Mond: hi peeps, had my tp Feb 2016, lots... - British Liver Trust

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Mond

Mondimoo profile image
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hi peeps, had my tp Feb 2016, lots of illness before, lots after

but seem to be finally on mend, but bones still hurt alot, and the chronic rib cage pain is really a problem I can't seem to get ANY help with. Ideas?????

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Mondimoo profile image
Mondimoo
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Isabelle2 profile image
Isabelle2

Hi

I had my tp a yr ago. I have had pain in my joints esp fingers and hands also shoulders. My rheumatologist reckons its the effects of advagraf or cellcept. Changed cellcept to myfortic but still hurts. It seems a bit less painful now - brain adapting to it? At first it was quite debilitating but now more of a nuisance. The problem is we need our immunosurpresseurs! I don’t know if this helps.

Hope it gets better

Isabelle

Litimag profile image
Litimag

I'm one year post transplant and still get some joint pain too. Chronic fatigue as well, coupled with a constant headache lol. I tend not to stress it too much when I am at the clinic though, I seriously don't want them messing with my Prograf levels or whatever because of some tolerable joint and head pain. It's a bit of a balancing act really.

Dorset1 profile image
Dorset1

Hi Mondoo

Had my TP October 16. Still get pain under ribs, some wound & back pain.

Am trying to be as active as possible. I have even started running (at 61)!!

I think it does help with the aches & pains & certainly with my state of mind.

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