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Hi Everyone,

I asked my Rheumy today if joint damage/crippling was inevitable and

she said no...that with the right combination of meds, the disease

could be controlled and joint damage prevented. I would appreciate any

opinions/comments on this. Is she right?

Thanks,

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Yes, she is right. The disease-modifying medications actually

prevent crippling damage from occuring. Even though you may continue

to have some flares and some swelling and some pain or stiffness, you

will be protecting your joints from permanent damage.

best regards,

sherry z

--- In , " " <cat1657@...>

> I asked my Rheumy today if joint damage/crippling was inevitable

> and she said no...that with the right combination of meds, the

> disease could be controlled and joint damage prevented.

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Hi ,

I don't have as long an experience as some, but I can tell you that in

my case. I caught the disease prior to experiencing any joint damage,

as so far, 5 years later, I still have no joint damage.

So I would say at least short term it is possible. Long term, I'll

have to wait and see, but others might be able to give more info.

Stay Well,

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Sherry, I guess what I am not understanding is, if these meds prevent

the permanent joint damage, then why do so many end up disabled?

--- In , " S. Zorzi "

> Yes, she is right. The disease-modifying medications actually

> prevent crippling damage from occurring.

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It can be controlled and joint damage rate reduced but I seriously doubt if

damage can be avoided.But I am not a Dr. and I only speak from my own experience

Walt

[ ] joint damage

I asked my Rheumy today if joint damage/crippling was inevitable and

she said no...that with the right combination of meds, the disease

could be controlled and joint damage prevented.

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One reason is that they are very expensive and so the insurance

companies make the doctors exhaust all the other possibilities before

approving them. In some countries they are not prescribed at all, or

very rarely. Many of our members from Great Britain have indicated

that it is next to impossible to get these more expensive meds.

Another reason is that it often takes SO LONG to get a proper

diagnosis. Many of us realize in retrospect that we had symptoms of

PA for many years before we actually got diagnosed. Depending on how

severe the inflammation was and how long it lasted and how often,

people can have damage before they even KNOW they have PA. Sometimes

it's the PA specific damage showing up on x-ray that finally makes

the GP or internist or orthopedist realize the person has PA and not

osteoarthritis. This is especially a problem for those who don't

have obvious P - maybe just " dandruff " or nail P, which goes

undiagnosed.

Also, many people are reluctant to take them because they do carry

risks. In some cases, people wait too long before telling their

rheumies that the current meds are not providing acceptable relief,

which slows down the whole process of getting to the " better " meds.

Finally, there is a type of PA called " mutilans " which causes very

destructive damage very quickly. Fortunately, this kind is VERY

RARE. But it is very, very damaging.

Oh, and there is also the problem that the meds often stop working

after some period of time. Our over-active immune systems find a way

around them. I've been on Humira for one year now, and I'm getting

worried that it may stop working any day now. If that happens, we

will have to hope that one of the other biologicals will work and

work quickly for me. Some people have some pretty bad periods

between times, which can increase the risk of damage.

That's the situation as I understand it. However, I'm not a doctor -

just a PA sufferer who's trying to learn as much as I can about PA so

I can better manage and monitor my own health care. I hope you will

ask the same question of the rheumatologist and let us know what

he/she says!

best regards,

sherry z

--- In , " " <cat1657@...>

> Sherry, I guess what I am not understanding is, if these meds

> prevent the permanent joint damage, then why do so many end up

> disabled?

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