My memory is shocking and I’m starting to worry. It’s been a gradual thing over the last 3 years. I laughed it off at first and blamed it on the menopause (I’m not even in the menopause) then I though it could be stress but it’s getting worse.
Could it be related to UAT? I read a deficiency in B12 could be the cause. How do I know what the range levels should be? I’m on 75mg levothyroxin.
Has anyone else suffered the same and did you manage to resolve it?
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Welly73
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You will see folks on here referring to brain fog. That is what you are describing. Can't think straight, forget words, forget what you were on about mid sentence, can't concentrate
Do you have recent blood test results to share. It could be you need a levo increase. Or it could be B12 or other vitamins so be good to check those levels too.
I’ve just added a copy of my last bloods to my post. Since increasing my dose we went into lockdown so the drs aren’t seeing anyone unless it’s urgent.
The tsh is too high for someone on levo. It should be 1 or lower. The ft4 result is not near the top of its range. I think you need and Increase of 25mcg levo to begin with.
I've started using a private blood test company called Thriva. My docs weren't doing any blood tests during lock down so gave them a try. I was really impressed with the service and was worth every penny to get that underactive thyroid diagnosis. Sent the readings to my docs and they put me on medication! (I'm not associated with Thriva in any shape of form, was just really pleased to get a great service!).
I've been like this. I started to catch myself doing things my partner's grandmother (with dementia) had been doing in her early days with the illness, and it was scary facing going to the doctor to raise the subject. I simply had a B12 deficiency, and the B12 supplements made a difference quite quickly.
It's up to you whether you test, I technically don't think there's any harm supplementing B12 on the off-chance it'll make a difference.
Other symptoms are tingling/numb toes, mouth ulcers, clumsiness.
My grandma had dementia too and It has made me worry but I think it’s more likely to be a symptom of UAT. As soon as the drs will see non-urgent cases I’ll be booking in for my bloods re doing.
None that I'm aware of, it's one of those supplements that's near impossible to overdose on. The only issue with it is that is can artificially inflate your blood levels if you do test, so you need to stop taking for a few weeks before a blood test. If you do manage to get a test soon, hold off on supplements until you're tested, if it will be a while until your tested, then you have nothing to lose. I take Cytoplan sublingual B12, it's not too expensive. Make sure you buy from a good brand (not holland and Barret's, but Cytoplan, solgar, BetterYou mouth spray)
we do need to be careful with vitamin B 12. B vitamins need to be in the correct proportions, if you take too much B12 you are likely to deplete other important B vitamins and develop other symptoms.
For full Thyroid evaluation you need TSH, FT4 and FT3 plus both TPO and TG thyroid antibodies tested. Also EXTREMELY important to test vitamin D, folate, ferritin and B12
Low vitamin levels are extremely common, especially if you have autoimmune thyroid disease (Hashimoto's) diagnosed by raised Thyroid antibodies
Have you had thyroid antibodies tested
Can see you have low vitamins and now supplementing
Ask GP to Retest vitamin levels
Recommended on here that all thyroid blood tests should ideally be done as early as possible in morning and before eating or drinking anything other than water .
Last dose of Levothyroxine 24 hours prior to blood test. (taking delayed dose immediately after blood draw).
This gives highest TSH, lowest FT4 and most consistent results. (Patient to patient tip, best not mentioned to GP or phlebotomist)
My last test was taken in the afternoon but now I know this top tip I will make sure I do it that way in future.
I was on 50mg and increased to 75g.
I’m not overly sure on the brand but will check first thing in the morning.
I haven’t been taking any supplements as I was worried to do so incase there were any side effects to taking them. I bought b complex should I start taking them do you think?
If you take b complex now and need a thyroid test the Biotin in it will effect the lab test, need to leave off for one week. If you want to know your b 12 levels any supplements will make it look falsely high.
If you have a low B12, you should ask for an 'intrinsic factor' blood test to diagnose if you have Pernicious Anaemia - a common autoimmune condition. I have P.A. and the P.A. forum will advise/help you. Don't supplement with B12 until you get the proper blood test.
Many on this forum have more than one autoimmune condition.
If you read through your last post of 5 months ago SeasideSusie explained the supplements you would benefit from based on your results. I would be starting them as soon as you can.
Click onto your username to find your previous post 🌻
Strongly recommend getting FULL thyroid and vitamin testing privately...assuming GP only tests TSH and Ft4
For full Thyroid evaluation you need TSH, FT4 and FT3 plus both TPO and TG thyroid antibodies tested. Also EXTREMELY important to test vitamin D, folate, ferritin and B12
Igennus Super B is good quality and cheap vitamin B complex. Contains folate. Full dose is two tablets per day. Many/most people may only need one tablet per day. Certainly only start on one per day (or even half tablet per day for first couple of weeks)
Or Thorne Basic B or jarrow B-right are other options that contain folate, but both are large capsules
If you are taking vitamin B complex, or any supplements containing biotin, remember to stop these 7 days before any blood tests, as biotin can falsely affect test results
Thank you so much. I’m going to call my gp on Monday morning g to get new bloods done if possible. I think it’s a good starting point. If they refuse due to the lockdown restrictions do you think I’ll be best getting them done privately?
Since these results gp increased Levo by 25mg. So I’m not sure what my vitamin levels are now.
Very important when you test - always get tested as early as possible in morning before eating or drinking anything other than water and last dose levothyroxine 24 hours before test
“According to the current TSH reference interval, hypothyroidism was not diagnosed in about 50% of the cases in the afternoon.”
“Further analysis demonstrated inadequate compensation of hypothyroidism, which was defined in 45.5% of the morning samples and in 9% of the afternoon samples”
TSH levels showed a statistically significant decline postprandially in comparison to fasting values. This may have clinical implications in the diagnosis and management of hypothyroidism, especially SCH.
Private tests are available as NHS currently rarely tests Ft3 or thyroid antibodies or all relevant vitamins
Agree with the b12 deficiency. I use betteryou vits. I suggest you do the same, They come in a liquid form, you spray, hence they’re easily absorbed and very good quality too.
You are also vit D deficient according to your results! That will also cause you big probs . I take both.
Betteryou vits are in holland & Barrett’s or you can sometimes get good deals on line. Good luck with that. Am sure you’ll soon notice a difference 👍
I can see from the photo of your (latest?) results that your TSH is not well suppressed.... and there is no result for T3*. The B12 result is a blur on my screen, but your folate and Vitamin D are both too low, barely scraping into the Normal ranges.
Note on supplements - the 'side effects' of taking a quality B complex are negligible compared to the really damaging effects of a deficiency. Vitamin D deficiency is very serious as it compromises immunity, mental health and our other (not just thyroid) hormones. To avoid side effects of too much vitamin D - it's a Calcium magnet - is to take Magnesium and Vitamin K2. The Magnesium helps vitamin D to work and fights inflammation and the K2 pulls any extra Calcium into the bones where it's needed and away from soft tissue and arteries. It's a trusted combination.
In order to have optimal vitamin D (you do with Hypothyroidism) results should be >75 nmol/l. See above link. Labs often use another scale which is in nanograms per ml (ng/ml)measurements, so be careful that you don't confuse them...
*I think I initially misread your T4 result... is that a 19, 18 or a 15? Well, it's only low - mid range, so you'd certainly benefit from a dose increase with that TSH over 3 and hypo symptoms. Your doctor needs to address this.
I agree with Slow Dragon that you should really have been tested after the increase (these results are quite old). Obviously, during full lockdown many of us put things like blood tests off, but I'd be getting on with it now, before the colder months kick in which is always harder for many of us.
I noticed in your posts five months ago, a lovely and very comprehensive reply from Seaside Susie about getting your vitamin levels sorted.
Now your t3 and antibody levels were never given, so, for all anyone knows you could be a poor converter. I would ask for t3 to be tested. Low t3 effects the brain. Having low vitamins or minerals is often the cause of poor conversion, also high antibodies.
If you chose to put off supplementing due to concern over side effects, or decided to go along with the GP and take 400 units of Vitamin D, and folic acid (rather than proper methylfolate which is much easier to absorb) then you won't see much improvement. I know the 'better' supplements may seem a bit of a stretch, but nutrition is really not part of a medic's training and there's a lot of experience on this forum about what's actually working.
Here's some evidence showing Free T3 to be low in Alzheimers. In the study, the TSH and T4 was the same as those without Alzheimers, but T3 was much lower. This is shocking, because clinicians don't always routinely test for T3, even in those on Levothyroxine. My mother-in-law ended up with dementia after years of needless suffering with hypothyroidism.
I had same around the time of menopause. Then as I got further away from the menopause my memory seemed to recover. I’m on 125 Levo. Hope you can relax and don't worry too much. I felt at that time too, I had so much to deal with it can be overwhelming.
Hi welly 73 i am having the same problem until recently i was on 75mg 100mg of levothyroxine on alternating days then it was decided by my gp that i should take 75mg and 50mg alternating days . Went to see my endo and he put the doses up to original dose and my b12 is awful. They also found a deficency in my vit d. But would not give me a loading dose as the gp told me i would have to buy it myself. Just awaiting new blood test to see how they are . Hope you feel better soon
Your GP sounds pretty cavalier going against your Endo's recommendations and lowering your dose. I'd be tempted to switch if there's someone else at your surgery. You could try posting your b12 results on the PA forum for advice.
Hi I feel your pain as I suffer from the same. I have spoken to the doctors but they just laugh it off. I have lost a lot of confidence especially my work life as sometimes I can’t string a sentence together. So I would also be interested to see what everyone says !
It’s a kind of relief to read others experience with symptoms that you suffer yourself. My husband has even commented on my inability to remember particular words to complete a sentence! It’s embarrassing when you just cannot remember which word you need to explain something. I’m hoping that when my recent full bloods are back, it will show a deficiency and that by supplementing my memory and muscle/joint aches and pains will increase/decrease respectively. I see that VLJones has at least got a supportive endo that has increased his/her Levo.
The B vitamins that have helped me with cognitive function are methylated b12, folate and coenzymated b6 which is called p5p. B5 is good for stress. Also, minerals like zinc and magnesium are good for cognitive as well as anxiety prevention (as magnesium acts as a buffer to cortisol spikes) and an iron rich diet for fatigue.
That’s fantastic, my endo doesn’t even know what dose of Levo I’m on. I wanted an increase of 25mcg which would take me to 50mcg and he refused for the moment. Then sent me a letter saying that he would like me to have bloods done in August before our September phone appt and to stay in the 50mcg that I am currently taking!!! He obviously cannot be bothered to read my notes, I’ve got no chance 😟 where do you live? Are you in the northwest by any chance?
I'd get your Free T4 and Free T3 tested (rarely done by GP). Free T4 is an inactive hormone and converts to T3. Free T3 is the Active thyroid hormone and we have millions of T3 receptor cells that enables our body to function, especially heart and brain have the most T3 receptor cells.
I had started to have memory problems that resolved with B12 injections but emerge again if I stop having the jabs. My mother had this too and also had Osteoporosis and Hypothyroidism. My theory is that B12 absorption is thwarted if the sufferer has metabolic disorders. Stands to reason really! I'm also vegetarian so need to get B12 some way other than in food. I'm currently trying a liquid form that is Vegan friendly and is supposed to be easier for the body to absorb and utilise. I have a hunch that B12 absorption deficiency might be implicated in Dementia.
My sister had terrible memory lapses. Turned out she had Pernicious Anaemia. She thought she had dementia (only 51). But being diagnosed and now having injections of B12 makes a HUGE difference.
My folate, B12 and vitD all drop low if I don’t supplement practically all the time.
The advice above is the best. Seaside Susie, Slow Dragon and others should not be ignored.
I would get new tests done before any supplementing.
Then repost on here, and get great advice.
You can have the supplements ready to start after the test results.
Folate, B12 and vitD being low will make you feel extra fatigued too, so hopefully you will see an improvement within a few weeks.
Although my memory has improved, I still write notes in a book. I find writing it down helps me to forget less. Sometimes I might have to read something several times for it to sink in. Don’t give up, keep reading, keep learning, and gradually you’ll feel more like your old self again.
I had my bloods done yesterday and the dr called to say the vote t years hasn’t been carried out, on the plus side the nurse did my antibodies instead off full thyroid test.
My dr had agreed to test FT3 AMA has also taken my memory aiatiarion seriously and gave me a memory test and is also doing me an ECG and colesterol for memory. Also inclination for my joint pain.
I’m going back in two weeks to get the other bloods taken so should have all my results to share then.
I was really surprised that my dr too my symptoms seriously so please contact your go if your having the same symptoms. So t be afraid of sounding silly.
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