Getting a diagnosis
About 14 years ago, a doctor had xrays of my spine taken as I was experiencing back pain, and he said it looked like I had arthritis in my spine. Nothing about that was written in my chart and I kind of forgot about it since i would rarely see doctors as doctors haven't been very helpful in my experience.
This past winter, I had horrible pain in my toes and noticed that my toes were all hugely swollen. The pain got so bad that walking is difficult. My regular doctor suspected it could be psoriatic arthritis and he gave me a referral to a rheumatologist.
I have the rheumatologist appointment scheduled for three days from now and want to be sure what I'm getting myself into. I worry about the costs associated with trying to get this diagnosed, because insurance in the United States is terrible, and they will rip you off any way they can. I'm assuming xrays would likely be covered by insurance but I'm guessing something like an MRI would not be fully covered and could potentially be a huge out of pocket expense.
For those who received a diagnosis of arthritis, how were you diagnosed? Was an MRI necessary? Was it hugely expensive with several doctor visits needed to get to a diagnosis? I know I should put my health first, but I just got most of my debts paid off this year after working hard to do that for the past 10 years. I worry about accumulating a bunch of debt now due to trying to get my arthritis diagnosed. Any information on this would be helpful.
Also, one of the reasons I would like a diagnosis is, if I ever get to the point where going into work is too difficult (which seems possible since currently just walking around in my house is difficult), I want to have a diagnosis to support any disability claims. For those who have claimed disability, was this very difficult to do? Were you required to take prescription medications in order to qualify for the disability? Most of the drugs prescribed for psoriatic arthritis are so toxic and have such bad side effects (from what I've read) that I would be scared to take them, but I don't know if you would be required to take them before I could legally claim disability.
Any comments or suggestions are appreciated.
注释
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Ellen ModeratorPosts:978
Good morning@chloe8596
我看到您将首次看到风湿病学家患有疑似的银屑病关节炎,并有很多查询。
不幸的是,我对美国医疗保健系统的了解不多,因为我们在这里非常幸运,我们拥有NHS,即使我们有时确实有长期等待的清单,也可以免费提供我们所有的测试。
This will help a little at least with what tests might be done:
As will this although again it is UK specific I would imagine there will be an overlap:
I can't help much with your welfare benefits either so very sorry, but here they are based on what help you need rather than what medications you are taking if that helps at all?
I really don't want you to be too frightened about the medications you might be offered though. Many many of us on here take them and we do just fine on them.
Please do come along in chat to our members though. There is so much experience here a fair few members have Psoriatic Arthritis and will be able to offer some reassurance to you.
Best wishes
Ellen.
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StickyWicket MemberPosts:26,703
嗨,克洛伊。我为你感到。一方面,我有一个长期存在的RA,另一方面是一个现在是美国公民的儿子,所以我了解医疗的担忧。
我认为,成本都取决于您拥有的医疗保险套餐。我的儿子曾经不得不为自己的针迹付出代价,然后包裹不包括运动伤害。几年前,他被告知他应该每6个月进行一次扫描,以检查他的肝脏的病变是否没有生长。但是这花费了200美元的时间,因此没有覆盖,因为他还被告知这可能只是他童年脑膜炎的疤痕,他不会打扰。在这里,我们有自由但已久的任命。这两个系统的组合将是不错的。
我确实找到了与约翰·霍普金斯(Johns Hopkins)的链接,约翰·霍普金斯(Johns Hopkins)是美国最好的医学院之一。我希望它有帮助。https://www.hopkinsarthritis.org/arthritis-info/psoriatic-arthritis/diagnosis/
I'd just add that, if you do have PsA, it's much better to ignore the scary stuff and take the meds. Meds problems are a slight possibility. Untreated PsA will do more damage.
Good luck and do let us know how you get on.
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chloe8596 MemberPosts:4
非常感谢!我很欣赏your comments. Just feeling a part of this community is already very helpful : )
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chloe8596 MemberPosts:4
Thank you! This is very helpful!
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StickyWicket MemberPosts:26,703
I'm thinking of you. Hope it goes well.
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