What is your history of diagnoses leading up to ankylosing spondylitis?

Had right SI joint issues as an early teen. Chiropractic helped. Started Powerlifting at 25, felt inflammation increase in the SI and had thought it was a bulging disc. Did rehab exercise routines for over a year and didn't get better. Traction just pissed it off even more as well. Eventually fell out of the exercise out of hopelessness.

Relevant note: I hooked up with girls from time to time, and apparently one day I contracted chlamydia. Symptoms didn't show immediately, but when they did I started and finished treatment with antibiotics.

So I was still suffering fro. SI pain, and recently I had learned that I could gain relief from sacrum adjustments by the Chiropractor even though they hurt initially.

So I was dumb and decided to do it myself at home. After I popped my own sacrum, I began walking funny, with pain getting progressively worse in the SI joint.

Little did I know that, in conjunction with the chlamydia bacterial infection, somehow that self adjustment would trigger a HUUUUUUUGE inflammatory response.

During that night, I jumped out of bed quickly to relieve myself like I normally did, and the inflammation was so bad, I realized I could not stand. I was in so much pain, I fell and was nauseated. I was on the floor for more than 24 hours before calling an ambulance. I was given Fentanyl just so I could be put onto a scoop stretcher. And I was given some steroids in the ER.

Once I switched to crutches, I went to Urgent Care to see if it was a disc issue. We weren't sure.

Went to an Orthopaedic clinic and saw a Nurse Practitioner. Put me on Gabapentin, Meloxicam, and a few others I don't remember off-hand. She eventually recommended I receive a shot in my lower back. Long story short, that didn't help.

I was pretty much bedridden for months, and in many moments just spasming in bed while not even moving, yelling in terrible pain. I noticed my knees swell up as well. I'm talking a huuge amount of swelling. This raised the practitioner's eyebrows, so I was then sent to a knee specialist.

At this point the SI has been under control (thank God) but the knees were the remaining issue. I gave him the story, and he mentioned very quickly the possibility of an autoimmune issue. We ruled out what we could through imaging and other poking/prodding. He said it looks autoimmune but should get blood tested.

Blood tests were a bit indefinite and vague. They just saw that I had alot of inflammation in me. They ended up recommending a Rheumatologist and so I went to her. She wanted another blood test to be sure of what's going on.

My C-Reactive protein was a whopping 132mg/ml and she said it definitely looks like AS. She put me on Cosentyx and symptoms got better after each weekly dose.

Weekly doses with Cosentyx extends only up to 5 weeks, then it should be taken monthly. The 5th week passed just fine. The 6th week came and I was still ok. A few days later after that 6 week mark and symptoms started worsening again in the knees. I'm still taking meloxicam as well so this was not comforting news to me.

One thing I noticed during all this ordeal was that when I didn't eat, inflammation amd pain would lessen. So I decided to do that and then begin a pretty solid paleo diet. Symptoms are improving since then but I hope to be in remission soon. Also, I'm really ready to take another dose of Cosentyx to see if it gets even better.

Ending note: Currently have Crepitus in the knees due to rapid decrease in swelling/inflammation. Also, forgot to mention thoracic spine was gaining inflammation earlier, that subsided greatly as well.

/r/ankylosingspondylitis Thread