Hi I am new here, Debbie

[Guest guest]

Hello, yes I am also one of the non identified PC objects out there and

I am also quite new here but I have already had so much help from the

network.

Nothing on tests, MRCPs ultrasound or whatever, but the symptoms are

there just like CP, and enzymes help and the antioxidanttherapy I was

recommended from the UK . I get attacks even with the enzymes, it comes

and goes, I never know. Dont hope too much for an answer, I did for 8

months, hoping and hoping, but never getting a result. It is more than

frustrating beeing without a diagnose and only be treated by symptoms.

It seems they dont really beleive you. I have to see a psychiatrist now

to get my sickleave prolonged. And I have been so sick, cramps,

pain,loosing a lot of weight, not able to get out of bed. Deadly tired,

and so on, my whole life collapsed. This site is a blessing I would not

have made it without all the support I have had by mail from so many.

And all the advice! Keep on chatting, asking, I have understood that at

least I am not alone, neither are you. I dont know where my CP comes

from, I have been drinking (not for the last year) it is part of my job

to be social, but I know of many who have consumed much more than me and

are not struck by this horror. So, dont blame yourself, who knows, I had

breastcancer too, from what, why? I understand you are asking yourself,

did I cause it myself, leave it, it only makes it worse, we never know

about any desease, people have smoked a lifetime and dont get

lungcancer…others dont and get it.. I had a good advice and that is to

try to find a Doctor specialized in Pancreas. Keep on mailing you´ll

feel the support, we are all in the same situation, more or less where

ever we come from. Lots of Love from Stockholm Sonja