Sarah,
Your visit sounds like it was very frustrating. I'm not a rheumatologist, but looking at the hands is an important part of the appointment. But only a part. You cannot tell if an individual has lupus or RA, or any other CTD without bloodwork. I had a similar experience with a GI doctor. I told her I had RA, and she grabbed my hands, looked at them for 5 seconds, and said you do not have RA. I informed her I had a positive RF, and she shut up real quick. Diagnosing these diseases is very tricky and it takes a good, solid physical exam, a detailed history from an expert interviewer, and lab tests to actually come to a diagnosis. My first rheumy visit was about 45 minutes long. The longest I've ever sat in a doctor's office. Good to know that you have a good PCP. I like your plan.
Elcamino
Current dx: Rheumatoid Arthritis
I think you should find another Rhuemy. My first one did do some blood work and some xrays. he spent about 15 minutes per visit (I saw him 3 times) and in the end told me I fibro and nothing else and on the 3rd visit told me he had done all he could (He is even an associate professor of rhuematology at a state medical school). The second rhuemy did all the blood work he did again and then some plus a host of other test and found many things including arthritis and bone spurs in lots of places. the first visit she moved every joint in my body to feel how it was working (My first and second visits were about an hour each). Not all doctors or rhuemys are alike and some of them make their decesions to fast just like the rest of us. Unfortunatly when they do that we pay. You know something is going on with your body and you need to keep looking till you find a doctor who will look hard enough to help you. You are as always in my prayers.
Mark
PS
Could be that he just thinks your short
(couldn't resist) hehehehe
We make a living by what we get; we make a life by what we give.
Sir Winston Churchil
Confirmed Diagnosis of - Psoriatic Arthritis/Spondylitis/Graves Disease/GERD/Scoliosis/Hiatal Hernia/Graves Disease of the Eyes/Chronic UTIs
Thanks
Thank goodness you have a great PCP. Do as directed and find another rhuemy in your plan to have ready to see when the time is right. An ortho and MRI is great as well. Good luck
**
Hi Sarah,
I had alot of trouble with my first rheumy, said once the insomnia gets under control the pain from the fibro would go away! Ha! He said I could not work any longer but that "he was not the guy to send the SSD paperwork to" I am now seeing a new rheumy, she checks all my joints for swelling, knots and motion. Come to find out I have RA, polyarthritis and Osteo! My RH factor is on the borderline, but she said by her physical examination that I do have RA. She placed me on methotrexate and plaqunel. If I do not improve by the next visit then she will start me on Enbrel or Humira.
Good luck to you Sarah, hope you find a good rheumy soon. I know you have been suffering for a while. I usually chat with you in the fibro chat.
Take care of you,
Tee
Trust in the Lord with all your heart, And lean not on your own understanding; In all your ways acknowledge Him, And He shall direct your paths. Proverbs 3:5-6
you're not alone with this one...so many people will relate to it trust me.
erin
Active, Severe Rheumatory Arthritis. Crohns. AS. Chiari Malformation & Right Brain venous anomoly. Partial complex seizures. Emphysema. Rheumatic Lung & Heart. MVP and Tricuspid prolapse. Had Lymes disease for 10 years.
Confirmed Diagnosis of - Psoriatic Arthritis/Spondylitis/Graves Disease/GERD/Scoliosis/Hiatal Hernia/Graves Disease of the Eyes/Chronic UTIs
My rheumy went from Mr. Hyde to Dr. Jekyll.. he was the nicest person today. Weird. He wants results of my blood tests from PCP faxed to him, along with my last back xray. I go tommorrow to PCP so I should know something a little more.
I did get clarification on the not treating me for fibro. He meant that since I'm already on lortab and other meds, and have a good stretching program... there isn't anything else he can do. I'm already doing it. So he wasnt being a total jerk. He just didn't explain it properly. He still stands by no RA or no Lupus. So I'm still in limbo as far as the cause of the fluid. Maybe the blood tests will show up with some type of something. It's a bad day when you hope your tests come back ABnormal, isn't it?
Thanks for all the replies, and the good wishes, and I will update as I know it.
Sarah
hey Sarah,
no, it's not bad. and believe it or not...doctors want positive bloodwork and abnormal crap to show up as well! nothing is more frustrating to a pt and an MD as a difficult-hard-to-crack treasure-hunt-case where there is no BOOM THERE IT IS IN YOUR FACE clinical findings.
Dr's like textbook pts. few like to put the energy into the search.
so the twisted as it may seem feeling of "the want for abnormal" is...TOTALLY NORMAL.
especially if there are things going on that don't exactly make sense or are odd. or rare. and autoimmune and rheumatics?...geesh, GodBless people going into that specialty. i mean, look at how complicated it is! to us!
so, in all...validation for what is wrong is kinda like....closure. and Sarah, it may take a lot of time. but if they are finding things & this doc is acting differently, you're in the right direction.
in my prayers.
sincerely,
erin
Active, Severe Rheumatory Arthritis. Crohns. AS. Chiari Malformation & Right Brain venous anomoly. Partial complex seizures. Emphysema. Rheumatic Lung & Heart. MVP and Tricuspid prolapse. Had Lymes disease for 10 years.