Delayedmail sent through England Suzie, chills

[Guest guest]

Sent: 09 December 2004 19:25

To: pancreatitis@...

Subject: To Suzie, freezing, chills

Dear Suzie, thanks for your answer even if it hurts it also helps to

hear someone else having the same problems. My doctors dont seem to want

or know how do deal with it. They dont at all connect it with my CP,

they regard me as weird, with multiple syndroms, they say its allergy

(mouth), some kind of reumaproblems with the chills in hands and feet.

Everything but not what I am trying to say, it comes with my eating,

left side pain and so on, CP symptoms. I get red spots on my face,

flaring up also in connection but they dont want to listen. I nearly

passed out in hospital and at home many times last year, they ignored it

and asked if I wanted something calming me down. I had spasm in all of

my body ones, thought I was dying and when it gets up towards my neck

and head, slow motion and hard to speak. It takes up to one hour or at

worst couple to get back to life again. Why on earth doesn´t anyone

listen to us and beleive us?

Thanks for your answer. Lots of Love from Sonja