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Jay, Hey, how did the rheumy go?

Take care,

Steph in VA

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Hi Namcy,

I did my first injection tonight. I am an EMT and do injections ans

IV's so I'm trained and used to it. Except it was on myself which

felt odd.

The needle and syringe is the same that diebetics use for insulin

injections.

I tend to agree with my RD that I am getting a more precise dose as

all the medicine is being absorbed and none being flushed out.

You can be trained to do the injections. it is very easy. Even I can

do it!!

Best wishes and God Bless,

Jay

--- In Rheumatoid Arthritis , " nmr " <nmr.01@t...>

wrote:

> Hi Jay,

>

> Do you have to go in weekly for the injection of Methotrexate or

are you to

> do it yourself? I find this very interesting as I'm currently

taking 25mg

> weekly in pill form.

>

> *hugs*

>

>

> ----- Original Message -----

> From: " Jay Bishop "

> Sent: Friday, August 29, 2003 5:39 PM

> Subject: Re: Jay

>

>

> > Hi Step,

> >

> > My Rheumy confirmed the DX of RA and made some changes in my meds.

> > He double my oral intake of Plaquinil to 200 mg daily. He

increased

> > my Methotrexate to weekly injection rather than oral and increased

> > the dosage from 10mg to 15mg. The reason for the injection is

there

> > is no real way of knowing how much the body is aborbing by the

> > intestines when taken orally, and I will get all of it by

injection.

> >

> > He also wants me to take between 1500 and 2000 mg of calcium with

Vit

> > D daily.

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  • 4 months later...

Thanks Jay,

Your message brought tears to my eyes.

Sierra

> > The bothersome side effects from Plquenil I described in an

earlier

> > post(light-headedness) seem to have nearly disappeared after 6

> weeks.

> > I'm grateful for that. I can take it with lunch at work and not

> have

> > to worry about seeming odd to others. I am seeing improvement

> > (decreased swelling and redness) in my hands. I still feel achy,

> but

> > Vioxx comes to the rescue there.

> >

> > Tonight I was doing some gentle yoga at home,wondering if I will

> ever

> > improve to the point of being able to keep up in a regular

exercise

> > class again. I really do not know what to expect. I guess we just

> > have to remain flexible (yoga joke) and accepting of whatever

> comes...

> >

> > I'd be interested in hearing people's experiences of coming to

> terms

> > with a diagnosis, if anyone wants to share.

> >

> > Sierra

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Sierra,

Your most welcome. My other daughters (older) also helped but the

little one carried me through when I wanted to just die get it over

with.

Hang in there, it will get better. It may take time but it will.

I am now on Enbrel and it has made a world of difference. Also

Methotrexate, prednisone, Plaquinil, Folic Acid, Trazadone (for

sleep), and Oxycodone for pain. I don't need much of the pain med

anymore and less Trazadone.

God Bless and good luck,

Jay

> > > The bothersome side effects from Plquenil I described in an

> earlier

> > > post(light-headedness) seem to have nearly disappeared after 6

> > weeks.

> > > I'm grateful for that. I can take it with lunch at work and not

> > have

> > > to worry about seeming odd to others. I am seeing improvement

> > > (decreased swelling and redness) in my hands. I still feel

achy,

> > but

> > > Vioxx comes to the rescue there.

> > >

> > > Tonight I was doing some gentle yoga at home,wondering if I

will

> > ever

> > > improve to the point of being able to keep up in a regular

> exercise

> > > class again. I really do not know what to expect. I guess we

just

> > > have to remain flexible (yoga joke) and accepting of whatever

> > comes...

> > >

> > > I'd be interested in hearing people's experiences of coming to

> > terms

> > > with a diagnosis, if anyone wants to share.

> > >

> > > Sierra

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  • 2 months later...
Guest guest

<<I saw your post Jay, here, did you miss it?

>>

I just checked the archives and it is there, however, it never came through back

to me. So, sorry about that.

Jay

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