Hi,
I am new to this board. I had my 2nd child in June and ever since I had him, I have had bad aching joint pain, mostly in my fingers (predominately in my left pinkie finger and now in my right pinky too). My knuckles ache, as do my elbows and my feet - mostly the knuckle joints of my toes. But also mostly near the pinky side of my feet (just like the pain is mostly on the pinky side of my hands).
I also noticed a small nodule on my left elbow, about the size of a lima bean, or perhaps a bit smaller. It does not hurt.
The pain is concentrated in my hands and elbows. I have a hard time opening jars of baby food sometimes. Advil and Alleve do not help.
I went to see my Internist a while ago and he told me that my aches were from carrying the baby. I disagreed. He did xrays of my left hand (it hurt more than my right at the time) and he told me it was fine. He did bloodwork too.
This is the result of my bloodwork:
Sed Rate by modified westergreen: 4
Anachoice screen w/refl to titer, ifa anachoice screen: positive
Anachoice antibodies, titer and pattern
ANA pattern: negative
Antinuclear antibodies <1:40 titer
(the above results may suggest the possibility of autoimmune antibodies. testing for ena antibodies (sm, sm/rnp, ssa, ssb, scl-70, jo-1) and ds-dna antibody should be considered if clinically indicated.
Rheumatoid Factor: 37 H reference range <14 IU/ml
I am going to see a Rheumatologist on monday but i'm totally worried. not sure if i need to be.
I am not sure why i ache to much....
And, when i was pregnant, i came down with PUPPPS, (google it), a rash seen in pregnant women who carry boys. It's an autoimmune thing too. This was in the spring of 2007.
thanks for any help.forgot to mention, my internist wrote on my lab results, which he mailed to me
"not suggestive of lupus"
"these are indeterminate. nothing bad found. perhaps RA but i doubt it. continue aleve for 1 month and if aches persist beyond that, we should have you see a rheumatologist"forgot, i am a 38 year old white woman in otherwise good health. no RA in family, but father has autoimmune problems.cnddream, it sounds like your internist is not proactive, which is unfortunate, but since you're seeing a rheumatologist at least you don't need to rely on him for an accurate diagnosis. My doctor sent me to the RD at the first sign of RA and my RF was only 17 or something like that. The RD said she loves my doctor because my doctor doesn't fool around and she catches the cases early.
Early, aggressive treatment is the number one thing for a better prognosis with RA. Even though RA is grossly underfunded for reasearch (compared to other chronic diseases) strides have been made in better treatment and more effective medications, so the future with it is not nearly as bleak as it used to be.
Welcome to the board, fellow Canadian. Hopefully you won't have to be here but if you need it it's a pretty good resource.
[QUOTE=cdndream]
I am going to see a Rheumatologist on monday but i'm totally worried. not sure if i need to be. [/QUOTE]As a sufferer of RA I see this as a good thing, it is way better to have this looked at now rather than later.
I can understand your apprehension about the visit but be assured that if you do have RA then the quicker you get onto medication the better you will in the long term.
Not saying you have it ..
Be calm, not long to go now.
My sed rate is in the hundreds, pretty bad. Your number is very low which is a good thing. You might want to be checked for Fibro as well.
It may be nothing, but I'm glad to hear that you have an appt. It is better to know early and get started on treatment. Jot down notes as to your symptoms. Quite often diagnosis is based on symptoms since bloodwork doesn't always tell the full story.
Good luck to both of the newbies on this thread.