Help me diagnose
Background and symptoms: I've been suffering from lower leg pain in both my legs (from knees to feet) for the past 3 years. The symptoms are mainly extreme pain, fatigue/ exhaustion with activities, and pins and needles and burning sensation most of the time, but no skin psoriasis, swelling, or other physical symptoms. This problem started all of a sudden after a long flight (approximately 8 hrs) on a plane where my seat was mechanically damaged, and I couldn't recline it; the guy in front of me reclined his seat entirely, so I didn't have any space to move my legs properly. I requested him, as well as the air hostess, to change my seat to no avail. The pain started after I got off the plane and increased exponentially as I walked through the airport. Since then, it's been a disaster. I don't have these symptoms anywhere else in my body, not even in my upper legs or anywhere else in my body. Before this flight, I never ever had this type of pain in my life.
Diagnosis so far: My initial treatment was done in the US. US healthcare is crap, but I didn't know until I got a first-hand experience. My dumb primary care provider put me on 200/400 mg Ibuprofen and then switched to acetaminophen of low strength despite my terrible symptoms. He didn't give me any stronger painkillers or local anesthesia despite my thousand requests; they just kept saying that it was an unusual pain throughout all our meetings. After 3 months, he realized that it's getting even worse so he thought it could be nerve issue so he gave me gabapentin and later switched to pregabalin which were also of very very low strength. Later, he told me to take only multivitamins as my reports (by that time, I had done blood tests, urine tests, an MRI of my lower legs and back, and CT angiogram of my legs) were ok. During this entire period, I consulted a few doctors of different specialties, but they said that as the reports are fine, we can't help you. Also, the wait time to schedule any test or appointment is extraordinarily long in the US and it definitely exacerbated my condition. That time my symptoms include-- achy pain, shooting and burning sensation. I couldn't stand for more than 30 minutes at all and couldn't walk for more than 15 minutes without terrible pain.
I came back to my native country after about a year as by that time I was told by my medical care team that I might be able to fly now and since then I consulted a few doctors of different specialties. My physical therapist suggested that the symptoms relate to arterial disease like intermittent claudication but, my test reports are normal. My Ultrasound says 30-40% blood flow reduction in the anterior and posterior tibial artery, but the Vascular surgeon said it's normal. I did the same tests in the US earlier, and the Vascular surgeon in the US said the same thing and also said that apart from the pain, nothing else matches with vascular problems, especially as I don't have any physical appearance similar to vascular disease. I was given Naftidrofuryl oxalate - a vasodilator for 2 months, which didn't abate the pain at all, so I believe it's not a vascular issue. I got all sorts of blood tests (HLA B27, RF factor, C reactive protein, CPK, lactate, uric acid, D-dimer, CBC test, almost any kind of blood test imaginable) and imaging tests(MRI, ultrasound, CT angiogram) done along with nerve tests (EMG and NCS). These tests have been done routinely and multiple times in different hospitals in 3 different countries, and the results are fine every time. The only test I couldn't get done is called myositis metabolic panel because it's not available where I'm now. My neurologist also said that it's not a nerve issue. Recently, 2 MRIs were done by my Rheumatologist and he found just a slight inflammation in my calves but the other MRI suggests that I have pretty good inflammation in my tendon and joint in my foot. My rheumatologist now says that it's peripheral spondylo arthritis. According to him, peripheral spondylo arthritis is observed through ultrasound or imaging tests rather than blood tests, hence nothing shows up in my blood tests reports. I asked him if it could be due to any infection but he denied that and said if it were due to any infection, then it would be found on a blood test by now. I know that ultrasound is a subjective thing that depends on the person who's performing it(technologist/doctor) but I'm just so confused and skeptical. I still have those symptoms- achy pain, burning sensation. Although sciatica is mostly found in one leg but I have these symptoms in both legs. I took pregabalin for 6 months but it dedn't help me at all. My EMG and NCS are also fine. My MRI which I got done here in my country suggests I have mild sacroilitis which I've attached here though the doctors said it's fine and not necessarily a dangerous sign.
I find it very weird that due to a bad flight, I developed arthritis/ sciatica all on a sudden. Does anyone relate to my symptoms? Has anyone ever had a similar experience? I need some suggestions, please!
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I wish you the best
Do you have a positive RF or elevated ANA, CRP, ESR or any other blood work that indicates suspicion of an autoimmune disease? Any persistent Back pain? If so, is it worse in the morning?
One of my diagnoses is spondyloarthropathy. I have axial inflammation in my spine and sacroiliac joint and imaging shows inflammation where tendons attach to bone in my shoulders (seen on xray and ultrasound) and inflammation in my gluteal muscles (seen on an MRI). I am negative for HLAB27 but have positive RF and elevated ESR and CRP. All my other panels including the myositis panel is negative. My symptoms are most improved on immune suppressants. Have any DMARDS or biologic drugs been suggested to address the peripheral spondyloarthritis that was diagnosed?
RF , ANA, CRP, ESR- all normal, done routinely. HLAB27 - negative. I'm not sure what's going on with me
@bbk186 No treatment prescribed for the SpA?
Okay. Don’t be mad but have you or anyone else considered a conversion disorder? And I’m not talking about hypochondria or psychosomatic illness. A conversion disorder occurs when your brain malfunctions and sends the wrong signals to your body. When no one could diagnose my physical problems (also involving serious physical pain) I looked into it. As a matter of fact, I was hoping that it was a conversion disorder since half the battle of “curing “ it is knowing that you have it.
It can cause severe pain and even blindness and deafness. It’s no joke.
But it’s treatable. Read up on it. There’s a fancy new name for it now but if you search for it, there’s lots of information. Mayo even wrote about it.
What you experienced on that plane was traumatic, plain and simple. I’m sorry for your experience and your pain and I hope you find the answers that you’re looking for.
What do you mean?
I have the exact same thing. Horrible shin pain. Mostly when walking or standing. I’m 68 and otherwise in excellent health. Upper body I feel like I’m 20! Had 2 cortisone injections in my l4 l5 with no help. Had back surgery (laminectomy) for spinal stenosis. My surgeon was 90% confident that’s what was causing my shin pain. Four months later the pain is worse than ever. Had vascular ultrasoundI’m that was normal and emg where they noticed a slight issue. Not closer now in finding the cause than 2 years ago. Living with horrible daily pain. Taking lyrica 3 times a day. Doesn’t really help. Have an appointment for yet another back injection and an appointment with a neurologist in July. Must have told my story to 5 doctors.
My son (53) was not able to have his issues (pain, muscle loss, rash, fatigue)diagnosed for over 2years. After years of testing, he is now doing a program removing parasites from his body. He did extensive research and continues to follow up . He is definitely improving. It is quite amazing, after using an anti parasitic program, how much better he is feeling.
So very sorry you are going through this. How frustrating for you! I don’t have any suggestions, but just wanted to tell you I care.
@mmmerrimac I hear you! I believe “difficult patient” is the go to “diagnosis” given by any doctor who can’t figure out what’s wrong with you. 🫤