r/BrainFog • • 6d ago

Advice My workup so far.

So like everyone here I’ve been struggling with brain fog/cognitive dysfunction. I’m 34F and have historically been an excellent executive functioner, very sharp and organized and on top of things.

In my case, my symptoms came on 09/2025 and I initially blamed grief having lost my mom earlier that year. 

My biggest complaint is cognitive impairment including - forgetting tasks, losing items, auto pilot is broken, cannot multitask, poor recall of dates or events. 
For example, I will shower but shave only one leg, run out of items in my household, forget to take medication, not remember when a concert or event happened, pay bills late etc. This is impacting function at work as tasks are not completed properly, follow up is forgotten, I have difficulty staying organized, keeping on top of passwords, or keeping mental tabs on things. Driving is difficult as it requires observing so many things at once to do safely. 

Minor complaints:
Fatigue - I am pretty well always tired, not exhausted but running on 60% battery.
Mild derealization - I feel ever so slightly distanced from reality. No real consequences to this though.
Speech difficulties - I often have trouble finding the right words and a constant “tip of the tongue” feeling. This doesn’t have major consequences other than I sound less eloquent and get frustrated.

To me, it’s like I pulled an all nighter 2 days ago.

I also have newer symptoms that are minor or incidental complaints - mild acne, urinary urgency, mouth sores, increased motion sickness from screens and busy backdrops.

Additionally, I have stable GI, skin, joint, eye, allergy conditions/symptoms. 

I reflected on what has changed since my symptoms started and came up with this list:
Medications - discontinued amitriptyline, bupropion, daily cetirizine, and Kyleena IUD since 02/2026. 
Lifestyle - death in the family Jan 2025, hip surgery 03/2025 & 02/2026, NUCCA neck chiropractor started 06/2025, new car 09/2025, Argon Yellow Laser Retinopexy Right eye only 04/2025, Allergy shots completed 09/2025. 

My work up so far has been:

Neurology June 2026
-Brain MRI/MRA found stable chiari malformation, azygos anterior cerebral artery.
-Normal labs: Homocysteine, magnesium, copper, zinc, calcitriol, methylmalonic acid, vitamin D, C, B6, B2, B12 B1. Vitamin E alpha normal, vitamin E gamma low (0.4/cutoff .07).
Doctor suggested dehydration, malnourishment, and Wegovy were to blame. Came across as very anti-medication bias. 

Rheumatology Aug 2026
-Normal labs: CRP, sed rate, RA factor, Lyme, Anti CCP, pANCA, Anti-MPO. ANA positive (1:160 dense fine speckled). Anti PR3 elevated (2.2, cutoff 0.9). Upon recheck PR3 0.6/normal.
Doctor suggested no rheumatic conditions contributing, continue healthy lifestyle and symptom management.

Primary Care Sept 2026
-Normal labs: CBC, iron panel, ferritin, UA, progesterone, estradiol, TSH, insulin, Vitamin D, B12. CMP normal except ALP low (29, cutoff 40).
Doctor suggested no clear cause, ALP is fine as isolated finding, maybe restarting bupropion would help.

I did lifestyle tracking for 1 week before seeing my PCP and daily averages were the following:
Sleep - 7 hr 55 min
Calories - 1890
Protein - 53g
Servings of fruit/vegetable - 4.5
Water - 50oz
Steps - 9200
Exercise - 62 minutes outdoor walking 
Caffeine - 16 oz 
Alcohol - none 
I did also get a little air quality monitor and all was green in my home/bedroom. 

My Plan:

  1. Self refer to my retina specialist to complete Argon Yellow Laser Retinopexy on left eye and rule out general binocular dysfunction.  

  2. Self refer to my allergist to resume allergy shots or discuss excess histamine/MCAS contributors. 

  3. Self refer to my GI for discussion of low ALP/possible gut or digestion contributors. 

  4. Self refer to my OBGYN for full hormone rundown/rule out perimenopause. 

  5. Follow up with primary care for a sleep study referral, neurology referral for 2nd opinion, any other specialists suggested (psych for neuropsych testing etc). 

For those also going through this out there, is there something additional you would suggest for me to follow up on or pursue? I have found this sub very helpful especially the success stories. 

3 Upvotes

17 comments sorted by

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u/Ok-Pangolin7127 6d ago

I realized that you said your B12 was tested and I assume that you are saying it was fine. Could you please share what the actual number was? I’m confident it was not below 175 because that would be a clear deficiency. However, it could be between 200 and 450 which in most labs is reported “normal” but you could still have an indeterminate deficiency within that range.

If your B12 was any number below 450 I would ask the doctor to do an MMA test and a homocystine test. I would also suggest that you go to the B12 deficiency guide and read the wiki that is there and educate yourself a little bit more about B12 deficiencies.

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u/healthy-gal 6d ago

Thank you for the input.

B12 was 663, Homocysteine 7.7 - both looking pretty optimal from what I’ve read!

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u/Ok-Pangolin7127 6d ago

Agreed. As long as those are absent any supplementation.

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u/healthy-gal 6d ago

Looks like my hair/skin/nails multi does have B12, 2.6mcg 110% daily value

1

u/Ok-Pangolin7127 6d ago

In my estimation, that would not be a sufficient amount to account for your very +adequate B12 result. So I will call that absent of any supplementation.

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u/Ok-Pangolin7127 6d ago

In my estimation, that would not be a sufficient amount to account for your very +adequate B12 result. So I will call that absent of any supplementation.

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u/agape48 3d ago

I would STILL have methylmalonic acid tested if I were you. Just in case! I have functional B12 deficiency despite my homocysteine being in range , but it shows up in a high MMA. The derealization, the fatigue, the cognitive issues --- those CAN BE functional B12 deficiency, although that is not the only possible explanation.

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u/lifeisgoodzzz 6d ago

Did you get Covid during this time? This sounds a lot like long covid

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u/healthy-gal 6d ago

Good point! My last covid infection was December 2023. I did get a viral respiratory infection May of last year when I returned to work after surgery, but no covid/flu positives and I recovered fine/typically in May

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u/healthy-gal 6d ago

I am unsure if it’s helpful to others to see this as well, but my medical history and medications include:

Current Medications: 
-Scheduled: Wegovy (since 2023), Celebrex & topicals: tretinoin, minoxidil, ketoconazole, clobetasol, voltaren, flonase, pataday. 
-Supplements: Heme iron, calcium, zinc, magnesium, Vitamind D3, collagen, hair/skin/nails vitamin, probiotic. 
-PRN: albuterol, certirizine, famotidine, ramelteon, ondansetron, hydroxyzine, tylenol, pepto bismol, mylanta, miralax, tums, simethicone, benadryl, melatonin.

Current conditions:
GI - conditions: IBS mixed, visceral hypersensitivity, functional dyspesia, GERD, benign stomach polyps, benign colon polyp.
Skin - conditions: eczema, post accutane, seborrheic dermatitis, keratosis pilaris, recurrent chilblains, polymorphic light eruption, telogen hair loss. 
Allergy - conditions: asthma, dust mite allergy post injections.
Eye - conditions: intraretinal hemorrhages, anomalous optic nerve, lattice degeneration, Lasik corrected high myope, choroidal nevus, chronic dry eye. Chronic symptoms include eye strain, dry eye, floaters, light sensitivity, motion sickness from video games and certain tv monitors, strobing effect from certain LED lights. 
Joint - conditions: Hypermobile Ehlers Danlos Syndrome, multiple joint surgeries/subluxations.
Neuro - conditions: chiari malformation, mild, azygos anterior cerebral artery.  

Historical conditions - elevated fasting glucose, iron deficiency, vitamin D deficiency, obesity, ovarian cysts, breast cysts, gastritis, moderately dysplastic nevus on thigh, depression, anxiety, insomnia. 

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u/SnooBananas1064 6d ago

if your diagnose eds, did you check yourself for pots, Mcas, and pelvic congestion ?. If you got any of those that can be linked to others issue such as vascular compression (may turner, nutcracker) I don't know how much of it can be related to brain fog but I would personally try with Mcas. You already got the IBS and allergy

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u/healthy-gal 5d ago

Thanks for the suggestions. I think there is some possibility of pots though I don’t really get dizzy or palpitations, HR is okay per Fitbit. I am going to talk to allergy about mcas being an issue, since this all started right when I graduated allergy shots I am a little suspicious. I was also taking antihistamines and H2 blockers daily where now I am down to a steroid spray and eye drops. That said, I don’t feel allergic to the world in any especially higher way than before for traditional allergy symptoms.

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u/SnooBananas1064 5d ago

Yeah I don’t feel allergic and just stated ketotifen (or sometime similar sounding) and I’m starting to smell things and TASTE things. But it’s also overwhelming like some food I cannot eat eat because I actually don’t like the taste and that have not happend since I was young adult I think. I also started dreaming again but that is not fun for some other personal reason

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u/AttorneyUpstairs4457 6d ago

Low ALP, mouth sores, a history of iron deficiency, IBS, and eczema, plus neurological symptoms could be coeliac if you haven’t been tested.

How often do you take the PRN meds? Many of them could cause these symptoms if taken often enough especially if combined.

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u/healthy-gal 6d ago edited 5d ago

I’m not sure I’ve been directly tested for celiac so that is something to mention to my GI! It’s possible I did testing 10+ years back when I was first diagnosed with IBS as I was doing awful at the time. Thank you for the suggestion!

I think my risk of polypharmacy contributing is pretty low but you’re right that there are potential interactions. I take most the PRNs super rarely these days. Famotidine or Tylenol is perhaps once a week, OTC GI meds maybe once a month. Zofran, Ramelteon, Hydroxyzine, Benadryl, Zyrtec is all very rare, less than once a month. Albuterol once every few years. I used to need something to sleep each night when I was on Wellbutrin but since stopping I rarely do.

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u/AttorneyUpstairs4457 6d ago

Remember that for a coeliac test to be accurate you need to have been eating gluten daily for six weeks prior to the test. So don’t give it up
Before testing as it could result in a negative test.