← Return to New to Autoimmune Diseases, concerned blurry vision

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@dianabanana

Hi,

Sorry about your blurry vision. I hope you are OK.

I am female 44 years old with autoimmune disease diagnosis scleroderma with very similar intermittent severe blurry vision problems (predominantly left eye), similar severe eye pain problems, including severe headaches/migraines, and intermittent color vision saturation loss, as well as morning uveitis (“red and veiny eyes”), intermittent photosensitivity (days to weeks of pain and severely hating office lights, and sunlight is too bright, etc.)

For me, it was elevated blood ammonia (hyperammonemia) contributing to my blurry vision issues and many other neurological issues.

What has helped me with reducing blurry vision and other neurological issues:

1. L-ornithine L-aspartate (LOLA): 6g-12g/day divided doses - to reduce ammonia

2. Eating 0.25 ounces of liver pate about every other day or so for “meat based” Vitamin A (retinol). Vegetable based Beta carotene or supplements didn’t work for me. I make the chicken liver pate at home from the $3 tubs of chicken livers at Whole Foods. Don’t eat too much liver, just a bit, otherwise Vitamin A (retinol) toxicity. Know that 0.25 ounces is just a small bite of liver pate.

3. Eating less protein overall, moderate protein diet - to reduce ammonia.

4. TUDCA tauroursodeoxycholic acid: 250mg-750mg/day - to help bile and fat soluble vitamins (A, E, D, K) digestion and eyes. You can read about TUDCA how it also helps with photosensitivity. It has taurine in it which also helps the eyes. It’s basically bile to help you digest to get nutrients to your eyes. I have autoimmune scleroderma so I have malabsorption issues of the stomach.

5. Probiotics (Lactobacillus GG, S. Boulardii, Bifidobacterium) - to reduce ammonia

6. Asking my doctor for alternate prescription drugs or dose reduction - to avoid drug-induced hyperammonemia. See WHO list of drug-induced hyperammonemia.

7. Re-assessing my use of over the counter pain killers that can also cause drug-induced hyperammonemia. See WHO a list of drug/induced ammonia.

8. Sometimes: Very low dose doctor prescribed Lactulose (2.5 to 5mL/day, approximately, which is the pediatric dose) - to reduce ammonia if neurological/vision symptoms severely worsens.

9. Blue-Blocker Sunglasses: I bought the orange tinted blue blocker overlay glasses for really bad days so I can at least drive and go to the grocery store and withstand the lights. I don’t need them as much anymore if I focus on reducing my blood ammonia and ensuring Vitamin A (retinol) to my eyes, by using the methods mentioned above.

All the above is for people with liver disease or overworked livers, who need to reduce their blood ammonia levels. I don’t have any of the biomarkers for liver disease and according to all the tests my liver is considered fine/normal…. but my mom had autoimmune primary biliary cirrhosis/cholangitis (PBC), so I could be on my way to eventually getting PBC. For now, besides autoimmune scleroderma, I have a diagnosis of what is known as “covert encephalopathy”, where blurry vision is one of my neurological symptoms. In addition to genetic issues, likely, some of my various medications over the years probably contributing to my ammonia inching up over time. See WHO list of drug-induced hyperammonemia. All these compounding factors can “add up” to elevated ammonia over time or at least intermittently.

Note that testing the blood levels of ammonia often don’t correlate directly to the severity of the encephalopathy in “covert encephalopathy” so my doctor and I have to go by my symptoms. Moreover, as an outpatient, it takes the lab 7 days to get ammonia results anyway.

It took me years to figure out my increasingly worsening “blurry vision” was associated with ammonia. Some of my eye damage is probably permanent, although I hope for improvement. For me, none of the MRI’s, CT’s or any of the opthamology or neurology tests ever revealed anything. Rarely, if ever, is a blood ammonia test ever done unless you have obvious “overt encephalopathy.”

Neurological symptoms of “covert encephalopathy” can easily be brushed off as fatigue/pain, emotions/stress, aging/being-tired, just a headache/migraine, just neck pain, etc. So, my blurry vision was brushed off as everything it wasn’t: allergies, dry eyes, too much cell phone use, stress, sleep, aging, etc.

Focusing on my liver health and methods of reducing ammonia helped reduce my blurry vision and my vision loss. My migraines, fatigue, pain, cognitive issues, emotional balance, etc. also improved. Again, I just say “reduce”, not “eliminate.” There is definitely more going on than just ammonia, but reducing my ammonia helped systemically with everything, my blurry vision included. I have to be satisfied with any improvements, even if not perfect resolution.

It is very frightening to experience blurry vision and potential vision loss, and light sensitivity can be very ‘emotionally frightening,’ to put it mildly.

I hope your vision is going to be OK. I surely don’t know, for sure, if it’s an ammonia issue for you, and I hope you have a receptive doctor who might consider “covert encephalopathy” as a possibility and who can advise you on what to do to help you. Maybe if you also have it, you can catch/reduce your elevated ammonia before it goes on unknown as “covert encephalopathy” for too many years like me. Good luck!

References
1. Drug-associated hyperammonaemia: a Bayesian analysis of the WHO Pharmacovigilance Database, 2022, Alexander Balcerac.

NOTE: I have mutated genes for porphyria (FECH) and retinitis pigmentosa (TRNT1 mitochondrial disease) so it is uncertain if my blurry vision problems are entirely ammonia-related or if those vision/light related mutated genes are factors. The belief is that my porphyria genes and mitochondrial disease genes could just be making my eyes more susceptible to the effects of the elevated ammonia. than what most other people without the genetic susceptibility and compounded by my autoimmune scleroderma disease would experience. I don’t know if you have ever had genetic testing. Either way - Regardless of whatever the genes say, all of the above ammonia reducing methods, and TUDCA, and meat-based Vitamin A (retinol) helped me improve my blurry vision and light sensitivity and headaches/migraines, neck pain, etc. Your eye issue seems very eerily similar to mine, which is why I’m writing such a detailed post. Best of luck with your doctors help!

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Replies to "Hi, Sorry about your blurry vision. I hope you are OK. I am female 44 years..."

Thank you so much for sharing your experience. I’m sorry you went through all you did.

Your post reminded me that years ago I was told I had a non-alcoholic fatty liver and found out there is also a family history of it. So now I’m going to read up on that and vision issues.

It helps to know that other people here, like you, understand how frightening blurry vision is. I’m so anxious to get to the bottom of and find this process of eliminating things to try to figure it out frustrating and depressing.

Again, thank you for sharing your experience in such detail. I’m going to look into all you mentioned and also mention to rheumatologist and makes sure he knows about my non-alcoholic fatty liver. Best of luck to you as well.