Is this Osteoarthritis? Are the doctors right? | Arthritis Information

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I have severe joint pain. The pain is most common in my neck, shoulders, knees, and hips. I was diagnosed with crepitus. This is when the cartilage around joints has eroded away and the joint ends grind against one another.
     Further evaluation including a blood test that was negative for rheumatoid arthritis, led them to diagnose me on a whim, with Osteoarthritis (degenerative).
     I was put on a steroid pack for 2 rounds with no effect. They put me on diclodenac. I was on diclodenac (50 mg. 3 times a day) with minimal improvement. I have been taking it for almost 6 months, and it's effectiveness has significantly wore off little by little. It no longer helps me at all.
     I was sent to an orthopedic surgeon because I had a bad "flare up" in my shoulder. My shoulder has always been the worst pain. At least this is what I kept telling the doctors. I say this because, I now know that the grinding or crepetis in my shoulder ( louder and more painful than in any of my other joints) was not the cause of my pain. What I did not realize that the problem was on my cervical spine. It feels to be most painful at my C7 vertebrae.
     Right on this spot, if I push I feel a pop, i feel a pop when I push in and another when I let go. The doctors told me this was a tendon popping in my neck. But I do not understand how that can be so coincidental, because this is the cause of a lot of my pain, this area in my neck is the worst and they have spend a lot of time trying to fix this, I think they lost sight of the big picture and all my other symptoms.
     X-rays were negative, cat-scans were negative. ( both tests on my skull cervical spine and left shoulder) I was sent to physical therapy. 4 weeks for my shoulder, no positive effect. Then a cortisone shot, again, did not help. Next I was ordered 6-8 weeks of physical therapy for my neck. I currently was ordered an MRI because the therapy was too intense for me.
     In therapy I underwent traction. Their theory was that I had a slipped disk. The exercises that usually relieve a slipped disks symptoms, did not relieve mine. They did not know what to do with me. They send me back to my orthopedic doctor after seeing me 3 times a week for 7 weeks.
     I was previously ( by my physician) diagnosed with kyphosis. I have what is referred to as a dowagers hump.
     I have an appointment for an MRI in a few days. I am hoping something that I never thought I would hope, I hope they find something. I want them to find something that is easily fixed. The problem is, I have a hard time believing they know what is wrong with me. I understand it is practicing medicine, but I have medical insurance and I want more tests to take place.
     My pain started when I was 13 or 14. I am now 19 and some days I can barely get out of bed. Doctors have told me things like "Its poor posture". The first doctor I saw had my mom CONVINCED that the pain was stress manifesting itself as pain. He had me referred to a child psychiatrist who put me on medication where I attempted suicide twice. Anyways...

     I want to know if anyone knows what this could be. I also would really like some advice on questions I should be asking my doctor. If this MRI (God forbid) come back negative, should I ask him to test for an auto immune disease? or a ask for a bone density test? I do not know what it could be but I am learning step by step what it is not.


     My other unrelated but possible related diagnoses, include
     -Cutis Marmatora
     -ADHD
     Bipolar Disorder

Other medications include
     -Adderall - ( 20 mg. a day, recently increased to 30)
     -Depakote which I took for one month, then stopped. (750mg)
The adderall and depakote were prescribed in feb. of this year. these medications did not effect my symptoms.



List of symptoms.

     Hips-
-Started at age 13.
-hurts to sit indian style
- hurts to sit on hard floor or chair
- flares to constant pain that lasts days sometimes a week but never more than a week.

Knee pain
-Swelling.
- Stiffness after standing for a long time
-If you put your hand on my knee as I move it, you can feel a squeaky grind.
-My knees use to dislocate often as a kid. My mom would just bend my leg straight out and a loud pop could be heard, and the pain would be gone. The last time I can remember my knee dislocation was when I was 17.

Hands/ wrist
- doing anything repetitively hurts. such as dishes, folding clothes.
- my hands are always cold, ice cold.

- my left toes go numb from time to time which leads me and the doctors to believe I have a pinched nerve.

Extreme fatigue.

Pain that was intensified with physical therapy.
-pins and needles feeling in left arm
-shooting pains in left arm
- numbness in my left fingers
- the feeling that I lost circulation in my left arm.
- my neck ( on the sore spot which is right on the c7 vertebrae) got very sore.
- cutis marmorata was more visible ( lines over legs, stomach arms, that was explained to be my capillaries swelling and contracting) I asked another doctor and he said this condition was an infant condition and it was VERY rare in adults, and is a common misdiagnoses for auto immune disease.

     So again,      I want to know if anyone knows what this could be. I also would really like some advice on questions I should be asking my doctor. If this MRI (God forbid) come back negative, should I ask him to test for an auto immune disease? or a ask for a bone density test? I do not know what it could be but I am learning step by step what it is not.
     This is effecting my everyday life. It is hard to get out of bed. I cannot wear a seat-belt in the car because I cannot sit up straight without slouching, sitting up straight makes my lower back very weak and sore. I am tired of being stiff and in pain. Please give me your advice.






Hi moon of harvest wish i could help with diagnosis but cant but after reading your post just felt i had to say something. You poor poor thing this must be terrible for you. Cant understand though why ra has been totally ruled out as i think it can sometimes be present with no obvious blood results try going on the ra forum and see if anyone ther is the same as you

 
best wishes for better health lynn

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