Wound up in the Emergency Room
#21
(Mon-04-08-2014, 20:27 PM)Caroline Wrote: Sorry Jim, mixed you up with Fred again.
You both look so alike !
Angel

Spank Spank Spank how dare you I'm much better looking Big Grin
Reply
#22
(Mon-04-08-2014, 20:17 PM)Caroline Wrote: Hello Sandra,

That does not sound good, all this pain in the past years. And in all those joints ! You seem to have the same Jim and I, PsA or psoriatic arthritis. But normally PsA sticks to the tiny joints of hands and feet.
Good that you now are seeing a rheumatologist, but beware, those doctors are old fashioned. With that I mean that they will probably try to set you on MTX, methotrexate, one of the worst psoriasis medications.
And more, it appears more and more that it does not help on PsA.
You can read the article [Post=610] on our own psoriasisclub, and you can google on methotrexate no better than placebo for psoriatic arthritis Dr. Christopher T. Ritchlin,

Take the research with you if you are going to the reumatologist, I have been there also, see also [post=2031] for a discussion, and other posts.

Keep us posted maybe we can be of further help to you.
Caroline
Hi Caroline and Jim
Thanks for the info. I will certainly go in armed with the research. I said it may take a few months as there is a 6-12 week wait for appointments and that's urgent. My joints seem to flare up when the psoriasis flares. Keeping active, moving is the only thing G.P. Can say at present, which I do, but I did say, "you try doing it when it feels like you are walking on glass" also reccomended rest! Again I work, and in a real catch twenty two situation as I can't take tramadol when driving, so can only take in the evening. Still moaning won't change it. Just got to get on with it and actually I do, most of the time. I was just so fed up with being diagnosed with all sorts and no connection made to the psoriasis.
Anyway moan over and thanks for the advice and support.
Sandra
Reply
#23
I think it's good to moan and get those frustrations out, we've all done it on here, that's the beauty of the forum, we have all been in the same situation, some of us lucky ones have found the treatment that works for us ..... Others like you are still looking, I'm sure there is something that will control yours if Fumaderm isn't for you there's plenty more in the armoury to try.

Has the Fumaderm done anything for you ( apart from make you hot and itchy?)
Did it affect the psoriasis in any way?

So your GP has said get exercise on your poor feet Doh and also to rest how contradictory .
Come back and moan anytime ( I do regularly ) thanks again for keeping us informed of how things work out
Jim Thumb
Reply
#24
(Tue-05-08-2014, 09:42 AM)jiml Wrote: I think it's good to moan and get those frustrations out, we've all done it on here, that's the beauty of the forum, we have all been in the same situation, some of us lucky ones have found the treatment that works for us ..... Others like you are still looking, I'm sure there is something that will control yours if Fumaderm isn't for you there's plenty more in the armoury to try.

Has the Fumaderm done anything for you ( apart from make you hot and itchy?)
Did it affect the psoriasis in any way?

So your GP has said get exercise on your poor feet Doh and also to rest how contradictory .
Come back and moan anytime ( I do regularly ) thanks again for keeping us informed of how things work out
Jim Thumb

Fred !! eh... Jim !!
You are mixing up yourself now. Doh Sandra is not Tanlou.
Sandra is on the phototherapy, not on Fumaderm. (yet....)
Reply
#25
(Tue-05-08-2014, 10:10 AM)Caroline Wrote:
(Tue-05-08-2014, 09:42 AM)jiml Wrote: I think it's good to moan and get those frustrations out, we've all done it on here, that's the beauty of the forum, we have all been in the same situation, some of us lucky ones have found the treatment that works for us ..... Others like you are still looking, I'm sure there is something that will control yours if Fumaderm isn't for you there's plenty more in the armoury to try.

Has the Fumaderm done anything for you ( apart from make you hot and itchy?)
Did it affect the psoriasis in any way?

So your GP has said get exercise on your poor feet Doh and also to rest how contradictory .
Come back and moan anytime ( I do regularly ) thanks again for keeping us informed of how things work out
Jim Thumb

Fred !! eh... Jim !!
You are mixing up yourself now. Doh Sandra is not Tanlou.
Sandra is on the phototherapy, not on Fumaderm. (yet....)

Oh dear I must put more water in my whiskey ( sorry for the mix up Sandra I'm gonna say it's due to my age Big Grin)
Reply




Users browsing this thread: 1 Guest(s)