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i had this the past two weeks, the rheumatologist gave me a fluid pill. i was

reading up on it, it said it would help the swelling but not what was causing

it. my feet looked like watermelons....my hands were so sore and swollen too.

stoddardtim <tstoddard@...> wrote: my hands and feet seem to swell up,

more so in the am

i dont know if this is normal or not. the pain still stays the same.

has anyone else had thi problem. thanks tim

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the tops of my feet swell all the time from everything from the weather, to

drinking thew wrong kind of liquid. The look like they have their own little

pillows! My doc lets me keep a water pill on hand so I can take if needed,

stoddardtim <tstoddard@...> wrote: my hands and feet seem to swell up,

more so in the am

i dont know if this is normal or not. the pain still stays the same.

has anyone else had thi problem. thanks tim

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My swelling is happening in the afternoons. But the soreness is

all day. Some one said it was because of barometric pressure. Is

that true with RA?

my hands and feet seem to

swell up, more so in the am

> i dont know if this is normal or not. the pain still stays the

same.

> has anyone else had thi problem. thanks tim

>

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  • 2 months later...
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> How common is it to have no visible swelling? I ask because

that's my

> situation and one of the major reasons (actually, it might be the only

> reason) I'm still in " official " diagnosis limbo.

I don't swell very badly until evening, and then you can only notice if

you know me. My knuckles do get hot, but not red. My rh dx'd me using

the thing where he squeezes my joints and sees how many hurt. There's a

scientific name for that, but I can't remember...

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