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Well, I went and saw my family doctor today and she can't understand

why my oncologist hasn't set me up with a pain pump yet..so I'm

going off to a Pain Management Unit and they will organise a pain

pump to use at home...About time..now I don't need to worry about

finding people to babysit my little girl while I'm in hospital

anymore...and will have decent pain meds to ease the attacks some

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,

This is such a positive step forward, to have a pain pump. You

must be so relieved. I hope it works well for you and enables

you to stay at home with your child....instead of having to run to

the ER every time your pain goes out of control.

Once you have it, let us know how it's going.

With hope and prayers,

Heidi

Heidi H. Griffeth

South Carolina

SE & SW Regional Rep.

PAI, Intl.

Note: All comments or advice are personal opinion only, and

should not be substituted for professional medical consultation.

I'm going off to a Pain Management Unit and they will organise a

pain pump to use at home...

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...so I'm going off to a Pain Management Unit and they will organise

a pain pump to use at home...About time..

,

I just saw the post about the pain pump. Are you talking about an

implantable pump or one on the outside where you need an IV line?

Just curious, because I have an implantable and wanted to caution you

to make sure the doc who puts it in knows what he'a doing. I had to

return to surgery because the catheter came out of my spine because

the first doc did not anchor it.

Be Blessed,

Diane H

TN State Rep

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I have no idea Dianne, I don't need it all the time, just when I

have an attack, about 3 days a week. I don't have any idea how they

work and haven't been told how it works yet. I thought it would just

go into my port and was wondering...how do I shower with it being

stuck in there..and other silly questions like that. I've left a

message with my doctor's nurse to call me back and will ask about

this then..thanks for that bit of info.

catherine

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