snip
>I am a pharmacist by profession, so hopefully
>I will be able to be of use if anyone has questions about medicines.
>Thanks for reading this far, and be well and free from pain,
>cheers,
>Pete
>(wow - my longest usenet post *ever*)
Welcome aboard Pete, although sorry you had to be here, but like you
say at least you know the score, so to speak. Did the RD or GP
prescribe folic acid with the methotrexate? If not check it out with
him/her and you'll probably be able to get a small bottle of folic
acid from work!!
I have RA, but I'm sure others like Chris R [with PA] will post
shortly.
Good luck
--
preceed with 2006 to email
no@emails.thx - 31 Jan 2006 01:13 GMT
>I have RA, but I'm sure others like Chris R [with PA] will post
>shortly.
(blushes)
ohh gosh ... I am famous ... at last!! Wohoo!! :oD
Chris R.
>I've just officially become an arthritis sufferer, so I thought I might
>drop in here and say hello.
Hello :o) Plenty of room inside - pull up a chair, pour a drink and
have a chat with the regulars :o)
>My problems began well over a year ago; pain and morning stiffness,
>starting with one ankle and one toe. This gradually worsened and spread
>to other joints.
> ... [snip]
Yup - your story sounds depressingly familiar - mine started with a
few 'funny' joints which were a bit stiff. Then my knee started
swelling dramatically and i was diagnosed with PA. Like you, I didn't
have Psoriasis to any great degree - just odd small patches.
>Anyway, he drained some fluid from the left knee joint - horrible at the
>time, but the immediate improvement in pain, swelling and stiffness made
>it worthwhile. He also injected some steroids into the knee.
Yeah - don't let anyone tell you "it's OK" ... or "we'll make sure it
won't hurt this time" ... they're damn liars! LOL I have had it done
twice and the second time they could have just injected the steroids
and not bothered trying to drain anything out - the fluid was as thick
as egg-white! Just thinking about that needle probing about is enough
to make me go white :oS
>have to wait weeks before I know if the MTX is helping, but at least
>something is happening to give me hope.
Well, don't look for any dramatic improvement from MTX ... it is more
of a stabilizer - with MTX the condition should be dampened down
considerably and you'll hopefully get less flare-ups and less joints
will head west. Also, whatever you do, don't think that you don't need
DMARDs. I stopped taking my MTX last Spring and spent the summer
regretting it and building my dose back up again.
If you're not reponding to just MTX + NSAID you could do worse than
try the combo I am on. My rheumy said sufferers often do better on
low/moderate does of MTX + Leflunomide (+NSAID). I just had constant
problems with lethargy and nausea when my MTX went about 10mg/week.
>Obviously I'm not exactly *happy* about receiving a diagnosis of a
>lifelong - and possibly life-changing - ailment, but at least I now know
>the enemy, and am feeling positive.
That's the thing to remember - knowledge is power - learn about it and
learn how to live with it. Also make sure you go to your
rheumatologist armed with the latest information so that you can show
him/her that you have an interest in your condition and can even
suggest which treatment you feel would suit your lifestyle best.
>Thanks for reading this far, and be well and free from pain,
>cheers,
Thanks Pete - and you too :o)
Chris R.
Robin Fairbairns - 02 Feb 2006 11:12 GMT
>>I've just officially become an arthritis sufferer, so I thought I might
>>drop in here and say hello.
[quoted text clipped - 11 lines]
>swelling dramatically and i was diagnosed with PA. Like you, I didn't
>have Psoriasis to any great degree - just odd small patches.
my first psoriasis was diagnosed when i went to the doctor with a
wound i thought wasn't healing. "the wound's gone, he said, that's
psoriasis". sure enough, it steadily spread: nothing much, ever, but
always something itching away somewhere.
the next time i went to the doctor (ca. 18 months later) it was
because several of my joints had seized up. he guessed it was pa, and
referred me -- the rheumatology dept confirmed his guess.
>>have to wait weeks before I know if the MTX is helping, but at least
>>something is happening to give me hope.
[quoted text clipped - 5 lines]
>DMARDs. I stopped taking my MTX last Spring and spent the summer
>regretting it and building my dose back up again.
mtx did nothing for me (over a very long period). then my liver
function started declining, and they switched me. i seem to have been
on lots of dmards (sufficiently many that i can't remember all of
them); i'm currently on azathioprine, which may or may not be
working. the best was cyclosporin[e?], but the blood test regime was
an awful bore. cyclosporin did a lot for the psoriasis, too, but it
all came back when i came off it. (it also made me *even* *hairier*,
something i wouldn't otherwise have thought possible -- cf picture on
http://www.cl.cam.ac.uk/~rf/ admittedly post cyclosporin)
i find the arthritis shifts its focus: i never actually know what's
going to "go" next. the plus side of this is that only a few joints
are "permanently" damaged (knuckles and huge bunions on my feet), the
the down side is not knowing how to limp from one day to the next :-)
(the day we buried my father, i had agonising pains in my chest: i
thought it must be a heart attack coming on, and was feeling guilty
about the effect it would have on my mother. however the pains just
stayed there for a few days, and then went away again. the rheums
said it might have been inflammation of the joint at the botttom of
the breast bone: i had never thought of that as a joint, and am still
a bit unclear what they were talking about.)

Signature
Robin Fairbairns, Cambridge
Hi Pete
... and welcome. Sorry about the arthritis - it can take a while to get a
diagnosis though can't it? I think it was about 18 months for me.
Good luck with the methotrexate - I take 10mg per week, combined with
Enbrel. A few years ago I was started on methotrexate alone, and was on
20mg. From memory (always risky!) it took about 12 weeks to work for me -
hope its not that long for you.
Jayne
> Hi all,
> I've just officially become an arthritis sufferer, so I thought I might
[quoted text clipped - 36 lines]
> Pete
> (wow - my longest usenet post *ever*)