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I am 24 and it is going to be 10 years since I was diagnosed RA, I am a medical student from Slovakia but study in Czech republic and also have to work for my living. I had very big problems at the beginning... couldn?t lie in bed and turn without pain, couldn?t get up, put on clothes, brush my hair, go to school, I slept all day (if I didnt have too much pain to fall asleep), was always tired, I couldnt even chew!!!.... I took MTX and prednison and had soo many side effects (too bad for one adolescent!) but I have to say that after some time (months or a year) it went better and better.... you just cant stop believe and give up! my mum helped me very much that time, she was more sad than me, couldnt reconcile to my disease. I am writing to you because all this started again and now I am feeling the same, feel desperate and hopeless, but I know that it will go away in some time and will be better, you just have to go through this... if you want some advices how to relieve the pain or just to talk, dont worry and write to me, I can understand how difficult it is for you... (and I am sorry for my english
)I can feel how worried and scared you are. I agree, it is very scary to get this diagnosis. Sometimes I get all caught up in it too.
Hopefully you will start getting treatments to help with everything. You might want to show your mom some educational stuff about RA. She probably doesn't want you to hurt either, and is worried about you.
Take care, and let us know how you are feeling about things.
I sure hope you can feel up to the museum and things like that soon. I know I'm not either. Heck, my husband does most of the grocery shopping lately. I've got to get back to being active. I'm hoping the methotrexate I just started will be kicking in soon.
Keep trying to find the good things in every day, as these are the things to focus on.
Other people will never understand and the one thing I have found with older people is they tend to be less understanding.... I know crazy. I have one lady at work who thinks that it's a competition. Well lady, you can win this one! Chronic pain and inflamation is awful and I wouldnt wish it upon my worst enemy. Your ANA shows you that it's not all in your head. Just take one day at a time, one step at a time and dont let people push you into doing things you just cant do. Who cares if that toy is on your floor for 3 days in the same spot. I will tell you one thing, RA will really show you whats important in life and whats not. This is coming from someone who's pretty OCD. Good luck!
I am new to this also. My diagnosis is "iffy" because not all my labs confirmed it. My Rfactor was 6 times normal, the ANA was positive, but all my other labs were normal. I have been symptomatic for some time, and having some wierd stuff happen. When I suddenly had extreme pain in bilateral hands, fingers and wrists I really knew something wasn't right, that's when they ran the tests. Are anyone else's lab results similar to mine? My rheumatologist was slow to diagnose me, but is starting me on Plaquinil. I am afraid to start it, in case I'm not, but afraid to wait and have more damage happen. Do I have it?
Janet
My RF is as high as yours and my anti-CCP was off the charts but I had normal inflammatory markers (normal sed rate and CRP). I was having pretty mild symptoms for about 2 months (painful feet, stiff elbow and shoulder, nothing major) but then woke up one morning and thought I had broken my arm in my sleep I was in so much pain. Within 2 weeks I was in a full on RA flare with severe morning stiffness, fevers, no energy, swollen head to toe but never had an elevated inflammatory marker. I was actually told there was no way it was RA because my inflammatory markers were normal but then the antibody tests came back and my doctor had to back pedal a lot. I'm also on Plaquenil and it's working great for me. I'm sorry you're having to go through this but I'm glad your doctor is taking you seriously and starting you on something! I hope you get to feeling better soon.
Thanks for sharing. do u think i'm in for a big flare? How strange that both our labs don't show inflammation. ?Do you know of others with similar labs as ours? I'm doing better right now, which always makes me think, " you wuss, you don't have it". I'd like to know your name. When he put you on Plaquinil, did he give you a diagnosis of RA? How long ago did you start the Plaquinil? So many questions.
Janet
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