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Hello Becky,

I'm so sorry you are feeling so low. You are at the right place for

receiving the advice and support you need. My CP is not gall-bladder

linked (it's hereditary) but there are plenty of people here with a

similar history to yours and I'm sure they'll be very willing to

share their experience. There are members who have had PICC lines,

of course.

All of us have gone through the misery of pancreatic pain and the

desperate search for a " cure " . There is no panacea but there are

ways in which the disease can be made easier to manage with a

greater degree of comfort for the patient.

I live in the UK so I'can't advise on specific docs. You are wise to

look for the best one possible, a really experienced

gastroenterologist or a specialist pancreatologist. CP is relatively

rare and few doctors see many cases, if any.

I sympathise about not being able to work or have an active social

life. That can be one of most devastating things about CP. However,

many people find themselves in that position and then improve under

certain treatment regimes. I'm sure there will be useful replies to

your post.

I do hope you soon get the help and advice you need and are moved

towards a less painful time. In the meantime, take heart from the

group. I don't know how I would have managed without everyone here

over the last 15 months since my diagnosis.

With very good wishes,

Fliss (UK)

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