newly DX: after covid i started... - Functional Neurol...

Functional Neurological Disorder - FND Hope

5,652 members2,948 posts

newly DX

nurseny profile image
7 Replies

after covid i started feeling unbalanced in my gait and my speech sometimes makes me sound like i'm drinking lots of wine i have already paid quite a bit in bills , so with that said I'm going on one year dx in july and my symptoms have not changed i'm trying to work out more and stay heathy but I have to wonder if this dx is the right one for me. So if I could get some feed back and referrals to other neurologist or tests to confirm dx i would appreciate it.

Written by
nurseny profile image
nurseny
To view profiles and participate in discussions please or .
7 Replies
bookish profile image
bookish

Covid may affect one-carbon metabolism, as in how you process vit B12 and folate, and also glutathione levels. This may or may not show in blood tests which are not at all conclusive for identifying B vitamin deficiencies, but it might be somewhere to start. There is no definitive test for a B12 deficiency, so low serum could rule in a deficiency but normal or high serum does not rule it out. Can be complex and won't bore you with all of it in case you've been there and done that! Balance and speech sounds like it could be B12 and/or folate to me (but please don't take folic acid alone until you have had the full gamut of B12 tests - serum, active (holo tc), gastric parietal cell antibodies, intrinsic factor antibodies, serum gastrin, methylmalonic acid, homocysteine - remembering that you can still have a functional deficiency with 'normal' levels of the whole lot. Best not supplement before testing as it skews results considerably and they don't all return to base when you stop, making a tricky diagnosis even trickier. Mine seems to be genetic as well as a glutathione absent gene. NAC is useful for me, for the latter. Best wishes

nurseny profile image
nurseny in reply to bookish

thank you are you a Doc just wondering

bookish profile image
bookish in reply to nurseny

No, no medical qualifications, just an interested patient who has done a lot of reading to try to help themself get better. Really helped me to always get a copy of my blood test results and try to find out what they actually mean. If no-one has tested things that might be useful then you can ask for them or pay and do them yourself if you have to. First thing - ask for copies, and make sure they have tested serum B12 and folate, and see what they were. Then ask for info to help you think about what to do next. The Pernicious Anaemia forum is a good place. Cheers

nurseny profile image
nurseny in reply to bookish

thank you i do have blood work cbc cmp and a bmp but no problems there next time i see the doctor i will focus on those again thank you

bookish profile image
bookish in reply to nurseny

cbc here doesn't routinely include even serum B12 or folate, but could be different with you. RDW, MCH, MCV etc may give you clues but likely need further testing. Best wishes

nurseny profile image
nurseny in reply to bookish

B12 and Folate were ok

bookish profile image
bookish in reply to nurseny

What did they test and do you have the actual results with ranges and units? Unless they did the lot they can't say that there is no deficiency with any degree of certainty - remember there is no test to rule out a deficiency. You can have a cellular deficiency of either with above range serum results. It does not need to be low, or be anaemic, or be macrocytic. And they do not know that, in most cases, so they will tell you that you are ok, when testing has not been adequate.

You may also like...

Newly diagnosed need advice

see a neurologist and was just given a website at the end of the appointment. His story is one night

Newly diagnosed

I saw FND). I know have a third neurologist who wants me to have an MRI which of course isn't...

Newly Diagnosed

the app, that it is FND. I'm been referred for cbt therapy but i'm already in private therapy so...

Newly diagnosed

as I am having a very bad brain fog day today. I'm fed up of people not understanding what I'm...

newly diagnosed

month ago. My story is a bit of a tough one. I got tinnitus from covid infection Nov 22 then woke...