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I have CP and just found this support group. I would really like to

hear from you, I really need help through this time in my life and I

just know all of you understand and can help me.

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Hi assistant2pdg,

and welcome to this site.

I am new here as well but I can tell from watching and listening the

people here are super and will help in any way possible...

as will I if I have anything you can use you are certainly welcome to

it!

Glad you are here and come on back,

Shelia

> I have CP and just found this support group. I would really like to

> hear from you, I really need help through this time in my life and I

> just know all of you understand and can help me.

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Hi assistant2pdg,

and welcome to this site.

I am new here as well but I can tell from watching and listening the

people here are super and will help in any way possible...

as will I if I have anything you can use you are certainly welcome to

it!

Glad you are here and come on back,

Shelia

> I have CP and just found this support group. I would really like to

> hear from you, I really need help through this time in my life and I

> just know all of you understand and can help me.

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> I have CP and just found this support group.

-------------------------------------------------------------

Hi Welcome aboard!! I am so sorry that you had to seek us out but am

very glad you found us. this is a wonderful group that has helped me

out so many time. I only hope that I can return the favor in some

small way.

Where do you live? Maybe there are some members in your area. Also,

whats your name..LOL. Ask anything you want; we talk about everything

here and between us all we have gone through it all.

Warmly,

(SC)

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Hi Teal,

Well, another hoosier, I keep telling you all there is something about the

upper midwest that is associated with this disease. Again, an x-hoosier (but

always there)

Best wishes, Poncho - GA

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Thank you. I am just glad to finally find people that understand. My name is

Teal and I live in Indiana. I still work (where I am now). I am reading all

your stories or questions and just cannot believe it, I have these problems and

it is very nice to learn I am not the only one. I never really realized how

alone I felt until I've been reading this. I will write more when I can (when I

finish my task at hand), I will tell you my story and hope to hear yours.

Teal

wrote:

> I have CP and just found this support group.

-------------------------------------------------------------

Hi Welcome aboard!! I am so sorry that you had to seek us out but am

very glad you found us. this is a wonderful group that has helped me

out so many time. I only hope that I can return the favor in some

small way.

Where do you live? Maybe there are some members in your area. Also,

whats your name..LOL. Ask anything you want; we talk about everything

here and between us all we have gone through it all.

Warmly,

(SC)

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Teal

I am from Indiana also. What part do you live in?

Patty Duley

Corydon, IN

" ---------------------------------

---------------------------------

Start your day with Yahoo! - make it your home page

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I live in Madison County - I've never heard of your city, where is

that?

Teal

> Teal

> I am from Indiana also. What part do you live in?

> Patty Duley

> Corydon, IN

>

> " ---------------------------------

>

>

>

>

> ---------------------------------

> Start your day with Yahoo! - make it your home page

>

>

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Hi,

Welcome. Come on in and share your story. I am Angie, I am 38. I live in SC.

I have had chronic pancreatitis for 2 years (diagnosed!). I had surgery in

ton to open up the ducts about 5 weeks ago. I have pancreas divisum. That

is what caused my cp. Let us know your story and how we can help. There are

some great people here with alot of info!

Angie in SC

" The happiest of people don't necessarily have the

best of everything; they just make the best of everything that comes along

their way. "

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Teal,

The surgery was not to awful but it is not the easiest thing I have ever had

either! It has helped some but I still will have chronic pain. It is not as

bad as before so I will take what I can get!

Ouch on the disk in your back being hit! That must have been horrible! I am

going to a pain doc for the first time on Aug. 4th and I wanted one who did

not do blocks right away. I want to get to know someone and research how they

have done and their " track record " so to speak before I let them do anything to

me!

It is so frustrating not have a definite diagnosis. I went like that for 2

and 1//2 years and finally when I went to ton to the docs at MUSC they

saw the divisum and said I needed surgery. They have been wonderful to me!

I hope they can get some answers for you soon! Now speaking of rambling,

look at what I have done! I am a horrible rambler! Sorry!

Take care,

Angie in SC

" The happiest of people don't necessarily have the

best of everything; they just make the best of everything that comes along

their way. "

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Hello -

How are you doing since your surgery? I am married and 30 years

old. I have had pain for most of my life however, just diagnosed in

2000. At this point in time, I am attempting to get a second

opinion from a dr in Cincinnati. I am very upset lately b/c the dr

told me that there was nothing more they could do for me. I have

been told that my pancreas is misshaped but so many of the drs have

used different terms and the term " divisum " is one they have used.

I have had 2 Celiac Plexus Blocks which neither worked. The last

one I had the drs " inadvertantly " hit a disk in my back, which

caused more pain than I was in before I had the block! Sorry I am

rambling.

Teal

Indiana

> Hi,

> Welcome. Come on in and share your story. I am Angie, I am 38. I

live in SC.

> I have had chronic pancreatitis for 2 years (diagnosed!). I had

surgery in

> ton to open up the ducts about 5 weeks ago. I have pancreas

divisum. That

> is what caused my cp. Let us know your story and how we can help.

There are

> some great people here with alot of info!

> Angie in SC

>

> " The happiest of people don't necessarily have the

> best of everything; they just make the best of everything that

comes along

> their way. "

>

>

>

>

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Angie:

I am glad to hear surgery helped a little bit. You are right in

this you take what relief you can get. The only reason they decided

to do the pain blocks was b/c the pancreatic surgeon was not sure if

surgery would help me b/c of how my pancreas " malfunctions " as well

as how it is physically misshaped. The only definite diagnosis they

have said was " idiopathic chronic pancreatitis " . During many of my

ERCP's they have talked about the " pressures " being very high...now

from reading and researching I think that means something else????

Idk I hope I can get into another dr very soon...I would like to at

least get on with the thought of getting better, does that make

sense? Also, I have went to one session with a massage therapist /

energy therapist yesterday. I don't know if it has helped yet, she

said it may take more than one session but it may help it may

not...she told me to wait and see how I felt over the next couple of

days. Now I am rambling again - sorry!

Teal

Indiana

> Teal,

> The surgery was not to awful but it is not the easiest thing I

have ever had

> either! It has helped some but I still will have chronic pain. It

is not as

> bad as before so I will take what I can get!

> Ouch on the disk in your back being hit! That must have been

horrible! I am

> going to a pain doc for the first time on Aug. 4th and I wanted

one who did

> not do blocks right away. I want to get to know someone and

research how they

> have done and their " track record " so to speak before I let them

do anything to

> me!

> It is so frustrating not have a definite diagnosis. I went like

that for 2

> and 1//2 years and finally when I went to ton to the docs

at MUSC they

> saw the divisum and said I needed surgery. They have been

wonderful to me!

> I hope they can get some answers for you soon! Now speaking of

rambling,

> look at what I have done! I am a horrible rambler! Sorry!

> Take care,

> Angie in SC

>

> " The happiest of people don't necessarily have the

> best of everything; they just make the best of everything that

comes along

> their way. "

>

>

>

>

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Teal, I have Botox, it works wonderfully! I know Baylor and s Hopkins does

botox, but I am not sure who else, It is worth asking. It lasts up to 6 months.

I got mine 9 March. So far so good. I get breakthrough pain, but it's not a big

deal, I just yoga breath my way through that and I am good to go. -Kathleen

assistant2pgd wrote:>

>

>

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Teal,

The massage therapy sounds wonderful, if nothing else than to relax and take

your mind off of the pain for a while! I think I could go for that!!

Angie in S C

" The happiest of people don't necessarily have the

best of everything; they just make the best of everything that comes along

their way. "

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It was very relaxing, I am not sure if it has helped my pain, it is

something that will take some time but other than the cost I'd love

to do it again.

Teal

> Teal,

> The massage therapy sounds wonderful, if nothing else than to

relax and take

> your mind off of the pain for a while! I think I could go for

that!!

> Angie in S C

>

> " The happiest of people don't necessarily have the

> best of everything; they just make the best of everything that

comes along

> their way. "

>

>

>

>

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