Yummmm and some other stuff

[Guest guest]

Okay, so I've convinced my husband to let me take my Geodon later than dinnertime, after another night ended up with me asleep on the couch at 10:30 and waking up at 2:30 to find he's still on the computer, and then me waking up at 7 not able to get back to sleep, and being antsy.  He says I can take my Geodon no later than 9:00, so I needed something I could eat at 9, since it has to be taken with food.  I've been craving brownies, so they are in the oven now.  Then at 9, I can just have a brownie with my Geodon. 

I still don't really know how to react to my MS doctor wanting me to see my local neurologist for pain control.  I mean, this is really the first time I've had bad pain, other than pain brought around from holding myself differently when I'm in a flare.  I guess I call my local neurologist Monday, and whichever doc I get into first (he usually is hard to get into, and I'm supposed to get scheduled for a follow up appointment with her once my blood test results are in to talk about Tysabri), I see what's going on.  But this makes me wonder, if I start having other problems related to my MS, is she just going to refer me back to him?

I think I may have started having problems with urinary retention, at least that's what it feels like.  My primary doc six months ago had referred me to a urologist because " people with ms have problems with their bladders " (this after my first UTI under his care).  I checked out fine at that appointment, but I'm due for a recheck, so I have a feeling I'd better keep it and get checked out.

Tina

[Guest guest]

Tina I will continue to keep you in my prayers.

Hugs

nne

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> Yummmm and some other stuff

>

> Okay, so I've convinced my husband to let me take my Geodon later than

> dinnertime, after another night ended up with me asleep on the couch at

> 10:30 and waking up at 2:30 to find he's still on the computer, and then

> me

> waking up at 7 not able to get back to sleep, and being antsy. He says I

> can take my Geodon no later than 9:00, so I needed something I could eat

> at

> 9, since it has to be taken with food. I've been craving brownies, so

> they

> are in the oven now. Then at 9, I can just have a brownie with my

> Geodon.

>

> I still don't really know how to react to my MS doctor wanting me to see

> my

> local neurologist for pain control. I mean, this is really the first

> time

> I've had bad pain, other than pain brought around from holding myself

> differently when I'm in a flare. I guess I call my local neurologist

> Monday, and whichever doc I get into first (he usually is hard to get

> into,

> and I'm supposed to get scheduled for a follow up appointment with her

> once

> my blood test results are in to talk about Tysabri), I see what's going

> on.

> But this makes me wonder, if I start having other problems related to my

> MS,

> is she just going to refer me back to him?

>

> I think I may have started having problems with urinary retention, at

> least

> that's what it feels like. My primary doc six months ago had referred me

> to

> a urologist because " people with ms have problems with their bladders "

> (this

> after my first UTI under his care). I checked out fine at that

> appointment,

> but I'm due for a recheck, so I have a feeling I'd better keep it and get

> checked out.

>

> Tina

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