Could I have RA and Ankylosing Spondylitis?

Thanks for replying. I asked my primary care doctor today if it could be osteoarthritis, and she said it wasn't bad enough, from the x-ray. Could it be from the RA? I thought RA didn't manifest in the back. Well, I made an appointment at the rheumatologist's office tomorrow (though they set me up with the PA); at least that's some progress. I'm bringing my x-ray with me.

What do they mean by "degeneration?" From what? Couldn't they get more specific? Doctors treat people like imbecilles. Take this pill, you'll be fine. No information. After a bottle of Flexeril, I'm pretty sure this isn't just a muscle strain.

I am so frustrated. I don't know what to tell my job. I'm thinking of going to a job website to look for a sedentary job in bookkeeping or data processing. I've been at my job for 3 years (mail clerk in a state prison), and I would lose all the good benefits, but I really can't see myself making it to 62 to get the retirement anyway (I'm 35). Even if this back problem gets better, I'ts getting harder and harder to deal with the RA hip pain with all the standing and walking.

I'm taking sulfasalazine. They haven't tried me on the biologics yet. Maybe it's time. It's kind of scary, though, with the possibility of cancer from them.

How did your visit go?  I hope you got some information to help you.  I also wanted to tell you a couple of things.  First of all, when you are young, they will want to get aggressive treating your disease.  If your current meds are not helping they should take up another med. Biologics are practically a miracle......Enbrel put my body almost back to normal. I have more upper resp. infections but I would rather have it than the pain so severe that I'm vomiting. Cancer never crosses my mind. There are side effects from every medicine, I am aware but certainly don't worry about it now. If you go with the arthritis unchecked your body could end up in worse shape. I was begging for Enbrel back in the beginning. They would not give it to me until my spouse called and threatened to sue them. (I switched Drs)  If you can, take a covered medical leave from your job. Either short term disability or FMLA.  Protect your job at all costs unless you have someone to completely support you. It is hell out here with no job. And under no circumstances do you tell a new employer that you have RA or whatever...

you are protected under FMLA  and it is a federal offense if an employer violates the policy.  Protect your job because you could get better medicine and feel better. It sounds crazy but true. Fight to change your meds. Lots of us love biologics, some don't. 

I talked to the rheumatologist's Physician's Assistant. She said that though some people can have two autoimmunes, AS and RA can't go together. That made me feel more hopeful. Though, you're telling me you have both? She should meet you, then. Why do I only get stuck seeing PAs? The doctor is always too busy, or something. Well, she seems to think my back problem is a disc, and supports my GP's process of wait and see if the physical therapy helps. I can't get an MRI, she says, because insurance companies won't pay until you've been in therapy a month. So, I'm back to just waiting and not knowing what to tell my job. No one will help me.

As for the bad hip pain, she did allow me to double my dose of Sulfasalazine. She said the doctor wouldn't even consider putting me on a biologic yet. I guess they wait 'til you're completely crippled and it's too late. Well, hopefully the 4 pills a day of sulfasalazine will help. 

Hi there, sorry you have feeling so rough. Next time you make an appointment don't let them make it with the PA.  Tell them you have seen the PA twice already and you want to see the doctor this time and that is your right.  They can't be too busy to see you when you call and make the appointment.  I would think also the doctor would see you the first time (i'm thinking this was your first visit????) before having the PA see you.  It shouldn't hurt the PA's feelings but the important thing is seeing who you want to see and are paying to see.   Hope you do well on the azulfidine and get to feeling better :)

That makes sense. I just went on WEbMD and read about psoriatic arthritis. I did have a rash on my left foot for a couple of years before I was diagnosed with RA. I told the rheumatologist about it on my first visit, but she didn't even look at it. Since I've been on the DMARDs, the rash went away. I also have the ridges on my fingernails. However, one of the main reasons for diagnosing me with RA was that my rheumatoid factor was elevated, which doesn't happen in psoriatic arthritis.

The PA told me my back pain wasn't from arthritis, because it would show up on an x-ray. Then, I went to a back pain specialist, and he told me it IS arthritis, and that it doesn't always show up on x-rays. Still, no MRI. I feel more confused and lost than ever now. No one will give me any answers. I got three different diagnoses from 3 different doctors, and still no one will do a test to find out what's wrong.