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Medical Forum / Diseases and Disorders / Arthritis / July 2004

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Started the Methotrexate

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R. Joanne Johnson - 22 Jun 2004 13:58 GMT
Hi everyone,
I gave myself my first injection on Friday night. I had no problem doing it
at all. My experience with Type I Diabetes stood me in good for that! (use
an pump now).

I felt just fine until late Sunday mrning when I felet tired and had a bit
of an off taste in my mouth bordering on a little bit of nausea. By Monday
(yessterday) just fine! The daily maintenance dose of Prednisone and Bextra
are helping until that begins to work.

A few questions.
How long before results with the mthx?

Is it true about the exposure to sick people (colds etc.)? I work in schools
(sub teacher now, part time computer teacher in an elemntary/middle school
in September) and wonder if being around kids will...well you know.

Really interested in experiences. I only started on 0.4 ml, but doctor said
that it is started small and will be built up.

Thanks everybody,
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RoseB - 22 Jun 2004 14:38 GMT
>How long before results with the mthx?

It can take awhile unfortunately.
>Is it true about the exposure to sick people (colds etc.)? I work in schools
>(sub teacher now, part time computer teacher in an elemntary/middle school
>in September) and wonder if being around kids will...well you know.
I teach First Grade and have been on mtx for ten years. I actually
didn't feel that I caught more colds, etc. In the past it seems like I
had one big cold that lasted almost all year, with mtx  that didn't
seem to be the case any more. We do become immune to certain types of
cold and flu after being exposed. There seemed to be more of a risk
with imuran, for catching colds and flu.
Rose
@}>-->>>
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R. Joanne Johnson - 24 Jun 2004 11:19 GMT
Hi Rose and thank you for chiming in!

I guess I asked that question because I saw on the drug info sheet to avoid
people with infedctions...ha, as if you could do that in life, right, LOL! I
know when I was teaching all those years full time and was int eh same
clkassroom day after day, the kids could be dropping around me with all
kinds of stuff and I never seemd to really get sick...had this theory that I
built up an immunity to the germs living in that classroom.

Guess it is a silly fear on my part but this is all so new to me.(the mtx)

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RoseB - 25 Jun 2004 01:06 GMT
>Guess it is a silly fear on my part but this is all so new to me.(the mtx)
I don;t blame you. It does sound really scary when you read the
literature. Some of what they say is more specific to the high dose
mtx used to treat cancer.

Because of this potential increased risk for us, it makes it that much
more important to teach good hygiene to the kids so that they are
doing appropriate self care when they have colds etc.,
ROse
@}>-->>>
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Newsgroup Spambuster - 22 Jun 2004 15:02 GMT
Joanne, one thing that has worked for many here that take mtx is to make
sure you are very well hydrated (lots of water!) the day you take your
mtx.   This often helps cut down on the nausea and such.  Also, many
people take it at night just before bedtime so that they sleep through
some of the side effects.   Just some thoughts.

It can often take quite a while for the mtx to kick in, especially at
lower doses.   Many people find that they really don't notice that much
of an effect until they reach the 15 mg. or higher mark with the mtx.  

As far as the working around children and getting sick more often, that
seems to be a highly individual thing for most.   Some don't notice any
more illness than normal, while others tend to get sick more often.  

Good luck to you and really hope the mtx does the trick for you!!!

Donna G
R. Joanne Johnson - 24 Jun 2004 11:22 GMT
Donna thank you for your good wishes! And also the good advice. I will make
sure to drink that water! I am taking only a small amount , injected 0.4 ml.
My doctor is going to build it up as we go seeing what the toleration is and
liver tests of the first month show.

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>
> Joanne, one thing that has worked for many here that take mtx is to make
[quoted text clipped - 14 lines]
>
> Donna G
edrina - 23 Jun 2004 21:53 GMT
> Hi everyone,
> I gave myself my first injection on Friday night. I had no problem doing it
[quoted text clipped - 17 lines]
>
> Thanks everybody,

Hi

My father had RA and I am also a carrier. He was on MTX for 2 years.  
I have since spoken to his Rhumatologist and was told that he should
have been on folic acid and should have had regular liver function
tests.   Unfortunately his GP was not very good about this.   Please
make sure that you get all the regular checks and also that you are
checked for folic acid requirements - you also need to consume plenty
of water.

Good luck with the treatment
R. Joanne Johnson - 24 Jun 2004 11:25 GMT
Thanks for the good wishes. I am sorry too, that thiungs did not work out so
well for your father. I am taking the folic acid and will be very faithful
about the tests monthly. I think I have a good Rheumatologist and will have
to trust him to do the right thing here. I am also picking up some good
information in this group. It is a whole new world to me.
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Harvey R. Stone - 24 Jun 2004 20:24 GMT
> Hi
>
> My father had RA and I am also a carrier.

Hhhm,,,  I find your use of the word carrier to be interesting and
confusing.   Would you explain to me what you mean or how you use the word.
Harv
Squirrely - 27 Jun 2004 07:26 GMT
Joanne,

I sure hope you do great on the MTX. congrats on doing your first shot. ;-)

I hope that is all you get from side effects of the MTX. That would be good.

I am glad the pred and Bextra are helping you too.

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Love and hugs to all
Good thoughts coming your way too.

Squirrely Jo

> Hi everyone,
> I gave myself my first injection on Friday night. I had no problem doing it
[quoted text clipped - 17 lines]
>
> Thanks everybody,
R. Joanne Johnson - 27 Jun 2004 13:14 GMT
Hi Sqirrely!
Now did my second shot on Friday and did what I read he...yesterday I forced
a lot of fluids! So far so good!

Thanks for the words of support...really makes me feel more comfortable with
the whole thing. I have positive feelings about it, I am hoping and praying
to retard this RA in its tracks.
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> Joanne,
>
[quoted text clipped - 29 lines]
> >
> > Thanks everybody,
Harvey R. Stone - 27 Jun 2004 14:30 GMT
> Hi Sqirrely!
> Now did my second shot on Friday and did what I read he...yesterday I forced
[quoted text clipped - 3 lines]
> the whole thing. I have positive feelings about it, I am hoping and praying
> to retard this RA in its tracks.

:-)   and so do we.   It was good for me for 7-8 years and got me out of bed
and back to work.  You would not believe how many of us were just as scared
of the medicine.   If we do nothing else,,,, its the disease we should be
afraid of.
Harv
Squirrely - 29 Jun 2004 19:55 GMT
Joanne,

Gld to hear your second shot went ok too.

Yeah isn't the group great at giving helpful info.

Good luck with this new meds and I hope it is the miracle drug for you.

Signature

Love and hugs to all
Good thoughts coming your way too.

Squirrely Jo

> Hi Sqirrely!
> Now did my second shot on Friday and did what I read he...yesterday I forced
[quoted text clipped - 3 lines]
> the whole thing. I have positive feelings about it, I am hoping and praying
> to retard this RA in its tracks.
R. Joanne Johnson - 30 Jun 2004 13:19 GMT
Hi Squirrely and Harvey,
Yes, Harvey, I am more afraid of what will happen without the medicine and
will deal with the side effects! Squ. Jo, yes, reading here has really given
me some information I was missing. Now I know why my doctor was dragging his
feet about treatment until he was absolutely positive.

Thank you !
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> Joanne,
>
[quoted text clipped - 14 lines]
> praying
> > to retard this RA in its tracks.
Squirrely - 02 Jul 2004 19:57 GMT
Joanne,

I hope the treatment keeps giving you good results with no side affects.

I am glad you got the info here from the group that you needed.

Signature

Love and hugs to all
Good thoughts coming your way too.

Squirrely Jo

> Hi Squirrely and Harvey,
> Yes, Harvey, I am more afraid of what will happen without the medicine and
[quoted text clipped - 3 lines]
>
> Thank you !
 
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