. Fosamax but that was stopped too, I

know the Rheumy wants that started as soon as possible. I see him on

Monday. I hope they put me to sleep. My son said it is the same as the

ERCP except at the end they use different instruments. This is the one day

he has to be at work, so my daughter-in-law is taking me. I'm okay with

this, actually if Ricky can't come Bonnie is an excellent one to go. She

will ask all the right questions and she will understand what he is talking

about.

Thank you for helping, it is a shame we have to take the drugs we take.

Without them though, our quality of life would not be as good. I know my

sister will say why do you take those drugs, but she can't understand she

doesn't have the disease.

Me Mom

----------

> From: ednettieolson@...

> egroups

> Subject: Re: [ ] University of Penn

> Date: Thursday, January 04, 2001 12:58 PM

>

> Me Mom :

>

> I am also glad you are having more testing done regarding your

intestines.

> Don't be afraid. The tests that they do are quite normal and they sedate

you

> so you will not feel anything. At least they may get to the bottom of

the

> problem. Please tell me what meds you are using for RA. My meds

bothered my

> stomach so so bad. It could perhaps be a combination of things. Good

luck

> and God Bless.

>

> Jeannette

>

> Our websites: http://rheumatoid.arthritis.freehosting.net/

> http://www.rasupport.webprovider.com/

> Change subscription options:

Link to comment
Share on other sites

-

Did I read one of your notes correctly- that your doctor

wants you to take FOSOMAX?! My GI problems and

irritation started with Fosomax- it is extremely hard on

the GI tract - especially when you take the crud we do.

My doctor switched me over to miacalcin- you inhale that

and I still had problems. You may want to bring up the

fosomax to the new guy and see if it is a good guy. If

someone charged me the deductible before I saw the

doctor- its the last time I'd see them. It would give me

a pretty clear picture of their priorities.

Hugs,

Link to comment
Share on other sites

Hi ,

I have been on Fosomax for two years. The Rheumy just gave me the once a

week pill. I have not been able to go on it though. I hope to know more

about this on Monday when I see him. I knew it was very hard on the

stomach. I am glad that now I know about some other drugs. I see my

primary today so I will bring it up.

Thanks,

Me Mom

----------

> From: k.j.choate@...

> egroups

> Subject: Re: [ ] University of Penn

> Date: Thursday, January 04, 2001 8:57 PM

>

> -

>

> Did I read one of your notes correctly- that your doctor

> wants you to take FOSOMAX?! My GI problems and

> irritation started with Fosomax- it is extremely hard on

> the GI tract - especially when you take the crud we do.

> My doctor switched me over to miacalcin- you inhale that

> and I still had problems. You may want to bring up the

> fosomax to the new guy and see if it is a good guy. If

> someone charged me the deductible before I saw the

> doctor- its the last time I'd see them. It would give me

> a pretty clear picture of their priorities.

>

> Hugs,

>

>

> Our websites: http://rheumatoid.arthritis.freehosting.net/

> http://www.rasupport.webprovider.com/

> Change subscription options:

Link to comment
Share on other sites

,

The paying of the fee before I saw the doctor is the first thing I thought

was strange. God forbid if you didn't have it. You can not see the doctor

until you pay. I am glad I am changing doctors.

Me Mom

----------

> From: k.j.choate@...

> egroups

> Subject: Re: [ ] University of Penn

> Date: Thursday, January 04, 2001 8:57 PM

>

> -

>

> Did I read one of your notes correctly- that your doctor

> wants you to take FOSOMAX?! My GI problems and

> irritation started with Fosomax- it is extremely hard on

> the GI tract - especially when you take the crud we do.

> My doctor switched me over to miacalcin- you inhale that

> and I still had problems. You may want to bring up the

> fosomax to the new guy and see if it is a good guy. If

> someone charged me the deductible before I saw the

> doctor- its the last time I'd see them. It would give me

> a pretty clear picture of their priorities.

>

> Hugs,

>

>

> Our websites: http://rheumatoid.arthritis.freehosting.net/

> http://www.rasupport.webprovider.com/

> Change subscription options:

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...