Unknown illness

Posted by supernat10 @supernat10, Mar 17 6:38pm

Hi all, I've been struggling with illness for a few years now with no proper diagnosis. The issues I have come and go. I'll be going along for a few months without any serious issues, and then they hit me all at once. I do have chronic issues as well, but no resolve. Just thought I'd see if anyone had suggestions for what to do next. I've been to every doctor, had every test, MRI/CT scan of my entire body multiple times.

To start with the facts, I'm a 45 yr old male, had reflux since I was 20 and have been on a single daily dose of nexium since then. When I stop, my stomach begins to hurt, and I don't mean burn from acid, I mean painful within hours of missing a dose. I've tried many times to quit. While there's no real evidence, I suspect a relation to being on this med for over 20 years.

One issue that has been seemingly getting worse is my double vision at distance. I only realized I had it about a year ago, but sometimes it is so bad, it's nerve wracking to drive, especially when looking off to the sides or up high (rear view mirror), where it gets much worse. The double vision is pretty much constant, some days worse than others. I was having considerable muscle weakness during one of my episodes last year, so I went to a neurologist about that as well as my eyes. They did an MRI, but found nothing. (actually, there are 3 spots on my brain MRI, which showed up in about 2017, but the surgeon felt they were likely there from childhood, and they've never gotten bigger). He tested me for several variations of myasthenia gravis which were all negative.

The episodes I get periodically, usually begin with a throbbing chest pain on my left side, just under my armpit. That pain can turn from throbbing to a constant soreness for days. This started over a decade ago in some form. It is now also on my right side and sometimes in the center of my chest. Usually a sharp, stabbing pain, and either with my heart rate or spasming, hard for me to tell, but it's not solid. I "believe" it's somehow tied to my esophagus, because it will sometimes wake me up in the middle of the night. I used to take a baby aspirin when it happened, thinking it was a blood clot or something, and it would go away. What I realized was just drinking the water caused it to dissipate, no aspirin needed. I've been to a cardiologist and the ER on 4 separate occasions, did have an elevated D-Dimer at the first ER visit in 2017, but they did an angiogram CT, and I was clear of blood clots. Cardiologists have done echos and 48 hour take home heart monitor, all normal.

My most recent version of this pain has seemingly moved. The throbbing was in my neck on my left side at the base, just next to my carotid. It throbbed all night, and the next day, the pain moved into the top back of my head (along with my neck still). Another ER visit, but they cleared me (chest xray, bloodwork, ekg). The following evening, I started eating some sushi, and within a few bites, I had a deep central stabbing throbbing chest pain again, for about 10 seconds, that was a level 9 and left me shaking for 10 minutes. After that episode, nothing for over 2 weeks. Fast forward 2 weeks, and back to the chest pains in the left/right walls near my armpits again. Also some random pains near my groin, in my lower right abdomen, in my arms.

Since the episode a couple of weeks ago, I've also had pins and needles in my right pointer finger, though it has mostly subsided. And a more generalized minor numbness in my left hand. I've also began monitoring my blood pressure, because the cardiologist asked me to. And this is something I've checked for a many years, and it's always been right at 120/80. The last week, it's been closer averaging to 100/70, with low of 95/66 and all under what I consider my normal bp. I noticed this "lower" BP also happened last time I had these chest pains start up.

When I had a CT a couple of years back on my brain for the neuro, they detected several thyroid nodules. I had those tested, and they were not cancerous. At the same time, my lymph nodes ballooned bigger than I've ever seen. They made me come back a month later, and they were back within normal range.

My right eye does droop a little, which is why I thought it might be MG, especially with the fact that I get muscle weakness sometimes for weeks on end, have difficulty standing after sitting for a while, feel wobbly, muscles are just generally sore. But those tests were normal.

At one point last year, I had to go to the bathroom every hour for over a week straight (literally 24 times a day), and had multiple urine tests, all come back normal. This happened to a smaller degree for a couple of days a few months before that. Nothing since then though.

I had a sparkly blue ball appear in my right eye, which then turned into a yellow circle in my vision for several days before turning gray and disappearing. They looked for floaters, but couldn't see any, and told me that must be what it was.

I have a pain in the front left side of my head when I receive any kind of IV. It burns as the liquid moves through. This was one of the reasons for my Neuro ordering a CT, but it was clean.

Probably unrelated, but more muscular issues. I threw my lower back out last year picking up something that I've picked up many times before, and have not been able to lift much of anything since then. I had dual inguinal hernia surgery in 2013, and also have a hiatal hernia.

Last year, my stomach was hurting so bad from just eating normal foods, I had an endoscopy done (and colonoscopy because of my age). All normal, but even now a year later, I have pain with my 2nd or 3rd meal of the day. Nearly instantly when eating. It's not severe, just a gnawing/minor pain, so I can live with that.

Lastly, I'll periodically get muscle spasms all over. Just before my neck started throbbing, I was having muscle spams in that exact spot several days before.

Another issue I deal with is difficulty taking a deep breath. No trouble breathing normally, just taking a deep breath like a sigh. I am very active, and don't lose my breath. This has been going on for many years.

I feel like I'm at my wit's end. I know my days are numbered, but I just want to know what's going on, what to avoid, how to process all of this. I'll go months feeling "okay", and then I'm slammed back into painful nights and days if not weeks of pain and anxiety not knowing what's around the next corner, running to multiple doctors with the same tests over and over again showing nothing wrong.

Thanks for listening.

Interested in more discussions like this? Go to the Autoimmune Diseases Support Group.

@supernat10, there are more neurological tests that can be done to check if you have central nervous system and peripheral nervous system issues causing your symptoms.

Did you ever have COVID or get the vaccine? I had both and got side effects from the vaccinations (2 doses and pain at back base of head plus lightheadedness). I am learning more about worsening neurological symptoms following COVID vaccines/illness.

https://med.libretexts.org/Bookshelves/Nursing/Nursing_Skills_(OpenRN)/06%3A_Neurological_Assessment/6.03%3A_Neurological_Exam
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I can relate to your undiagnosed and anguished situation. I have Parkinson’s-like symptoms that come and go. I do not have Parkinson’s but what do I have? Myasthenia Gravis??
Whatever this is now affects the sound of my speech and
Causing loss of hearing in my left
Ear. I can no longer listen to music.
I, like you, have periods of time where depression sets in. So,what’s a person to do?? Keep trying to find answers! Do not give up!! Do everything you can to find a cure and a way to live with this.
I wish you success in finding your answers.

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Do you have a plan of care for yourself, with these new symptoms? You may have to stop driving, look into transit or carpooling. Is there another diet plan you can try, or, if drinking water helps are there acidic drinks you can stop or slow down on? Can you talk to someone who knows you well and ask for their suggestions?

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@seniormed

A good plan to stop nexium and get a script for another
acid blocker. There are other options and what if nexium
is a contributing factor.?

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I'm absolutely planning to discuss this with my gastro next month. Thanks!

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@dlydailyhope

@supernat10, there are more neurological tests that can be done to check if you have central nervous system and peripheral nervous system issues causing your symptoms.

Did you ever have COVID or get the vaccine? I had both and got side effects from the vaccinations (2 doses and pain at back base of head plus lightheadedness). I am learning more about worsening neurological symptoms following COVID vaccines/illness.

https://med.libretexts.org/Bookshelves/Nursing/Nursing_Skills_(OpenRN)/06%3A_Neurological_Assessment/6.03%3A_Neurological_Exam

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I did have covid twice, once in Dec 2019 and once May of 2022, and after that May, my symptoms really doubled down. It's after that I noticed the eye problems and my stomach started to hurt daily. I also have chronic vertigo when I lay flat which started with that. I'm sorry you had bad reactions, an all too common story among people I know. Best wishes getting well!

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@dlydailyhope

@supernat10,
I can relate with your experience and symptoms.

I am in the process now of getting a new neurologist to test me for MS and CIDP. I have had vision blurriness, brain fog, cough, trouble breathing deep/singing at church, chronic extreme fatigue, full body pain at different times, arm/hand/leg/feet pain/weakness/numbness and pins/needles, muscle spasms/twitches, dizziness and balance issues, tinnitus, memory issues (feel like I am getting dementia at 54 years old), difficulty speaking/finding words and swallowing at times, etc.

I had pressure and pain around my chest (MS hug?). I have gastritis and esophagitis and take omeprazole and recently had a HIDA scan which showed my gallbladder stopped functioning (need to have it removed because it causes pain near my liver/gallbladder which runs across my rib cage after eating). Have you had your liver/gallbladder checked? It could be tied to autonomic nerve dysfunction which can affect heart, lungs and digestion. Have you had a small fiber neuropathy punch biopsy done to see if that may be causing some of your problems?

Good luck!

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@dlydailyhope thank you so much for sharing. This makes me feel like I'm not alone in this, and I hope the same for you. I will talk with my gastro next month about the HIDA scan. I have had liver workups in the past that were basic and normal, not sure about my gallbladder. I just ordered an extensive liver/gallbladder test online though, which will break the bank, but I feel like I have to look out for myself at this point. I have not had a fiber punch done, will discuss that with my rheumy when I find one. The last one I went to told me everything was from sitting wrong on my couch while working on my laptop. I stopped doing that though, and unsurprisingly had no improvement. My primary thinks I have fibro, and has for a long time, but I'm not convinced. Most of my pains center around my gastric system. Anyway, thanks for writing, and keep me up-to-date on how you're doing, and I'll do the same!

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@lavendercottage

Do you have a plan of care for yourself, with these new symptoms? You may have to stop driving, look into transit or carpooling. Is there another diet plan you can try, or, if drinking water helps are there acidic drinks you can stop or slow down on? Can you talk to someone who knows you well and ask for their suggestions?

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Thank you for your response. I stopped driving about 8 years ago but for a different reason. I also appreciate your suggestion that I drink more water. So I will add this to my action plan, And I do have someone who knows me pretty well to question.
Best of luck in your quest for relief.

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@supernat10

@dlydailyhope thank you so much for sharing. This makes me feel like I'm not alone in this, and I hope the same for you. I will talk with my gastro next month about the HIDA scan. I have had liver workups in the past that were basic and normal, not sure about my gallbladder. I just ordered an extensive liver/gallbladder test online though, which will break the bank, but I feel like I have to look out for myself at this point. I have not had a fiber punch done, will discuss that with my rheumy when I find one. The last one I went to told me everything was from sitting wrong on my couch while working on my laptop. I stopped doing that though, and unsurprisingly had no improvement. My primary thinks I have fibro, and has for a long time, but I'm not convinced. Most of my pains center around my gastric system. Anyway, thanks for writing, and keep me up-to-date on how you're doing, and I'll do the same!

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@supernat10
You are definitely not alone!!! We are here to help each other to fill in the gaps of support for those with chronic, complex illness.

You will want to have your neurologist do the small fiber neuropathy skin punch biopsy. They took a very small skin sample at top of thigh and calf of the same leg. It showed I had significant nerve damage/loss and was considered idiopathic because at the time they did not know what caused it. SFN could be causing autonomic nervous system dysfunction for you. My journey has been 7+ years trying to get answers and diagnoses and can be exhausting and expensive, that is for sure!

My gastro did bloodwork and abdominal ultrasound and both were normal. Despite taking omeprazole for gastritis for some time and stopping NSAIDs/ibuprofen, I still had pain near my liver and across my lower chest/upper abdomen. The HIDA scan showed visually my gallbladder function which was 7% when it should be a minimum 35%-40%! It basically just stopped working. I see the surgeon today to discuss removing it.

https://www.mayoclinic.org/diseases-conditions/autonomic-neuropathy/symptoms-causes/syc-20369829https://my.clevelandclinic.org/health/diseases/17479-small-fiber-neuropathy
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@supernat10

@dlydailyhope thank you so much for sharing. This makes me feel like I'm not alone in this, and I hope the same for you. I will talk with my gastro next month about the HIDA scan. I have had liver workups in the past that were basic and normal, not sure about my gallbladder. I just ordered an extensive liver/gallbladder test online though, which will break the bank, but I feel like I have to look out for myself at this point. I have not had a fiber punch done, will discuss that with my rheumy when I find one. The last one I went to told me everything was from sitting wrong on my couch while working on my laptop. I stopped doing that though, and unsurprisingly had no improvement. My primary thinks I have fibro, and has for a long time, but I'm not convinced. Most of my pains center around my gastric system. Anyway, thanks for writing, and keep me up-to-date on how you're doing, and I'll do the same!

Jump to this post

@supernat10
Have you had a colonoscopy to check if colon is causing any issues? Endoscopy can check esophagus, stomach and duodenum small intestine but your colon is right at the bottom of your liver/gallbladder/pancreas and stomach. In addition to these exams not sure if there are other functional test that could be done to determine root cause of your gastro/abdominal pain.

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@dlydailyhope

@supernat10
Have you had a colonoscopy to check if colon is causing any issues? Endoscopy can check esophagus, stomach and duodenum small intestine but your colon is right at the bottom of your liver/gallbladder/pancreas and stomach. In addition to these exams not sure if there are other functional test that could be done to determine root cause of your gastro/abdominal pain.

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@supernat10
Here are diagram pictures from my gastro surgeon’s office.

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