Rheumatoid Arthritis Support Group
Rheumatoid arthritis is a chronic, inflammatory, multisystem, autoimmune disorder. It is a disabling and painful condition which can lead to substantial loss of mobility due to pain and joint destruction. The disease is also systemic in that it often also affects many extra-articular tissues throughout the body including the skin, blood vessels, heart, lungs, and...
Tami
She's "concerned" but wants to wait 6 more months? What's that going to accomplish? Is she sending you for labs or imaging? Was your first rheumy nuts, too?
Are you in an urban area with lots of choices, or are you having to drive two hours to see these people? Do you have a good PCP?
Sorry for all the questions and no answers. We can tell the difference between "aches and pains" and something being really wrong. We believe you.
I am in a very urban area, so my options are almost limitless. My PCP is a wonderful man, but he wanted an expert to do something. I will call him tomorrow.
She means EXERCISE, baby. I used to run and cycle long distances - she means THAT.
Yes, my first rheumy was nuts too.
I have had the panel of tests. All negative/ normal except for one positive ANA. My plain xrays were... Yawn...
It's not enough. She wants to see swelling. I have some swelling! I call it puffiness. But it still isn't enough. In seven months I have gone from bilateral foot pain to include, all bilateral, ankle, hips, knees, thumbs, and wrists.
I've been crying on and off since 3:00.
Tami
Tami
All I can add is my support and to let you know you are not alone - and to tell you to listen to RASally's advice - she is SO on-the-spot with this kind of thing - her advice is worth more than gold, and has gotten me through a mess more than once.
Hugs to you, confoosed, for having to endure this BULL. I'm so sorry. Don't give up, please. We are all behind you.
RASally, as the kids say, you're The Bomb. I will call my PCP later today.
My visit was the typical interview/physical exam/verdict thing.
Yep, I tried everything to at least get the rheumy to do SOMETHING and only ended up crying in frustration.
Pain control: she flat out refused to give me steroids. She changed my diclofenac to "prescription strength" naproxen. I am devouring Ultram like tictacs. (Staying within the limits, of course.)
No way, they both ache, not to the degree I do.
Yes see if your PCP can help you thru this 6 month period.
My goodness just awful. My heart goes out to you.
Perhaps a journal/diary over this period may help. Take it with you
To what ever doctors you are seeking help from.
Some find it very helpful, any good doctor should.
Grasping for anything that may help you get some help.
The very best of luck.
Sammy
One thing you can try with your primary doc is to get a round of prednisone. Like 3 weeks worth. Take it and see if it greatly improves your status. If it does, then autoimmune disease is probably your culprit. At least then, you will have more to go on.
I took prednisone for shingles in '07. It was euphoric! I'd had strange bouts of RA "flares", but this cured everything, man!
When I add how great it helped to the 6 years (YES 6 YEARS) of symmetrical symptoms, I was sure I had RA.
Another test your PC doc can give you is anti-ccp. Although many people will be sero negative, this test is one that might catch the proof you need. If it's negative too, well, then sero negative it is.
Good luck!
I have had prednisone three times in 7 months and it has been an overnight miracle drug for me each time. This rheumy said it "is not indicated."
Sammy,
Thank you for your input especially about your daughters. I had two pages of notes, condensed from a diary of sorts. I also had two pages of diagrams with details about exactly where I hurt. I did not convince her. I really feel like I held nothing back..
To add to my anger I have my PCP and a friend who is a NP WITH RA telling me I have arthritis that is serological,