Ankylosing Spondylitis: A long wait for treatments that barely work
Published 17 Oct 2019 • Updated 19 Aug 2020 • By Louise Bollecker
Carole suffers from Ankylosing Spondylitis. For years, her complaints of chronic pain were not taken seriously and were blamed on her weight. She recounts her battle for an accurate diagnosis and how she has been since, as she continues to wait for her treatment to take effect.
Mysterious Pains and Misdiagnosis
I’ve suffered from multiple sprains since I was 8 years old, and then when around the age of 17, I underwent an operation on two subclavian arteries.
Fifteen years ago, I started having back pains, but only in the morning when I got up. My doctor told me, after doing an MRI and X-rays, to change my mattress, take up a sport and try to lose some weight. But despite changing my mattress and losing weight, I didn’t get better, my back was still killing me in the morning…So I decided, “Oh well, I’m going to put myself out a bit” and every day I got up at 7 AM just to avoid the back pain.
“One thing was certain: I was a fat hypochondriac”
I moved house due to job change and so I had to change my GP as well. Unfortunately, the first one thought I was a nutcase and that my pain was all due to my weight; the second one sent me to an endocrinologist after conducting a load of tests on me. The endocrinologist, told me, without even examining me, to lose some weight and I’d feel better. So, one thing was certain: I was a fat hypochondriac. That was the only explanation they had for my chronic pain.
I moved again for my work and got a sprain that took three months to heal. By then, the back pain was waking me up in the middle of the night and keeping me from getting back to sleep. So, I made a list of all the problems I was having and gave them to my new GP. He took a look at my list and told me: “You have a few symptoms that do not match with my initial prognosis, so let's keep searching.”
A Series of Test to Diagnose Ankylosing Spondylitis
So we got to testing: blood sample to check the rheumatoid factor: extremely high CRP and VS levels. Tested to see if it wasn’t sleep apnoea. The doctor said there were only two possibilities left: Ankylosing spondylitis or arthritis and since I was “too young” to have arthritis, it could only be AS. To get final confirmation, I had to get an MRI of my sacroiliac joints and make an appointment with a specialist. In the meantime, my doctor gave me anti-inflammatories to reduce the pain.
I waited for months to get an appointment with the specialist. I gave him a letter from my GP and showed him the results of all the tests that I had taken since I was a little girl. I told him about the multiple sprains, I showed him the MRI which showed a bilateral of the sacroiliac joint and the blood tests. Even though he still insisted on telling me that the CRP And VS levels could have been due to my weight, he confirmed the initial diagnosis, telling me “If you hadn’t done the MRI, I wouldn’t have seen it, but it’s there. There’s no doubt about that. You have AS.” I left his office with a diagnosis that took me years to get…I could finally put a name on it. I still had to a test for the BLA B27 gene, which I was positive for.
The internist talked to me about treatment options and decided to try three NSAIDs (Nonsteroidal anti-inflammatory drugs), and I was put on 3 months sick leave for yet another strain. A few months later, I came down with acute shoulder tendinitis (which meant carrying my arm around in a sling). At my 3rd appointment, the internist told me that the condition had evolved and that I should switch to a biopharmaceutical treatment. I did the necessary tests, took a vaccine I needed and in July 2019, I started on Simponi.
I’m on my second injection. The first one allowed to get a full night’s rest…my lower back doesn’t give me any more trouble. However, after the second one, my pain is back and my hips and knees are swollen despite taking NSAIDs twice a day. A radiography showed pinching in both my knees and the left hip.
I’m not on my third sick leave in 3 months and I can’t walk around without a cane. My GP told me to be patient and wait until my third injection. But it’s a long time to wait.
The Psychological Effects of a Chronic Illness
As far as my family goes, I’d say my daughters are supportive, my partner tries to help me however he can, but my own family has had a rough time of it. It’s an unseen illness, so one of my sisters is convinced I’m just a hypochondriac and my mother thinks I’m just making it up. Even when I showed her the official diagnosis, she still didn’t believe me…I just let it go, I don’t even try to explain anymore. I go to see them when my health permits, but we don’t talk about it.
As for my morale, it’s really hard to feel like you can’t do much. Even though I see a chiropractor, not seeing any improvement in my condition really gets me down. Especially when you have to move about, but you’re tired and your legs just don’t respond. So, I joined a few internet support groups. It helps to get the suffering out in writing even if I still get down about not being able to run, hike, bike…Sometimes, I have hope, sometimes I’m completely demoralised, but I’m happy that those web sites exist.
My advice for patients suffering from AS
Be strong and don’t let go. And especially, if your doctor doesn’t believe you, get a new doctor. He probably just doesn’t know enough about this condition.
Thank you, Carole for sharing your experience. What about you? How were you diagnosed with AS? What treatments have worked for you?
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